earn
•••nun
PHYSICO-CHEMICAL CONSTANTS.
MELTING AND BOILING POINT
TABLES.
BY
THOMAS CARNELLEY, D.Sc. (Lomx), B.Sc. (Vicr.), F.C.S., F.I.C.,
PROFESSOR OF CHEMISTRY IN UNIVERSITY COLLEGE, DUNDEE.
VOL. II.
LONDON:
PUBLISHED BY HARRISON AND SONS, 59, PALL MALL,
$oakatUm to % $urai anb f .^J. % frmee of Malts.
1887.
LONDON :
HARBISON AND SONS, PRINTERS IN ORDINARY TO HER MAJESTT,
ST. MARTIN'S LANE.
[ iii ]
PREFACE.
The issue of this second volume of Melting and Boiling Point Tables completes a labour of ten
years. It contains more than 32,000 melting and boiling point data, which, with those given in the
h'rst volume, make a total of over 51,000.
For the data published by Eegnault in the Memoires de I'Acad&mie, in reference to the vapour
tension of substances at different temperatures, and for Brock's tables calculated from Eegnault's
results, I am indebted to Landolt and Bornstein's excellent " Physikalisch-Chemische Tabellen."
The alphabetical index of Eoot-Carbon Compounds contains not only those for which the melting
and boiling point data are known, but also others, in order to render the index more complete for all
root-carbon compounds ; for these, and for the idea of such an index, I must acknowledge my
indebtedness to Eichter's admirable " Tabellen der Kohlenstoff-Verbindungen."
The paging of Volume II. has been made continuous with that of Volume I., in order that the
two may be bound together if desired.
The portion of Part II. contained in the present volume brings the data down to the Autumn
of 1885, while Part III. brings the data down to near the end of 1886.
THOS. CAENELLEY.
University College, Dundee.
June, 1887.
TABLE OF CONTENTS OF VOL. II.
MELTING AND BOILING POINT TABLES.
PART II (continued).
Organic Compounds.
III. Compounds containing Four Elements :-
/. CHFO
2. CHClBr
CHC1I
3. CHC10
4. CHC1S
CHClSe .- . . .
CHClTe
5. CHC1N
6. CHC1P
CHClAs
CHClSb
CHCIBi
7. CHBrI
8. CHBrO
9. CHBrS .
CHBrSe
CHBrTe
10. CHBrN
//. CHBrP
CHBrAs
CHBrSb
12. OHIO
13. CHIS (,T .
CHISe
CHITe .
PAGE
353
353
353
356
383
383
383
383
390
391
391
391
391
392
418
418
418
419
425
426
426
426
429
429
429
PAGE
III. Compounds containing Four Elements
(continued) : —
14. CHIN 429
15. CHIP 432
CHIAs 433
CHISb 433
16. CHOS 434
17. CHOSe 441
18. CHON 441
19. CHOP 592
CHOAs 594
CHOSb 595
20. CHSN . . 595
CHSP 604
CHSAs 605
CHSSb . .605
CHSBi 605
21. CHSeN 605
CHSeP 605
CHNP 605
CHNAs 605
22. CClBrO 606
CC1IO 606
CC10S 606
CC10N 606
CBrOS . . 606
TABLE OF CONTENTS.
PART II (continued).
Organic Compounds.
III. Compounds containing Four Elements
(continued) : —
CBrON
CI03ST
COSN
CSNT
IV. Compounds containing Five Elements :-
CHFON
CHClBrI
CHClBrO
CHClBrN
CHClBrP
CHC1IO
CHC1IS
CHC1IN
CHC10S
CHC10N
CHC10P
CHClOAs
CHClOSb . . .
CHC1SST . . . .
CHC1SP
CHClSAs
CHC1NP .
CHClNAs .
CHClNSb
CHBrlO
CHBrlS
CHBrIN
CHBrOS
CHBrON
CHBrOSb
CHBrSN
CHIOS
CHION
CHIOP
CHIOAs
CHISN
CHOSN
CHOSP
CHOSSb
.
CHOSeN
CHOSeP
PAGE i PAGE
IV. Compounds containing Five Elements
(continued) : —
606 CHONP 677
606 CHONAs 678
606 CHONSb 678
606 CHSNP 6J8
CClBrOS 678
607 CClBrON .678
607 CC10NP 678
607 CBrOSN 678
609 V. Compounds containing Six Elements : —
609 CHFC10S 679
610 CHFOSN 679
610 CHClBrlO ........ 679
610 CHClBrlS 679
610 CHClBrOS 679
614 CHClBrON 681
633 CHClBrOP 681
634 CHClBrSN 682
634 CHC1IOS 682
634 CHC1ION 682
635 CHC10SN 682
635 CHClOSeN 685
635 CHC10NP 685
635 CHClONSb 685
635 CHBrlON 685
635 CHBrOSN 685
635 CHBrONP 689
635 CHIOSN 689
635 CHOSNP 689
637 CClBrOSN 689
656 VI. Compounds containing Seven and Eight
656 Elements : — •
656 CHClBrOSN 690
656 CHC10SNP 690
659 CHClBrOSNP 690
659 VII. Compounds containing Special Ele-
659 ments : —
660 Compounds containing Ag . . . 691
676 „ „ Al . .' . 691
677 „ „ An ... 691
677 „ B. . . . 692
677 Ba 694
TABLE OF CONTENTS.
PART II (continued).
Organic Compounds.
PAGE
VI I. Compounds containing Special Ele-
ments (continued) : —
Compounds containing Be . . . 694
Ca . . . 694
Cd . . . 694
Cr . . . 694
Cu . . . 695
Pe . . . 695
Hg . . . 695
K . . . 698
Li ... 698
Mg . . . 698
PAGK
VII. Compounds containing Special Ele-
ments (continued) : —
Compounds containing Na . . . 699
Pb . . . 699
Pt . . . 700
Si ... 703
Sn . . . 706
Ti . . . 708
Tl . . . 708
V . . . 708
W . . . 708
Zn 708
PART III.
I. Vapour Tensions and Boiling Points
of Simple Substances 712
II. Vapour Tensions and Boiling Points
of Mixed Substances : —
A. Of Aqueous Solutions . . . 740
B. Of Solutions other than those
in Water 761
III. Freezing and Melting Points of Mix-
tures, including Cryohydrates :—
A. Of Mixtures with Water . . 763
B. Of Mixtures with Benzene . 776
C. Of Mixtures with Naphthalene 777
D. Of Mixtures of Carbon disul-
phide and Ethyl alcohol . . 777
III. Freezing and Melting Points of Mix-
tures, including Cryohydrates (con-
tinued) : —
E. Of Mixtures with Ethylene
dibromide 777
P. Of Mixtures with Formic acid 777
G. Of Mixtures with Acetic acid 777
H. Miscellaneous Mixtures . . 778
IV. Miscellaneous Melting and Boiling
Point Data (Fats, Oils, &c.) ... 780
V. Volumes and corresponding Tears of
Issue of the more important Chemi-
cal and Physical Periodicals . . . 782
VI. Alphabetical Index of the Root Com-
pounds of Carbon 788
The following abbreviations are in addition to those given in Volume I. : —
n. = normal.
n.c. = non-condensable.
n.d. = non-decomposable.
A. J. American Journal of Pharmacy.
B.r. Itcferate der Berichte der Deutschen
Chemischen Gesellscliaft zu Berlin.
4*.
353
III.- COMPOUNDS CONTAINING FOUR ELEMENTS.
(l.) CHFO.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Acetone hydrofluoride
C3H6O.HF
C3H7FO
55
....
Landolf
C. R, 96, 580
44, 655
„ dihydrofluoride
C3H6O.2HF
C3H3F20
— 15 to —12
)i
)»
JJ
Difluobenzoic acid
C6H3Fa.COOH
C7H4F202
232 u. c.
Jackson & Harts-
B., 18, 1993
48, 1224
horn
Benzoyl fluoride „.
C6H5.CO.F
C7H5FO
161-5 (745)
Borodine
A., 126, 60
ii., 671
Fluobenzoic acid
C6H4F.COOH=1.2
C7H5F02
117-118
Paternd & Oliveri
G. I. [1882], 85
42, 614
„ ,, ••" ••••
=1.3
)J
....
133
Paternd
G. I., 11, 90
40, 598
»» ,,
)) )I
»)
123-124
Paternd & Oliveri
G. I. [1882], 85
42, 614
„ ,,
= 1.4
j)
....
180-181
,,
)»
j>
»» „
» »»
J)
....
182
,»
G. I., 11,90
40, 598
„ „
»1 »
))
.... \
182
Schmitt & Gehreii
J. p. [2], 1, 394
24, 368
Methylic fluobenzoate
C6H4F.COOMe=1.3
C8H7FO2
192-194
Liquid
Patern&
G. I., 11, 90
40, 598
» »
») »
»
192-194
Liquid
Paternd & Oliveri
G. I. [1882], 85
42,614
Fluotoluic acid
C6H3.Me.F.COOH= ?
»
....
160-161
,,
)1
,»
Fluoanisic acid
C6H6.OMe.F.COOH=l.?.4
C3H7F03
204
,,
I»
42, 615
Ethylic fluobenzoate
C6H4F.COOEt=1.4
C9H9FO2
cf. G.I. 11,90
Cryst.
Schmitt & Gehren
J. p. [2], 1, 400
vii., 164
(2.) CHClBr and CHC1I.
1
Chlorobromoform
....
CHClBr3
121-125
Dyson
43, 46
„
....
))
123-135 t. d.
Liquid
Jacobsen and Neu-
B., 15, 601
42,938
meister
Bromochloroform
....
CHCLBr
91-92
Liquid
i»
)>
»
a-Chlordibromethylene
CHBr : CBrCl
C2HClBr2
141-142 (734
L— 20
Denzel
B., 11, 1741
36, 213
a-Chlortetrabromethane
CHBr2.CBr2Cl
C2HClBr4
200-205 (285
32-33
,,
B., 11, 1739
»
a- „
„
»
240 (735)
....
»
A., 195, 210
36, 369
a- „
j»
J)
....
33
Mabery
A. C. J., 5, 255
46,663
a- „
,,
))
32-33
Wallach & Bischof
46, 663
Dichlorbromethylene
....
C.jHCl.Br
110-115
A., 216, 261
„
n
114-116
Liquid
Henry
C. E., 98, 370
46, 979
a- „ ,
CHBr:CCl2.
»
114-116 (740)
L— 20
Denzel
B., 11, 1741
36, 214
a-Dichlortribromethane
CHBrj.CBrC]2
C2HCloBr3
215-220
L— 20
),
B., 11, 1740
36, 213
Trichlordibromethane
....
C2HCl3Br2
200 (760) p.d
....
Patern6
G. I., 1, 590
vii., 308
,,
....
»
93-95 (14)
„
jy
j,
a-Chlorbromethylene
CHj : CClBr
C2H2ClBr
55-58
....
Miiller
As., 3, 287
„
»1
»
62-63 (750)
Liquid
Denzel
B., 11, 1740 ; A.,
36, 213
195, 206
,,
»»
JJ
62-63
....
Henry
C. E., 97, 1491
46, 571
,,
»»
)»
63
Liquid
,,
C. R., 98, 680
46, 830
,,
JT
)»
62
Miiller
[1864]
&-
CHC1 : CHBr
I)
80-83
....
....
A., 216, 258
,,
»
>i
81-82
Liquid
Plimpton
41, 394
»»
H
»
81-82
Henry
C. E., 98, 741
46, 831
?
....
(C2HsClBr).
140
Solid
Demole and Diirr
B., 11, 1304
34, 846
a-Chlortribromethane
CH2Br.CBr2Cl
C2H2ClBr3
200-201 (735)
L— 20
Deuzel
B., 11, 1735
36, 213, 369
p. d.
,,
>»
)>
170-171 (335)
,,
A., 195, 210
»
,, ....
ji
))
165-167 (285)
j,
»
„
a-Dichlordibromethane
CH2Br.CBrCls
C<2 iigO 12-01*2
176-178
1.— 20
»
B., 11, 1740
36, 213
(3-
CHClBr.CHClBr
»
195-200
....
A., 216, 257, 262
Trichlo^ )ror.".jthaue
CCl3.CH2Br.
C2H2Cl3Br
151-153
Liquid
Henry
C. E., 98, 370
46, 978
a-Chlordibromethane
CH3.CClBr2
0,,H.1ClBr2
123-124 (753)
1.— 20
Denzel
B., 11, 1739
36, 213
„
»)
))
124
....
,,
A., 195, 210
36, 30!)
2 z
354
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
/3-Chlordibromethane
CHj-Br.CHClBr
CsH3ClBr2
162-5-163
1.— 20
Denzel
B., 11, 1739
36, 213
o-Dichlorbromethane
CH3.CCl.2Br
CjHjCljBr
98-99 (758)
1.— 20
„
B., 11, 1740
n
P-
CH,Br.CHCl2 (?)
„
137
Lescosur
B. S. [2], 29, 483
34, 718
„
„
„
137-138
Henry
C. E., 97, 14H1
46, 571
„
„
„
138
....
„
C. E., 98, 370
46, 979
y- .
CHClBr.CHjCl
n
139-140 c.
Perkin
45, 535
i-
„
151
Lescceur
B. S. [2], 29, 483
34, 718
11
....
» (?)
158-162
„
„
Ethylidene chlorobromide ...
CH3.CHClBr
C,H4ClBr
81-82
Eeboul
A., 155, 215
vii., 489
.. 11
„
„
84-5 (765)
1.-19
Lescoeur
B. S. [2], 29, 483
34, 718
IT 1»
11
„
84-84-5(750
1.— 20
Denzel
B., 11, 1739
36, 213
IT 11
n
n
85
....
„
A., 195, 210
36, 368
,, »
•J
„
85
Plimpton
41, 397
Ethylene chlorobromide
CyfigC'ltO'.ii.^.Br
„
105
Denzel
A., 195, 210
36, 369
n i>
n
„
106-107
James
35, 806
n »
n
u
106-108
„
47, 366
T. »
i.
ii
108
Henry
C. E., 98, 370
46, 979
TT >>
„
ii
107-108
„
A., 156, 16.
» »
a
ii
107-109
....
Demole
B., 9, 556
30, 283
JT 11
a
ii
108
....
Plimpton
41, 397
!> 17
n
ii
104-108
Liquid
Lescoeur
B. S. [2], 29, 484
34, 718
,1 71
„
»
107-109
James
43,37
n 11
„
„
108-110
Simpson
P. E. S., 20, 118
38, 456
1
....
C3HClBr2(?)
a. 150
....
Pinner
B., 8, 1324
29, 554
Dichlorbromallylene
C3HCl2Br
143
....
„
B., 5, 205
26, 495
„
„
143
„
A., 179, 45
29, 549
Dichlortribrom propylene ....
C3HCl2Br3
....
207
„
B
11
1
....
C3H2ClBr
100-110
n
B., 8, 1325
29, 554
Dichlordibrom propyleue ....
C3H2Cl2Br2
190 p. d.
Kramer and Pinner
A., 158, 37
24, 558
Dichlorbrom propylene
a. C3HCl2Br
C3H3Cl2Br
143
Pinner
A., 179, 45
Dichlortribrom propane
Of. C3HCl2Br3
C3H3Cl2Br3
207
„
I!
Chlorbrom propylene
C3H4ClBr
105
....
A. 112, 237
.,,
CH,.CCi:CHBr
)>
100-110
Friedel
A. C. [4], 16, 343
vii., 1019
orCH2:CCl.CH2Br.
a-Bromallyl chloride
CH2 : CBr.CHjCl
„
120
Liquid
Henry
B., 5, 186, 482
vii., 50; 25,686
a-Chlorallyl bromide
CH3.CCl.CH,Br
II
121
C. E., 95, 849
44, 173
Chlorbromglycide
CHC1 : CH.CH2Br
JI
126
....
....
As., 6, 375
ii., 899
i)
„
136-127
Eeboul
As., 1, 230
vii., 1020
Chlortribrompropane
03H4ClBr3
238 p. d.
....
„
As., 1, 231
ii., 899
Allylenedichlordibromide ....
....
C3H4Cl2Br2
190
....
....
J. [1872], 323 ;
A., 179, 44
Dichlordibrotnpropane
CH2Br.CClBr.CH2Cl
11
200-205
Friedel and Silva
C. E., 74, 955
24, 1190
"
»
II
205
....
„
C. E., 73, 958
vii., 1020
»
11
„
SOS
C. E., 75, 81
25, 805
,,
CH2Cl.CBr2.CH2Cl
„
212
....
Hartenstein
J. p. [2], 7, 313
26, 1218
„
....
M
220-221
Eeboul
As., 1, -231
ii., 899
11
i>
220-225
Friedel and Silva
C. E., 75, 81
25, 805
Chlordibrompropane
CH3.CClBr.CH2Br
C3H5ClBr2
169-170
Eeboul
A. C. [5], 14, 453
36, 128
"
"
»
169-170 c.
„
C. E., 82, 377
29, 894
"
"
ii
170
Friedel
A., 112, 236
vi., 968
»
II
CHa.CHBr.CHClBr
u
n
170-175
177-177-5 c.
Eeboul
A. C. [4], 16, 343
C. E., 82, 377
vii., 1019
29, 894
"
"
H
177-177-5
....
11 >
A. C. [5], 14, 453
36, 128
"
n
195
....
Oppenheim
J. [1867], 569
vi., 968
„
(Bromallylchlorbromide)
ii
197-199
197-200
....
Simpson
P. E. S., 27, 118
B. S., 31, 410
38, 456
OH2Cl.CHBr CH2Br
.,1
195-200
Darmstiidter
A., 153, 319
vi., 433
11
"
»
abt. 200
....
J. [1857], 476
i., 894 •
"
D
ii
202
....
....
i., 898
"
....
11
202-203
....
Eeboul
J., 13, 461
Dichlorbrom propane
C3H5Cl2Br
200-205
156-160
....
Friedel and Silva
C. E., 84, 955
A., 138, 123
24, 1190
COMPOUNDS CONTAINING FOUR ELEMENTS.
355
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dichlorbrompropane
....
CiHDCl2Br
abt. 176
J. [1857], 477
i., 894
;>
»
180-187
....
Simpson
P. E. S., 27, 118
38, 456
a-Chlorbrompropane
Me.CClBr.Me
C3H6ClBr
93-95-5(745)
Eeboul
B., 7, 1037
27, 977
"- »
u
»
93
....
»
A. C. [5], 14, 453
36, 128
"- >.
))
»
93-93-5(745)
)5
A. C. [5], 14, 482
36, 131
8- „
Me.CH2.CHClBr
i)
112-113
Sawitscli
C. E., 52, 399
vii., 1018
fl- „
J»
n
112-113
Reboul
A., 155, 216
3- „
M
JH
abt. 110
»
C. E., 78, 1775
27, 977
«- „
u
n
abt. 110
)i
A. C. [5], 14, 453
36, 128
s- „
11
»?
110-112
n
A. C. [5], 14, 487
36, 131
y- ..,
Me.CHBr.CH2Cl
j>
120
»
B., 7, 1037
vii., 1019
7- .»
>»
v
121
....
»
A. C. [5], 14, 453
36, 128
>- »
Me.CHCl.CH2Br
u
119-121
Liquid
Friedel and Silva
B. S. [2], 17, 532
25, 890
y- ,.
»»
3J
118-120
Simpson
P. E. S., 27, 118
38, 456
«-
CHa01.CH2.CH!,Br
1)
140-141 (746)
Eeboul
C. E,, 78, 1773
27, 976
5- „
1)
J*
140-142(746)
j»
A. C. [5], 14, 487
36, 132
?
C5H8Cl2Br2
C5H0Cl2Br2(?)
232-236
Pinner
B., 8, 1326
29, 554
Dichloramylene dibroruide ....
....
CsH8Cl2Br2
230-240
A., 179, 37
Methylchlordibrompropyl-
CHMeBr.CClBr.CHMeCl
))
140-145 (31)
....
Thurnlackh
A., 223, 149
46, 1118
carbinyl chloride
Dichlortribrombenzene
Cls.Br3=1.3.2.4.6
C6HCl2Br3
....
121
Langer
B., 15, 1332
Trichlordibrombeuzene
Bra.Cl,= „
C6HCl3Br2
149
M
B., 15, 1330
42, 1058
,,
„ = »
J»
....
119
....
A., 215, 119
Chlortribrombenezene
Br3.Cl=1.3.5.6
C6H2ClBr3
....
80
Silberstein
J. p., 27, 116
44, 661
„
5» »
)J
....
82
Langer
B., 15, 1065
42, 954
Chlorbrombenzene
Cl.Br=1.4
C6H4ClBr
196-3(756-12)
67-4
Kbrner
G. I., 4, 305
29, 215
»»
» =1-3
JJ
196
....
j»
»
29, 220
Chlordiallyltetrabromide ....
C6H9ClBr4
....
Liquid
Henry
C. E., 87, 171
36,34
Chlorhexylene dibromide ....
....
C6HuClBr2
218-220
....
Destrem
B., 16, 229
Chlorbenzyl bromide
C6H4.Cl.(CHsBr)=1.4
C7H6ClBr
48-5
Jackson and Field
B., 11, 905
36, 62
5) » •"•
» »
1>
....
48-5
»
A. C. J., 2, 85 ;
40, 806
3, 252
» »
J' )^
)J
....
48-5
Jackson and White
B. 13, 1217
38, 879
Cinnyl chlordibromide
Ph.C3H4Br2Cl
C9H9ClBr2
96-5
Grimaux
C. E., 76, 1598
26, 1139
o-Trichlordibromnaphthalene
C10H3Cl3Br.,
....
166
....
iv., 13
a-Dichlordibromnaphthalene
....
C10H4Cl2Br2
170
....
»
0-
....
M
....
166
....
»
Dichlorbromnaphthalene ....
....
C10H5Cl2Br
80
Beilstein
Org. Chem. 1205
iv., 11
Chlordibromnaphthalene
CioHsdsBrj
....
150
5J
Org. Chem. 1206
iv., 10
tetrachloride
Chlorbromnaphthalene
al> "2
C10H6aBr
....
115
....
B. S., 26, 540
Ohlorbromnaphthalene tetra-
C10H6ClBr5
110
Beilstein
Org. Chem. 1205
bromide
Dichlornaphthalene tetrabro-
C10H6Cl2Br4
....
a. 100+
j)
Org. Chem. 1206
iv., 10
mide
Dibromnaplithalene tetra-
....
C-ioH6Cl4Br2
....
abt. 155
«
>»
)1
cliloride
Bromnaphthalene dichloride
....
C10H7CI2Br
165
Gerhardt
....
iv., 8
Trichlorbromisocymene
Me.PrJS.Cl3.Br.=1.3.(?)4
C10HioCl3Br
65
Kelbe
B., 16, 619
Dichlordibromanthracene ...
....
C14H6Cl2Br2
251-252
Schwarzer
B., 10, 377
32,493
Diclilorbromanthracene
....
C14H7Cl2Br
168
»
)J
»
Di(bromphenyl )dichlorethy-
CCl2:C(CcH4Br).,
C14H8Cl.2Br2
119-120
Zeidler
B., 7, 1180
28, 148
lene
Dichloranthracene tetrabro-
....
C14H8Cl2Br4
166
Schwarzer
B., 10, 376
38, 493
mide
Di(bromphenyl)-trichlor-
CCl3.CH(C6H4Br)!i
Clt'ELtClJBtt
139-141
Zeidler
B., 7, 1180
28, 148
ethane
Di(bromtolyl)trichlorethane
C013.CH(C6H.iBrMe)2
C16H1.,Cl3Br2
148
Fischer
B., 7, 1192
28, 154
a-Tetrachlortribromdinaph-
C10H4Cl2Br2.C10H5C]2Br
C20H9Cl4Br3
74-76
Faust and Saame
A., 160, 69
vi., 846; 25, 05
thyl
0-
»
71-73
3)
A., 160, 71
1)
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
lodochloroform
CHC13I
131
Liquid
....
A., 22, 229; 126,
i., 913
239
Methylene chloriodide
....
CH2C1I
109-109-5
Liquid
Sakurai
47, 198
(760-4)
jj jj »•»•
....
JJ
129
jj
41, 362
Chloriodoethyleue
CH3:ccn
C2H2C1I
101-102
Henry
C. R, 98, 518
46, 719
,j
jj
JJ
100-101
Liquid
j»
C. R, 98, 680
46, 831
(759) p.d.
>» .... ....
f !HC1 : CHI
JJ
114-116
....
A., 216, 263
,, .... ....
JJ
JJ
119c.
Liquid
Plimpton
B., 16, 79
41, 392
jj .... ....
D
J)
119
...
Henry
C. R, 98, 741
46, 831
Dichloriodoethane
C2H3C12I
171-172 s. d.
Liquid
»
C. R, 98, 518
46, 719
(774)
Ethylidene chloricxlide
CH3.CHC1I
C2H4C1I
117-119
Simpson
P. R S., 27,118
38, 456
jj u
JJ
JJ
118
Plimpton
41, 397
Ethylene chloriodide
CHsCl.CH.,1
JJ
137-138
....
Meyer and Wurster
B., 6, 964
jj »
JJ
JJ
140-143
Simpson
....
37, 180
jj jj — •
JJ
1J
140-1 (759-3)
s. f. m.
Thorpe
37, 180
jj »
JJ
)J
146 (753)
»
JJ
j» jj ••••
J)
JJ
141
Plimpton
41, 397
I? j>
JJ
JJ
141
Plimpton & Graves
)!
j» u •»•
JJ
JJ
145
Simpson
J., 16, 485
jj » ••••
J)
JJ
146
Maumen6
J., 22, 345
jj jj
}J
JJ
147
....
Simpson
P. E. S., 11,390
ii., 579
a-Chlorallyliodide
C3H4C1I
150 (760)
Eomburgh
R. T., 1, 233
44, 449
jj
JJ
92-95 (40)
»
B., 16, 393
0- „
CHOI : CH.CH2I
JJ
162 p. d.
»i
B., 16, 392
(760-4)
Dichloriodopropane
....
C3H5C12I
SOS
Liquid
Henry
B., 4, 702
24,907;vii.,320
•j
JJ
205-210
Simpson
P. R S., 13, 540
vi., 92
Ohloriodopropane
CH3.Cai.CH3
C3H6C1I
110-130(10)
Oppeuheim
As., 6, 360
vi., 826, 968
,,
CHj.CHCLCHjI
JJ
149 (760)
Friedel and Silva
B. S. [2], 17, 536
vii, 1019
jj .... ....
JJ
)J
40-43(10-12)
»
JJ
»
Chloriodobenzene
C,H4.C1.I=1.2
C6H4C1I
a. 233
Liquid
Korner
G. I., 4, 305
29, 215
jj
JJ JJ
JJ
229-230
Liquid
Beilstein and Kur-
B., 7, 1395
28, 364
batow
?j
» =1-4
)J
236-227
56-57
3>
B., 7, 1395
28, 363
j)
JJ )J
JJ
227-6(751-26)
Solid
Korner
G. I., 4, 305
29, 215
o-Chloriodotoluene
C7H6C1I
242-243
1. —14
Wroblewsky
A., 168,211,2.0.
27, 55; vii.,
....
[2], 6, 164
1166
0- „
»
240
8. 10
»
J)
D
'- »
Me.I.Cl=1.2.?
»
240
1
Beilstein and Kiihl-
Z. C. [2], 6, 102
vii., 1177
berg
(3.) CHC10.
Trichloracetaldehyde (chloral)
CC13.COH
C2HC13O
94
Liebig
A., 1, 195
37, 191
jj >j
JJ
JJ
944
»
....
i., 881
j» j>
JJ
JJ
—75
Berthelot
G. J. C., 1878
jj j>
JJ
JJ
95-100
Detsenyl
C. G, 1873, 767
27, 572
jj j)
)J
JJ
96-97 (750)
Briihl
G. J. G, 1880
jj jj
))
?:
96-4 c. (760)
Thorpe
37, 191
» j>
J>
j)
97-2 c. (760)
15
jj
jj D
JJ
jj
97-73 c. (760)
Passavant
....
39, 55
jj jj
J)
j)
98-1-99
Kopp
A.
37, 191
(745-9)
» j>
JJ
jj
98-6
»
....
1., 881
Dichloracetyl chloride
CHC12.CO.C1
)j
108
....
Bogomoletz
B. S. [2], 34, 330
40, 401
jj jj ••"
JJ
j)
107-108
Liquid
Otto and Beckurts
B., 14, 1618
40, 1030
COMPOUNDS CONTAINING FOUR ELEMENTS.
357
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Walts' Diet.
& J. Ch. Soc.
Parachloralide
....
CoHClaO
182
• •.*
Cloez
iv., 341
Trichloracetic acid
CCL..COOH
CJHC1A
a. 180
Henry
B., 12, 1846
„ • ,,
„
„
194-195
Solid
Tommasi & Meldol
....
27, 314
„ „
„
„
195
44-8
Judson
Z. C. [2], 7, 40
vii., 9
„ „
„
„
195
44-8
Clermont
C. B., 83, 112
24, 812
„ „
„
„
....
45
....
J. p. [2], 27, 16
„ „
„
„
195-200
46
Dumas
A., 32, 109
i., 878
,, „
„
„
....
46-5
Bichter
Tabellen
,, „
„
„
....
52
Beckurts and Otto
B., 14, 588
,, ,, .... ....
„
„
195
52-4.
Clermont
A. C. [5], 2, 401
27, 1154
Chloracetyl chloride
CH2C1.CO.C1
C2H2C120
105
....
Wurtz
A., 102, 96
vi., 22
„ „
„
„
105-107
Bogomoletz
B. S. [2], 34, 330
40, 401
„ „
„
>i
107-108
Henry
C. B., 100, 114
48,372
Uichloracetaldehyde
CHC12.COH
„
89-90
Paterud
G. S. P., 5, 123
vi., 76
,, .... ....
„
„
88-90
....
Paternd and Pisati
G. I., 1, 461
24, 1190
Paradichloracetaldehyde
....
(CSH,CLO).
....
129-130
Jacobsen
B., 8, 87
28, 631
Metadichloracetaldehyde ....
„
....
n.f. 200
Friedrich
A., 206, 253
40, 407
Dichloracetic acid
CHC12.COOH
CjHjCljO,
189-191
s. 0
Wallach
B., 9, 1212
31, 59
„ „
„
„
195
Manmene
J., 17, 316
vi., 19
Chlorethylene oxide
CHC1.CH2.0
C2H3C10
89-92
A., 216, 269
C'hloracetaldehyde
CHjCl.COH
i)
85-5 c. (738)
43-45
Bichter
B. K. T.
.... ....
„
„
MM
65-75
„
J)
„ (polymer)
(CH2Cl.COH)n
„
....
87-87-5 c.
Natterer
M. C., 3, 461
42, 1046
Acetyl chloride
CHj.CO.Cl
„
50-9 (746-1)
....
Thorpe
....
37, 188
„ „
J)
„
50-93 (746-3)
„
...
„
„ „
J!
„
55
....
Gerhardt
J., 5, 444
i., 35
„ „
„
„
53-5-55
Schall
B., 17, 2204
„ „
„
„
51-52 (720)
....
Briihl
G. J. C., 1880
,, „
„
„
55
....
Gal
A. C. [3], 66, 187
vi., 23
„ „
„
„
55-56
Kopp
A., 95, 208
37, 188
„ „
„
„
55-56
Perkin
41, 269
Chlormethylic formate
H.COO.CH2C1
C2HaC10s
abt. 100
Henry
B., 6, 742
vii., 807
Methylic chlorocarbonate ....
C1.COOCH,
„
66-5-67-5
Meyer and Wurster
B., 6, 965
)) !>
„
,,
71-4
....
Bose
A., 205, 229
40, 252
» !!
„
11
71-71-5(150)
....
Klepl
J. p., 26, 447
44, 311
Chloracetic acid
CH2C1.COOH
„
180
Geuther
A., 132, 171
vi., 22
,, „
„
„
185-187-5
s. 62
Hofmann
J., 10, 348
i., 876
(755-7)
,, „
„
j»
180-187
....
Heutschel
B., 17, 1286
46, 990
,, ,, — ....
„
„
183-9 (747)
62-64-5
Tollens
B., 17, 665
„
n
H
„
...t
a. f. 53-54
„
„
„
n
„
„
187
...•
Gal
A. C. [3], 66, 187
vi., 23
„ „
„
n
185
....
„
G. J. C., 1862
,, „
„
„
187
61
Conrad & Guthzeit
B., 15, 606
42, 946
„ „
JJ
„
188
....
Cahours
G. J. C., 1863
„ „
„
n
....
62
Briihl
G. J. C., 1880
:'richlorethylalcohol
CClj-CHyOH
C2H3C1,0
151 (737)
17-8
Thurnlackh
A., 210, 67
42, 295
,,
„
„
150-152
a. f. m.
Mering
B., 15, 1020
iVichlormethyl oxide
„
abt. 130
....
Regnault
A. C. [2], 71, 401
Chloral hydrate
CC13.CH(OH)2
C3H,C1,02
95
....
Vlartius&Bartholdy
B., 3, 443
vii., 313
M „
„
„
97
Personne
C. B., 69, 1363
„
„ „
,j
„
97
....
Jungfleisch, Le-
J. Ph. [4], 208
„
baigne, & Boucher
» »)
„
„
97-5
49-53
fTluckiger
Z. C., 6, 432
„
„ „
„
,)
99
50-51
Jacobsen
A., 157, 243
24, 257
„ „
»
„
95
....
Martins and Men-
G. J. C., 1870 ;
delssohn
Z. C.
H
„
95
....
Senry
B., 4, 101
24, 256
„ „
—
„
58
Ger. Phann., 1882
„ 5)
„
„
97-5
57
Meyer and Dulk
B., 6, 449
26, 878
„ „
„
„
....
57
^riedrich
A., 206, 251
40,407
358
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Chloral hydrate
CC13.CH(OH)3
CjHjClA
115 (755)
s. 40-2
Thomsen
Z. (1, 13, 156
vi., 432
?! » ••••
t»
J)
145
56
Koussin
Z. 0., 13, 96
,, ,,
?J
))
145
50
Persoime
Z. G, 13, 172
Isochloril hydrate
....
»
....
80
Meyer and Dulk
A., 171, 74
27, 461
,, ,,
....
M
....
80
Meyer
B., 6, 449
26, 878
Dichlormethyl oxide
....
c.H4(a2o
105
Eegnault
A. C. [2], 71, 398
Dicliloracetaldehyde hydrate
CHCL.CH(OH)2
C2H4Clj02
98-100
43; 57
Friedrich
A., 206, 251
40,407
j» »
»
»5
118-121
50-57
Denaro
G. I., 14, 117
46, 1283
Chlormethyl oxide
CH2C1.O.CH3
CSH5C10
79-5 (759)
....
Friedel
C. E., 84, 247
32, 424
Ethyleue hydroxychloride ....
CH2C1.CH2.OH
»»
128
Wurtz
A., 110, 125
ii., 578
» »
«
U
128-131
Demole
B., 9, 555
» »»
J»
»
130-131 (760)
....
Henry
B., 7, 70
Ethylidene hydroxychloride
CH3.CHC1.0H
J)
25-30 (10)
Liquid
Hanriot
A. C. [5], 25, 219
42, 590
Ethylic hypochlorite
EtO.Cl
Jl
36 (752)
Liquid
Sandmeyer
B., 18, 1768
48, 1045
Methyl oxide+HCl
....
C2H7C1O
—2
Liquid
Friedel
C. E., 81, 152
28, 1245
|3-Dichloracrylic chloride
cci2:cH.coci
CjHCljO
a. 145
....
Wallach & Hunaiis
B., 10, 569
32, 591
Trichloracetyl carboxylic acid
CC13.CO.COOH
C3HC1303
89
Hofferichter
J. p. [2], 20, 195
38, 35
Pentachloracetone
CHC12.CO.CC13
C3HC16O
185
Liquid
Cloez
B. S. [2], 39, 636
46, 580
j» .... ....
n
•>
190
Stadeler
A., 109, 277
i., 30
„
1)
»
192
Liquid
Cloez
B. S. [2], 39, 636
46, 580
„
»
)1
182
....
....
A., Ill, 181
+4H20 ....
»
....
....
15-17
....
A., Ill, 295; 122,
120
/3-Dichloracrylic acid
CClj : CH.COOH
C/gJigOlgOj
75-77
Wallach
A., 203, 83 ; B.,
38, 799; 29,
8, 1580
551
ft- »i j,
)!
)»
76-77 ; a. f.
Wallach & Hunaus
B., 10, 568
32, 591
63-64
a- „ „
CHC1 : CC1.COOH
»
....
85-86
Bennett and Hill
B., 12, 656
36, 617
n- „ „
p
»»
85-86
Hill and Mabery
A. C. J., 4, 263
44, 309
"• » »
»J
»>
....
85-86
Ciamician & Silber
G. I., 13, 320
46, 176
Tetrachloracetone+4H2O ....
....
C3H2C14O
....
35
Bouis
A. C. [3], 21, 111
i., 30
» » •»>•
JJ
177-180
38-39
Bischoff
B., 8, 1342
29, 559
Hexachloracetone hydrate ....
CO(CC13)2.H3O
C3H2C1602
15
A., 122, 120
a-Chloracrylic acid
CH2:CC1.COOH
C3H3C102
Liquid
Pinner
B., 8, 964
«- „ „
n
5)
176-181
Liquid
Beckurts and Otto
B., 10, 1949
34, 291
"• i. »
J>
J)
63
Wallach
A., 203, 83
38, 799
"- „ „
J»
))
64-65
Werigo & Melikoff
B., 10, 1499
34, 290
°- » »
V
)1
65
Otto and Beckurts
B., 18, 239
48, 510
°- i) „
»)
))
65 u. c.
Werigo and Werner
A., 170, 163
27, 242; vii.,
1012
ft- » »
CHOI: CH.COOH
»
84
Bandrowski
B., 15, 2702
0- „ »
»
J)
....
84-85
Wallach & Hunaus
B., 10, 569
32. 592
ft- » .,
»»
)J
....
84-85
Wallach & Eeincecke
B., 10, 2128
34, 404
Chlormalonic acid
CHC1(COOH)2
C3H3C104
....
133
Conrad & Guthzeit
B., 15, 605
42,946
a-Dichlorpropionyl chloride....
CH3.CC12.COC1
C3H3C13O
105-115
Beckurts and Otto
B., 11, 388
34, 488
Trichloracetone
CH3.CO.CC13
))
d.
Bouis
A. C. [3], 21, 111
i., 30
j,
)>
»)
170-172
Kramer
B., 7, 257
27, 676
,,
I»
)»
170-172
Bischoff
B., 8, 1338
29, 558
+2H20 ....
)>
»
....
43
u
B., 8, 1338
+2H20 ....
»
n
44
Kramer
B., 7, 257
27, 676
Trichlormethylic acetate
CH3.COO.CC13 (?)
C3H3C1302
145 d.
Laurent
A. C. [2], 73, 25
i., 23
Methylic trichloracetate
CCl3.COOMe
»
154
Henry
C. E., 101, 250
48, 1122
!> Jl
j»
Clermont
C. R., 96, 437
Trichlorpropionic acid
....
)i
....
60
A. C. [3], 16, 67,
72, 82
Trichlorlactic acid
CC13.CH(OH).COOH
C3H3C1303
105-110
Bischoff and Pinner
B., 5, 208
25, 485
>i it
)1
f}
105-110
A., 179, 79
29, 555
Isotriclilorglyceric acid
CC13.C(OH)2.COOH
C;1H3C1A
102
Claisen & Antweiler
B., 13, 1938
40, 154
Dichlorvinyl methyl oxide ...
a-Chlorpropionyl chloride ...
CC1S : CH.O.CH3
CH3.CHCI.CO.C1
C3H4C120
»»
109-110
109-110 (744)
Liquid
Denaro
Henry
G. I., 14, 117
C. E., 100, 114
46, 1283
48, 372
ft- » »
ft.
CH2C1.CH2.CO.C1
»?
143-145 (763)
Liquid
»)
j>
17
» J)
))
»
a. 140
....
Hi., 466
COMPOUNDS CONTAINING FOUR ELEMENTS.
350
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dichloracetone
CH3.CO.CHC12
C3H4C120
115-117
Friedel & Ladenbur
A., 159, 259
24, 919
)» .... ....
n
»
116-5
Stadeler
A., Ill, 301
i., 30
,, , •"• ••••
?!
M
119-120
....
Glutz and Fischer
J. p. [2], 4, 52
24, 921
„
D
))
120
Wroblewsky
Z. C. [2], 4, 565
vi., 27
M .... ....
13
)i
120
Liquid
Mulder
B., 5, 1009
vii., 14; 26, 380
i) * •' ••"
11
»
120
....
Borsche and Fittig
A., 133, 112
„
11
J)
120
Liquid
Bischoff
B., 8, 1330
29, 557
»»
•J
I]
120
Liquid
Grabowsky
B., 8., 1438
11
i>
))
j>
120
Conrad
A., 186, 236
29, 370
•
32, 436
"
1»
»
120-121
Markownikoff
B., 6, 1210
11 •••• ••••
1?
1)
121-5
....
Fittig
J., 12, 345
i., 30
11 .... ....
11
))
121-5 c.
Theegarten
B., 6, 897
» (polymer) ....
....
n
130-140
Grabowsky
B., 8, 1438
29, 557
i) »
....
)j
132-135
Bischoff
B., 8, 1332
29, 558
11 11
»
135-140
Mulder
B., 5, 1009
)i •••• ••••
CHaCLCO.CHjCl
?)
170-171
Liquid
Bischoff
B., 8, 1332
,,
»
)5
170-171
Liquid
Glutz and Fischer
J. p. [2], 4, 52
vii., 14; 24, 922
,,
»
)1
170-171
....
Bischoff
B., 8, 1332
11
i»
»
172-172-8 c.
42-5
Eichter
Tabellen
i) ••" ""
»>
))
168-169 (723)
43
Hermann
B., 13, 1708
„
j>
»»
171-172
42-43
Henry
C. R, 94, 1428
42, 1039
11 .... ....
»
))
43
Markownikoff
B., 6, 1210
vii., 318 ; 27,
241
11 •*•• *'"
»
3)
140-170
44
Barbaglia
B., 7, 468
27, 790
))
»
)I
167-5
45
Markownikoff
A., 208, 355
40, 1121
Chlorethylic chlorformate ....
C1.COO.C2H4C1
C3H4C1202
150-160
Liquid
Nemirowsky
J. p. [2], 31, 173
48, 741
Methylic dichloracetate
CHClj.CO.OCH3
11
143-144
....
Wallach
A., 173, 299
28, 351
11 »
J)
11
144
....
Henry
C. E., 101, 250
48, 1122
Dichlormethylic acetate
CH3.CO.OCHC12
))
145-148 p. d.
Malaguti
A. C. [2], 70, 379
i., 23
a-Dichlorpropionic acid
CH3.CC12.COOH
11
185-190
1.-8
Beckurts and Otto
B., 9, 1877
32, 180
n- „ „
n
)1
185-190
....
M
B., 10, 264
32, 182
a- „ „
31
»
186-190
....
»
B., 10, 1952
34, 291
a- „ „
»
>1
190-195
Liquid
D
B., 9, 1593
31, 298
a- „ „
»)
192-194
-4
Ciamician & Silber
B., 18, 1764
a- „ „
j>
11
....
a. 15
Beckurts and Otto
B., 10, 2039
34; 290
0-
CH2a.CHCl.COOH
)1
S10 (762)
abt. 50
Henry
B., 7, 414
27, 679
o
p- i, »
J)
))
210 (762)
50
>j
J. p. [2], 10, 185
28, 347
0- ,1 5)
11
»
50
Werigo & Melikoff
B., 10, 1499
34, 289
3- i, »
1»
)»
....
50
Melikoff
B., 13, 274
38, 627
ft- » »
»
11
50
»j
C. C. [1881], 354
42, 38
Dichlorlactic acid
CHC12.CH(OH).COOH
C3H4C12O3
219-231
75-78
Grimauz and Adam
B., 10, 903
29, 65
11 »
)»
n
....
76-5-77
....
B. S., 34, 29
CH3.CO.CH2C1
C3H6C10
117
Riche
C. E., 49, 176
i., 30
J., 12, 339
vi., 27
116-120
Liquid
M^arkownikoff
28, 443
i>
j>
118-120
Henry
B., 5, 190, 966
26, 379
j>
118-121
Bischoff
B., 5, 864
26, 159 160
••
»
....
119
Linnemann
A., 134, 170
vi., 27
119
Mulder
B., 5, 1009
vii., 13
120
Liquid
Barbaglia
B., 6, 318
26, 877
j,
j)
119-120
Glutz and Fischer
J. p. [21 14 52
24, 921
120-5-121-5
Markownikoff
Jr L J) >
0. E., 81, 668,
29, 339
)>
728, 776
120-125
Klriwaksim
B., 4, 563
26, 160
Epichlorhydrin
CH2a.CH.CH2.0
)5
»)
115-118
....
Miinder and Tollens
Z. C. [2], 7, 252
25, 999
n
»
I>
116-56 (760)
Thorpe
37, 206
11 ....
5J
5J
117 (755-5)
....
Darmstadter
J., 21, 454
11 .... ....
n
»
117
....
Gegerfeldt
B., 6, 721
26, 1123
1) ....
»i
J1
117-118
....
Markownikoff
A., 208, 349
40, 1120
„
19
»J
118
....
....
....
ii., 898
360
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Epichlorliydrin
CH2C1.CH.CH2.O
Q,H5C1O
118-119
Lowe
G. J. C., 1870
vii., 48
„
„
H
118-119
Reboul
J., 13, 456
37, 207
„
„
„
115-8 (758)
Schiff
G. J. C., 1881
„
„
„
120-130
Berthelot
i., 894
n-Chlorallyl alcohol
CH2:CC1.CH2.OH
.,
136 (763)
Henry
C. R., 95, 849
44, 178
u- „ „
„
„
136-140
....
Romburgh
R. T., 1, 233
44,450
ft- ii ii
CHC1 : CH.CHj.OH
„
153 c.
Liquid
„
B. S., 36, 549
42,376
Propionyl chloride
CHyCH^COCl
„
abt. 80
Buchamp
J., 9, 429
„ ii
„
„
80
Sestini
B. S., 11, 470
„ „
"
>'
77-S-78-3
Brtihl
G. J. C., 1880
.^
,, „ .... ....
„
11
79-5
„
44, 990
/3-Chlorpropionie aldehyde ....
CH2C1.CHS.CHO
„
....
34-5-35-5
Krestownikoff
B., 12, 1487
38, 234
ft-
„
„
170-175
33-5
Grimaux & Adams
B. S. [2], 36, 22
40, 888
(12-15)
9- „ „
„
„
....
32
Geuther & Cartmel
....
i., 57
Ethylic chlorocarbonate
Cl.COOEt
C3H5C1O2
94
....
Dumas
A. C. [2], 54, 230
i., 916
Chlormethylic acetate
CH3.COO.CH2C1
„
115-116
Henry
B., 6, 740
vii., 807;
26, 1117
Methylic chloracetate
CH2C1.COO.CH3
„
126-127 (757)
Liquid
„
B., 6, 742
26, 1117
,, ,,
„
„
129
Liquid
Meyer
B., 8, 1153
29, 372
., ii
„
„
ISO (740)
A., 179, 8
>! 1,
„
11
130
Henry
C. R., 101, 250
48, 1122
a-Chlorpropionic acid
CH3.CHC1.COOH
„
180-185
....
„
C. R., 1203, 1258
28, 443
a- „ „
„
,,
186
L— 18
Buchanan
Z. C. [2], 4, 523
vi., 960
ft' 11 »>
CH2C1.CH2.COOH
„
*•>*
33-5-41
Richter
Tabellen
ft- ii 11
„
„
203-205 (764)
37-38
Henry
C. R., 100, 114
48, 372
ft- ii »
J)
„
....
40-5 c.
Linnemann
A., 163, 96
vii., 27; 25, 689
p- „ „
„
„
58
Richter
vii., 27
ft- i> n
„
„
....
65
Wiehelhaus
....
vi., 960
a-Chlorlactic acid
CH2(OH).CHC1.COOH
C3H5C103
Liquid
Melikoff
B., 13, 273, 956
38, 627
"- ,, „
„
,,
Liquid
„
B., 13, 2153
40, 154
ft- 11 II
CH2C1.CH(OH).COOH
....
71
Frank
A., 206, 344
40, 417
ft- 11 »
u
i)
....
77
Richter
J. p. [2], 20, 193
38,32
0- ,, „
„
);
....
78
Melikoff
B., 13, 2153
40, 154
ft- ii >.
ji
„
....
78
„
C. C. [1881], 354
42,38
p~ ,, j,
„
);
....
78-79
B., 13, 273
38, 627
Trichlorpropyl alcohol
CCl3.CHMe.OH
C3H5C13O
150-160
49-2
Thurnlackh
A., 210, 78
42,295
Propylphycite trichlorhydrin
....
)J
172-173
Wolff
Z. C., 12, 465
Chloral methylate
CCl3.CH(OH)(OMe)
C3H6C1302
98
50
Bartholdy & Martius
B., 3, 445
vii., 314
II ,) ....
„
106
50
Jacobsen
A., 157, 244
24, 257
Allyl alcohol dichloride
CH2C1.CHC1.CH2OH
C3H6C120
180-184
....
Tollens and Hen-
B. S. [2], 11, 394;
vi., 91; vii., 48
ninger
A., 156, 164
II )) I!
•i
'i
183
....
Hiibner and Muller
A., 159, 179
24, 906
" " »
11
.,
182
Miinder and Tollent.
Z. C. [2], 7, 252
25, 999
Glycerol diehlorhydriu
CH2C1.CH(OH).CH2C1
"
183
158
....
Gegerfeldt
Clans
B., 6, 721
A., 170, 125
27, 243
" "
11
„
171-171-5
Markownikoff
B., 6, 1211
27, 241
" "
•i
„
171-171-5
„
A., 208, 349
40, 1120
(765) =
175-8-1 76-3 c.
•
"
.'
„
172-174
Miinder and Tollens
Z. C. [2], 7, 252
25, 999
" "
n
n
172-174
Hiibner and Muller
Z. C. [2], 7, 232
„
" "
11
„
174
„
A., 159, 173
34, 906; vli., 48
ii ii ....
"
„
174
....
Friedel and Silva
C. R,, 75, 81
25, 805 ; vii.,
.
1020
" "
»
- „
176-177
....
Hiibner and Miillei-
Z. C. [2], 6, 344
vii., 317
" "
»
n
176-177
Gegerfeldt
B., 6, 721
26, 1123
11 ,1
"
11
176-177 c.
Watt
B., 5, 258
25, 612
" "
11
„
175-180
Henry
A., 155, 324
1" J!
"
i.
174-186
....
Hiibner and Mullei
Z. C. [2], 6, 344
vii., 317
COMPOUNDS CONTAINING FOUR ELEMENTS.
301
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Glycerol dichlorhydrin
CH201.CH(OH).CH.,C1
C3HBC120
178
b. —35
....
i., 894
» »
»
»
178
Glaus
A., 160, 42
26, 1120
I! 1)
....
>»
179-180
Henry
J. p. [2], 10, 185
28, 346
,» )»
....
Jl
180
Eeboul
J., 13, 458
ii., 898
J5 »
....
JJ
180-183
....
Gegerfeldt
Z. C., 13, 672
,) ,1
....
I»
182
Hiibner and Miillei
Z. C. [2], 7, 232
25, 1000
» »
....
>»
183
....
Gegerfeldt
B., 6, 720
26, 1123
1) ))
....
J»
182 (760)
....
Kahlbaum
B., 17, 1260
', »J
....
)»
104 (75)
>»
))
•.» )1
....
»I
951 (50)
»
)»
)I I!
....
»
83-2 (25)
....
»i
))
1) )) "••
....
»
79-1 (20)
....
M
))
J! )1
....
)1
74-6 (15)
....
)!
))
V I!
....
»1
68-8 (10)
....
»
J)
V >!
....
))
64-2 (5)
»»
)»
»» ?J •"•
....
»»
56-6 (0)
»
»
Propylene chlorhydrin
CH3.CH(OH).CH2C1
C3H;C1O
126-128
Oppenheim
J., 21, 340
vi., 968
» n "••
ji
JJ
127
....
Oser
B. S. [1860], 235
vii., 1021
,> «
»
H
127-7 c.
Markownikoff
C. E., 81, 668,
20, 339
728, 776
11 !>
)»
))
127-128
....
Morley and Green
47, 132
)) >!
CH2(OH).CH2.CH.!a
)>
160 c.
....
Eeboul
C. E., 79, 169
27, 1154
)» »
»
»
160-162
....
»
A. C. [5], 14, 491
36, 128, 133
a-Glycerol chlorhydrin
CH2C1.CH(OH).CH2(OH)
C3H-C102
227-
1. —35
Berthelot
J., 6, 456
i., 893
a- „ „
n
1»
139 (10)
....
Hanriot
C. E., 86, 1139
34, 656
a- „ „
»
*)
139 (20)
....
)5
A, C. [5], 17, 62
36, 1030
8- „ „
CH2(OH).CHC1.CH2(OH)
»
144-146 (10)
Liquid
I»
C. E., 86, 1139
34, 656
8- „ „
»
>»
148 (20)
....
»
A. C. [5], 17, 73
36, 1030
a- „
»)
>J
145-146 (20)
....
)»
)>
))
B- „ „
H
>J
159 (100)
....
)1
B. S. [2], 27, 256
32, 301
8- „ „
))
n
220
....
Henry
B., 5, 449
8- „ „
)»
»»
230-235
»
J. p. [2], 10, 185
28, 346
Heptachlorethyl acetate
....
C4HC17O2
....
b. 100
Leblanc
i., 22
Maleyl chloride
C2H2(CO.C1)2
C4H2C12O2
70-71 (11)
Liquid
Anschiitz and Wirtz
B., 18, 1947
47, 900
Fumaryl „
»
))
60 (14)
....
)> »>
»
1)
„ „ .... ....
»>
)»
160
KekuM
As., 2, 86 ; A.,
ii., 747
112, 26
Muco-chloric acid
....
C4H2C1203
....
125
Schmeltz& Beilstein
As., 3, 280
iv., 764
„ ,, ....
....
JJ
125
Bennett and Hill
B., 12, 656
Trichlorerotonyl chloride ....
CC13.CH:CH.COC1
C4H2CI4O
162-166
Liquid
Judson
Z. C. [2], 7, 40
vii., 398; 24,
233
?
....
)!
196
••••
Paternd
G. S. P., 5, 123
vi., 77
Tetrachlorethyl oxide
(C2HC14)20
0^,0,0
189-7 (857-5)
Pa tern 6 and Pisati
G. I., 2, 333
26, 158
Chlorsuccinic anhydride
CH2.CHC1.CO.O.CO
C4H3C10,
130-131
38-41
Anschiitz& Beumerl
B., 15, 642
42, 828
(14-15);
125-126
(11-12)
Chlorf umaric acid
COOH.CH I CC1.COOH
04H3C104
abt. 190 d.
178
Bandrowski
B., 15, 2695
44, 313
« »
»
J)
....
191
Kander
J. p. [2], 31, 1
48, 652
Chloromaleic acid
C2HC1(COOH)2
))
....
171-172
Carius
B., 3, 334
vi., 798
Trichlorcrotonic aldehyde .. .
CC13.CH : CH.COH
C4HSC130
163-165
....
Kramer and Pinner
A., 158, 37
vii., 35; 24,
557
,, »
....
i)
163-165
• *..
Goldberg
J. p. [2], 24, 97
42, 28
Trichlorcrotonic acid
CC13.CH:CH.COOH
C4H3C1A
234-236
....
Kramer and Pinner
A., 158, 37
24, 558
)> !>
1»
))
236-238
44
Judson
Z. C. [2], 7, 40 ;
24, 233 ; vii.,
B., 3, 785
397
Trichlorethylidenic glycollate
O.CH2.COO.CH.CC13 (?)
C4H3C130S '
....
41-42
....
A., 193 ; 36
n-y-dichlorcrotonaldehyde ....
CH2C1.CH : CC1.CHO
C4H4C120
86-87
s. in C02 and
Natterer
M. C., 4, 539
44,965
snow
a-Chlorcrotonyl chloride ....
CH3.CC1 : CH.COC1 or
»>
142
Liquid
Sarnow
B., 4, 731
24, 1047
CH3.CH : CC1.COC1
3 A
362
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Billing
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Tetrolyl chloride
C4H4CLO
171-172 p.d
Liquid
Demar<;ay
C. R., 88, 126
36, 458
„ „
,,
172
Liquid
ii
B..S., 33, 524
38, 626
„ ,,
„
172-174
Pawlow
B., 16, 486
Succinyl chloride
COCl.CHj.CHs.COCl
C4H4Cl2Oj
abt. 190
Gerhard t & Chiozz
C. R., 36, 1050
v., 462
Dichlorcrotonic acid
CHClj.CH : CH.COOH
J)
215-5 u. c.
64
Gottlieb
J. p. [21 12, 1
29, .562
Action of Cl on tetric acid ..
....
C4H4C140
....
48-48-5
Demarcay
C. R., 88, 126
36, 458
Action of Cl on tetroly]
....
„
49
„
B. S., 33, 524
38, 626
chloride
Trichlorbutyryl chloride ...
03H4C13.COC1
„
162-166
Judson
B., 3, 787
Tetrachlorethylic acetate ...
CH3.COO.CHC1.CC13
C4H4C14O2
185
....
Meyer and Bulk
A.J 171, 67
27, 460
.. ..
„
r
186
Curie and Millet
C. R., 83, 745
31, 188
,, ,.
„
„
188-189
....
Z. C. [1870], 345
Tetrachlor butyric acid
(\H3C14.COOH
„
140
Pelouze and Gelis
A. C. [3], 10, 449
i., 694
Hexachlorethyl oxide
CHC!2.CH2.O.CC1,,CH2C1 or
c4H4a6o
250
....
Paterno
G. S. P., 5, 123
vi., 77
.
CHC12.CHC1.O.CHC1.CHC12
» ii
....
- „
250
....
Z. C. [1869], 394
a-Crotouic chloride
CH3.CH:CH.CO.C1
C4H5C10
123-128
Pawlowsky
B., 5, 331
a-Chlorcrotonic aldehyde ...
CHjCLCH : CH.COH
„
147-148
....
....
A., 179, 31
11 11
„
„
abt. 147
Pinner
B., 8, 1322
29, 553
Chlormethacrylic acid
fr. CH2:CMe.COOH
C4H6C102
58-5
Morawsky
J. p. [2], 12, 375
29, 563
» ,.
„
„
59
Gottlieb
J. p. [2], 12, 20
29, 562
i) »»
„
„
59-60
„
J?
);
|3-Chlor-/3-crotonic acid
CHa : CC1.CH2.COOH
„
194-8 c.
59-5
Frohlich
Z. C. [2], 5, 270
vi., 512
0- „ „
„
n
....
59-5
Friedrich
B., 15, 218 ; A.,
44, 968
219. 322
0-
„
„
59-5
Kahlbaum
B., 12, 2339
p- „ „
/3-Chlorcrotonic acid
II
CH3.CC1 : CH.COOH (2)
j)
59-5
93
Claus and Lischke
Alberti
B., 14, 1089
I. D., Strassburg,
-
1876
0-
„
„
206-211
94
Frohlich
Z. C. [2], 5, 270
vi., 512
P- „ „ ....
„
»
206-211 p.d.
94
Geuther
J. p. [2], 3, 431
24, 813
a- 11 „
„
„
206-211
94
„
J. Z., 6 ; pt. 4
vii., 399
3- „ „ ....
„
„
94-5
Kahlbaum
B., 12, 2337
3- „ „
„
ii
94-5
Friedrich
B., 15, 218 ; A.,
42, 945 ; 44,
219, 322
968
*" 11 11 •«••
„
„
....
97
Thurnlackh
A., 213, 379
42, 1279
'- .. i
CH3.CH : CC1.COOH
n
206
94
Sarnow
B., 4, 732
24, 1046
"" » »
"
»
212
96
»
B., 5, 468
vii., 398; 25,
11 „ ....
J)
„
97-5
Kahlbaum
B., 12, 2338
°- )! 11
M
)J
....
97-5
Friedrich
B., 15, 218 ; A.,
42, 945 ; 44,
Ethylic chloroxalate
COCLCOOEt
C4H6C103
128
Morley and Saint
219, 322
968
43,400
» "
II
„
131
Richter
C. C. [1878], 446
36, 139
,, ,, .... ....
.1
„
140
Henry
B., 4, 600
24, 820; vii.,
883
Ohlorsuccinic acid
Prichlorethylic acetate
Ethyldichloracetyl chloride....
Irichlorvinylethyl oxide
COOH.CHC1.CH2.COOH
CH3.COO.CHC1.CHCL
C2H5.CC12.COC1
C4H6C104
C4H5C1302
C4H5C130
250-280
152
154-8 c. (755)
151-5-152
Anschiitz & Beumert
Kessel
jfeuther
Patern6 and Pisati
B., 15, 642
B., 10, 1999
I. [1864], 317
G. I., 2, 333
42, 828
vi., 22
vii., 2 ; 26, 159
»! 11
Trichlorbutyric aldehyde ....
)»
CC18.CH2.CH2.CHO
))
154-156
164-165(750}
Liquid
Busch
Engel & Moitessier
B., 11, 446
C. R., 90, 1075
34, 487
40, 407
Ethylic trichloracetate
Trichlorethylic acstate
CH2C1.CHC1.CHC1.CHO
CCl3.COOEt
CH3.COO.CH2.CC13
C4H"ci302
163-165
164
167 (736) ;
Liquid
s. —78
Liquid
Kramer and Pinner
^atterer
Vlalaguti
Thurnlackh
B., 3, 386
M. G, 4, 539
A. C. [3], 16, 62
A., 210, 69
44, 965
i., 879
42, 295
71 (18-3)
ii ii ....
Trichlorisobutyric acid
Trichlorbutyric acid....
CH3.COO.CHC1.CHC12
fr. (CH3)2.CH.COOH
fr. CH3.CH2.CH2.COOH
I»
164
250-280 p.d.
50
58
L/eblanc
Vessel
Gottlieb
rimrnlackh
A. C. [3], in, 207
B., 10, 1999
J. p. [2], 12, 1
A., 213, 374
34, 133
29, 561
42, 1279
" "
»
„
....
60
....
Z. P. C., 6, 494
....
COMPOUNDS CONTAINING FOUR ELEMENTS.
363
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Trichlorcrotonicaldehyde hy-
CC13.CH:CH.CH(OH)2
C4H5C1302
....
78
Kramer and Piimei
A., 158, 37
24, 557 ; vii.,
drate
400
J> 11
JJ
JJ
....
78
Pinner
A., 179, 21
29, 548
Trichlorethylglycollic acid ...
CC13.CH2.O.CH2.COOH
C4H5C1303
....
69-5
Thurnlackh
A., 210, 72
42, 295
Pentachlorethyl oxide
CC13.CC12.O.C2H5
C4H5C150
190-210 p.d.
Liquid
Busch
B., 11, 446
34, 487
i» ji
„
)J
•••*
Liquid
Jacobsen
B., 4, 217
24, 515
» 1>
CC13.CHC1.O.CH2.CH2C1
JJ
235
....
Henry
B., 7, 763
27, 979
Dichlorbutyric aldehyde
C3H5C12.COH
C4H6CLO
200
....
i., 689
» »
GH2Cl.CH2.Cn2 COH
JJ
225-230
Saytzeff
A., 171, 251
27, 570
d-Chlorbutyryl chloride
CH3.CH2.CHC1.COC1
JJ
129-132
Markowiiikoff
A., 153, 241
....
Uichlorethoxyethylene
CHCKCCLOEt
JJ
128-2 c.
....
Geuther&Brockpofl
J. Z., 7, 359
vii., 487 ; 26,
867
Dichlorethylic acetate
CH3.COO.C2H3C12
c4Heci2o2
110
Malaguti
A. C. [2], 70, 368
....
)1 J5 ""
JJ
JJ
125
....
Curie and Millet
C. B., 83, 745
31, 188
>J )»
CH3.COO.CHC1.CH2C1
JJ
146-148
Liquid
>!
B., 9, 1611
»
» )!
JJ
165
....-
....
M. C., 3, 453
....
E thy lie dichloracetate
CHClj.OOO.CjH5
JJ
150-160
Liquid
Wallach
B., 10, 1527
....
» »
JJ
JJ
153
....
Fischer & Geuther
J., 1864, 316
vi., 19
ii i>
JJ
JJ
154-157
....
Wallach
B., 6, 114
vii., 310 ; 26,
627
v »» '•••
JJ
JJ
156
....
Mttller
vi., 19
» i) ••••
JJ
JJ
158
»
G. J. C.. 1864
....
i) »j
JJ
JJ
156
....
Curie and Millet
C. E., 83, 745
31, 188
i> )j ••••
JJ
JJ
156 (738)
...,
Briihl
G. J. C., 1880
» ii
JJ
JJ
156
Conrad
A., 186, 232
32, 436
Chlorethylic chloracetate ....
CH2C1.COO.CH,.CH2C1
JJ
180-210 d.
Liquid
Mulder and Bremei
B., 11, 1959
36, 303
jj »
JJ
JJ
145 (i. v.)
....
u
)j
j»
i» »
JJ
J)
197-198 u.c.
Liquid
Henry
C. R, 97, 1308
46, 421
Methylic dichlorpropionate....
CH3.CCl2.COO.CH,,
»»
143-1 44 u.c.
Liquid
Beckurts and Otto
B., 9, 1878
32, 181
i) »
C^Cl^COOCHa
JJ
158
...«
Ciamician & Silber
B., 18, 1764
....
Dichlorhy droxy isobuty ric
CHCl2.CMe(OH).COOH
C4H6C1A
82-83
Bischoff
B., 8, 1334
29, 558
acid
» »
(CH2C1),,C(OH),COOH
JJ
90-92
Grimaux and Adam
C. JJ., 90, 1252
38, 801
Tetrachlorethyloxide
CC13.CHC1.0.C2H5
C4H0C140
185-190
....
Henry
B, 4, 101
24, 255; vii.,
314
»
JJ
JJ
185- 190 u.c.
H
B., 4, 436
24, 696
(755)
,5 ....
JJ
JJ
189-7 (757)
Paternd and Pisati
G. I., 2, 333
vii., 484
Ethoxychlorethylene
CHC1 : CH.OEt
C4H7C1O
122-123
....
Geuther
Z. C. [2], 7, 128
24, 515 ; vii., 8
Ethylidene acetochloride ....
CH3.CHClAc
JJ
121-5 (746)
....
Franchimont
E. T., 1, 243
44, 452
Chlorcrotyl alcohol
JJ
158'3c.(742-5)
a. f. m. of ice
Thurnlackh
A., 213, 376
42, 1279
and CaCl2
Butenylglyceryl epichlorhy-
....
JJ
125-5 c. (738)
Liquid
Zikes
M. C., 6, 348
48, 1046
drin
Isobutyryl chloride ....
Me^CH-COCl
»!
92
....
Markownikoff
Z. C., 1866, 501
vi., 378, 381
i) i>
5)
)1
91-5-92-5
....
Briihl
A., 203, 19
....
(748)
Butyryl chloride
CH3.CH2.CH2.COC1
JJ
abt. 95
....
Gerhardt
J., 5, 445
i., 699; vi.,381
,, ,,
JJ
JJ
99-101 (734)
Briihl
A., 203, 19
....
11 „
JJ
JJ
100-101-5
Linnemann
A., 161, 179
25, 395
Chlorbutyric aldehyde
C3H6C1.COH
JJ
141
i., 689
3- „ 11
CH3.CHC1.CH2.COH
JJ
....
96-97
Kekul6
Z. C. [2], 5, 57i
vi., 513, 25, 616
A., 162, 100
Ethylene chloracetin
CH2Cl.CH2.OAc
C4H7C102
143-145
Liquid
Ladenburg and De-
B., 6, 1024
mole
11 u
JJ
»
143-145
....
Henry
B., 7, 70
27, 457
11 ?i
M
»>
145
....
Simpson
J., 12, 487
ii., 568
Ethylglycollic chloride
»
127-128
Henry
B., 2, 276
Propylic clilorocarbonate ....
CLCOOPr*
i)
115-2 c.
Rose
A., 205, 229
40, 252
» jj
1>
)?
120-130d.
**"
Roemer
B., 6, 1101
27, 39
3 A 2
364
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Ethylic chloracetate
CHXlCOO.CjHj
C4H7C1O2
141-142-5
....
....
M. C., 2, 696
,, „ .... ..
»
)»
143-S
....
Wilm
A. C. [3], 49, 97
i., 877
„ „
)»
n
144-146
Briihl
G. J. C., 1880
„ „
»
»
142-147
....
Menschutkin and
Z. C. [2], 7, 5
24, 150
Jermolajew
Chlorethylic acetate
CH3.COO.CHC1.CH3
»
90-140
....
Simpson
C. E., 47, 174
i., 109
i> »
?)
jj
120
Wurtz
C. E., 73, 528
84,1056;vii.,35
1) )!
j>
»
120-124
....
...
A., 109, 156
»> „
»
»
121-5 (746)
Franchimont
B., 16, 402
Methylic a-chlorpropionate...
CH3.CHCl.COOMe
»
130-131
A., 208, 342
» »
)»
j»
ISM
....
Kahlbaum
B., 12, 344
36, 521
» ' ft- n
CH2Cl.CH2.COOMe
)>
155-157
....
Henry
C. R, 100, 114
48, 372
a-Chlorisobutyric acid
(CH3)2.CCl"cOOH
j>
abt. 190
»»
B. S., 25, 23
30, 397
7
ji »
C3H6C1.COOH
»
230-235 p. d
106-107
Melikoff
B., S., 41, 311
40, 1301
/3-Chlorbutyric acid
CH3.CHC1.CH2.COOH
»
200. d.
7
Pinner
B., 12, 2056
38, 99
a- ,, »
))
»j
200-201
98-99
Markowuikoff
Z. C. [2], 4, 621
vi., 380
Methylic chlorlactate
CH2Cl.CH(OH).COOMe
C4H7C103
185-187
....
Frank
A., 206, 347
40, 417
Chlorhydroxybutyric acid ...
C3H5C1(OH).COOH
))
....
53-56
Erlenmeyer and
B., 15, 49
44,969
MUller
?> »
JJ
»
....
62-63
Melikoff
B.,16, 1268; B. S.
44, 969 ; 46,
41, 311; 43, 115
1301; 48, 650
>? »
M
J)
82
»
))
»
»> »
»
J>
....
82-83
}»
»
»
» »
CH3.C2H2C1(OH).COOH
»
....
85
))
J)
)»
» M •"•
....
)»
m. p. error
98-99
Jt
B., 15, 2586
44, 311
for 82-83
Acetone chloroform
CMe2.CCl3.OH
C4H.C130
167 u. c.
96-97
Willgerodt
B., 14, 2456
42, 492
») »
JJ
)>
cf. B 15,2305
96
»
B., 16, 1585
44, 1079
» » +|H2O
»)
))
80-81
D
»
»
Trichlorbutyl alcohol
C3H4C13.CH2OH
»
120 (45)
61-5-62
Thurnlackh
B., 14, 2759 ; A.
42, 824, 1279
213, 372
» »
» -
)1
199-200
60-61
Mering
B., 15, 1021
42, 952
Chloral ethylate
CCl3.CH(OH)(OEt)
C4H7C1302
112-5 (740)
46
Lieben
B., 3, 909
24, 345
»» „
»
»
114-115
43-46
»j
»
vii., 313
„ >»
)5
J)
113-5
Jungfleisch, Le-
J. P. [4], 11, 208
vii., 313
baigne, &Eoucher
?» »
J)
»
....
44-46
....
26, 879
„ „
I»
»1
115
....
Senry
B., 4, 102
24, 256
•» ?» ••-• .««•
)J
»
115
56
itoussin
C. E., 69, 1144
vii., 313
„ „
)>
))
115-116
S. 40
Vlartius and Barth-
B., 3, 444
»
oldy
» »
»
))
115-117
56-57
Tacobsen
A., 157, 244
24, 257
» „ ....
>»
J)
116
Wurtz
C. E., 85, 53
32, 878
Butylchloralhydrate
C3H4C13.CH(OH)2
»)
v.t. 100 (860)
....
Cngel & Moitessier
U. E., 90, 1075
40, 407
Dichlorethyl oxide
(CH3.CHC1)2O
C4H8C12O
116-117
jieben
J., 11, 291
i., 599
,, „
))
»
15-117
....
lessel
A., 175, 46
28, 554
» »
»
5J
52(40)
Liquid
lanriot
A. C. [5], 25, 219
42, 590
)? » ••••
CH2C1.CHC1.O.C2H6
»
40-147
)arcet
A., 28, 82
i., 540
» j,
jj
))
40-147
jieben
J., 12, 446
vl., 596
>» ji
»
)>
V
Wislicenus
A., 192, 106
34, 777
Action of HC1 on aldehyde....
....
))
8-60 (40)
....
lanriot
C. E., 92, 302
40, 404
Dichlorbutylhydrin
....
J»
05-107(30)
jiquid
/jikes
M. C., 6, 348
48, 1046
Dichlorisobutylhydrin
C4HrCl(OH)Cl
»
43-5-(764)
jiquid
Ecominedes
G E., 92, 1235
40, 793
Erythrol dichlorhydrin
C4H6C12(OH)2
C4H8C1202
....
45?
)e Luynes
A. C. [4], 2, 385
vi., 583
» n ••••
CH2C1.[CH(OH)]2.CH2C1
»
....
25-125-5
••rzybytek
B., 17, 1092
46, 979
)> H
5)
»
....
24-125
M*l
J. E., 13, 171
Chloraldehyde hydrate
(CH2C1.CHO)2+H2O
C4H8C1203
5-5 cor.
3-50
Natterer
M. C., 3, 442
42, 1046
» 5» "•
)J
)>
5-100
4-75
Glinsky
Z. C., 6, 647
vii., 36
Chlorethyl oxide
CH^CHCl.O.CjH,
C4H9C1O
7-98
....
acobsen
B., 4, 215
vii., 481 ; 24,
513
„ „
»
»
05
jiquid
lenry
C. E., 100, 1007
48, 883
,. „
CH2C1.CH2.O.C2H5
ji
07-108(o.p.)
....
D
u
»
COMPOUNDS CONTAINING FOUR ELEMENTS.
365
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc
u-Chlorisobutyl alcohol
(CH3)2.CC1.CH2.OH
C4H9C1O
128-130
.<>•
Henry
B. S., 25, 23
30, 397
11 II
))
1)
137
....
Butlerow
A., 144, 26
vi., 376
Chloraldehyde alcoholate ..
CH2Cl.CH(OHXOEt)
C4H9C102
95-96
....
Jacobsen
B., 4., 216
vii., 481 ; 21,
514
ii 11
»
*1
93-95
....
A., 164, 219
Hydroxychlorethyl oxide ..
CH3Cl.OH(OH)OEt
))
151-152
Abeljanz
A., 164, 197
26, 156 ; vii.,
482
Butenylglyceryl chlorhydrin
C4H7C1(OH)2
J)
1 34-1 36 c. (28
Liquid
Zikes
M. C., 6, 348
48, 1046
>i "
11
'»
180-185
....
A. C. [3], 67, 290;
69, 339
Action of HC1 on aldehyde..
....
C4H10C1202
25 (40)
....
Hanriot
C. R, 92, 302
40, 404
Chloralide
CC13.CH.O.CO.O.CH.CC13
C5H2C1603
....
112-114
Kekul6
A., 165, 293
i., 884
11
)»
»
• ••*
112-114
Wallach
B., 6, 118
vii., 310
„
*>
?)
272-273
114-115
ii
ii
26, 627
„
Jj
)>
268 (734)
114-115
Grabowsky
B., 8, 1434
29, 551
Parachloralide
>»
182
Cloez
J., 12, 434
Pyromucyl chloride
C4H3O.COC1
C5H3C102
170
«...
Lies-Bodart
....
iv., 765
„ „
»
)J
160-180
Liquid
Wallach
B., 14, 753
40, 715
Chlorpyromecenic acid
C5H2C10.0H+H20
»
MM
174
Hilacbein
J. p. [2], 32, 129
48, 1208
Chlorcitraconic anhydride ...
....
C5H3CI03
212
98-100
....
J., 1873, 583
11 ii
>1
....
100
Gottlieb
J. p. [2], 8, 73
27, 358
Trichlorphenomalonic acid ...
CC13.CO.CH : CH.COOH
C5H3C1A
131-132
Kekule & Stfecker
A., 223, 181
46, 1122
» »
)J
))
....
131-132
Carius
A., 140, 317; 142,
129
» »
)>
»»
C6H3C1302(?
Krafft
B., 10, 798
Mesaconyl chloride
C3H4(COC1)3
CdH4Cl202
80 (17)
....
Petri
B., 14, 1635
40, 1032
Itaconyl „
»
))
89 (17)
....
ii
;i
)J
Citraconyl chloride
COC1.CH : CMe.COCl
»
83 (17)
....
11
ll
ii ii
i>
»
95 (17-5)
Liquid
Strecker
B., 15, 1640
42, 1281
ii ii
ii
»
175 d.
....
Gerhardt & Chiozza
A., 87, 294
Trichlorethylidene lactate ....
CCl3.CH.O.CHMe.COO (?)
C5H5C1303
222-224
45
....
A., 193, 36
Trichlorangelactic acid
CHC1 : CCl.CHCl.CH(OH)
)>
140
Bischoff and Pinner
B., 5, 213
vii., 400 ; 25,
COOH
486
ii ii
» »
n
cf.C5H7Cl3O3
140
n
A., 179, 99
29, 556
Acetyl trichlorlactic acid ....
Ca3.CH(OAc).COOH
C5H5C1304
....
65
Pinner and Fuchs
B. 10, 1061
Pentinic chloride
....
C5H6C120
189-191
....
Demarjay
B. S. [2], 33, 575
40, 255
11 ii ••••
»)
189-192
....
11
C. R, 88, 126
36, 458
Ethylic #-dichloracrylate ....
OC12 : CH.COOEt
C5H6C1203
173-175
Liquid
Wallach & Hunaus
B., 10, 569
32, 591
Glutaryl chloride
COC1.(CH2)3.COC1
M
216-218
Liquid
Eeboul
C. R, 82, 1502 ;
30, 508; 36,
A. C. [5], 14, 501
134
Pyrotartryl chloride
COC!.CH2.CHMe.COCl
H
190-195
Liquid
Hjelt
B., 16, 2624
46, 297
Allyl tetrachlorethyloxide ...
CC13.CHC1.OC3H5
C5H6C140
195d.
....
Oglialoro
G. I, 1874, 463
28, 878
Tetrachlorvaleric acid
C4H5C14.COOH
C5H6C1402
b.-15
Dumas and Stas
A., 35, 145
v., 978
a-chlorallylic acetate
CH2:CCl.CH2.OAc
C5H7C10,
140-145
Henry
B., 5, 454
a- ,, 11
»
»
145
ii
C. E., 95, 849
44, 173
£- 11 ii
CHCi:CH.CH2.OAc
J)
56-159
Martinoff
B., 8, 1318
29, 541
3- 11 11
J)
»
57-158
....
Henry
C. E., 95, 849
Ethylic £-chloracrylate
CHC1 : CH.COOEt
))
43-145
....
Wallach & Hunaus
B., 10, 569
32, 592
11 "
>T
))
45-146
Pinner
B. 7, 250
27, 682
11 11
»
»
45-146
Pinner & Bischoff
A., 179, 74
29, 556
Methylic a-chlorcrotonate ...
CH3.CH : CCl.COOMe
»
60-8
....
Kahlbaum
B., 12, 344
36, 521
„ j3-chlor-/3-crotonate
CH2:CCl.CH2.COOMe
))
42 c.
jiquid
Frohlich
Z. C. [2], 5, 274
vi., 512
Chlormethylcrotonic acid ...
r. CH3.CH : CMe.COOH
))
09-210
7
Demargay
C. R, 84, 1087
32, 591
11 "
M
»
9'5
Riicker
B., 10, 1954
34, 292
ii 11
)»
1)
MM
8-69
Otto and Beckurts
B., 18, 825, 847
18, 755
a-methyl-|3-chlorcrotonic acid
CH3.CCi: CMe.COOH
V
....
9-5
Friedrich
B., 15, 218
12, 945
Chlorangelic acid
Me.CCl : CH.CH2.COOH
»
03-104
Pinner and Klein
B., 11, 1499
36, 43
Ethylic malonyl chloride ..
COCl.CH2.COOEt
C6H7C103
170-180
....
Van t'Hoff
B., 7, 1572
28, 358
Chlorangelactic acid
....
ii
....
16-116-5
Pinner and Klein
B., 11, 1496
n 11 •— . »
n
...*
40
Pinner
B., 7, 589 '
27, 787
366
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Mesachloryprotartaric acid ...
...
C5H7C10<
....
129-130
Schwartz
Z. C., 1866, 724
vi., 821, 981
Itaclilorpyrotartaric acid
....
j)
225-235
140-145
11
Z. C., 1866, 721
vl., 980
Chlorcitramalic acid
....
C6H7C10S
....
100
Gottlieb
A., 160, 101
25,78
Chloritamalic acid
....
3)
....
150
Bichter
R. K. T.
Hydrochloroxycitraconicaeid
))
160-162 d.
Morawski
J. p. [2], 9, 430
28, 1253
Trichlormethy Ipropy 1 ketone
CCl3.CO.Pr
C5H-C13O
186 (753)
....
Grabowsky
B., 8, 1439
29, 557
Methyl trichlorpropy 1 ketone
CH3.CHC1.CC12.CO.CH3
»>
192
....
Thurnlackh
A., 223, 149
46, 1118
Trichlorhydroxy ethyl allyl
CC13.CH(OH).OC3H5
C^CIA
116
20-5
Oglialoro
G. I. [1874], 463
28, 878
oxide
Propylic trichloracetate
CCl3.COOPr«
))
187
Clermont
C. R, 96, 437
44, 729
Trichlorvaleric acid ....
C4H6Clj.COOH
))
....
b. — 18
Dumas and Stas
A., 35, 145
v., 978
Ethylic trichlorlactate
CCl3.CH(OH).COOEt
C5H7C1303
66-67
Bischoff and Pinner
B., 5, 218; A.,
25, 485 ; 29,
179, 83
555
Trichlorvalerolactic acid
CH2C1.(CHC1)2.CH(OH).
J)
cf.C.H^O.,
140
>!
A., 179, 99
29, 556
COOH
n 11
)?
)1
....
140
Pinner and Klein
B., 11, 1492
Glycerol acetodichlorhydrin
C3H6.Cl2(OAc)
C5H8C1A
188-190
Franchimont
B., 16, 394
11 11
)»
»
194-195
Liquid
Henry
B., 4, 704
24, 908
11 n
!»
)J
205
....
Berthelot and Luca
A- C. [3], 53, 460
i., 25
11 11
))
)>
202-203
Truchot
J., 18, 503
Ethylic a-dichlorpropionate....
CH3.UCl£.COOEt
)J
155-160
Beckurts and Otto
B., 11, 388
34, 488
11 «- ii
H
»
156-157
....
11
B., 9, 1878
32, 181
11 «- »
H
»
158
....
11
B., 9, 1E93
11 «- D
))
))
160
Liquid
Klimeuko
B., 3, 466
vii.,1012,1033
» «- 11
»
)»
155-160
....
Eichter
B., 10, 684
32, 441
11 "- 11
»
))
160
....
Beckurts and Otto
B., 10, 1952
34, 292
>! P- „
CH2Cl.CHCl.COOEt
)J
180 (750)
Henry
B., 7, 414 ; 10,
1854
» ft- 11
11
J)
183-184
Werigo & Melikoff
B., 10, 1500
34, 289
11 £• 11
11
»J
180-190
Werigo & Werner
A., 170, 163
vii., 1012 ; 27
242
11 »
....
J)
185-190
Werigo & Okulitsch
A., 167, 49
26, 1020
Chlorethylic-jS-chlorpro-
CH2C1.CH2.COO.C2H4C1
))
210-215
Liquid
Henry
C. R., 100, 114
48, 372
pionate
Ethylic dichlorlactate
....
C6H8CIS03
205-206
....
J. R., 7, 162
n 11
....
)!
219-221
....
A., 179, 88
11 11 ....
?J
219-222
....
B. S., 34, 29
a-Chlorallyl ethyl oxide
CH2 : CCl.CH2.OEt
C6H9C1O
110
Friedel and Silva
C. R., 75, 81
26, 805
11 11 11
H
11
110
....
Henry
vii., 1020
"" 11 11 11
CHC1 : CH.CH2.OEt
>J
120
....
11
B., 5, 189
vii., 50
P" 11 11 n
7>
J)
120-125
Friedel and Silva
C. R., 75, 81
25, 805
Methylchlorallyl carbinol ....
CH3.CH : CCl.CHMe.OH
))
158
Liquid
Thurnlackh
A., 223, 149
46, 1118
Acrolein+ethyl chloride ....
CH2 : CH.CClEt.OH
))
115-120
....
As., 3, 182
Isovaleryl chloride
(CH3)2.CH.CH2.COC1
>r
115-120
Bechainp
J., 9, 429
v., 979
11 11
»
ji
11 3-5-1 14-5
Briihl
A., 203, 24
Trimethacetyl chloride
CMe3.COCl
j»
105-106
Liquid
Butlerow
A., 173,373; B.,
27, 1084; 28,
7,728
250
Chlorvaleric aldehyde
CHMe2.CHCl.CHO
)i
134- 135
....
Schroader
B., 4, 402
24, 560; vii.,
-
1195
Chlorruethylisopropyl ketone
CH2Cl.CO.CHMe2
jj
120 p. d.
Etard
C. R., 84, 951
32, 427
Methylchlorpropyl ketone ....
CH,.CO.CHC1.C.,H5
))
130
....
Wislicenus and
B., 8, 1038
29, 371
Conrad
n n
»
jj
130
Liquid
Conrad
A., 186, 242
32, 436
Ethylidene propioehlorhydrin
Propylene acetochloride
CH3.CHC1.(O.C8H50)
CH3.CH(OAe).CH,Cl
C5H9C1O3
„ "(1)
135 u. c.
151 c.
Kiibenchamp
Morley and Green
A., 225, 267
47, 132
48, 136
Isobutylic chlorocarbonate ....
Cl.COO.CH,,CHMe2
11
130-1 40 p. d.
Liquid
Mylius
B., 5, 972
26, 266
11 11
>»
11
128-8 c.
Rose
A., 205, 230
40, 252
Propylic chloracetate
CH2Cl.COOPr«
n
161 (740)
....
....
A., 197, 8
11 11
Ethylic a-chlorpropionate ....
J)
CH3.CHCl.COOEt
11
11
161-162(765)
143-5
Liquid
Liquid
Henry
Briihl
C. R., 100, 114
B., 9, 35
48, 372
29, 700
11 "- „
11
11
144
Wichelhaus
A., 148, 169
vi., 900
11 a- 11
H
11
146
Briihl
A., 203, 24
COMPOUNDS CONTAINING FOUR ELEMENTS.
367
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Ethylic a-chlorpropionate ....
CH3CHCl.COOEt
C5H9C103
150
....
Wurtz
A., 107, 193,
iv., 736
„ -0-
CH2Cl.CH,.COOEt
)»
150-160
....
vi., 960
,, -0- 11
»»
))
162-163(765)
Henry
C. R, 100,114
48, 372
Glycerol aceto-ehlorhydrin ....
CH2(OAc).CHCl.CH2.OH
C5H9C1O3
230
11
J. p. [2], 10> 185,
28, 346
11 11
1?
aht. 250
....
i., 25
Ethylic /3-chlorIactate
CH2Cl.CH(OH).COOEt
)J
205 u. c.
37
Frank
A., 206, 347
40, 417
11 11 11
11
)J
160-185 (174)
Melikoff
C. C. [1881], 354
42,38
„ ?-
11
5)
144
Wurtz
J., 11, 254
„ »- „
....
»
150-160
Rudneff
B., 8, 434
Methyltrichlorpropy I carbine!
CHMeCl.CCLCHMe.OH
C5H9CI3O
123 (41)
50-5
Thurnlackh
A., 223, 149
46, 1118
Allylethyl clichlorhydrin ....
....
q,H100120
165
Markownikoff
J. [1865], 492
vi.. 99
/3-dichlorpropionic aldehyde
CILCl.CH01.eH(OH)(OEt)
C5H10C12O2
150-155
As., 3, 192
alcoholate
Amylene chlorhydrin
....
C5H,,C10
155
....
Carius
A., 126, 19»
vi., 121
Dariv. of chlorinated ether....
^)
117-118
Liebeu and Bauer
J., 15, 394
Methylethyl chloracetal
C.;H3Cl(OEt)(OMe)
C5HnC102
abt. 137
Lieben
J., 20, 546.
vi., 598
Glycerol ethoxychlorhydrin
C3H5Cl(OEt)(OH)
»
180
....
Eeboul
....
ii , 883
i) 11
11
J>
183-185
....
Henry
Z. C. [2], 6* 575 ;
vii., 49; 25,
R, 5, 449
686
11 »
11
J»
183-185 (758)
11
J. p. [2], 10, 185
28, 346
11 11
11
J)
188
....
As,, 1, 236
Allylethyl chlorhydrin
J>
220
....
J. [1872], 331
Ethylic chlorlevulinate
....
C5HHC103
225-230
Liquid
Conrad & Guthzeit
B., 17, 2287
48,43
Trichlorquinone
C6HC1302
160
Stadeler
A., 69, 327
v., 28
11
....
H
....
164-166
Stenhouse
[2], 6, 208
vi., 987
11 •••• ••••
....
»
....
165-1G6
Krafft
B., 10, 799
32, 748, 749
Pentachlorphenol
C6C16.OH
C6HC16O
....
183-184
Beilstein
B., 11, 2183
36, 463
11
»>
n
....
186
Ruoff
B., 9, 1495
"
)»
)T
....
186-187
Merz and Weith
B., 5, 458
vii., 906 ; 25,
701
Pentachlorresorcinol
c,a4(oa)(OH) =1.3
C6HC1502
92-5
Steuhouse
P. B. S., 20, 78
26, 298 ; vii.,
1042
?
....
»
65
....
A., 160, 265
Pentachlorphenol dichloride
c6ci6(OH) : ci2
c6naro
....
68-5-70
Beilstein
B., 11, 680
34, 585
11 11
n
»
78-5-80
11
B., 11, 2182
36, 463
j3-Dichlorquinone
CfrHaCUIO^ 1.3,2.5
C6H2C1202
....
119
Guareschi and Dac-
B., 18, 1170
conio
ft- ,i
i? >»
M
....
120
Armstrong
....
24, 1121
ft- „
»> r>
»»
....
120
Faust
A., 149, 153
))
ft- „ ,
n »
ji
....
120
11
Z. C. [1867], 727
vii., 1036
n- 11
=1.4.3.6
jj
....
154
Levy and Schultz
B., 13, 1428
38, 888
a- „
)) ^
»
....
150
i)
A., 210, 150 ; B.,
42, 510
18, 2367
«- 11
) »
)i
159
Schultz
B,, 15, 656
«- 11
» J»
»
....
160
Stadeler
A., 69, 309
v., 28
a- 11
»» »
>»
164
Kraffts
B., 10, 800
32, 749
Dahydromucic chloride
04H2O(COC1)2
C6H2C1203
sb. 100
80
Klinkhardt
J. p. [2], 25, 46
42, 498
Dichlorcomanic acid
C5HC1A.COOH
C6H2C1204
217
Ost
J. p., 27, 293
44, 796
11 11
}»
)»
217
11
J. p., 29, 57
48, 49
Trichloroehloroxybenzene ....
C6H2C13.OC1
C6H20140
....
119
Benedikt
M. C., 4, 233
44,985
Tetrachlorquinol
C,C14.(OH), =6.5.3.2. 4.1
C6H,,C1402
a. 220
....
iii., 216
Chlorquinone ...
C6H,C1 : 0, = i
C«H,C1O«
37-38
Schulz
B., 15, 654
6^^3 2
„ =(2 or 5).1.4
6 3 2
57
Levy and Schultz
A., 210, 144
42, 509
»»
57
B., 13, 1428
38, 888
(?)
)' »
l<
»>
....
120
11
Laubenheimer
B., 9, 770
(0
....
»
160
Stadeler
A., 69, 300
v., 28
Chlorcomauic acid
CiHjClOj COOH
C0H3C104
....
247
Ost
J. p. [2], 29, 57
48, 49
Trichlorphenol
OH.Cla — 1
C6H3C130
250
44
Laurent
iv., 393
11 •••• "•*
„ =? 3.2.1
11
248-5-249-5
54-1-54-5
Hirsch
B., 13, 1908
40, 164
u. c.
11 "••
„ = »
11
58
Piria
iv., 393
11
„ =1.2.4.6
11
67
Daccomo
B., 18, 1163
vii., 929
368
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet
& J. Ch. So<
Trichlorphenol
OH.C13=1.2.4.6
C6H3C130
244
67-68
Faust
B., 6, 136
26, 635
»
>i )>
)>
24.T5-244-5
67-6S
u
Z. C. [2], 3, 727
vi., 909
p. d.
Trichlororesorcinol
(OH)S.C13 =1.3.4 (?)s
C6H3C1302
....
69
Claasen
B., 11, 1441
34,868
„
>» 1>
JJ
....
73
Eeinhardt
J. p. [2], 17, 336
34, 727
,, .... .
» J)
>T
83
j>
))
»
,,
» 7)
»)
....
83
Benedikt
M. C., 4, 224
44, 984
Trichlorquinol
„ =1.4.2.3.5
»
a. 130 +
....
A., 69, 321
iii., 216
,,
» V*
))
....
131-132
Krafft
B., 10, 797
32, 748
?i
F
1> X
JI
133-134
n
B., 10, 797
32,748
» ....
1! I)
J>
134
....
As., 6, 214
vi., 987
Trichlorpyrogallol
(OH)3.C13=1.2.3. 4.5.6
C6H3C1303
177 d.
Webster
45, 206
i, -i-3H3O «
» »
J»
....
115
>»
»
Trichlorphloroglucol....
„ =1.3.5.2.4.6
1}
136 u.c.
j>
47, 424
Phenaconic chloride
....
H
165
....
Carius
....
vi., 905
Dichlorphenol
OH.C12=1.2.4
c6H4ca2o
209-210
4S-43
Fischer
Z. C. [2] 4, 386
vi., 908, 921
»
JI >»
j»
209-211
41-42
Chandelon
B., 16, 1749
44, 1109
«
»» >t
))
....
42-43
Beilstein and Kur
B., 10, 270
31, 706
batow
»
»» »
»
213-214
42-43
PJ
B., 8, 693
28, 1037
>T .... ...
)> )J
ji
209-210
43
Faust
B., 6, 136
26, 635
J»
)> »1
jj
210
43
Petersen
A., 157, 171
24, 251
v
J) 11
)>
cf. vii, 926
43
Post
B., 7, 332
27, 800
« .**• ....
„ =1.3.5 (?)
»
....
54-55
Hirsch
B., 11, 1982
36, 315
t*
.. = (?)
)j
213-215
»«•«
Longuinine
C. R, 86, 1392
34, 832
>» .... ....
„ =1.2.6
n
217-219
63
Chandelou
B., 16, 1752
44, 1109
» ....
»» ji
»>
cf. vii, 929
65
Post
B., 7, 332
27,800
»* ....
» »»
j)
$18-820
65
Siefart
Z. C. [2], 5, 450
vi., 909
»»
» »
H
218-220
65
Petersen
A., 157, 171
24, 251
» .... ....
» »
»j
218-220
65
Faust
B., 6, 135
26, 634
Dichlorresorcinol
(OH)2.a,!=1.3.(?)2
C6H4C1202
249
77
Keinhardt
J. p. [2], 17, 328
34, 726
)» -... ....
„ =1.3.(?)2
))
....
100
»
B., 10, 1525
34,222
Dichlorqiiinol
„ =1.4.2.6
»
....
157-158
.... •
A., 149, 154
*» ....
„ =1.4.2.5
»
164
....
....
iii., 216
)>
»< »
)»
....
164
Levy and Schultz
B., 13, 1428
38, 888
j> .. . ....
» »
»J
166
»
A., 210, 148
42, 509
» .... ....
» = (0
J»
....
172
Kraflft
B., 10, 800
32, 749
Dichlormucouic acid
C6H4C1204
w.m. 260 p.d.
Bell
B., 12, 1272
36, 917
Malic chloranilide chloride....
C6H4C1404
a. 200
....
A., 193, 44
Chlorphenol
OH.C1=1.2
C6H5C10
....
liquid
Petersen
B., 6, 368
26, 1133
» »»
ti
173
jiquid
Beilstein and Kur-
B., 7, 1398 ; A.,
28, 363
batow
176, 39
»» »»
)>
74
jiquid
ji
B., 7, 488
27, 806
» j?
H
175-176
Fischli
B., 11, 1463
34, 866
)> i»
H
75-177
'TK.K 177
....
Miiller
A. P. [3], 3, 103
27, 157
» i»
i» '»
u
jj
/ O i>— 1 i t
176
5>
ilasse
»
B., 10, 2192
»
34, 416
IT •'"
>» »
»
175-5-177
. —15
Faust and Miiller
B., 5, 777
26, 65 ; vii.,
>7V^ 177
Ai *7^ "^riQ
906
»» 17
» »>
»
jj
/ j *j — i / 1
175-5-177
nr. T QA
. —15
-liquid
j»
?aust
•j l/o, oUo
B., 6, 136
Rl t'Q
28, 156
26, 633
» )>
»
/u— loU
jiquid
scnniitt
, 1, OH
26, 634
»
J» '»
)>
180
*Yft ivyfyfin}
....
Post
B., 7, 332
A1 TO OOl
27, 800
» »
)»
/ O— L / /^/ Ot/;
iranier
., 1/0, d<3l
vii., 906, 929 ;
28, 157
>» *••> «... ....
» >1
>j
76-177
<7
Sorner
G. I., 4, 305
29, 235
» =1.3
J» .
2-T4 c.
jiquid
Beilstein and Kur-
B., 7, 1395; A.,
28, 364
n /(
batow
176, 45
» »>
»j
214
Corner
G. I., 4, 305
9, 235
>1 • ..
» »
5)
215
Q «K
jonguinine
Tl 1
C. R., 86, 1392
4, 832
JJ r>
)1
211-212 u.c.
at
Jnlemaim
B., 11, 1161
34, 978
,, =1.4
)1
218
Armstrong
....
8, 520
COMPOUNDS CONTAINING POUR ELEMENTS.
369
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Chlorphenol ....
OH.C1— 1.4
C6H5C1O
217
36
Beilstein and Kur-
B., 7, 487; A.,
27, 806 ; vii.,
,j -...
„ .... ....
11 11
11 11
7)
»»
217
220
218
37
38-5
batow
11
Bahr-Predari
Schmitt
176, 30
B., 7, 1396
Z. C. [2], 6, 246
B., 1, 68
905, 918
28, 363
vi., 908
218
Faust
B., 6, 1022
41
Beilatein and
B., 5, 478
26,72
41
Kiihlberg
Petersen
B., 6, 378
26, 1133
41
Peters,
A., 176, 186
28, 762
41
Hasse
B., 10, 2190
34, 416
218
Post
B., 7, 332
27, 800
818-219
41
Petersen & Predari
A., 157, 125
24, 241
218
41
Faust
B., 6, 136
26, 633, 634
218
41
Korner
G. I., 4, 305
20, 235
abt. 220
41
Dubois
Z. C. [2], 3, 205
vi., 908
Chlorresorcinol
Ch.lorqu.inol ....
OH.OH.C1=1.3.?
—1.4.5
C6H5C102
255-256
89
Reinhardt
Wohler
J. p. [2], 17,322
A.,51,155; 69,307
34,726
98
Levy and Schultz
B., 13, 1427
103-104
Schulz
B., 15, 654
263 p.d.
106
Levy and Schultz
A., 210, 137
42,509
Chlorniceic acid
Malic chloralide
COOH.CH,,CH.COO.
C6H5C1306
215 »
150
137-138
St. Evre
Wallach
J., 1, 529
B., 9, 1215
31,60
» »
?
Tritetrachloracetone + 6H2O
» »
a-dichlorpropionic pyruvic
anhydride
Chlorethylic crotonate
Chlorphlorone
Dimethylic chlorfumarate ....
Trichlormeaityl oxide
Ethylic trichlorcrotonate ....
Quercittrichlorhydrin
Trichlorethylidenediacetate
Trichlorphenoiualic acid
Dichlordumasin
Allylic a-dichlorpropionate ....
11 11
Manitol anhydride dichloride
Ethylic acetodichloracetate....
Ethin dichlordiacetin
Dichloradipic acid
?
Chlorethylic trichlorbutyrate
Ethylic chlormethacrylate ....
„ chlor-|3-crotonate ....
a
,, ,i ~'J~ ii
>, >i ~P~ ))
11 » ~P~ ii
» ii ~a~ ii
i) 11 -o- „
Chlorcrotylic acetate
CH(CC13).O
))
Me.CCl2.CO.O.CO.CO.Me
C3H5.COO.CHC1.CH3
C2HCl(COOMe)2
CC13.CH : CH.COOEt
CCl3.CH(OAc)2
CH3.CC3j.COO.C3H5
c6H8o2.ci2
OH3.CO.CCl2.COOEt
C2H2(OCl)2(OAc)2
COOH.CClMe.CClMe.COOH
CCl2:C(OEt)(OC2H3Cl,,)
C3H4C13.COO.CHC1.CH3
fr. CH2:CMe.COOEt
CH2:CCl.CH2.COOEt
ii
fr. CH2:CH.CH2.COOEt
fr.CHj.CH: CH.COOEt
»
CH,Cl.CH:CH.CH2.OAc
C^CIA
C6H5C1702
11
C6H6C12O4
C6H6C1403
C6H7C102
C6H7C104
C6H7C130
C6H7C13O2
c6H7ci3o4
C6H7C130S
0^0,0
(W3A
)»
C6H8C1203
C6HSC1204
})
C6H8C14O3
C.H/310,
J)
»
n
»
T»
i»
it
160-170
220
223-225
206-208
212
221-222 u.c.
150-155
176-178 d.
215-220
143 (43)
205-207
120 (20)
153-159
220
155-158
161-4
184 c.
176
176-178
168-169 c.
(741-1)
139-140
129
30-32
35
Liquid
Liquid
b. 100
Liquid
Liquid
155
Liquid
131-132
49
Liquid
185
Liquid
Liquid
159 u. c.
160-5
Liquid
Liquid
Liquid
Liquid
Grabowsky
Biachoff
Bouis
Beckurts and Otto
Pinner
Bad
Kauder
Grabowsky
Judson
Meyer and Dulk
Carius
Beckurts and Otto
Fauconnier
Conrad
Prudhomme
Beckurts and Otto
Friedel
Morawaky
Claus and Lischke
Geuther
Frohlich
Geuther
Sarnow
Thurnlackh
A., 193, 42
B., 6, 1071
B., 8, 1341
A. C., 21, 111
B., 18, 234
A., 179, 21
A., 151, 158
J. p. [21 31, 1
B., 8, 1441
Z. C. [2], 7, 40
A. C. [5], 15, 56
B., 4, 966 ; A.,
171, 73
A., 142, 140
A., 110, 22
B., 9, 1878
A., 167, 230
C. E., 95, 991
A., 186, 234
C. E., 70, 1137
B., 10, 1503 ; 18,
847
C. C., 1875, 514 ;
B., 8, 642
A., 179, 41
C. C. [1877], 131
B., 14, 1089
Z. C. [2], 5, 273
J. p. [2], 3, 431
B., 5, 469
A., 164, 101; 173,
301
A., 213, 379
27,46
29, 559
48, 507
29, 549
vi., 929
48, 652
29, 557
24, 233; vii.,
398
vii., 312; 25,
247; 27,461
vi., 918
ii., 351
32, 181
44,306
32, 436
vii., 11
34, 290; 48,
754
30,66
34, 213
vi., 512
24, 814
vii., 398
25, 690
42, 1279
3 B
370
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Chlorvinyl dimethylacetic
CH2:CCl.CMe2.COOH
C6H9C102
....
63-64
Demarcay
C. R., 84, 1087
32, 591
acid
Chlorethyl-crotonic acid
C,H4C1.C3H4.COOH
„
74-75
„
„
„
Ethylic acetochloracetate ...
CH3.CO.CHCl.COOEt
c6H9ao3
193-195
Liquid
Allihn
B., 11, 569
34, 566
Trichlorcaproic aldehyde ...
C6H3C13.CHO
C6H9C130
212-214
Liquid
Pinner
B., 10, 1053
32, 586
„ „
„
„
215-220
„
B., 8, 1321
29, 554
Isobutylic trichloracetate ...
CCl3.COO.CH2.CHMe2
C6H9C1302
187-189
....
Judson
B., 3, 784
vii., 10
Trichlorbutylic acetate
C3H4Cl3.CH2.OAc
„
130-132 (70)
Liquid
Thurnlackh
B., 14, 2759
42, 824
» .,
„
„
131-132 (70)
....
„
A., 213, 373
42, 1279
» >i
„
„
217-5 (730)
....
„
„
,,
Trichlorcaproic acid
C6H8C13.COOH
„
....
64
Pinner
B., 10, 1054
32, 587
Trichlorhydroquercite
MM
„
....
155
Prunier
A. C. [5], 15, 5 ;
36, 241 ; 34,
C. R., 86, 338
400
Chloral ethylate acetate
CCl3.CH(OEt)(OAc)
C6H9C1303
198 u.c.
....
Meyer and Bulk
B., 4, 965 ; A.,
vii., 314 ; 25,
171, 70
247 ; 27, 461
Phenose trichlorhydrin
„
10
A., 136, 324
Pentachloracetal
CCl3.CH(OEt)(OC2H3Cl3)
C6H9C1502
186-189
Friedel
C. C. [1875], 514
30, 66
?- alcohol
(CH2)2.CH(CH2C1).CC1.CH2.
C6H10C120
115-119(20)
Liquid
Natterer
M. C., 5, 567
48, 497
OH
Leucic chloride
....
,,
90-100
....
Lippmann
A., 129, 81
vi., 118
Dichlorpinacolin
JJ
178
51
Fittig
A., 114, 61
iv., 647
Isobutylic dichloracetate ....
CHC]2.COO.CH2.CHMe2
C,H10C1202
182-184
Wallach
A., 173, 300
28, 351
Metacrolein dihydrochloride
C6H802-2HC1
„ (?)
....
50
Geuther&Cartmell
i., 57
Ethylic dichlorhydroxyiso-
CHCl2.CMe(OH).COOEt
C6H10C1203
208-215 p.d.
....
Bischoff
B., 8, 1336
29, 558
butyrate
» »
(CH2C1)2 : C(OH).COOEt
„
225-230
Liquid
Kelly
B., 11, 2223
36, 306
Chlorhexylene alcohol
C6H10C1.0H
c6Huao
165-168
Liquid
Natterer
M. C., 5, 567
48, 498
» ,.
CH2C1.CH(OH).CHS.C3H5 or
„
183-187
Liquid
Lopatkin
J. p. [2], 30, 389
48, 497
CH2Cl.CH(C3H6).CHj.OH
» »
„
185-187
Destrem
B., 16, 228
Allylethyl chlorcarbinol
C3H6.CClEt.OH
„
133-135
....
....
A., 162, 99
Capronyl chloride
CH3.(CH2)4.COC1
„
136-140
..-.
A., 130, 364
Diemethylethylacetyl chlo-
CMe2Et.COCl
„
132
....
Wischnegradsky
B., 8, 541
28, 878
ride
1
....
„
145-150
....
Etard
B., 10, 236
?
....
„
150
....
„
C. R., 84, 127
31, 585
Ethylene butyrochlorhydrin
CH2C1.CH2(O.C4H7O)
C6HnClO,
190
....
Simpson
A., 113, 119
ii., 571
Ethylidene „
CH3.CHC1.(O.C4H,O)
„
149 u.c.
....
RUbencamp
A., 225, 267
48, 136
Isoamylic chlorocarbonate ....
Cl.COO.C5Hn
„
154-3 c.
....
Rose
A., 205, 230
40, 252
Ethylic a-chlorbutyrate
CH3.CHj.CHCl.COOEt
„
156-160
Markownikoff
A., 153, 241
„ ft- „
CH3.CHCl.CHj.COOEt
i»
150-160
....
Hemilian
B., 6, 562
26, 1021
>> P- ji
1)
„
168-169
....
....
J. R., 11, 252
„ p- „
n
„
168-169(741)
1. —20
Balbiano
B., 10, 1749;
34, 134, 658
G. I., 8, 90
„ o-chlorisobutyrate ....
Me2Ca.COOEt
„
148-5-149-5
Liquid
M
G. I., 8, 371
36, 615
c. (749)
Chloraldehyde ethylateacetate
CH2Cl.CH(OEt)(OAc)
C6HuClO3
170
....
....
A., 134, 176
Dulcitol chlorhydrin
C6H7(OH)4C1
CA.CIO,
90
....
A. C. [4], 27, 178
Quereitol chlorhydrin
C6H7(OH)4C1
M
198-S02
Prunier
A. C. [5], 15, 54
36, 241
» „
it
n
....
198-200
C. R., 86, 338
34,400
Trichloracetal
CCl3.CH(OEt)2
C,HUC1S02
197
Liquid
Byasson
C. R., 87, 26
34, 967
"
"
"
199-201 ;
Liquid
Wurtz and Vogt
C. R., 74, 277
vii., 2
H
„
199-201 ;
....
Paternd and Pisati
G. I., 2, 333
26, 158
204-8 c.
(758-9)
»
n
„
230
....
Henry
B., 4, 101
24, 255 ; vii.,
314
„ (polymer?) ....
Ca3.CH(OEt)2
,,
230 p.d.
72
Paternd
C. R., 67, 765
vi., 4 ; vii., 2
" »
n
„
72-74
Paternd and Pisati
G. I., 2, 333
26, 158
» »
JJ
83
Krey
J. Z., 10, 84
31, 295
Dichlorhexyl alcohol
....
C6H12C12O
205-210
....
Destrem
B., 16, 228
COMPOUNDS CONTAINING FOUR ELEMENTS.
371
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Dichloracetal . ....
CHCl2.CH(OEt)2
C6H,oCLO0
abt. 180
Lieben
J., 10, 436
i., 5
180
Krey
J. Z., 10, 84
31, 295
"
183-184
./
A., vols. 149, 150,
and 179
180-187
Jacobsen
B., 4, 217
"
186
Jacobsen and Neu-
B., 15, 600
"
meister
185-190
Goldberg
Jp. [21 24, 100
42, 28
Diglycerol dichlorhydrin ....
c6H10a2o3
230-235
jr t Ji *
A. C. [3], 67, 303
Mannitol dichlorhydrin
C6H8C12(OH)4
C6H12C1204
174 d.
Bouchardat
C. R., 75, 1187 ;
vii., 774 ; 26,
A. C. [4], 27, 174
161
Hexylene chlorhydrin
C,;H12CLOH
C6H13C10
Liquid
Domac
M. C., 2, 319
40, 1114
„ a-chlorhydrin
CHMe(OH).CHCl.CH2.Et
„
abt. 170
Liquid
Henry
C. R., 97, 261
46, 34
„ /3- „
CHMeCl.CH(OH).CH2.Et
.,
170-171(761)
Liquid
„
„
„
Tetramethylethylene chlor-
CMe2a.CMe2.OH
„
....
55
Eltekoff
B., 16, 399
44, 567
hydrin
Ethylchlorbutyl oxide
Et.O.C2H3Cl.Et
ji
137
Lieben and Bauer
J., 15, 393
vi., 597
» ,,
JI
„
141
A., 123,133; 133,
288
Chloracetal
CH2Cl.CH(OEt)2
C6H13C1O2
155
Liebeu
i., 5
150-160
J., 10, 437
"
150-160
Goldberg
J. P. [2], 24, 98
42, 28
Ji
155
Klien
J. Z., 10, 67
31, 291
5?
"
156-8 c.
Paterno & JMazzara
G. I., 3, 254
26, 1217
T>
154-159
TCrev
J. Z., 10, 84
31, 295
Ethoxyethyl chlorethyl oxide
D
C2H4Cl.O.C2H4.OEt
)5
159
..AV.J
Lieben
A., 133, 287
iv., 288
!. » ,1
CHMeCl.O.CHMe.OEt
)J
146
Liquid
Hanriot
A. C. [5], 25, 219
42, 590
Triethyleneglycol chlorhydrin
....
C6H13C103
222-223
A. C. [3], 67, 292
Diglycerol chlorhydrin
....
C6H13C104
270
A. C. [3], 67, 303
Trichlorbenzoyl chloride
C6H2C13.COC1 =5.4.3.1
C7H2C14O
36
Salkowsky
A., 163, 32
vii., 164 ; 26,
715
•J 5J
=6.4.2.1
„
272
abt. 41
Beilstein and Kiihl-
A., 152, 238
vi., 313
berg
Tetrachlorbenzoic acid
COOH.C14 =1.2.3.4.6
C7H2C14O2
187
„
A., 152, 245
33
Chlormeeenic acid
HO.C5C10(COOH)3
C7H3C106
+H20
165 d.
Hilsebein
J. p. [2], 32, 129
48, 1202
Dichlorbenzoyl chloride
C6F3C12.COC1 =4.3.1
c7H3a3o
242
Beilstein and Kiihl-
A., 152, 228
vi., 312
berg
» »
=6.2.1
5)
244
Liquid
Schultz
A., 187, 273
32, 782
/3-Trichlorbenzaldehyde
CCH2C13.CHO= 2
„
90
Seelig
B., 18, 425
48, 770
a- „
=6.4.2.1
„
112-113
„
„
„
a- „
= „
J)
110-111
Beilstein and Kiihl-
A., 152, 238
berg
0-Trichlorbenzoic acid
OOOH.C13 = 2
c7H3a3o2
129
Seelig
B., 18, 425
48, 770
1) !>
=1.2.4.6
„
....
160
Janasch
Z. C. [2], 3, 404
ii., 313
„
„ „
.,
168
Beilstein and Kiihl-
A., 152, 234
vi., 313; 24,
berg
555
» »
=1.3.4.5
„
203
Salkowsky
B., 4, 224
25, 715
)) J)
11 J>
3J
SOS
51
A., 163, 33
vii., 164
Pentachlorbenzyl alcohol ....
CeCl^.CH^OH
C7H3C160
193
Beilstein and Kiihl-
A., 152, 246
vi., 335
berg
Pentuchlororcin
....
C7H3C1502
....
120-5
Stenhouse
P. R. S., 20, 72 ;
25, 297 ; vii.,
A., 163, 175 ;
878.
169, 265
Chlorbenzoyl chloride
CeH4Cl.COCl =1.4
C7H4C12O
220-222
Liquid
Emmerling
B., 8, 881
28, 1261
» „
=1.3
.,
225
....
Limpricht & Uslar
A., 102, 263
i., 567
i, „
=1.2
3»
235-238
Liquid
Emmerling
33.J 8, 883
28, 1261
» „
= »
3,
285
....
Limpricht & Uslar
A., 102, 262
i., 567
Dichlorbenzaldehyde
C6H3C12.CHO =4.2.1 (?)
„
230-233
57-58 u.c.
Gnehm
B., 17, 753
46, 1028
i> ....
=4.3.1
3»
....
68
Beilstein and Kiihl-
A., 152, 228
berg
-
3 B2
372
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Dichlorbenzaldehyde
C6H3Cl5.CHO =5.3.1
C-H4C13O
65-65-5
Gabriel
B., 15, 2001
Dichlorsalicylaldehyde
C6H2Clj.OH.CHO =(?)2.2.1
C7H4C1203
25
Lowig
P. A., 36, 383
v., 171
Dichlorbenzoic acid
COOH.Clj =1.2.6
JJ
....
122
Arouheim & Die trie!
B., 8, 1404
20, 392
jj jj ••••
jj jj
J»
....
126-5
Schultz
A., 187, 270
32, 782
j» »
„ =1.2.3 or 4 or 5
JJ
....
150
Wilkins and Hack
A., 222, 166
46, 602
„ ,, ....
jj »
JJ
301
150
Beilstein
B., 8, 814, 925
28, 1194
i) j)
jj jj
JJ
abt. SOI
150
j»
A., 179, 287
29, 252, 587
I) )!
jj »
JJ
....
152
Gnehm
B., 17, 753
46, 1028
}, jj
jj jj
JJ
....
155-156
Claus
B., 8., 949
)» )) "••
jj «
J>
....
156
jj
B., 6, 722
26, 1141
)) )) ••••
jj jj
Ji
....
156
Claus and Pfeifer
B.j 5, 658
29, 252
,, „
jj i>
JJ
....
156
Schultz
A., 187, 268
32, 782
j, jj ....
= 1.3.4
JJ
....
196-197
Otto
A., 122, 147
vil., 163
)l JJ ••••
» jj
»
....
SOI
Beilstein and Kiihl
Z. C. [2], 5, 180
vi., 312 ;
berg
Z. C. [2] 6, 417
vii., 163
JJ JJ •••• ••
jj u
JJ
201
Claus
B., 6, 723
26, 1141
JJ »
jj u
JJ
....
201
Beilstein
B., 8, 924
29, 252
JJ JJ ••••
jj jj
JJ
201
Doebner
B., 9, 130
29, 932
» ))
jj u
J)
....
201
Schultz
A., 187, 268
32, 782
Dichlorsalicylic acid
COOH.OH.C1, = 1.2.3.5
C7H4C1203
....
214
Loxner
J. p. [2], 13, 430
JJ JJ ••••
u jj
))
....
214
Rogers
T. D. Gottigen
1875
1> )) ••••
u »
»
....
914
Smith
B., 11, 1226
34,879
JJ )) ••••
= 1.2.(»),
J)
224
u
B., 11, 1225
JJ
Dichlorhydroxybenzoic acid
= 1.4.(%
JJ
156 u. c.
Claus and Eeimann
B., 16, 1600
44, 1112
JJ JJ
» »)
)>
255-256
Loxner
J. p. [2J, 13, 434
30, 283
Dichlorhydroiytoluquinone
Me.Cl2.OH : O2 = ?.C02.1.2.5
JJ
....
157
Steuhouse & Groves
B., 13, 1306
Chlorbenzotrichloride
C6H4C1.CC13==1.4
c7H4a4o
240-260
•Ml
Klepl
J. p., 28, 193
46,447
Tetrachlorcresol
CH3.OH.CI4 = 1.3.2.4.5.6
»
150
Lallemand
J. [1856], 621
v., 795
Pentachlororcinhypochlorite
C7H3C1!)O2.HC1O.
C7H4C1603
....
140-5
Stenhouse
P. R, 20, 72
25, 297
A., 163, 181
vii., 878
Benzoyl chloride
c6H5.coci
C7H6C10
196
MM
....
A., 98, 235
i., 566
» »
jj
J)
....
— 1
Lieben
A., 178, 43
29,80
» )>
j»
)>
195
....
Malaguti
A. C. [2], 70, 376
» »
M
)J
196-1
....
Schall
B., 17, 2203
D jj
j)
J»
195-200
....
Uahours
J., 1, 532
» JJ "••
>J
ij
198
....
Sarnitzky
G. J. G, 1864
» »
tj
JJ
198
....
D. P., 256, 144
48, 944
„ ,,
JJ
n
198-198-3
....
Kopp
A. [1855]
jj jj — • •»•»
)J
jj
198-7
....
Buff
....
44, 990
Chlorbenzaldehyde
C6H4C1.CHO = 1.2
j)
210-220
Liquid
Henry
J., 22, 509
„
= 1.3
jj
206
Liquid
MUller
D. P., 255, 356
48, 850
„
= 1.4
j>
210-220
Berlin
A., 151, 140
vi., 329
}) .... ....
JJ JJ
M
210-213
••••
Sintenis
B., 4, 699
jj
JJ »
9}
....
47-5
rackson and White
B., 11, 1043
34, 729
Chlorbenzoic acid
COOH.a = 1.2
C.H5C102
....
130
Chiozza
A. C. [3], 36, 102
i., 555
» H
JJ J>
jj
....
136-5
jellmann
B., 17, 536
46, 1133
,, „
JJ JJ
»
....
137
3eilsteiu and Schlun
J. [1865], 330
vi., 311
JJ »)
JJ JJ
jj
....
137
'etersen
B., 6, 368
26, 1133
» j)
JJ JJ
jj
....
137
{ichter
B., 4, 463
JJ JJ
JJ JJ
jj
....
140
Limpricht & Uslar
A., 102, 264
.,555
„ „
JJ JJ
jj
....
140
f olbe & Lautemann
A., 115, 183
vi., 311
» J)
= 1-3
jj
....
151
Wroblewsky
Z. C. [2], 5, 460
jj
JJ »
J> JJ
jj
....
152
lichter
B., 4, 463
jj jj ....
JJ JJ
jj
....
152-5
Jeilsteinand Schlun
J. [1865], 330
v., 341
jj jj
>! !>
jj
....
153
'etersen
B., 6, 368
6, 1133
jj jj
JJ JJ
jj
....
153
lubner
A., 222, 67
46, 315
jj „
JJ JJ
jj
....
153
'aternci
G. I., 11, 90
0, 598
,, ,,
„ = 1.4
jj
233
ackson and Field
A. C. J., 2, 85
0, 803
j, j,
" !!
n
233-234
ackson and White
B., 11, 1043
4,729
jj jj
55 JJ
'j
234
Dmmerling
B., 8, 880
8, 1261
jj j, .... ....
JI JJ
jj
.... i
235
MUller
Z. C. [2], 5, 137
i., 311
COMPOUNDS CONTAINING FOUR ELEMENTS.
373
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Chlorbenzoic acid
COOH.C1=1.4
C7H5C1O2
235-236
Beilstein & Geitner
A., 139, 336
„ „
j> >i
J)
236
Beilstein and Schlun
J. [1865], 330
iv., 341
» >j
JJ JJ
Jl
236
Paternd
G. L, 11, 90
40, 598
,, ,,
J) JJ
J)
237
Petersen
B., 6, 368
26, 1133
» »
5J JJ
1>
....
252 (sic.)
Michaelis & Panek
B., 14, 408
40, 604
Chlorhydroxybenzaldehyde
CHO.OH.C1=1.4.?
)>
148-149
Herzfeld
B., 10, 2196
34, 423
Chlorhydroxybenzoic acid ...
COOH.OH.C1=1.2.5
C7H5C103
....
163
Lossuer
J. p. [2], 13, 418
30, 282
» jj
J» JJ
jj
....
167-168
Hasse
B., 10, 2190
34, 416
» »
J» JJ
)>
....
167-5
Beilstein
B., 8, 816
» i>
JJ )»
»
170-171
Hubner and Weiss
B., 6, 175
i) »
JJ >J
jj
....
172
Smith
B., 11, 1227
34, 879
jj i> —
)J »
j»
....
172-5
Hubner & Brenken
B., 6, 174
26, 756
» !)
=1.4.3
»
....
164-165
Hasse
B., 10, 2192
34, 416
JJ »
JJ U
)j
....
169-170
Lossner
J. p. [2], 13, 432
30, 283
J) JJ
J» JJ
ji
....
187-5-188
Peltzer
A., 146, 287
vl., 900
Chlordihydromecenic acid ...
HO.C5H2C10(COOH)2
c,H5ao6
....
145 p.d.
Hilsebein
J. p. [2], 32, 129
48, 1203
Trichlorcresol
CH3.OH.C13=1.3.(?)3
C.H5C130
270
96
....
J., 1856, 620
Trichlororcinol
Me.(OH),.Cl3= ?
CjSjcsA
....
123
Stenhouse
P. K., 20, 72
26, 297 ; vli.,
878
159 or 59 ?
Eichter
E. K T., 140
iv., 214
Triehlortoluquinol
» »
t)
197
A., 172, 211
„
=1.2.(?)
:j
....
211-212
South-worth
A., 168, 275
27, 62 ; vi.,
1106
„
JJ >J
JJ
....
211-212
Glaus and Eiemann
B., 16, 1602
44, 1112
Hydroxybenzaldichloride ....
C6H4.OH.CHC12=1.2
C;H6C12O
82
Henry
Z. C. [2], 5, 371
vi., 507
Dichlorbenzyl alcohol
C6HjClj.CHO=1.4.6
)J
....
77
A., 147, 351
vi., 335
C6H2.Me.OH.a2=1.4.(?)j
39 u.c; 42 u.c
Glaus and Riemann
B., 16, 1599
44, 1112
jj .... .... ....
=1.2.(?)2
JJ
n
I
55 u.c.
jj
B., 16, 1601
44, 1112
Dichlortolu-o-quinol
C6HCl,,Me.(OH)s
c7H6a2o2
119-121
Southworth
A., 168, 274
27,62
„ -m- jj
JJ
)J
167-169
A., 168, 271
Trichlorvalerolactinic chloral-
....
C7H6C1603
295-299
87-88
....
A., 193, 37
ide
Trichlorlactic-butyrchloralide
....
)>
106-107
....
A., 193, 47
Chlorbenzyl alcohol ....
C6H4.(CH,OH).C1=1.4
C7H7C1O
....
66
Beilstein and Kiihl-
A, 147, 344
vi., 335
berg
)> »
» »
n
....
70-5
Jackson and Field
A. C. J. [2], 88
40, 806
Chlormethoxybenzene
C6H4CI.OMe=1.4
JJ
abt. 200 u.c.
Liquid
Henry
B., 2, 711
vi., 916
»
Jj JJ
>J
198-S02
L— 18
Beilstein and Kur-
B., 7, 1396
vii., 905 ; 28,
batow
363
jj
» JJ
))
190-193
....
Herold
B., 15, 1687
42, 1287
C6H3Me.OH.Cl:=1.4.?
abt. 240
56
Biedermann
B., 6, 326
26, 898
Chlorterebilic acid
CMe2.O.CO.CCl : C.COOH
c7H7ao4
200-203
Roser
A., 220, 254
46, 460
i i
Methylic malic chloralide ....
c7H7a,o6
....
85
....
A., 193, 45
Oxyheptic dichloride
....
C7H8C1S0
21 d. (sic)
Demarcay
C. E., 86, 1138
34,662
Chlorterebic acid
....
C7H8C1O4
....
168 d.
Frost
A., 226, 363
48, 393
jj jj •••• ••••
....
)>
....
160-170
Eoser
B., 15, 296
„ „
CMe2.COO.CH2.CCl.COOH
JJ
189-5-190
Williams
B., 6, 1097
27,72
i i
,, ,, ....
jj
JJ
191
Eoser
B., 15, 296
Acetchloral allylate
CCl3.CH(OAc).O.C3H6
C7H9C13O3
105-107
Liquid
Oliveri
G. L, 14, 13
46, 1118
Lactic butyrchloralide
....
J>
260-262
....
....
A., 193, 47
Acetyltrichlorvalerolactinic
C4H6Cl3(OAc).COOH
C7H9C1304
+H20
84
Pinner and Klein
B., 11, 1492
acid
Pimelic chloride
C5H10(OOC1)2
C7H10C130S
210 p.d.
....
Kachler
A., 169, 173
27, 155
Acrolein acetyl chloride
C3H40.2C2H3OC1
C7H10C1203
140-145
....
Arontein
As., 3, 184
vl., 56
Methylchlorallylcarbinol
CHMe : CCl.CHMe.OAc
C7HUC103
172
....
Thurnlackh
A., 223, 149
46, 1118
acetate
Ethylchlormethyl crotonate
fr. CH3.CH ; CMe.COOEt
J)
173-157
....
Eiicker
B., 10, 1954
34, 292
j> jj
jj
5>
178-180
....
Demarcay
C. E., 84, 1087
32, 591
Chloriapropylcrotonic acid ...
))
s. —25
jj
jj
jj
Chlorpropylcro tonic acid
JJ
....
Liquid —28
jj
u
j»
374
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soo.
Ethylic chlorangelactate ...
C4H9C10.COOEt
C7HUC103
230 d.
Liquid
Pinner and Klein
B., 11, 1497
36,42
Diethylic chlorraalonate
CHCl(COOEt)2
C-HnClO,
220-5-221-5
....
A., 209, 221
» , »
»
>»
221—292
Liquid
Conrad & Bischoff
B., 13, 600
38, 629
Glycerol diacetochlorhydrin
C3H5.Cl(OAc)2
»»
abt. 245
Berthelot & Luca
A. C. [3], 53, 433
i., 26
)» »
»
)J
245
cf. B, 16, 394
Truchot
J., 18, 503
Trichlordiisopropylketone ...
....
C7H,,C130
228-229
Liquid
Barbaglia & Gucci
B., 13, 1571
40,34
Amylic trichloracetate
CC13. COOCjH ! i
C7HnCl302
217
Clermonfc
C. R., 96, 437
44, 729
Methyltrichlorpropylcarbinol
CHMeCl.CCl2.CHMe.OAc
)I
227
Liquid
Thurnlackh
A., 223, 149
46, 1118
acetate
Ethylic trichlorhydroxy-
C4H5Cl3(OH).COOEt
c7Hua3o3
225
40
Pinner and Klein
B., 11, 1492
36,42
valerate
Dichlordiisopropyl ketoue ....
C7H12C12O
175-176
Liquid
Barbaglia & Gucci
B., 13, 1571
40, 34
Glycerol butyro-dichlorhydrin
C3H5C12(OC4H70)
07H12C1202
226-227(738
Truchot
A., 138, 298
....
Isobutylica-diehlorpropionate
CH3.CCl2.COOBu3
)J
183-185
....
Backunts and Otto
B., 9, 1879
32, 181
Chlordi-isopropyl ketoue ...
....
c7H:l3cio
141-142
Liquid
Barbaglia and Gucc
B., 13, 1570
40, 34
Chlorethylic valerate
C4H9.COO.CHC1.CH3
C7H13C102
118-128 d.
....
Simpson
P. E. S., 27, 120
38, 459
Ethylidene valerochlorhydrin
CH3.CHC1.O.C5H9O
It
162 u. c.
Eubencamp
A., 225, 267
48, 136
Chloral iso-amylate
CC13.CH(OH)(OC5H,,)
C7H13C1302
143
s. 25
Bartholdy & Martius
B., 3, 443
vii., 314
)> »
....
»
14S-147
50
Jacobsen
A., 157, 244
24, 257
Heytylene chlorhydrin
C7H14C1.OH
C7H15C10
206-208
Clermoiit
B. S. [2], 13, 404
vii., (544, 868
Glycerol diethyl chlorhydrin
C3H5Cl(OEt)2
C,H15C1O2
184
Eeboul & Loureii9o
A., 119, 237
Trichlor-phthalic anhydride
o : (co)2 : c6HCi3=i.2.3.4 ?
CgHCl303
157
Claus and Kautz
B., 18, 1370
48, 972
>» »
» »
)>
....
157
Atterberg& Widman
B., 10, 1843
34, 322
t
/
C8HC11304
115-120
Cahours
A., 67, 29
v., 463
Dichlor-phthalic anhydride
o : (co)3 : c6H2ci2=i.2.(?)2
C8H2C1203
185-186
Atterberg
B., 10, 547
32, 623
» j>
»» »J
5»
187
Faust
A., 160, 64
25, 76; vii., 978
Tetrachlor-phthalic acid
(COOH)2.C14=1.2.3.4.5.6
CSH.2C1404
250
Claus and Spruck
B., 15, 1404
Chlorphthalic anhydride
o : (C02) : c6H3ci=i.2.4
C3H3C1O3
89
Cleve
B. S. [2], 29, 499
34, 736
n »
>! !>
))
....
95
Alen
B. S. [2], 36, 434
43, 409
n ,1
" ')
)»
95 u. c.
Claus and Dehne
B., 15, 320
» ;>
1» »
1)
95
Kriiger
B., 18, 1759
48, 1053
It „
= 1.2.3
n
122
j»
)«
15
)J v
>1 »
)i
140-143 (?)
J., 1880, 862
Phthalic chloride
C6H4(COC1)2=1.2
C8H4CL02
268
s. 0
Wischin
A., 143, 260
vi., 944
„ „
*> '»
»»
268
Liquid
Schreder
B., 7, 705
27, 990
„ „
1» 11
H
270
8.0
Miiller
Z.C.P.[1863],257
iv., 633
» » .•" "••
11 11
i)
270
Liquid
Ad or
A. C. [4], 26, 41 7;
vii., 979 ; 26,
A., 164, 229
66, 392
„ „
)) 11
i>
270
Piccard
B., 7, 1785
28, 570
Isophthalic chloride
=1.3
j>
276
41
Schreder
B., 7, 708
27, 991
Terephthalic chloride
=1.4
)5
259 u.c.
77
Berger
B., 10, 1743
>» » ••••
» ))
))
....
78
Schreder
B., 7, 708
27, 991
Dichlorpiperonal .... „.
C6H3C12.O.CO.CHO
C8H4C1203
90
A., 159, 147
Dichlorphthalic acid
C6H2C12.(COOH)2=(?)2.2.1
C8H4C1204
....
183-185
Faust
A., 160, 64
25, 76; vii., 978
» )>
!> »
J»
• ••»
183
Claus and Kautz
B., 18, 1370
48, 972
/3-phthalide chloride
C6H4.CC13.COC1=1.2
C8H4C140
262 p.d.
47
Gerichten
B., 13, 419
38, 474
°- » «
c6H4:(cci2)2: 0=1.2
))
275 p.d.
88
))
B., 13, 418
38, 473
Dichlorpiperonal chloride ....
C6H3C12.O.CO.CHC12
C8H4C1403
abt. 280 d.
Liquid
A., 159, 147
vi., 948
Tartaric chloralide
[.CH.COO.CH(CC13).O]2
C8H4C1606
122-124
Wallach
B., 9, 1215
31, 60
Chlorphthalic acid
(COOH)2.C1=1.2.4
C8H5C1O4
....
130-134
Kruger
B., 18, 1759
48, 1053
»» „ ....
» »
»»
148
Claus and Dehne
B., 15, 320
sj j>
» »
i»
149-150
Al&n
B. S. [2], 36, 434
» ji ....
=1.2.3
))
....
179-181
Kriiger
B., 18, 1759
48, 1053
Chlorisophthalic acid
=1.3.5
;»
27S
Beyer
J. p. [2], 25, 506
42, 1296
Trichloracetoxybenzene
OAc.Cl3=1.2.4.6(?)
CsHsCljO,
261-262
As., 7, 184
Dichloracetophenone
C8H6C120
250-255
Dyckerhoff
B., 10, 532
32, 481
Fi-om polyporic acid
)»
109
Stalilschmidt
A., 195, 365
36, 383
Dehydracetyl chloride
C.HiClA
101
Precht
B., 9, 1100
30, 506
Piperonal dichloride
C0H5.O.CO.CHC1.,
)>
230-240 d.
Liquid
Fittig and Eemsen
Z. C. [2], 6, 97 ;
vi., 948 ; 24,
A., 159, 147
938
COMPOUNDS CONTAINING FOUR ELEMENTS.
375
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Phenyl dichloracetic acid ....
Ph.CCl2.COOH
OSH.CIA
50-55 d.
Claisen
B., 12, 631
JJ JJ JJ
1)
H
69
Radziszewski
B., 2, 209
vi., 1102
Dichloracetoxybenzene
OAc.Cl2=1.2.4
n
244-245
....
A., 23, 60; As., 7,
184
Dichlortoluic acid
Me.COOH.Cl2=1.3(?),
j»
160-161
....
A., 144, 269
Dichlorxyloquinone
C6Me,Cl2:O2
»»
175
Carstanjeii
J. p. [2], 23, 432
42, 612
Methylic dichlorsalicylate ....
OH.COOMe.CL=1.2.(2)2
C3H6C1203
..:.
142
Smith
B., 11, 1226
....
Dichlormethsalicylic acid ....
OMe.COOH.Cl3=1.2.(?)
)I
....
abt. 100
Cahours
A. C. [3], 10, 343
v., 163
» »
)J JJ
)»
104
Procter
J. Ph. [3], 3, 257
JJ
Dichloranisic acid
OMe.COOH.Cl2=1.4.(?)
))
196
Reincecke
B. S. [2], 7, 177
vi., 173
Tetrachlor-/3-oreinol
C6Me2Cl2(OCl)2
C3H6C1402
109 or 190
Stenhouse& Groves
A., 203, 291
37, 399
Tetrachlordimethylquinol ....
C6Cl4(OMe)2
»
153-154
Habermaiin
B., 11, 1035
34,728
Chloracetophenone
Ph.CO.CH2Cl
C9H7C1O
246
41
Graebe
B., 4, 35
24, 222
jj
1)
»
344-245 u.c.
58-59
Staedel
B., 10, 1830
34, 419
Acetochlorpheaone
C6H4C1(CO.CH3) = 1.4
J)
230-231
20
Gautier
B. S., 43, 602
48, 1061
Toluyl chloride
CcH4Me.COCl = 1.2
1»
211 (733)
....
Ador and Rilliet
B., 12, 2301
j» jj .... ••"
= 1-3
)j
218 (724)
j»
B., 12, 2300
>» jj •*••
= 1-4
>»
224-226(720)
....
)>
B., 12, 2298
,, ,, .... ....
jj jj
5)
214-216
....
Cahours
A., 108, 316
v., 864
Chlorisobutaldehyde (?)
....
C8H7C102
173
106
Boquillon
J. P. [5], 11,654
48, 962
Phenylic chloracetate
CH2Cl.COOPh
)»
230-235
40-2
Prevost
J. p. [2], 4, 379
vii., 9 ; 25, 144
Phenylchloracetic acid
Ph.CHCl.COOH
J»
78
Radziszewski
B., 2, 208
vi., 1102
jj u
1*
I>
78
Meyer and Boner
B., 14, 2392
Methylic chlorbenzoate
COOMe.Cl = 1.4
'1
42
Emmerling
B., 8, 883
28, 1261
Anisyl chloride
C6H4.OMe.COCl = 1.4
>»
262
....
Cahours
A. C. [3], 23, 351
i., 306
Chlora-a-toluic acid
C6H4C1(CH2.COOH) = 1.4
11
60
Beilstein & Kiihl-
A., 147, 346
40, 806
berg
ii jj
» »
J)
68
Radziszewski
B., 2, 208
jj
jj jj
J1 JJ
»»
103-5-104
Jackson and Field
A. C. J., 2, 89 ;
40, 804
B. 11, 905
jj jj ••••
»J »
11
105-106
....
Z. P. C., 7, 27
Chlortoluic acid
COOH.Me.Cl = 1.2.4
»»
....
130
Kriiger
B., 18, 1758
48, 1053
„ „
= 1.2.3
))
154
»
jj
jj
,f „ .... ....
= 1.2.5
)*
....
166
»i
jj
jj
jj jj
= 1.4.5
»»
....
184-186
Kekule & Fleischer
B., 6, 1090
27,66
jj jj •••• •*••
»» JJ
n
....
194-195
Gerichten
B., 10, 1249
34, 49
» jj •••• ••••
»' )I
i>
194-196 u.c.
u
B., 11, 366
34, 571
199-201 c.
i) jj ••••
= 1.3.4
H
203-204
Vollrath
A., 144, 266
v., 864
»j jj •••• •"•
1» »
>i
204 c.
Remsen & Kuhara
A. C. J., 3, 424 ;
42, 608
B., 15, 951
j) jj •— •>••
» »»
»»
203-204
Beilstein & Kreusler
A.., 144, 182
JJ J) .... '"•
)1 U
»
209-210 c.
Jacobsen
B., 18, 1761
48, 1052
Chloryxloquinone
CeHMe2Cl : O2
»)
48
Carstanjen
J. p. [2], 23, 431
42, 612
Methylic chlorsalicylate
COOMe.OH.Cl. = 1,2.5
C8H;C1O3
....
48
Smith
B., 11, 1227
Chloranisic acid
COOH.OMe.Cl. = 1.4.6
H
....
176
....
A., 56, 312
i., 302
» »
!> ))
I)
....
180
....
B. J., 23, 421
jj jj
= 1.4.5
»>
214-215
Schall and Dralle
B., 17, 2528
48, 146
Chlordehydracetic acid
C8H7C1O4
93
Precht
B., 9, 1101
30, 506
(?)
CPhCl2.COH+HCl
C8H7C130
begins 265 d.
..*.
Combes
C. R., 98, 678
46, 837
Ethoxytrichlorbenzene
C6H2Cl3.OEt = ?
N
240
43-44
Faust
Z. C. [2], 3, 727
vi., 909
jj —
„ = 1.2.3.4
j»
....
67-68
Petersen
A., 157, 171
24, 252
Ethoxydichlorbenzene
CeHjCLj-OEt = ?
c8H8a3o
226-227
Liquid
Fischer
Z. C. [2], 4, 386
vi., 908
jj ....
= 1.3.4
jj
236-237
....
....
A, 23, 60; As., 7,
183
Dichlordimethyl resorcinol ....
C6H2(OMe)2Cl2 = 1.3.(?)2
CSH8C1202
d. 140
Liquid
Honig
B., 11, 1040
34, 727
„ qninol
= 1.4. a)2
»»
126 u.c.
Habermann
B., 11, 1035
34, 728
Dichlor-^-orcinol .... ....
C6Me2(OH)2Cl2
1»
142
Stenhouse & Groves
A., 203, 292
37, 399
Dichlorxyloquinol
n
n
148-150
Carstanjen
J. p. [2], 23, 431
42, 612
» ..
»
11
175
....
A., 151, 171
Phenylchlorethyloxide
Ph.O.CH,,.CH2Cl
C8HSC10
221 (754)
25
Henry
C. R., 96, 1233
44,802
376
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J.Ch. Soc.
Ethoxychlorbenzene
C,H4.OEt.Cl = 1.2
C8H9C1O
208-208-5
Liquid
Beilatein and Kur-
B., 7, 1398 ; A.
vii., 906; 28,
batow
176, 39
363
„
11 11
„
•210
Liquid
Henry
Z. C. [2], 6, 247
vi., 916
ii ••••
= 1-4
„
210-212
21
Beilatein and Kur-
B., 7, 1396 ; A.
vii., 905; 28,
batow
176, 31
363
Chlormethoxytoluene
CjH3Me.OMe.Cl = 1.3.4 or 6
„
185
....
....
A., 151, 115
ii
= 1.4.5
J)
213-215
Liquid
Schall and Dralle
B., 17, 2529
48, 146
Ethylic chlorniceate
C8H9C102
230
....
St. Evre
J., 1, 530
Chlordimethylreaorcinol
C6H3(OMe)2Cl = 1.3.?
„
....
118
Hbnig
B., 11, 1039
34, 727
Chlorxyloquinol
C6HMe2(OH)2Cl
„
....
147
Carstanjen
J. p. [2], 23, 43
42, 612
ii ••••
„
n
148-150
....
A., 151, 166
Acetotrichlorethylidene
....
C8H9C1A
154-158
Liquid
Mathews
43, 203
acetic ether
(24-26)
Crotonic chloral diacetate ..
C3H2Cl3.CH(OAc)2
C3H9C1S04
240-250 p.d.
Liquid
Pinner
A., 179, 21
29, 549
Ethylic malic chloralide
....
C3H9C1305
45-46
....
A., 193, 45
Diethylic chlormaleate
C2HCl(COOEt)3
c8Hnao4
843-845
....
Glaus
A., 191, 80
34,857
ii 11
„
It
250-260
....
Henry
A., 156, 179
Action of HC1 on aldehyde...
C8H12CJ20
100
....
Hanriot
C. R., 92, 302
40, 404
? — acetate
(CH2)2.CH(CHSC1).CC1.CH2.
C8H12C12OS
122-123
Liquid
Natterer
M. C., 5, 567
48, 498
1 ' OAc
Diethylic maleate diehloride
C8H12C1204
243-245(735)
MM
Glaus and Franck
B., 10, 928
33, 740
? — acetate
CH2Cl.CH(OAc).CHs.C3H5
C3H13C102
203-207
Liquid
Lopatkin
J. p., 30, 389
48, 49
or
CH2Cl.CH(C3H5).CH2.OAc
Ethylic ethylacetochlor-
CClEtAc-COOEt
C3HI3C103
215-220 d.
....
Wislicenus and
A., 186, 241 ; B.,
29, 370
acetate
Conrad
8, 1034
Diethylic chlorsuccinate
COOEt.CH2.CHCl.COOEt
c8Hl3ao4
234-235
Anschiitz
B., 18, 1952
Diglycerol acetrichlorhydrin
.*..
C8H13C1303
190 (20)
Z. C., 1866, 513
Glycerolisovalerodichlorhy-
C3H5.(OCSH9)OC12
C8H14C1202
245 (737)
Truchot
A., 138, 298
v., 980
drin
Hexylene acetochlorhydrin ...
C6H12C1.0Ac
C8H1SC102
188-190
Liquid
Senry
C. R., 97, 260
46,34
Triethoxydichlore thane
C2HCl2(OEt)3
C8H16C1203
205
.».
J., 1864 and 1873
?
0(C2H3C1.0Et)2
11
163-165
Abeljanz
A., 164, 220
26, 156
?
O[CH(OEt).CH2Cl]2
ii
abt. 165
Jacobsen
B., 4, 216
vii., 481; 24,
514
Octylenechlorhydrin
«...
C8H17C10
204-208
Clermont
iv., 173
Glycerol isoamyl chlorhydrin
C3H5(OC5Hn)(OH)Cl
C8H17C102
235
Reboul
J., 13, 464
ii., 884
Tetrachlorcoumarin
....
C9H2C1402
144-145
Perkin
24, 45
vi., 500
a-Chlorcoumarin
....
C9H5C102
....
122-123
11
24, 44
ft' „
....
j(
162
Saisecke
A., 154, 84
Chlortrimesic acid +H2O
C6H2C1(COOH)3 =6.5.3.1
C9H,,C106
278
J. p. [21 15, 310
J)
a-Trichlorcinnamic acid
C6H2C13.CH I CH.COOH
....
200-201
Seelig
r L Jj 7 "•*"
B., 18, 425
48, 770
P- ii ,,
„
n
185
Trichloracetophenone benzoic
acid
C6H4(CO.CC13).COOH =1.2
C9H6C1303
144
Jabriel & Michael
B., 10, 1556
34, 430
Salicylic chloral
....
j j
124-125
A., 193, 41
Dichlorethylene protocate-
O.C2H2Cl2.O.CfH3.COOH
C9H6C1204
118-121
....
A., 168, 109
chuic acid
=43.1
Cinnamyl chloride
C6H5.CH:CH.COC1
C9H7C10
262
....
Cahours
A., 178, 214
.,990
Chloratropic acid
a-Chlorcinnamic acid
Fr. C6HS.C(COOH) I CH2
Ph.CH:CCl.COOH
9)
C9H7C1O2
170-171 (58)
r. water
35-36
85
137-138
^laisen & Antweiler
jadenburg
3erkin
B., 13, 2124
B., 12, 948
47, 258
40, 169
36, 720
ii n
»
„
'r. petroleum
11$
11
„
ii n
»
11
....
138-139
Torrer
B., 16, 854
ii 11
»
ii
....
142-143
Jutz
B., 15, 788
42, 1073
11 ii
11
„
....
142
PlochI
B., 15, 1946
44, 195
ft- ii 11
S-
Ph.CCl : CH.COOH
11
....
114
Jutz
B., 15, 788
42, 1073
11 11 ....
II
11
....
114
?erkin
47, 258
n 11 ....
C1.(CH : CH.COOH =1.3
H
167
Gabriel & Herzberg
B., 16, 2036 ;
44, 1123 ; 48,
C. C. [1884], 35
661
' "
=1.2
11
....
200
ii n
J)
jj
ii 11
=1.4
„
....
240-242
COMPOUNDS CONTAINING FOUR ELEMENTS.
377
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Chlorcinnamic acid
?
C9H7C102
....
132
....
A., 70, 7
i., 987
Acetylic chlorsal icy late
C6H3a(OH).COOAc =?.2.1
C9H7C104
....
149
Smith
B., 11, 1227
Chlormethylnoropianic acid
CcHCl.OMe.OH.CHO.COOH
C9H7C1O6
206
Prinz
J.p., 24, 370
42, 403
Ethylic chlormecenate
HO.C,.C10(COOH)(COOEt)
C9H7C106
....
148
Hilsebein
J.p. [2], 32, 129
48, 1202
From polyporic acid
....
C9H7C1202(?)
....
108
Stahlschmidt
A., 195, 365
36, 383
Ethylic trichlorbenzoate ....
Cl3.COOEt =6.4.2.1
C9H7C130!!
....
65
Beilstein and Kiihl-
A., 152, 237
vi., 313
berg
11 11 ••••
„ =5.4.3.1
JJ
....
86
Salkowsky
A., 163, 32
vii., 164 ; 88,
715
Propionoxytrichlorbenzene....
CI3.(O.C3H50) =6.4.2.1
•*»
262-5-264-5
Liquid
Daccomo
B., 18, 1163
48, 889
u.c.
Phenyl dichlorpropionic acid
Ph.CHa.CHCLCOOH
C9H3C12O2
....
162-164 d.
Erlenmeyer
B., 14, 1867
Dichlorbenzylic acetate
C6H3Cl2(CH2.OAc) =1.4.?
»1
259
....
Beilstein and Kiihl-
A., 147, 350
vi., 336
berg
Ethylic dichlorbenzoate
C6H3CLCOOEt =4.3.1
)»
262-263
Liquid
11
A., 152, 227
vi., 312
11 11
'„ =4.2.1
)j
271 c.
Liquid
Beilstein
B., 8, 435, 813 ;
28, 1194 ; 29,
A., 179, 283
587
Ethylic dichlorsalicylate
C6H2Cl2.OH.COOEt =(?),.2.1
C9H8C1A
47
Smith
B., 11, 1226
Xylylic chloride
Me.Me.COCl =1.2.4
c9H9ao
234-236
25-5-26-5
Ador and Meier
B., 12, 1970
38, 252
Methylic phenylchloraeetate
Ph.CHCl.COOMe
C9H9C1O2
248 c. ; p.d.
Liquid
Meyer and Boner
B., 14, 2392
Chlorethylic benzoate
Ph.COO.C2H4Cl
»>
260-270
....
A., 113, 121
n-Chlorhydratropic acid
CH2Cl.CHPh.COOH
5J
....
78-74
Merling
A., 209, 20
40, 1143
ft- 11 11
CH3CClPh.C!OOH
>»
....
85
Ladenburg
B., 12, 948
ft- » 11
J)
»I
....
86-88
Merling
A., 209, 4
40, 1143
ft- 11 11
»>
•)•)
89
Spiegel
B., 14, 237
40, 277
Chlorphenylpropionic acid ....
a.(CH2.CH2.COOH) =1.2
)1
....
96-5
Gabriel & Herzberg
B., 16, 2036 ;
44, 1123 ; 48,
C. C. [1884], 35
661
11 11
=1.3
)•
....
77-78
11
71
11
11 11
=1.4
H
....
12Jf
11
JJ
11
11 11
» J>
»
....
126
A., 147, 95
Ethylic chlorbenzoate
COOEtCl =1.2
51
237-241
Emmerling
B., 8, 883
28, 1261
11 11
>' ))
3»
948
....
....
A., 143, 96; 117,
153
11 11 ••••
„ =1.3
)1
238-242
Liquid
Kekul6
B., 1861, 308
vi., 311
11 11
;» »>
1)
S45
*•••
Limpricht & Uslar
A., 102, 263
i., 555
Chlorbenzylic acetate
C6H4Cl(CIL,.OAc)=1.4
»J
240
....
Neuhof
Z. C. [2], 3, 467
vi., 336
Phenyl chlorlactic acid
....
C9H9C103
....
104
....
A., 147, 79
11 11 11
....
J»
+H20
78-80
11
Chlortropic acid
CHs(OH).C!ClPh.COOH
))
....
128-130
Ladenburg and
B., 13, 377
38, 472
Eugheimer
Ethylic chlorsalicylate
COOEt.OH.Cl =1.2.4 or 5
)1
•«••
110
Smith
B., 11, 1227
p-Cresol chloral
C6H4.Me.OH + CC13.COH
Og-tlgC/ljjOj
....
52-56
Mazzara
G. I., 13, 269
46, 187
Trichlorvalerolactic bntyr-
....
C9H10C1663
300-310
84-86
....
A., 193, 48
chloralide
Phenyl chlorcarbinol ethyl
Ph.CHCl.OEt
C9HnClO
210-212
Hubner and Bente
B., 6, 805
27, 152
oxide
Chlorbenzyl ethyl oxide
C6H4Cl(CH2.OEt) =1.4
»»
....
Liquid
Jackson and White
B., 13, 1218
38, 879
11 11 11
11 11
JJ
....
Liquid
Jackson and Field
A. C. J., 2, 85
40, 808
1, 11 1*
11 11
5)
215-218
Liquid
Neuhof
A., 147, 339
11
1< 11 11
11 11
))
215-220
Liquid
Naquet
As., 2, 251
v., 855
11 11 11
11 11
1>
215-220
....
Beilstein and KUhl-
A., 161, 335
vi., 336
berg
a-Ethoxychlortoluene
C6H3MeCl.OEt
»)
210-220
Liqxud
Wroblewsky
Z. C. [2], 6, 164 ;
vii., 867; 27,
A., 168, 210
55
ft-
11
J»
210-220
Liquid
11
11
11
Anhydrocamphoronic chloride
....
C9HUC104
....
130
Kachler & Spitzer
M. C, 6, 173
48, 808
Diethylic trichlorethylidene-
CC13.CH : C(COOEt)2
C9HUC1304
160-164 (23)
Liquid
Kommenos
A., 218, 145
46, 423
malonate
Diethylic chlorethenyltricar-
COOH.Ca(COOEt).CH2.
C9H13C1O6
205-215 (160)
Bischoff
A., 214, 44
44, 45
boxylate
COOEt
Isobutylic chlorangelacetate
....
C9H15C103
235-240
Pinner and Klein
B., 11, 1497
36, 42
-
3 c
378
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference,
"Watts' Diet.
&J.Ch.Soc.
Diethylic ethylchlormalonate
Et.CCl (COOEt)2
C9H15C104
Liquid
Guthzeit
A., 209, 232
42,39
» »
»
)J
228
Liquid
Conrad
B., 14, 618
Diethylic itachlorpyrotarta-
C3H5Cl(COOEt)2
»»
250-252 d.
Liquid
....
Z. C., 1866, 722
vi., 980
rate
Parachlorpropaldehyde
....
C9H15CI303
170-175
33-5
Grimaux & Adam
C. B., 92, 300
40, 406
(12-15)
Pelargonpyl chloride
C8H17.COC1
C9H17C1O
220
....
Cahours
A. C. [3], 39, 207
iv., 371
Tetrachlornaphthaquinone ....
C14 ; O2=a! a2 ft $2 ; a, a3
C10H2C14O2
160 u. c.
Claus and Lippe
B., 16, 1018
44, 921
Trichlornaphthaquinone
CioH3Cl3 . Oj
C10H3C1302
250
Claus and Spruck
B., 15, 1404
42,1211
„
i»
>I
250
Claus and Lippe
B., 16, 1017
+xH,0
»
n
95
»
»
» »
»
»>
95
Claus and Spruck
B., 15, 1404
42, 1211
/3-Dichlor-a-naphthaquinone
c10H4ci2:o2
C10H4C12O2
....
152-153
Plagemami
B., 15, 485
"- » -"- i)
»
i»
188
Carstanjen
B., 2, 633
a- ,, -«- »
jj
»»
189
Plagemann
B., 15, 485
a- ,j -<*- »
*>
»j
189
Graebe
A., 149, 3
vi., 853
»- » -»- »
j)
»
....
190
Darmstadter and
B., 2, 114
Wichelhaus
Chlor-a-naphthaquinone
c10H5a : o2
C10H5C102
109-111
Plagemann
B., 15, 485
Chlorhydroxynaphthoqui-
C10H4C1(OH) : O3
C10H5C103
200
....
....
vi., 853
none
Dichlor-a-naphthaquinol
C10H4C12(OH)3
010H6C1202
....
135-140 d.
Grsebe
A., 149, 6
vi., 857
Diacetyltetrachlorquinol
C6Cl4(OAc)2=(?)4.4.1
C10H6C1404
....
245
»
A., 146, 20
vi., 988
a-naphthoic chloride....
C10H7.COC1
C10H7C10
297-5
Solid
Hofmann
: vl., 851
Chlornaphthol
Ci0H6.Cl.OH=aj ; o2
J)
....
57
Claus and Ochler
B., 15, 314 J 42, 736
»» ....
= »/3
»
....
68
Schall
B., 16, 1901 44, 1109
»» ....
= ?a
)1
....
109
Grimaux
B. S. [2], 18, 208 26, 70
»
= 1.9
ft
....
115
Claus and Zimmer-
B., 14, 1484
40, 915
mann
Mandelic chloralide
Ph.CH.COO.CH(CCl3)O
C10H7C1303
305-310 p. d.
59
Wallach
B., 9, 1215
31,60
» » ••>•
....
n
305-310 d.
82-83
A., 193, 40
Diacetyltrichlorquinol
C6HCl3(OAc)2=(?)3.4.1
C10H7C1304
153
Grsebe
A., 146, 28
vi., 988
1
....
C10H8C1202
195-196
....
J. [1872], 424
Diacetyl dichlorquinol
<OAc)rCls=1.4.2.5
C10H8C1204
....
138-140
Schulz
B., 15, 653
H V
» )i
»
....
Ul
Levy and Schultz
A., 210, 148
42,509
» » •"•
„ =1.4.3.5
»
....
66-5
Levy
B., 16, 1445
44, 1117
Methoxyphenylacryl chloride
C,H4.OMe.(C,,H,,.COCl)=1.4
C10H9C102
abt. 50
Perkin
J. [1877], 792
31, 410
Diacetyl chlorquinol
(OAc)2.Cl=1.4. 2 or 5
C10H9C104
....
72
Levy and Schultz
B., 13, 1427
38, 888
»i i, .... ....
» )>
»)
72
»
A., 210, 140
42,509
)> »
Jl )>
1J
....
72
Schulz
B., 15, 654
Chlormeconin.... . .
....
1)
175
Anderson
A., 98, 48
iii., 863
Ohloropianic acid
C6H.(COH).Cl.(OMe)2.COOH
C10H9C105
210-211
Prinz
J. p., 24, 367
42, 403
Butyryl trichlorphenol
(O.C4H70).C13=1.2.4.6
C10H9C1302
272-275 u. c.
Liquid
Daccomo
B., 18, 1163
48, 889
Pentachlorthymol
....
C10H9C160
98
Lallemand
A. C. [3], 49, 158
v., 795
Dichlornaphthalene aceto-
C10H6Cl2.Cl3.OAc
C10H9C1602
195
Widmann
B., 12, 1714
38, 47
chloride
Ethylic phenyldichloracetate
Ph.CCl2.COOEt
^ioSi0Cl3O3
263-266
Claisen
B., 12, 630
36, 648
Glycerol benzodichlorhydrin
C3H5Cl2(OBz)
))
222 (40-50)
A., 138, 298
Dichlorthymoquinone
Dichlornaphthydreneglycol....
....
»J
H
99
155-156
Andresen
J. p. [2], 23, 176
B. S., 18, 207;
40, 590
19, 396
Dichlorethoxyquinone
Ethylic dichlororsellinate ....
CeC^OEt^O,,
C6Me.COOEt.(OH)2Cl2
C10H10C1204
»)
107
162
Stenhouse
Hesse
23,6
A., 117, 315
vi., 989
iv., 237
Deriv. of Valeral
....
C10HIOC140
208-210
....
Schroeder
B., 4, 401
24, 560; vii.,
Diethyl tetrachlorquinol ....
QA(dBt),
C10H10C1402
112
Grtebe
A., 146, 19
1195
vi., 988
Chloranethol
C6H4.C3H4C1.0Me=1.4
C^H^CIO
258
—6
L/adenburg
Z. C. [2], 5, 575 ;
vi., 157 ; vii.,
As., 8, 91
72
" » >i
Cuminyl chloride ! C6H4.Pr.COCl
Benzylchlormalonamide ... CCl(CH2Ph)(CONH2)0
u
»
CioHnC102
228-230
256-258
d. 210-220
3-4
abt. 80
uandolph
Cahours
Bischoft' & Emmert
C. R, 82, 226
A. C. [3], 23, 347
B., 15, 1113
29, 705
ii., 184
42, 1208
COMPOUNDS CONTAINING FOUR ELEMENTS.
379
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Ethylic chlortoluate
COOEtMe.Cl=1.3.J
C10HUC102
260-265
A., 144, 267
Chlortolylpropionic acid
(CH2.CH2.CO2H)ClMe=1.2.
)>
122-123
Gerichten
B., 11, 365
34, 570
Benzochlorhydrin
C3H5(OH).C1.(OC7H60)
Ci0HiiC103
—40
Berthelot
A. C. [3], 41, 302
i., 547
Chlorhydroxythymoquinone
C6MePr«.OH.Ci:O2
j>
....
122
Ladenburgand En
B., 10, 1222
34,' 60
gelbrecht
Trichlorthymol
Me.Pi-.OH.Cl3
C10HUC130
250
45
A. C. [3], 49, 157
„
»
»
61
jj
v., 795
Diethyltrichlorquinol
C6H(OEt)2Cl3=1.4.(?)3
Ci0HnCl302
68-5
Grsebe
A., 146, 28
vi., 988
?
....
c)0H12a2o
98-99
Auwers
B., 17, 2978
48, 381
Diethylic dichlormuconate ...
C4H2Cl2(COOEt)2
C10H12C1204
95-96
Bell
B., 12, 1273
Deriv. of Valeral
....
C10H12C16O
203-204
Schroeder
B., 4, 401
a*, 559
Trichlorcamphor
Ci0H13Cl3O
....
54
Cazeneuve
C. R, 99, 609
48, 59
Dichlorcamphor
....
C10H14C120
263d.
93
D
C. R, 94, 730
48, 738
„
J)
96
Cazeneuve&Didelo:
C. B., 94, 1058
42, 864
»
Isomer
»
77 ; si. 70
Cazeneuve
C. R, 94, 1360
42, 1107
Chlorcamphor
....
C10H15C10
244-247
83-84
»
C. R, 94, 1530 ;
44, 214 ; 48, 58
99, 609
„ ....
)J
93-94
SchiffandPuliti
B., 16, 888
3,
)I
244-247 s. d.
100 ; sf. 95
Cazeneuve
C. R, 95, 1358
44, 599
,,
)>
95
Wheeler
S. J. [2], 45, 48
vi., 387
Chlorhexylene diacetate
C,H,a(OAo),
C10H5C104
140 (20)
Liquid
Natterer
M. C., 5, 567
48, 498
Triethylic chlormethintricar-
CCl(COOEt)3
CIOH16C10,
210 (140)
....
Conrad
B., 14, 618
40, 577
boxylate
Camphor dichloride
....
C10H16C12O
....
70
Pfaundler
B., 11, 364
34, 586
„ ,,
»
150-155
Spitzer
»
)>
,, ,, ....
)»
155-155-5
»
B., 11, 1819
36, 168
Campholic chloride
C9H|7.COC1
C10H17C10
222-226
....
A., 126, 265
1
CioHisCljOj
98
Kekulo
A., 162, 102, 309
vii.,34;25,617
Capryl chloride
C9H19.COC1
C10H19C10
200-220
Liquid
Grimm
A., 157, 272
24, 361 ; vii.,
249
Hydrochloride of worm seed
C10H1SO.HC1
5)
30-35
Hell and Eitter
B., 17, 1977
46, 363
oil
Octylene acetochlorhydrin ....
C8H16Cl.OAc
C10HI9C1O2
225
Clermont
A., 152, 322
vi., 880
Isovaleraldehyde +2HC1 ....
(C5H10C1)20
C10H20C120
180
Bruylants
B., 8, 414
Terpenehydratedihydrochlor-
C10H20C120(?)
49
Flavitzky
B., 12, 2355
38, 403
ide
Diglycerol diethylchlorhydrin
O : (C3H5)(OEt)3(OH)Cl
C10H21C104
285
....
Reboul & Lourengo
C. R, 52, 401
ii., 894
Dichlor-j3-naphthoic acid ....
C10H5C12.COOH
CiiH0Cl2O2
....
291
Ekstrand
B., 17, 1605
46, 1361
a-Naphthoyl chloride
C10H-.COC1 = a
C,,H7C1O
297-5
Liquid
Hofmann
B., 1, 41
£- „ „
= 0
)J
304-306
43
Weith
A., 180, 317
30,86
Dichloroxysacchulmide
CnH8Cl206
d.w.m. 200
Sestini
G. I. [1882], 292
42, 1182
Ethylic acetylchlormecenate
AcO.C6ClO (COOH) (COOEt)
CnH,C107
70
Hilsebein
J. p. [2], 32, 129
48, 1203
Diacetyltrichlortoluquinol ....
C6MeCl3(OAc)3
CnH9Cl304
....
114
Borgmann
A., 152, 253
vi., 1106
Diacetyl-ru-dichlortoluquinol
C6HMeCl2(OAc)2
CiiHioCl2O4
122-124
Southworth
A., 168, 271
27, 62
Valeryltrichlorphenol
(O.C5H90).C13 = 1.2.4.6
CnHuClgO,
281-284 u.c.
Liquid
Daccomo
B., 18, 1163
48, 889
Isobutylic dichlorsalicylate....
COOBuP.OH.Clj = 1.2.(?)2
CHH12C12O3
188
Smith
B., 11, 1226
Diethyltrichlortoluquinol ....
C6MeCl3(OEt)2
3irHMCa,O|
107
Borgmann
A., 152, 254
vi., 1106
Camphocarboxy lie chloride ....
C10H14.OH.COC1
CnH.^lO,
44
Kachler and Spitzer
B., 13, 1413
38, 892
Triethylic chlorethenyltricar-
C2H2Cl(COOEt)3
CUH17C106
290 p.d.
Bischoff
B., 13, 2162
40, 156
boxylate
Glycerolchloracetyltriacetin
C3H5(OAc)3.AcCl
CnH17C107
240 (20)
Z. C. [1866], 513
Triglycerolacetotetrachlorhy-
02(C3H5)3(OAc)Cl4
CnH18Cl4O4
230 (20)
»
drin
Diethylic isobutylchlormalo-
C4H9.CCl(COOEt).,
cllallcio4
845
Conrad and Bischoff
B., 13, 600
38, 629
nate
!) !>
»
jj
245-247
Guthzeit
A., 209, 237
42,40
Octochlordiphenol
C12C18(OH)3
C12H2C1802
233-5-234-5
Weber & Sollscher
B., 16, 884
Tetrachlor-y-diphenol
C6H2C12(OH).C6H2C12(OH)
C12H6C1402
233
Magati
B., 13, 227
38, 644
Tetrachlorquinhydrone
C12H6C1404
120
....
A., 69, 316
+2H20
From naphthalene
C10H6CI2(OAc).Cl.,
C12H9C1602
195
Widmann
B., S. [2], 28, 507
32,900
Diethylic tetrachlorphthalate
C6(COOEt)2.Cl4 = 1.2.3.4.5.6
C12H10C1404
60
Grebe
B., 16, 861
3 c 2
380
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diethylic tetrachlorphthalate
C,,Cl4.COO.C(OEt)2 = 1.2.(?)4
C12H10C1404
124
Graebe
B., 16, 861
Cumenylacrylcliloride
C6H4.Pr(C2H2.COCl
C12H13C10
....
abt. 25
Perkin
J. [1877], 790
31, 399
Diethylic chlorisophthalate...
(COOEt)2.Cl= 1.3.5
C12H13C104
....
abt. 45
Baeyer
J. p. [2], 25, 514
42, 1296
Thymol chloral
C6H3.Me.Pr.OH + OC13.COH
C12H15C13O2
130-134
Mazzara
G. I., 13, 269
46, 187
?
C12H25C104
275-285
....
A. C. [3], 67, 310
Lauryl chloride
0] 1X123.0001
C12H23C1O
142-5 (15)
—17
Krafft and Burger
B., 17, 1378
46, 1125
Dichlordiphenylene ketoue ...
C.H3Cl.CO.CjH3Cl = 1.4.5 ;
CI3H6CL,0 (?)
....
103-104
Hodgkinson and
43, 171
5.4.1
Matthews
» >l
» !I
»
158
?»
43, 170
Benzoxytrichlorpheuol
OBz.Cl3 = 1.2.4.6
C13H7C1302
70
Daccomo
B., 18, 1164
48, 889
Chlordiphenyl ketone
Ph.CO.CcH4Cl
C13H9C1O
a. 300
75-5-76
Kollarits and Merz
B., 6, 547
vii., 939 ;
26, 1036
Benzoxychl orbenzene
C6H4C!.OBz
C13H9C1O2
87
A., 53, 96
i., 554
Ethylic dichlor-/3-naphthoate
C10H6Cl2.COOEt.
C13H10C1202
66
Ekstrand
B., 17, 1605
46, 1362
Benzyloxychlorbenzene
C6H5.CH2.O.C6H4.C1
C13HUC1O
...
70-71
A., 161, 345
vii., 180
„ ....
»
JJ
71-71-5
Sintenis
B., 4, 700
24, 909
Ethylic chlor-a-naphthoate ....
C10H6Cl.COOEt
CuHudo,
42
Ekstrand
B., 17, 1604
46, 1361
Chlorhydrin of ethylic aceto-
OHPhCl.CHAc.COOEt or
C13H15C103
41
Claisen & Matthews
A., 218, 170
46, 443
benzilidene acetate
CH2Ph.CAc01.COOEt
n »
j»
>?
...
71
»
!>
tt
Penta-chloranthraquinone ....
....
C14H3C1502
w.m.
Diehl
B., 11, 181
34, 430
Tetra-
....
C14H4C1402
320-330
j»
B., 11, 180
34, 429
n » ••••
c6a4:(co)2:c6H4
»
191
Kircher
B., 17, 1167
46, 1039, 1040
Tetrachloralizarin
C14H2C14(OH)2:02
CHH4C1404
260
Diehl
B., 11, 189
Trichloranthraquinone
....
c14H5a3o2
....
284-290
)>
B., 11, 180
34, 429
Pentachloroxytolidene
....
C14H5C1502
....
187-190
A., 153, 128
Dichloranthraquinone
C14H6C1202
261
Kircher
B., 17, 1169
46, 1040
Dichloralizarin
c,4H4ci2(OH)3:o2
C14H6C1204
«...
208-210
Diehl
B., 11, 188
34, 428
Acetyloctochlordiquiuol
C6Cl4(OH)J.C6Cl4(OAc)(OH)
C14H6C180S
230
Hesse
A., 114, 294
iii., 216
Ohloralizarin . ..
C14H5C1(OH)2:02
C14H7C104
244-248
Diehl
B., 11, 187
34, 428
Trichlorxytolidene
....
C14H7C1302
87
• »*
A., 153, 128
•
Anthraquinone dichloride ....
C{H4.CO.C6H4.CC12
C14H8CL,0
132-133
Thorner and Zincke
B., 10, 1479
34, 231
Phenanthradichlorketone ....
C6H4.C6H4.CO.CC12
H
165
Lachowicz
B., 16, 331
44, 667
Octochlorethyldiquinol
C6Cl4(OH)2.C6Cl4(OEt)(OH)
Cijifajo.
236
Hesse
A., 114, 292
iii., 216
Chlorphenanthrene
....
c14H9ao
....
122-123
Lachowicz
J. p. [2], 28, 168
46,82
Chloroxytolidene
....
CJ4H9C1O2
57-58
A., 153, 127
Benzoylbenzenyl trichloride
C6H4.Bz.C013 = 1.4
C14H9C13O
....
107-107-5
Thorner
B., 9, 483
30, 198
» »
» )!
))
111-111-5
j)
A., 189, 92
34, 68
Benzoylbenzylene dichloride
Cf,H4.Bz.CHCl2 = 1.4
C14H10C120
....
94-95
J)
B., 9, 483 '
30, 197
» »
» >i
)J
....
a.s. 85-86
))
A., 189, 91
34,68
Clilorbenzil ....
....
))
71
Ziniu
A., 119, 177
vi., 305
DichlordiacetoxjTiaphthalene
C10H4Cl2(OAc)2
C14H10C1204
236
Grsebe
A., 149, 7
vi., 857
Benzoylbeuzyl chloride
C6H4.Bz.CH2Cl = 1.4
C^HuClO
....
97-98
Thorner
B., 9, 482
30, 197
» )>
» )»
>j
a.a. 93-94
A., 189, 89
34, 68
Chlorbenzilic acid
....
C14HUC102
270
Cahours
A. C. [3], 23, 350
i., 915
Diphenoltrichlorethane
CC1,.CH(C6H4.OH),
C14HnCl303
202 d.
Meer
B., 7, 1201
28, 158
Tetracetoxydichlorbenzene ....
C6Cl2(OAc)4
C14H12C1,08
235
Grsebe
A., 146, 34
vi., 990
Diaeetoxydichlordihydro-
C10H6Cl(OAc)2
C14H14C1204
130-131
Grimaux
B. S. [2], 18, 208
26, 69
naphthalene
Diethylic benzylchlormalo-
nate
(Ph.CH2.CCl(COOEt)2
C14H17C104
305 p.d.
Liquid
Conrad
B., 13, 2159
40, 168
Chlorthymyldiacetate
C6HClMePr(OAc)2
))
87-88
Schulz
B., 15,657
42, 838
Ostruthin hydrochloride
Anthraquinone carboxyl
chloride
C14H17O2.HC1
c14H7:o.,.coci
C^H^CIO^O
clsH7eio3
100
147
Gorup-Besanez
Liebermann and
Glock
A., 183, 321
B., 17, 889
31, 717
46, 1188
Benzylidenephenyl ketone
hydrochloride
CHPhCl.CHj.CO.Ph
or CHjPh.CH01.CO.Ph
C1SH13C10
quick heat
slow heat
119-120
110-112
Claisen and Clapa-
rede
B., 14, 2464
42, 512
Trichlorsantonin
TT
C15H15C13O3
213
....
B. S., 5, 202
v., 191
COMPOUNDS CONTAINING POUR ELEMENTS.
381
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Metasantonic chloride
....
C15H19C103
....
139
Cannizzaro and
G. I., 8, 309
36, 331
Valente
Santonic chloride
....
}J
....
170-171
n
Alantic chloride
C14H20(OH).OOC1
C15H31C102
....
140 d.
Kallen
B., 9, 156
29, 917
Myristyl chloride
C14H2-.COC1
C1SH27C10
168 (15)
—1
Krafft and Burger
B., 17, 1379
46, 1125
Ciruicyl chloride
....
JJ
....
abt. 44
Carius
A., 114, 154
I., 964
Dichlordiphthalyl
....
C16H6C1204
....
248
Ador
A., 164, 245
26,68; vii., 980
Dicacetoxyoctochlordipheuyl
C,Cl4(OAc).C6Cl4(OAc)
C16H6C1804
193-194
Weber & Sollscher
B., 16, 885
Dichlor-n-naphthylene pheu-
fr. C,H4.O.CI§H.
C16H8C120
245
Arx
B., 13, 1727
40, 282
ylene oxide
1 '
Diphthalyldichloride
(.CC1.C6H4.CO.O)2=(1.2)0
C16H8CI2O4
«...
245
Grsebe and Schmal
A., 228, 126
48, 798
p i
zigang
1
C16H9C1305
17
Ador
A., 164, 229
26,69; vii., 981
Hydropiperom chloride
C7H502.CHC1.CHC1.C7HA
C16H12C1204
....
198
Kemsen and Fittig
A., 159, 132
vi., 949 ; 24,
935
1
..«
C16H12C14O2
....
109-110
....
A., 195, 371
Ethyloxanthranyl chloride ....
C6H4.CO.C6H4.CClEt
C16H13C10
88-89
Liebermann and
B., 14, 459
40, 609
Landshoff
,, ..
„
„
88-89
Liebermann
A., 212, 87
42, 862
C H CIO
117
Stadel
B.,9,1759;13,83
31, 459
8-
16 13 3
154-155
J)
H
Carboxylphenylmethyltri-
Me.eeH4.C2HCl3.C8H4.COOH
C16H13C1A
173-174
Fischer
B., 7, 1192
28, 155
chlorethane
Dichlorhydrocoerulignone ....
C12H2Cl2(OMe)4(OH)2
C16H16C1206
220
Hayduck
B., 9, 929
30, 516
Dulcitol aceto-chlorhydrin ....
....
CuB-aClO.,,
160
....
A. C. [4], 27, 154
Tetrethylic chlorethyl acetyl-
(COOEt)2CCl.CEt(COOEt)2
C16H25C108
d.
Liquid
Bischoff and Each
B., 17, 2786
48, 244
ene tetracarboxylate
Palmityl chloride
C15H31.COC1
C16H3,C10
192'5(15)s.d
12
Krafft and Burger
B., 17, 1379
46, 1125
„ „
„
„
....
50
Villier
B., 9, 1932
Cetene chlorhydrin
C16H32C1(OH)
C16H33C10
abt. 300
b.— 15
Carius
A., 126, 201
vi., 421
Leucogallol +2H2O
....
C18H,,C112O12
....
104 d.
Stenhouse & Grove
A., 179, 240
28, 709
C,aH,Cl,,O,n
109 p.d.
A., 179, 237
28, 707
Phthalyltrichlorphenol
c6H4:o2:(o.c6H2ci3)2=i.2
is 7 H 10
C18H8CLp4
••>.
193-194
Daccomo
B, 18, 1164
48, 889
(1.2.4.6)2
Chlordehydrobenzoylacetic
cci : c : cph.o.GPh : C.COOH
C18HUC103
....
150-151
Perkin
47, 293
acid
Tetrachlorhydropolyporic
....
C18H14C1404
....
108
A., 195, 372
acid
Diacetoxyphenyltrichlor-
CCl3.CH(C6H4.OAc)2
C18H15C1304
....
138
Fischer
B., 7, 1202
28, 158
ethane
From benzoic ether ....
....
C18H16CleO3
188-190
•*«•
Malaguti
A. C. [2], 70, 374
i., 567
Isobutyl oxanthranyl chloride
C6H4.CO.C6H4.CClBu/3
CI8H17C10
....
78
Liebermann
A., 212, 87
42, 862 .
,1 I! »
„
„
....
78
Liebermann and
B., 14, 463
40, 610
Walder
?
....
C18H17C103
....
57
Limpricht and
A., 160, 177
25, 137
Schwanert
Tetrachlorcarotin
....
C13H=0C140
....
120
A., 117, 228
Dichlorole'ic acid
....
C13H32C12O2
begins 190
....
Lefert
J. Ph. [3], 24, 113
iv., 194
Stearyl chloride
17 3»
C.gHjjClO
215 (15) d.
23
Krafft and Burger
B., 17, 1380
46, 1126
Isoamyl oxanthranyl chloride
C6H4.CO.C6H4.CC1.C6HU
c,9H19ao
....
85
Liebermann and
B., 14, 459
40, 609
i p
Landshoff
Dichlor-a-dinaphthaleue
....
C20H10C12O
....
150-151
Knecht & Unzeitig
B., 13, 1725
oxide
„ -£- „
....
„
....
245
„
B., 13, 1726
40, 281
Fluorescein chloride
c6H4:(co.c(iH3ci)2:o
C2,H10C12O3
....
252
Baeyer
A., 183, 18
31, 198
„ ,, ....
„
n
252 u.c.
Fischer
B., 7, 1212
28, 159
Dibenzoyltetrachlorquinol ....
C6Cl4(OBz)2 =1.2.4.5.3.6
C20H10C14O4
....
230
Levy and Schultz
B., 13, 1429
38, 888
„
!, ».
„
....
233
„
A., 210, 156
42,510
„ trichlororesorcinol
C6HCl,(OBz), =(?)2.4.3.1
C20HnCl304
133
Reinhard
J. p. [2], 17, 346
4,727
„ trichloroquinol ....
„ =5.3.2.4.1
„
....
174
Levy and Schultz
B., 13, 1429
8, 888
»» j« •"•
,,
» -
....
174
..
A., 210, 153
42,510
382
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet'
& J. Gh. Soc.
a-Dichlorphenylanthranol ....
....
0^0,0
abt. 170
Baeyer
A., 202, 95
38, 656
Phenol phthalein chloride ...
C,H4(CO.C6H4C1)2
C20H12C1202
....
155-156
j>
B., 9, 1233
31, 308
„ phthalidein chloride
see B., 9, 1238
))
156
)j
B., 9, 1236
31, 309
Phthalin of fluorescem chlo-
0(C6H3C1)2 : CH.C6H4.COOH
C20H12C1203
....
226
»
A., 212, 352
42, 1097
ride
=(1.1.1), ; 1.2
» » ?>
» )»
J>
....
229-230 u.c.
Fischer
B., 7, 1213
28, 159
» ?> »i
....
»»
....
229-230
Baeyer
A., 183, 21
31, 198
Dibenzoyl-dichlorquinol
(OBz)2.Cl2=1.4.3.5
C20H12C1204
105
Levy
B., 16, 1446
44, 1117
j> >»
„ =1.4.3.2 or 6
))
....
185
....
A., 210, 149
„ -dichlororesorcinol
„ =1-3.(0,
»
127
Reiuhard
J. p. [2], 17, 335
34, 726
„ -chlororesorcinol ....
(OBz)a.Cl=1.3J
C20H13C104
98
)>
J. p. [2], 17, 327
j>
„ -chlorquinol
» =1-4-5
»
130
Levy and Schultz
B., 13, 1428
38, 888
» »
J) )>
>*
....
130
j)
A., 210, 142
42, 509
Phenol hydrophthalidin chlo-
C,H,C1.CH(OH).C,H4.CH.
C2UH14C12O
....
56
Baeyer
A., 202, 97
38, 656
ride
CfffZ
Dichlortriphenylmethane car-
(C,H4C1)2CH.C6H4.COOH
C2oHi4012O2
....
195
i)
A., 202, 84
38, 655
boxylic acid
»» >» »
»
)>
....
205-206
)>
»
j)
i
....
C20H15C13O2
137
Liebermann
B., 6, 953
26, 1242 ; vil.,
1061
Dichloracetyl-hydroccerulig-
C12H2Cl2(OMe)4(OAc)2
C20H20C12O8
172
Hayduck
B., 9, 929
30, 516
none
Arachidyl chloride
0 j g Jj-gg. OOO1
CjoH^ClO
....
66-67
Tassinari
B., 11, 2031
36, 307
Benzene resorcinphthale'in
C6H3(OH)2CPh.C6H4.COO
C2iH15Cl3O4
Cryst.(fr.
113-114
Pechmann
B., 14, 1860
+CHC13
CHC13)
Glycerol stearochlorhydrin ....
C,H5(C1A,0)a(OH)
C21H4IC103
28
Berthelot
A. C. [3], 41, 225
v., 425
Dithymol trichlorethane
CCl3.CH(C6H2Me.Pr.OH)2
C22H27C13O2
+C3H60
194
Jager
B., 7, 1197
31, 262
Naphthalfluorescem dichlo-
....
C24H12C12O3
....
283
Terrisse
A., 227, 133
48, 667
ride
Dibenzoxydichlortetrahydro-
C10H4.H4.(OBz)2.Cl2
C.yH^CLO,
....
148-150
....
B. S., 18, 208
naphthalene
Dibenzoyldichlorthymoquinol
C6Cl2Me.Pr.(OBz)2
C24H20C1204
....
190-191
Schulz
B., 15, 658
42, 838
Dibenzoylchlorthymoquinol
C6HCl.Me.Pr.(OBz)2
C24H21C104
116-118
»
»
1
C24H25C104
184-186
Liquid
Boquillon
J. P. [5], 11, 654
48, 962
Dithymoltrichlorethane
CCl3.CH(C6H2MePr.OH).,
C2.iH33Cl3O3
....
194
Jager
B., 7, 1197
31, 262
+C2H60
Lignocerylchloride ....
CggH.^' COC1
C24H47C1O
48-50
Hell and Hermann
B., 13, 1720
40, 250
Diacetyl dichlorcatechin
C21H16Cl207(OAc)2
C25H22Cl2On
....
169
Liebermann and
B., 13, 695
40,53
Tauchert
Heptachlorcholesterin
....
C26H37C120
....
60
A., 59, 110
Octochlorlepidine
....
C28H12CI8O
97
Dorn
Z. C. [2], 5, 597
vi., 781
Hexa- „
....
c*al4cif)
80-90
»
A., 155, 356
)}
Penta- „
....
CMH1SC150
186
»
A., 155, 355
»
Chloride of diphenic anhy-
....
c«H16aA
....
128
Graebe and Men-
B., 13, 1304
38, 812
dride
sching
Dichlorlepidine
....
C28H1SC120
....
156
Dorn
Z. C., 2 [5], 597
vi., 781
,,
....
)>
169
Zinin
B., 5, 1106
26, 489
Isodichlorlepidine
....
JJ
166
j>
B., 8, 696
28, 1005
Dichloroxylepidine
....
C^H^C^O,
178
Dorn
Z. C., 2 [5], 597
vi., 781
j)
....
))
202
Zinin
B., 5, 1106
26, 489
„
....
>j
»..
230
»
B., 8, 696
28, 1005
Chlorlepidine
CjsHuClO
143-146
Dorn
A., 153, 355
Chloroxylepidine
....
CWH19C102
185
Ziniu
B., 5, 1105
26, 489
Hydrodichloroxylepidine
....
C^HjoClA
•«..
261
»
B., 8, 696
28, 1005
Dichloroxylepidine ....
....
L • Og rl ogOl oOg
182
3J
i)
)»
From Isohydrobenzoin an-
C^H-aClO
153
Breuer and Zineke
A., 198, 168
38, 117
hydride
» » »
C23H24C120(!)
....
87(?)
)) JT
)1
)»
From quassin
C32H39C15O3
119d.
Oliver! and Denaro
G. I., 15, 6
48, 907
Glyceroklipalmitochlorkydrii
C3H5.C1.(O.C16H310)2
C35HWC104
44
Villier
B., 9, 1933
Tetrachlorabictic acid
....
C^4H60Cl4O5
124
J., 1861, 391
Chlorobastin ....
f1 TT PI A
b-i f\r\
/~1 1 "D
.41 i no
i-'alib^lcUd
. 100
Uross and _t>evan
•rtlj lUi/
COMPOUNDS CONTAINING FOUR ELEMENTS.
383
(4.) CHC1S, CHClSe, and CHClTe.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch.Soc.
Dichlorthiophene
C4H2C12S
170
Weitz
B., 17, 795
46, 1130
Octochlorethyl sulphide
(C2HC14)2S
C4H2C18S
160 p.d.
Riche
A. C. [3], 43, 297
ii., 546
)! »
»
»
160 p.d.
Begnault
A. C. [2], 71, 406
i) 11
)j
217-222
Eiche
A., 92, 360
Chlorthiophene
....
C4H3C1S
130
....
Weitz
B., 17, 794
46, 1130
Hexachlorethyl sulphide ....
(C2H2C13)2S
C4H4C16S
189-192
....
Eiche
A., 92, 359
ii., 545
Tetrachlorethyl sulphide ....
(C2H3C12)2S
C4H6C14S
167-172
....
»
A. C., 43, 297
!»
Chlorphenylsulphhydrate ....
C6H4C1.SH
C6H5C1S
53-54
Glutz
A., 143, 109
vi., 919
Dichlor-;3-ethylthiophene ...
C4SHCL..Et
C6H6C12S
235-237C
Liquid
Bonz
B., 18, 551
48, 767
Chlorbenzyl sulphhydrate ....
C6H4C1(CH2.SH)=1.4
C7H7C1S
19(?) ; 19-20
Jackson and White
B., 13, 1218 ;
38, 879 ; 40,
A. C. J., 2, 167
807
)i i)
» J»
»
....
77-78
Beilstein
A, 161, 348
» »> •••*
» JT
»)
84-85
»
>i
i> u
)J )>
)1
84-85
Neuhof
A, 147, 346
Dithienyl dichlorethylene ....
CCL, : C(C4H3S)2
CioH6CI2S2
Liquid
Peter
B., 17, 1343
46, 1001
„ trichlorethane ....
CC13.CH(C4H3S)2
C10H7C13S2
76
»»
B., 17, 1342
)1
?
....
^10^20^*2^2
240-250
....
Guthrie
A, 121, 108
v., 1077
Dichlorphenyl sulphide
(C6H4C1)2S
(_y|2-D.8012O
88-89
Krafts
B., 7, 1165
28, 153
Dichlorphenyl disulphide ....
(C6H4C1)2S2
C12H9C12S2
71
Glutz
A., 143, 111
vi., 919
Chlorbenzyl sulphide
(C6H4C1.CH2)2S=?
C14H13012S
Liquid
Pauly
A, 167, 187
» i»
=(1-4),
»
....
42
Jackson and White
B., 13, 1217
38, 879
„ disulphide
(C6H4C1.CH2).,S2=(1.4)2
C14H,2C12S2
....
59
»
A. C. J., 2, 166
40, 807
Dichlorthionessal
....
C23H19C12S
....
219
Dorn
A., 153, 351
vi., 1087
Dimethyl selenio-dichloride
Me2Sea2
C2H6Cl2Se
d. 70
59-5
Jackson
B., 8, 110
28, 553
Dimethyl telluro-dichloride ...
MejTeCL,
C.,H6Cl2Te
....
97-5
Wohler and Dean
A., 93, 233
iii, 992
(5.) CHC1N.
Triehlorguanidine
CH2C13N3
115-120
Beilstein and Kur-
B., 7, 731
27, 1097
batow
Methyl nitrogen dichloride....
CHj-NCl,
CH3C1JN
59-60 u.c.
Liquid
Kohler
B., 12, 771
36, 781
Formamidiue hydrochloride
NH:CH.NH2+HC1
CH5C1N.,
....
81
Gautier
A, 145, 118
» »
»
)J
....
81
Claisen & Matthews
B., 16, 310
41, 266
Methylamine hydrochloride .
NH2Me+HCl
CH.C1N
abt. 100
Wurtz
C.E.,28,223&322
iii., 997
Dichloracetonitril
CHC12.CN
C2HC12N
112-113
....
Bisschopinck
B., 6, 732
26, 1128
„ ....
....
(C2HC12N),
....
69-70
Weddige & Korner
J. p. [2], 31, 176
48, 739
Chloracetonitril
OH2C1.CN
C2H2C1N
126-127 p.d.
....
Engler
B., 6, 1003
27,76
„ .... ....
))
»
123-124
....
Bisschopinck
B., 6, 732
26, 1128
Ethyl nitrogen dichloride ....
C2H5.NC12
C2H5013N
91
Wurtz
A. C. [3], 30, 474
ii., 558
»» »
)J
»
88-89 (762)
liquid— 30
Tscherniak
B., 9, 147
29, 913
» »
))
J»
86-91
....
Kohler
B., 12, 771
36, 781
Dichlorethylamine
CH2C1.CHC1.NH2
)J
....
136
Abeljanz
B., 4, 986
25, 607
Hydrogen cyanide sesqui-
2HCN+3HC1
C2H5C13N3
....
180 d.
Claisen & Matthews
B., 16, 309
hydrochloride
Acetamidine hydrochloride....
NH:CMe.NH,+HCl
02H7C1N2
....
164-165
Pinner
B., 17, 178
46, 723
Ethylamine hydrochloride ....
NHjEt+HCl
C2H,C1N
abt. 80
Kohler
B., 12, 1871
» »
)»
»»
315-320
76-80
Wurtz
C. B., 28, 223, 323
ii., 557
?
HCN+(CN)2Clj
C3HC12N3
20
....
i)
A, 44, 308; 79,280
ii., 280
a-Dichlorpropionitril
CH3.CC12.CN
C3H3C12N
104-107
Otto
A., 116, 199
ii.,532;iv.,736
„
is
»
103-107
Liquid
Backunts and Otto
B., 9, 1593
31, 298
JT ....
)T
)1
105
Liquid
>!
«
»
„
....
(C3H3C12N)U
....
73-5
Beckurts and Otto
B., 10, 263
32, 182
„ I:
....
))
....
73-5
)i
B., 10, 2040
34, 285
„
....
J»
74-5
Otto
A., 116, 199
ii.,532; iv.,736
384
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
a-Chlorpropionitril
CH3.CHC1.CN
C3H4C1N
121-122
Liquid
Backunts and Otto
B., 9, 1592
31, 298
Propionitril hydrochloride ...
C2H5.CN+HC1
C3H6C1N
....
121
Gautier
C. R., 63, 921
vi., 524
Propionamidine hydrochlo-
NH:CEtNH2+HCl
C3H9C1N2
d. 230
133
Pinner and Klein
B., 11, 1484
36,47
ride
jj »
)»
JJ
129
Pinner
B., 17, 178
46, 723
Isodimethyl fonnamidine
NH:CH.NMe2+HCl
JJ
....
168-169
*?
B., 16, 1650
44, 1090
hydrochloride
Propylamine hydrochloride...
Me(CH2)2.NH2+HCl
C3H10C1N
....
a. 100 +
Mendius
A., 121, 129
v., 891
jj >j
n
JJ
....
139-5
Gautier
C. R., 67, 723
vi., 966
» »
jj
JJ
....
156-158
Linnemann
A., 161, 43
25, 236
Tetrachlorpyrroline
....
C4HC14N
....
110 d.
Ciamician & Silber
B., 16, 2391
46, 292
a-Chlorcrotonitril
CH3.CH:CC1.CN
C4H4C1N
136
Liquid
Sarnow
B., 5, 470
25, 690
Chloroxalmethyline
C4H5C1N2
204-S05
Liquid
Wallach
A,, 184, 53
32, 185
,,
...»
1»
205
....
Wallach & Schulze
B., 14, 422
40, 572
Ethylcyanide -f cyanogen-
Et.CN+CNCl
JJ
60-68
Henke
A., 106, 289
il., 280
chloride
Trichlorbutylidenimide
CCl3.CH2.CHi,CH:NH
C4H6C13N
d. 192
164-165
Pinner and Klein
B., 11, 1491
36,42
ji ...
i)
1J
169-170
Schiff
B., 11, 2167
36, 452
Dichloracetethylimidechlo-
CHCl2.CCi:NEt
JJ
161-164
Wallach and
B., 13, 517
38, 547
ride
Kamenske
Hydropyrroline hydrochlo-
C4H7:N+HC1
C4H8C1N
...»
173-174
Ciamician & Denn-
B., 16, 1539
44, 1142
ride
stedt
Butylamine hydrochloride ....
CH3.(CH2)3.NH2+HC1
C4H12C1N
....
195
Linnemann & Zotta
A., 162, 3
vii., 222; 25,
475
Isobutylamine hydrochloride
CHMeEt.NH2+HCl
)J
....
b. 100
Wurtz
A., 93, 124
v., 737
» »
»»
JJ
....
160
Linnemann
A., 162, 3
25, 477
» »
»
J)
160
Brauner
A., 192, 65
34, 779
Butylamine hydrochloride ....
CMe3.NH2+HCl
Jl
....
a. 250
Linnemann
A., 162, 7
vii., 223; 25,
477
!> »
»
M
....
270-280
Brauner
A., 192, 65
34, 779
Trichlorpyridine
....
C6H2C13N
48
Konigs and Geigy
B., 17, 594
46, 1195
i)
....
))
.$9-50
»
B., 17, 1834
46, 1369
?
....
C5H2C14N2
....
212
Pechmann & Stokes
B., 18, 2291
48, 1202
Dichlorpyridine
..,,
C5H3C12N
....
66-67
Konigs and Geigy
B., 17, 1833
46, 1369
?
C6H3C13N2
157-5
Pechmann & Stokes
B., 18, 2291
48, 1202
Chlorpyridine (cf. B., 15, 1179)
N.C1=1.2
C5H4C1N
14S (743-5)
....
Ciamician & Denn-
B., 14, 1154
40, 826
stedt
»
Chloroxalmethylethyline ....
J»
1)
C5H,C1N3
147-148
212-213
Liquid
))
Haitinger & Lieben
Wallach and West
M. C., 6, 279
B., 9, 264
48, 966
30, 184
»
>»•
j)
212-213
ii
Wallach
A., 184, 72
32, 187
Diethylformamidine hydro-
NEt2.CH : NH+Ha
C5H13C1N2
125
Pinner
B., 17, 180
46, 724
chloride
Piperylhydrazine hydrochlo-
C6H10N.NH2+HC1
j;
162
Knorr
B., 15, 860 ; A.,
42, 1115 ; 46,
ride
221, 297
467
Hexachlor-a-picoline
C5HC13N.CC13
C6HC16N
....
60
Ost
J. p., 27, 277
44, 793
i) »
))
60
Bellmann
J. p. [2], 29, 1
46, 841
Pentachloraniline
C6C16.NH2
C6H,C15N
....
235
Langer
B., 15, 1331
42, 1058
)>
1)
232
A., 215, 120
Trichlormethylpurine
C5N4MeCl3
C6H3asN4
174
Fischer
B., 17, 331
46, 996
Tetrachloraniline
NH2.C1.,=1.2.3.4.6
C6H3C14N
cf. B., 10, 270
88
Beilstein and Kur-
B., 11, 1863; A.,
31, 707; 36, 144
batow
196, 236
"
„ =1.2.3.5.6
)1
»
90
5)
»
51
» ....
„ =1.2.3.4.5
118
Trichloraniline
NH2.C13=1.2.3.4
C6H4C13N
u
292 c.
67-5
1)
)I
ji
j»
?I
D
» jj
»
cf. 10, 270
67-5
»
B., 9, 1688
31, 473, 707
jj
„ =1.2.4.6
5J
77
Langer
B., 15, 1064
j» ....
'> JJ
Jl '
....
77-5
Korner
....
31, 706
jj .... ....
» JI
)»
....
78-79
Pierson and Heu-
B., 16, 1049
44, 915
niann
»
" JJ
!»
77-05
Mills
P. M. [4], 49, 21
28, 648
jj ....
» JJ
»
77-068
51
P. R. [1831], 205
COMPOUNDS CONTAINING FOUR ELEMENTS.
385
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Trichloraniline
NH2.C13=1.2.4.6
C6H4C13N
260 c. (752)
77-5
Beilstein and Kur-
B., 8, 1656
29, 713
batow
»
11 »
»
262 c.
77-5
u
B., 11, 1862
36, 143
„
11 »
))
80
Wegenhoffer
J. p. [2], 16,_451
34, 297
„
„ =1.2.4.5
I
94-95
Beilstein and Kur-
B., 9, 579
30, 294
batow
„
1J »1
»
95
j»
B., 9, 1688
31, 473
„
»1 »'
J»
95-96
D
B., 11, 1860
36, 143
„ .... ....
)1 11
»»
270
96-5
Lesimple
A., 137, 125
vi., 921
Quinoue dichlordiimide
C6H2C12.NH.NH
C6H4C12N2
124 d.
Krause
B., 12, 48
i i
Tetrachlor-diaruidoboizene....
(NH0)2.C14=1.4.2.3.5.6
C6H4C14N2
p. d. 200
218 u. c.
u
B., 12, 51
36, 462
NH3 on (trichloracetonitril)n
C6cf7N3(NH2)2
C6H4C17N5
....
165
Weddige
J. p. [2], 28, 188
46, 35
Dichloraniline
NH2.C13 = 1.2.3
C6H6C12N
252 c.
23-24
Beilstein and Kur-
B., 10, 2090 ; 11,
34, 299; 36, 143
batow
1861 ; A., 196,
217
fj .... »««•
„ =1.2.6
)»
....
39
»)
B. S. [2], 30, 25;
34, 974; 36, 143
A., 196, 219;
B., 11, 1861
„
„ = *
»
....
49-5
Laubenheinier
B., 7, 1601
28, 759
,, .... ....
„ =1.2.5
J>
251
50
Jungfleish
A. C. [4], 15, 252
ji ...» ....
>1 »
)J
251
50
Beilstein and Kur-
A., 196, 215 ;
31, 473 ; 34,
batow
B., 9, 1688; 10,
299 ; 36, 143,
2089; 11, 1861,
231
2057
>i •••• "••
„ =1.3.5
»
259-260
50-5
»
11
»
(740-6)
,, .... ....
» )»
)1
50-5
Witt
B., 8, 145
„ ....
„ =1.2.4
j»
....
63-64
Pierson and Heu-
B., 16, 1049
44, 915
mann
)i .... •«
It >1
11
....
6V9
Korner
G. I., 4, 305
29, 215
,, ....
11 )1
»
239 u. c.
62-5
Witt
B., 7, 1602
28, 759
,,
)> )»
»)
2Jf5 c.
63
Beilstein and Kur-
A., 196, 219; B.,
28, 451, 1037 ;
batow
7, 1761; 8, 693;
31, 706 ; 34,
10, 270, 2089;
299 ; 36, 143
11, 1861
ji .... ...
„ =1.3.4
272
71-5
>»
11
»
NH3.C1 = 1.2
CfiHfiClN
207 c.
Liquid — 14
B., 7, 487, 1395
27, 806; 28,
^^6*^6
363
Liquid
Jungfleish
A. C. [4], 15, 186
vii., 145
„
JJ *>
„ = 1.3
))
11
230 c.
Liquid
Beilstein and Kur-
B., 7, 1399
28, 364
batow
Liquid
Korner
G. L, 4, 305
29, 233
)» »»
= 1.4
j»
Solid
11
»
J1
1)
64
Griess
vi., 921
64
Heumann
B., 5, 915
26, 168
1) >*
64
Gabriel
B., 11, 2260
36, 323
Jl »
11
a. 200
65
....
vi., 439
1» )*
>1
69-5
Laubenheimer
B., 9, 1827
31, 594
)) Jl
11
69-706
Mills
P. E. [1881], 205
'1 J>
11
69-69
P. M. [4], 49, 21
28, 648 ; vii.,
)> **
11
905
230-231 c.
69-70 ; a. s.
Beilstein and Kur-
B., 7, 1395 ; A.,
28, 362 ; 80,
)1 1*
70-71
batow
182, 94
361
231
Solid
U
B., 7. 487
27, 806
»» .... .... ...
)J »
)»
70
WaUach and Huth
B., 9, 425
30,97
Chlor-a-picoline
1»
164-165 u. c.
21
Ost
J. p. [2], 27, 278
44, 793
Chlorpicoliiie
id. with preceding
>1
160-170
....
Ciamician and
B., 14, 1162
40, 827
Dennstedt
Dichlordiamidobenzene
(NH2)2.C12= 1.2.3.5
C6H6C12N2
60'5
Witt
B., 7, 1604
28, 759
»
= 1.4.2.6
H
123-5
»!
B., 8, 145
3 D
386
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet-
& J. Ch. Soc.
Chlordiamidobenzeue
(NH^Cl = 1.2.4
C6H7C1N2
72
Beilstein and Kur-
B.,8,693; 9,634
28, 1037; 30,
batow
309
)!
!) >!
„
72
Laubenheimer
B., 9, 773
30, 295
)»
= 1.3.4
„
.86
Beilstein and Kur-
B., 11, 1939; A.
36, 144
batow
197, 76
Aniline hydrochloride
C6H5.NH2 + HC1
n o ^^y t
C6H8C1N
....
192
Pinner
G. J. C., 1881
Picoline „
C6H.N.HC1
„
....
160
Ramsay
P. M. [5], 2, 271
36, 263
Chlorcyanmethine
....
C6H8C1N3
+ 3H2O
165 u. c.
Baeyer
B., 4, 176
Chlorcyanmethine dichloride
C6H9C1N3.C12
C6H8C13N3
s. b. 200
Keller
J. p. [2], 31, 363
48, 961
Chloroxalethyliue
....
C6H9C1N2
217-218
s. f. m.
Wallach
B., 7, 327
27, 985
„
....
„
217-218
ord. temp.
„
A., 184, 40
32, 184
Di(chlorallyl)amine
(C3H4C1)3NH
C6H9CLN
194 d.
....
Engler
B. S. [2], 9, 134
vi., 95
„ hydrochloride
+ HC1
CfiH10d3N
b. 100
„
„
„
a-methylpiperidine „
C6H13N + HC1
C6H14C1N
189
Ladenburg & Roth
B., 18, 48
48, 557
Capronamidine hydrochloride
NH : C(C5HU).NH3 + HC1
C6HlbClN3
106-107
Pinner
B., 17, 178
46, 723
Isobutylbiguauide „
NH(CH2Pr0).C(NH).NH.
C6H16C1N6
....
216
Smolka
M. C., 4, 815
46, 288
C(NH).NH2 + HC1
„ dihydrochloride
+ 2HC1
C6H17C13N5
....
194
M
1)
„
Chlorbenzonitril
C6H4C1.CN = 1.2
C7H4C1N
232 u. c.
42-43
Henry
B., 2, 493
„
= 1.3
„
....
39
Griess
B., 2, 370
vii., 427
„
= '
„
b. 40
Limpricht
i., 564
From o-nitrobenzaldehyde ....
„
82-84
Rudolph
B., 13, 311
38, 469
Isocyanophenyl chloride
Ph.N:CCl2
C7H6C13N
211-212
Liquid
Sell and Zierold
B., 7, 1229
28, 270
,i i)
„
„
212
....
Hofmann
B., 12, 1127
36, 805
Trichlortoluidine
Me.Cl:,.NH2=1.2.4.6.3
C7H6C13N
....
91
....
A., 187, 278
„
„ =1.2.4.5.?
J)
....
94-95
Seelig
B., 18, 423
48, 770
„
=1.2.3.4?
J)
....
105
„
„
11
Dichlortoluidine
Me.Cl2.NH2=1.2.4.6
C7H7C12N
*259
88
Wroblewsky and
Z. C. [2], 6, 164
vii., 1167, 1177
Pirogow
„
» ,.
„
259
88
Wroblewsky
A., 168, 213
27, 56
Trichlordiamidotoluene
Me.Cl3.(NH3)2=1.2. 4.5.3.6
C7H7C13N2
....
196
Seelig
B., 18, 423
48, 770
„
„ =1.2.3.4.5.6
„
195-207 d.
n
,,
„
Chlormethylaniline
Cl.NHMe=1.3
C7HSC1N
240
Liquid
Coste and Bodewig
B., 18, 431
48, 793
Chlorbenzylamine
C1.(CH2.NH2)=1.4
„
Liquid
Jackson and Field
A. C. J., 2, 95
40, 806
„
=1
11
Liquid
Berlin
A., 151, 144
vi., 338
Chlortohiidine
Me.Cl.NH2=1.3.4
„
222
Liquid
Wroblewsky
Z. C. [2], 5, 322 ;
vi., 1104; 27,
A., 168, 197
54
„ =1.4.6(2)
i.
236
Liquid
Henry and Radzis-
Z. C. [2], 5, 542
vi., 1104
zewsky
„
» ,,
„
238
Liquid-14
Wroblewsky
Z. C. [2], 6, 683
vi., 1105
..
*> »
„
238
Liquid -20
„
A., 168, 197
27, 55
„
=1.4.3
„
18
Engelbrecht
B., 7, 797
27, 986
„
= 1.2.?
„
26
Lellmann
B., 17, 535
46, 1133
„
=1.4.6(2)
IT
28-29
Engelbrecht
B., 7, 797
27, 986
»
» »
„
241
29-5
Beilstein and Kiihl-
Z. C. [2], 6, 102
vii., 1177
berg
»
=1.4?
„
241
83
Wroblewsky
Z. C. [2], 6, 683
vi., 1105
»
" J)
H
241
83
„
A., 168, 147
27, 55
»
». ,,
„
237-242
....
„
Z. C., 12, 684
»
» ,,
„
243
85
Henry and Radzis-
Z. C. [2], 6, 157
vi., 1105
zewsky
Chlormethylaniline hydro-
Cl.NHMe=1.3
C7H,CL,N
164
Coste and Bodewig
B., 18, 430
48, 793
chloride
Chlorbenzylamine hydro-
C1.(CH.,.NH.,)=?
I)
197
Berlin
A., 151, 144
vi., 339
chloride
» ..
,, =1.4
J1
239-241
Jackson and Field
A. C. J., 2, 95
40, 805
Benzylamine „
Ph.CH2.NH2+HCl
C7H10C1N
235-240
Spica
G. I., 10, 515
40, 262
Glyoxalisoamyline „
C7H13N3+HC1
C7H13C1N2
135-136
ladziszewsky & Szul
B., 17, 1291
46, 985
a-y-hydrolutidine „
C7H16N + HC1
C7H1BC1N
235
Ladenburg & Roth
B., 18, 919
48, 816
Phenyldichloracetonitril
C6H5.CC1.,.CN
223-224
Claisen
B., 12, 626
Chloroxiiidole chloride
CsH4.CCi:CCl.NH=1.2
i j
D
cf.B.,15, 786
103- 104
Baeyer
B., 12,458
36, 535
COMPOUNDS CONTAINING FOUR ELEMENTS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Chlorphenylacetonitril
C,H4C1(CHS.CN)=1.4
C8H6C1N
....
Liquid
Neuhof
A., 147, 347
40, 806
„
„ „
„
....
29
Jackson and Field
A. C. J., 2, 85
40, 803
Tolyldichlorcarbimide
CH3.CNC1£=1.2
C8H7C12N
218
Lachmann
B., 12, 1349
36, 935
Trichlordimethylaniline
NMe2.Cl3=1.2.4.6(?)
CSH8C13N
257
32
Krell
B., 5, 879
26, 279
l)ichlordimethylaniline
NMe.2.Cl2=1.2.4(?)
C8H9C12N
234
Liquid
„
„
„
Acetanilide chloride
Ph.NH.CCl2.CH3
„
b. 50
Wallach and Hof-
B., 8, 1570 ; A.,
29, 604
niaim
184, 88
Chlordimethylaniline
NMe2.Cl=?
C8H10C1N
212
Liquid
Krell
B., 5, 879
26, 279
„
„ =1.3
„
231-233
Liquid
Baur and Sta'del
B., 16, 32
44, 579
Chloreth y laniline
NHEt.Cl=1.4
„
Liquid b. 0
Hofmann
A., 74, 143
iv., 451
Chlorxylidine
Me2.NH2.Cl=1.3.4.?
„
89
Tawildarow
Z. C., 1870, 419
„
=1.4.5.?
11
....
92-93
Jannasch
A., 176, 55
„
„ =1.4.5.2
,,
....
92
Kluge
B., 18, 2098
Chlorethylphenylamine
NHPh.C2H4Cl + HCl
C8H,,C12N
158
Nemirowsky
J. p. [2], 31, 173
48, 741
hydrochloride
Phenylethylamine hydio-
Ph.CH2.CH2.NH2+HCl
C8H12C1N
217
Filati
G. I., 8, 446
36, 719
chloride
11 <i
„ „
11
217
Filati and Piccini
B., 12, 1308
36, 922
,1 .»
11 11
,,
217
Spica
G. I., 9, 555
38, 241
Xylylamine hydrochloride ....
Me.C6H4.CH2.NH2+HCl
„
185
Pieper
A., 151, 129
vi., 1132
11 )>
J! "
„
a. 230 d.
Colombo and Spica
G. I., 1875, 124
28, 895
Chloroxalpropyline
C8H13C1NS
235
....
Wallach & Schulze
B., 13, 516
38, 547
,,
•
236
....
„
B., 14, 423
40, 572
Di(chlorallyl)ethylamine
(C3H4Cl)2N.Et
CSH13C12N
s.a. 200
Engler
B. S. [2], 9, 134
vi., 95
Hydro-a-isopropylpyridine
....
C3H14C1N
....
208-210
Ladenburg
B., 18, 1589
48, 992
hydrochloride
a-isopropylpiperidine hydro-
CTT XT _L TirM
8±±17ll -f-ilv^l
C8H18C1N
206
„
B., 17, 1679
46, 1386
chloride
Coniiue hydrochloride
„
,.
C8H,6C1N(?)
218
„
„
„
Copellidine ,,
„
„
....
171
Diirkopf
B., 18, 923
48, 817
Trichlorquinoline
C9H4C13N
107-5 u.c.
Rugheimer
B., 17, 738
46, 1050
„ ^
H
....
140
Feer and Konigs
B., 18, 2396
48, 1235
11
f)
....
160-5
Friedlander and
B., 15, 1425
42, 1209
Weinberg
a-y-dichlorquinoline
11.0.01=0,8,0., ;
C9H5C12N
....
67
Baeyer and Bloem
B., 15,2150,2152
44, 196
,, „
1> >!
H
280-282
67
Friedlander and
B., 15, 2683
Weinberg
,, „
„ =0,8,8., ;
„
....
104
„
B., 15, 2679
44, 351
a-i- „ .... -~^T
>i >i
„
....
104-105
Baeyer
B., 12, 1321
36, 946
p- >.
„ ="i ! a,a:
„
92-93
Coste
B., 15, 561
42, 979
m- „ '
jj 1 ' lr^'2
„
....
103-104
„
„
„
Chlorquinoline
N.Cl=ai ; 82
U9H6C1N
256
Liquid
»
B., 15, 559
11
„
„ =meta
„
264-266
Liquid
Coste and Bodewig
B., 17, 926
46, 1197
„
_ai)3i .
M
266-267
37-38
Friedlander and
B., 15, 334
42,732
Ostermeier
Anhydroamidotolyloxamic
11 * j
CBH,Me.N : CC1.CC1 : N
i6 ; i
C,H6C12N2
114-115
Hinsberg
B., 16, 1533
44, 1129
chloride
=1.3.4
Methylchloroxindole
C,H4.Ca : CCl.NMe=1.2
C9H7C12N
....
58-59
Baeyer
B., 15, 786
42, 1103
Tetrachlorcyanconine
C9H10C13N2C1
C9H10C14N2
Liquid
Riess
J. p. [2], 30, 145
48, 236
Dimethylbenzamidochloride
Ph.CCl2NMe,
C9H,,C12N
36
Hallmann
B., 9, 846
30, 418
Tetrahydroquinoline hydro-
CaHnN + HCl
C9H12C1N
180-181
Hoffmann and
B., 16,729
44, 1143
chloride
Konigs
Trichlorcyanethine ....
C,H12C13N3
....
110
Riess
J. p. [2], 30, 145
48, 236
Propyl|)henylamine hydro-
C6H4.Pr«.NH2=1.4
C9H14C1N
203-204
Francksen
B., 17, 1221
46, 1007
chloride
C'uniidiiie hydrochloride
C,H4.Pr0.NH2=?
„
....
62
Schaper
Z. C. [2], 3, 12
vi., 516
Triacetonamine hydrochloride
CMe2.CH2.CO.CH2.CMe2. NH
C9H18C1N
293
Fischer
B., 16, 650
44, 790
Methyltrichlorquinoline
C9NH3MeCl3
C10H6C13N
134
Rugheimer and
B., 17, 741
46, 1023
Hoffmann
/3-dichlornaphthylamine
C10H6C12.NH2
C10H7C12N
104
Widmann
B. S. [2], 28, 510
32, 900
3 D 2
388
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
ij-dichlornaphthylamine
C10H6C12.NH2
C10H7C12N
94
Cleve
B. S. [2], 29, 500
34, 736
Chlornaphthylamine
NH2.Cl=a,a,, ;
CiaH3ClN
85-86
Atterberg
B., 10, 548
„
„ =0; ; a.
„
93-94
„
„
„
i> »>
n
93-94
„
B., 9, 1731
,,
11 ^ *
„
98
Seidler
B., 11, 1201
34, 983
Methychlorquinoline
N.Me.Cl=a,/3,aj ;
„
290
59
Knorr and An trick
B., 17, 2878
48, 274
f-diehlordiamidonaphthalene
Cl ; Cl
C10H8C12N2
204-205
A16n
B. S. [2], 36, 433
42, 410
Quinoliue methochloride
C9H7N.MeCl + H2O
C10H10C1N
126
Ostermeyer
B., 18, 593 ;
48, 672
C.C., 1884, 970
Tetrahydroquinoline metho-
C9HnN.MeCl+H,0
„
244
3)
„
„
chloride
Chlor-a-naphthonitril
C10H6C1.CN
CUH6C1N
145
Ekstrand
B., 17, 1604
46, 1361
Tetrachlordispoline (tetra-
....
CnH7Cl4N
135
Zorn
J. p. [2], 8, 304
27, 484
chlorcryptidine)
?
CPh : N.CCl.CH.CMe : N
CUH9C1N0
71
Pinner
B., 17, 2520
48, 159
i j'
Ethylchlorquinoline
N.Cl.Et=alS1/32 ;
CnH^CIN
72-73
Baeyer & Jackson
B., 13, 120
38, 407
|3-naphthiniidoamide hydro-
C10H7.C(NH2) : NH+HC1
CnHjjClNj
224-226
Pinner and Klein
B., 11, 1486
36, 48
chloride
Quinoline ethochloride
C9H7N.EtCl+H20
CnH12ClN
92-5
Claus and Tosse
B., 16, 1278
44, 1009
Octochlorcarbazole
C6C14.NH.C6C14
C12HC18N
275
Knecht
A., 202, 29
38, 661
L. J
Hexachlorcarbazole
C12H3C16N
225 d.
„
A., 202, 28
„
Dichlorazophenylene
Fr.C,H4.]fc6H4N
C12H6a2N2
144
Claus
B., 8, 604
28, 899
i i
Trichlorcarbazole
C12H6C13N
180
Knecht
A., 202, 28
38, 660
Tetrachlordiphenylamine ....
NH.(C6H3C12)3
C12H7C14N
133-134
Gnehm
B., 8, 1040
29, 265
Azoaraidodichlorbenzene
C6H3C12.N2.C6H2C12.NH2
C12H7C14N3
126-5
Griesa
A., 121, 275
iv., 460
Dichlorazobenzene ....
C6H4C1.N2.C6H4.C1=(1.3)2
C12H8C12N2
101
Laubenheimer
B., 8, 1625
29, 578
»
=(1.4),
„
183 u.c.
Willgerodt
B., 14, 2637
„
11 11
„
183
Heumann
B., 5, 914
vii., 150
»
11
„
184
Hofmann & Geyger
B., 5, 918
26, 168
„
11 11
„
....
183
Calm & Heumann
B., 13, 1182
38, 880
„
11 11
„
185
Willgerodt
B., 14, 2635
42, 396
Dichlordiphenylamine
NH(C6H4C1)2
C12H9C12N
80 u.c.
Claus and Schaare
B., 15, 1286
Azoauiidod ichlorbenzene
C,H3C1.N2.C6H4C1.NH2
C12H9C12N3
124-5
Griess
A., 121, 271
if., 460
Chloramidodiphenyl
C6H3.Ph.NH2.Cl=1.2.?
C12HIOC1N
48
Liiddens
B., 8, 872
Di-chlorhydrazobenzene
(C1.C6H4.NH.)2=(1.3)2
C12H10C12N2
94
Laubenheimer
B., 8, 1624
29, 578
11 »
=(1-4),
„
....
122
Hofmann & Geyger
B., 5, 918
26, 169; vii.,
151
» n ....
» 11
„
122
Calm & Heumann
B., 13, 1181
38, 880
Dichlordiamidodiphanyl
(C6H3C1.NH2)2=(14.1)2
„
60
Schultz
B., 17, 464
46, 903
>i
=(4.3.1),
,,
....
163
D
B., 17, 465
„
11
11 11
11
....
163
Laubenheimer
B., 8, 1625
29, 578
Ethyl /3-naphthylamine hy-
C10H7.NHEt+HCl
C12H14C1N
....
235
Henriques
B., 17, 2669
48, 168
drochloride
Trimethylquinoline „
C9NH4Me3+HCl
n
260
Pfitzinger
J. p. [2], 32, 240
48, 1246
p-dimethamidoquinoline
C,NHs.NMej+MeCl
C12H"5C1N2
+H20
244
Ostermeyer
B., 18, 596; C.C. 48, 672
methochloride
1884, 970
Hydro- p-dimethamidoquino-
C9NH10.NMe2+Mea
C12H19C1N2
+2H2O
220
B
M
(j
line methochloride
Chloroxalisoamylene
....
C12H21C1N2
267-870
Liquid
Wallach
A., 214, 316
44,49
)!
....
265-270
Liquid
Wallach & Schulze
B., 13, 516
38, 547
Methyltetrachlordiphenyl-
NMe(C6H3Cl!!)2
C13H9C14N
••««
96-97
Gnehm
B., 8, 1041
29, 265
amine
Benzanilideimide chloride
Ph.CCl:N.Ph.
C13H10C1N
abt, 310
39-40
Wallach & Hofmann
B., 8, 313
28, 1031
Diehlordiphenylguanidine ...
C13HnCl2N3
140-141
B. S., 32, 170
a-amidotolyl-phenylhydro-
chloride
Fr. C6H4PhMe=1.4
C13H14C1N
280-283 p.d.
Carnelley
29, 21
?-
....
200
Jackson
B., 10, 961
32, 606
Benzylidene plienyldiamine
NHPh.CHPh.NH2+HCl
C13HI5C1N2
223-224-5
Bernthsen and
B., 13, 918
38, 639
hydrochloride
Szymansky
COMPOUNDS CONTAINING FOUR ELEMENTS.
389
Name.
Consttiution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
a-, 8-,y-, and 8- Dichlordiben-
NH(CH2.U6H4C1)2= ?
Oj4iij3012^
Liquid
Berlin
A., 151, 141
40, 806
zylamine
°" » >! »
=(1.4)2
»
....
29
Jackson and Field
A. C. J., 2, 94
40, 805
Trichlorethylidene diphenyl
CCl3.CH.(NHPh)2
C14H13C13N2
100-101
Wallach
B., 5, 251 ; A.,
vii., 311 ; 25,
dianiine
173, 274
611 ; 28, 349
)» 51 »
J)
»)
• ...
100
Amato
G. I., 5, 461
30, 637
a-dichlordibenzylainine by-
NH(CHj.C,H4Cl)s=(1.4)2
C14H14C13N
288-289
Berlin
A., 151, 141
vi., 338
drochlnride
a~ » v '»
T» )»
H
....
288
Jackson and Field
A. C. J., 2, 85
40, 805
P>~ V » 5?
= »
)>
225-228
Berlin
A., 151, 141
vi., 338
y- » . » »
» )>
)1
218-220
u
»
»
» »I »
M »»
»
221-222
»
5)
j)
Trichlorethylidene dipheuyl-
C013.CH(NHPh)2+HCl
C14H14C14N2
196
Amato
G. I., 5, 461
30, 638
diamine hydrochloride
» « »
CCl3.CH(NHPh)2+2HCl
C14H16C15N2
w.m.
»
»
))
Dibenzylamine hydroohloride
(C6H6.CH2)2HN+HC1
C14H16C1N
250
Limpricht
A., 144, 304
vi., 337
)» »
»
V
255-256
Spica
G. I., 10, 515
40, 262
?
....
CI6H9a2N
162-1C3
Gabriel
B., 18, 2450
48, 1231
Cinnamaldehyde anilide hy-
Ph.CH:CH.CH : NPh+HCl
C15H1401N
149
Peine
B., 17, 2117
46, 1345
drochloride
Methy lacridine methochloride
C13H8NMe+MeCl
C15H16C1N
....
130-135 d.
Bernthsen
A., 224, 1
46, 1356
Ainidomethyl dihydro anthra-
C14H10Me.NH2-)-HCl
C15H16C1N
....
245
Roemer
B., 16, 1633
44, 1137
cene hydrochloride
? hydrochloride
C16H16N6+HC1
C16H17QN6
....
252
Berger
M. G, 5, 451
48, 387
Dimethylphenylbenzylam-
(Ph.CH2.NPhMe2)Cl
C15H18C1N
+H20
110
Michler& Gradmaim
B., 10, 2079
moniutn chloride
Dibenzylguaiiidine hydro-
NH : CCNH-CHsiPh^+HCl
C15H19C1N3
176
Strakosch
B., 5, 696
vii., 182, 582
chloride
Triarnylamine hydrochloride
(CVH^N+HCl
C15H34C1N
b. 100
Plimpton
C. R., 91, 433
40,34
Quinoline benzylchloride ....
?» »
C6H4.CH : OH.C : NCl.CH2Ph
C16H14C1N
1»
+ 2H2O
170
129-130
Clauss and Tosse
i)
B., 16, 1277
»
44, 1009
»
i) :i
» i)
)» JJ
J1
))
130
)>
»
»
j> »
>i "
JI
+3H2O
65
D
»)
»»
i) >i
11 I!
»J
)»
65
Glaus & Himmel-
B., 13, 2046
mann
I
Ph.N:CMe.CH2.OCi:NPh
C16H15C1N2
116-117
Wallach & Hof maun
B., 8, 1570; A.,
29,604;32,188
184, 95
Trichlorethylidene di-p-tolyl-
C«l3.CH(NHC6H4Me)2
C16Hl;a3N2
114-115
Wallach
B., 5, 252; A.,
vii., 311,1179;
amine
173, 279
25, 611 ; 28,
350
From Zu-ethide on benzo-
C16H18N2+HC1
CKH19C1N2
257
Frankland & Evans
....
37, 565
nitril
'
Diphenylethylamine hydro-
(Ph.CH3.CH2)2NH+HCl
C16H20C1N
265
Fileti and Piccini
B., 12, 1308
chloride
» »
»
»
quick Ht.
260
Spica
G. I, 9, 555
38, 241
)' »
»
»J
slow Ht.
265
j»
»
))
Dixylylamine hydrochloride
(Me.C6H4CH2)2NH + HC1
)»
198
Pieper
A., 151, 129
vi., 1133
Butylacridine hydrochloride
013H8N.04H9+HC1
C17H18C1N
191
Bernthsen & Traube
B., 17, 1509
46, 1183
Tetramethylbeuzidineiuetho-
Me2N.C6H4.C6H4.NMe3Cl
C17H23C1N2
....
228
Michler& Pattinson
B., 17, 117
46, 747
chloride
=(1.4)2
Acutamide on pheuylcyan-
C18H17N6+HC1
C18H18C1N5
softens 240
256-264 u.c.
Berger
B., 14, 1256
40, 810
araide
Base from aceto-o-toluide ...
....
C18H19C1N2
....
52-53
Wallach
A., 214, 208
44, 48
» »
J-
71-72
D
B., 9, 1214
31, 92
Trichlorethylidene dixylyldi-
CCla.CH(NH.C6H3Me2)2
C18H21C13N2
95-99
j>
A., 173, 283
28, 350
amine
Ethylene dipheuyldimethyl-
C2H4(NClMe2Pli)2
C18H26C12N2
124
Hiibner, Tolle, and
A., 224, 331
46, 1318
auimoninm chloride
Athenstadt
?
C19H13N+HC1
C,9H14C1N(?)
a. 220
Bernthsen
A., 192, 1
34, 789
Dichlorbenzenyldiphenyl-
NPh2.CCl2.Ph
C19H15C12N
cf. B.I 5, 1285
149
Claus
B., 14, 2369
42, 178
ainine
-
300
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Methylenediquinoiil hydro
CH2(C9H6N)2+2HC1
C19H16C12N2
168
llhousopoulos
B., 16, 2005
44, 1150
chloride
Benzenylisodiphenylamidine
NPhj-CPhiNH+HCl
C19H17C1N2(
223d.
Beruthsen
A., 192, 1
34, 788
hydrochloride
Triphenylmethylamine hy
CPh3.NH2+HCl
C19H18C1N
....
244
Elba
B., 16, 1276
44, 1000
drochloride
Triphenylguanidine hydro
PhN : C(NHPh)2+2HCl
C19H19C12N3
207
Sell and Zierold
B., 7, 1231
28, 270
chloride
Cinchonine chloride
....
C19H21C1N2
52
Koenigs
B., 13, 287
38, 674
» »
....
)>
....
72
»
B., 14, 1854
Diquiuoline methochloride ..
CI8N2H12+2MeCl
C20HIS012N2
+ 6H2O
260
Osteruieyer
C. C., 1884, 970
48, 672
Triphenylethylamine hydro
CPh3.CH2.NH2+HCl
C^H^CIN
....
247
Elbs
B., 17, 700
46, 1031
chloride
Chlorhydrobenzamide
isomeric
C21HI7C1N2(?
183
A., Ill, 158
»
jj
., (»
186
A., Ill, 146
Lophine hydrochloride
C21H16N2+HC1.
»
160
Kiihn
....
iii., 735
!) )!
....
)»
155
Brunner
A., 151, 135
vi., 793
Trichlortribenzylamine
N(CH2.CfiH4Cl)3=(1.4)3
C21H18C13N
S8-89
Berlin
A., 151, 139
vi., 338
n
»
)»
78-5
Jackson and Field
A. C. J., 2, 92
40, 805
„ hydro-
N(CH2.C6H4C1)3+HC1
C21H19014N
abt. 196
»
»»
>»
chloride
=(1-4),
» i»
» )i
)J
170-175
Berlin
A., 151, 139
vi., 338
Tribenzylamine hydrochlo-
(C6H6.CH2)3N+HC1
C21H22C1N
....
227-228
Spica
G. I., 10, 515
40, 262
ride
?
....
C-^H^CIN,
....
162-163
Berlin
A., 151, 136
Phenylbenzo-3-naplithacri-
C6H4.CPh.C10H6.N + HCl
C23H16C1N
235
Claus and Kichter
B., 17, 1596
46, 1359
dine hydrochloride
|
j8-dicyano-p-phenyl-p-ditolyl-
....
C^CIN,
....
110-115
Landgrebe
B., 11, 975
guanidine
Leuco-base from trichlor-
C.H.Cl.N,
....
128-129
Tischer
D. P., 252, 78
46, 944
benzaldehyde
Triphenylethylamine hydro-
(Ph.CH2.CH3)3N+HCl
C^HjjCON
>...
137-138
Spica
G. I., 9, 555
38, 241
chloride
Trixylylamine hydrochloride
(Me.C6H4.CH2)3N+HCl
))
212
5ieper
A., 151, 129
vi., 1133
Triphenylmethylbenzyl-
Ph.CH2.NH.CPh3+HCl
C26H24C1N
....
249
Elbs
B., 17, 703
46, 1031
amine hydrochloride
Hydrocinnamide hydrochlor-
(Ph.CH:CH.CH2)3N2
C27K,5C1N2
+3H2O
220-221
'eine
B., 17, 2111
46, 1344
ide
Benzylamarine ethochloride
C21Hl;(CH2Ph)N2+EtCl
C30H29C1N2
125 u.c.
Glaus & Kohlstock
B., 18, 1854
48, 1133
Ethylbenzylamarine hydro-
C21H16Et(CH2Ph)N2+HCl
)»
135 u.c.
»i
j)
1)
chloride
Benzylamarine benzochloride
C21H17(CH2Ph)N2
C^CIN,
45
n
B., 18, 1853
-fPh.CHX!!
» -)
» »
?)
40-75
Dlaus and Elbs
B., 13, 1420
8,882
(6.) CHOP, CHClAs, CHClSb, and CHC1BL
Ethylphosphotetrachloride ....
Isopropylphosphodichloride
PEtCl4
PPrfCl,
C2H5C14P
O.HyCljP
135
100 d.
Liquid
Michaelis
B., 13, 2175
40, 158
Phenylphosphodichloride ...
PPhCl,
C6H5C12P
140-142 (57)
)1
Michaelis and Coste
B., 18, 2109
11
55
))
220-222
Kohler & Michaelis
B., 10, 813
32, 451
jj
Jl
»5
222 u. c.
Liquid
Michaelis
B., 6, 602, 816
26, 1148; 27, 168
n
»
»
222
»>
C. C., 4, 548
37, 347
u
Phenylphosphotetrachloride
Triethylphosphodichloride ....
PPh014
PEt.,( 1,
»)
C,H5C14P
CBH,5C1,,P
224-6 (763-6)
73
100
Thorpe
Michaelis
37, 347
B., 6, 817
27, 168
iv., 611
Tolylphosphodichloride
C6H4Me.PCl.= 1.2
v^6 16 2
C.H7C12P
944
Liquid— 20
Michaelis & Panek
A., 212, 212
42, 959
>' „ =1.4
J)
245
20
V
B., 13, 655
38, 641
COMPOUNDS CONTAINING FOUR ELEMENTS.
391
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Tolylphosphodichloride
C6H4Me.PCl2=1.4
C7H7C12P
245
25
Michaelis & Panek
A., 212, 212
42, 959
„
>! !)
1)
240
Liquid
Michaelis
B., 12, 1009
36, 721
Tolylpliosphotetrachloride ...
C6H4Me.PCl4=1.2
C-H7C14P
....
Solid
Michaelis & Panek
A., 212, 216 ; B.
38, 641; 48, 900
13, 653
)»
= 1.4
i)
....
42
»
D
»
Phenylmethylphosphochlo-
PPhMeCl
C7H8C1P
160
KShler & Michael i
B., 10, 814
32, 451
ride
Xylylphosphodichloride
C6H3Me.2PC',,
C8H9C12P
260-290 (?)
Liquid
Michaelis & Panek
A., 212, 236
42, 964
» ....
C6H3Me2.PU4
C8H9C14P
270
Liquid — 18
»
1»
D
Naphthylphosphodichloride
CIOHr.PCl2
C10H7C12P
a. 360 p. d.
Kelbe
B., 11, 1500
„
1»
11
a. 250
•«••
»
B., 9, 1051
Diphenylphosphocliloride ....
PPh2Cl
C12H10C1P
320
Liquid
Michaelis and Linl
A., 207, 208
42, 306
,,
1»
»
300
Liquid
Michaelis
B., 10, 627
32, 453
»
11
11
210-215(57)
....
Michaelis and Coste
B., 18, 2109
Diphenylphosphodichloride...
PPh2C13
CijHiQUljF
....
Solid
Michaelis
B., 10, 627
32, 453
Triphenylbenzylphosphochlo-
PPL3(CH2Ph)Cl
CjjHMpLP
+H20
287
Michaelis & Soden
A., 229, 334
48, 1135
ride
Tetrabenzy Iphosph ochloride
P(CH2Ph)4Cl
C^H^CIP
224-225
Letts and Collie
T. E., 30, 181 ;
40, 722; 42,
P.E.S.E., 11, 46
724
Methylarsendichloride
AsMeCl2
CH3Cl2As
133
Baeyer
A., 107, 279
i., 401
Ethylarsendichloride
AsEtC'l2
C2H5Cl2As
156
Coste
A., 208, 34
Dimethylarsenchloride (caco-
AsMejCl
C2H6ClAs
a. 100
b.— 45
Bunsen
A., 37, 31 ; 42, 22
i., 405
dylchloride)
Phenylarsendichloride
AsPhCl2
C6H,,Cl2As
252-255
Liquid
Michaelis
B., 9, 1567
31,311
»
n
*»
249
»
B., 8, 1317
29, 610
Phenylarsentetrachloride ...
AsPhCl4
C6H6Cl4As
cf. B., 9, 1568
45
»
B., 10, 622
32, 452
Tolylarsendichloride....
C6H4Me.PCl2=1.2
C7H7CLAs
264-265
Liquid
Coste and Michaelis
B., 11, 1889; A.,
36, 1(53
201, 248
,, ....
= 1.4
J)
267
31
»
»
)»
Naphthylarsendichloride
C10H7.AsCl2
C10H7Cl2As
....
63
Michaelis & Schulte
B., 15, 1954
Phenyldiethylarsendichloriile
AsPhEt2Cl2
C10H15Cl2As
Crystalline
Michaelis
B., 10, 626
32, 453
Diphenylarsenchloride
AsPhjCl
C12H10ClAs
333
Liquid
Coste and Michaelis
B., 11, 1885; A.,
36, 162; 38, 396
201, 215
»
11
11
330
Michaelis
A., 207, 195
Diphenylarsentrichloride ....
AsPh2Cl3
C12H10C13AS
cf.A.,201,222
174
»
B., 9, 1569
31, 311
Ditolylarsenchloride ....
(C6H4Me)2AsCl=(1.4)2
C14H14ClAs
340-345
Coste
A., 208, 18
Diphenylethylaraendichloride
AsPh2EtCl2
C14H15Cl2As
....
137
Michaelis
A., 201, 235
Triphenylarsendichloride
AsPh3Cl3
P TT PI A a
^18-LJ-15^-12"-a
cf.A.,201,242
171
Coste and Michaelis
B., 11,1888
36, 162
Tritolylarsendichloride
As(C6H4Me)3Cl2=(1.4)3
C21H21C12A8
....
214
Coste
A., 208, 27
40, 905
Triethylstibine dichloride ...
SbEt3Cl2
C6H16012Sb
b. 12
A., 88, 323; 97,
i., 342
332
Tritolylstibine dichloride ...
Sb(C6H4Me3)Cl2=(1.4)3
tvgj ji gjv/laO D
....
156-5
Hichaelis &Genzken
B., 17, 925
46, 1136
Ethylbismuthdichloride
BiEtCl2
C2H,,ClsBi
....
Crystalline
A., 92, 376
(7.) CHBrl.
Dibromiodomethane
CHBrJ
6
....
A, 22, 233
i., 680
Dibromiodethylene
CIBrlCHBr
C3HBr,I
....
66
Homolka and Stolz
B., 18, 2285
48, 1198
a- Bromiodethylene ....
CH2 : CBrI
C2H2BrI
128-130p.d.
Liquid
Henry
C. E., 98, 680
46, 830
(764)
0-
CHBr:CHI
>»
142
Beboul
vii., 491
»- „
»
n
150 c.
s. 8
Plimpton
B., 16, 79
41, 395
a- „
»
»i
150
....
Plimpton & Graves
43, 123
B- ,.
»
)>
150
Henry
C. E., 98, 741
46, 831
0- i,
»
D
140-150 d.
A., 216, 266
392
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
/3-Bromiodethylene
CHBrlCHI
CjH2BrI
162
Reboul
vii., 491
»- „
jj
u
150 p.d.
25
Lagermark
B., 6, 1211
JJ
lode thy lenedibromide
CH2Br.CHIBr
C-jH^Br^
170-180 d.
Simpson
P. R. S., 22, 51
27, 564
Ethylidene iodobromide
CH3.CHIBr
C2H4BrI
141-142 (735
Reboul
A., 155, 213
vii., 489 ; 27,
240
»» j»
»J
ft
142
Plimpton
41, 397
jj »»
JJ
)1
141-142
Gargariu
B., 7, 734
27, 1075
jj »» ••
n
JJ
142
Friedel
C. R., 79, 164
27, 1150
jj j»
»j
1)
142-143
Liquid — 18
Lagermark
B., 7, 913
27, 1151
JJ » •*
>j
J»
142-144
Simpson
P. R. S., 27, 118
38, 456
Ethylene ,,
CH2Br.CH2I
J)
145-147
25-5
Lagermark
B., 7, 908
27, 1151
jj 11
JJ
J)
150 p.d.
25-5
jj
B., 6, 1211
27, 240
jj ji ••-
JJ
JJ
162-167
28
Simpson
P. R. S., 22, 51
27, 564
v .,
JJ
JJ
162-167
28
Gargarin
B., 7, 733
27, 1075
)i u •••
JJ
)J
163
....
Plimpton
41, 397
11 jj
JJ
)>
163
27-r
Friedel
B., 7, 655 ; C. R.,
27, 1151
79, 164
jj u (impure)
»J
J)
160-162
Liquid
Lagermark
B., 7, 914
jj
>» jj »
»J
JJ
160 p.d.
Liquid
Eeboul
A., 155, 214
vii., 489
Bromiodpropane
CH3.CBrI.CH3
C3H6BrI
147-148 c. ;
jj
C. R., 74, 944;
25, 683 ; 36,
P.d.
B. S., 16, 50 ;
131 ; vii., 51,
A. C. [5], 14, 483
1017
55 ....
CH3.CBr CH2I(2)
JJ
160-168 p.d.
Liquid
Simpson
P. R. S., 22, 51
27, 564
Tribromiodobenzene
Br3.I=1.3.5.6
C6H2Br3I
....
103-5
Silberstein
J. p. [2], 27, 119
44,661
Bromidobenzene
C6H4BrI=1.4
C6H4BrI
251-5(754-44)
91-9
Korner
G. I., 4, 305
29, 215
jj
» =1-3
J>
252 (754-44)
Liquid
jj
jj
jj
U .... • ....
» =1-2
J>
257-4(754-44)
Liquid
jj
j>
jj
Dibronuliiodotoluene
Me.Br2.I2=1.3.5.2.4
C7H4Br2I2
«...
68
Wroblewsky
B., 9, 1055
30, 511
Dibromiodtoluene
Me.Br2.I=1.3.5.4
C7H5BrsI
270
86
jj
A., 168, 190; 192,
27, 54 ; 34, 978
209
lodobenzyl bromide
C6H4I.CH2Br=1.2
C7H6BrI
52-53
Mabery & Robin-
A. C. J., 4, 101 ;
42, 1057
son
B., 15, 1758
» u
=1.4
J)
....
78-75
Mabery & Jackson
B., 11, 55 ;
34, 421
A. C. J., 1, 103 ;
2, 250 ; 3, 252
Bromiodotoluene
Me.Br.I=1.2.3 or 5
J)
260
Liquid —20
Wroblewsky
Z. C. [2], 7, 240 ;
24, 713 ; 27, 52
A., 168, 164
»j
„ =1.3.4
JJ
265
Liquid — 14
jj
Z. C. [2], 6, 164 ;
vii., 1166; 27,
A., 168, 159
51
Bromiodonaphthalene
C1()H6BrI=a^2 ;
310H6BrI
....
68
Meldola
47, 523
jj
„ =aja2 ;
jj
83-5
jj
jj
jj
„ =a1/3l. ;
jj
....
94
jj
?j
(8.) CHBrO.
Tribromacetaldehyde
CBr3.COH
Ci!HBr3O
a. 100
Lb'wig
A., 3, 305
i., 666
(Bromal)
»» 11
jj
jj
120-180
Liquid
Pinner
A., 179, 69
29, 550
>» »i
»j
jj
172-173
Liquid —20
Schaffer
B., 4, 366
24, 558 ; vii.,
209
» j»
j»
jj
174 (760)
Kahlbaum
B., 17, 1260
« »)
u
jj
103-9 (75)
....
jj
J!
ji i>
>»
jj
92-4 (50)
jj
JJ
5» >5
u
jj-
77-7 (25)
.
jj
JJ
>» JT
u
jj
74-1 (20)
jj
11
J! JJ
»
jj
68-7 (15)
....
jj
J!
« J!
i»
jj
62-3 (10)
....
jj
11
» V
»
jj
53-4 (5)
jj
11
" JJ
>j
jj
40-6 (0)
....
jj
)>
COMPOUNDS CONTAINING FOUR ELEMENTS.
393
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Parabromalide
....
C2HBr3O
200 p.d.
67
Cloez
A., Ill, 178
iv., 340
Dibromacetyl bromide
CHBr2.COBr
„
194
....
Gal
B. S., 5, 172
vi., 21
Tribromaeetic acid
CBr3.COOH
C2HBr302
....
128-130
Wiedel and Gruber
B., 10, 1150
32, 780
„ „
„
„
245
130
Schaffer
B., 4, 370
24, 559
11 11
„
„
250
135
Crofts
A., 129, 56
vi., 18
11 »
„
„
....
136
Petrieff
B., 8, 731
Dibroinacetic aldehyde
CHBr2.COH
C2H2Br20
140-142
Liquid
Pinner
B., 7, 1500 ; C. C.
28, 1174
[1875], 3
11 "
)J
11
142
Liquid
„
A., 179, 70
29, 550
Bromacetyl Bromide
CHoBr.COBr
11
150
Hiibner
A., 124, 321
vi., 21
11 »
„
„
149-150
....
Naumann
A., 129, 263
11 51
„
„
150-155
Samosadsky
Z. C. [2], 6, 105
vii., 10
Dibromacetic acid
CHBr2.COOH
C2H2Br2O2
b. 200
....
Demole
B., 11, 319
11 11
„
„
225-230
....
Perkin and Duppa
12, 3
i., 666
,
„
„
235
43-48
Bouchardat
C. R, 100, 452
48, 499
„ ^ „
„
„
232-234 p.d.
45-50
Schaffer
B., 4, 368
24, 559
Acetyl bromide
CH3.COBr
C2H3BrO
81
Gal
B. S., 5, 172
vi., 20
„ „
„
JJ
81
Hitter
J., 8, 504
Bromethylene oxide
CHBr.O.CH2
»
89-92
Demole
B., 9, 51
29, 693
Bromacetic acid
CH2Br.COOH
C2H3Br02
205-209
„
B., 9, 561
„ „
„
11
203
53
Hofmann
B., 16, 588
„ „
„
„
208
Geuther
A., 132, 171
vi., 22
,, ,,
JJ
„
208
b. 100
Perkin and Duppa
11,22
i., 665
Bromal hydrate
CBr3.CH.(OH)2
C2H3Br3O2
53-5
Schaffer
B., 4, 366
24, 558; vii.,
209
Dibromethyl alcohol
CHBrj.CHj.OH
CTT "D_ f\
n±l,J&ln\J
179-181
....
Demole
B., 9, 49
29, 692
?
Me.CBr(OBr)OH
C2H4Br2O2
....
36-37
Hell & MUlhauser
B., 10, 2105
34, 289
Ethylene Bromhydrin
CH2Br.CH2.OH
C;H6BrO
147
Henry
A. C. [4], 27, 243
11 11 ••••
„
„
145-150
Demole
B., 9, 48
?
....
C2H7BrO3
89-91
40-45
„
B., 9, 50
Tribromacrylic acid
CBr2:CBr.COOH
C3HBr3O2
115-118
Mabery and Lloyd
A. C. J., 4, 92
42, 1049
,, I, .... ....
11 '
„
117
Mauthner & Suida
M. C., 2, 109
40, 890
„ „
„
„
....
118
Hill and Mabery
A. C. J., 3, 172 ;
40, 1125; 44.
4, 263
309
Tribrompyruvic acid
CBr3.CO.COOH
C3HBr303
....
90
Grimaux
C. R, 78, 974
27, 887
i) 11
„
J)
+ 2H20
104
11
B. S., 21, 393
27, 888
Pentabromacetone
CHBr2.CO.CBr3
C3HBr6O
75
Mulder
J. p., 91, 472
vi., 27
„
„
„
76
Benedikt
C. C. [1878], 101
34, 499
Pentabromomethylic .acetate
CH2Br.COOCBr3
C3HBr502
....
74
Steiner
B., 7, 505
27, 886
, (Bromoxaform)
„ „
„
„
....
74-5
Lagermarck
Z. C. [2], 6, 299
vii., 213
„ ,,
„
„
75
Cloez
A., 122, 121
i., 996
„ „
„
,,
'
77
Cahours
A., 64, 352
vi., 17, 370
j3-Dibromacrylic acid
CBr2:CH.COOH
C3H2Br202
....
83-84
Jackson and Hill
B., 11, 1674
36, 224
11 11 11
„
„
243-250
85
Petri
A., 195, 70
36, 373
11 11 i)
„
„
....
85
Mauthner & Suida
W. A., 83, 273
40, 889
11 11 11
11
„
85-86
Bandrowski
B., 15, 2703
44, 314
11 11 11
„
„
85-86
Hill
B., 12, 660
36, 616
1) 11 >!
„
„
85-86
Hill and Andrews
A. C. J., 4, 177
42, 1187
11 11 11
„
„
85-86
Hill and Mabery
A. C. J., 3, 172
40, 1124
Dibrompyruvic acid
CHBr2.CO.COOH
C3H2Br2O3
89-91
Wichelhaus
B., 1, 264
vi., 980
11 11 ••••
„
11
....
abt. 93
Clermont
B. S. [2], 19, 105
vii., 1033 ; 26,
495
Dibromomalonic acid
CBra.(COOH)2
C3H2Br2O4
....
126-128
Petrieff
B., 7, 402
27, 787
Tetrabromacetone ....
....
C3H2Br4O
+2H20
42-43
Mulder
J. p., 91, 472
vi., 27
Tetrabrompropionic acid
CHBr2.CBr2.COOH
C3H~Br402
....
125
Mauthner & Suida
W. A., 83, 273
40, 889
11 11
,,
,,
125
Hill and Mabery
B., 14, 1681
40, 1030
11 »
„
„
....
125-126
11
A. C. J., 4, 263 ;
44, 309
B., 16, 80
11 11
CBr3.CHBr.COOH
„
118-120
Mabery
A. C. J., 5, 251
46, 664
'S-Bromaerylic acid
....
C3H3BrO2 .
53
Bandrowski
B., 15, 2702
o n
394
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
a-Bromacrylic acid
CH3 : CBr.COOH
C3H3Br03
....
69-70
Wagner & Tollens
B., 6, 512
26, 1220
„ „ .,
J)
M
....
69-70
Plnlippi and Tollens
A., 171, 333
27, 680
/3- „ „
CHBr : CH.COOH
M
115-116
Wallach & Eeincke
B., 10, 2130
34, 404
Brompyruvic „
CH2Br.CO.COOH
C3H3Br03
....
Liquid
Wichelhaus
B., 1, 265
vi., 980
Tribrompropionic acid
CBr3.CH2.COOH
C3H3Br302
....
53
Fittig and Petri
A., 195, 73
40, 800
„ „
CH2Br.CBr2.COOH
„
92
Michael and Norton
A. C. J., 2, 18
11
?j u
„
ta
....
93
Linnemann & Penl
B., 8, 1098
„ „
„
n
....
95
Mauthner & Suidn
W. A., 83, 273
40, 889
„ „
CHBr3.CHBr.COOH
„
....
118
Hill and Andrews
A. C. J., 4, 177
42, 1187
I! >!
„
„
....
118
Hill
A. C. J., 4, 273
Tribromlactic acid
CBr3.CH(OH).COOH
C3H3Br303
141-143
Wallach & Eeinckt
B, 10, 2129
34, 403
Dibromacetone
CH2Br.CO.OH2Br
C3H4Br20
24
Volker
A., 11)2, 1)7
34, 781
a-brompropionic bromide ....
Me.CHBr.COBr
„
154-155
Kaschirsky
C. C. [1881], 278
42, 36
Dibrompropionic aldehyde ....
CH2Br.CHBr.COH (?)
„
79-85 (5-6)
Liquid
Grimaux and Adam
B. S. [2], 36, 136
40, 1029
,, „
„
J?
150-170
....
Aronstein
As., 3, 188
vi., .-,(;
u u
....
( „ ).
....
59
Henry
B., 7, 1113
28, 1 43
„ 5*
....
„
....
60; 66
Linnemann & Penl
B., 8, 1097
)J I) ••••
„
66
Volker
A., 192,89
34, 781
a-a-Dibronipropionic acid ....
CH3.CBr2.COOH
C3H4Br2O2
220-S21 *. d.
61
Phillip! and Tollens
B., 6, 516
26, 101!)
V )» M •*••
„
„
227
65
Friedel & Machuca
C. E., 54, 220
vii., 1010
» ,, »
„
I*
.*.*
65-66-5
Tollens
Z. C., 14, 305
24, 1040
a-0-
CH,Br.CHBr.COOH
„
....
58
Schmoger
J. p. [2], 24, 43
42, 40
V )» » ""
f
lowly heated
64 •>
Tollens
B., 8, 1452
29, 561
1
Quickly „
a.f. 51 J
„ „
. »>
„
....
63-64; a.f. 51
Linnemann & Penl
B., 8, 1099
29, 64
» „ »
„
,,
240 d.
63-64
Phillip! & Tollens
B., 6, 516
26, 1019
» „ „
„
„
....
63-64
Wagner andTolleus
B., 6, 514
26, 1221
„ ,,
„
„
220-240
64-64-5
Miinder and Tollens
B., 5, 73
25, 402
,. » „
„
„
....
69-70
Phillipi and Tollens
B., 6, 518
» ,, ,,
„
„
+7H20
s.— 5
Linnemann & Penl
B., 8, 1098
29, 64
Dibromlactic acid
...
C3H4Brz08
....
98
„
B., 8, 1101
Propionyl bromide
CH3.CH2.COBr
C3H5BrO
96-98
Sestini
B. S. [2], 11, 468
vi., 962
„ „
„
,,
103-104
Bruyn
C. C., 1885, 356
48, 963
„ „
„
„
104-106
Kaschirsky
C. C., 1881, 278
42,37
Epibromhydriu
CH2Br.CH.CH2.0
„
138
Berthelot & DeLuca
J., 9, 600
i., 668
„
„
139
....
ii., 898
„
„
M
138-140
Henry
A., 154, 363
vii., 210
Bromacetone ...
CH3.CO.CH2Br
1 Aft—l A*** H
Eiche
„,
a-Bromallyl alcohol
CH2 1 CBr.CH2.OH
"
155
Henry
B., 5, 453 .
vii., 50, 1018
„ ,, ,,
„
M
152 (776)
• „
B., 14, 404
25, 686
Methylic bromacetate
CH2Br.COOMe
C3H5BrO2
144 d.
....
Perkin and Duppa
11, 22
i., 065
a-Brompropionic acid
CH3.CHBr.COOH
M
202-205-5 c.
s. —17
Kekule
A., 130, 17
iv., 733-
») »» ji
„
„
202
Kaschirsky
C. C. [1881],' 278
42,37
v ,, ,,
„
„
190-210
....
Friedel & Machuca
C. E., 53, 408
iv., 733
?» 11 »
„
190-210
Beckurts and Otto
B., 18, 222
0-
CH2Br.CH2.COOH
9)
it..
6V5
Bichter
Z. C. [1868], 450
„ „ „
„
•n
61-62
Beckurts and Otto
B., 18, 227
48, 506
/3-Bromlactic acid
CH2Br.CH(OH).COOH
q,H.BrQ,
89-90
Melikoff
B., 13, 958
38, 800
Dibrompropyl alcohol
CH2Br.CHBr.(JH2.OH
C3H6Br2O
212-214
Eichter
E. K. T.
V M
»
„
217
Aronheim
B., 7, 1382
28, 246
)» „
TJ
,,
219
Weger
A., 221, 61
46, 11
V )1
„
219
....
Morkownikoff
J. [1864], 490
vi., 91
Dibromhydrin
C3H5Br2.OH
f|
219
Berthelot and Luca
J., 8, 627
i., 668
»
D
„
219
„
J., 9, 601
»
,i
u
214-220
Zotta
A., 174, 96
Trimethylene glycol bromhy
CH2Br.CH2.CH2.OH
C3H7BrO
98-112(185)
Liqviid
Fruhling
M. C., 3, 697
44, 42
drin
Pn.pylene „ „
OH3.CHBr.CH2.OH
145-148
Z. C. [1870], 423
a-Glycerol-bromhydrin
CH2Br.CH(OH).CH.,(OH)( ?)
C3H7BrO2
180 (10)
Berthelot and Luca
A. C. [3], 48, 304
i., 668
*•*' » )i
CH2(OH).CHBr.CH2(OH)(?)
„
160 (66)
L. —15
Veley
C. N., 47, 39
1
C3H8Br40
210
....
Henry
A., 154, 363
vii., 210
COMPOUNDS CONTAINING FOUR ELEMENTS.
395
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Bromorualelc anhydride
C,HBr.CO.O.CO
i" i
C4HBrO3
212
Liquid
Kekule
A., 131, 1
iii., 787
j) »
»
))
214
Liquid
Pictet
B., 13, 1670
40, 253
!) )I
»
»
$16
Liquid
Anschiitz
B., 10, 1884
34, 136
„ )»
Polymer ?
J)
....
108-110
Carius
A., 149, 265
vi., 797
Bromomucobromic acid
C4HBr3O2
....
53-54
Jackson and Hill
B., 11, 1673
36, 224
)J 5)
....
))
....
55-56
Hill
B., 13, 737
Bromomaleic acid dibromide
?1
....
55
Hill and Sanger
B., 17, 1761
46, 1305
u-Dibromfurfurane ....
CH:CBr.O.CBr:CH
C4H2Br2O
164-163(764);
9-10
Hill and Hartshorn
B., 18, 448
48, 762
i i
62-63 (15)
„ „
,»
)>
165-167
Liquid
Canzoneri & Oliveri
G. I., 15, 113
48, 1144
Mucobromic aldehyde
C.,Br,(COH)2
C4H3Br2O2
88
Tonnies
B., 12, 1203
36, 918
Isodibromosuccinic anhydride
CBr0.CH3.CO.O.CO
C4H2Br2O3
32
Pictet
B., 13, 1670
40, 253
i " i
Dibromsuccinic „
CHBr.CHBr.CO.O.CO
))
....
100
Kekule
As., 2, 85
v., 459
i i
Mucobromic acid
5J
....
130
Schmelz & Beilsteiu
As., 32, 78
iv., 764
,, „
....
»
120-121
Jackson and Hill
B., 11, 1671
36, 224
n ,, .... ....
....
)>
120-125
Hill
B., 13, 734
26, 625
„ ,,
»
120-130
Limpricht
A., 165, 293
vii., 828
Dibromomaleic acid
C2Br,!(COOH)3
C4H2Br2O4
108
Kekule
A., 130, 3
38, 160
., „
i)
»»
....
112
>»
A., 131, 1
iii., 788
», j> •••• ••••
))
))
108-120
Limpricht
A., 165, 294
vii., 828; 26, 625
„ ,,
JJ
)»
....
120-123
Hill
B., 13, 736
„ ,,
)»
)J
....
123-125
Hill and Hartshorn
B., 18, 450
48, 762
>j „
JJ
»
....
123-125
Ciamician & Silber
G. I., 14, 31 ; B,
46, 1117
17, 553
Dibromfumaric acid
(3OOH.CBr : CBr.COOH
»
Blackens 217
219-220 p.d.
Bandrowsky
B., 12, 2213
38, 160
Hexabromethylmethyl ketone
CBr.,.CH2.CO.CBr3
C4H2Br6O
89-90
Demole
B., 11, 1712
36, 220
a-Dibromfurfurane tetrabro-
CH Br.CBr2.O.CBr3CHBr
J1
....
110-111
Hill
B., 16, 1132
44, 912
mide
i i
n » »
»
»
....
110-111
Hill and Hartshorn
B., 18, 449
48, 762
?
....
5»
....
55
J» !»
J>
u
Pentabromethylic bromace-
CH2Br.COO.CBr2.CBr3
C4H2Br602
195-198
Liquid
Kessel
B., 11, 1923
36, 1.38
tate
Octobromethyl oxide
(CBr3.CHBr)20
C4H2Br8O
132-135
»
B.. 10, 1668
34, 128
(450-470)
?
....
C4H3Br02
84
Limpricht
A., 165, 292
vii., 1032 ; 26,
625
Bromsuccinic anhydride
CH2.CHBr.CO.O.CO
C4H3BrOb
137(11)
26-31
Anschiitz & Bennert
B., 15, 643
42, 828
i " i
?
)»
....
109
....
J. p. [2], 23, 441
Acid from mucobromic acid
C4H,Br04
111-112 (?)
Hill
B., 17, 240
46, 731
Bromomaleic acid
CJIBr.(COOH)2
V
abt; 120
Carius
A,, 149, 265
vi., 797
„ „
1)
'I
....
125-126
Kekule
A., 131, 87
iii., 787, 788
» ,,
J»
»
125-126
Anschiitz
B., 10, 1884
34, 136
>» » •"• •• •
IT
5»
126-127
Kekule
A., 130, 1
v., 458
>, )i
)»
1>
127-128
Pictet
B., 13, 1670
40, 253
ji )> •••> ••••
1?
ji
128
Petri
A., 195, 62
36, 373
„ „
))
»
129-130
Bandrowski
B., 12, 345
36, 524
I»o- „ „
It
»»
160
Kekul6
A., 131, 1
iii., 788
1) )> »
»
>»
165
Carius
A., 149, 265
vi., 797
Bromfumaric acid
COOH.CH : CBr.COOH
»)
172
Kekule
A., 130, 1
v., 458
,1 n ""
))
))
172
Bandrowski
B., 12, 345
36, 524
)) ,, •••• ».»•
1)
»
174-175
Hill and Sanger
B., 17, 1761
)) ,» •••> ••••
>J
)»
176-177
»
B., 17, 1763
46, 1306
,, v
)>
,,
177-178
Bandrowski
B., 15, 2697
Tribromsuceinic acid
COOH.CHBr.CBrj.COOH
C4H3BrsO4
136-137
Petri
A., 195, 70
36, 373
51 i) ••"
?
»
d.w.m. 200
Burgoin
('. R, 78, 1111
37, 786
Tetrabromethylic bromace-
CHjBr.COO.CBrj.CHBr,,
C4H3Br502
175-177
Liquid
Kessel
B., 11, 1921
36, 138
tate
Dibromomethacrylic acid ....
fr. CH,:CMe.COOH
C4H4Br202
78
Cahours
A. C. [3], 67, 129
vi., 510, 511
Dibroincrotonic acid
....
j)
i 95-97
Pinner
B., 14, 1081
3 E -2
396
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Broniacetic anhydride
(CILBr.COkO
C.H.BrA
245
Liquid 0
Gal
C. R, 71, 273
vii.,ll;24,232
Dibromsuccinic acid ....
COOH.CHBr.CHBr.COOH
CjH^BrA
....
d.w.m.
....
G. H., 524
Isodibromsuccinic acid
COOH.CH2.CBrj.COOH
J)
....
160
Kekule
As. 2, 89
v., 459
Tetrabrombutyric acid
C3H3Br4.COOH
C4H4Br4O2
....
115
Limpricht
A., 165, 296
vii.,828;26,(;2.-,
Bromomethacrylic acid
CHBr I CMe.COOH
C4H5BrO,.
228-230 p.d.
60
Cahours
A. C. [3], 67, 29
vi., 511
» »i
JJ
»»
....
62-63
Kichter .
R. K. T.
>! 11
»)
«
....
65
Kekul6
As., 2, 85
»
11 11
J)
)»
....
65
Friedrich
A., 203, 351
40, 413
Isobromotnethacrylic acid
CHs:C(CH2Br).COOH
»)
65-66
Krusemark
A., 206, 12, 22
40, 416
0-Bromcro tonic acid
CH3.CBr:CH.COOH
))
....
90
....
J. p. [2], 25, 388,
394
ft- „ „
>»
)J
92
Michael & Norton
A. C. J., 2, 15
40, 799
«- >i 11
CH3CH:CBr.COOH
;j
106-5
»
>i
»
11 11 11 •••• ••••
)»
jj
cf. B., 15, 49
107-109
Bischoff & Guthzeit
B., 14, 617
Ethylic oxalyl bromide
COOEt.CO.Br.
C4H5Br03
abt. 150
....
Kichter
C. C., 1875, 446
36, 139
Bronisucciuic acid
COOH.CHBr.CH2.COOH
C4H5BrO4
159
A.
11 „ .... ....
»
>»
....
160
Anschiitz & Bennert
B., 15, 643
11 11 .... ....
»>
))
....
160
Fittig
B., 9, 122
29, 898
Aldehyde broraal
CBr3.CHO+OH3.CHO
C4HsBr3O2
abt. 175
Liquid
Schiitzenberger
B. S. [2], 19, 8
26, 487
Ethylic tribroinacetate
CBr3.COOEt
JJ
225
Gal
B. S., 5, 172
vi., 21
Tribrombutyric acid
C3H4Br3.COOH
))
....
111
Michael & Norton
A. C. J., 2, 162
40, 799
„ ,1 ....
»
J)
114
i?
ji
)J
n-Bromisobutyric bromide ....
CMe2Br.COBr
C4HfiBr2O
162-164
Kaachirsky
C. C., 1881, 287
42,37
a-Brombutyric „
CH,.CH2.CHBr.COBr
j»
172-174
11
1)
»i
Ethylic dibromacetate
CHBrs.COOEt
C4H6Br202
192
Liquid
Schaffer
B., 4, 369
11 11
)>
>»
194
....
Gal '
B. S., 5, 172
vi., 21
11 11
))
»
192-195
....
Remi
B., 8, 695
28, 1004
Bromethylic bromacetate ....
CH2Br.COO.OH2.CH,!Br.
»J
230-240 d.
....
Demole
B., 9, 557
30, 283
11 11
CH2Br.COO.CHBr.CH3
)J
180-240 d.
Kessel
B., 10, 1995 ; 11
34, 133
(o.p.);130-
1917
135 (360)
Dibromethylic acetate
CH3.COO.CHs.CHBr2
»
193-195 u.c.
Demole
B., 9, 51
Methylic-a-a-dibrompro-
CH3.CBr2.COOMe
»T
175-179
....
Philippi
A., 171, 323
pionate
Methylie-a-/3-dibrompro-
CH2Br.CHBr.COOMe
»
203 (745)
Liquid
Miinder & Tollens
B., 5, 74 ; A.,
25, 402 ; vii.,
pionate
167, 229
1012
u 11
11
J?
205-8
Weger
A., 221, 61
46,11
a-Dibrombutyric acid
....
n
d.
8. —15
Schneider
A., 119, 279
vi., 380
11 11 11
....
JT
....
Liquid
Michael & Norton
A. C. J., 2, 12
11 11 11 ••••
J^
150 (3)
Liquid
Friedel & Machuca
As., 2, 76
vi., 379
«-/3-
CHj.CHBr.CHBr.COOH
,,
....
78
Bulk
A., 139, 69
11 11 11 ••••
)i
»J
....
87-90
Kolbe
J. p. [2], 25, 385
397
11 i> 11 •»••
»»
»»
....
87
Michael & Norton
A. C. J., 2, 12
11 jj 11 ....
11
»>
90
Korner
A., 137, 234
vi., 510
Dibromisobut}7ric acid
»
232 (760)p.d.
45-48
Cahours
R, 4, 145
vi., 379
11 11
....
)1
48
Kolbe
J. p. [2], 25, 373
44,573
Methyl bromallyl oxide
CHs.O.C3H4Br
C4H.BrO
115-116
Henry
Z. C. [2], 6, 575 ;
vii., 50 ; 25,
B., 5, 455
687
Isobutyric bromide ....
CHMe2.CX)Br
Jl
116-118
Kaschirsky
C. C., 1881, 273
42,37
Butyric bromide
CH3.CH2.CH2.COBr
•)J
126-127
»i
i>
D
11 )) .•«« ....
M
I»
128
J., 1857, 344
Bromisobutyric aldehyde ....
....
(04H7BrO)n
128-129
A., 211,353
Bromethylic acetate....
CH3.COO.CHBr.CH3
C4H7BrO2
135-145 p.d.
....
Tawildarow
B., 7, 731
27, 1080
11 11
CH3.COO.CH2.CH.,Br
i)
161-163
....
A., 171, 121
Ethylic bromacetate
CH2Br.COOEt
?»
159
Aronstein
B., 14, 606
11 11 .... ..••
>i
)» .
759
Perkin and Duppa
11, 22
i., 665
11 11 •«•« ....
11
j)
159
Gal
B. S., 5, 172
vi., 21
o-Brombutyric acid
C:H3.CH2.CHBr.COOH
jj
110 (3)
Friedel & Machuca
As., 2, 76
vi., 379
i» 11 11 •••• •»••
)»
V
180
Liquid — 15
Schneider
A., 119, 279
vi, 379
11 11 11 ••>•
J»
»»
200
....
Naumann
A., 119, 115
»
,* »i 11 ....
»>
sir p.d.
....
Friedel & Machuca
A., 120, 279
11
COMPOUNDS CONTAINING FOUR ELEMENTS.
397
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
a-Brombutyric acid ....
CH3.CH2.CHBr.COOH
C4H7BrO2
214-217
• >••
Kaschirsky
C. C. [1881], 278
42, 37
i3-Bromisobutyric acid
CH2Br.CHMe.COOH
„
....
ft
Engelhorn
A., 200, 65
38, 379
a- „ „
Me,.CBr.COOH
11
....
42
Markownikoff
A., 138, 361
vi., 379
n 11 11 ••••
„
„
....
45
Engelhorn
A., 200, 65
38, 379
11 11 11
„
„
45-46
Thomson
A., 200, 75
38, 380
11 11 11
„
„
198-200 p.d.
48
Hell & Waldbauer
B., 10, 448
32, 313
11 11 11
*)
,.
....
48
Kaschirsky
C. C., 1881, 27
42, 37
Bromhydroxybutyric acid ....
C3H5Br(OH).COOH
C4H7BrO3
90
Melikoff
B. S., 43, 115
48, 650
11 11 ••••
3J
„
100-102
....
J. R., 7, 179
Bromhydroxyisobutyric acid
CH2Br.CMe(OH).COOH
„
....
100-101
Kolbe
J. p. [2], 25, 376
44, 573
>! 11
„
„
....
101
Melikoff
B. S., 43, 115
48, 650
Acetone bromoform ....
COMe2+CHBr3
C4H.Br3O
....
167
Willgerodt
B., 14, 2458
42, 492
11 11
11
„
....
175
Willgerodt&MUller
C. C. [18S4], 808
48, 648
„ „
n i
„
+xH20
165-167
11
V
„
Bromal alcoholate
CBr3.CH(OH)(OEt)
C4H7Br302
....
44
Schaffer
B., 4, 367
24, 558 ; vii.,
209
Glycerol methyldibrom-
C3H5Br2(OMe)
C4H8Br20
185
Henry
B., 5, 455
25, 687
hydrin
Ethylene oxybromide
....
C4H8Br202
95
65
....
A. C. [3], 69, 317
ii., 580
Erythrol dibromhydrin
C4H6Br2(OH)2
„
....
130
Champion
C. R., 73, 114
24, 811 ; vii.,
471
Bromethyl oxide
CH2Br.CH2.OEt
C4H9BrO
127-128(755)
Liquid
Henry
C. R., 100, 1007
48, 882
Diethyleneglycol bromhydrin
CH2Br.CHj.O.CH2.CH,.OH
C4H9BrO2
205
....
....
A. C. [3], 67, 286
?
(C2H4O2)2.Br2.HBr.
C4H9Br304
....
8d.
Steiner
B., 7, 184
27, 566
Ethyl oxide + bromine
Et2O+Br3
C4H10Br30
....
22
A., 167, 86
Tribrompyromucic acid
O.CBr I CBr.CBr : C.COOH
i j
C5HBr303
218-219
Hill and Sanger
B., 17, 1763
43, 1306
Dibrornpyromucic acid
O.CBr : CH.CBr : C.COOH
C5H2Br203
168
m
B., 17, 1762
46, 1305
»> 11 ••••
O.CH : CBr.CBr '. C.COOH
185
Canzoneri & Oliveri
G. I., 14, 172
48, 245
i 1
11 11
11
„
184-186
Tonnies
B., 11, 1088
34,786
11 11 ••••
11
J)
192
Hill and Sanger
B., 17, 1762
46, 1305
Tribromethylidene tribrom-
CBr3.CH.O.CH(CBr3)COO
C5H2Br603
158
Wallach & Reiucke
B., 10, 2129 ; A.,
34, 404
lactate (Bromalide)
i j
193, 52
Bromcitraconic anhydride ....
C3H3Br.CO.O.CO
C5H3Br03
....
95
Richter
R. K. T., 69
1 — ._!
11 11
„
„
200
97-98
Lagermarck
Z. C. [2], 6, 299
vii., 349
11 11
„
„
225
....
Kekule
As., 2, 92
11 11
,.
„
....
99-100
Richter
R. K. T., 69
/3-Brompyromucic acid
O.CH . CH.CBr I C.COOH
constit. cf.
128-129
Hill and Sanger
B., 17, 1762
46, 1306
> i
B. 11,1840
y- » 11
O.CH : CBr.CH : C.COOH
,;
^
155
Canzoneri & Oliveri
G. I., 14, 172
48, 245
1 1
11 11 I* *.'•
„
11
155
Schiff & Tassinari
B., 11, 843
34, 721
11 11 n ••••
„
„
„
156-157
„
G. I., 8, 297
8-
O.CBr : CH.CH I C.COOH
V
180
M
B
36, 308
i i
11 11 *i
„
„
,,
183-184
Hill
B., 16, 1131
44, 912
11 11 11
11
„
„
183-184
Hill and Sanger
B., 17, 1763
46, 1306
?
....
C.H.BrO.
+H20
d. 120
....
J. p. [2], 23, 441
8-Brompyromucic acid tetra-
O.CBr2.CHBr.CHBr.CBr.
C5H3Br603
....
170 d.
Hill and Sanger
B., 17, 1763
46, 1306
bromide
i i
COOH
Itadibrompyrotartaric anhy-
C3H4Br2.CO.O.CO
C5H4Br203
50
Petri
B., 14, 1637
40, 1032
dride
r' " J
Pyromucic acid tetrabromide
O.CHBr.CHBr.CHBr.CBr.
C5H4Br40,
159-160 d.
Tonnies
B., 11, 1086
34,786
i i
COOH
Bromitaconic acid
....
C5H5Br04.
....
164 d.
....
J., 1873, 584
Tribromethylidene lactate ....
CBr3.CH.O.CHMe.COO
C5H6Br303
95-97
Wallach & Keincke
B., 10, 2130
34, 404
i i
11 11
„
95-97
Kilimenko
J. p. [2], 13, 100
29,900
Ethylic tribrompyruvate
CBr3.CO.COOEt
„
95-97
....
J. R., 8, 125
Tribrompyrotartaric acid ....
CTT T>_ //"1/^/~\TT\
•1 Ll-,L>T'A \..'\J\J fl l.y
C5H6Br3O4
w.m. 240
Lagermarck
Z. C. [2], 6, 303
vii., 1034
Ethylic /3-dibromacrylate ....
CBr2 : CH.COOEt
<;5H6Br202
212-214
Liquid
Petri
A., 195, 72
36, 373
398
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dibromvalerolactone
....
C5H6Br202
....
81
Wolff
A., 229, 24!)
48, 1121
Dibromlevulinic acid
....
C5H6Br203
d. 130-140
112-113
Hell and Kehrer
B., 17, 1982
46, 1298
Methylic dibromsuccinate ...
COOMe.CHBr.CHBr.COOH
CiH.Bri04
d. w. m. 24">
Glaus
B., 15, 1846
Itadibrompyrotartaric acid...
....
))
240-250 (o.p.
....
Petri
B., 14, 1637
d.; 174-175
(i.v.) d.
Dibromglutaric acid
fr. COOH.(CH2)3.COOH
)J
....
101-103
B. S., 27, 348
Dibrompyrotartaric acid
....
))
....
127-128
Bischoff & Emmert
B., 15, 1107
42, 1191
Citradibrorupyrotartaric acid
....
J)
....
150
Fittig
A., 187, 42
38, 738
?J »
JJ
d. 165-170
150
)»
B., 10, 517
32, 430
» »
....
)J
....
193-194 d.
A., 206, 2
Meta-dibroinpyrotartaric acic
....
>J
...,
170 d.
jj
B., 10, 517
32, 430
'» » »?
....
))
....
170
i)
A., 187, 42
32, 738
>» » »
1>
....
204 d.
....
A., 206, 2
Ethylic |8-bromacrylate
CHBr I CH.COOEt
C5H7Bi-02
155-158-5
Wagner and Tollenb
A., 171, 350
27, 681
Bromallylic acetate ....
CH2 : CBr.CH2.OAc
»
163-164
Henry
B., 5, 453
25, 686 ; vii.,
50, 1018
Bromvalerolactone
»
))
....
1.-15
Messerschmidt
A., 208, 101
42, 35
Bromlevulinic acid
....
C5H;Br03
59
Wolff
A., 229, 249
48, 1124
Bromethylmalonic acid
CH2Br.CH2.CH(COOH)2
C5H7BrO4
116
Fittig and Boeder
B., 16, 373
44, 730
!) !)
»
»J
....
11G
Boeder
A., 227, 13
48, 653
» H
)»
)»
....
116-117
Perk in
47, 814
Itabrompyrotartaric acid ...
CsHjB^COOH).,
))
abt. 250 d.
130-134
....
Z. C., 1866, 722
vi., 981
« »
51
»
....
137
Landolt and Fittig
B., 9, 1193
31,61
)> »
JJ
I)
137
Fittig
A., 187, 42
32, 737
Bromisopyrotartaric acid _..
C^Br.CHCCOOH),,
»
....
141
Glaus
B., 10, 824; A.,
32, 593 ;34, 857
191, 80
Citrabrompyrotartaric acid....
C3H5Br(COOH)2
))
....
148
Fittig
A., 187, 42
32, 738
» »j
)J
)>
....
146 d.
Fittig and Landolt
B., 9, 1193
31,61
Brompyrotartaric acid
fr. COOH.CH2.CHMe.COOH
J»
202-204
Guthzeit & Bischofl
B., 14, 616
40, 579
Hydroxybrompyrotartaric
C,H4Br(OH)(COOH)3
C5H7Br05
....
156 d.
Scherks
A., 227, 233
48, 513
acid
Ethylic tribromlactate
CBra.OH(OH).COOEt
C5H7Br303
....
44-46
Wallach
A., 193, 52
34,403
Ethylic u-dibrompropionate
CH3.CBr2.COOEt
C5H3Br202
190-191
Philippi and Tollens
B., 6, 517
vii., 1011; 26
1019
i) ?) »
»
))
191-192
Tollena
A., 171, 324
,, o/3-
CH2Br.CHBr.COOEt
))
211-214
Miinder and Tollens
B., 5, 73
25, 404
>1 !> )>
»
)»
211-214(746)
....
»
A., 167, 230
vii., 1012
)» )» 51
»
)>
210-214
Philippi and Tollens
B., 6, 517
26, 1019
J> » )>
»
)J
214-6
Weger
A., 221, 61
46, 11
Dibromvaleric acid
fr. CHS.(CH2),.COOH
)T
....
57-58
Messerschmidt
A., 208, 110
42,35
j) ,,
fr. Angelic acid
))
76 p. d.
Jafte
A., 135, 291
vi., 157
j, n
C2H4Br.CMeBr.COOH
»
82-83
Berendes
B., 10, 836
32, 593
5j D «•>• • •••
»
)»
82-83
Schmidt
A. P. [3], 13, 213
36, 223
)) ))
»
)»
83-83-5
Fittig
B., 10, 516
)» jj
CH3.CHBr.CBrMe.COOH
»
86-5
Schmidt
B., 12, 255
)» » •"• ••••
»)
)»
....
86-86-5
Pagenstecher
A., 195, 123
36, 456
Broiuallylethyloxide
CH2:CBr.CH,,.OEt
C5H9BrO
130-135
Liquid
Henry
B., 5, 189
vii., 50
Isovaleric bromide
CHMe2.CH2.COBr
)}
143
Buchamp
C. E., 42, 224
v., 979
Ethylic a-brompropionate ....
CH3.CHBr.COOEt
C5H9Br02
158
M. C., 2, 543
;» »
J»
)»
159-160 d.
Henry
A., 156, 176
)) »
)»
)»
160-165
A., 197, 13
») 5)
>»
»»
162
....
A., 216, 31
»l »»
)»
129-132(160)
A., 206, 319
Methylic a-brombntyrate ....
Me.CH2.CHBr.COOMe
|]
165-172
Duvillier
C. E., 88, 598
36, 523
a-Bromisovaleric acid
CHMe2.CHBr.COOH
226-230
Gahours
As., 2, 78
v., 978
Q-Broni-ni6thylethylacetic
( 1W PIT PTLf^U nr\/^TT
^n3.^n2.OJMer>r.(JOOM
))
66-66-5
Pagenstecher
A., 195, 110
36, 455
acid
Glycerol acetobromhydrin ....
C3HsBr(OAc)(OII)
C5H9Br03
175 (100)
J., 1878, 523
„ ethyldibromhydrin
C3H5Br2(OEt)
CsHjoBijO
193-195
Morkownikoff
Z. C., 1865, 554
vi., 99
Tribromquiuone
G,HBr,:0,
C6HBr302
108
....
A. C. [5], 15, 67
)> ....
JJ
JJ
147
Sarauw
A., 209, 120
40, 1136
COMPOUNDS CONTAINING FOUR ELEMENTS.
399
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Tribromhydroxyquinone ....
C6Br3(OH) : 02
C6HBr303
..«
206-207
Barth and Schreder
M. C., 5, 589
48, 520
Bromoxytetrabrombenzene ...
C6HBr4.OBr
C6HBrsO
121
....
M. G, 1, 361
Pentabromphenol
C6Br5.OH
„
....
225
Korner
A., 137, 210
vi., 908
Pentabromresorcinol
C6Br4 OH.OBr— 6 5.4 2 3.1
C6HBr5O2
113-5
Stenhouse
P. E., 20, 72; A.,
25, 298; vii.,
163, 184
' > J
1042
Phlorobromin
CcHBr0O
152
Benedikt
A., 189, 166
34, 499
Brom. deriv. of Bromanil-
C6HBr, O
110-5
Stenhouse
As., 8, 22
vi., 986
aminic acid
Dibromquinone .... ....
C H Br " O ? ? 4 1
C H Br O
76
J. p. [21, 24, 465
ii
88
r L J" )
A. C. [5], 15, 67
„
ii i
ji
122
Levy and Schultz
A., 210, 157
42, 510
„
!> 1
«
188
Schulz
B., 15, 655
,,
„ ,,
„
188
Sarauw
A., 209, 113
40, 1136
Bromoxylbromcomenic acid
C6H2Br206
+3HS0
d. 105
J. p. [2], 26, 467
Bromoxytribrombenzene ....
C H Bi3.OBr
C6H2Br40
....
109
Benedikt
A., 199, 128
„
„
J)
118
„
M. C., 1, 360
38, 246
Tetrabromphenol
C6HBr,.OH=6. 4.3.2.1
„
120
Korner
A., 137, 209
vi., 908
Tetrabromresorcinol.. .
CcBr4(OH)2=6.5.4.2.3. 1
C6H2Br402
163
Claassen
B., 11, 1440
34,867
„
„ „
„
167
Benedikt
M. C., 1, 366
Tetrabrompyrocatechol
„ —6.5.4.3.2.1
187
Stenhouse
C. E., 29, 95
27, 587
Tetrabromqxiinol
„ =6.5.3.2.4.1
JJ
244
A.
Bromphenylene oxide
C6H3Br:0
C6H3BrO
....
195
Marker
A., 124, 250
v., 161
Bromqumone . ....
C,H3Br I O2=5.4.1
C1 H BrO
55-56
Sarauw
A.. 209, 102, 106
40, 1135
55-56
Schulz
B., 15, 656
CO
» \*)
I
abt. 88
A. C. [5], 22, 218
40, 583
Bromeoumalinic acid
C4HJBr(NH2)(COOH)2
C,H,Bi04
....
176
Pechmann
B., 17, 2397
48, 175
Di bromeitraconimide
C4H2Br2:(CO)2:NH
C6H3Br202
....
142-144
Mendini
G. I., 15, 182
48, 1126
Tribromphenol
C6H2Br3.OH=6. 4.2.1
C6H3Br80
89-90; 91
Baumann & Brieger
B., 12, 805
36, 789
„
ii ii
11
92
Post
A., 205, 66
„
11 11
„
....
92
Werner
C. E., 98, 1333
46, 900
„
H 11
„
abt. 93
Armstrong& Brown
25, 858
„
11 11
M
94
La Coste
B., 13, 2177
„
11 11
„
....
94-95
Michaelis & La Coste
B., 18, 2112
„
„ „
„
....
95
Sintenis
A., 161, 340
vii., 929
„
11 i>
„
95
Korner
A., 137, 208
vi., 908
Tribromresorciuol
C6HBr3(OH)2=('024.3.1
C6H3Br,02
+xH20
104
Typke
B., 10, 1578
„
„ „
„
J»
111
....
A., 130, 357 ;
M. C., 2, 474
Tribromquinol
„ =5.3.2.4.1
„
....
136
Sarauw
A., 209, 116
40, 1136
Tribromphlorglucinol
C6Br3(OH)3=6. 4.2.5.3.1
C6H3Br303
148 u.c.
Webster
47, 424
Bromeitraconimide
C4H3Br:(CO)2:NH
C6H4Br02
....
179-182
Mendini
G. L, 15, 182
48, 1126
Dibromphenol
C6H3Br2.OH=4.2.1
C6H4Br20
154 (11)
40
Korner
A., 137, 205
vi., 908, 929 ;
24, 252
„
„ „
„
154 (47)
40
Werner
C. E., 98, 1333
46, 900
„
11 11
„
....
40
Baeyer
A., 202, 36
38, 658
„
=6.2.1
„
....
55-56
„
A., 202, 36 ; B.,
31, 308 ; 38,
9, 1232
658
„
11 11
„
55
Mohlau
B., 15, 2494
3-Dibromresorcinol ...
C6H2Br2(OH)2=?.?.3.1
C6H4Br202
83-85
Zehenter
M. C., 2, 479
42, 194
«- ,i
11 >!
11
92-93
Hofiuann
B., 8, 64
28, 571
„ ,,
11 11
,,
93-93
Baeyer
A., 183, 57
31, 204
Isodibromquinol
11 — ....4.1
ii
....
86-87
Sarauw
A., 209, 109
40, 1136
(=C6H3Br.OH.OBr ?)
Dibromquinol
=?.3.4.1
„
185-186
Wichelhaus
B., 12, 1505
38, 42
186; 186-187
Sarauw
A., 209, 100, 107
40, 1135, 1136
" "
188
Schulz
B., 15, 655
Acetylic mucobromate
JT 11
C3HBr2O.COOAc
C6H<Br.04
53-54
Jackson and Hill
B., 11, 1673
36, 224
Broniphenol . . .
Or,H4Br.OH=1.2
G-H-BrO
236-238
Liquid 10-12
Fittica
J. p. [2], 28, 176
46, 55
Vy6 5
194-195
Liquid
Fittig and Mager
B., 8, 363
„
11 11
11
235
Liquid
Hiibner& Brenken
B., 6, 170
vii., 905
Liquid
Korner
G. I., 4, 387
29, 228
11
n
132(22)118(9)
Liquid— .18
A., 137, 197
vi., 907
400
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
C6H4Br.OH=1.3
CLH.BrO
Liquid
Korner
G. I., 4, 305
29, 228
V^gJJ.JJJ»
227-229
Wiirster & Nolting
B., 7, 905
27, 1163
JJ JJ
?)
— 18
Petersen
A., 159, 71
24, 249
» )I
)>
236-236-5
32-33
Fittig and Mager
B., 8, 364
» I)
1>
236-236-5
32-33
Fittica
J. p. [2], 28, 176
40, 55
IT 5)
=1.4
yi
235-236
63-64
Hiibner & Brenkeu
B., 6, 173
26, 751
))
»
%38
63-64
Fittig and Mager
B., 7, 1177
28, 147
)' »>
M
63-64
Post
B., 7, 332
27, 800
T» ))
»)
63-64
Bako wski & Lepperi
B., 8, 789
28, 1197
)) ?1
)»
238
64
Fittica
J. p. [2], 28, 176
46, 55
)) '>
»»
137 (28)
64
Werner
C. E., 98, 1333
46, 900
JJ )»
))
66 '4
Korner
G. I., 4, 387 ; J.,
29, 228 ; vii.,
>J )?
II
[1875], 636
905
Bromquinol .
C6H,Br(OH)2 = 5.4.1
C.H.BrO,
110
Sarauw
A., 209, 100, 105
40, 1135
^^6 5 2
110-112
Wichelhaus
B., 12, 1504
38, 42
,, .... ....
» »>
» »»
1»
»
....
110-112
Schulz
B., 15, 655
Ethylic mucobromate
C3HBr2O.COOEt
C6H6Br203
....
50-51
Jackson and Hill
B., 11, 1672
36, 224
Tetrabromadipic acid
C4H4Br4(COOH)2
C6H6Br404
....
200-211
Limpricht
A., 165, 271
vii., 29 ; 26,
623
Methylic brommaleate
C2HBr(COOMe)2
C6H7Br04
237-338 u.c.;
Liquid
Auschiitz
B., 12, 2284
126-129
(30-40)
„ bromfumarate
»
»
30
)>
>j
Bromhydromucouie acid
....
))
....
183
Limpricht
A., 165, 265
26, 622 ; vii.,
827
Tribromadipic acid
C4H6Br3(COOH)2
C6H7Br304
....
177-180
»
A., 165, 269
vii., 28 ; 26,
623
Dibromallyl oxide
(C3H4Br)20
C6H8Br20
212-215
....
Henry
B., 6, 729
26, 1123
Allylic a-^-dibrompropionate
CH2Br.CHBr.COO.C3Hs
C6H8Br203
215-220
....
Miinder & Tollens
A., 167, 230 ; B.,
25, 402 ; vii.,
(746-5)
5,73
1012
Dibromhydrosorbic acid
....
M
....
94-95
Kachel and Fittig
A., 168, 287
27, 44
Ethylic dibromsuccinate
COOH.CHBr.CHBr.COOEt
C6H8Br204
275 u.c.
Glaus
B., 15, 1844
44,44
Dimethylic „
COOMe.CHBrCHBr.COOMe
>1
61-5-62
Anschiitz
B., 12, 2282
» t) ....
H
J)
....
62-5
C'laus
B., 15, 1846
» » •»•>
»
I)
....
62-64
J. E., 11, 288
Dibrompropylmalonic acid ....
C3H5Br,,CH(COOH)2
»
....
119-121
Hjelt
B., 15, 624
42, 947
Dibromadipic acid
C4H6Br2(OOOH)2
)>
....
115-122
A.., 165, 266
j) ,,
)»
»
175-190 d.
Limpricht
A., 165, 253
vii., 28 ; 26,
623
„ ,, ....
J)
))
205
Ador
B., 4, 627
Tetrabromcaproic acid
C5H7Br4.COOH
C6H8Br4O2
....
178-179
Barringer & Fittig
A., 161, 325
vii., 1091
i» »
))
))
183
....
A.,168,277; 200,58
Etliylic bromomethacrylate
fr.CH2:CMe.COOH
C6H9BrO3
192-193
Liquid
Cahours
As., 2, 349
vi., 511
Hemibromhydriu
....
D
b. 200
Berthelot and Luca
A., 101, 72
i., 669
Propylic a-dibrompropionate
CH3.CBr2.COOPr«
C6HlnBr,Os
200-204
....
Philippi
A., 171,324
«-0-
CH2Br.CHBr.COOPr«
H
233
Weger
A., 221, 61
46, 11
Ethylic dibrombutyrate
C3H6Br2.COOEt.
fj
191-193
....
vi., 380
Dibromcaproic acid ....
C5H9Br2.COOH
»j
....
68
Fittig
B., 9, 120
29, 897
1» 5)
)J
l»
68
Fittig and others
A., 200, 44
38, 377
J) JT •*" ....
Et.CH2.CHBr.CHBr.COOH
j»
....
77
Markownikoff
B., 6, 1176
» » •». ....
»
ij
80-5
Fittig and others
A., 200, 35
38, 376
)» )) •'•• ....
C2HBr2MeEt.COOH
I)
.»•
97-6
....
M. G, 4, 77
°- )! » •- »~.
99
Mulck
A., 180, 54
29, 924
Dibromisocaproic acid
....
>i
*«««
99-100
Geisler
A., 208, 46
42, 42
)i »
Etliylic a-bromisobutyrate ....
Me2.CBr.COOEt.
»
C6HnBrO2
157-160
90-91
Engelhorn
Markownikoff
A.,161,314; 200,46
B., 6, 1440
27, 359
n »
JJ
>»'
158-159
Hell & Wittekind
B., 7, 320
11 !)
»
jj
160 u.c. ;
Hell & Waldebauer
B., 10, 449
32, 313
162-7 c.(746)
I! »
»
)i
1 60 u.c. ; 163-6
Markownikoff
A., 182, 336
(761-9)
„ a-brombutyrate
C^^CHBr-COOEt
j)
\ ' " **/
169-174
Hell & Miihlhimser
B., 13, 474
COMPOUNDS CONTAINING FOUR ELEMENTS.
401
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Ethylic a-brombutyrate
C2H5.CHBr.COOEt
C6HnBr02
170-172
....
Hell and Lauber
B., 7, 561
27, 887
I* )>
»
H
171-172
....
....
26, 495
11 11
?)
11
175-178
....
Cahours
J., 15, 248
vi., 379
11 11
11
11
178 c.
Tupoleff
A., 171, 249
27, 565
n 11
11
11
175-185
....
....
26, 495
,, h ,,
03H6Br.COOEt
11
abt. 185 p.d.
Schneider
A., 119, 115
vi., 379
Bromcaproic acid
CH3.(CH2)3.CHBr.COOH
11
abt. 240
Cahours
As., 2, 78
vi., 395
11 55
C2H4Br.CHEt.COOH
11
Liquid — 18
Fittig
B., 9, 121
29, 897
,, ,, ....
11
11
Liquid — 18
Fittig and others
A., 200, 42
38, 377
„ „
C3H5EtBr.COOH
11
....
25
»
A., 200, 24
38, 375
jj „
C5H10Br.COOH
11
85-86
J. B., 11, 128
Mannitol bromhydrin
C6H8Br(OH)3:0
CfiHuBrO.,
....
100
Bouchardat
A. C. [5], 6, 122 ;
vii., 776 ;
C. E., 75, 1187
26, 161
Dulcitol „
11
11
....
143
A. C. [4], 27, 184
Dibromhexylalcohol
C6HnBr2.OH
C6H12Br20
252-254
....
Destrem
B., 16, 228
Mannitol dibromhydrin
C6H8Br2(OH)4
C6H12Br204
....
178 d.
Bouchardat
A. C. [5], 6, 120 ;
vii., 774;
C. E., 75, 1181
26, 161
Hexylene bromhydrin
Me.CHBr.CHPr.OH
06H13BrO
188-190(769)
Liquid
Henry
C. E., 97, 260
46, 34
Bromacetal .... ....
CH2Br.CH(OEt)2
C-H,,BrO,
170 p. d.
Pinner
B., 5, 149
vii., 1; 25, 406
b~^l3 2
JT
171
Wislicenus
A., 192, 112
34, 777
Triethylene glycol bromhy-
11
11
C6H13Br03
250
....
A. C. [3], 67, 286
drin
Pentabrombenzoic acid
C6Br6.COOH
C7HBrbO.,
234-235
Eeinecke
Z. C. [2], 5, 110
vi., 310
Tribrombenzoic acid
C6H2Br3.COOH = ?
C7H3Br302
178
Hiibner
B., 10, 1705
34, 149
11 „ ....
,, =1
11
....
186-5
n
B.T 10, 1708
D
„ „ ....
= 7.4.3.1
11
195
)»
B., 10, 1706
jj
M ,, ....
= 1
11
....
234-235
Eeinecke
Z. C. [2], 5, 110
vi., 310
Tribromtoluquinone
C6Me.Br3 : O2 = 1.3.4.6.2.5
11
235-236
Canzoneri & Spica
G. I., 12, 469;
44,330
B., 16, 793
Tribromdihydroxybenzoicacid
COOH.(OH)2.Br3= 1.3.5.2.4.6
C7H3Br3O4
183
Barth and Senhofer
A., 159, 225
vii., 433
Pentabromorcinol
....
C7H3Br502
....
126
Stenhouse
P. E. S., 20, 72;
25, 297 ; vii.,
A,, 163, 180;
879
169, 252
Dibrombenzoic acid
COOH.Br.Br= 1.2.3
C7H4Br202
146-148
Neville & Winther
B., 13, 965
37, 435
„ „
» »»
)i
148
Glaus and Lade
B., 14, 1170
40, 814
„ „
n n
j)
150
Hiibner & Lawrie
B., 10, 1706
34, 149
„ ,)
» JJ
11
153
)>
B., 10, 1705
34, 148
„ „
= 1.2.5
11
149-151
Neville & Winther
37, 435
,, j, .... ....
)) )»
11
151 ; a. s.
Eichter
B., 7, 1147; 8,
28,73
151-152
1422
,, ,, .... ....
11 11
11
151-153
Neville & Winther
B., 13, 963
37, 435
„ „
11 11
11
153
Hiibner
A., 222, 67
46, 316
i) 11 •••• ••••
11 11
11
....
153
Glaus and Lade
B., 14, 1170
40, 814
„ ,,
= 1.2.6
11
....
150-167
Neville & Winther
37,441
,, „ .... ....
= 1.2.4
11
....
166-168
B
B., 13, 972
37,443
„ »
11 11
11
168-170
M
11
37,442
„ „
„ -1.3.5
11
....
207-210
»
B., 13, 967
37, 437
D „
» 51
11
208-209
»
«
37, 438
v i
» 11
11
208-209
Eichter
B., 8, 1423
,, ,, .... ....
11 11
11
213-214
lesemann&Kochler
A., 222, 166
46,600
,, ,, .. ....
11 11
11
223-227
Hiibner
Z. C. [2], 5, 514
vi., 310
•>•> 11
11 11
11
2S3-227
Hiibner and Anger-
A., 158, 10
24, 364
stein
„ „
= 1.3.?
11
....
228
Hiibner & Lawrie
B., 10, 1705
34, 148
11 11 •••• ••••
-1.3.4
11
223
Halberstadt
B., 14, 2215
42, 183
11 11 •••• •••
11 11
11
228
»
B., 14, 908
11 11
11 11
'11
....
229
Hiibner and Smith
B., 10, 1706
34, 148
11 11 •••• ••••
11 11
11
229-230
Burghard and Beut-
A., 222, 166
44, 600
nagel
11 11
11 11
11
229-230
Burghard
B., 8, 559
2, 892
11 11 •••• ••••
11 11
11
232-233
Neville & Winther
B., 13, 970
37, 439
3 F
402
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dibromtoluquiuone .... .*
C6HMe.Br2 : (X,
C7H4Br3O2
...«
85
Canzcmeri & Spica
G. I., 12, 469 ;
44, 331
B., 16, 793
Dibromsalicylic acid
COOH.OH.Br2=1.2.(?)2
C7H4Br303
abt. 150
Cahours
A. C. [3], 7, 102
v., 156
JJ JJ "'•
„ =1.2 or 6.3.4
?»
218
Hiibner and Smitl
B., 10, 1706
34, 149
J) JJ .... ..
=1.2.(?)2
»
219
HUbner & Kollwag
B., 10, 1707
jj
„ ,, ....
»» »>
It
221
Hiibner and Lawri
B., 10, 1706
34, 148
J> JJ •"•
=1.2.3.5
M
....
223
Lellmann & Groth
B., 17, 2728
48, 265
maim
Dibromhydroxybeuzoic acid
= 1.4.(0,
)j
....
266-268
Balbiano
G. I., 13, 65
44, 1125
Dibromdihydroxybenzoic
(X)OH.(OH)2.Br3=1.2.6.3.4
C7H4Br2O4
....
214 d.
Zehenter
M. C., 2, 475
42, 193
aci
Dibromgallic acid
COOH.(OH)3.Br2=1.3.4.5.2.
C7H4Brs05
+H20
140
Grimaux
As., 5, 235
ji »
J» »J
»
jj
150
Etti
B., 11, 1882
Tetrabromcresol
Me.OH.Br4=1.4.2.3.5.6
C7H4Br40
....
108-110 d.
Baumann & Briege
B., 12, 804
36, 789
Benzoyl bromide
C6H5.COBr
C7H5BrO
218-219
0
Claisen
B., 14, 2473
42, 514
Brombenzaldehyde ....
C6H4Br.COH=1.2
)»
Liquid
....
A. C. J., 3, 32
n
=1.3
)J
Liquid
JJ
„
= 1:4
!»
....
57
Jackson and White
B., 11, 1043
34, 729
Brombenzoic acid
OOOH.Br=:1.2
C7H5BrO,,
....
90(?)
Richter
Z. C. [2], 5, 457
vi., 310
j» »» ••••
» ii
JJ
sb. 250
100
Peligot
A., 28, 246
i., 555
»» » ••••
)> )»
»»
....
137-5
Richter
B., 4, 462, 465
24, 688
j> j>
^» »
))
137
Hiibner & Eetschy
Z. C. [2], 7, 631
vii., 1173 ; 25,
697
,, „ .... ...
>» »»
J>
143-144
Bedson
37,95
J» M
M »»
>J
147-148
Schramm
B., 18, 1273
,, „ ....
» I»
»»
148
Zincke
B., 7, 1502
38, 119
„ „
»' t>
J>
....
150
Rahlis
A., 198, 99
tf
„ ), .... ....
» ))
»>
....
152
Lennep
Z. C. [2], 7, 67
24,370
JJ )j .... ....
M »
M
....
153
Wroblewsky
Z. C. [2], 5, 322
vi., 280
J» J» "••
)J *»
»
158
Schultz, Schmidt
A., 207, 348
40, 912
and Strasaer
)» )f
„ ='•
»>
....
152-153
Eeinecke
Z. C. [2], 5, 109
vi., 309
,» j,
= 1.3
Jj
151
Jackson
B., 9, 932
30, 512
„ „
» »
)j
153
Sandmeyer
B., 18, 1496
)) ,,
» J)
....
153
Hiibner and Anger-
A., 158, 5, 19
24, 363; vii.,
stein
161
»t >J ....
JT M
jj
wn
153
Wroblewsky
Z. C. [2], 7, 135
24, 564; vii.,
1177
» )) ....
» »J
•JJ
....
154
11
B., 8, 574; A.,
28, 886; 34,
192, 196
977
»» IJ
*t
•JJ
....
154
Korner
G. I., 4, 305
29, 216
,, „
)» J)
i)
....
155
Hiibner & Retschy
Z. C. [2], 7, 631
25, 697 ; vii.,
1173
M |,
»J »J
)>
....
155
Hiibner
A., 162, 71
25, 624; vii.,
1065
,, n ... ..,.
= 1.4
jj
....
239-240
Jackson
B., 9, 931
30, 512
11 JJ •••• ."
n >*
jj
....
240
Schramm
B., 17, 2923
JJ >J
>» jj
)i
....
245
Eiibner and Post
A., 169, 1
27, 56
M J)
» »
jj
248
Jarnelley & Thom-
47, 587
son
»? JJ •»•
ii j>
JT
248-251
Hiibner
B., 10, 1707
34, 149
»T «) .... ....
jj jj
J)
....
248
Raveill & Hiibner
A., 222, 166
46, 600
r» ,,
» 11
))
a. 250
Weith and Landolt
B.,7, 1746; 8, 717
28, 1200
jj )» ••••
JJ !>
»T
250
Etard
C. R., 87, 989
36, 320
)» jj
11 U
JJ
....
251
HUbner and Oily
J. [1866], 347
vi., 310; vii.,
161
»> j»
JJ 11
)J .
....
251
Jadziszewski
Z. C. [2], 5, 356
vi., 1102
n »
JJ JJ
J»
....
251
liibner and Anger-
A., 158, 1
24, 363
steiii
,T „
" JJ
»»
....
251
Hiibner & Retschy
Z. C. [2], 7, 631
vii., 1173; 25,
697
jj >» •». .».
>J JJ
JJ
251
3urghard
B., 8, 558
28, 892
COMPOUNDS CONTAINING FOUR ELEMENTS.
403
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Brombenzoic acid
COOH.Br=1.4
C7H5BrOs
....
251
Etard
A. C. [5], 22, 218
40, 581
„ ,, —
ji 11
51
251
Halberstadt
B., 14, 910
j, ,,
11 1)
))
251
Schramm
B., 18, 1273
Bromsalicylic aldehyde
CHO.OH.Br=1.2. ?
?J
98-99
Henry
B., 2, 275 ; Z. C.
vi., 1008
[2], 5, 371, 478
Bromhydroxybenzaldehyde....
=1.4. ?
>J
179-180
Herzfeld
B., 10, 2198
34, 423
Bromhydroxybenzoic acid ....
COOH.OH.Br=1.2.5
07H5Br03
....
164-165
Hiibner and Hein-
Z. C. [2], 7, 711
25, 894
zerling
51 11
*» Jl
)»
sb. 150-155
164-165
Henry
B., 2, 275
11 11 ••••
T» )>
)i
....
165
Lellmann and
B., 17, 2729
48, 265
Grothmann
1) 11
=1.2.3
>l
....
184
»*
B., 17, 2726
)»
11 11
» )1
J1
....
219-220
Hiibner and Hein-
Z. C. [2], 7, 711
25, 894
zerling
Hydroxybromtoluquinone ....
C6HMe.Br.(OH).:02
»
196-197
Spica & Magnanimi
G. I., 13, 312
46, 175
Bromdihydroxybenzoic acid
COOH.(OH).j.Br =1.2.6. ?
O.H5BrO4
184 d.
M. C., 2, 480
„ 11 •••
„ =l.a5. ?
)r
253
Earth and Senhof er
A., 164, 115
25, 1015; vii.,
433
Bromgallic acid .... **
COOH.(OH)3.Br =1.3.4.5.6.
C7H5BrO5
....
a. 200 d.
Grimaux
B. S. [2], 7, 479
vi., 628
Tribrommethoxybenzene ....
C6HsBr3.OMe
C7H5Br30
87
Eeinecke
B. S..[2], 7, 177
vi., 173
Tribromomethoxyphenol ....
OMe.OH.Br3=1.2.(?)3.
C7H5Br3O2
102
Tiemann & Koppe
B., 14, 2017
42, 54
it D
=1.3.(?),
V
99
....
M. C., 1, 368
11 11
)> '1
)»'
104
Tiemann and Par-
B., 13, 2364
40, 270
risius
Tribromorcinol
Me.(OH)2.Br3 =1.3.5.2.4.6
Q
....
98
Hesse
A., 68, 96
iv., 214
,, .... ....
u »i
>i
103
Lamparter
A., 134, 257
M
Tribromtoluquinol
„ =1.2.5.3.4.6
I)
....
201-202
Canzoneri & Spica
G.I., 12, 469;
44, 331
B., 16, 793
Methylic bromcoumalinate ....
C5H3BrO2.COOMe
C7H6Br04
....
134
Pechtnann
B., 17, 2379
48, 176
Dibrommethoxybenzene
OMe.Br.Br =1.2.4
C7H6Br20
54
Cahours
A., 52, 331
i., 305
11 11
11 11
))
272
59
KSrner
A., 137, 206
vi., 908
Bromomethoxybenzene
OMe.Br =1.4
C7H7BrO
220 u. c.
Liquid
Henry
B., 2, 711 ; Z. C.
vi., 916
[2], 6, 247
11 u •"*
u n
)»
223 c.
Korner
A., 137, 203
vi., 907
Brombenzylalcohol ....
(CH,OH).Br=1.4
))
69
Jackson & Lowery
B., 10, 1209
34, 64
„ „
(CH2.OH).Br =1.4
)5
....
77
11
A. C. J., 3, 246
„ „
» )»
^J
77-77-5
Schramm
B., 17, 2923
11 i»
=1.2
>^
80
Jackson and White
B., 13, 1218;
38, 879
A. C. J., 2, 316
Bromcresol
Me.OH.Br =1.4.5
»1
213-214
1. f. m.
Schall and Dralle
B., 17, 2530
48, 146
=1.4.6
>»
218-220
17-18
Vogt & Henuinger
C. E., 94, 650
42, 729
=1.3.5
»
....
56-57
Neville & Winther
B., 15, 2991
41, 421
=1.2.?
»
88-5.
Wroblewsky
Z. C. [2], 7, 135 ;
24, 565 ; 27, 62
A., 168, 165
Me.(OH)2.Br =1.3.5.?
C7H7BrO5
....
135
Lamparter
A., 134, 258
iv., 213
Ethylic pyromucate tetrabro-
CHBr.(CHBr)0.O.CBr.COOEt
i " i
C7HsBr403
46-48
Tonnies
B., 11, 1086
34, 786
mide
Bromterebic acid
C.H9BrO4
151 d.
Frost
A., 226, 363
48, 393
Methylic ethylic dibrom-
COOMe.(CHBr)j.COOEt
C7H10Br204
62-5 u. c.
Glaus
B., 15, 1846
succinate
Ethylic bromlevulinate
C4H6BrO.COOEt
CjE.^^
240 p. d.
Conrad & Guthzeit
B., 17, 2286
48, 43
Glycerol dicetobromhydrin ....
C3H6Br(OAc)2
CVH.^rO^?
170-180(100)
Hanriot
A. C. [5], 17,62
36, 1030
Isobutylic a-dibrompropio-
CH3.CBr2.COOBu3
C7H12Br2O2
213-218
Philippi
A., 171, 324
nate
Ethylic dibromvalerate
fr. CHMeEt.COOEt
ji
185
Jaff6
A., 135, 298
Bromamylene ethylate
C6H8Br.OEt.
C7H13BrO
177-180
Bauer
Z.C.P.(1861),673
vi., 1-20
11 11
is
J>
177-180
Eeboul
A., 133, 84
Isoamylic bromacetate
CH2Br.COOC5Hn
CyH^BrO.,
207
.i.*
Perkin and Duppa
11,22
i., 666
Ethylic a-bromvalerate
CH3.(CH2)2.CHBr.COOEt
»
190-192
Liquid
Juslin
B., 17, 2504
4:8, 137
„ a-bromisovalerate ...
CHMe2.CHBr.COOEt
»
190-194
....
Borodine
A., 119, 121
v., 978
Bromoenanthic acid
»»
250
....
....
As., 2, 83
(ilycorol diethylbromhydrin
C3H,Br.(OEt)2
C7H14Br02-
195-205
Liquid
Henry
B., 4, 704 24, 908
3 K 2
404
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Tribromphthalic anhydride
C6HBr3:(CO)2: 0=14.3.2.1
C8HBr3O3
....
157
Flessa
B., 17, 1484
46, 1186
Dibromphthalic „
C6H2Br2:(CO)2:0=(?)2.2.1
C8H.Br203
207-5-208
Guareschi
A., 222, 262
46, 842
» >.
11 11
„
....
SOS
Bliinileiu
B., 17, 2491
48, 163
Tetrabromphthalic acid
C6Br4(COOH)2 =6.5.4.3.2.1
C8H2Br404
266 d.
„
B., 17, 2494
48, 164
Bromphthalic anhydride
C6H3Br:(CO)2: O=3.2.1
C8H3BrO3
....
60-65
Pechmann
B., 12, 2126
,. >,
=4.2.1
„
....
125
Smith
J. [1879], 143
35, 792
n n
11 ii
„
....
132
Guareschi
A., 222, 262
46, 843
,i »
ii ii
„
....
134-135
Meldola
47, 511, 512
,i »
ii ii
„
....
138-140
Faust
A, 160, 62
„
ii 11
„ =?.2.1
„
v. C8H2Br2O
207-5-208
Guareschi
G. I., 7, 24 ; G. I
31, 712; 42,
[1881], 542
734
Tribromphthalic acid
(COOH)2.Br3=1.2.3.4.?
C8H3Br304
....
190-191
Flessa
B., 17, 1484
46, 1186
Dibromphthalide
....
C8H4Br202
....
188-189
Guareschi
A., 222, 262
46, 842
Dibromphthalic acid „
(COOH)2.Br2 =1.2.(?)2
C8H4Br204
135
„
„
„
,, „ ....
ii ii
„
206
Blumlein
B., 17, 2490
48, 163
Dibromterephthalic acid
=1.4.5.?
„
....
320
Glaus and Wimme
B., 13, 904
38, 632
Bromcoumarone
fr. C,H4.CH : CH.O
C8H6BrO
....
36
Ebert
A., 226, 347
48, 391
r i
Brompiperonal
C6H2Br(COH).O.CH2.O
C8H6Br03
129
Fittig and Mielck
A., 152, 49
vi., 948
=?.1.3.4
Bromphthalic acid
(COOH)2.Br =1.2.3
C8H6Br04
....
135
Guareschi
B., 10, 294 ; G. I
31, 712 ; 43, 3
7,24
i. ,,
ii n
„
....
138-140
Faust
A., 160, 62
„ „
11 11
„
300-330
138-140
Pechmaun
B., 12, 2126
,, 11
=1.2.4
„
cf. C8H3BrO3
174
Meldola
47, 511, 512
,i
11
„
„
174-176
Guareschi
A., 222, 262
46, 843
„ ,,
11 11
„
„
197 u.c.
Carnelley & Thorn
47, 591
=203 e.
son
Bromisophthalic acid
=1.3.4
„
....
205
Schultz
B., 17, 469
Bromterephthalic „
=1.4.5
„
304-305
Fischli
B., 12, 619
36, 639
I» V •"•
11 11
„
290-295 u.c.
Carnelley & Thom-
47, 590
=304-309 c.
son
Brompiperonylic „
C6H,,Br(COOH).O.CH2.O
„
....
204-205
Fittig and Mielck
A, 172, 158
27, 899
=?.1.3.4
Tribromresorcinol acetate ....
OH.OAc.Br3 =1.3.(2)3
C8H6Br303
114
Claassen
B., 11, 1442
Pentabromethylphenol
C6H4.OH.(CBr2.CBr3)
C8H6Br60
....
103-106 d.
....
A., 216, 284
Dibromacetophenone
Ph.CO.CHBr2
C8H6Br20
....
36
Eunnius
B., 10, 2010
34, 147
., »
„
„
.;..
36-37
A., 195, 161
Dibromethylenephenol
HO.C6H4.C2HBr2
„
240-250 s.d.
37-38
A., 216, 283
?
„
d.
68-69
Jannasch
Z. C. [2], 7, 453
25, 241
Coumarone dibromide
C6H4.O.CHBr.CHBr
"
....
86
Fittig and Ebert
A., 216, 169
44, 474
Dibromphenyl acetic acid ....
C6H3Br2(CH2.COOH)
C8H6Br202
114-115
Bedson
37,97
Dibromtoluic acid
COOH.Me.Br2 =1.3.(!)
11
185-186
Fittig, Ahrens, and
A, 147, 36
vi., 1100
Mattheides
n »
„ =1.4.3.6
„
195
Schultz
B., 18, 1762
48, 1054
Dibromxyloquinone
C6Me2Br2:02=1.3.(?)4
„
174
....
A., 195, 273
ii
=1.4.(?)4
„
184
J. p. [2], 23, 434
Methyldibromsalicylic acid ....
OOOH.OMe.Br2 =1.2.(?)2
C8H6Br203
145
Cahours
A. C. [3], 10 339
v., 163
Dibromanisic acid
COOH.OMe.Br2=1.4.(?)2
....
207-208
Keinecke
B. S. [2], 7, 177
vi., 173
*i ii «... ....
„ „
„
13-5-214-5 c.
Crespi
G. I. [1881], 219
42, 192
Dimethoxydibromquinone ....
C6Br2(OMe)2:02
C8H6Br204
175
lofmann
B., 8, 67
28, 56!)
ii 11
»
n
.75
n
B., 11, 332
34, 418
Tetrabromethylphenol
....
C8H6Br40
58-59
....
A., 216, 283
" "
•i •
105-106
....
A., 156, 255
•
„
138
lantzch
A., 215, 51
44,84
Teti'abrom-/3-orcinol
C:6Me2Br2(OBr)2
C8H6Br402
....
101
Stenhouse and
A., 203, 293
37, 401
'
Groves
'
....
C8H7BrO
212-216
38-39
annasch
Z. C. [2], 7, 453
25, 242
COMPOUNDS CONTAINING FOUR ELEMENTS.
405
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Gh. Soc.
Acetophenone bromide
Ph.CO.CH2Br
C8H,BrO
of. B. 11, 931
50
Emmerling and
B., 4, 148
24, 258
Engler
?) >»
»
»T
....
50
Staedel and Klein-
B., 13, 837
38, 660
schmidt
j» »
||
»)
....
50
Bottinger
B., 14, 1238
40, 815
i» »
u
*)
50
Hunnius
B., 10, 2008
j) D ••••
>1
)»
50
Mohlau
B., 15, 2466
Acetylenebromphenylin
J)
220 ; d. 240
....
A., 216, 278
Bromoxystyrolene
))
265
M. C., 1, 181
Phenylbromacetic acid
Ph.CHBr.COOH
CsH-BrO3
382
83-84
Glaser and Kadzis-
Z. C. [2], 4, 142 ;
vi., 1101
zewski
B., 2, 208
Methylic brombenzoate
COOMe.Br=1.2
)»
246-247
Liquid
Eahlis
A., 198, 109
38, 119
5> »
=1.3
u
....
31-32
....
A., 159, 14
Brom-a-toluic acid
(CH2.COOH).Br=1.4(?)
5)
Mixture, of.
76
Radziszewski
B., 2, 208 ; Z. C.,
vi., 1102
37,96
[2], 5, 358
>» »
=1.3
»'
....
100-100-6
Gabriel
B., 15, 841
42, 1071
„ „
= 1.2
)T
102-5-103
Jackson and White
B., 13, 1219 ;
38, 879
A. C. J., 2, 316
„ „
» »
I>
103-104
Bedson
37,95
„ „
=1.4
55
114-115
j>
37,94
,, ,,
» J»
)I
114-5
Jackson & Lowery
B., 10, 1210 ;
34, 64
A. C. J., 3, 246
Bromomethoxybenzaldehyde
COH.OH.Br=1.2. 1
•»
....
113-114-5
Perkin
A., 145, 304
vi., 1008
ji
=1.4. ?
))
Solid
Cahours
A. C. [3], 14, 486
i., 306
Bromtoluic acid
COOH.Me.Br=1.3.6
V
140-145
Jacobsen
B., 14, 2352
42, 185
» „ ....
=1.3. ?
))
155
Kelbe
B., 15, 42
42, 619
,, ,, .... ....
= 1.2.6
J»
167
Jacobsen & Wierss
B., 16, 1956
44, 1121
» „
=1.2.5
))
....
174-176
Jacobsen
B., 17, 2375
48, 143
7» „
=1.3. 1
))
....
185-189
....
vi., 1100
,, ,,
= 1.3.4
)»
205-206
Fittig and Abrens
A., 147, 32
»
„ „
» »
;j
205-206
Ahrens
Z. C., [2], 5, 106
vii., 1175
„ ,,
r ?»
»
205-207
Bottinger& Ramsay
A., 168, 258
27, 69
„ »»
v »
»)
....
209
Jacobsen
B., 14, 2351
42,185
»i }) •••• ••••
» JT
»»
208-209 c.
Remsen & Kuhara
A. C. J., 3, 424
42, 608
„ ,,
H ))
v
....
210-5
Kelbe
B., 15, 41
42,619
„ „
= 1.4.3
)»
203-204
Landolph
B., 5, 268
vii., 420; 26,
473
„ ,,
'1 5!
)»
203-204
Morse and Ram sen
B., 11, 225
34, 571
»> „
» )J
Jj
203-5-204
Jannaschand Diek-
A., 171, 83
27, 477
mann
D »
*» »J
»
304
Bruckner
B., 9, 407
30,85
Bromphenoxyacetic acid
C6H4Br.O.UH3.COOH
C8H7BrO3
153-154
Fritzsche
J. p. [2], 20, 295
38, 320
Methylic bromsalicylate
COOMe.OH.Br=1.2. ?
» t
265-266
36-38
Henry
B., 2, 276 ; Z. C.
vi., 1003
[2], 5, 479
Methylbromsalicylic acid ....
COOH.OMe.Br=1.2. ?
;»
....
55
Cahoui-s
A. C. [3], 10, 339
v., 163
Bromanisic acid
=1.4. ?
)j
205
Laurent
R. S., 10, 6, 362
i., 301
,, v .... ....
= 1.4.5
»
....
211-5-212 c.
Balbiano
G. I. [1881], 396
42, 169
71 )5 *•" ••••
V »)
)5
213-214
Schall and Dralle
B., 17, 2531
48, 146
,, „
») »
H
213-214
Salkowski
B., 7, 1013
28,65
» Jl •"• ••"•
= 1.4.6
j»
....
218-218-5
Balbiano
G. I. [1881], 396
42, 169
Bromethylene pyrogallate ....
Brom vanillin ....
fr. C6H3(OH):02:C2H4
COH.OH.OMe.Br= 1.4.5. ?
ji
67
160-161 u. c.
Magatti
Tiemann & Haar-
B., 12, 1862
B., 7, 615
38, 250
27, 896
ij
161
mann
Carles
B. S. [2], 17, 12
vii., 1201
Bromdehydracetie acid
1J ) J
f r. CH2 Ac.C : CH.C(COOH) : C.
1 1
>J
C8H7Br04
134
Oppenheim and
B., 9, 1101
30, 506
OH
Precht
M >* *•"
»
))
....
136-137
Perkin and Bern-
B., 17, 1524
46, 1121
hardt
Bromvanillic acid
COOH.OMe.OH.Br=1.3.4. ?
»1
+ H20
192-193
Matsmoto
B., 11, 139
34, 503
Ethylic bromcomenate
C6HBrO2(OH)(COOEt)
C8H7Br06
140-141
Mennel
J. p. [2], 26, 471
406
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Ethoxytribrombenzene
C6H2Br3.OEt
G8H7Br30
72-5
Mohlau and Oeh
J. p., 24, 484
48, 396
michen
Ethyltribromphenol
C6HBr3Et.OH.
11
53-5-55
....
A., 156, 256
Tribromxyleuol
Me2.OHBr3= ?
„
141
Wroblewsky
Z. C. [2], 4, 232
vi., 1129
„
„ =1.3.5.2.4.6
„
162-5
Thol
B., 18, 362
48, 522
11
„ =1.2.4.3.5.6
„
169
Jacobsen
B., 11, 28
34, 412
11
„ =1.3.2.4.5.6
„
....
175
„
B., 11, 26
11
i,
„ =1.4.2.3.5.6
„
175
„
B., 11, 27
„
„ .... ..
„ =1.3.4.2.5.6
J)
179
11
B., 11, 25
34, 411
Ethoxydibrombenzene
C6H3Br2.OEt=1.3.5
G8H8Br,0
268
Liquid
Mohlau and Oeh
J. p. [2], 24, 483
42,396
michen
Dibromxylenol
Me2.OH.Br2=1.3.4.(2)2
„
73
Jacobsen
B., 11, 25
34,411
„
=1.3.(2)3
„
....
80
Armstrong anc
B., 9, 950
Gaskell
„
)>
„
....
176
Fittig& Hoogewer
Z. G. [2], 5, 170
vi., 1129
Dibromdimethylpyrocatecho
(OMe)2.Br2=1.2.(?)2
C8H8Br2O2
....
83-84
Matsmoto
B., 11, 137
34, 502
11
11 »
„
92
Merck
N. J. T., 21, 134
v., 997
11
11 1!
„
....
92-93
Tiemann & Koppe
B., 14, 2018
42, 54
Dibromdimethylresorcinol ...
n ^1>3.(*)2
„
137-138 u. c
Honig
B., 11, 1041
34, 727
11
11 11
„
141
Tiemann&Parrisiu
B., 13, 2365
40, 270
Dibromdimethylquinol
=1.4.5.?
„
142
Habermann
B., 11, 1036
34, 728
Dibromomethylorcinol
Me.OMe.OH.Br2=1.3.5.6.(?)
„
146
Tiemann & Streng
B., 14, 2002
42, 52
Dibrom-|8-orcinol
Me2.(OH)2.Br2=?
„
155
Stenhouse & Grove
A., 203, 296
37, 402
Dibromxyloquinol
„
„
184
Carstanjen
J. p. [2], 23, 421
42, 612
?
C8H6Br40(?)
C8H8Br40
....
138
Hantzsch
A., 215, 51
44,84
Phenylbromethyloxide
Ph.O.CH2.CH2Br
C8H9BrO
350-260 p. d
39
Henry
C. B., 96, 1233
44, 802
„
Ph.O.C2H4Br
n
240-250 p. d.
39
Weddige
J. p., 24, 241
40, 1137
Bromhydroxystyrolene
C6H5.C2H3Br(OH)
H
265
Liquid
Suida and Plohu
W. A., 81, 245
40, 268
Ethoxybrombenzene
C,H4Br.OEt=?
|(
130 = 230?
....
Grimaux
B., 2, 715
„
„ =1.4
233
Liquid
Lippmann
W. A., 62, 605
24, 1040
Methoxybromtoluene
Me.OMe.Br=1.4.5
225-227
Liquid
Schall and Dralle
B., 17, 2531
48, 146
Bromxylenol .... . .
Me2.OH.Br=1.3.4.?
I jl( 1 lilt 1
Jacobsen
B. 11 25
34 41 1
n
....
OT*I -iii
11 =1.4.5.?
71
B. S. 27 140
"
)j
....
74
Adam
B. S. 41 288
* *
11 11
j)
87
Jacobsen
B., 11, 27
34, 412
Diethylic bromomaleate
C2HBr(COOEt)2
C^ErO,
56(o.p.),u.c.
Anschiitz
B., 12, 2284
143 (30-40)
Brommalophthalic acid
....
C8HnBr05
....
d. 180
A., 166, 353
Tribromdipropylacetolactone
....
C8HnBr,Os
f. A., 216, 76
Liquid— 13
Hjelt
B., 15, 628
42,946
1
C8HnBr303
....
42-43
Spatzky
J. E. [1885], 61
48, 512
Diethylic dibromsuccinate ....
COOEt.(CHBr)2.COOEt
CsH12Br!!04
40-150 p. d.
58
KekulS
As., 1, 358
v., 459
n ,i
„
„
58
Anschiitz
B., 12, 2281
11 n
„
„
....
o9
Glaus
B., 15, 1845
11 ii
„
68
jehrfeld
B., 14, 1820
Dibromsuberic acid
C6H10Br2(COOH)2
72-173
Gantter and Hell
B., 15, 149
42, 716
Bromdipropylacetolactone ....
....
C8H13BrO2
f. A., 216, 73
jiquid — 13
Hjelt
B., 15, 628
42,946
Diethylic bromsuccinate
COOEt.CH2.CHBr.COOEt
C H BrO
25-226 d.
J. R, 9, 277
Bromsuberic acid
CeH.^COOH),
J?
.A., 155,251
02-103
Jantter and Hell
B., 15, 148
42, 716
» »
I)
„
d. 140-150
00-101
lell and Eempel
B., 18, 814
48, 755
1
....
J9H20Br6O2
Od.
. 22
Schiitzenberger
B. S. [2], 19, 8
26, 487
Xanthogallol ....
C18H4Br1406(?)
C9H2Br703(?)
22
Stenhouse
C. N., 29, 96
27, 586; vii.,
1031
Tribromumbelliferone
C6Br3(OH).CH.CH.COO
C9H3Br308
94
'osen
B., 14, 2746
42, 839
Tribromoesculetin
=(?)3.1.2.?
C9H3Br304
240 d.
jieberruann and
B., 13, 1592
40, 108
Knietsch
0-Dibromcoumarin
fr. C6H4.CH : CH.COO=1.2
C9H4BfnO2
176
'erkin
24,42
vi., 500
' ~ |
"' »
C6H3Br.C2HBr.COO=1.2
„
....
174
Ebert
3, 370
5» •••• ....
" ')
11
179
11
A., 226, 350
« „
"
183
11
....
4,40; vi.,500
COMPOUNDS CONTAINING FOUR ELEMENTS.
407
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Fr. Amidonaphthaquiuon-
....
C3H4Br2O2
173
Kronfeld
B., 17, 721
46, 1037
imicle
Dibromoesculetin
C9H4Br204
233
Liebermann anc
B., 13, 1594
40, 108
Knietsch
a-bromcoumarin
fr. CfiH4.CH : CH.COO=1.2
i i
C9H5Br02
110
Perkin
23, 371 ; 24, 37
vl., 499
(3- „
C6H3Br.C2H2.COO=1.2
M
160
Ebert
A., 226, 349
i i
8- „
i» 11
)»
•••>
160
Perkin
24,42
vi., 500
Bromomethylenephthalyl ...
C6H4:(CO)2:CHBr.=1.2
11
132-133
Gabriel andMicha
B., 11, 1011
34, 734
Bromocoumarilic acid
fr. C6H4.CH I C(COOH).0
i i
C9H5Br03
a. 250
Perkin
24,48
vi., 498
=1.2
11 11
....
»
250-251
Ebert
A., 226, 350
Bromomethylenephthalyl
C9H5Br302
117-5-118-5
Gabriel andMichae
B., 11, 1007
34, 735
dibromide
u. c.
Tribromacetophenone car-
C,H4(CO.CBr3).COOH=1.2
C9H5Br303
159-5-160
11
B., 10, 1555
34, 229
bonio acid
Coumarin dibromide
....
C9H6Br202
abt. 100 p. c
Perkin
23, 369
vi., 499
i> 11
C6H4.CHBr.CHBr.COO=l.
)>
105
A., 216, 163
Methylene phthalide dibro-
C6H4.COO.CBr.CH,Br=1.2
))
98-99
Gabriel
B., 17, 2523
48,164
i i
mide
Bromcinnamic aldehyde
Ph.CBr:CH.COH
C9H7BrO
72-73
Zincke and Hagen
B., 17, 1815
46, 1344
11 11 ••••
M
....
112
Gossing
C. C. [1877], 193
34, 318
Bromatropic acid
Ph.C(COOH):CHBr
C9H7Br02
....
130
Fittig and Wiirste
A., 195, 162
36, 380
0-bromcinnamic acid
Ph.CH : CBr.COOH
1}
120
Glaser
A., 143, 336
vi., 468
£- „ „
H
)>
....
120
Barische
J. p. [2], 20, 173
38, 43
»- » i.
Ph.CBr : CH.COOH
11
130-131
Glaser
A., 143, 333
vi., 468
a- „ „
11
tt
....
131
Bariscbe
J. p. [2], 20, 182
38,43
o- „ „
)1
»
131
Leuckart
B., 15, 17
Bromcinnamic acid .... ....
C6H4Br.(CH : CH.COOH)
)J
211-213]
Gabriel
B., 15, 2295
44, 195
=1.2
„ „
= 1.3
11
....
178-179
11
B., 15, 2297
11
11 11 .... ....
=1.4
11
251-253
11
B., 15, 2300
44, 196
Brommelilotic anhydride ....
fr. O.C6H4.(CH2)2.CO.O=1.2
11
106
Hochstetter
A., 226, 355
48, 390
Phenoxybromacrylic acid ....
CHBr:C(OPh).COOH
C9H7BrO3
....
138
Hill and Stevens
A. C. J., 6, 187
48, 532
Na-ethylate on bromacrolein
....
)»
....
140
Grimaux and Adam
B. S. [2], 36, 136
40, 1029
Brom-o-aldehydophenoxy-
fr. C6H4(COH).O.CH2.COOH
C9H7Br04
....
163
Rossing
B., 17, 2992
48, 388
acetic acid
a-phenyltribrompropionic
Ph.CBr2.CHBr.COOH
C9H7Br3O2
132
Glaser
A., 143, 335
acid
0- 11 »
Ph.CHBr.CBr2.COOH
>»
45-48
u
A., 143, 338
0- 11 »
Ph.C3HBr3.COOH
11
151
Kinnicutt & Palmer
A. C. J., 5, 583
46, 603
Tribromhydratropic acid
fr. Ph.CHMe.COOH
i»
....
150
Fittig and Wiirster
A., 195, 163
36, 380
Propionoxytribrombenzene ....
C6H2Br3(O.C3H50)
»
65
juareschi and Dac-
B., 18, 1174
48, 891
como
Cinnamaklehyde dibromide....
Ph.CHBr.CHBr.COH
CsHsBr.O
....
100 d.
Zinck6 and Hagen
B., 17, 1814
46, 1343
Dibrorntolyluiethylketone ....
fr.C6H4Me.Ac=1.4
»
100
Vlichaelis
B., 15, 186
42,970
Dibromhydratropic acid
Ph.CBr(CH2Br).COOH
^g-tlgJjrgOd
....
115-116
Fittig and Wiirster
A., 195, 159
36, 379
Phenyldibrompropionic acid
Ph.CHBr.CHBr.COOH
)»
....
195
....
A.
» 11
3»
1?'
....
196
A.nschiitzand Kin-
B., 12, 538
36, 645
nicutt
Methylicdibromphenylacetate
C.ftBrj.CH.j.COOMe
)»
20-230(d.p.)
....
3edson
37,96
Ethylic dibrombenzoate
COOEt.Br2=1.3.4
11
....
38-38-5
iurghard
B., 8, 560
28, 892
11 I* ....
17 11
11
....
38-38-5
iurghard and Bent-
A., 222, 166
46, 601
nagel
THbroTnmesitylenic acid
COOH.Me2 Br2— 1 3.5.2.4.or6
94-195
iussencfuth
A. 215 249
4, 470
}>
Dibromatrolactic acid
CHBr2.CPh(OH).COOH
C9H3Br203
....
67
Jottinger
B., 14, 1236
40, 815
Phenyldibromlactic acid
Ph.C2HBr2(OH).COOH
1)
....
84
Cinnicuttand Pal-
A. C. J., 5, 583
46, 603
mer
Methylic dibromanisate
COOMe.OMe.Bra=1.4.(?)2
11
....
1-5-92
ialbiano
G. I., 13, 65
4, 1125
408
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dibromhydrocoumaric acid,..
(CH2.CH2.COOH).OH.Br2
C9H8Br2O3
107
Stohr
A., 225, 57
46, 1350
„
'» I)
..
....
115
Zwenger
A., 25, 116
vi., 716
Dibrommethoxytoluic acid ...
COOH.OMe.Me.Br2
193-194
Paternd and Can-
G. I., 10, 233
38, 884
=1.2.4.(?)s
zoneri
Methylacetophenone bromide
C9H9BrO(?)
C9H10Br20(?
55
Bottinger
B., 14, 1598
40, 1036
Phenylbromallyl oxide
Ph.O.CH2.CBr:CH2
„
240 s.d.
Liquid
Henry
C. E., 96, 1233
44, 803
a-Bromhydratropic acid
CH2Br.CHPh.COOH
C9H9BrO2
....
93
Fittig and Wurster
A., 195, 152
36, 379
» )j *••
„
„
93-94
Merling
A., 209, 13
40, 1143
ft- » »
CHj.CBrPh.COOH
„
93-94
„
A., 209, 10
„
Phenyl a-brompropionic acid
Ph.CH2.CHBr.COOH
„
137-5
Anschiitz and Kin-
B., 12, 537
36, 645
nicutt
.. >! »
„
„
138
Fittig
B., 9, 1195
31, 61
,, „
„
„
....
137
Fittig and Binder
A., 195, 132
36, 378
» » »
„
„
d. 143
137-138
Fittig
B., 10, 519
33, 431
Bromphenylpropionic acid ...
Br.(CH2.CH2.COOH)=1.3
„
74-5-75
Gabriel
B., 15, 2294
44, 195
,, » ~
=1.8
„
....
97-99
„
B., 15, 2296
„
» >. -
=1.4
„
....
136
Glaser
A., 143, 341
» »> ••••
» .,
„
136
Gabriel
B., 13, 1682
,, » •-
» »
„
....
135
Goring
C. C. [1877], 793
34, 318
Ethylic brombenzoate
COOEt.Br=1.2
„
254-255
Liquid
Eahlis
A., 198, 109
38, ] 19
» »
=1.3
,,
259
Liquid
Engler
B., 4, 707
24, 923
Brombenzylic acetate
C6H4Br.(CH2OAc)=1.4
j?
250-260 d.
Liquid
Jackson & Lowery
B., 10, 1209
Bromethylsalicylol ....
COH.OEt.Br.=1.2. ?
„
67-68
Perkin
A., 145, 308
vi., 1009
Bromxylic acid
COOH.Me2.Br=1.2.4.5
„
....
172-173
Sussenguth
A., 215, 244
44, 469
,, „
» .1
„
....
174.
Gunter
B., 17, 1608
„ „
„ =1.2.5. 1
,,
189
„
B., 17, 1609
46, 1347
a-Bromomesitylenic acid
COOH.Me2.Br=1.3.5.6
„
....
146 a.f. 138
Schmidt
A., 193, 172
36, 156
ft- » »
„ =1.3.5.4
„
212
Sussenguth
A., 215, 246
44, 469
ft- » I!
.; »
„
....
214-215
Schmidt
A., 193, 174
36, 156
Phenylbromlactic acid
Ph.C2H2Br(OH).COOH
C9H9Br03
125
Glaser
A., 147, 83
>. »
„
„
+H20
120-122
„
„
a-Bromphenoxypropionic acid
CH3.CH(O.C6H4Br).COOH
„
105-106
Saarbach
J. p. [2], 21, 157
38, 393
Methylic bromanisate
COOMe.OMe.Br=1.4. ?
,,
gentle ht.
Laurent
A., 56, 314
1., 301
Brommelilotic acid
OH.(CHj.CHa.COOH)=1.2
„
....
141-142 d.
Hochstetter
A., 226, 355
48, 390
Bromveratric acid
COOH.(OMe)2.Br=1.3.4. ?
C9H9Br04
183-184
Matsmoto
B., 11, 136
34, 502
Isopropoxytribrombenzene ....
C6H2Br3.OPr/s
C9H9Br3O
....
93
Silva
B. S. [2], 13, 27
vi., 917
Methoxytribromxylene
Me2.OMe.Br3— 1.3.4.2.5.6
120
Jacobsen
B., 11, 26
Bromacrolein ....
IT "
' ' . ,
B. S. [21 36 136
40 1029
Stycerin dibromhydrin
Ph.C3H4Br2.OH
C9H10Br20
«...
74
Grimaux
C. E., 74, 1598
26, 1139
Methylacetophenone bromide
„
C9H9BrO (?)
55
Bottinger
B., 14, 1598
40, 1036
Dibrompseudocumenol
Me3.OH.Br2=1.3.4.5.2.6
„
....
148-149
Edler
B., 18, 630
48,772
Dibrompseudocuminol
„ —1.34625
1 4Q_1 r.n
T> ,
B., 11, 30
34, 413
i*±ij 1UV
Dibrommesitol
„ =1.3.5.2.4.6
....
150
Jacobsen
A.. 195, 271
36, 529
Dibromdimethylorcinol
Me.(OMe)2.Br2=1.3.5.2.4or6
C9H10Br2O2
K.I
160
Tiemannand Streng
B., 14, 2001
42, 51
Dimethyldibrommethylpyro-
Me.(OMe)j.OH.Br2=?
C9H10Br203
....
126
Hofmann
B., 12, 1375
38, 249
gallol
Dibromnono-dilactone
(CH2Br.C.COO.CH2)2
C9H10Br204
130
Hjelt
B., 14, 627; 15, 625
40, 577; 42, 946
Isopropoxybrombenzene
C6H4Br.OPris=1.4
C9HnBrO
236 (760)
Liquid
Silva
Z. C. [1870], 250
vi., 917
Brompseudocuminol
Mea.OH.Br=1.3.4.6.2 or 5
B
250 d.
32
Reuter
B.,11, 29
34, 413
Bromomesitol....
, Q R O y(
A 1 f\K O*-/\
» — ....
"
80
Jacobsen
A., 195, z/0
36, 529
"
J)
81
Biedermann aud
Ledoux
-D.. O. OU
Brom-mesityleneglycol
(CH2.OH)2.Me.Br=1.3.5.2
C9HuBr02
126
C'olson
C. E, 97, 177
46, 57
or 4
Phorone tetrabromide
(Me2CBr.CHBr)2CO
C9Hl4Br4O
88-89
Claisen
A., 180, 12
29, 896
» »
Me2CBr.CHBr.CBrMe.
„
86-88
„
B., 7, 1168
28, 161
CHBrAc
Diallylcarbinolacetate tetra-
(CH2Br.CHBr.CH2)2CH.OAc
C9H14Br4O2
L.f.m.
Saytzefi'
A., 185, 137
32, 297
bromide
COMPOUNDS CONTAINING FOUR ELEMENTS.
400
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Ethylic itabrompyrotartrate
....
C9H15BrO4
270-275 p.d.
....
Z. C. [1866], 722
vi., 981
?
....
C9H16Br202
42
Fittig
B., 17, 3014
48, 376
Ethylic a-bromoananthylate....
C5Hu.CHBr.COOEt
C9H17BrO2
220-225 p.d.
Liquid
Hell and Schiile
B., 18, 625
48, 757
Tetrabrom-a-naphthaquinone
....
C10H2Br402
....
265
Bliimlein
B., 17, 2489
48, 163
» -°~ D
„
164
Flessa
B., 17, 1482
46, 1186
Pentabrom-n-naphthol
C10H2Br5.OH
C10H3Br60
....
238-239
Blumlein
B., 17, 2488
46, 163
.. -#- »
„
„
237
Flessa
B., 17, 1481
46, 1186
Dibrom-a-naphthaquinone ....
Br^Oj^fta^;
C10H4Br202
....
149-5 ; a.s
Diehl and Merz
,B., 11, 1065
34, 736
151;5
., „
„ =^l/31ai«2 :
„
218
Miller
B. S., 43, 125
48, 667
» -?- „
„ = ?
„
....
171-173
Guareschi
A.', 222, 262
46, 842
Dibromfuril
C H Br O
183-184
Fischer
B., 13, 1339
38, 798
10 4, J 4
185
A.,' 211, 225
42, 500
Tetrabrom-3-naphthol
C7H3Br4.OH.
C10H,Br4O
156
Smith
i35,"791
Bromhydroxy-a-naphthoqui-
HO.Br: 05=3,^0,;
C10H6BrO3
196-5
Diehl and Merz
B., 11, 1066
34, 737
none
-«- »
„ ,,
„
196-197
Baltzer
B., 14, 1901
» -a- .1
» >>
„
....
201-202
Miller
B. S., 43, 125
48, 667
Bromfuril
C10HjBrO.
Cry st&ll in6
Fischer
A. 211 227
42 500
Phthalylbromacetic acid
C6H4:(CO)2:CBr.COOH=1.2
»
...
232-235
Gabriel & Michael
B., 10, 2200
34, 426
Pentabromsafrol
....
C10HbBr502
169-170
Grimaux & fiuotte
A., 152, 90
vi., 1014
Dibrom-a-naphthol
C19H6Br2.OH
C10H6Br2O
....
111
Biedermann
B., 6, 1119
27, 161
„ -a- „
„
»
111
Meldola
C. N., 47, 536
44, 536; 45, 161
Br on diamidonaphthol
C1(,H6Br203
175
Diehl and Merz
B., 11, 1068
34, 737
Tetrabromresorcinol .diacetate
(OAc)2.Br4=1.3.2.4.5,6
C10H6Br404
169
Claasen
B., 11, 1441
34, 868
Furil octobromide
....
C18H,Br804
....
185 d.
Fischer
B., 13, 1338 ; A.,
38, 798; 40, 500
.an, 214
Brom-/3-naphthol
ClpH6Br.OH=a1/31 ;
C10H7BrO
84
Smith
B., 12, 6bO
35, 790
„ .,
„ „
„
84
Armstrong
B.,'l5, 202
36, 722
3-Brompropionic coumarin ...
....
C10H7Br02
....
146
Perkin
Ji [1875], 591
28, 13
Methoxybromphenylpropiolic
C,H3Br (OMe)C i C.COOH
C10H,Br03
abt. 168 d.
„
39, 419
acid
=1.2.1
Phenoxymucobromic acid ....
CHO.CBr : C(OPh).COOH
C10H7Br04
....
104-105
Hill aoid Stiven
A. C. J., 6, 187
48, 532
Bromhydroxy-(3-methylcou-
HO.C.H2Br.CMe :C(COOH).O
i i
H
221 d.
Peeh,niann & Cohen
B., 17, 2135
46, 1332
marilic acid
=1.2.4.3
Phenoxybrommalei'c acid ....
C2Br(OPh)(COOH)2
C10H7Br06
....
103-104
Hill and Stiven
A, C. J., 6, 187
48, 532
Tribromresorcinol diacetate
(OAc)2.Br3=1.3.4.(?)2
C10H7Br304
108
Claasen
B., 11, 1439
34, 867
Benzoyldibrompropionic acid
Bz.CHBr.CHBr.COOH
CloH8Br203
....
135
Pechmann
B., 15, 888
42., 1074
Carboxylphenyldibrompro-
COOH.(CHBr.CHBr.COOH)
C10H9Br.,04
....
212-21,3
Gabriel & Michael
B., 10, 2204
34,427
pionic acid
=1.2
11 )) :i
=1.4
„
....
d.w.ni.sv 300
Low
B., 18, 949
48, 799
Dibromquinol diacetate
(OAc)2.Br2=1.4.5.2
„
159-5 ; 161
Schula
B., 15, 654, 655
Dibromphenylene dioxyacetic
C6H2Br2(O.CH2.COOH)j
C)0H9Br206
249-25o'd-
Gabriel
B,, 12, 1640
38, 34
acid
=(?)2.3.1
2
C10H8Br402
183
Fittig & Barriuger
Aw 161, 307
25, 488
Methoxydibromphenyldi-
(CHBr.CHBr.COOH).OMe.
C10H8Br403
200-202
Perkin
39, 421
brompropionic acid
Br2=1.2.())2
Methoxyphlenylbromacrylic
(C2HBr.COOH).OMe.Br
C10H9BrO3
169/5-171
„
39% 423.
acid
=1.2.?
» »
»J 1)
„
169
„
39, 426
Methylic bromterephthalate
(COOMe)2.Br=1.4.5
C10H9Br04
a. 300
42
Fischli
B.x 12, 620
36, 639
Bromquinol diacetate
(OAc)2.Br=1.4.5
„
....
71-73
Schulz
B., 15, 655
Brompiperopropionic acid ....
CH2:O2:C6H2Br(CH2)2.
n
...*
139-6
Weinstein
A., 227, 31
48, 665
COOH
Bromomeconin
M
....
167
Anderson
A., 98, 48
Hi., 863
Bromacetovanillic acid
COOH.OMe.OAc. Br= 1 .3.4
CioH9BrO5
....
165-167
Matsmoto
B., 11, 138
34, 502
Bromopianic acid
„
....
192
J. p. [2], 24, 367
„ ,,
„
204
Wegscheider
M, C., 4, 268
44,997
„ „
....
,,
....
250-251
„
„
M
Methoxybromphenyldibrom-
(CHBr.CHBr.COOH).OMe.
CloH9Br303
185-188
Perkin
39, 418
propionic acid
Br=1.2.?
-
3 o
410
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Benzylidene acetone dibrom-
Ph.CHBr.CHBr.CO.Me
C10H10Br20
....
124-125
Claisen & Claparede
B., 14, 2462
42, 512
ide
Methylic phenyldibrompro-
Ph.CHBr.CHBr.COOMe
C10H10Br.,Oj
....
117
Anschiitz and Kin-
B., 11, 1220; 12,
34,981; 36,645
pionate
nicutt
538
Phenyldibrombutyric acid ....
Ph.CHBr.CHBr.CH2.COOH
i»
138
Jayne
A., 216, 107
44, 473
Ethylic dibromtoluate
COOEt.Me.Br,=1.4.3.6
„
310
49
Schultz
B., 18, 1762
48, 1054
Dibrompropylbeuzoic acid or
Pr».COOH.Br2=1.4.(?)3 or
„
....
152-153
Claus and Wimmel
B., 13, 903
38, 632
dibrom toluene propionic acid
(CH2.CH2.COOH).Me.Br2
Dibrommethylbenzylacetic
....
w
....
135
• •••
A., 193, 316
acid
Dibromeugenol
(CH : CHMe).OMe.OH.Br2
is
59
Chasanowitz & Hell
B., 18, 824
48, 779
=1.4.3.(?)s
Dibromthymoquinone
Me.Pr« : O2.Br2=1.4.2.3.5.6
„
73-5
Carstanjen
J. p. [2], 3, 55
24, 351 ; vii.,
1156
Methoxyphenyldibrompro-
(CHBr.CHBr.COOH).OMe
C10H10Br2O3
....
abt. 156 d.
Perkin
A., 216, 160
39, 420
pionic acid
=1.2
Ethylic dibromanisate
COOEt.OMe.Brs=1.4.(?)3
„
88 c.
Crespi
G. I. [1881], 419
42, 193
Methyldibromatrolactic acid
....
„
....
163
Bottinger
B., 14, 1597
40, 1036
Ethylic dibromorsellinate ....
COOEt.(OH)3.Me.Br2
C10H10Br204
144
A., 117, 315
iv., 237
Dibromeugenol dibromide ....
(CHBr.CHBrMe).OMe.OH.
Ci0H10Br4O2
118-119
Chasanowitz & Hell
B., 18, 824
48, 779
Br.,=1.4.3.(?)3
Brompropylphenylketone ....
Ph.CO.CHj.CH2.CH2Br
C10HnBrO
37-39
Perkin
47, 843
Phenylbrombutyric acid
Ph.CHBr.CH5.CHj.COOH
Ci0H,,BrO2
69
Jayne
A., 216, 102
44, 472
Ethylic bromtoluate
CH3.COOEt.Br=1.3.?
„
270-275
s. —5
Pittig and Ahrens
A., 147, 34
vi., 1100
Bromcumic acid
COOH.Pr«.Br=1.4.5
t,
....
146
Naquet and Longui-
C. R, 62, 1031
vi., 515
nine
„ „
» .,
„
151-152
Gerichten
B., 11, 1719
36, 230
Ethylic bromanisate
COOEt.OMe.Br=1.4.?
C10HnBrO.,
gentle heat
Laurent
A., 56, 313
i., 302
„ ,, .... ....
=1.4.2 or 3
„
53-60-5
Balbiano
G. I. [1881], 396
42, 169
„ „
„ =1.4.3 or 2
,,
73-5-74
„
„
B
„ „ .... ....
». ,,
„
73-5-74
Crespi
G. I. [1881], 419
42, 192
„ bromphenoxyacetate
C6H4Br.O.CH2.COOEt
„
59
....
J. p. [2], 20, 298
?
....
„
83
Magatti
B., 12, 1863
38, 250
Anethol dibromide
(CHBr.CHBr.Me).OMe=1.4
C,0H12Br,,0
abt. 65
Ladenburg
As., 8, 95
vi., 157; vii., 72
Bromcamphoric anhydride ....
C8HuBr:(CO),:0
C10H13BrO3
215
Wreden
A., 163, 330
25, 896
Tribromcamphor
....
C10H13Br30
64
Swarts
B., 15, 1625
42, 1300
„
....
„
63-64
Royere
B., 15, 1621
a-Dibromcamphor
C10H14BrsO
....
57-61
Swarts
B., 15, 1622
„
a- ,,
....
;,
59-61
M
B., 15, 1621
»- •>
II
57
Montgolfier
B. S., 23, 253
42,527
"• »
....
»
....
57
Armstrong and
[1877]
Matthews
a- .,
....
j(
57
Schiff
B., 14, 1379
„
n- ,.
„
.".i.
60-61
Zepparovitch
M. C., 3, 231
42, 865
"- »
„
....
61
Kachler & Spitzer
M. C., 3, 205
42, 864; 44, 961
B 16, 1311
0- i)
....
„
285 p.d.
114-5
Swarts
Z. C. [2], 2, 628';
vi., 387
B., 15, 1622, 2135
42, 1300
3- „
„
....
114-115
Kachler & Spitzer
M. C., 3, 205 ; B.,
42, 864
15, 1343
P- jj
....
„
114-115
Zepparovitch
M. C., 3, 231
42, 865
Bromcamphor
C10H15BrO
274
76
Perkin
....
vi., 387
„
274 p.d.
76
Maisch
C. C. [1873], 437
27, 582
"
„
....
76
Silva
B., 6. 1093
27, 70
....
„.
2~4
76
Kachler & Spitzer
M. C., 3, 205
42, 864
....
"
274
....
Swarts
J. [1862], 463
B1 A 1 0*7*7
vi., 387
,,
I
76
Schroder
., 14, 1,377
B., 13, 1072
"
"
....
76
Montgolfier
B. S., 23, 230
COMPOUNDS CONTAINING FOUR ELEMENTS.
411
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dibromcaprio acid
Bu0.(CHBr)2.CHMe.CH2.
C10HI3Brs02
,.,.
135 u.c.
Hell and Schoop
B., 12, 194
36, 521
COOH or BuP.CHBr.CBr
PrP.COOH
?
C,0H180+HBr
C10H19BrO
33-35
Hell and Bitter
B., 17, 2610
48, 172
Tetrabrom-u-naphthoic acid
C10H3Br4.COOH
CnH4Br402
....
239
Hausemann
B., 9, 1523
31, 321
» ~P" !> » "••
H
»
259-260
M
)»
n
Tetrabromacetyldaphnetin ....
C6Br2(OH)(OAc).CBr : CBr.
CuH4Br405
.•*
290 d.
Stilnkel
B., 12, 113
36,469
i
co.o
Tribrom-£-naphthoie acid ....
C10H4Br3.COOH
CnH5Br302
269-270
Hausemann
B., 9, 1522 .
31, 320
Brom -a- „ „
C10HjBr.COOH
CnH.BrO2
242
M
B., 9, 1517
31, 318, 319
,, -P- >! ))
....
11
....
256
)»
B., 9, 1518
31, 319
Couuiaroxyacetic anhydride
C6H4.(CHBr)2.COO.CO.CH20
CnH8Br204
213
Bossing
B., 17, 3002
48, 389
dibromide
=1.2
Methyl /3-methylbromumbel-
MeO.CeHjBr.CBrMe.
CuH9Br303
233-235
Pechmann & Cohen
B., 17, 2134
46, 1332
liferone dibromide
CHBr.COO=U.4.5
Tribromorcinol diacetate
Me.(OAc)2.Br3=1.3.5.2.4l6
CnH9Br304
...i
143
Claassen
B., 11, 1440
Bromphenylmethylfurfuraue
fr.Ph.CBr.(CHBr)2.CBrMe.O
CuH9Br50
bl^kens 200
208-210
Paal
B., 17, 2760
48, 249
tetrabromide
Coumaroxyacetic acid dibro-
COOH.(CHBr)2.C6H<.O.CH2.
CiiH10Br3O5
219-220
Bossing
B., 17, 2999
48, 389
mide
COOH=1.2
Dibrommethoxyphenyl di-
C6H2Br2(OMe)(CHBr.
CuH10Br403
abt. 200
Perkin
39,434
brombutyric acid
CBrMe.COOH)=(?)j. 1.2
Ethylic j3-bromeinnamate ....
Ph.CBr.CH.COOEt
^^..BrO.,
290-292
....
Barisch
J. p. [2], 20, 185
38,43
Ethoxyphenylbromacrylic
OEt.(CjHBr.COOH)=1.2
CnHnBrO3
164
Perkin
39, 428
acid
Dibromallylacetophenone ....
Ph.CO.(CH8)2CHBr.CH2Br
Ci.H.jBrp
121-122
»
45, 189
Ethylic phenyldibrompro-
PLCHBr.CHBr.COOEt
C11H12Br20!
69
Anschiitz and Kin-
B., 11, 1221
34, 981
pionate
nicutt
)) »
ji
n
....
69
»
B., 12, 538
36, 645
)) !>
n
>»
69
Perkin
45, 172
Dibromphenylvaleric acid ....
Normal
)»
108-109
Baeyer & Jackson
B., 13, 122
38, 407
Stycerinacetodibromhydrin....
Ph.C3H4Br2.OAc
)1
85-86
Grimaux
C. B., 76, 1598
26, 1 139
Methylic /3-methoxyphenyl
MeO.C8H4.C2H2Br2.COOMe
CuHjjBrgOa
68
Perkin
39, 425, 427
dibrompropionate
=1.2
» a~ »
» »
»
....
125
»
39,425 426
Ethoxyphenyldibrompro-
EtO.C6H4.C2H2Br2.COOH
H
....
155 d-
Ebert
A., 216, 158
44,472
pionic acid
=1.2
Methylbromeugenol
(CH:CHMe)(OMe)2.Br
CuHlsBrO2
185 (44)
Liquid
Wassermann
C. B., 88, 1206
36, 790
=1.3.4. ?
„
» »
»i
190 (20)
»j
B., 10, 237
„ dibromide
(CHBr.CHBrMe).(OMe)2.Br
Cj.H^BrA
77-78
»
C. B., 88, 1206
36, 790
=1.3.4. ?
Dimethyl propyldibrompyro-
CeBrjPrCOMeJ^OH)
CnH14Br2O3
108-109
Hofmann
B.,8, 67; 11,331
gallol
Bromcamphocarbonic acid ...
C,0H14BrO.COOH
^llH|5BrO3
109-110
Silva
B., 6, 1093
27,70
Dibromundecylenic acid
010H19Br2.COOH
CnHjoBr/X
38
Becker
B., 11, 1413
34, 853
, ,1
»
»
38
Kraflft
B., 10, 2035
34, 292
Dibromdiphenylene oxide ....
....
C,,H6Br2O
185
A., 159, 215
»
....
»)
....
185
Kreysler
B., 18, 1721
Bromrosoquinol
C12H4Br4(OH)2
C12H6Bri02
264
Baeyer & Schraube
B., 11, 1301
34, 869
T etiubrom-y-diphenol
(.C6H2Br2.OH)2=[l.(?)J.4]:!
»
....
264 u.c.
Magatti
B., 13, 225
88, 643
Didromphenyl oxide
C,2H8Br2O
a. 360
53-55
Hoffmeister
A., 159, 210
vii., 941
» !>
....
jj
....
58
Niedei-hausern
B., 15, 1124
11 !)
....
»
58-5
Merz and Weith
B., 14, 191
Dibrompiperide
C12H8Br204
136
Fittig and Mielck
A., 172, 139, 151
3 o 2
412
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Dibromoxypiperide
CH2 : (Oa) : C6H2Br.CHBr.
CI2H8Br206
....
181-182-5
Fittig and Mielck
A., 172, 156
27, 899
CH : C(OH).CH.COO or
i 1
CH2 : (O) : C6H2Br.CHBr.
CH(OH).CH : C.COO
i_ |
Bromnaphthalic acid
C10H6Br(COOH)2
C12H.BrO;
....
210
Blumenthal
B., 7, 1095
Benzofuril tetrabromide
....
C^H.BrA
....
127^128 p.d.
Fischer
A., 211, 230
42, 500
Bromphenylphenol oxide ...
C,H4Br.O.C6H4.OH
C12H9BrO2
....
Liquid
Bohmer
J. p. [2], 24, 473
42, 398
Brom-yS-acetonaphthol
C10H6Br.OAc
>J
215 (20)
Liquid
Canzoneri
G. I., 12, 424
44, 68
Bromoxypiperide
CHa : O2 : C6H3.CHBr.CH :
C12H9BrO6
....
131-5-132
Fittig and Mielck
A., 172, 144
27, 898
C(OH).CH.COO or
1 1
CH2 : O2 : C6H3.CHBr.
CH(OH). CH : C.COO
L. 1
Tetrabrompiperonic acid
C12H10Br404
....
160-165 d.
>>
A., 172, 137
Tetrabromoxypiperonie acid'
....'
C12H10Br406
d. 100; 155 d.
u
A., 172, 154
Ethyl brom-a-naphth6'l
C10H,(Br.OEt
C12HuBrO
48
Machetti
G. I., 9, 504
38, 261
» » ~P~ »
»
»j
....
96
Koelle
B., 13, 1954
40, 178
Brom-S-hydropiperic acid ....
....
C12HnBrO4
170-171
Buri
A., 216, 177
44, 485
Cinnamenylvinylmethylke-
Ph-C^Br^CO-Me
C12H12Br2O
....
173-5 d.
Diehl and Einhorn
B., 18, 2323
48, 1221
tone dibromide
Diethylic dibromterephtha-
(COOEt)2.Br2=1.4.3.6
Cl2H12Br204
335
121
Schultz
B., 18, 1763
48, 1054
late
Dibromhydropiperic acid ....
....
•»)
....
13'5-136
Fittig and Mielck
A., 172, 159
27, 900
j> i» ••••
....
»»
137-140
Buri
A., 216, 177
Dibrommethoxyphehyl di-
CcH2Br2(OMe)(CHBrV
C12H12Br403
abt. 159 d.
Perkin
39, 437
brom valeric acid
CEtBr.COOH)=(?)2.1.2
Phenylhomoparae'onic acid
C12H1SBKV
....
149
Fittig
B., 14, 1825
42, 190
hydrobromide
i> I?
....
»
....
149 d.
Penfield'
A., 216, 123
44, 473
Diethylic bromphthalate ....
(COOEt)2.Br=1.2.3'
J)
295 d.
....
....
A., 160, 64
Propylic phenyldibrompro-
PhlCHBr.CHBr.COOPr*
C12H14Br20,
....
23
Anschiitz and Kin-
B., 12, 538
36, 645
pionate
nicutt
Brompropylene ethylphefiyl-
....
c^HyfeOi
230 p.d.
Morley and Green'
47, 136
ketate
Bromcumenylpropionic acid
n
....
S5-87
Perkin
J. [1877], 379
32, 661
Ethylbromeugenol
C3H6;OMe.OEt.Br=1.4.3.?
>»
48
Wassermann
A., 179, 386
29, 707
Ethylbromeugenol dibromide
C3H5Br2.OMe.OEt.Br
C12H16Ur3O2
....
80'
j»
A., 179, 385
))
=±1.4.3.?
Dipropylbromresbrcinol
(OPr«)2.Br=1.3.?
C-j2HjyKrO2
70-71 u.c.
Kariof
B., 13, 1679
40, 270
Heptabromdiphenylene
06HBr3.C6Br'4.CO'
C13HBr7O
«...
136
Salzmann and
B., 10, 1402
34,80
ketone
1 1
"Wichelhaua
Hexabromdiphenylene
C6HBr3.C6HBr3.CO(?)
C13H2Br60
black 225
nf. 280
»
)>
»
ketone
i : 1
Dibromdipheuylene ketone....
fr. C,-H4.C6H4.CO=2
C13H6Br20
....
142-5
Holm
B., 16, 1081
44, 921
>• 11
= 1.2; 1.2
»
....
197
H
)1
»
» i)
» »
»
....
198
Hodgkinson ami
B., 16, 1103
43, 165
Matthews
Dibromdiphenylene ketone
»)
C13H6Br202
....
210
Perkin
43, 190
oxide
" ;>
i>
))
....
211-212
Behr and Dorp
B., 7, 399
27, 798
Tetrabromdihydroxybenzo-
CO.(C6H2Br2OH)2
^i3H6Br4Oa
213-214
Baeyer and Bur-
B., 11, 1299
34, 887
phenone
kardt
»
)J
>»
....
213-214
Baeyer
A., 202, 131
38, 658
Bromdiphenylene ketone ....
C6H3Br.C6H4.CO=!.1.2 ; 1.2
C13H7BrO
....
104
Hodgkinson and
B., 16, 1103
43, 165
Matthews
Benzoyltribromphenol
OBz.Br3=1.2.46
C13H7Br302
81-5
Daecomb
B., 18, 1168
48, 890
Diacetyltribromcesculetin ....
C8HBr3O,,(OAc),,
C13H.Br306
180-182
Liebermann and
B., 13, 1592
40, 108
Knietsen
Dibromphenylbenzoic acid ....
....
C13H8Br203
212
Holm
B., 16, 1082
44,922
a~
C6H4Br.C6H3Br.COOH
n
201-5-203-5
Carnelley and
47, 589
=1:4 ; l.(2 or 3):4
Thomson
COMPOUNDS CONTAINING FOUR ELEMENTS.
413
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
jS-Dibromphenyl benzole acid
C6H4Br.C6H3Br.COOH
ClaH8Br202
....
232 ; af. 231
Carnelley and
47, 589
=1.4 ; l.(3 or 2).4
Thomson
Diacetyldibromoesculetin ....
C9H2Br2O2(OAc)2
Cl3H8Br2O6
177
Liebermann and
B., 13, 1595
40, 108
Knietsen
Tetrabromdihydroxydi-
CH2(C6H2Br2OH)2
C13H8Br402
225
Beck
A., 194, 326 ;
34, 421 ; 36,
phenylmethane
=[1.(?)2.4]2
B., 10, 1839
325
Bromdiphenyl ketone
06H4Br.CO.Ph
C13HaBrO
81-5
Kollaritzand Merz
B., 6, 547
vii., 939 ; 26,
1036
Phenylio brombenzoate
COOPh.Br.=1.3
C13H9BrO2
65
J. [1879], 676
Dibrombenzhydrol
fr. Ph.CH(OH)Ph
CuH10Br/)
163
A., 133, 12
iv., 478
Dibrombenzylphenol
fr. Ph-CH^CeH^OH
»•
abt. 175
Paternd and Fileti
G. I., 3, 121, 251
27, 373
Benzylbromphenyloxide
Ph.CH2.O.C6H4Br
ClsHuBrO
....
59-59-5
Sintenis
B., 4, 700; A.,
24, 909 ; vii.,
161, 344
180
Bromdiethyloesculetin
fr. C6H2(OEt)2.CH : CH.COO
C13H13Br04
res'
Will
B., 16, 2118
46,69
i i
Bromdiethyldaphnetiu
ii
115
Will and Jung
B., 17, 1085
46, 1042
Ethylic phenylacetyldibrom-
Ph.CHBr.CBrAc.COOEt
Ci3H14Br2O3
97
Claisen
B., 14, 347
40, 405
propionate
Benzylidene mesityl oxide
....
C,3H14Br40
118
Claiseu and Cla-
B., 14, 2461
tetrabromide
pare"de
Ethylic ethoxyphenyldi-
C6H4(OEt)[(CHBr)2.COOEt]
Ci3H16Br2Ob
78
Perkiu
39, 428
brom propionate
=1.2
Isoamylic dibromresellinate
....
CI3H16Br2Q4
73-8
A., 139, 40
A cetyldimethylpropyldi-
C6Br2Pr(OMe)2(OAc)
n
....
101-5-102-5
Hofmann
B., 11, 331
34, 417
brompyrogallol
Hydrobromcumenyl crotonic
C6H4.Pr(CH2.CHBr.CH3.
VisH-i-rBrQi
148-150 p.d.
Perkin
J. [1877], 380
32, 662
acid
COOH)
Bromsalicin ....
CLH.-BrO,
160
Schmidt
Z. C. [2], 1, 320
,,i 1 f\f\l
V-'J3-M-M7'^ 7
v**i lUvl
Pentabromanthraquinone ....
....
C14H3Br6O2
....
w.m.
Diehl
B., 11, 183
34, 430
Tetrabromauthraquinbne ....
....
C14H4Br402
295-300
jj
B., 11, 182
»
i»
....
n
....
nf. 370
Hammerschlag
B., 10, 1213
34, 76
Tribromanthraquinone
....
C14H6Br302
186
Diehl
B., 11, 181
34, 430
»
...;
»
....
365
Hammerschlag
B., 10, 1213
34, 76
Tribromflavopurpurin
....
C14H5Br306
284 d.
Schunck & Roemer
B., 10, 1823
34, 322
Peiitabromoxytolidene
.._
C14HsBr502
....
206
......
A., 153, 127
a-Dibromanthraquinone
....
C14H6Br202
....
145
Perkin
37, 555
0-
)>
174-175
n
37, 555
»-
....
))
....
236 u.c.
Diehl •
B., 11, 181
?-
....
'»'
....
270-272
Auerbach1-
B., 15, 2918
Dibromphenanthrene qui-
fr. CO.C6H4.C6H4.CO
H
....
230
Limpricht
B., 6, 533 ; A.,
26, 898
none
=2,1 ;.1.2
167, 185
Dibrom-?-quinone
=2.1 ; 1.4
»>
166u.c.;170c
Carnelley &Thomson
47, 592
Dibrom hydroxy anthra-
C6H4,:(CO)s:C6HBra.OH
CI4H6Br203
....
207-208
Baeyer
A, 202, 136 ; B.,
31, 308
quinoue
=2.1 ; 1.2.3.5.4
9, 1231
Dibromalizarin
....
C14H6Br204
168-170
Diehl
B., 11, 190
34, 428
Dibromxanthopurpuriu
....
»
....
227-230
Plath
B., 9, 1205
31, 87 ; 33, 424
»
....
»
231
Schunck & Roemer
33, 424
Fr. dibrom-o-p-ditolyl
C14H8Br204(?)
»
197-1 98 u.c.;
Carnelley&Thomson
47, 592
201-202 c.
Tetrabromoxytolidene
• t* •
C,4H6Br402
150
A., 153, 127
Bromanthraquinone
C6H4:(CO)2:C6H3Br
C14H7BrO3
187
Greebe and Lieber-
As., 7, 290
vi., 180
=2.1; 1.2.4
mann
»
=2.1; 1.2.3
J)
188
Pechmann
B., 12, 2127
Bromalizarin ....
C14H5Br(OH)2O2
C,4H,BrO,
a. 280
Diehl
B., 11, 190
34 49S
Brompurpurin
^14 7*^ ^^4
C14H7BrO5
275
D. P., 228, 263
"^, ^t^Q
34, 737
i, .... ....
....
)>
275
jieberniann& Platte
B., 10, 1620
34, 78
„
....
I)
....
276
Schunck & Roemer
B., 10, 564
31, 673 ; 32, 625
Dibromoxytolidene ....
....
C14H8Br202
121
A., 153, 125
Dibromdiphenylene glycollic
....
CI4H8Br203
abt. 225
Friedliinder
B., 10, 537
32, 493
acid
Fr. dibrom-o-p-ditolyl
v. C14H6Br204
O^ilyDl'gO 4
....
....
....
414
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference,
'Watts' Diet.
& J. Ch. Soc.
Dibromdiphenic acid
C12H6Br2(COOH)j
C14H8Br204
....
295-296
Ostermayer
B., 7, 1091
Bromsalicylic anhydride ...
[C6H3Br(OH).CO]2O=(..2.1)2
CI4H8Br206
....
164-165
Henry
Z. C. [2], 5, 479
vi., 1003
Dibromresorcinphthalein ...
CTTT>_ f( \~\~\\ C^C\ f 1 TT
g-d-Droi wxi jq.v-'w.Vj'c-cij.
„
....
218- 220
Baeyer
A., 183, 56
31, 204
COOH=(?)2. 1.3.2; 1.2
Brombenzoylbenzoic acid ...
COOH.Bz.Br.=1.2.3 or 6
CuHjBrOj
219-221
Pechmann
B., 12, 2126
Bromdiphenic asid
CcH4(COOH).C6H3Br.COOH
C14H9BrO4
....
208u.c.;215c
Carnelley & Thom-
47, 591
=4.1; 1.4.2
son
Pentabromcurcumin dibro-
C14H9Br704
cf. B., 16, 573 abt. 120 d.
Jackson and Menke
A. C. J., 4, 360
44, 482
mide
Dibromdeoxybeiizoin
C14H10Br20
....
87
Zinin
A., 126, 221
vi., 332
„
ii
110-112
Limpricht and A., 155, 70
vii., 174
Schwanert
Tetrabromethylene phenyl-
....
Ci4H10Br4O2
....
b. 100
....
Z. C. [1869], 447
oxide
Bromdeoxybenzoin
....
C14HuBrO
...»
50
Limpricht and
A., 155, 68
vil., 174
Schwanert
Bromdihydroanthrol (?)
....
!> (?)
....
92-94
Perger
J. p. [2], 23, 137
40, 608
Brombenzylidene benzoate ....
Ph.CHBr.OBz
C14HnBr02
69-70
Claisen
B., 14, 2475
42, 514
Benzoxydibromtoluene
Me.OBz.Br2=1.4.3.5
C14HnBr202
....
91-91-5
Schall and Dralle
B., 17, 2532
48, 146
Ethylene diphenol tetabro-
....
C,4H14Br4O2
....
a. 100
vi., 917
mide
Curcumin tetrabromide
....
C14H14Br404
cf. B., 16, 573
185 d.
Jackson and Menke
A. C. J., 4, 360
44, 481
Dibromthymoquinol diace-
C6Br2MePr(OAo)3
C14H16Br204
MM
121-122
Schulz
B., 15, 658
tate
Diacetyl dibrompicomar
C6Br2Pr(OAc)2.OMe
CMHleBr206
....
78
.,..
M. C., 4, 185
Bromthymoquinol diacetate
C6HBrMePr(OAc)2
C,4H17BrO4
91
Schulz
B., 15, 658
42, 838
Tetrabrommorin
....
C,,H6Br407
+2JHSO
258
Benedikt & Hazura
M. C., 5, 667
48, 554
Brombenzylidene phthalide
C6H4.COO.C. CBrPh=1.2
C15H9BrO2
160
Gabriel
B., 18, 2444
48, 1230
From ethobromcodeine
„
121; 121-122
Gerichten and
B., 15, 1485, 2179
42, 1113; 44,
Schrotter
222
Methylbromhydroxyanthra-
C6H4;: (C0)j.. C6H.Me.OH.Br
C16H9BrOs
305
Fraude
A,, 202, 165, B.,
36, 635
quinone
Br.OH.Me=1.2.3
12, 237
Benzylidene phthalide di-
C6H4.COO.CBr.CHBrPh
C16H.0Br202
146
Gabriel
B., 17, 2521
48, 165
bromide
=1.2
Tetrabromphloretin
«...
C16H10Br405
205-210 d.
Hlasiwetz
A., 119, 104
iv., 492
Bromcresolphthalein
C6H2BrMe(OH).OC.C6H4.
C15H,,Br04
228
Fraude
B., 12, 240
36, 635
COOH=?,1.2.?; 1.2
Benzylidene phenylketone
CHBrPh.CHBr.CO.Ph
C-sH-^O
156-157
Claisen & Claparede
B., 14, 2464
42,512
dibromide
Dibrom-a-pyrocressol
215
Schwarz
B., 16, 2143
46, 79
Dibromdimethoxybenzophe-
fr. CO(CaH4.OMe)2=(1.4)2
C.sHuBrA
....
181
Bosler
R, 14, 329
40, 422
none
Dibromhydrocotoi'n
C15H12Br204
95
Jobst and Hesse
A., 199, 59
38, 328
Tetracetyldibromgallic acid
C6Br2(OAc)3.COOAc
C15H12Br209
+ 2H20
91
•»»t
B., 3, 643
=6.2.5.4.3.1
Bromlapachic acid
CloH4(C8H9);02.OBr
C16H13Br03
cf.B., 16, 801
139-140
Paterno
G. I., 12, 337
44, 211
Bromhydrocotoin
....
C15H13Br04
147
Jobst and Hesse
A., 199, 59
33, 328
Dibromoesculin
C15H14Br209
....
193-195 d.
Liebermann and
B., 13, 1594
40, 108
Kuietsch
Brompicrotoxin
C15H15Br06
....
d.w.m. 240-
Paterno & Oglioloro
G. L, 7, 193, B.,
32, 790
250
10, 1100
"
H
245
Schmidt & Lowen-
B., 14, 819
40, 741
hardt
Dibrom-a-metasantonin
C16H16Br203
....
184
Cannizaro and Car-
G. I., 10, 461
40, 286
neluti
» ~P~ „
.... •
186
Brom-/3-metasantonin
Ci5H17BrO.,
114
„
H
G. I., 8, 318
M
36, 330
" "
....
„
....
114
„
G. L, 10, 461
40, 285
!) ~a~ »
....
,,
....
212
.,
M
40, 286
"
212
"
G. L, 8, 318
36, 330
COMPOUNDS CONTAINING FOUR ELEMENTS.
415
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Santonyl bromide
....
Ci5Hi9BrO3
145-5
Cannizaro and
G. I., 8, 31)9
36, 331
•
Valente
Dibrora-a-naphthylene phe-
....
C16H8Br,0
cf. A., 209, 144
284
Arx
B., 13, 1727
40, 282
nylene oxide
Diphthalyl dibromide
C6H4.COO.CBr i CBr.C6H4.
Cl6H8Br2O4
4:
begins 220 d.
Greebe & Schmal-
B., 15, 1674
48, 1298
COO=(I.2)2
zigang
Dibrom-m-acetoxyanthaqui-
C6H4 : (00), : C6H(OAc)Br2
t
cf. A., 202, 137
189-190
Baeyer
B., 9, 1231
81, 308
none
Dibromocampheride
....
C16HIOBr206
224-225 d.
Jahns
B., 14, 2389
42, 209
Diacetyltetrabrom-y-diphenol
(C6H2Br2.OAc),=(l.U4)2
C16H10Br404
245
Magatti
B., 13, 225
38, 643
Tetrabromlecanoric acid
....
C16H10Br407
abt. 157
Hesse
A., 139, 28
vi., 778
Ethylic dibromdiphenylene
fr. C6H4.C6H4.C(OH).COOEt
C16Hi2Br2O3
150-151
Friedlander
B., 10, 537
32, 493
glycollate
Dibromhsematoxylin
....
C,,H12Br206
d. a. 120
Dralle
B., 17, 373
48, 1043
Dibromlecanoric acid
....
C16H12Br207
175 ; 179 c.
Hesse
A., 139, 28
vi., 778
Diacetyldibromrhamnetin ....
C13H,Br,Os(OAc),
»
211-212
Liebermann and
B., 11, 1621 ; A.,
36, 272
Hermann
196, 322
?
C14H10Br.Ac
C16H13BrO
107
Limpricht and
....
vii., 1163
Schwanert
Bromdioxyretistene
....
CI6H13Br02
210-212
Z. C. [1869], 74
Fr. tolane dibromide
C14H10Br.OAc
»
....
107
Limpricht and
B., 4, 380
Schwanert
Dibromethyl deoxybenzoin....
fr. Ph.CH2.CO.C6H4Et=1.4
C16Hl4Br20
113
Sollscher
B., 15, 1681
42, 1292
Methylic diphenyl dibrom-
Ph.CHBr.CBrPh.COOMe
Ci6H14Br2O2
105-108
Cabella
G. I., 14, 14
46, 1348
propionate
Tetrabromhydrocoerulignone
C12Br4(OMe)4(OH)2
C16H14Br406
217-218
Hayduck
B., 9, 930
30, 517
Dibromhydrocoerulignone ....
C12H2Br2(OMe)4(OH)2
C16H16Br2O6
....
262
5»
)1
»
Brompalmitolic acid ,.,
Cl5H26Br.COOH
C16H27Br02
31
Schroeder
A., 143, 31
vi., 896
Bromhypogceic acid
C^H^Br.COOH
C16H29Br02
....
19-23
)5
A., 143, 26
vi., 727
Tribrompalmitic acid
CjsHjsBrj.COOH
C16H29Br302
39
»
A., 143, 27
»
Dibrompalmitic acid
C15HJ9Br2.COOH
C16H30BrA
29
>»
A., 143, 24
vi., 726
Ethyl tetrabrommorin
C15H,,Br4EtO7 + 3H2O
C17H10Br407
135
Benedikt & Hazura
M. G, 5, 667
48, 551
From bromcinnamic acid ....
....
C17H12Br202
a. 340
Leuckart
B., 15, 19
42, 615
Tetrabromevernic acid
....
C17H12Br4O7
161
Stenhouse
P. R S., 17, 222
vii., 496
Bromdehydracetonebenzil ....
....
C17H13Br02
172
Japp and Miller
47, 29
Pentabromdurylbenzoyl
....
C17H13Br50
224-225
J. [1879], 372
Dibenzylidene-acetone tetra-
CO(CHBr.CHBrPh)2
C17H14Br40
206-208
Claisen and Clap-
B., 14, 2461
42, 511
bromide
ardde
Benzylidenephthalidebromide
Ph.C2HBr(OEt).C6H4.COO
Ci7H15BrO3
149
Gabriel
B., 17, 2527
48, 165
ethoxide
> 1
=1.2
Acet.ylbromhydrocoto'in
....
C17H15BrO3
166
Jobst and Hesse
A., 199, 61
38, 328
Brom a-ditolylpropionic acid
f r. (Me.C6H4)2.CHMe.COOH
C|7Cj7BrO2
143-144
Haiss
B., 15, 1478
42, 1071
=(1.4)2
Ethylic phenyldibrompro-
CHBrPh.CHBr.CO.CEt2.
C^H^BrA
55
Claisen and Mat-
A., 218, 170
46, 444
piony Idi ethy lacetate
COOEt
thews
»> >i »
» »
J5
54-55
Matthews
43, 206
Erythropyrocatechol
C18H,BrI00
139 d.
Stenhouse
A., 177, 197
28, G ; vii., 1029
Xanthogallol
....
C18H4Br14Oc
122
,,
A., 177, 193
28, 6; vii., 1031
?
C18H7Brn09
130
D
n
28, 4; vii., 1031
Dibromchyrsoquinoiie
C18HsBr202
....
160-165
Adler
B., 12, 1892
38, 263
Dibromethylenebenzoyl car-
C6H4 : (CO), : CH.CBr2.OC.
C18H10Br2O5
285-287
Gabriel & Michael
B., 10, 1561
34, 230
bonic anhydride
C6H4.COOH=(1.2)2
Dibromethylene dibenzoyl
fr. (.CH2.CO.C6H4.COOH).2
C18H12Br2O6
270-272
u
B., 10, 2209
24, 428
carbonic acid
=(1.2),
Tribrompyrogiiajacol
Ci8H13Br3O3
172
Wieser
M. C., 1, 601
40, 813
Phenyldibrompropylic cin-
Ph.CH:OH.COO.CH.
C18H16Br202
151
Miller
B., 9, 275
29, 939
namate
(CHBr)2.Ph
Dibromhexmethoxyd iphenyl
fr. (MeO)3C6H2.C6H2(OMe)3
C^BrA
138-140
Ewald
B., 11, 1623
36, 253
Dibromoleic acid
cf. A., 140, 56
C18H3!,BrA
200
....
Lefort
J. Ph. (3), 24, 113
iv., 194
416
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Tetrabromstearic acid
C17H31Br4.COOH
C|8H32Br4O2
cf. A., 140, 56
abt. 70
Marasse
Z.C. (2), 5, 571
vi., 1038
Broraoleic acid
C17H32Br.COOH
C.sH^BrO,
cf. A., 140, 47
35-36
Overbeck
J. p., 97, 159
vi., 881
Dibromoelai'dic acid ...
C^H^Br^COOH
C18H34Br202
cf.A.,140,6
27
Burg
B. S. (2), 3, 191
vi., 550
Bromstearie acid
CjjH^Br.COOH
C18H35BrO2
....
41
Oudemanns
J. p., 89, 1957
v., 419
From isoamyloxanthranol ..
....
C19H18Br20
120 d.
....
A., 212, 95
Dibromdiacetylpicrotoxide
....
19 IS 2 8
180
Paternd & Oglialorc
G. I., 9, 57
36, 729
or Diacetylpicrotoxide di-
or
bromide
C19H2(1Br208
Ethyl brompodocarpic acid ..
....
C19H25BrO3
....
158
A., 170, 237
Pentabromquinol phthale'in
fr.C.H4:[OO.C,H,(OH)],:0
' -, i i ' - i^rsOt
....
a. 300
Ekstrand
B., 11,716
34, 676
=1.2 ; (7.1.4),
Pentabromresorcinol oxale'in
O.C6H2Br(OH).CO.C : (C6H
Oj.jii_ J3l*r O*
d.w m. 230
Glaus
B., 14, 2567
42,399
i i
Br,.OH),:O=U.3. ?;
Dibrom-/3-dinaphthalene
^ [(?)3.1.3].2
vyn/i-tLin-DrnO
cf.A.,209,140
247
Knecht & Unzeitig
B., 13, 1726
40, 281
oxide
» -<"- ., 11
„
cf.A.,209,137
287
H
B., 13, 1725
„
Dibromphenolphthalei'n an-
....
CjoH^Bi'A
....
255-258
Baeyer
A., 212, 347
42, 1096
hydride
Dibromfluorescei'n
....
020HJOBr2O5
260-270
„
A., 183, 38
81, 200
Tetrabromphenol phthale'in...
C6H4(CO.C6H2Br2.OH)2=1.2;
C20HloBr404
220-230
„
B., 9, 1231
31, 308
» •>
.1 »
„
220-230
„
A., 202, 77
38, 654
Tetrabromphenolphthalideln
cf. B, 9, 1238
jj
....
a. 280
„
B., 9, 1237
31, 309
Dibromhydroxydiphenyl
t ji i ;^i
C6H2Br2(OH).CPh.C6H4.COO
i i
C»HItBr,Q,
196
Pechmaim
B., 13, 1615
40, 96
pntnalide
Dibromphenylresorcinphtha-
fr. C6H3(OH)2.CPh.C6H4.COO
CsoH12Br204
219
„
B., 14, 1861
42, 184
lein
i i
=1.3.7; 1.2
Tetrabromphenolphthalin ....
C6HsBr2(OH).CH(OH).C6H4.
C20H12Br4O4
140
Baeyer
R, 9, 1233
31, 308
CO.C6H2Br.,OH
» j>
....
J"
205
,,
A., 202, 85
38, 655
Tetrabrompurpurogallin
C20H12Br409
202-204
Clermont ftdbautan
C. E., 94, 1362
42, 1066
Hexabromdiresorcinoltetra-
C6Br3(OAc)2.C,Br3(OAc)2
C'.,0H12Br6O8
259
....
M. C., 1, 356
acetate
Tetrabrom-/3-diresorcinol-
C6HBr2(OAc)2.C6HBr2(OAc)2
C20H14Br4Os
195
....
M. C., 1, 353
tetracetate
Tribromerythrol
C20H19Br301,
+ 1^H2O
139
A., 117,310
Dibromdiacetylhydroccerulig-
C12H2Bri.(OMe)4(OAc)2
C^H^BrijO,
178
Hayduck
B., 9, 930
30, 516
noue
a-Dibenzoyldithymol
....
C20H24Br2O2
....
215
Dianin
J. E. [1882], 130
42, 624
Hexabromresocyauin
....
C2iH12Br6O6
250 d.
J. p., 24, 127; 25, 83
Bromphthalacene oxide
C21H13BrO
200
Gabriel
B., 17, 1398
46, 1190
Brombenzylcurcumin
C14H13(CH2.C6H4Br)04=1.4
C21H19Br04
cf.B.,15,1761
78 ; sf. 76
Jackson and Menkt
A. C. J., 4, 77
42, 1108
Alcoholate of ethylbrompodo-
....
C21H31Br04
....
a, 80
A., 170, 213
carpinic acid
Acetyl tetrabromfluovescein
....
C22H10Br406
278
Baeyer
A., 138, 1
31, 203
7 bromhydrin dibromide
C22H12Br(OH).Br2
C22H13Br30
d.w.m. 280
Rousseau
A. C. (5), 28, 145
46, 180
Dibromacetoxydiphenyl -
"!6H2Br2(OAc).CPh.C6H4.COO
C22H14Br2O4
....
170-172
Pechmann
B., 13, 1616
phthalide
i .--i
Tribromcotoin
....
C22H15Br3O6
114
Jobst and Hesse
A., 199, 26,
38, 326
Dibromorthocresolphthalein
fr. C6H4(CO.C6H3Me.OH)2
C22H16Br2O4
cf.A.,202,158
255
Fraude
B., 12, 239
36, 635
= 1.2 ; (7.1.2),
Dehydroacetophenonebenzil
....
C22H16Br402
....
110-115
Japp and Miller
47,36
tetrabromide
Dibrom-o-cresolpbthaliu
....
C22HlsBr204
236
A., 202, 170
Dibromerucic acid .... . ...
....
46-47
Hausknecht
A., 143, 44
vi., 257
Tetrabrombehenic acid
C22H40Br4On
77-78
A., ] 43, 45
Bromerucic acid
C22H41BrO2
33-34
A., 143, 50
vi., 581
Tribrombehenic acid....
31-32
1}
Brassidic acid dibromide ..
C22H,2Br2O.,
54
A., 143, 57
vi., 367
Dibrombehenic acid
42-43
Otto
\., 135, 227
vi., 581
COMPOUNDS CONTAINING FOUR ELEMENTS.
417
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diethyltetrabromaurin
C19H8Et2Br403
C23HlsBr4O3
110-115
Ackermann
B., 17, 1627
46, 1340
Tetrabrornphthalfluorescem
C24H10Br405
a. 310
Terrisse
A., 227, 133
48, 667
(naphthaleosin)
Tetrabromfluorescein diace-
....
C24Hl2Br40-
278
....
A., 183, 53
tate
Tetrabromquercetin
fr.C24H1409:(O.C6H1204)2:0
C24H12Bi-,On
218
Liebermann and
B., 12, 1185
Hamburger
Diacetyldibromfluorescem ....
....
C34H14BrA
208-210
Baeyer
A., 138, 1
31,200
Dibromfluorescein diacetate
...
C24H14Br,07
208-210
A., 183, 38
Diacetyltetrabromphenol-
C6H.,Br,(OH).6!c6H4.C
C24Hl4Br405
....
256
Baeyer
A., 202, 95
38, 656
phthalidin
1
r
(OH).C6HBrs.OAc
Diacetyltetrabromphenol-
....
C24H14Br406
134
„
A., 202, 80
38, 654
phthale'in
Diacetyltetrabromphenol-
cf. B., 9, 1238
„
cf. A., 202,
182-183
„
B., 9, 1237
31, 310
phthalide'in
108
Diacetyltetrabromphenol-
fr. C6H2Br2(OH).CH(OH).
C24H16Br4O|.
....
165-166
„
B., 9, 1234 ; A.,
31, 309 ; 38,
phthalin
C6H4.CO.C8H2Br2,OH
202, 36
655
Tetrabromtetracetylbrazilin
C16H6Br405Ac4
C24HI9Br409
220-222
Buchka and Erck
B., 18, 1141
48, 907
Tribromtetracetylbrazilin ....
C16H;Br3OiAc4
C24H19Br3O,,
145-147
„
B., 18, 1140
„
?
C6H4(CH2.O.CHBr.C6H4,
C24H20Br204
80
Low
B., 18, 2073
48, 1208
COH)2=1.4;(1.4)2(?)
Diethylic tetrabromrosolic
QwH 10Et2Br4O.,
C24H20Br403
110-115
Ackermann
B., 17, 1627
46, 1340
acid
Bromtetracetylbraziliii
C16H9Br06Ac4
C24H21BrO9
203-204
Buchka
B., 17, 685
46, 1044
Diacetylbromcaitechin
C21H17Br07(OAc)2
C2iH23BrOH
....
120
Liebermaim and
B., 13, 696
40,53
Tauchert
Pentacetyldibronicesculin ....
C15H9Br204(OAc)s
C25H24Br2014
203-206
Liebermaim and
B., 13, 1594
40, 108
Knietsch
Fr. benzophenone
....
C26H15BrsO2
125
Linnemann
A., 133, 6
iv., 478
Pentacetylbromhsematoxylin
C16H8BrO6.Ao6
CjuHaBrO,,
210
Buchka
B., 17, 684
46, 1043
Tribrombaphinitone ....
C26H23Br3Ofi
180-2 c. ; ,d.
Anderson
....
30, 585
Br-deriv. of styrogenin
C26H39Br30 (?)
C.6H37Br30(?)
260
Myhus
B., 15, 945
Cholesterin dibromide
C26H44Br20
113-114
Liebermaim
B., 18, 1807
48, 1075
Tetrabromdiacetylquercetin
C24HIOBr4011Ac:.
CMH16Br4O13
....
226-228
Liebermann ami
B., 12, 1185
36, 946
Hamburger
Dibromlepidene
.....
Ca.H^Br.p
185
••••
A., 153, 131
,,
....
_
....
190
Zinin
J. [1867], 31b
vl., 781
Dibromoxylepidine ....
' \>s 1 ! |8Br2O2
222
....
J. [1876], 425
„
239
„
Tetracetyldibromgallein
....
CjgH^BrjO,,
234
Buchka
A., 209, 266
42, 61
Dibromdiacetylquercetin
O24H12Br;Ac2O11
O^HigBrgOj-j
218
Liebermann and
B., 12, 1184
36, 945
Hamburger
a-Tribrompyrocressol
C28H23Br3O2
cf.B.,15,2206
s. 200
Schwarz
M. C., 3, 738
44, 207
y- »
....
„
s. 183
„
„
n
Bromlaserpetiu
....
CjoH^BrjOg
90
Kulz
A. P. [3], 21, 161
46, 183
Bromechicerin
....
C30H47Br02
116
A., 178, 63
Bromoquassiin
....
C31H4,-IBT-IO9
75
Christensen
A. P. [3], 20, 481
42, 1302
Dibrompalmitone
.....
C31HmBr20
55
Herez
A., .186, 257
32, 427
,, hydrobro-
....
C31H6,Br3O
5-5
„
J)
>!
inide
Tetrabromdibenzoylhydro-
C32H28Br4O8
....
84
Jobst and Hesse
A., 199, 56
38, 327
cotin
Dibromdibenzoylhydrocotin
....
C32H30Br2Os
147
„
A., 199, 55
„
Fr. quassin
C32H41Br309
155 d.
Oliveri and Denaro
G. I., 14, 1
46, 1192
Bromechitin ....
C32H51Br02
100
A., 178, 68
Tetrabromleucotin ....
....
C34H28Br4O10
157
Jobst and Hesse
A., 199, 42
38, 326
Tetrabromoxyleucotin
....
C^H^Br.O,,
....
159
n
A., 199, 51
38, 327
Dibromleucotin
...
034H30Br201(,
187
„
A., 199, 41
38, 326
Dibromoxyleucotin
....
C34H30Br2012
190-192
„
A., 199, 50
38, 327
3 II
418
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Dibromstearone
Br on dioxyretistine.... . „«
....
UMHwBr30
C40H31Br405
C^Hc-Br-jO.
....
72
234-235
150
Ekstrand
J. [1855], 517
A., 185, 102
A., 176, 72
v., 425
32, 498
Dibromabietic acid .... „„
....
C44H,2Brs05
134
Emmerling
B., 12, 1443
38, 265
(9.) CHBrS, CHBrSe, and CHBrTe.
Tribromthiophene
C4HBr3S
259-260 c. j 29
Rosenberg
B., 18, 1774
48, 1051
Dibromthiophene
S.Br2=1.2. ?
C4H2Br2S
203-207
Liquid
Meyer and Stiidlei
B., 18, 1490
48, 972
„
1» »»
11
205-207 u. c.
Liquid
Langer
B., 17, 1566
46, 1133
„
» »»
))
206-206-5
Liquid
Meyer
B., 16, 1470
44, 1091
u. c. ;
210-5-211 c.
Brorathiophene
....
C4H3BrS
149-151 u. c.
....
»
B., 16, 1472
?)
,, ....
....
J>
149-151
....
Meyer and Stadler
B., 18, 1490
48, 972
Diethylene dithiotetrabro-
C2H4:SBr2:SBrj:C3H,
C4H8Br4S2
....
96 d.
Husemann
A., 126, 287
vi., 607
mide
Tribrom-thiotolene
S.Me,Br3= ?
C6H3BrsS
34
Volhard & Erdman u
B., 18, 455
48, 763
>i •»- ,,
„ =1.2.3.4.5
))
74
Meyer and Kreis
B., 17, 787
46, 1131, 1132
j> -ft- „
„ =1.3.2.4.5
»)
....
86
Egli
B., 18, 545
48, 766
Dibrom-a-th iotolene
S.Me.Br2=1.2.(?)2
C5H4Br2S
227-229
Liquid
Meyer and Kreis
B., 17, 787
» -«- »
*) 5)
JJ
227-229 n. c.
Liquid
Meyer
B., 16, 2970
46, 586
Brombenzene sulphhydrate
O8H4Br.SH=l,4
C,H6BrS
74
Hiibner & Alsberg
A., 156, 327
36, 803
» *>•
it n
J)
75
»
Z. C. [2], 6, 389
vii., 153
j» »»
)> )>
»
230-231
74-75
Baumann& Preusse
Z. P. C., 5, 319
42, 756
Tribrom-/3-ethylthiophene ....
S.Et.Br3=1.3.2.4.5
C6H5Br3S
....
108
Bonz
B., 18, 550
48,766
Dibromthioxylylbromide ....
SiMe.Br2,CH,,Br=1.2.3.4.5
)»
142-144
Paal
B., 18, 2253
48, 1206
Dibrom-|3-ethylthiophene ....
S,Et.Br2=1.2.(?)2
C6H6Br2S
Liquid
Bonz
B., 18, 550
48, 766
Dibromthioxylene
S.Me2.Br2=1.2.5.3.4
))
246-247 u. c.
46
Messinger
B., 18, 564
48, 767
„
» »
M
....
50 ; sf. 47
Paal
B., 18, 2253
48, 1206
Bromthioxylene
S.Me2.Br=1.2.5.3
C6H7BrS
193-1 94 u. c.
Liquid
Messinger
B., 18, 1637
48, 1052
Brombenzylsulphhydrate ....
C6H4Br,(CH2.SH)=1.4
C^H^rS
24
Jackson and Harts-
A. C. J., 5, 264
46, 665
horn
Bromtoluene sulphhydrate ....
Me.Br.SH=l.a?
»
246 p. d.
L,— 20
Hubner & Wallach
Z. C. [2], 5, 500
vi., 290
»> „
» »
n
245 p. d.
7
»
J)
)»
Dithienyldibromethylene ....
CBr2:C(C4H3S)2
CioHfiBr.jS,,
Liquid
Peter
B., 17, 1344
46, 1001
Dithienyltribromethane
CBr,,.CH(C4H3S)2
C10H;Br3S3
101-102
»
»
jj
Dibromphenyl sulphide
S(CGH4Br)2
C^HgBr^S
109-110
Krafft
B., 7, 1164
28, 153
„ disulphide ....
S2(C6H4Br).2=(1.4)2
C12HsBr2S.j
....
93
Nbtling
B., 8, 1310
28, 264
?
....
CI4H6Br2S2
n. f. 250
Limpricht
B., 6, 534
26, 1032
Brombenzyl sulphide
(U6H4Br.CH::),!S=(1.4)2
C14H12Br2S
59
Jackson and Harts-
A. C. J., 5, 264
46, 665
horn
„ disulphide
(C6H4Br.CH2)2S2=(1.4)2
C14H12Br2S2
87-88
u
J)
1*
Bromtolyl disulphide
(C,H3MeBr)2S2=1.2.3 or 5)
,,
56-58
Hubner and Poat
A., 169, 42
27, 59
Bromphenylmercaptole of
CMe2(S.C6H4Br)2=(1.4)2
C15Hl4Br2S2
89-90
Baumann
B., 18, 888
48, 749
acetone
Bromphenylmercaptal of
Ph.CH(S.C6H4Br)2=(L4.)2
CigfH14Br2S2
79-80
»»
B., 18, 885
J)
benzaldehyde
Bromphenylmercaptal of
Ph.CH :CH.CH(S.C6H4Br)2
C21H16Br2S2
105-107
,,
)»
p|
cinnamaldehyde
=(l-4)3
Tribromthionessal
C2sH17Br3S
....
265-270
Fleischer
A., 144, 194
vi., 1087
Dimethylselenio-dibromide....
Me2SeBr2
C2H6BraSe
cf. A., 179, 5
82 d.
Jackson
B., 8, 110
28, 553
Diniethyl-telluro-dibrotnide
Me.2TeBr3
C,H6Br,Te
89
Wohler and Dean
A., 93, 233
COMPOUNDS CONTAINING FOUR ELEMENTS.
419
(10.) CHBrN.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Dibromacetonitril .... „..
CHBr^CN
C2HBr2N
142
Van t'Hoff
B., 7, 1571
Bromacetonitril hydro-
CH2Br.CN+HBr.
C2H3Br2N
sb. 65
65
Engler
A., 133, 139; 142
vi., 523
bromide
69
Acetonitril cKhydrobromide
CH3.CN+2HBr.
C2HiBr2N
sb. 49
47-50
?)
II
t)
Tribromglyoxalin
C3HBr3N2
214 d.
Wyss
B., 10, 1371
Brompropionitril hydrobro-
C3H4BrN+HBr
C3H5Br2N
64
Engler
A., 142, 65
vi., 524
mide
1
Propionitril dihydrobromide
Me.CH2.CN+2HBr
C3H7Br2N
....
50-55
»
»
jj
Tribromomethlyglyoxaline ....
C3Br3N.NMe
C4H3Br3N2
88-89
Wallach
B., 16, 537
44, 911
»» ••••
j)
M
88-89
Wyss
B., 10, 1372
Tribromparoxalmethyline ....
....
M
258
Eadiszewski
B., 15, 2707
44, 308
n-Dibrompyridine
N.Cla=1.2.?
C6H3Br3N
108
Ladenburg
B., 15, 1030
«- »
» »
H
....
109-110
Hofmann
B., 12, 989
36, 734
"- .,
JJ Ji
M
109-110
Gerichten
A., 210, 101
48,315
« ,.
»> >J
»
110
Schotten
B., 16, 649
"- „
» »
)»
110-5
Ladenburg
B., 15, 1142
«- »
1) »
»j
GO
112
Hofmann
B., 16, 588
44, 813
|3- „
„ = 1
))
....
164-165
Fischer and Reim-
B., 16, 1184
44, 923
erschrnid
J3- „
J> >'
»
164
KSuigs and Geigy
B., 17, 593
46, 1195
Brompyiidine
N.C1=1.2
C5H4BrN
169-5(760-5)
Liquid
Cianiician & Denn-
B., 15, 1174
42, 1214
stedt
(cf. B., 15, 943)
)> 1)
)J
169-170
Liquid
Danesi
G. I., 12, 150
42, 867
»» .... ....
ii Jl
})
170
....
Hofmann
B., 12, 990
36, 734
» — •
1» »)
»
173
Liquid
»
B., 16, 589
NH;) on phlorobromine
....
C6II4Br6N2
120
Beiiedikt
C. C. [1878], 101
34, 499
?
....
»
....
124
....
A., 189, 167
Tribromethylglyoxaliue
(C3Br3N)NEt
C5HbBr3N2
....
61-62
Wallach
B., 16, 537
44, 911
»
»»
«
....
61
Wyss
B., 10, 1372
Tribronidiazobenzenimide ....
C0H2Br3.N.N : N=1.3.5.6
C6H2Br3N3
....
59
Silbersteiu
J. p., 27, 116
44,661
Peutabromaniline
CeBr6.NH2
C6H2Br5N
Not b. 220
Korner
G. I., 4, 305
29, 218
)i
»
»
**8
....
J. [1875], 344
Tribronidiazobenzenimide
C6H2Br3.NBr.NBr2 = 1.3.5.6
C6H3Br6N2
....
98-5
Silberstein
J. p., 27, 118
perbromide
Diazodibromphenylimide ....
C6H2B2.N2.NH
C6H3BriN3
....
62
Griess
P. T. [1864], 700
iv., 484
Tetrabromaniline
Br4.NH2=1.2.3.5.6
C6H3Br4N
115-3
Korner
G. I., 4, 305
29, 212
„
» »
)1
....
116-117
Wiirster & Nolting
B., 7, 1564
29, 389
p-Diazobromphenylimide ....
C6H3Br.N2.NH
C6H4BrN3
20
Griess
P. T. [1864], 700
iv., 483
Trbiromaniline
Br3.NH2=1.3.5.6
C6H4Br3N
116-22
Mills
....
28, 648
i» ....
» »)
I)
....
116-319
»*
P. B. [1881], 85
ji •••• ••••
11 »
»
abt. 300
117
Fritzsche
J. p., 28, 204
iv., 436
»
» )>
J»
....
117
Hofman
B., 15, 411
42, 951
M .... ....
» )'
»)
118
Korner
G. I., 4, 305
29, 212, 227
J» ....
» '»
)J
118-5
Zander
A., 198, 1
38, 124
,, ....
)» >J
)»
....
119
Nolting and Kohn
B., 17, 357
„ .... ....
)) J)
»
119
Nolting & Scholler
B., 8, 819
29, 928
,,
»» )J
»>
....
119
Losauitsch
B., 15, 471
42, 954
,,
11 )}
5)
....
119
Baumann and Tie-
B., 12, 1192
36, 936
niann
,,
)» )»
)J
....
119
Limpricht
B., 10, 1541
,}
)> J>
»>
119-120
Fittig and Buclmei
A., 188, 26
34, 50
,, ....
„ =1,2.3.5
)1
d. a. 130
n. f. 130
Korner
G. I., 4, 305
29, 223
Dibromaniline
NH2.Br2=1.2.5
=1.3.5
CsHsBr2N
51-53
56
Langer
A., 165, 181
B., 15, 1329
JJ
»
56-5
Korner
G. I., 4, 30
29, 218
» »
= 1
ji
50-60
Hofmann
A., 53, 47
iv., 436
»
=1.2.6 (?)
)^
70-71
Limpricht
B., 10, 1541
34, 221
)) \ /
=1.2.4
»>
78'82
Mills
P. M. [4], 49, 21
28, 648
)J
)>
L J) >
3 H 2
420
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dibromaniline
NH2.Br2=1.2.4
11 n
i» )i
11 i»
11 i»
1» 11
—1 34
C6H5Br2N
11
»i
J5
)1
«
fi
; *)
n
11
C6H6Br4N
))'
»1
C6H6BrN
j^
jf
»
11
11
•si
f1
»1
51
»J
Jf
11
>1
51
rt
si
11
i)
*;
11
)i
i>
*:
i»
11
11
C6H"Br3tf
C6H7BrN2
C6n"BrN
CcH8BrN3
C6H8-Br2N2
C6H14BrN
CyH.BrN
C7H4Br2N3
C7H3BrN2
241'5
241-5
241-5
251
229
cf. 28, 147
cf. 29, 212
+3H2O
abt. 225
78-833
79-5
79
79
79-4
79-5
80
80'4
84
89-90'
108
90
90
190
Liquid
Liquid
16
16
16
18-18-5
a, 30
31
31
31-31-S
50
57
61
61 -871
61-62
61-62
61-8
63
63
63
63
63
63-64
63-5
63-64
64
64-5
65
66-4
d. 250
63
68
187
141-142 u.c.
38
182
38
239
124
Mills
Griess
Tiemann and Piest
Wurster
Korner
Remmers
Spiegel berg
Korner
Limpricht
Fittig and Bucliner
Ladenburg
Bell
»
Gattermann
Griess
Petersen
Wurster and Gru-
beumann
Wurater & Notling
Wurster
Fittig and Mager
Korner
Hiibner & Alsberg
Petersen
Fittig and Mager
Hofmann
Griess
Gabriel
Mills
Richter
Klinger
Mills
Fittig and Mager
Anschiitz & Schultz
Notling & Scholler
Fittig and Biichner
Calm and Heumann
Baltzer
Keramers
Weith and Landolt
Petersen
Gabriel
Korner
Remmers
Hiibner & Retschy
Ramsay
Bayer
Wallach
Ladenburg & Roth
Engler
Fischer and Tafel
Fischer and Tafel
P. R. [1881], 205
A., 121, 267
B., 15, 2032
B., 6, 1491
G. I, 4, 305
B., 7, 348
A., 197, 257
G. I., 4, 305
B., 10, 1541
A., 188, 23
B,, 15, 1030
B., 10, 1863
B., 11, 1812
B., 16, 635
[2], 5, 857
B., 6, 368
B., 7, 418
B., 7, 905
A., 173, 145
B., 8, 364
G. I., 4, 305
Z. C, [2], 6, 639
B., 6, 368
B., 7, 1179
«
A., 53, 42
P. T. [1864], 713
B., 12, 1638
P. R. [1881], 205
B., 4, 460
A., 184, 261 ; B.,
8,311
P. M. [4], 49, 21
B., 7, 1175
B., 9, 1399
B., 8, 819
A., 188, 23
B., 13. 1182
B., 14, 1902
B., 7, 347
B., 8, 716
B., 6, 368
B., 11, 2261
G. I., 4, 387
A., 210, 99
C
B., 7, 347
B., 6, 796, 797
P. M. [5], 2, 271
B., 4, 178
B., 16, 537
B., 18, 49
B., 4, 708
A., 227, 303
A., 227, 303
iv., 436
27, 369
29, 212
27, 696
38, 799
29, 218
34, 221
34, 50
36, 526
44, 796
vi., 921
26, 1133
27, 691
27, 1163
28, 757
29, 232
vii., 143
26, 1133
vii., 944 ; 28,
147
iv., 435
vi., 921
38, 41
24, 687
31, 710 ; 28,
1025
28, 648
vii., 904, 944
29, 928
34,50
38, 880
28, 1194
26, 1133
vii., 143
36, 324
vii., 904
27, 696
26, 1147
36, 263
48, 557
24, 924
48, 541
48, 541
.,
>y ? *
» = *
» '= '
Me combined with N
CBr : CBr.CBr : CBrNEt
i J
Dibrommethylpyridine
Tetrabrommethylpyrrol
»
Tribromaniline hydrobrom-
ide
Bromaniline
n
(NH2.Br3=1.3.5)+HBr
NH2.Br = 1.3
1) 1»
)) 1)
» J)
1» 11
>» 1*
NHs.Br=l,2
» !>'
l» »'
!) II1
NH2.Br =1.4
» »
» )>
» )»
» n
)> )»
)') >>
»' «
>' »
i) n
>^ n
» !<
» )t
»» 1>
I» )1
JJ >*
)>' H
if i*
« *)
NHj.NH2.Br =1.2.4
» *j
C6H7N.HBr.
fr,C3H2MeN.NEt
C6H4Br.CN =L3
C6H3Br.CBr.NHN
L |
11 •"*' •"• »"•
,,
j) .... ... ....
Methyldibrompytidylium
bromide
Bromdiamidobeiizene
,,
Picoline hydrobromide
Bromcyanmethine
Dibromoxalethyline ....
a-Methylpiperidine hydro
broinide
Brombenzonitril .... ,.,.
Dibromindazole
Bromindazole...
COMPOUNDS CONTAINING FOUR ELEMENTS.
421
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Tetrabromtoluidine ....
Me.NH2.Br, =1.3.2.4.5.6
C;H3Br4N
223-224
Neville & Winther
B., 13, 975
37, 449
» •*••
„ =1.4.2.3.5.6
11
226-227
J»
B., 14, 418
39, 86
Tribromtoluidine .... . ;...;
Me.NH2.Br3= ?
C7HaBr3N
72
Sch offer
A., 174, 366
28, 370, 463
11 ....
11 n
11
....
82
si
A., 174, 362
28, 370
11
„ =1.4.2.3.5
,,
82-o-SS
Neville & Whither
B., 14, 418
39, 86
„
„ =1.3.2.5.6
ri "
....
93-94
11
B., 13, 974
37, 448 ; 39, 8li
11- ••••
=1.3.(?):l
11
95 ; a.s. 101
....
Limpricht
B., 7, 450
27, 901
„ ....
11 11
11
95; a.s. 101
....
Lorenz
A., 172, 177
28, 81
,, .... —
=1.3.4.5.6
,,
96-96'S
Neville & Winther
B., 13, 974
37, 447 ; 39, 8(i
«
„ =1.3.2.4.6
•i
....
97
Wroblewsky
Z. C. [2], 7, -2\0,
vii., 1177 ; 24,
271 ; A., 168, 19f
1062; 27, .54
11 ....
!) 11
11
....
100-101-6
Neville & Winther
B., 13, 975
37, 440 ; 39, 86
11
= 1.8.0),
11
....
105-106
Gerver
A., 169, 379
27, 167
,, ....
ji i»
>!
112
Limpricht
B., 6, 1009
27,73
)! J)
!>
112
Gerver
A., 169, 378
27, 167
11 .... ....
=1.4.2.3.?
1)
113
....
A., 173, 217
„ ....
„ =1.4.2.3.6
11
118-11S-6
Neville & Winther
B., 14, 418
39, 86
Beuzonitril dihydrobromide
C6Hs.CN + 2HBr.
C7H7Br,N
70
Engler
A., 149, 307
vi., 525
Dibromtoluidine
Me.NH2.Br3=1.3.2.6
»1
....
33-35
Neville & Winther
B., 13, 971
37, 440 ; 39, 8(i
„ ....
=1.2.3.5
)1
....
43-44
11
37, 630
„
» »
1)
cf. 39, 86
45-46
11
B., 13, 966
37, 436, 627
n
V 11
11
....
46-47
it
B., 14, 419
37, 630
„
» )'
11
50
Wroblewsky
Z. C. [2], 7, 210 ; vii., 1177 ; 24,
A., 168, 187
564 ; 27, 54
„
" 11
11 '
50
Mohlau & Oemiclien
J. p., 24, 478
42, 395
11 *••• •• •
=1.(2 or 4).5.6
11
52-53
Neville & Winther
37, 435 ; 39, 8(i
,, .... v ....
„ =1.3.4.5
11
cf. 39, 86
58-59
11
B., 13, 975
37, 447
11 "•• ••••
„ =1.3.2.5
11
cf. 39, 86
72-5-73-1
11
B., 13, 974
37, 448
11
„ =1.4.3.5
)1
....
73
Wroblewsky
Z. C. [2], 5, 460
vi., 1104
51 11
11
....
73
11
A., 168, 189; 173,
vii., 1165
216
1) •••• ••••
11 1>
)1
cf. 39, 86
73
Neville & Winther
....
37, 436, 632
11 ...* ....
)! 11
11
....
76
Wroblewsky
37, 436
,,
»1 1»
11
73
Mazzara
G. 1^ 10, 370
38, 879
D .... ....
51 11
))
....
74
Limpricht
B., 7, 719
27, 991
>1
=1.3.4.6
>1
cf. 39, 86
~4'6'-75'5
Neville & Winther
B., 13, 971
37, 440, 443
,j .... ....
„ =1.3.5.6
»1
••••
83
Wroblewsky
Z. C. [2], 7, 135
24, 564
1>
!! »
11
....
83
11
Z. C. [2], 6, 239
vii., 1165, 1177
11 •••• •"•
11 11
»1
....
83-85 Neville & Whither
....
37, 434
11
11 11
Jl
cf. 39, 86
86-4
11
B., 13, 964
11
D .... ....
=1.4.2.5
)1
....
83
Wroblewsky
A., 168, 186
27, 53
j, .... ....
11 !»
H
84-85
Neville & Winther
....
37, 451
,, ....
11 J)
11
cf. 39, 86
84-6-85
11
B., 13, 963
37, 445
= 1.4.2.6
11
cf. 39, 86
87-88
11
B., 13, 962
37, 446
11 .... .. .
= 1.2.4.5(?)
....
92-5
Wroblewsky
A.,168,184;Z.C.
24, 1062; 27,
[2], 6, 239; 7,
54; vii., 1165
271
1177
11 .... ....
» 11
11
95
»i
11
11
))
11 11
ji
cf. 39, 86
97-98
Neville & Winther
B., 13, 970
37, 451
Brombenzylamine
CllH4Br(CH,!.NH.!)=1.2
C-H8BiN
....
Liquid
Jackson and White
B., 13, 1219
38, 879
i»
=1.4
11
Liquid
Jackson & Lowery
A. C. J., 3, 247
42, 170
Brommethylaniline
C6H4Br.NHMe=1.4
11
259-260
Liquid
Wiirster & Scheibe
B., 12, 1817
38, 107
Bromtoluidine
Me.NH2.Br=1.2.3
»)
....
Liquid 0
Hiibner atid Roos
B., 6, 801
11
.. 0)
11
253-257
Liquid
Hiibner & Wallach
Z. 0-12], 5, 22, 530
vi., 1103
51 ....
11 11
11
240
Liquid
Wroblewsky
Z. C. [2], 7, 606
25, 698
11 .... ....
» :>
11
cf. 39, 86
Liquid
Neville & Winther
B., 13, 1945
37, 630
11
„ =1.3.2
Jl
240
Liquid
Wroblewsky
Z.C.[2],7,135,60()
25, 698; vii.,
1
1177
.-,
= 1.4.6
11
....
25-3S
Neville & Winther
B., 14, 418
39, 86
„
= 1.4.5
Jl
cf. 39, 86
Liquid
11
| 37, 438, 630
11 11
11
220
....
Wroblewsky
Z. C. [2], 5, 276
vi., 1104
422
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Bromtoluidine
Me.NH2.Br— 1.4.5
C7H8BrN
240
8. 8
Wroblewsky
A., 168, 154
27, 51
« .... ..
» »>
»1
26
Claus & Steinberg
B., 16, 914
i»
=1.2.4
Jl
....
a. —2
Wroblewsby and
Z. C. [2[, 7, 165
vi., 1104; vii.,
Kurbatow
1167, 1176
)> .... ..
)> »
„
s. —2
Wroblewsky
A., 168, 177
27, 53, 165
»
)» 1'
Ti
30
Heynemann
A., 158, 340 ;
24, 681 ; vii.,
Z. C. [2], 6, 402
1167, 1176
»( .... ..
» »
?»
cf. 39, 86
30-31
Neville & Winther
37, 442
»> •"•
') . »
)»
32
Hiibuer and Eoos
B., 6, 799
27, 165
»> .... ..
=1.3.5
,,
255-260
Liquid— 20
Wroblewsky
B., 8, 573 ; A.,
28, 886 ; 34,
.
192, 196
977
yl .... ..
)) 11
)>
....
34-5-37
Neville & Winther
37, 433
T)
>» »>
))
35-35-2
n
»
)) .... ..
» >»
»»
....
35-37
i)
37,449
)» ...» ..
»> ))
1)
cf. 39, 80
85-6-36
u
B., 13, 964
37, 433
»)
» »T
1)
....
36-6
yj
37, 433
»>
=1.2.5
))
54-57
»
37, 630
J>
1) I>
))
cf. 39, 86
55-56
»
37, 431, 631
»
» »
»
240 d.
57
Wroblewsky
Z. C. [2], 7, 135
24, 564 ; 27,
A., 168, 163, 173
51; vii., 1177
» .... ...
») )»
))
....
56
Grete
A., 177, 249
29, 73
)» «" ...
» »
»J
....
57-5-58
»
B., 8, 567
28, 888
>» *•*• ...
=1.3.4
»»
cf. 39, 86
30-6-32
Neville & Winther
B., 13, 972
37, 442
,,
» »
»)
....
67
Wroblewsky
A., 168, 177
27, 53
5)
» »
))
....
67
Wroblewsky and
Z. C. [2], 6, 165 ,
vi., 1104 ; vii.,
Kurbatow
J. [1875], 627
1167,1176
» ...
II >!
»
....
75
Hiibner and Boos
B,, 6, 800
27, 166
>,
=1.3.6
»)
240
....
Wroblewsky
A., 168, 173
27,53
)>
» »»
)>
....
76-77
Neville & Winther
37, 440
))
>» »»
))
76-78-5
»
37, 431
>t •••• ...
»J »
JJ
77-78
,i
«
» •"> ...
)) )«
))
78-79
»i
B., 13, 963, 969
39, 86
»
» >»
I)
78-4-78-8
M
M
»
Diamidobromtoluene
Me.Br.(NH2)2=1.4.2.3
C7H9BrN2
59
Hiibner & Schiipp-
B., 17, 776
46, 1143
haus
» •••
=U.2.4
))
104
Buhemann
B., 14, 2659
42,392
»
„ =1.5.2.4
»
107
Grete
A., 177,262; B.,
28, 888 ; 29,
8,567
73
Tribromglyoxalisoamyline ...
C7H9Br3N2
....
216-217
Kadziszewski and
B., 17, 1293
46, 986
Szul
Luticline hydrobromide
C7H9N+HBr
CrH10BrN
d. 230
Ladenburg & Roth
B., 18, 1592
Dibromglyoxalisoamyline ....
....
C7H10Br2N2
....
157-158
Badziszewski and
B., 17, 1293
46, 986
Szul
Glyoxalisoamyline hydro-
C7H12N3+HBr
C7H13BrN2
100
H
B., 17, 1292
46, 985
bromide
Bromdiazobenzene cyanide....
C6H4Br.N2.CN+HCN=1.4
C8H5BrN4
127-5
Gabriel
B,, 12, 1638
38,41
Phenylbromacetic nitril
Ph.CHBr.CN
C8H6BrN
d. 150
Liquid
Beimer
B., 14, 1798
Brom-a-toluic nitril
C6H4Br.(CH2.CN)=1.2
»
....
Liquid
Jackson
A. C. J., 2, 316
j) j»
=1.4
H
....
46
Jackson and Lowry
B., 10, 1210
34,64
»» D
'1 )5
47
H
A. C. J., 3, 246
Ethenylbromodiamidoben-
zeiie
06H3Br.NH.CH2.CH : N
C^BrNj
206
Bemmers
B., 7, 348
27, 696
=11.2
Bromformanhydroisodi-
C6H2MeBr.N : CH.NH
})
....
187
Hiibner & Schiipp-
B., 17, 777
46, 1143
amidotoluene
i i
haus
=1.4.2.3 or 1.4.3.2
Phenylbromacetimid bro-
Ph.CHBr.CBr.'NH
C8H7Br2N
...
200 d.
Reimer
B., 14, 1797
42, 169
mide
Dibroiuiiaphthylamine
NH2.Br2=a,/3s ; a
I)
101-102
yieldola
47, 514
jj
„ =ao3, ; /5
)1
105
D
47, 511
Bronidimethylaniiine
C6H Br.NMe2=1.3
C3H10BrN
259 c.
11
Wiirster & Scheibe
B., 12, 1818
38, 108
•>
=1.4
»
....
55
Weber
B., 8, 715
28, 1200
)i ..-.
>i
);
55
31aus and Howitz
B., 17, 1326
46, 1000
COMPOUNDS CONTAINING FOUR ELEMENTS.
423
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Bromdimethylaniline
C6H4Br.NMe2=1.4
C8H10BrN
SfT (722)
55
Merz and Weith
B., 10, 763
32, 603
»i
» »
)»
264 c.
55
Wiirster and Beran
B., 12, 1820
38, 108
Bromxylidine
Me2.NH2.Br=1.3.4.5
»
96-97
Genz
B., 3, 225
vii., 1210
Fr. dimethyl-p-diamidoben-
....
CsHuBrN2
146
Wiirster and
B., 12, 1803, 2071
88, 110
zene
Sendtners
Bronicyanmethethiue
....
C3H12BrN3
155 d.
Eiess and Meyer
J. p. [2], 31, 112
48, 646
Hydro-a-isopropylpyridine
....
C8HMBrN
230-233
Ladenburg
B., 18, 1589
48, 992
+HBr
a-isopropylpiperidine + HBr
....
C8H19BrN
216
s»
B., 17, 1679
46, 1386
Coniine+HBr
C8H16BrN(?)
,, (?)
207
»
»
»
Copellidine+HBr
....
»
165
Diirkopf
B., 18, 923
48, 817
Tetrethylammonium tri-
NEt4.Brs
C8H20Br3N
78
Marquart
J. p. [2], 1, 429
vii., 485
bromide
Hexabromquinoline
....
C9HBr,N
88-89
Weidel
A., 173, 95
28, 88
Tetrabromquinoline
....
C9H3Br4N
119 u.c.
Clauss and Istel
B., 15, 820
42, 1110
Tribromquinoline
....
C9H4Br3N
173-175
Lubavin
Z. C. [2], 5, 690
vi., 430 ; vii.,
A., 155, 318
307
„ ....
....
))
173-175
Hoffmann & Konigs
B., 16, 737
Dibromquinoline
N.Brs=l ; 1.3
C9H6Br2N
100-101
Coste
B., 15, 559
42,978
„
„ =1 ; 1.4
»
124-126
)>
B., 14, 917 ; 15,
40, 742 ; 42,
559
978
,, ....
» »»
ii
....
127-128
Metzger
B., 17, 188
46, 757
Bromquinoline
N.Br=?
C9H6BrN
270
Coste
B., 14, 916
40, 741
»» ••••
„ =1 ; 3
11
276-278
....
)>
B., 15, 558
42, 978
Amidobromquinoline
)i >»
C9HrBrN2
164
i»
B., 15, 1920
44,91
Propenyltribromphenylene
C6HBr3.NH.CEt:N=(?)3.1.2
C9H7Br3N2
257-262
Smith
A. C. J., 6, 172
48, 525
diamine
i i
Quinoliue tetrabromide
....
C9H7Br4N(?)
cf. B. S., 38,
88
Grimaux
C. E., 95, 85
124
Propenyldibromphenylene
C6H2Br2.NH.CEt:N=(?)2.1.2
C9H§Br2N2
224-226
Smith
A. C. J., 6, 172
48, 524
diamine
Quiuoline dibromide+HBr
C9H9Br3N
cf. B. S., 38,
86
C. E., 95, 85
42, 1215
124
Dibromtetrahydroquinoline
C9H9Br2N
05-66
Clans and Istel
B., 15, 823
42, 1110
Bromtetrahydroquinoline
....
C9HnBr2N
192 d.
Hoffmann and
B., 16, 737
44, 1145
+ HBr
Konigs
Ethylmethylbromaniline
C6H4Br.NMeEt=1.4(?)
C9H12BrN
265
s. b. 0
Clans and Howitz
B., 17, 1327
46, 1006
Dimethylbromtoluidine
Me.NMe2.Br=1.2.?
»)
244
Liquid
Michler & Sampais
B., 14, 2173
42, 177
»
=1.3.?
)»
276
08
Wiirster & Kiedel
B., 12,1801, 1825
38, 109
Tribromcyanethine ....
....
C9H12Br3N3
126
Riess
J. p. [2], 30, 145
48, 236
Propylphenylamine+HBr ....
C6H4.Pr.(NH2.HBr)=1.4
C9H14BrN
213
Francksen
B., 17, 1222
46, 1008
Bromcyanethine
C9H14BrN3
152-153
Meyer
J. p. [2], 26, 339
44, 353
j) ....
)»
153
Riess
J. p. [2], 30, 145
48, 235
Methylcopellidine-fHBr ....
C8H16MeN+HBr
C9H20BrN
151
Diirkopf
B., 18, 926
48, 817
Dibromnaphthylamine
NH2.Br2=a1o231 ;
C10H7Br2N
118-119
Meldola
B.,12, 1961
38, 260 ; 43, 4
» ....
» =ft«
»
121
Laws on
B., 18, 2424
48, 1239
Bromnaphthylamine
NH2.Br=a.^, ;
C10H8BrN
62
Meldola
47, 510
„
,> =0i»i ;
M
63
j»
43, 5
47, 523
j) ...
» D
)i
63
Cosiner
B., 14, 59
40, 606
,,
„ =a1 ; 0! or /32
ft
....
63-64
Guareschi
A., 222, 262
46, 843
,5
„ =£i"2 ;
)»
71-5
Meldola
47, 509
,, ....
„ =3^, ;
tt
71-5
j»
47, 523
» ...
„ = »
i»
85
Guareschi
A., 222, 262
46, 843
)>
„ =«i"2 ;
)»
94
Rother
B., 4, 850
n
» J»
)j
1
94
Meldola
43, 5
47, 523
Broniacetamidobenzyl-
NHAc.Br.(CH2.CN)=l.?.4
C10H9BrN2
127-129
Gabriel
B., 15, 840
42, 1070
cyanide
Bromam idoacenaphthal ide ....
(NH2)2.Br=a1a201 ;
)»
222
Meldola
47, 501
Quinoline dibromide metho-
CaNHjEr^MeBr
CwHwBrIN
• •••
123
Ostermeyer
C.C. [1884], 970;
48, 672
bromide
B., 18, 594
Pyridine dibromide hydro-
(C6H5Br2N)2.HBr
C10HllBr6N2
125-12(5
Grimaux
C. R., 95, 85
42, 1216
bromide
-124
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diethylbromaniline ....
C6H4Br.NEt2=1.4(?)
C10H14BrN
270
33
Glaus and Howitz
B., 17, 1324
46, 1006
Brom-a-naphthoic nitril
....
CnH6BrN
147
Hausamann
B., 9, 1516
31, 318
„ -ft- „
....
JJ
....
148-149
„
B., 9, 1517
„
Quinoline ethobromide
C9H7N.EtBr+H80
G,,H12BrN
80
Glaus and Tosse
B., 16, 1277
44, 1009
Decabromdiphenylamine
NH(C6Br6)2 (?)
C12HBr10N
a. 310
Gessner
B., 9, 1512
31, 301
Octobromdiphenylamine
C12H3Br8N
302-30o
„
„
31, 302
Hexabromdiplienylamiue ...
....
C12H3Br6N
218
Gnehm
B., 8, 926
29,83
Hexabromdiazoamidoben-
C6H.,Br3. Nj. NH.l'sH.Br.,
C12H6Br6N3
....
158 d.
Silberstein
J. p. [2], 27, 120
44, 661
zene
=1.3.0.6; 6.5.3.1
Tetrabromazobenzene
C12H,Br4N2
320
Werigo
A., 165, 200
26,385;vii.,148
Azimido-dibromdiphenyl ...
C12H7Br2N3
206
Schultz
B., 17. 466
46, 903
Tetrabromdiphenylamine ....
NH(C6H3B,2)i
C,2H7Br4N
cf. A., 132,166
182
Gnehm
B., 8, 925
29, 83
Diazoamidodibrombenzene ....
....
C12H7Br4N3
167-5
Griess
A., 121, 273
iv., 460
Bromcarbazole
....
G12H8BrN
199
Ciamician & Silber
G. I., 12, 272
42, 1104
Dibromazobenzene
C6H4Br.N2.C6H4Br=(1.3)2
C12H8Br2N2
125-5
Gabriel
B., 9, 1407
31, 307
= (1.4),
„
205
Schultz
B., 17,465
iv.,412;vi.,270
>• »
.,
of. A., 135,179
205
Werigo
A., 165, 199
26, 384; vil, 148
„
»> 1)
205
Calm & Heumann
B., 13, 1182
38, 880
Phenauthroline dibromide ....
tl
149
Skraup & Vortmann
M. C., 3, 582
44,87
Tribromdiazoamidobenzene
C6H2Br3.N2.NHPh=1.3.r>.6
C12H3Br3N:i
104
Silberstein
J. p. [2], 27, 121
44, 661
Tetrabrbmbenzidine
G12H8Br4N2
284-286
Glaus and Risler
B., 14, 86
40, 605
Phenanthroline octobromide
CHBr.(CHBr)1,.N : G.C ;
C,.H.BrsN,
176-178
Skraup & Vortmann
M. C., 3, 570
44,87
! 1
(~1 "VT * f ~*TTR». /f^"TTTJ*.\ /"" *
V^.-L1 . \-^il -Dr.! ^>iiJ5r )g.V^ .
•
1
CHBr.CHBr
Ethenylbrom-u-|8-naplitha-
C10H5Br.NH.CMe:N
C12H9BrN3
202
Meldola
47, 505
lene diamiue
i j
Bromethenyl naphthalene
CNH.CMe : N?C.CH :
229
Prager
B., 18, 2160
48, 1239
diamine
i i
i
CBr.CBH4
Phenanthroline hydrobro-
>...
);
....
278-280
Skraup & Vortmann
M. C., 370
44,87
mide
Dibromdiphenyilamine
NH(C6H4Br)i!
C12H9Br2N
107
Lellmami
B., 15, 830
42, 1060
Dibromaniidoazobenzene
CI2H9Br2N3
145
Griess
A., 121, 269
iv., 460
!,
..,,
cf. B.,17, 1403
152
Berju
C. C. [1884], 871
46, 11 48; 48, 660
Dibromhydrazobenzene
C6H4Br.(NH)2.C6H4Br
C12H10Br2N2
107-109
Gabriel
B., 9, 1406
31, 307
=(1.3),
V
„ =(1,4)5
„
. ..
ISO
Werigo
A., 165, 192
26, 384; vil., 148
„
„
jj
130
Calm & Heumann
B., 13, 1182
38, 880
Dibromdiamidodiphenyl
89
Fittig
A., 132, 207
iv., 411
,,
(.C6H3Br.NH2)2=(?.1.4),
M
108 c.
Schultz
B., 17, 466
46, 903
>,
=(U.3)2
151-5-152
Gabriel
B., 9, 1407
31, 307
Benzenylbromphenylene ami-
C6H3Br.N : CPh.N
C13H9BrN2
200
Johnson
B., 10, 1710
1 i
ume
Tctrabrommethyldiphenyl-
NMe(C6H3Br2)_,
C13H9Br4N
129
Gnehm
B., 8, 926
29,83
amine
Tribrommethyldiphenyl-
C6H3Br2.NMe.C6H4Br
C13H10Br3N
98
„
„
„
amine
Oxaldipropylisoamyline bro-
(XH.|Pi*N^Pf"Br
C13H23BrN,
162-163
Radziszewski and
B., 17, 1295
46, 986
mide
Szul
Pheuyldibromanilidoacetic
C6H3Br,(NH.CHPh.CN)
G14H10Br2N..
92
Tiemann and Piest B., 15, 2032
44, 198
nitril
=1.3.4
Benzylidene dibronitoluidine
C14HuBr2N
160-165 d.
J. [1880], 566
Tetrabroin-p-ditolylamine
(Me.C6H2Br2)2NH
C14HnBr4N
162
Lehue
B., 13, 1545
40, 41
Diniethamidoazotribromben-
C,HsBr,.Ns.C,H4.NMes
C14H12Br3N:,
..'.
161
Silberstein
J. p. [2], 27, 124
44, 662
zene
= 1.3.5.6; 1.?
Bromazotoluene
Me.C6H4.N2.C6H3Br.Me
C H BrN
136
Petrieff
B., 6, 557
26, 1027
Dibromdibenzylamine
(C6H4Br.CH2)2NH=(1.2)2
CHHMBr,N
36
Jackson and White
B., 13, 1219
38, 879
"
=(1.4),
„
cf.A.,151,: 70 50
Jackson & Lowery A. C. J., 3, 247 42, 171
COMPOUNDS CONTAINING} FOUR ELEMENTS.
425
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Uibenzylamine hydrobromide
(C6H5.CH2)3NH+HBr
C14H16BrN
266
Limpricht
A., 144, 304
vi., 337
Quinoline amylbroniide
C9H7N.C5HnBr
C14H19BrN
....
140
Claus and Tosse
B., 16, 1278
44, 1009
j> i>
11
))
+.rH2O
87
»
»
»*
?
....
C14H18Br2N:
57-5
Werigo
Z. C. [1865], 631
vi., 285
Picoline ethylene dibromide
(C6H7N)3.C2H4Br2
)»
27,6
Ramsay
P. M. [5], 2, 279
36, 263
/3-Lutidine dibromide + HBr
(C7H9NBr2)2+HBr (?)
C14H19Br5N2
64
Grimaux
C. K., 95, 85
42, 1216
Bromphenylquinolinamine ....
N.(NH.C6H4Br)=1.2 ; (1.4)
C16HnBrN2
146
Friedlander and
B., 18, 1533
48, 990
Weinberg
Phenylhydrazine f Bromcin-
Ph.CBr:C2H2:N2HPh
C15H13BrN2
....
129-130
Zincke and Hagen
B., 17, 1815
46, 1344
namaldehyde
Tetrabrom-/3-naphthyl-
fr. C10H7.NHPh
C^H^r^N
cf. A., 209, 15!
19.8
Streiff
B., 13, 1853
40, 177
phenylamine
Tribrom-a-naphthylpheny.l-
. J)
C16H10Br3N
cf. A., 209, 155
137
u
B., 13, 1852
40, 176
amine
Dibrom-/3-naphthylpl'enyl-
i)
C16HuBr3N
cf.A.,209,15f
140
n
B., 13, 1853
40, 177
amine
Methyldiphenylbrompyr-
C3N2BrMePh2
C16H13BrN3
....
75
Knorr and Blank
B., 18, 316
48, 556
azene
Brombenzylquinoline dibro-
C,H7N.C7H7Br.Brs
C16H14Br3N
100 u. c.
Glaus
B., 18, 1306
48, 908
raide
Dixylylamine Ijydrobromide
(Me.C6H4.CH3)sNH+HBr
C16H20BrN
.... |
195-19,6
Pieper
A., 151, 129
vi., 1133
Tetrabrpnxtolyjnaphthyl-
fr. C10H..NH.C6H4Me
C17HnBr4N
168-169
i Friedlander
B., 16, 2080
46, 80
amine
=£; 1-4
?
C9H6N.CHBr.CHBr.Ph
C17H13Br3N
173-174
Wallach & Wiisten
B., 16, 2009
44, 1097
Dibromdiquinoline
(C9NH6Br)2=a1 ; /32-a, ; a,
C18H)0Br2N.,
n.f. 280
Fischer
M. C., 6, 546
48, 1247
Bromdiquinoline
C18HnBr^2
....
150-155
Ostermeyer and
B., 17, 2149
48, 174
Henrichsen
Dibromtetramfthyldiamido-
Me2N.MeBrC6H2.C6H2BrMe.
C18H33Br2N3
,117
Michler and Sam-
B., 14, 2173
48, 177
ditolyl
NMej=1.2.('02;(?)2.2.1
paio
Methylphenam,idoazotri-
G6H2Br,.N2.C6H4.NMePh
C19H14Br3N
.I?8
Silberstein
J. p. [2], 27, 98
44, 662
brombenzene
=1.3.5.6 ; 1.?
Pentabromazonaphthalene ....
....
C20H9Br5N2
a. 320
Klobukowski
B., 10, 576
32, 623
Tribromtribenzylamine
(C6H4Br.CH2)3N=(1.4)3
C3lH18Br3N
78-79
Jackson & Lowery
B., 10, 1211
34,65
») ....
» i»
»J
cryst. fr. ethei
76^78
)»
A. C. J., 3, 247
42, 171
. »»
>i »
n
cryst. fr. pe-
92
»)
»
u
troleum
,, ....
.=(1.2),
. »»
....
121-5
Jackson and White
B., 13, 1219
38, 879
Tribrombeiizy lamine + H Br
=(1.4)3
C21H19Br4N
270
Jackson & Lowery
B., 10, 1211
34, 65
Brom-deriv. of phenanthroline
C24Hl6Br3N4
176-178
Skraup & Vortmanu
M. C., 3, 581
» n
....
C24H17Br3N
176-178
«i
M. C., 3, 581, 583
5> I)
C12H8NsBr2+C12HsN2.HBr
C24H17Br3N4
....
178
5)
M. C., 3, 370
44,87
Tetrabromtetrimidazoan-
[C6H4:(C:NH)2:C6HBr2]3:N2
C28H14Br4N6
....
233
Glaus &Dierufellnei
B., 14, 1336
42, 523
thracene
Tetrabromdibenzylene di-p-
(Ph.CH)3(N.C6H2Br3Me)3
C^Bir.N,
....
160-165, d.
Mazzara
G. I., 10, 370
38, 879
tolylamine
Diphenyldiisoindolazotri-
(— CH.CPh.N.C6H4.Nj.
C40H34Br6N6
....
149-^50
Mohlau
B., 15, 2491
44, 342
brombenzene
C,HjBr3),=L2;. 6.5.3.1
(11.) CHBrP, CHBrAs, and CHBrSb.
Phosphenyl dibromide
Ph.PBr2
C6HsBr2P
255-257
Liquid
Michaelis & Kohler
B., 9, 519
30, 4-20
„ tetrabromide ....
Ph.PBr4
C6H5Br4P
....
207
M
B., 9, 521
u
„ hexabromide ....
Ph.PBr6
C6H6Br6P
sb. a. 110
solid
11
»
*>
Bromethyltriethylphosphon-
PBrEtj.C,H3Brj
G8Hl9Br2P
235 d.
Hofmann
As., 1, 154
iv., 618
ium bromide
Bromethy [dimethyl phenyl-
PBrMe3Ph.C3H4Br
C10H16Br2P
173
Gleichmann
B., 15, 199
42, 958
phosphonium bromide
- '
3 I
426
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Ethylene tetramethyldi-
CaH4(PMe2PhBr)2
Cj.HJBr.P.
a, 300
Gleichmann
B., 15, 199
42, 958
pheiiylphosphonium di-
broraide
Tetrabromide of above
C2H4(PMe!!PhBr).!.Br4
CiSH26Br6P2
171
»
B., 15, 200
»»
Triphenyl benzylphosphon-
Ph.CH2.PPh3Br
C25HS2BrP
274
Michaelis & Soden
A., 229, 334
48, 1135
ium bromide
Tetrabenzyl phoaphonium
(Ph.CH2)4PBr
CjsHjgBrP
216-217
Letts and Collie
T. E., 30, 181
42, 724
bromide
Ethylene di(triphenylphos-
C2H4(PPh3Br)2
C38H34Br3P2
a, 300
Michaelis & Gleich-
B., 15, 804
42, 1062
phonium bromide)
mann
Arsenpheuyl dibromide
Ph.AsBr2
CeHsBrjAs
285 s.d.
Liquid
Michaelis
A., 201, 203; B.,
32, 452
10, 625
Arsendiphenyl bromide
Ph2AsBr
C12H10BrAs
356 in CO,
Liquid
Coste and Michaelis
A., 201, 230 ; B.,
36, 162
11, 1886
Stibtriethyl dibromide
Et3SbBr2
C6Hi5Br2Sb
....
s. — 10
Lowig & Schweitzer
J. [1850], 475
i., 342
Stibtritolyl „
(C6H4Me)3SbBr2=(1.3)3
C51H21Br2Sb
113
Michaelis and
B., 17, 925
46, 1136
Genzken
n **
=(1.2)3
)»
178; 210
»
)i
>»
!) 1!
=(1-4),
>r
233-234
»
)»
»
(12
.) OHIO
Triiodacetaldehyde (lodal) ....
CIj-COH
CSHI3O
25-115
iii., 280
„ » ••••
„
„
110
....
Johnson
P. M. [3], 2, 415
„
Tetriodmethyloxide
(CHI,)/)
C2H2I4O
181-182
s. —6
Bruning
J., 10, 434
CH3.COI
C2H3IO
108 (757)
cf. A. ,'103.
Guthrie
P. M. [4], 14, 184
i Ti
., oo
335
104-105
cf.A.,95, 209
Cahours
J. 10, 344
lodacetic acid
CH2I.COOH
C2H3I02
82
Perkin and Duppa
P. M. [4], 18, 55
iii., 279
Methyl iodide hydrate
(CH3I)2,H20
C2H9I20
....
—4
Fourcraud
C. E., 80, 1491
40, 32
lodopropargylic acid
CI : C.COOH
C3HI02
....
140
Baeyer
B., 18, 2274
48, 1199
,, »
J)
J)
140
Homolka and Stolz
B., 18, 2282
Triiodacrylic acid
CL/CLCOOH
C3HI302
207
H
B., 18, 2286
48, 1198
3-diiodacrylic acid
CIS:CH,COOH
C.HAO.
....
133
11
B., 18, 2284
H
<i-/3- „ „
CHI : CI.COOH
,,
106
„
H
lodacrylic acid
CHI : CH.COOH
C3H3I02
139-140
Bandrowsky
B., 15, 2703
48, 510
Diiodacetone . , ...
CHjI.CO.CHJ
C3H4I O
,>, ... fjo.e
Viilkov
Ai ' t •' vi
^_
....
DJ. O~Oi O
V 1 H Kt I
., 1 •' — . OC7
*5^) iOL
Propionyl iodide
CH3.CH2.COI
C3H5IO
127-128
Sestini
B.S. [2], 11, 469
vi., 963
lodallyl alcohol
C3H4I.OH
„
....
160
Hiibner and Lell-
B., 13, 461
38, 5.38
mann
„ „
„
„
160
„
B., 14, 208
40, 242
Epi-iodhydrin
O.CH2.CH.CH.,I
..
160-180
Liquid
Reboul
As., 1, 227
Methylic iodacetate
CHjI.COOMe
C3HSI02
169-171 c.
Aronstein & Kruin ps
B., 14, 604
a-Iodopropionic acid
CHjCHLCOOH
„
Liquid
Wichelhaus
A., 163, 1; 144,
vi., 960
352
3-
CHjI.CHj.COOH
n
82
Beilstein
A., 120, 231
iv., 733
13- „
„
tt
82
Melikoff
B., 13, 2154
40, 154
B-
„
„
....
82-6
„
B., 13, 906
38, 800
'n-Iodolactic acid
CH3.CI(OH).COOH
C3H5I03
84-85
Glinsky
B., 6, 1257
8- „ „
CH2I.CH(OH).COOH
„
100-101
Melikoff
B., 14, 937
40, 712
Glycerol diiodhydrin
C3H5I2.OH
C3H6I20
d. 70-76
s. -16 to -20
aaus
A., 168, 25 ; B.,
25, 684 ; 26,
5, 355
1122
Diiodopropyl alcohol
CjH3Ij.CH,OH
,,
....
45 d.
Hubner and Lell-
B., 14, 207
40, 242
mann
Propylene gtycol iodhydrin....
C3H.IO
106 (60)
....
Z. C. [1870], 424
lodofumaric acid
COOH.CH : CI.COOH
C4H.IO4
182-184
Bandrowski
B. 15, 2697
44, 313
COMPOUNDS CONTAINING FOUR ELEMENTS.
427
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Methyl iodopropargyl oxide
C3H2I.O.Me
C4H5IO
s. 12
Liebermann
A., 135, 288
vi., 959
Crotonyl iodide
„
131-133
Liquid
Lieben and Liesel
W. A., 82, 960
40, 711
Butyryl iodide
Me.CH2.CH2.COI
C4H7IO
146-148
Cahours
J., 10, 344
i., 699
Ethylic iodacetate
CH2I.COOEt
C4H7IO2
178-180
cf. A., 112,
Butlerow
B., 5, 479
127
Methylic /3-iodopropionate ....
CH2I.CH2.COOMe
„
188 (756)
Liquid
Hem-y
C. E., 100, 114
48, 372
a-iodobutyric acid
„
....
110
Alberti
B., 9, 1194
/3- „ u
,,
Liquid
„
„
lodoisobutyric acid
CH2I.CHMe.COOH
„
37
Fittig
B., 9, 122
29, 898
11 11
H
„
3d
Engelhorn
A., 200, 65
38, 379
„ „
„
,,
36
Fittig
A., 187, 42
32, 736
lodethyl oxide
CH,I.CH2.OEt
C4H9IO
154-156
Liquid
Baumstark
B., 7, 1173
28, 141
„ „
J)
„
154-155
....
Demole
B., 9, 744, 746
lodopyromeconic acid
C5H3IO3
cf. A., 92, 321
a. 100
Brown
P. M. [4], 8, 201
iv., 761
Ethylic iodopropargylate ....
ci ; c.cooEt
C5H5I02
....
68
Baeyer
B., 18, 2274
48, 1199
Itaiodopyrotartaric acid
C6H7IO4
....
135
Z. C. [1866], 722
vi., 981
Isovaleric iodide
CHMej.CHj.COI
C6H9IO
168
....
Cahours
C. E., 44, 1252
v., 980
Propylic iodacetate
CH2I.COOPr«
C6H9I02
198 (756)
Liquid
Henry
C. E., 100, 114
48, 372
Ethylic |3-iodopropionate ....
CHjI.CHj.COOEt
„
202
....
A., 216, 128
11 H •'•
„
„
198-200(754)
Liquid
Henry
C. E., 100, 114
48, 372
s. d.
,1 11
„
,,
180-200
Beilstein
A., 122, 368
iv., 736
» 11
ji
„
160-170
....
J. p. [21 20, 166
Hydriodoangelic acid
„
46
Schmidt
B., 12, 252
36, 618
!, »
j.
....
46
H
A., 208, 254
40, 1126
j3 iodisopropylacetic acid
Me2.CI.CH2.COOH
,,
....
79-80
Schirokoff
J. p. [2], 23, 285
40, 414
lodovalerianic acid ....
fr. MeEt.CH.COOH
„
86-5
Berendes
B., 10, 836
32, 593
Hydriodotiglic acid
MeEtCI.COOH
„
86-5
Schmidt
A. P. [3], 13, 213
36, 222
,1 11 •*•« *•••
H
„
86-5
11
B., 12, 255
36, 618
11 u ••'• ••••
„
„
86-5
„
A., 208, 254
40, 1126
Diiodoqumone
C6H2I2:02=?.U.4
C6H2I202
178
Seifert
J. p. [2], 28, 437
46, 431
Triiodophenol
OH.I3=1.2.4.6
C6H3I30
150
Schiitzenberger
A., 120, 307;
vi., 909
131, 232
156
Korner
A., 137 214
vii., 929
Triiodoresorci ii ol
(OH)2.I3=1.3.4.6.?
C6H3I3O2
s.b. 190 d.
145 u. c.
Michael & Norton
B., 9, 1752
31, 464
„ —
„ =1.3.4.(?)2
„
154
Claassen
B., 11, 1443
34, 868
Diiodophenol
OH.I2=?
OHIO
on
Schall
B. 16 1902
v^g-LJ ^±2^-'
DO
abt. 110
Schiitzenberger and
C. E., 54, 197
iv., 394
Sengenwald
=1.2.4
i *\ci
lilaswitz and
B. 2 525' W. A.
vi Qlft
11 •
j)
LtJ\J
VX.| ty i\f
Weselsky
60, 290
/r)TT\ T 1 4 K 0
C* TT T O
, , r
Seifert
J. p. [21 28, 437
46, 431
lodophenol
OH.I=1.2
C H IO
1 23
Lobanoff
B., 6, 1251
27, 260 ; vii.,
^-^gij.^j.'w/
907
11 ••" ••••
>i ..
„
Liquid
Korner
G. I., 4, 305
29, 235
11 •••• •"•
,, »
„
43
Nolting and Wrze-
B., 8, 820
vii., 929
sinski
=1 3 (?)
q j.j
ICorner
G. I. 4 305
29, 235
"
,, i.t».yi/
»
ooim
11 •••• ••• • •••
.1 „
ji
64-66
Lobanoff
B., 6, 1251
27, 260; vii.,
907
=1 4 (1)
cf. A. 137 213
o 1-1
K.orner
G. I. 4 305
29 235
"
)» *-'^'\*J
»
ooiid
QQ
Lobanoff
B. 6 1251
27, 260 ; vii.,
l}
)) »J
*>
....
O€7
907
lodoresorcinol
(OH)2.I=1.3.?
C6H6I02
67
Stenhouse
P. E., 22,53; A.,
27, 586
171,311
Ethylic a-iodobutyrate
CH3.CH2.CHI.COOEt
C6HnI02
190-192 d.
««*«
Hell
B., 6, 30
26, 495
Triiodosalicylic acid
COOH.OH.I3=1.2.(?)3
C7H3I3Oa
157 d.
Lautemann
A., 120, 306 ;
v., 158
174, 104
Diiodosalicylic acid ....
COOII.OH.I2=1.2.(?)2
C7H4I203
d.w.m. 193
Liechti
As., 7, 141
vi., 1003
11 11
11 11
tt
d.w.m. 212
Lautemann
A., 120, 304
v., 158
„
u 11
„
d. 215
Birnbaum and
B., 15, 459
1
Eeinherz
i
3 i 2
428
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diiodosalicylic acid
COOH.OH.I2=1.2.(?)3
C7H4IS0S
220-230 d.
Demole
B., 7, 1439
lodobenzaldehyde
COH.I=1.4
C7H6IO
73
Jackson and White
B., 11, 1043
34, 729
lodobenzoic acid
COOH.I=1.2
C7H5I02
150-155
Mabery & Robinson
A. C. J., 4, 101
42, 1057
,, ,, ....
)> »
»
152
Griess
B., 4, 521
24, 702 ; v.i.,
164
„ „
n »
„•
150-157
Kekule
B., 7, 1007
28,64
„ ,,
» !>
„
155-156; '157
Richter
B., 4, 553, 554
24, 824
,. „
„ =1.3
ji '
172-5
Kbrner
Z. C. [2], 4, 327
24,825; vi.,313
„ „
» .,
»»"
185
Griess
B., 4, 522
24, 702; vii.,
164
„ „
„ „
„-
186
Birnbaum and
B., 15, 458
42,970
Reinherz-
t» >T •"•
i.' i» '
„
187-
Ounze and Hiibner
A., 135, 108 ;
vi., 313
136, 201
„ ,,
„ =1.4
„"
u.i. 250
Korner
Z. C. [2], 4, 327
vi., 313 ; vii.,
164
,. „
i. «>
„
....
250-251-
Glassner1
B., 8, 562
28, 888
,, ,, .... ....
JJ H
„•
256
Schmidt & Schultz
A., -207, 333
„
,, ,.
1J
257
Louis
B., 16, 111
»
» »
„••
262
Pahl-
B., 17, 1234
46, 1009
,, „
„ „
„
263
Michael & Norton
B., 18, 137
„ „
»' „• '
it'
265-266 '
Bdran
„•
48, 523
„ „
„ „ •
»•
....
267
Richter
B., 4, 554
24, 824
lodohydroxybenzaldehyde ....
COH.OH.I=1.4.?
„
198-199
Herzfeld'
B:, 10, 2198
34, 423
lodohydroxybenzoic acid ....
COOH.OH.I=1.4,?
C7H5IO:)
160
Peltzer
A., 146, 288
vi., 900
lodosalicylic acid
=1.2.5
»
mixture ?':
184
Liechti1
As.; 7, 136
vi., 1003
„ „•
,, „
„
„
184
Demote
B., 7, 1437, etseq
28, 253
» „'
,, i.-
j>
193-5'
Frankland'
31, 749
vi., 1003
,, .... ...:
11 )J
„
196
Lautemann
A., 120, 302
v., 158
» :,'
11 )»
„
196
Hiibner
B., 12, 1347
36, 928
» ,,
»' it"
»»
196'
Goldberg
J. p. [2], 19, 368
36, 929
,, „
,, !,
„ •
197'
Miller
B;, 16, 81
41, 404
„ „
=1.2.3
»
198
„
„.
„
Diiodocresol
Me.OH.I2=1.4.3.S
C7H6I30
61-61-5
Schall and Dralle
B., 17, 2534
48, 146
lodobenzyl alcohol
(CH2OH).I=1.4
C,H7IO
cf. A. C. J.,
71-75
Mabery & Jackson
B., 11, 56
34, 421
2, 251
lodorcinol
Me.(OH)2.I=1.3.5.?
C7H7IOS
.... '
86-5
Stenhouse
P. R., 22, 53;
vii., 879; 26,
C. N., 26, 279 ;
275 ; 27, 585
A.,- 171, 310
Acetyldiiodophehol'
C6H3I2.OAc
f~1 TT T f\-f
\J g XT g L a \Jf>
107 u.c.
Schall
B., 16, 1902
44, 1109
Methylic iodobenzoate
COOMe.T=1.4
C8H7I02"
114
Schmidt & Schultz
A., 207, 333
,, „
» »
Jl
....
114
Louis
B:, 16, 111
» » '
>J »
J)
115
Pahl
B., 17, 1234
40, 1010
lodo-a-toluic acid
C6H4I.(CH2.COOH)=1.2 '
„
95-96
Mabery &Robinson
A. C. J., 4, 101
42, 1057
„ ,,
=1.4
)J
cf. A. C. J.,
135
Mabery & Jackson
B., 11, 56
34, 422
2, 253
lodanisic acid
COOH.OMe.I.=1.4.5
C8H7IO3
234
Peltzer
B. S: [2], 9,' 148
vi., 173
.... ....
.,
„-
....
334-B
„
A.; 146, 302
vi., 901
1) !»
» >»
,,•
234-235
Schall and Dralle
B.; 17, 252$'
48, 146
lodovanillin
COH.OH.OMe.I.=1.4.5.?
....
n i
Bo Pol 17 i n
-,ii 1 ^Al
j>
Carles
. io. [ - |, l.lj 1 -
B*7 ft! R
Vll., lZ\JL
n"
Xiemann &' Haar-
mann
., /, OlO
27,8'.
Methoxyiodotoluene
Me.OMe.I=1.4.5
C8H9IO
237-238 '
Liquid
Schall and Dralle
B., 17, 2533
48, 146
Iodo-j3-orcinol ....
C6HIMe2(OH)2
C8H9I02
93.
Stenhouse & Groves
A.; 203, 298
37, 404
lodocinnamic acid
C.H.I.CCH : CH.COOH)=1.2
CjHylO,
....
212-214
Gabriel & Herzberg
B., 16, 2036;
44, 1123; 48,
C. C. [1884], 35
661
„ „
=1.3
JJ
181-182-
„•
„
j)
!! !)
=1.4
Jl
d. w. m. 255
H
B
H
Ethylic iodobenzoate
COOEt.I=1.2
C9H9IOS'
Liquid
vi., 313
» »
„ =1.3
Jl'
Liquid
A., 135, 110
" "
„ =1.4
•
Liquid
A., 207, 333
COMPOUNDS CONTAINING FOUR ELEMENTS.
420
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Phenyliodopropionic acid ....
Ph.C2H3I.COOH
C9H9I02
....
119-120 d.
Fittig and Binder
B., 9, 1195; A.,
31, 61 ; 36, 378
147, 97; 195, 133
lodohydrocinnamic acid
C6H4I.(CH2.CH2.COOH)
J>
....
102-103
Gabriel & Herzberg
B , 16, 2036 ;
44, 123; 48,
= 1.2
C. C. [1884], 35
661
11 ;i
= 1.3
»»
....
65-66
11
D
»!
l» 11
= 1.4
)1
140-141
11
11
U
Ethylic iodosal icy late
COOEt.OH.I=1.2.?
C,H,IQ,
....
70-71
J. [1864], 385
Acetoxydiiodotoluene
Me.OAc.I2=1.4.3.5
C9H9T2O3
62-62-5
Schall and Dralle
B., 17, 2534
48; 146
lodonaphthol.... .... »..
OH.I=?
C10H;IO
88
Ostermeyer-
C. C.' [1884], 937
48,672
.. ^— /J, (1 J
94-5
Meldola'
47, 525
DiacetyltriioJoresorcinol
(OAc)2.I3=1.3.4.(i)2
n
CioHyl-jO,
....
170
Claesson
B., 11, 1443
34, 868
lodomeconin ....
ClnHJO4
112
Anderson1
A., 98, 49
iii., 863
HI on Cantharidiu
i.*.
10 9*1 V4
^loHiJjlO.,
131
Piccard
B., 12, 577
36, 655
lodocamphor
C10H15IO
....
43-44
Haller
C. B., 87, 695
36, 329
Diiododiphenylquinol
C6H3I(OH).C6H3I(OH)
C12H8IS02>
abt. 150
Kammerer & Ben-
B., 11, 557
34, 574
zinger
Bsnzoyldiiodophenol
C6H.,I2 OBz
C13H8I20
95-96
Schall
B., 16, 1903
44, 1109
Diiododipheuic acid ....
(C6H3I.COOH)2=(1.4.2)2
C14H8I2O4 ,
....
abt. 260
Schultz
B., 11, 217
34, 511
i) 11
I> )>
>i
262
)J
B., 12, 236
36, 653
Benzoxydiiodotoluene
Me.OBz.I2=1.4.3.5
C14HnIA
....
129-5-130
Schall and Dralle
B., 17, 2534
48, 146
Santonic iodide
....
C,,HlfIQi.
136
Cannizzaro and
G. I., 8, 309 '
36, 331
Valente
Benzaldide oxyiodide
C2iH13I4O;
....
28
Geuther&Cartmell
A., 112, 22
1., 572
(13.) CHTS, CHISe, and CHITe.
Diiodothiophene
C4H2I2S
40-5 ::
Meyer and Kreis
B., 17, 1558
46, 1131
lodothiophene
....
C4H3IS
182 u.c.
Liquid
)!
B., 17, 1559
))
Diethylene disulphotetriodide
(C2H,)2S2I4
C4H8I4S2
132-133 d.
Husemann
A., 126, 289
vi., 607
Iodo-^-ethylthiophene
C4SH2IEt
C6H7IS
....
Liquid
Bonz
B., 18, 551
48, 767
lodothioxylene
C4SHIMe2
)>
....
Liquid
Messinger
B., 18, 1638
48, 1052
Triethyl sulphuro-iodide
SEtJ
C6H15IS
a. 100
Dehn
As. -4, 95
v., 882
Diiodophenylsulphide
S(C6H4I)2
tt|2H8I2S
....
138-139
Krafts
B.,- 7, 1165
28, 154
Triethyl seleno-iodide
SeEt3I
C6H,5ISe
w.m. 80-126
Pieverling
A., 185, 333
34, 130
Benzyldimethyl seleno-triio-
Ph.CH2.SeMe2I3
C,H13I3Se
65
Jackson
A., 179, 19
29, 581
dide
Diethyltellurod iiod ide
TeEt2I2
C4H10I5Te
50
Maleet
A., -79, 223
ii., 550
Triethyltelluroiodide
TeEt,!
C6H16ITe
90-92
Becker
A.,-180, 263
30, 46
": (14
) CHIN
-
Hydrocyanic hydriodide
HON. HI
CHjIN
v. 350-400
A., 138, 36
Ethylguanidine hydriodide....
NHEt.C(:NH).NH2+ HI
C3HlnIN3
...i
149 d.
Letnii
B., 8, 767
29, 911
Tetriodopyrroline
C4I4:NH
C4HI4N
....
d.w.m. 140-
Ciamician & Denn-
B., 15, 2584
44, 351
150-
stedt
Pyridiue periodide
C5HSN.HI.I4
C6H6I6N
....
89
Dafert
M. 0., 4, 496
44, 980
Trimetliylethylammonium
NEtMe3I3
C6H14I3N
64
Muller
A.; 108, 1
iii., 1000
triiodide
>! 11
J)
))
....
64
Dafert
M. C., 4, 496
44, 978
Trimethylethylamnionium
NEtMe3I5
C6H14IiN:
....
68'
»'
11
11
pentiodide
11 11
)t
»'
68
MUller
A., 108, 3
iii., 1000
Triiodaniliue ...
NHn.L=1.2.4.6
C.H.I.N-
185-5'
Michael & Norton
B., 11, 111
34, 406
-
430
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
NH2.I2=1.2.4.
C6H5I2N
95-95-5
Michael & Norton
B., 11, 111
34, 406
M
96
Rudolph
B., 11, 79
34, 422
lodaniline .... .... ...
NH2.I=1.3
c6n"iN
....
25
Griess
J. [1866], 457
vi., 921
25
Korner
G. I., 4, 305
29, 233
„ =1.4 or 1.2
60
Hofmann
A., 67, 65
iv» 444
;i
GO
Griess
J. [1866], 457
vi., 921
60
Korner
G. I., 4, 305
29, 233
„ „
,,
60
Michael & Norton
B., 11, 108
34, 406
60
Gabriel
B., 11, '2261
36, 324
=1.4 (f)
j>
83
Hiibuer
B., 10, 1717
Picoline diiodide + HI
,, — j.,nr y i j
C.HJ.N
79
Ramsay
P. M. [5], 2, 273
36, 263
Ethylglyoxalinemethiodide....
(C3H3N)NEt.MeI
C6HnIN2
....
74-75
Wallach
B., 16, 535
44, 911
Methylhydropyrroline meth-
C4H6MeN.MeI
C6H12IN
286 d.
Ciamician & Denu-
B., 16, 1542
44, 1142
iodide
stedt
Pipecoline hydriodide
NH.(CH2)s.CHMe.CH2+HI
C6H14IN
131
Hesekiel
R, 18, 912
48, 812
L J
Triethylazonium iodide
C6H17IN2
74-78
Fischer
B., 11,2208
36, 451
lodobenzonitril
C,H4I.CN=1.3
C7H4IN
....
41
Griess
B., 2, 370
vii., 427
Diiodotoluidine
Me.NHj.I2=1.4.3.5
C7H7I,N
124-5
Michael & Norton
B., 11, 115
34,407
lodobeuzylamine
C6H4I.(CHj.NH2)=1.2
C7H9IN
Liquid
A. C. J., 4, 101
»
=1.4
„
Liquid
A. C. J., 2, 257
lodotoluidine....
Me.NH2.I=1.2.4
„
273d.
48-49
Heymann
Z. C. [2], 6, 402 ;
24, 681 ; vii.,
A., 158, 338
1167, 1177
„ .... ....
=1.3.4
„
188-189
Glassner
B., 8, 562
28, 897
Picoline methiodide
C6H7N.MeI
C7H10IN
226-5-227u.c.
Ramsay
P. M. [5], 2, 277
36, 263
Picoline methiodide diiodide
C6H7NIs,.MeI
C7H10I3N
129
„
P. M. [5], 2, 278
J)
Methyltriethylammonium
NEtjMeL,
C,H18I3N
62
Muller
A., 108, 1
ill., 1000
triiodide
lod-a-toluic nitril
C,H4L(CH,.CN)=1.4
C8H6IN
50-5
Mabery & Jackson
B., 11, 56
34, 422
Dimethyliodaniline
C,H4LNMe2
C8H10IN
79
Merz and Weith
B., 10, 757, 765
32, 603
Picoline ethiodide
«..
C8H12IN
b. 100
Anderson
A., 94, 361
Hydro-a-isopropyl pyridine
....
C8HUIN
242-243
Laden burg
B., 18, 1589
48, 992
+HI
Tropidine periodide
C8H14I3N
92-93
B., 14, 232
lodotrimethylpiperidine
MM
C8H16IN
....
60
Fischer
B., 17, 1796
46, 1291
Trimethylpiperylium iodide
(CsHgMey'Me^I
C8H18IN
200
Hofmann
B., 14, 663
40, 621
Trimethy lamylammoni um
NMe.CQ.HJLI,
C8H20I3N
80
Muller
A., 108, 1
lli., 1001
triiodide
Tetrethylammonium triiodide
NEt4I.I2
Jj
142
Dafert
M. C., 4, 496
44, 978
lodoquinoline
N.I=ai/3, ;
C9H6IN
52-53
Friedlander and
B., 18, 1531
48, 990
Weinberg
»
» = '
JJ
300+
62-63
La Coste
B., 18, 782
48, 815
Quinoline diiodide
C9H7I2N(?)
67
Dafert
M. C., 4, 496
44, 980
» J!
jj
90
Claus and Istel
B., 15, 824
42, 111
lodocyanethine
C,H14IN3
152
Riess
J. p. [2], 30,145
48, 236
Trimethylphenylammouium
NMe3PhI.I2
C9H14I3N
116
Dafert
M. C., 4, 496
44, 978
triiodide
,,
Trhnethylphenylammonium
NMe3PhI.I4
C,H14ISN
87
pentiodide
J)
Oxalmethylisoauiyline meth-
C7H,1MeN1,MeI
C,H,7INS
169-170
Radziszewski and
B., 17, 1294
46, 986
iodide
Szul
lodotetramethylpiperidine ...
C9H181N
90
Fischer
B., 17, 1792
46, 1290
Iod-o-methyl quinoline
C9NH5MeI
C10H8IN
73-74
La Coste
B., 18, 785
48, 815
Quinoline methiodide
C9NH;.MeI
C10H10IN
72
„
B., 15, 192
Dimethylethylphenylammo-
NPhMe2EtI
C10H16IN
72
124-5
Ostermeyer
Claus & Rautenberg
B., 18, 594
B., 17, 1325
48, 672
46, 1005
nium iodide
» „
„
126
Claus and Howitz
Dimethylconylammonium
iodide
C8H16 1 NMe2I
C10H22IN
100
Hofmanu
JJ
B., 14, 708
40, 745
Dimethylcopellidinium iodide
C8H16Me2NI
«
267-268
Diirkopf
B., 18, 926
48, 817
COMPOUNDS CONTAINING FOUR ELEMENTS.
431
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
/3-Methylquinoline methio-
C10H,N.MeI
C,,H13IN
221
Dobner and Miller
B., 18, 1642
dide
?
N.Me=a,/3, ;
))
....
195
»
B., 16, 2468
46, 184
Ethyl quinazole methiodide
G'mH.jNo.Mel
CnH15IN2
192 d.
Fischer & Kuzel
A., 221, 261
46, 442
Ethylanhydracetdiamido-
C6H3Me.N : CMe.NHEtI
)1
+H.O
141-5-143-5
Hiibner
A., 210, 328
42, 505
toluene iodide
i i
Diethylaniline methiodide ...
NPhEt2MeI
C,,HI3IN
....
102
Clans and Howitz
B., 17, 1326
46, 1006
Methylamylpiperylammo-
C6H10N(C5Hu).MeI
C,,H24IN
195
Schotten
B., 15, 422
42, 982
nium iodide
Diiodoazobenzene ...
C6H4I.N2.C6H4I=(1.3)2
C12H8I2N2
150
Gabriel
B., 9, 1410
81, 307
„
=(l-4)2
ij
237
!>
B., 9, 1409
?»
Diiodohydrazobenzene
C6H4I.N2H2.C6H4I=(1.3)3
^12^10^2^2
....
89-90
?)
B., 9, 1410
11
11
=(1.4),
»
a. 100
5)
B., 9, 1409
11
Ethyl (or dimethyl) quino-
CuHuN.MeI
C12H14IN
203
Ntilting and Wein-
B., 18, 1342
48, 978
line methiodide
gartner
Ethyltetrahydroquinoline
C9H10EtN.MeI
C12H18IN
179 u.c.
Clausand Stegelitz
B., 17, 1331
46, 1051
methiodide
Trimethylpropylphenylam-
C6H4Pr.NMe2+MeI=1.4
C12H20IN
168
Glaus and Howitz
B., 17, 1328
46, 1006
monium iodide
Triethylphenylammonium
NEt3PhI.I2
C12H20I3N
....
81
Dafert
M. C., 4, 496
44, 978
triiodide
Triethylpheuylainmonium
NEt,PhI.I4
C.sH^N
....
68
?>
>r-
u
pentiodide
Tetramethyldiamidotoluene
Me.(NMei)2=1.2.5
C12H21IN2
160
Wurster and Riedel
B., T2;'J802
38, 109
methiodide
Ethvlmethylquinoline meth-
N.Et.Me=a,/31/32 ;
0I3HI6IN
196 p.d.
Dobner and Miller
B., 17," 17 15
46, 1375
iodide
E ih eny Idiethyltoluy leneami-
• •••
C13H19I3N2
Ill
A., 210, 376
dine triiodide
Methylbenzylpiperyl ammo-
C5H10N.C7H7+Met
C13H201N
145
Schotten
B., 15,423
42, 982
nium iodide
Triethylbenzylamine perio-
NEt3(CH2Ph)I3
C13H.,2I3N
87
Ladenburg& Struve
B., 10, 46
dide
/3-Naphthoquinoline methio-
C13H9N.MeI
C14H12IN
200-205
Skraup & Cobenzl
M. C., 4, 436
44, 1011
dide
Diiododibenzylamine
(C6H,I.CH2)2NH=(1.4).2
C14H13I2N
76
Mabery & Jackson
B., 11, 58
34, 422
Uibenzylamine hydriodide ....
(C6H5.CH2)2NH.HI
C14H,r.IN
....
224
Limprieht
A., 144, 304
vi., 337
Dimethykliethyldiamidoben-
C6H4.NMe2.NEtj+2MeI
C14HS6I3N2
218
Lippmann &Fleiss-
M. G, 4, 788
46, 178
zene dimethiodide
3*1.4
ner
Methylacridine methiodide ..
C13H8NMe.MeI
C15H14IN
185 d.
Bernthsen*>
A., 224, 1
46, 1356
Dimethylanhydrobenzodi-
C6H4.N : CPh.NMe.,1
015H15IN2
280
Hiibner.-
A., 201, 365
42, 505
amidobenzene iodide
1 1
Diiuethylanhydrobeuzodi-
C'r,H4 N : CPh.NMe,I3
*--i5Hi5I3N2
140-5
ii
)>
11
amidobenzene triiodide
1 ___ 1
Azobenzenetrimethylam mon -
Ph.N2.C6H4.NMe3I
C16H18IN3
173-174
Berjiv
B., 17, 1402 ;
46, 1148 ; 48,
mm iodide
C.C. [1884], 871
660
3-Methylquinoline amyl-
C10H9N.C5HUI
C15HMIN
....
215
Dobner and Miller
B., 18, 1643
iodide
Benzenyldimethdiamidoto-
....
<'16H17I3N2
101
Hiibner
A., 210, 368
luene triiodide
Flavoline methiodide
N.Ph.Me=n,31n2 ;
C17H16IN
185 d.
Bernthsen an d Hess
B., 18, 34
48, 559
Methyldiphenylpyrazene
C3HN2Ph2Me+MeI
C17H17IN,,
187
Knorr and Blank
B., 18, 315
48, 556
methiodide
lao-methyldiphenylpyrazene
)T
»
....
192
»i
B., 18, 935
48, 811
methiodide
Trimethylanthrammonium
C14H9Me3NI
C17H18IN
....
215 d. ; u. c.
Bollert
B., 16, 1637
44, 1139
iodide
Diethylanhydrobenzoyldi-
C.H4.NEt2I.CPh : NI,
C17H19I3N2
154-155
Hiibner and Simon
B., 12, 1342 ;
36, 923
amidobenzene triiodide
A., 210, 358
)» )i
}»
»J
....
154-155
Hiibner & Pichler
B., 10, 1722
34, 145
Tetramethylbenzidine
MesN.C0H4.C6H4.NMe.JT=
C17H23IN2
2G3
Michler and Pat-
B., 14, 2163;
42, 199 ; 46,
methiodide
(1.4)2
.
tinson
B., 17, 117
747
432
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Benzenyldiethyltoluylene-
....
C19H21I3N2
128-129
A., 210, 373
amidine triiodide
Diethylene-ethyldiamidodi-
....
c19HBm,
100
J. [1858], 353
iv., 456
phenyl iodide
?-Diquinoline luethiodide ...
(.C9NH6)2=/32 ;,-,-«.,;«,
C19H15IN2
126 ; sf. 83
Fischer
M. C., 6, 546
48, 1247
°-
= '
»
280-286 d.
Weidel
M. C., 2, 499
46,70
Dimethylbenzoylpseudo-
(C,HMe3Bz.NMe2+MeI
C19H2JN
187 d.
Frohlich
B., 17, 2675
48, 154
cumidine methiodide
= 1.3.4.2.6
Diquiuoliue dimethiodide ..
C)8HI2N3.2MeI
C20HlbI2N2
a. 290
Fischer
M. C., 5, 417
48, 399
» >i
(.C9NH6)2=(/32 ; „,),
M
300 d.
Koser
B., 17, 1819
46, 1372
Cinchine methiodide....
C.jH^Nj-Mel
Cj.HalN,
186
Comatock & Kouigs*
B., 18, 1221
48, 910
Nicotine sesquiiodide
(CIOH14N2)2I3
CsoH^N,
100
Wertheim
iv., 47
Triiodotribenzylamine
(C6H4I.CH2)3N=(1.4)3
U21H13I3N
....
114-5
Mabery & Jackson
B., 11, 57
34, 422
Dimethylcyanine iodide
C19N2H13Me2I
C?1H19IN2
291
Hoogewevff& Dorp
R. J., 2, 317
48, 674
Phenylbenzaldehydine ethio-
C6H4(NC7ps)2+EtI=1.2
C22H21INS
....
211-213
Ladenburg and
B., 11, 1654
36, 235
dide
Engelbrecht
Tolubenzaldehydine methio-
C6H3Me(N.C:II,)2+MeI=
»
209 d.
Ladenburg
B., 11, 594
34, 572
dide
1.3.4
Diquinoline diethiodide
(.CfcNH,),^ ; a,),
CS.HSJI.N,
270 d.
Roser
B., 17, 1819
46, 1372
Dimethamidotriphenyl- •*
Ph2CH.C6H4.NMe2+ Mel
C22H24IN
....
184-185
Fischer and Roser
B., 13, 675 ; A.,
38, 661 ; 40,
methane methiodide
206, 115, 157
588
Benzenyldiisoamylphenylene-
....
C23H21I3N2
111-112
A., 210, 363
ainidine triiodide
Tolubenzaldehydine ethio-
C6p3Me(NC7H6)2+EtI=
C23H23IN2
180-181
Ladenburg
B., 11, 593
34, 572
dide
1.3.4
Methylamarine methiodide
....
J)
246
Claus and Elbs
B., 13, 1419
38, 882
Diethylcyanine iodide
C19jN2H13Et2I
)»
271-273
Hoogewerff & Dorp
R. X., 2, 317
48, 674
Tolubenzaldehydine ethio-
C6H3Me(NC7H6)2+EtI,I2=
^23 "23 ^3^ 2
123-135
Ladenburg
B., 11, 593
34, 572
dide+I2
J.3.4
Ethyltribenzylamine iodide
(C6H5.CH2)3N.EtI
C23H26IN
....
190
Vasca-Lanza ,
B.,-7, 82
Diamylanhydrobenzoylami-
C6H4.N(C5H11).)I.CPh:NI2
C23H31I3N2
....
111-112
Hiibnerand Simon
B., 10, 1720 ;
34, 145; 36,
dobenzene triiodide
i i
B., 12, 1344
923
TetramethdiamidotripheTiyl-
Ph.CH(C6H4.NMe2)2+]VreI
^25*r*3^Ii^'2
218-222
Fischer
B., 12, 1686; A.,
38, 40
methane methiodide
206, 127, 151
!> J!
»»
)l
cf. A., 217,
231 d.
Doebner
B., 13, 2228
40, 166
256
Methane triquinoil+'HI
CH(C9H.NI)S
028H22I3N3
65
Rhoussopoulos
B., 16, 202
44, 600
Quinoline iodooyaniae
i
028H35IN2
100 d.
Nadler and Merz
J. p., 100, 129
vi., 430
Tetramethdiamjidopropyltri-
Pr.C6H4.CH(C6H4.NMe.)2
asH39T2N2
200
Zeigler
B., 13, 787
38, 640
phenylmethane methiodide
- + MeI
Benzylamarine methiodide
C21Hl?(CH2Ph)N.!.MeI
C29H27IN3
....
130 u. c.
Clans & Kohlstock
B., 18, 1855
48, 1133
,, ethiodide
C21H17(CH2Ph)N2.EtI
CaoHoglN.j
182 u. e.
n
B., 18, 1854
»
(15.) CHIP, CHI As, and CHISb.
Tolylphosphonium iodide ...
C6H4Me.(PH2.HI)=1.4
C7H10IP
340inCO2(?)
Michaelis & Paneck
A., 212, 235
43, 963
Trimethylphenylphosphon-
NMe3PhI
C9H14IP
205
Ananoff
A., 181, 363
ium iodide
Dimethylethylpheuylphos-
....
C10HJ6IP
• >».
137
,»
A., 181, 362
phonium iodide
Trimethyltolylphosphonium
C;6H4Me.(PMeJl) = 1.4
»
255
Czimatis
B., 15, 2015
44, 57
iodide
Methyldiethylphenylphos-
PMeEtjPhI
CHH18IP
95
Ananoff
B., 8, 49£ ; A.,
28, 1204
phoiiium iodide
181, 358
TriPthylphenylphosphoniuni
PEt,,PhI
CISH20IP
....
115
. »
>»
H
iodide
Methyldiethyltolylphospho-
CfiH4Me.(PEt,Mt-I)=1.4
)>
137
Czimatis
B., 15, 2016
44, 58
nium iodide
COMPOUNDS CONTAINING FOUR ELEMENTS.
433
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J.Ch. Soc.
Methyldiethylxylylphosphon-
C6H3Me2.(PEtjMeI)
C13H22IP
SO
Czimatis
B., 15, 2016
44, 58
ium iodide
Diphenyldimethylphosphon-
PMejPhJ
C14H16IP
241
Michaelis and Link
A., 207, 210
42, 306
ium iodide
!) !!
n
*J
245
Michaelis and Coste
B., 18, 2117
Triethylxylylphosphonium
C6H3Mea.(PEt3I)
C14H24IP
....
136
Czimatis
B., 15, 2016
44, 58
iodide
Ethylene hexethyldiphos-
C2H4 : PEt6I.:
Ci4H34I2P2
....
231
As., I, 188
iv., 622
plionium iodide
Diphenylmethylethylphos-
PMeEtPh2I
C15H13IP
....
181
Michaelis and Link
A., 207, 212, 215
42, 306
phonium iodide
Diphenyldiethylphosphon-
PEt,Pli2I
C16H2(^P
204
ji
A., 207, 214
n
ium iodide
Naphthyltriethylphosphon-
PEt/C..!!.)!
C16H22IP
....
209
Kelbe
B., 11, 1502
36, 68
ium iodide
Triphenylphosphonium
PHPh3I
CI8H16IP
cf. B., 15,
215 p. d.
Michaelis & Soden
A., 229, 334
48, 1134
iodide
803
Triphenylmethylphosphon-
PMePh3I
C19H18IP
165-166
Michaelis & Gleich-
B., 15, 803
42, 1062
ium iodide
mann
Triphenylethylphosphonium
PEtPh3I
C20H20IP
....
165
'Michaelis & Soden
A., 229, 334
48, 1134
iodide
Triphenylpropylphosphon-
PPr'Pli,!
PnHMIP
201-5
»j
•«
48, 1135
ium iodide
Triphenylisopropylphosphon-
PPr^PhjI
*»
+2ILjO
191
»i
J)
»
ium iodide
Tripheny] isobutylphosphon-
PBu0Ph.tI
^H24IP
176
~*i
Ji
i)
ium iodide
Triph eny lisoamylphosphon-
P(C5Hu)Ph3I
^tflnff
174
i>
«
i»
ium iodide
Triphenylbenzylphosphon-
P(CH3Ph)PhJ
•C-J5-H.J2IP
253
ij
»
»
ium iodide
Methylenehexaphenylphos-
CH.2(PPh3I)2
C3:H32I3P2
230-231 d.
Michaelisi& Gleich-
B., 15, 804
42, 1062
phonium iodide
mann
Arsemnethyldiiodide
AsMeI2
CH3I2As
a. 200
25
Baeyer
A., 107, 285
i., 401
Arsendimethyliodide(caeodyl
AsMe2I
C2H6IAs
a. 100
b. — 10
Bunsen
A., 37, 35; 92,
i., 407 .
iodide)
362 .
Tetramethylarsenium iodide
AsMe4I+AsI,,
C4H12I4As.2
170
....
Cahours
C. R, 49, 87
i., 410
+AsI3
Arsenphenyl diiodide
AflPhI2
C6H5I2As
....
Liquid
Michaelis & Schulte
B., 14, 913 ; 15,
40, 723
1953
Phenyltrimethylaisenium
AsMe3PhI
C9H14IA«
....
244
Michaelis and Link
A., 207, 205
42, 306
iodide
Diidoarsenobenzene
C6H5.AsI.AsI.C6H5
C12HWI2A83
crystalline
Michaelis & Schulte
B., 14, 913; 15,
40, 723
1953
Phenyltriethylarsenium
AsEtjPhI
C.jH^IAs
cf. A., 201
112-113
Coste and Michaelis
B., 10, 622 ; 11,
33, 453; 36,
iodide
213
1883
162
Diphenyldimethylarsenium
AsMe2Ph2I
C14H16IAs
109
Michaelis and Link
A., 207, 204
42, 305
iodide
Diphenylethylmethylarsen-
AsMeEtPh2I
C15H18IAs
170
»
A,, 207, 196
»>
ium iodide
Uiphenyldiethylarsenium
AsEt2Pb2I
C16HMIA8
....
184
....
A., 201, 236
iodide
Stibtriethyl diiodide
SbEt3I2
C6H16I2Sb
cf. A., 97, 331
70-5
Buckton
13, 116
1., 342
„ „
>J
»1
....
70-5
Lowig& Schweitzer
J., 75, 339
Stibtritolyl „
(C6H4Me)3SbI,=(1.4)s
C21H21I2Sb
182-5
Michaelis&Genzken
B., 17, 925
46, 1130
434
ORGANIC COMPOUNDS.
16. CHOS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts Diet.
& J. Ch. Soc.
Thioformic acid
H.CO.SH
CH2OS
cf. A,, 91, 125
120
Limpricht
A., 97, 361
v., 778
Methylsulphonic acid
CH3.S03H
CH403S
d. 130
Richter
R. K. T.
Methylic hydrogen sulphate
MeHSO4
CH4O4S
....
Liquid —30
Claesson
J. p. [2], 19, 240
36, 776
Thiacetic acid
Me.CO.SH
C2H4OS
95
....
....
v., 771
„ „
)J
»
93
....
Ulrich
J., 12, 355
Sulphacetic acid
HO3S.CH2.COOH
CSH406S
cf. A., 52, 278
62
Melsens
A. C. [3], 5,392;
v., 475
10, 370
„ „ .... ...
J)
))
....
68-70; 72
Carl
B., 14, 65
Ethionic anhydride
c2H4:(so3)2
C2H406S2
80
Magnus
P. A., 47, 509
ii., 523
Dimethyl sulphoxide
Me2SO
C2H6OS
Solid
Saytzeff
A., 144, 148
vi., 827
„ sulphone
Me2SO2
C2H602S
238
109
i)
D
vi., 827
Dimethylic sulphite
Me2SO3
O2H6O3S
121-5
Carius
A., 110, 219
v., 556
,, sulphate....
Me2SO4
C2H604S
188
Dumas and Peligot
A. C. [2], 58, 32
v., 626
Ethylene disulphonic acid ...
HSO3.CH2.CH2.SO3H
C2H,06S2
....
94
Husemau
A., 126, 272
v., 566
„ trisulphonic acid ...
HS03rCH2.CH(S03H)2
C2H609S3
80-1 10 pd.
Monari
B., 18, 1346
48, 970
„ dithiocarbonate ...
C2H4;COS2
C3H4OS,,
31
A., 126, 269
Mythylic thiacetate
....
CjHtOS
62-68
B. S., 25, 562
>» „
CH3.(X).SMe
)»
95-86
Wallach&Bleibtreu
B., 12, 1062
36, 786
Trimethylene oxysulphide ...
....
C3H6OS2
+iH20
80
Bartoli & Papasogli
G. I., 13, 287
46, 170
Dimethylic dithiocarbonate...
CO(SMe)2
J>
169
Liquid
Schmitt and Glutz
B., 1, 169
„ xanthogeiiiite ....
MeO.CS.SMe
JJ
167-168
Salomon
J. p. [2], 7, 114
27, 363
» jr
»
JJ
170-172
....
Cahours
A. C. [3], 19, 160
v., 501
Thiolactic acid
CH3.CH(SH).COOH
C3H602S
b. 100
Schacht
A., 129, 1
iii., 462
» it ••••
)»
n
....
141
Bottinger
B., 9, 1062
30, 624
» rt *>«•
)?
jj
....
141-142
»
A., 188, 321
34, 33
Methyl ethyl sniphon«
Me.SO2.Et
C3H802S
....
36
Beekmaim
J. p. [2], 17, 455
36, 39
Methylic ethylic sulphite- ....
MeEtSO;,
CjHsOjS
140-141-5
....
Carius
A., 111,93
v., 55 6
„ ethylsulphonate ...
C2H5.S03Me
197-5-200-5
....
J. [1870], 728
Isopropylsulphonic acid
Me2.CH^O3H
»
....
b. 100
Claus
B., 5, 660
Thiosuccinyl ....
CO.CH2.CH2.CO.S
C4H4OaS
31
Wesilsky
B., 2, 521
vi., 1042
Thiophene sulphiuic aeid ....
C4SH3.S02H
C4H402S2
....
67
Weitz
B., 17, 800
46, 1131
/3-thiophene sulphonic acid ....
C4SH3.SO,3
C4H403SS
....
Cryst.
Langer
B., 18, 554
48, 765
Thioglyoxylic acid
...
C4H4068
....
78-82
—
A., 198, 212
j8-thiophene disulphonic acid
C4SH2(S03H)2
C4H406S3
....
Cryst.
Lauger
B., 18, 553
»
Sulphethylic ether
....
C4H6OS3
....
120-123
Malaguti
A. C. [2], 70, 338
a, 541
Thiacetic anhydride
(Me.CO)2S
C4H602S
121
....
Kekulo
A., 90, 311
v., 772
>i »
)1
))
121
....
Saytzeff
Z. C. [2], 4, 642
vi., 20
Acetyl disulphide
(Me.CO)2S2
C.HeO^,
....
20
Kekul6 and Lin-
A., 123, 278
v., 772
nemann
Thiodiglycollic acid
S(CHa.COOH)5I
C4H604S
....
126
Wisliscenus
Z. C. [1865], 621
v., 776
»j ?» ••>•
»
J)
....
ISO
Schulze
Z. C. [1865], 77
»
» j, ....
»
n
129
Loven
B., 17, 2818
Dithiodiglycollic acid
S2(CH2.CX)OH)2
C4H604S2
....
100
Claesson
B., 14, 409
40, 580
Sulphoue diacetic acid
SO2(CH2.COOH)2
C4H606S
d. 200
182
Lov^n
B., 17, 2819
48, 241
Ethylic thiacetate
CH3.CO.SEt
C4HSOS
abt. 80
....
Kekul6
A., 90, 313
28, 259, 761 ;
v., 772
)) 5»
y>
I)
114-116
....
Michler
B., 7, 1313 ; A.,
28, 258, 761
176, 182
1 », .... ....
....
)J
115-117
....
Wallach and Bleib-
B., 12, 1062
36, 786
treu
J) „ ....
.«.
))
117
Saytzeff
Z. C. [2], 14, 642
vi., 20
Thiobutyric acid
C3H-.CO.SH
j)
130
Ulrich
A., 109, 280
i., 694
Aldehyde + thioaldehyde
C2H40+C2H4S
»
35 d.
—2
Pinner
B., 4, 258
24, 383; vii., 37
Ethylic methylic dithiocar-
....
C4H8OS2
179
»»
Chancel
A. C. [3], 15, 468
v., 500
bonate
Ethylic methylic xanthoge-
MeO.CS.SEt
J)
184
Liquid
Salomon
J. p. [2], 7, 115
27, 362
nate
» » »
MeS.CS.OEt
)T
184
»
J. p. [2], 7, 116
)>
Ethylic thioglycollate
CH2(SH).COOEt
C4H802S
a. 155 d.
Liquid
Claesson
A., 187, 124
32, 595
COMPOUNDS CONTAINING FOUR ELEMENTS.
435
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
C4H8O2S
145
Couerbe
A., 40, 297
Ethylic sulphonacetic acid ...
Et02S.CH2.COOH
C4H804S
Liquid
Claesson
B. S. [2], 23, 144
29, 568
Thiodiethylene glycol
HO.C2H4.S.C2H4.OH
C4H1002S
....
60
Carius
A., 124, 263
ii., 582
Diethyl sulphone
EtjSO2
»)
2J#
70
Oefele
A., 127, 370
ii., 968 ; vi.,
598
» !>
»
n
„.
70
Frankland and
B., 12, 845
35, 246
Laurance
Ethylic thioethylsulphonate
Et.SO2.SEt
C4H10O2S2
130-140 d.
Liquid
Otto
R, 15, 122
42,832
Diethylic sulphite
(EtO)aSO
C4H1003S
150-170
....
Ebelmann aud
A. C. [3], 17, 67
Bouquet
,, „
JJ
»i
abt. 150
Ogier
C. B., 94, 446
42,696
v 1,
»
»)
160-3
....
Pierre
C. R, 27, 213
v., 554
,, J!
i»
i»
161-3
Carius
J. p. [2], 2, 285
11 1>
Jl
»
161
....
Michaelis & Wagner
B., 7, 1074
28, 139
Ethylic ethylsulphonate
CjHs.SOj-OEt
»»
207
11
»
28, 140
„ ,,
)1
n
207-5 (746-9)
Carius
J. p. [2], 2, 269
>i :>
»
i»
213-213-5 c.
Nasiui
B., 15, 2884
(761)
11 l!
)>
»
2134
Kurbatow
A., 173, 7
Diethylic sulphate
(EtO^Oj
C4H1004S
110-120
....
Wetherill
A., 66, 117
v., 625
„ „
J)
)I
120-5 (45) ;
]
falls 2°-5
U.— 24-5
Villiers
C. R, 9, 1291
38, 797
for each (5)
J
„ „
JJ
»»
SOS p. d.
Liquid
Claesson
J. p. [2], 19, 231;
36, 776 ; 38, 28
B., 12, 1720
3-Thiophenic aldehyde
CH:CH.S.CH:C.COH
C5H4OS
-•
Liquid
Peter
B., 18, 537
48, 765
n- „ acid
S.CH : CH.CH : C.COOH
C5H402S
258 c.
IIS
Meyer and Keis
B., 16, 2174
46,46
„ „ ,,
»
A
118
Peter
B., 18, 542
48, 765
., „ „ .... ....
»)
n
.
118
Bonz
B., 18, 2309
ft- n 11
CH : CH.S.CH : C.COOH
L J
9'
„..
121 ; a.s. 123
>i
B., 18, 2305
,, „ „
)»
r»
125-5
11
B., 18, 2306
,, „ „
»?
j^
124-5-125
Nahnsen
B., 18, 2304
n 11 j>
»>
T?
....
124-5
Peter
B., 17, 2646
48, 142
„ „ „
»»
n
124-5
ji
B., 18, 542
48, 765
„ „ „
Ji
»
126-5
11
B., 17, 2646
48, 51
„ „ ?i
)>
i?
126-127
Paul and Tafel
B., 18, 456
48, 764
„ „ „
n
»»
260 c.
129 c.
Nahnsen
B., 17, 2194
Propylic thiacetate
CH3.CO.SPr"
CjH.oOS
135-137
....
Wallach & Bleibtreu
B., 12, 1062
36, 786
Isopropylic „
CH3.CO.SPr0
»
124-127
....
11
J)
11
Diethylic dithiocarbonate ....
(EtS)jCO
C^j.08,
196
Liquid
Solomon
J. p. [2], 4, 433
26, 620
)> i>
n
))
196-197
Schmidt and Glutz
B., 1, 167
„ xanthogenate
EtS.CS.SEt
n
200
Liquid
Debus
A., 75, 125
v., 500
ii v
H
j>
200
Solomon
J. p. [2], 4, 445
26, 620
11 11 ••••
»
»>
210-212
....
Zeise
A., 55, 310
,, thiocarbonate
EtS.CO.OEt
CSH10O.S
150-156
Liquid
Solomon
J. p. [2], 4, 436
26, 617
M ii
n
)»
156-159
....
Liebermanu
A., 207, 121
42, 298
11 11 •
EtO.CS.OEt
1)
161
Liquid
Solomon
J. p. [2], 4, 441
26, 620
11 »!
»
»)
162
Debus
A., 75, 136
Ethylic thiolactate
CH3.CH(SH).COOEt
1)
150-160
....
Lov6n
B., 16, 790
|3-Thienylglyoxylic acid
C4SH3.CO.COOH
C6H403S
....
86 ; sf. 78
Peter
B., 18, 537
48, 764
Thiophene dicarboxylic acid
C4SH2(COOH)2= ?
C6H4O4S
....
n. f. 295
Bonz
B., 18, 2307
» 11 11
=1.2.5
))
w. m. 350
Messinger
B., 18, 567
48, 767
Phenol sulphhydrate
C6H4.OH.SH =1.2
O.H.OS
216-217
5-6
Haitinger
M. C., 4, 170
44, 989
(750-7)
Acetothienone
C4H3S.CO.Me
1>
213-5 c.
1.— 15
Peter
B., 17, 2644
48, 141
Benzene sulphinic acid _ „..
Ph.SO2H
C,H.O,S
68
Otto and Ostrop
A., 141, 365
vi., 275
11 11 »! •"•
)l
11
....
b. 100
Kalle
A., 119, 153
v., 565
Methylthiophene carboxylic
CH : CMe.S.C(COOH) : CH
1 1
11
sb. 120
142
Paal
B., 18, 2254
48, 1206
acid
.
•
3 K 2
430
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Thiopyroracemic acid
....
C.HAS
....
87 d.
Bottinger
B., S), 404; A.,
30, 70 ; 34, 33
188, 325
Diethylic trithiodicarbonate
S(CS.OEt)2
CjH^OiSj
....
55
Welde
B., 9, 1045 ; J. p.
30, 624 ; 32,
[2], 15, 45
315
„ dioxytetrathiocar-
02(CS2Et)2 (?)
C6H,0O2S4
....
28
....
A., 72, 5 ; 82, 253
bonate
„ thioxalate
COOEt.CO.SEt
C6H1003S
211u.c.;217c.
....
Morley and Saiut
43, 401
Thiodilactic acid
S(C2H4.COOH)2
C6H1004S
M«f
125
Lovuii
B., 16, 790
Sulphone dipropionic acid ....
SO2(CHMe.COOH)3
C6H1006S
..«
155-156
51
B., 17, 2822
48, 241
Isobutylic thiacetate
CH3.CO.SBuP
C6H12OS
148-150
....
Wallach & Bleibtreu
B., 12, 1062
36, 786
Isoamylic xanthogenate
C5HnS.CO.SH
C6H,2OS2
187
Liquid
Johnson
5, 142
i., 206
Duplothiacetone „
»
183-188 c.
....
Wislicemis
Z. C. [2], 5, 534
vii., 12
?
....
»
Hit
43-56
....
J. [1866], 422
?
.„.
»
....
45-60
B. S., 38, 129
Ethylic ethylthioglygollate....
EtS.CHj.COOEt
C6H1202S
187-189
Liquid
Claesson
B., 8, 121
29, 567
?
+H20
C6Hi2O,>S4
180-185
80-82
A. C. [5], 17,307
Dipropyl sulphone
(CH3.CH2.CH2)2SO2
C6H1402S
....
29-30
Spring&Winssinger
B., 16, 329
Di-#-isopropyl sulphone
(Me2CH)3.SO2.
)»
36
Beckmann
J. p. [2], 17, 459
36, 38
Ethylene diethyl „
C2H4 : S02Et2
»
136-5
j)
J. p. [2], 17, 469
36, 39
„ ,, sulphoxide
C2H4(SOEt)2
C,H14OA
170
Ewerlof
B., 4, 717
24, 1189
Glyceric sulphaldehyde
(C3H6S20)2H20.
C6H1403S4
180-185
sf. 80-82
Benard
C. R., 82, 562 ;
30, 64 ; 38, 25
A. C. [5], 16, 289
n-Thiobenzoic acid
C6H5.COSH
C7H6OS
....
24
Engelhard t,
Z. C. [2], 4, 3.^3
vi., 324
Latschinoff, and
Malyscheff
Hydrothiobenzoic acid
C6H4.SH.COOH =1.3-
C7H602S
146-147
Frerichs
B., 7, 793
27, 9iX)
Sulphobenzoic acid
C6H4(S03H)(C02H)=1.3
C7H606S
....
80
Kammerer & Cai ius
A., 131, 156
vi., 323
>* »
= 1.4
»r
....
abt. 200 A.
Rerosen
Z, C. [2], 7, 297 ;
24, 1053; £9,
A., 178, 275
258
11 :r .—
!! >r
»
....
abt. 200
Wiesinger & Voll-
B., 10, 1715
brecht
» n
= 1.2
»
240 d.
Fahberg & Eemsen
B., 12, 473
Sulphosalicylic acid ....
COOH.OH.S03H=1.2.?
C7H606S
120
Mendius
A., 103, 39
v., 525
Sulphohydroxybenzoic acid....
= 1.3..?
)J
208
Senhofer
A., 152, 102
vi., 890
Disulphobenzoic acid
COOH.(S03H)2=1.2.4
C7H608S2
a. 285
Fahlberg
A. C. J., 2, 188
40, 818
Methylphenyl sulphone
CjH5.SOj.Me
C7H802S
88
Michael & Palmer
A. C. J., 6, 253
48, 536
» »
J1
)r
....
88-89
Otto
B., 18, 156
48, 536
Toluene sulphinic acid
C6H4Me.SOjH=1.4
)j
....
84
Otto & Damkohler
J. p. [2], 30, 321
48, 53.8
» » ir
53 )»
T)
85
Otto
B., 15, 131
5) n »
TJ )i
))
....
85
Otto and Eossing
B., 18, 2505
n » »
V »»
)J
86
Otto
Z. C. [1866], 655
v., 861
Ethylic 0-thiophenate
CH : CH.S.CH : C.COOEt
))
218 c.
Liquid
Nahnsen
B., 17, 2195
48, 52
„ thiocarbacetacetate....
s : c : CAc.cooEt
C7H803S
sf. 152
150-162
Norton and Oppen-
B., 10, 703
heim
Toluene sulphonic acid
C,H4Me.SO,H=I.2
»
....
91-92
Hiibner and Miiilei
Z. C., 14, 299
24, 1055
Cresol sulphonic acid
Me.OH.SO3H=1.2.4
C7H804S
....
80-81
J. [1879], 758
it » ,,
„ =1.4.6
n
anhydrous
187-188 ;
Jenssen
A., 172, 237; B.,
27, 480; 28, 77;
+5H20
98-5
7,57
vii., 932
Toluene trisulphonic acid ...
Me.(S03H)=?
C7H809S3
+6H2O
145
Claessou
B., 14, 308
40, 429
2
....
C7H12O3S2
165
Cech and Steiuer
C. R., 81, 155
28, 1255
Isobutylic ethylic xantho-
EtS.CS.OBuS
C7H14OS2
227-228
....
Mylius
B., 5, 975
26, 266
genate
Ethylic isobutylic thiocar-
Bu0S.CO.OEt
C7H1402S
190 193
73
B., 6, 313
26, 872
bonate
Isobutylic ethylic thiocar-
EtS.CO.OBuS
3)
190-195
1)
jj
JJ
bonate
Isoamylethyl sulphoxide
Et(C5Hu)SO
C7H18OS
s. —16
Saytzetf
A., 139, 354
vi., 123, 599
£-isoamyl ethyl sulphone ....
(Me2CH.CH2CH,).S02.Et
C7H1602S
270
13-5
Beckmann
J. p. [2], 17, 450
36, 38
Ethylic amylic sulphite
Et(C5Hn)S03
C,H1603S
210-225 p. d.
C'arius
A., 106, 291
v., 555
Thiophthalic anhydride
C6H4.CO.OCS=1.2
L J
CSH4O2S
284
114
Grsebe & Zschokke
B., 17, 1176 46, 1025
Isophthalosulphonic acid
(COOH),,SO3H=1.3.4
C8H607S
....
235-240
Jacobsen & Toinnes
B., 13, 1556 40, 50
COMPOUNDS CONTAINING FOUR ELEMENTS.
437
Name.
Constitution,
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Isophthalosulphonic acid
(COOH)2.S03H=1.3.4
C8H607S
....
fj$&44
Coale and Eemsen
A. C. J., 3, 204
40, 1038
» »>
= 1.3.5
))
257 d.
Tonnies
B., 13, 704
40, 50
Thiophenol acetate ....
C6Hs.SAc
C3H8OS
218-220 u.c.
...•
Michler
B., 7, 1312
28, 258
227-229 c.
„ ,, .... ....
»
»»
228-230 c.
Liquid
»
A., 176, 177
28, 761
Phenyl thioglycollic acid ....
PhS.CH2.COOH
C8H8O2S
....
43-5
Claesson
B. S. [2], 23, 441
29, 567
» » » ••••
1»
)»
61-62
Gabriel
B., 12, 1639
,, sulphinacetic acid ....
Ph.SO.CHj.COOH
C8H803S
74
Claesson
B. S. [2], 23, 446
29, 568
„ sulphonacetic acid ....
Ph.S02.CH.2.COOH
C8H804S
....
109
u
»
i»
ij )> »
»J
)>
110-111
Gabriel
B., 14, 834
40, 716
Dimethylic thiophene dicarb-
C4SH2(COOMe)2=1.2.5
))
142 ; sf. 137
Messinger
B., 18, 567
48, 767
oxylate
U Jl 11
)) 11
)1
....
145
>»
B., 18, 1639
48, 1052
?) )1 51
= I
J»
....
145-5
Bonz
B., 18, 2307
Sulphotoluic acid
COOH.Me.SO3H=1.4.2
C8H805S
cf.A.,172,32£-
190
Fittica
B., 6, 942
26, 1228
„ ,,
= 1.4.!
»
....
d. w. m.,
Fischli
B., 12, 617
36, 639
185-190
Acetothioxylene
C4SHMe2Ac=1.2.5.3
C8H10OS
223-224 c.
Liquid
Messinger
B., 18, 2301
48, 1205
Phenyl ethyl sulphone .... Ph.SOj.Et
CsH.oO^
41-42
Otto
B., 18, 161
48, 537
1J 1) >1 "••
5*
>J
42
Beck m aim
J. p. [2], 17, 457
36, 39
H » »1
J)
1»
a. 300
41-43
Otto
B., 13, 1274
38, 810
Metliyltolylsulphoue
C6H4Me.(SO2.Me)=1.4
)»
....
86-87
»
B., 18, 161
48, 537
Xylene sulphinic acid •
Me2.S02H=1.3.4
»
mixture ?
42-50
Jacobsen
B., 10, 1011
» 11 i>
= 1.2.4
T»
....
83
»
M
32, 601
» 11 i> ••••
=1.4.5
Jl
....
84-85
>!
B., 11, 22
34, 411
„ sulphonic acid
Me2 SO3H=1.3.4
C8HI00:,S
....
53 Limpricht
B., 18, 2188
Diethylic dithiosuccinate ....
(.CH,.COSEt)2
C8H14OjS2
270-271
Liquid
Seifert
J. p. [2], 31, 462
48, 1057
Ethylene ethyl xanthate
C2H4(S.CS.OEt)z
C8H1403S4
....
42
Welde
B., 9, 1047 ; J. p
30, 624 ; 32,
[2], 15, 55
137
Diethylic thiodiglycollate ....
....
C8H1404S
240-250
....
Schulze
Z. C. [1865], 78
11 11
....
?J
267-268 <:
....
Wisliscenus
Z. C. [1865], 261
v., 777
„ dithioglycollate ....
(.S.CH2.COOEt)3
C3H1404S2
280 d.
Liquid
Claesson
B., 14, 411
40, 581
Sulplioue dibutyric acid
SO2(CHEt.COOH)j
C,H1406S
....
152
Loven
B., 17, 2824
48, 241
„ diisobutyric acid ....
SOj(CMe.,.COOH)2
Jj
188
n
B., 17, 2825
»
Dibutyl oxysulphide
(Me.CH2.CH2.CH2).,SO
C8H1SOS
cf.B.,7, 1650
32
Grabowsky
A., 175, 349
28, 629, 1 1 75
Diisobutyl oxysulphide
(Me2CH.CH2)2SO
r»
....
41
Saytzeft' and Gra-
A., 171, 257
27, 565
bowsky
i» « >••-
»
»
68-5
Beckmann
J. p. [2], 17, 439
36, 37
„ aulphone....
(MejCH.CH2)2SOj
C8H1803S
205
17
i>
J. p. [2], 17, 448
36, 38
Dibutyl sulphone
(Me.CHj.CHj.CH.-X.SO.
IT
cf.B.,7, 1650
43-5
Grabowsky
A., 175, 350
28, 629, 1175
Thiocinnamic acid
Ph.cn : CH.COSH"
C9H8OS
250 p.d.
....
Engelhardt, Latschi-
Z. C. [2], 4, 359
vi., 470
notf, & MalyschefF
Sulphocinnamic acid
(S03H)(CH:CH.COOH)
C9H905S
+5H2O
100
Rudneu
A., 173, 12
28, 76
=1.4
Ethylic thiobenzoate
Ph.CO.SEt
C9H10OS
242-243
Liquid
Engelhardt, Latschi-
Z. C. [2], 4, 356
vi., 325
noff, & Malysclieff
Benzylthioglycollic acid
Ph.CHj.S.CHj.COOH
C9H100.,S
58-59
Gabriel
B., 12, 1641
38, 34
Sulphotolylene ethylene
J)
....
75-76
Otto
A., 143, 205 ;
v., 861 ; vi.,
Z. C. [1866], 655
1060
a-Hydroxy a-thiophenylpro-
PhS.CMe(OH).COOH
C9H1003S
v. 100
87
Baumann
B., 18, 263
48, 514
piouic acid
Toluene sulphonacetic acid ....
Me.(SOj.CH2.COOH)=1.4
C9H10O4S
117-118-5
Gabriel
B., 14, 834
40, 716
» »i »
» »
n
117-119
Otto
B., 18, 161
48, 537
Phenylpropyl sulphone
Ph.S02.Pra
C-yH^OgO
....
45
Michael & Palmer
A. C. J., 7, 65
48, 986
Tolylethyl sulphone
CH3.C6H4.S02.Et=1.4
))
55-56
Otto
B., 18, 161
48, 537
„ ,, ....
*> )»
5»
....
56
»
B., 13, 1276
38, 811
Mesitylene sul]>hinic acid ....
Me3.SO2H= 1.3.5.6
I)
98-99
Holtmayer
Z. C. [1867], 687
vi., 301
Pseudocumene sulphinic acid
=1.3.4.6
»
98
Budloif
B., 11, 32
34, 414
Hydroxyethyleue tolyl sul-
HO.C2H4.SO. .C6H4Me= 1 . 4
C9H1203S
54
Otto & Damkohler
J. p. [2], 30, 321
48, 538
phone
Ethylic toluene sulphonate ...
C6H4Me.SO3Et
M
....
32
....
v., 860
Mesitylene sulphonic acid ...
Me3.SO3H— 1.3.5.6
u -
+ 2HjO
77
Rose
Z. C. [2], 6, 341
it., 787
438
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Mesitylene sulphonic acid ...
Me3.SO3H=1.3.5.6
C9H1203S
abt. 100
Jacobsen
A., 145, 85
vii., 787
Sulphocamphoric acid
....
C9H1606S
160-165
Walter
A. C. [3], 9, 177
v., 490
Diisobutylic xanthate
Bu0O.CS.SBu0
C,H19OS2
247-250
....
Mylius
B., 5, 975
26, 266
Ethylic isoatnylthioglycollate
C6H11S.CH2.COOEt
C9H1802S
230
cf. B., 8, 122
Claesson
B. S., 23, 446
29, 568
a-Naphthalene sulphinic acid
C10H7.S02H
C10H802S
High temp.
Gessner
B., 9, 1500
31, 315
/3- „ sulphonic acid
JJ
„
105
11
B., 9, 1502
31, 316
"- » 11 11
C10H7.S03H
C10H8O3S
85-90
....
....
v., 560
a-Naphthol sulphonic acid ...
C10H6(OH).SOSH
C10H804S
d. 100
Schaffer
B., 2, 93
n- „ ., „ ...
„
„
101 d.
51
A., 153, 293
vi., 860
«- „ „ „ -
n
„
101
Clcve
B. S. [2], 26, 241
31, 208
P" 11 11 11
1)
„
12Z
Ebert and Merz
B., 9, 611
30, 410
P~ 11 11 11 •••
M
„
cf. 39, 135
196
Sehaffer
A., 153, 296
vi., 860
Phenylene dithiacetic acid ...
C6H4(S.CH2.COOH)2=1.3
C10H10O4S2
....
127
Gabriel
B., 12, 1639
38, 33
Trimethylic thiophentricar-
C4SH(COOMe)3=1.2.3.?
C10H1006S
118
Messinger
B., 18, 2303
48, 1205
boxylate
Ethylic phenylthioglycollic
PhS.CH2.COOEt
C10H1202S
275-285
....
Claesson
B. S. [2J 23, 441
29, 567
acid
11 11 11
„
„
S76-278p.d.
M
„
Ethylic methylthiosalicylate
C6H4.OMe.COSEt=1.2
„
197-198 (80)
Liquid
Seifert
J. p. [2], 31, 462
48, 1058
Phenylsulphonethylic acetate
Ph.SO2.C2H4.OAe
C,10H,2O4S
....
1. -12
Otto & Damkohler
J. p. [2], 30, 171
48, 262
Ethylic phenylsulphonacetate
Ph.SO2.CH2.COOEt
„
45
Michael & Comey
A. C. J., 5, 116
46, 319
Diethylic thiophendicarboxy-
C4SH2(COOEt)2= 1.2.5
„
....
46
Messinger
B., 18, 1639
48, 1052
late
a-Cymene sulphonic acid
Me.Pr«.SO3H=1.4.2
C10H14O3S
50-51
Spica
B., 14, 654
40, 602
n* 11 11 11
= 1.4.3
„
86-87
11
B., 14, 635
„
?- „
Me.Pr.SO3H=1.3.2
„
86-87
„
B., 16, 792
P~ >) » >j
Me.PrP.SO3H=1.3.?
„
....
88-90
Kelbe
A., 210, 26, 31
42,300
a~ » )1 » «••
Me.Pr«.SO3H=1.4.3
„
....
130-131 u. c.
Glaus
B., 14, 2143
42, 196; 44, 320
" .1 11 n
=1 4.2
„
177
Fittica
B., 7, 1361
28, 266
tl~ n 11 11 ••••
11 n
„
....
220
Glaus
B., 14, 2143
a- „ ,, „
11 »
„
-H3H2O
78-79
„
M
11 11 n ••••
Me.Pr0.S03H=1.4.2
n
270
Fittica
....
40, 602
Isodurene sulphonic aeid ...
Me4.SO3H = 1.2.3.5.6
,,
+^H2O
100
Bielefeldt
A., 198, 381
38,37
Thianissic acid
C10H14O4S
+2H20
b. 200
Stiidler & Waehter
A., 116, 163
v., 774
Tsobutylic isoamylie xanthate
Bu0O.CS.SC6Hn
C10H20OS2
265-270 p. d.
c. f. B., 5, 975
Mylius
B. S., 19, 221
26, 266
Diisoamyl sulphoxide
(C5Hn)sSO
C10H22OS
....
37-38
Satyzeff
A., 139, 355
vi., 116
„ sulphone
(Me2CH.CH2.CH2)2SO2
CjoH^OjS
295 p. d.
31
Beckmaiin
J. p. [2], 17, 441
36, 38
Diamylic sulphite
(C5Hn),S03
C10H23O3S
230-250
Carius
A., 106, 291
v., 553
Phenyl thienyl ketone
Ph.CO.C4H3S
CnH9OS
abt. 300
55
Comey
B., 17, 791
46, 1168
•y-Sulphonaphthoie aeid
S03H.COOH=£a ;
CnH806S
182-185
Strumpf
A., 188, 7
34, 74
ft- n 11
11 =pa ;
„
218-222 d.
M
A., 188, 5
n
8- 11 11
=a/3;
11
229-230 d.
„
A., 188, 10
11
°- v ,1
11 =aa ;
„
230-240
Battershall
A., 168, 114 ;
vii., 838; 25,
Z.C. [2], 7, 673
699
"• 11 11
11 11
„
235
Strumpf
A., 188, 3
34, 74
Ethylic thiocinnamate
Ph.CH:CH.COSEt
CUH12OS
250 d.
MM
Z.C. [1868], 359
Toluene dithiacetic aeid
Me.CBH3(S.CH2COOH),,
CUH12O4S2
....
151-151-5
Gabriel
B., 12, 1640
38,33
Ethylic benzylthioglycollate
Ph.CH2.S.CH2.COOEt
275-290
>. ii
„
B., 12, 1641
38, 34
Diethylic sulphosalicylate ....
OH.COOEt.SO3Et=1.2.?
CnH14O6S
MM
56
Mendius
A., 103, 62
v., 526
Isobutyltoluene sulphonic
Me.Bu0.SO3H=1.3.?
C,,H16O3S
75-76
Kelbe and Baur
B., 16, 2559
46, 300
acid
Diisoamylic dithiocarbonate
CO(S.C5Hn)2
CnH22OS2
281
Liquid
Schmidt and Glutz
B., 1, 169
Diphenylene sulphone
C6H4.S02.CfH4
C12H,AS
....
230
....
A., 156,334; 174,
188
Diphenylene disulphone
caH4:(so2)2:c6H4
C12HSO4S2
....
a. 300
Grwbe
A., 179, 182
29, 579
Phenyl sulphone
Ph.SO2.Ph
C12H10O2S
100
Mitscherlich
P. A., 31, 628
v., 486
11 11
11
„
124
Beckhurts and Otto
B., 11, 2067
36, 242
11 11
,i
„
....
126
Stenhouse
P. R. S., 14, 351
v., 489
11 11
11
„
125-126
Knapp
Z. C. [2], 5, 41
vi., 276
11 11
11
„
....
128
Freund
A., 120, 81
v., 486
n D •«•• ....
"
»
....
138-129
Otto
A., 135, 154
>'
COMPOUNDS CONTAINING POUR ELEMENTS.
439
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Isophenyl sulphone
....
C12H1002S
....
230
Stenhouse
P. R. S., 18, 543
vi., 277; vii.,
941
Dipheny] sulphinic acid
C6H5.C6H4.S02H
11
....
d. 70
Gabriel & Deutsch
B., 13, 388
38, 477
Phenol sulphide
S(C6H4.OH)2
i>
143-144
Krafft
B., 7, 1165
28, 154
Phenylic thiobenzene sulpho
Ph.S02.SPh
C12H10O2S2
36
Otto
A., 145, 318
vi., 919
nate
» 11 »
)»
11
....
45
Pauly and Otto
B., 9, 1640
31, 463
» >• "
»
11
....
45
Otto and Rossing
B., 18, 2500
Diphenol disulphide
S2(C6H4.OH)2=(1.2)2
11
a. 200 d.
Liquid
Haitinger
M. C., 4, 166
44, 988
Phenylic phenylsulphonate...
C,Hs.S03Ph
C12H10O3S
....
35
Schiaparelli
G. I., 11, 65
40, 602
Oxysulphobenzide
S02(C6H4.OH)2
C12H1004S
....
293 or 239
Annaheim
A., 172, 28
27, 796
Diphenj'l disulphonic acid ....
(.C6H4.S03H)2
C12H10O6S2
....
72-5
Fittig
A., 132, 209
v., 565
Benzyl sulphone .... m.
(CeH^CH^O,
C12HU02S
150
Vogt & Henninger
A. C. [4], 25, 129
25, 1097
Ethylic thioisophthalate
C6H4(COSEt)2=1.3
C12H1402S2
....
easily
Luckenbach
B., 17, 1428
46, 1158
Isoamylic thiobenzoate
Ph.COSC5Hu
C]2H16OS
271 p. d.
Liquid
Engelhardt, Lats-
Z. C. [2], 4, 356
vi., 325
chinoff, and Maly-
scheff
Ethylic ethylpheuylsulphon-
Ph.SOj.CHEt.COOEt
Ci2H16O4S
....
62
Michael & Palmer
A. C. J., 7, 65
48, 986
acetate
Toluylene amylene disul-
C6H10:(S02)2:06H3Me
C12H16O4S2
35-36
Otto
A., 143, 223,
vi., 1060
phone
?
C12H,,O6S2
78-79
11
A., 143, 224
»1
Dipropylbenzene sulphourc
Pr«2.S03H=1.4.5
Ci2H18O3S
....
62
Korner
B., 11, 1864
36, 142
acid
Ethylic acetoacetate sul-
S(CHAc.COOEt)2
CuHi8O6S
....
80-81
Buchka
B., 18, 2092
48, 1200
phide
Diisoamyldisulphocarbonic
(C6HU0)2CS4
C12H2_,O2S4
187
....
Johnson
5, 142
v., 496
sulphide
Ethyleue diisoamyl sulphone
C2H4(S.006Hn)2
C12H,,6O2S2
....
14&-150
Ewerlof
B., 4, 717
24, 1189
Benzophenoue sulphone
C,H4.OO.C6H4.S02
C]3H8O3S
....
174-175
Beckraann
B., 8, 992
29, 583
11 »
)»
i»
186-187
11
B., 6, 1112
27, 157
Phenylic thiobenzoate
C6H5.COSPh
C13H10OS
._.
56
Schiller and Otto
B., 9, 1634
31, 468
Sulphobenzid carbonic acid....
Ph.SO2.C6H4.COOH=1.4
Ci3Hi0O4S
a. 300
Michael and Adair
B., 11, 119
34, 415
Phenyl tolylsulphone
C6H4Me.(S02.Ph)=1.4
<AsH,aO3S
124-5
11
B., 11, 116
11
»i i'
>i 11
11
124-125
Beckurts and Otto
E., 11, 2068
36, 243
Diphenylmethane disul-
C13H10(S03H)2
C13H12O6S2
59
Doer
B., 5, 796
26, 170
phonic acid
Ethylic allylphenylsulphon-
Ph.SO2.CH(C3H6).COOEt
GUH,6O4S
....
64-5
Michael & Palmer
A. C. J., 7, 65
48, 986
acetate
Erythrohydroxyanthraqui-
c6H4:(co)2:c,H2^o2.o
CJ4H606S
d. b. 100
Lifschutz
B., 17, 900
46, 1189
none sulphonic anhydride
1
Thiobenzoic anhydride
(Ph.CO)2S
C14H10O2S
....
48
Jngelhardt, Latschi-
Z. C. [2], 4, 357
vi., 325
noff, & Malyscheff
Benzoyl disulphide
(Ph.CO)3S2
CiiH10OjSj
...
120
Cloez
A., 115, 27
v., 775
11 ii
It
11
....
128
Sngelhardt, Latschi-
Z. C [2], 4, 358
vi., 326
nofF, & Malyscheff
Dithiohydroxybenzoic acid ....
S2(C6H4.COOH):,=(1.3);I
Ci4H1004S2
....
242-244
Trerichs
B., 7, 794
27, 990
11 I! •—
» »)
ji
....
242-244
Jiibner and Lipp-
Z. C-i 1870, 294
vii., 1115, 1155
inann
)! II ••••
» »
»
242
Griess
J. p. [2], 1, 103
vii., 168
Sulphobenzid-dicarbonic acid
S02(C6H4COOH)2=(1.4)2
CuHi0O6S
a. 300
Michael and Adair
B., 11, 121
34, 415
Benzylic thiobenzoate
C6H5.COS.CH2Ph
C14HIaOS
....
39-5
lichter
R. K. T.
Tolylic thiobenzoate
C6H6.COS.C6H4Me=1.4
n
....
75
Schiller and Otto
B., 9, 1636
31, 469
Diphenyl sulphacetic acid ....
Ph.C6H4.S.CH2.COOH
C14H12O2S
....
169-170
Gabriel & Deutsch
B., 13, 389
38, 477
Phenylmercaptane-benzoyl-
PhS.CPh(OH).COOH
C14H,2O3S
....
68-5
iaumaun
B., 18, 891
48, 749
forraic acid
Benzyl oxysulphide
(Ph.CH2)2OS
C14H14OS
....
130
Marcker
A., 136, 90
v., 859
ii ii
)>
))
....
33
Otto and Luders
B., 13, 1284
38, 811
Benzyl sulphone
(Ph.CH,)aSOj
014HuOaS
50
11
B., 13, 1277, 1284
»)
„ „
)»
»?
....
50
Vogt & Henninger
A. C. [4], 25, 129
vii., 185
Benzyltolyl sulphone
Ph.CH2.SO.,.C6H4Me=1.4
>i
f
44-145
Otto
B., 13, 1278
38, 811
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Tolyl sulphoue
(06H4Me)2S02=(1.4)2
C14H1402S
....
155-156
Otto and Grubert
A., 154, 193 ;
vi., 289 ; vii.,
Z. C. [2], 6, 33
185,1125
11 11 .... •••*
11 11
„
....
158
Beckurts and Otto
B., 11, 2068
n ,1 »..» «••'
„ „
„
404-5-40.V2
158
Otto
B., 12, 1177
36, 926
(714)
Phenylxylyl sulphone
Ph.SO2.C6H3Me.
„
80
Bjckurts and Otto
B., 1 1, 2069
36, 243
Toluene disulphexide
C6H4Me.SO2.S.C6H4Me
C14H14O2S2
74
Marcker
A., 136, 83
v., 859
=(l-4)2
11 11
••»! -M
„
....
74-75
Otto and Eossing
B., 18, 2505
48, 1232
•i 11 "••
11 >1
„
74-76
Otto
B., 15, 131
11 11
»1 11
„
....
76
Otto, Lowenthal
Z. C. [2], 4, 623
vi., 289
and Grubert
Dimethoxyphenyl d {sulphide
S,,(C6H4.OMe)2=(1.2)2
„
119c.
Haitinger
M. C., 4, 168
44, 988
Ethylic diphenylsulphonate
C6H5.C(iH4.SO3Et
C14H]4O3S
73-74
Gabriel & Deutsch
B., 13, 388
38, 477
Methyl oxysulphobenzide ....
SO2(C6H4.OMe)2
C14HI404S
130
Annaheim
A., 172, 45
27, 796
Ethylene diphenylsulphone....
C2H4(S02.Ph)2
C14H14O4S2
....
179-5-180
Otto
B., 13, 1280
38, 811
.1 11
„
„
....
179-5-180
Otto and Dam-
J. p. [2], 30, 171
48, 262
k6hler
Benzyltoluene disulphonic
fr. Ph.CH2.C6H4Me=1.4
C'14H14O,;S2
38
Zincke
B., 5, 685
25, 1005 ; vii.,
acid
183
Phenylcournarin .sulphouic
C16H9O2.S03H
C15H10O6S
+ 2JH2O
262 d.
Curatolo
G. I., 14, 257
48, 539
acid
PhenylcouruariB tiisulphonie
C16H*02(S03H)2
C15H10O8S.2
+6H2O
18
11
„
n
acid
(i-Dithiophenyl propionic
(PhS)2CMe.COOH
c,5H14o2a,
....
113-114
Baumann
R, 18, 65
48, 514
acid
Plienylsulphonethyl benzoate
Ph.S02.C2H4.OBz
C15H,,04S
....
124-125
Otto & Damkfihler
J. p._[2], 30, 171
48, 262
Ethylene phenyltolylsul-
Ph.SO3.C2H4.SO2.C6H4Me
C15H16O4S2
....
162
11
„
42,263
phone
=1.4
Atronine sulphene
....
C16H1002S
193
Fittig
A., 206, 63
40, 427
o-Naphthyl phenyl sulphone
C10H7.SO2.Ph
C16H12O2S
99-5-lOQ-o
Michael and Adair
B., 10, 585
32, 613
P* H 1} 11
„
„
115-116 u.c.
„
B., 10, 587
„
11 11 11 11
„
„
....
121
Chrustschoff
B., 7, 1167
28, 162
Atronylene sulphonic acid ...
C16HU.SO3H
C,6H12O3S
258 p.d.
Fittig
A., 206, 61 ; B.,
38, 120; 40,
12, 1739
427
Atronol „ „
C16H13.SO3H
Cj6H14O3S
130-131 p.d.
„
A., 206, 52
40, 427
Diphenyldisulphacetic acid ....
(.C6H4.S.CH2.COOH)2
C16H14O4S2
252
Gabriel & Deutsch
B., 13, 390
38, 477
Tolylsulphonethylic benzoate
i|Bzp.C2H4.S02.C6H4Me= 1 .4
C1BH1604s"
175
Otto & Damkohler
J. p. [2], 30, 321
48, 538
Ethyl oxysulphobenzide
•S02(C6H4.OEt)2
159
Annaheim
J.p. [2], 1,14; 2,
vii., 886 ; 27,
385; A., 172,52
797
Ethylene ditolyl sulphone ...
C2H4(S02.Cr,H4Me)2 =(1.4),
016H18O4S2
200
Otto & Damkohler
J. p. [2], 30, 321
48, 537
Diphenylsulphonethyl sul-
S(CaH4.SOa.Ph),
C16H1SO4S3
123
11
„
phide
,i oxide....
0(C2H4.S02.Ph)2
C16H,AS2
69-70
„
J. p. [2], 30, 171
48, 263
11 »
....
88
B
J. p. [2], 30, 321
48, 537
Sulphocetenic acid
....
C16H32O3S
....
18
Lasarenko
B., 7, 125
Ethylic benzylphdiiyl sul-
PhSO2.CH(CH2Ph).COOEt
017Hi8O4S
95-96
Michael & Comey
A. C. J., 5, 116
46, 319
phon acetate
?
Ph.S02.C6H4.O.S02.Ph
C18H14O;,S2
123
Schiaparelli
G. I., 11, 65
40, 603
Ditolylsuphonethyl sulphide
(C6H4Me.S02.C2H4)2S
C^OA
150-160
Otto & Damkohler
J. p. [2], 30, 321
48, 538
Ditolylsulphonethyl oxide ....
(C6H4Me.S02.C2F4)20
W>A
....
83
„
.i
11
?
CsoHjA +S03
OeHuOjS
140-150
Baeyer
A., 183, 1
31, 199
Dinaphthyl sulphoxide
SO(C10H7)2
C^OS
162 u.c.
Ekstrand
B., 17, 2603
48, 171
„ sulphone
(C10H7)2S02
C20H1402S
70
....
v., 522
«- „
i.
11
cf. B. 9, 683
123
Stenhouse & Gi-oves
C. N., 32, 151
30, 518
P" 11 n
11
„
„
177
„
„
)(
11 11 11
„
H
cf. B. 10, 1723
175-5
Cleve
B. S. [2], 25, 356
30, 81 ; 34, 154
Phenylmercaptole of benzoyl
(PhS)aCPh.COOH
C,0H16O2Si
142
Baumann
B., 18, 891
48, 749
formic acid
Phenylmercaptal of piperonal
(W>,:(SPh),
,5
48
,,
B., 18, 886
COMPOUNDS CONTAINING FOUR ELEMENTS.
441
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Galipeine sulphate
C.20H2103N + H2S04
C2(,H2307S(?)
+ 7H20
15
K6rner& Bohringer
G. I., 13, 363
46, 341
Amyl oxysulphobeuzide
S02(C6H4.OC5Hn)2
GftHjoQJS
98
Annaheiin
A., 172, 55
27, 797
Methoxycymene sulphone ....
SO2(C6H2MePr.OMe)2
1)
150-151
Paterud
G. I. [1875], 13
28,639
Diphenyl sulphone .... ^..
S02(C6H4.C6H5)2
C^I^AS
214-216
Gabriel and Deutscli
B., 13, 387
38, 476
Ethylic dibenzylphenyl sul-
PhS02.C(CH2Ph)2.COOEt
C24H24O4S
118
Michael and Comey
A. C. J., 5, 116
46, 319
phonacetate
/3-Naphthalene diuaphthyl-
C10H,:SO(C10H7)2
CvayU-OyOfe
....
111 u.e.
Ekstrand
B., 17, 2602
48, 170
sulphoxide
Carvol + H,S
(C,,H140)2.SHZ
^/32-*"*3o^2"
....
187
Beyer
A. P. [3], 21, 283
46, 331
Meliiiointriaulphonic acid ....
C34H1703(S03H)3
C^H^O^S.,
n.f. 300
Trzcinski
B., 16, 2837
46, 590
Excretin
p rr s~\ q
96
JV1 ctrcct
P. E. S. 9 308
ii., 614
78 W6*"*i^
Trinkerite (fossil resin)
C.HbOA
168-180
Tscherniak
J.p. [2], 2, 258
vii., 1183
Phenol + SO2
>»
140
25-30
Holzer
J.p., 25, 462
44, 585
(17.) CHOSe.
Methyl selenious acid
Me.SeO.OH
CH4O2Se
122
A., 97, 6
Benzyl „ „
Ph.CH2.SeO.OH
C7H8O2Se
....
85
Jackson
A., 179, 13 ; B.,
28, 154 ; 29,
7, 1278
581
1
....
-
....
88
M
B., 8, 111
28, 553
(18.) CHON.
Nitroform
CH(N0j)3
CH06N3
15
Schischkoff
A., 103, 364
iv., 110
Methylazaurolic acid
CH3.N.O.N
CH2ON2
....
d. a. 100
....
A., 214, 336
Methylnitrolic acid ....
HO.N:CH.NO,,
CH2O3N2
G4, d.
Tscherniak
B., 8, 115; A.,
28, 561 ; 29,
180, 168
903
Formamide
H.CO.NH3
CH3ON
192-195
Liquid
Hofmann
16,72
11., 681
(cf. A., 128, 335}
„
„
150 (i. v.)
....
J. [1863], 319
Methylic nitrite
Me.O.NO
CH3O2N
— 13
Bertoni and Truffi
G. I., 14, 23
46, 1110
„ ,,
„
„
— 12
Strecker
C. E., 39, 53
iv., 75
Nitromethane (Nitrocarbol)
Me.N.O.O
l i
"
99
Meyer
A., 171, 32
vii., 893
.. %
H
„
99
Liquid
Meyer and Stuber
B., 5, 517
26, 804
"
„
101
Liquid
Kolbe
J. p. [2], 5, 427
vii., 893 ; 25,
» !»
997
Methelic nitrate
Me.O.NO2
CH303N
66
....
Dumas and Peligot
A. C. [2], 58, 37
iv., 109
Isuretine
CH4ONS
....
104-105 p. d.
Lessen & Schiffer-
A., 166, 295 ;
vii., 707; 25,
decker
Z. C. [2], 7, 594
500
Carbamide (urea)
CO(NH2)2
.,
....
120
....
v., 951
„ ,, .... ....
„
n
n. v.
130
Michler
B., 8, 1664
29, 702
i, ), .... ....
„
„
133
Lubavin
G. J. C., 1870
Hydroxyl urea
NH2.CO.NH(OH)
CH4O2N2
cf. A., 182,214
128-130
Dressier and Stein
Z. C. [2], 5, 202
vi., 725
Paracyanformic acid
....
(C2H02N)n
....
a. 250 d.
J. p. [2], 10, 212
Cyanformamide
NC.CO.NH,
C2H2ON2
60
J. E., 7, 99
Nitracetonitril
N02.CH2.CN
C2H2O2N.,
abt. 40
Steiner
B., 9, 781
30, 289
v
...
( » )n
216 d.
B
B., 9, 783
Methylic isocyanate
O I C : N.Me
C2H3ON
Liquid
Cloez
I. D., Paris, 1866
vi., 519
„ „
H
„
40
....
Wurtz
A. C. [3], 42, 59
„ „
„
„
43-45
A., 149, 313
Methylic cyanate
N'CO.Me
jj
90
Wurtz
A. C. [3], 42, 43
11., 196
>i „
( „ ).
98
Hofmann
B., 3, 766
Glycocinimide anhydride ....
CH2.NH.CO
i i
„ or
sb. 280
280
Curtius
B., 16, 755
44, 1087
( * )*
3 L
442
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Diazoacetamide
,,
Amidodicyanic acid ....
Oxamic acid ....
N:N.CH.CO.NH.,
i — i
(CN)2(OHXNH2)
CO(NH2).COOH
CH3.CH.KO.N
NH2.CO.NH.COH
H.CN(OH).CN(OH)H
CO(NH2).CO(NH2)
CHrNO.O.NO.CH,,
02H3ON3
»
»
CaH3O3N
C3H4ON2
C2H4O2N2
)*
C2H403N2
»
M
C2H404N2
)>
C2H5ON
)»
1)
»1
5»
5*
)>
»)
»>
1»
C2H602N
1)
>»
1J
1»
)9
)>
))
»
)l
)»
»)
H
i»
i)
>»
C2H5O2N3
?>
J)
U
C2H503N
»
»»
H
>»
cf. B., 8, 709
cf. A., 214, 329
180-181 ;
185-186 c.
180-185
190 (HO)
221
221
282 c.
218-220
220
114-115
114-115
16-4
16
16
16-6-17-8
17-5-18
18
18
29-30
111-113
111-113
111-113
113-114
177
+2H20(?)
85
86-3
87-2
83-85
87
97
114 d.
d. 100
173
142 d.
159
178
n. f.
58-60
80-81
81-82
81-82 d.
37-5
Liquid —17
Liquid
78
78
^8
82
82-83
Liquid
Liquid
52-55
120
120
170
232-236 d.
177
185
190 d.
190
190.
85-86
Curtius
»
Hallwachs
Toussaint
Meyer & Constam
Geuther, Schertz,
aud Maish
VVitteuberg& Meyei
Henry
Lecco
Meyer
5)
»
Semenoff
ter Meer
Linnemaun
Bodeker
Dumas & Malaguti
Wichelhaus
Kiindig
Cahours
Hofuiann
»
Petraczek
Meyer and Janny
Liebig
Meyer and Stiiber
Knecht
Brown
Mohr
Bertoni and Trufli
Dumas and Boullay
Kissel
)j
Meyer
Meyer aud Stiiber
j>
Heintz
Beckurts and Otto
Curtius
Baeyer
n
Wiedemann
Hofmann
Hup}>ert & Dogiel
Playfair&Wanklyn
Millon
Kopp
Wittstein
Henry
Kauisay
B., 17, 958
B., 18, 1287
A., 153, 295
A., 120, 237
B., 14, 1457
Z. C. [2], 4, 300
B., 16, 506
C. R, 100, 943
B., 9, 705
B., 7, 429; A.,
180, 170
B., 6, 1497
A., 175, 98
Z.C.P.[1864],129
B., 8, 1080; A.,
181,4
J. [1869], 601
W. A., 60, 44
G. J. C., 1860
C. B., 25, 657
B., 3, 848
A., 105, 277
G. J. C., 1863
B., 15, 981
B., 14, 2729
B., 15, 2784
B., 15, 1526
A., 30, 143
B., 5, 404
B., 10, 978
J., 9, 575
J., 7, 561
G. I., 14, 23
A. C. [2], 37, 15
B. S., 42, 319;
J.E. [1882], 226
»
A., 171, 19
B., 5, 401
A. C. [4], 28, 138
A., 79, 110
A., 123, 315
B., 14, 578
J. p. [2], 26, 155
A., 130, 154
j)
A., 68, 323
B., 4, 264
B., 4, 476
A. C. [3], 8, 236
A., 64, 320 ; 98,
367
J., 18, 470
G. J. C. [1874]
35, 472
46, 988
48, 884
vii., 406
iv., 279
vl., 1110
44, 804
48, 886
30, 287
27, 678 ; vli.,
895
27, 365
28, 558
vi., 605
29, 67 ; 30,
186
vi., 619
i.,5
vii., 3
24, 407
42, 822
44, 569
vii., 894
25, 682
32, 569
46, 1110
iv., 75
42, 935 ; 48,
364
u
vii., 894
25, 682
i., 751
ii., 908
ii., 909
44, 337
iii., 414
24, 716
iv., 108
Ethylazurolic acid
Formyl carbamide
Glyoxime
Oxamide
Methazonic acid
Ethyl uitrolic acid
» » »
» j> »
Ethylenic nitrite
Dinitroethane
Methylformamide
„
Acetamide
CH3.CO.N:O2;NH(?)
CH3.C(N02):NOH(?)
O2N.CH2.CH2.NO2
CH3.CH(NO!1)!
H.CO.NHMe
CH3.CO.NH2
>»
»
>1
»>
»
CHMe:N,OHorCHMe.
i
NH.O
»
m.o.N;o
»
M
H
M
v>
H
Et.NO2
)J
»)
>1
NH2.COOMe
CHS(OH).CO.NH.
»J
CH2(NH2).COOH
)>
NH2.GO.NH.CO.NH3
n
n
j»
»>
EtO.NO2
)»
)>
»1
»»
M
Ethylaldoxime (uitroso-
ethane)
•> !>
Ethylic nitrite
„ ,,
a 3» ...» ....
>« „
i» » >••• ••••
:» v
jt „
? _
Nitroethane
Methylic carbamate
Glycollamide ....
Atuidoacetic acid (glycocoll)
» »
Biuret
Ethylic nitrate
» j»
?i i) •.-.
V • , ....
J« >,
1! 1!
COMPOUNDS CONTAINING FOUR ELEMENTS.
443
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Hydroxylbiuret .... »..
HM
C2H5O3N3
....
134
Dressier and Stein
Z. C. [2], 5, 202
vi., 725
Diraethylnitrosamine
NMe,,NO
C~H6ON2
148-5 (724)
Liquid
Renouf
B., 13, 2170
40, 152
Methyl carbamide ....
NH2.CO.NHMe
1)
....
100-101
Hofmann
B., 14, 2734
42, 822
„ j,
))
)>
109
Fischer
B., 14, 1913
Ethenylamidoxime .... .;,.
NH2.CMe I N.OH
)J
135
Nordmann
B., 17, 2748
48, 239
Ethyl hydroxylamine
NHEtOH
C2H7ON
(58
Liquid
Gurke
A., 205, 274
40, 572
Ammonium aldehydate
)»
100
70-80
Liebig
A., 14, 144
i., 107
Hydroxylamine acetate
(NH2.OHXC2H4O2)
C2H7O3N
....
87-88
Lossen
Z.C.[2] —
vl., 723
Ethylenediamine hydroxide
C2H4(NH3.OH),
C3H1202N2
117
Hofmann
» »
)>
))
118
10
ihouspolos & Meyer
A., 212, 251
48, 940
Ammonium acetate -{- am-
AcO(NH4)+3NH3
C2H1602N4
—18
Troost
C. E., 94, 789
42, 1162
monia
51 » JJ
Ac.O(NH4)+6NH3
C,H,0SN7
—32
u
u
»
Acetyl cyanide
CH3.CO.CN
C3H3ON
93
Liquid
Hubner
A., 120, 334; 124,
vi., 22
315
., ,, .... ....
)J
»1
93
Fileti
G. I., 5, 391
29, 570
» » •••• ••••
( „ )«
....
120
»
»
D
Cyanacetic acid
NC.CH3.COOH
C3H303N
55
Richter
R. K. T., 31
» „
j>
>)
d. 165
80
Van t'Hoff
B., 7, 1382
28, 251
Methylic cyanocarbonate ....
NC.COOMe
1)
100-101
Weddige
J. p. [2], 10, 199
28, 448
» »
( „ )„
134
»
J. p. [2], 10, 214
28, 449
Nitrosomalonia acid
HO.N : C(COOH)2
C3H306N
126 d.
Meyer and Miiller
B., 16, 608
44, 790
,, ,, .... —
»
)>
125-129
Corirad
»
»
» n
))
»>
d.
Conrad & Bischoff
B., 13, 599
38, 629
C'yanacetamide
NC.CHj.CO.NHj
C3H4ON3
105
Van t'Hoff
B., 7, 1383
28, 251
Paracyanocarbomethylamide
....
( „ )n
250
Weddige
J. p. [2], 10, 217
28, 449
Glycolylcarbamide (hydan-
CH2.CO.NH.OO.NH
C3H402N2
206
Baeyer
A., 130, 158
vi., 702
to'in)
i 1
»» v
)1
J)
216
»
B., 8, 614
» i>
'»
1)
216
Hofmann
Zoochemie, 509
)) i)
5)
)»
216
Schulze & Barbieri
B., 14, 1834
Ethylic isocyanate
COINEt
CjHjON
GO
Wurtz
A. C. [3], 42, 43
ii., 195
» »
11
»«
....
G5
Zotta
A., 179, 101
29, 570
„ „ (polymer)
(C3H5ON)3(?) q.v.
))
95
Hofmaun
B., 3, 766
Ethylene cyanhydrin
C2H4(OH).CN
»l
220-222
....
A., 191, 275
Lactic nitril
CH.,.CH(OH),CN
i*
182-184 d.
b. —21
Z. C. [1867], 660
vi., 75
Lactimide
CHMe.CO.NH
275
Preu
A., 134, 372
vi., 773
i i
j»
Allylic nitrite
CH2 : CH.CH2O.NO
C3H602N
85 ; 93 (?)
Brackebusoh
B., 7, 226, 1142
27, 573
Nitropropylene
C3H5.N03
»j
96 ; 107 (?)
»
j»
J)
Nitrosoacetone
CH3.CO.CH2.NO
))
....
65
Meyer and Ziiblin
B,, 11, 695
34,660
„
n
^
....
G5
Treadwell & West-
B., 15, 2788
44, 572
enberger
Acetyl formimide
NH : CH.OAc
)'
70
Pinner
B., 16, 1653
44, 1090
Acetyl formamide
CH3.CO.CO.NH3
)>
124-125
Claisen & Shadwell
B., 11, 1566
36, 45
Allylic nitrate
C3H5.O.N : O
C3Hb03N
106
Liquid
Henry
B., 5, 452
25, 686
Methyloxamic acid ,...
CO(NHMe).COOH
J5
140
Wallach
A., 184, 69
32, 186
,, ,,
»
))
140
Wurtz
A. C. [3], 30, 443
« )» .... ....
>»
»
145-146
Hantzsch
B., 17, 2920
a-Nitrosopropionic acid
Me.CH(NO).COOH
)"
d. w. m. 177
Meyer and Ziiblin
B., 11, 694
34, 659
/3-Nitropropiouic acid
CH2(NO2).CH2.COOH
C3Hb04N
66-67
Lewkowitsch
J. p. [2], ?0, 169
38,33
Tartronamic acid
CH(OH).CO(NH2).COOH
»»
....
160 d.
Menschutkin
A., 182, 82; J. E.,
30, 627 ; 32,
8, 177
323
Glyceryl trinitrite
C3H606N3
150-154
cf. B,, 6, 1290
Masson
43, 350
„ „ (nitro
C3H6(N03)3 .
C3HS09N3
....
s. —4
Kern
C. N., 31, 153
glycerin)
)> n »
)1
»
....
11
de Vrij
G.J.C. [1855], 620
)> )> )?
»
1»
185
Champion
G. J. C. [1871]
Ethylidene carbamide
CH3.CH.NH.CO.NH
C3H6ON3
154
A., 151, 204
1 __[
Propylazaurolic acid
•••*
»1
. ...
127-5
Meyer and Coustam
A., 214, 334
44, 41
Methyloxamide
CONH2.CONHMe
C3HC02N3
227-229
Wallaoh and West
B., 9, 265
30, 185
„
»
»
227-229
Wallach
A., 184, 70
32, 186
3L2
414
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Malonamide ....
CH2(CO.NH,),
C3H..OoN2
168-170
Henry
C. R, 100, 943
48, 886
•^^2\ ' •*~*'2/z
3 o f^ z
770
J. [1875], 528
Acetylcarbamkle
))
NH2.CO.NHAc.
)»
112
Moldenhauer
A., 92, 405
i., 753
,,
»
»I
200?
Ziuin
A., 94, 100
)J
Acetoximic acid
OH3.CH(NO).CH2(NO)
»»
153
Tread well & West-
B., 15, 2786
44, 572
enberger
» )?
J)
)J
....
153
Meyer and Janny
B., 15, 1166
42, 1185
Propyl nitrolic acid .... '•'„.
CH3.CH2.C(NO2) : N.OH
C,H603N2
60
Meyer and Locher
B., 7, 672
27, 983
» »
»
Jl
60
Meyer
A., 175, 114
28, 558
„ ,, .... ' ...
n
»>
60
Meyer and Lecco
B., 9, 395
30, 72
Propyl pseudonitrolic acid ...
CH3.C(NO)(NO2).CH3
5)
68
Kissel
B., 16, 960
tt I?
»
»
70
Meyer and Locher
B., 7, 789
27, 983
») „
>»
»
76
Meyer
A., 175, 120
28, 559
»? »
»
)>
.-,.
76
Meyer and Locher
B., 7, 1509
28, 1183
Dinitropropane
CH3.CH2.CH(N02)2
C3H604N2
182-5 u.c. ;
1. -17
ter Meer
B., 8, 1080 ; A.,
29, 68 ; 30, 186
189 c.
181, 19
Dinitroisopropane
CMe2(NO,,)2
)1
187 u.c.
50
Bredt
B., 15, 2323
44, 176
»»
)>
)»
181-5 u.c. ;
53
Meyer and Locher
B., 7, 1617; A.,
28, 445 ; 29, 905
185-5 c.
180, 149
Ethyl formamide
H.CO.NHEt
C3H.ON
196-197
1. -30
Linnemann
W. A., 60, 44
vi., 619
,, „
»
)J
199
....
Wurtz
J., 7, 567
vii.,492
ij ,,
)J
)»
199
Hofmann
B., 5, 247
25, 502
Methylacetamide
CH3.CO.NHMe
»1
207
26
?»
B., 14, 2730
42, 822
»
)»
)1
906
28
»
))
5)
Propionamide
CH3.CH2.CO.NH2
>»
75-76
Sestini
Z. C. [2], 7, 34 ;
24, 234 ;
Cimento 4, 21
vii., 1009
»
II
»»
75-76
Hofmann
B., 15, 981
Dimethylacetoxime (acetox-
CMe2 : N.OH
J»
134-8 u.c.
59-60
Janny
B., 15, 2779
44, 58
ime)
» !)
>»
»»
134-8 c. (728)
59-60
Meyer and Janny
B., 15, 1324
48, 1047
Propylaldoxime (nitroso-
CH3.CH2.CH5.NO (?)
J)
130-132
Liquid
Petraczek
B., 15, 2784
propane)
Propylic nitrite
CHS.CH2.CH.,O.NO
C3H;O2N
43-46
Cahours
C. B., 77, 745
27, 39
j, ,, .... ....
»J
»
44-5
G. I, 14, 23
46, 1110
(?) ....
1»
v
55
Kissel
B. S., 42, 319
48, 364
i) ,, .... ....
Jl
))
57
Bertoni and Truffi
G. I., 14, 23
46, 1110
Isopropylic nitrite
(CH3)2CH.O.NO
i»
43-44
Kissel
J. E. [1882], 226
42, 936
» » .»•• ...
))
n
45 (762)
Liquid
Silva
Z. C., 12, 637
vi., 966
Nitroisopropane
(CH3)2CH.NO2
»
112-117
Liquid
Meyer and Choj-
B., 5, 1036
26, 262
nacki
„
))
)»
115-118
Schiff
B., 7, 1141
„
»
»j
115-118
Kissel
J. E. [1882], 226
48, 936
,, .... ....
)5
it
115-118
Meyer
A., 171, 39
vii., 895
Nitropropane
CHVCH2.CH2.NO2
?;
122-127
Liquid
i>
A., 171, 36
)1
„
»
»
122-127
Liquid
Meyer and Killiet
B., 5, 1033
26, 261
,, — ....
)T
»»
125-128
Liquid
Cahours
C. B., 76, 133
26, 366
Lactanride
CH3.CH(OH).CO.NH.,
74
A., 104, 197; 133,
u
( ^
257
Methylic methylcarbamate....
NHMe.COOMe
}»
92
Schreiner
J. p. [2], 22, 353f
40, 88
Ethylic carbamate (urethane)
NH2.COOEt
»
47-50
McOeath
B., 8, 384
" )>
»»
H
49
Ponornareff
B., 15, 515
» V
75
))
ISO
b. 100
i., 751
a-Amidopropionic acid (al-
CH3.CH(NH2).COOH
»
abt. 200
Strecker
A., 75, 29
i., 63
anine)
0- ,, „ (fl-al-
NH2.CH2.CH2.COOH
1)
....
180; 190
Mulder
B., 9, 1904
32, 312
anine)
0-
»J
jj
195
Hertz
A. P. [3], 8, 234
31, 479
Methamidacetic acid (sar-
NHMe.CH2.COOH
>»
....
sb. a. 100
Liebig
A., 62, 310
v., 198
cosiue)
» n i)
>i
»
100+
Strecker
A., 123, 263
COMPOUNDS CONTAINING FOUR ELEMENTS.
445
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
i
Reference.
"Watts' Diet.
&. J. Ch. Soc.
Methamidacetic acid (sar-
NHMe.CH2.COOH
C3H7O2N
....
210-220 d.
Meylius
B., 17, 286
46, 994
cosine)
Amidomalonamide ....
NH2.CH(CO.NH2)2
C3H702N3
....
182
Conrad & Guthzeit
B., 15, G07
42, 946
Isopropylic nitrate ....
UHMe2.O.N02
C3H70,N
100-102(760
Liquid
Silva
A., 154, 256
vi., 966
Propylic nitrate
CH3.CH2.CH2.O.NO2
i)
110-5
....
Wallach & Schulze
B., 14, 422
40, 572
Ethyl carbamide .... ...
NH2.CO.NHEt
C3H8ON2
....
92
Wurtz
B. [1862], 199
ii., 564
„ ,,
»
»
n v.
92
Michler
B., 8, 1665
29, 702
Dimethyl carbamide
NHMe.CO.NHMe
)J
....
.97
Wurtz
C. K., 32, 414
i., 754
„ „
)J
»
....
97-100
Maly & Hintereggei
B., 14, 726
40, 747
,, ,,
11
J)
273-288
99-5
Wurtz
R. [1862], 199
iii., 1003
1, „
?)
»
268-270
102-5
u
»
»
a-Amidopropionamide
CH3.CH(NH2).CO.NH2
)}
cf.A.,173,344
a. 250
Baumstark
B., 6, 883
26, 1243
Ethyl semicarbazide
....
C3H9ON3
...
105-106
....
A., 199, 294
Dinitropyrroline
C4NH3(N02)2
C4H304N3
152
Ciamician & Silber
B., 18, 1462
48, 993
Nitropyruvinure'id
....
)»
a. 200 d.
A. C. [5], 11,378
Methylparabanic acid
CO.NMe.CO.NH.CO
i i
C4H403N2
147
Maly & Andreasch
M.C., 3, 107
42, 633
» »
»»
»I
148
Maly and Hinte-
B., 14, 728
40, 747
regger
V 11 ""
»»
)1
149
Mabery and Hill
B., 13, 740
40, 39
» J»
»»
?)
149
Andreasch
B., 14, 1449
40, 897
»» )> ."•
»
I)
....
149-S
Hill
B., 9, 1094
Diisonitrosuccinic acid
OOOH.(C : N.OH),.COOH
C4H406N2
128-130 d.
M tiller
B., 16, 2986
46, 584
Cyanacetone ....
CH3.CO.CH2.CN
C4H5ON
120-125
I^tatthews and
B. 15 2679
Hodgkinson
„ (polymer)
»
166
J. p. [2], 1, 141
*
Allylic isocyanate
CO I N.C3H5
i»
82
Liquid
Cahours and Hof-
P. T. [1857], 555
ii., 195
mann
Propionic cyanide
CH3.CH2.CO.CN
)>
108-109
Claiaen and Moritz
37, 692
,, „
5»
)>
108-110
Liquid
»
B., 13, 2121
40, 154
Epicyanhydrin
0 : C3H5.CN
)5
....
162
Pazschke
J. p. [2], 1, 98
vii., 466
'?
....
11
d. 280
A., 213, 174
Ethylic cyanocarbonate
NC.COOEt
C4H5O2N
115-110
Liquid
Weddige
J. p. [2], 6, 117;
26, 381 ; 28,
10,197; A., 184,
448 ; vii.,
12
415
Ethylic paracyanocarbonate
(NC.COOEt)n
»»
165
»»
J. p. [2], 10, 208
28, 449
Succinimide ....
CH2.CO.NH.CO.CH.,
Jl
287-288
....
Menschutkin
A., 162, 166
vii., 1102
»)
))
....
1S5-12G
Erlenmeyer
Z. C. [2], 5, 175
vi., 1042
)»
»)
210
Fehling & Teuchert
v., 461
Cyanacetyl carbamide
CN.CH2.CO.NH.CO.NH2
C4H502N3
200-210 d.
Mulder
B. S. [2], 29, 531 ;
34, 786; 36,
B., 12, 466
619
Diglycollimide
....
C4H603N
142
Wurtz
A. C. [3], 69, 342
vi., 642
Fumaramic acid
NH2.CO.C2H2.COOH
J>
217 d.
Michael and Wing
A. C. J., 6, 419
48, 968
Acetyl oxatnic acid ....
NHAc.CO.COOH
C4H604N
54
....
J. p. [2], 9, 299
Amidomaleic acid
C2H(NH2).(COOH)2
)>
180-182
Glaus and Voeller
B., 14, 153
40, 254
Tartrimide
CH(OH).CO.NH.CO.CH(OH)
i i
)J
230 d.
Arppe
A., 93, 352
v., 698
Oximidosuccinic acid
COOH.C2H2(N.OH).COOH
C4H605N
d. 126
Ebert
A., 229, 45
48, 1123
Allanic acid ....
C4H605N5
+H20
d. 210-220
A., 159, 353
Nitrosopyrroline
C4H6N.NO
C4H6ON2
37-38
Ciamician and
B., 16, 1543
44, 1142
Dennstedt
Diethylic dicyanate
C2N2O,Me2
C4H602N2
98
Hofmann
B., 3, 766
24, 136
Lactyl cyanamide
CH3.CH(OH).CO. NH.CN
»
212
Mertens
J. p. [2], 17, 34
34, 398
Fumaramide
NH2.CO.CH : CH.CO.NH3
i)
232
Curtius and Koch
B., 18, 1298
48, 885
Glycocollimide anhydride ....
CH2.NH.CO.CO.NH.CH2
»
....
sb. 280
Curtius
B., 16, 755
Lactyl carbamide
CHMe.CO.NH.CO.NH
)*
125
Urech
A., 165, 99; B.,
vii., 724 ; 26,
i i
6, 1114
380 ; 27, 148
», >1 .... ....
n
»
140
Heintz
A., 169, 120
27, 149
„ „
i>
)»
145
Urech
B., 6, 1114
27, 148
Methyl hydantoin
CH2.CO.NH.CO.NMe
H
145
Neubauer
A., 138, 291
vi., 703
i 1
446
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Methyl hydantoin
CH2.CO.NH.CO.NHMe
C.HAN,
145
Hoppe-Seyler and
B., 7, 34
27, 464
Baumann
,, ,, .... ....
„
„
....
145-146
Baumann
B., 7, 239
27, 578
„ „
!»
11
151-152
„
>!
„
„ „
„
„ .
....
156; 157-158
Salkowski
B., 7, 119
27, 464
„ „
11
„
159-160-5
Guareschi & Mosso
J. p. [2], 28, 504
46, 618
Nitroerythromannitol
C4H6(NO,,)4O4
C4H6012N4
61
Stenhouse
P. T. [1849], 399
ii., 505
Isopropylic cyanate
....
C4H7ON
67
Hofmanu
B., 15, 756
vii., 1016
„ „
CHMe2.CNO
„
74
Silva
B. S. [2], 17, 97
26, 367
Hydroxyisobutyronitril
CMe2(OH).CN
„
abt. 120
Urech
A., 164, 257
26, 59
y-hydroxybutyronitril
CH,(OH).CH2.CH2.CN
„
240-250
M. C., 3, 699
Ethoxyacfctonitril
CH,(OEt).CN
11
132-133
....
Norton & Teherniak
C. E., 87, 27
34, 972
„
»
„
134-135 (750)
Liquid
Henry
B., 6, 261
26, 879
Crotonamide .... . .
Liouid
Beilsteiu & Wie£?and
B., 18, 483
48, 740
(0
„
....
149-152
Pinner
B., 17, 2008
46, 1292
Me.CH : CH.CO.NH2
159
B., 12, 2056
38, 99
Ethylleucazone
C4H7ON3
158-158-5
) J
Meyer & Coustam
A., 214, 341
44, 40
Nitrobutylene
Me2C : CH.NO2 or
C4H702N
154-158 p. d.
Liquid
Haitinger
W. A., 77, 428
36, 701
CH2 : CMe.CH2.NO2
Nitrosomethyl acetone
CH3.CO.CH(NO).CH3
„
185-186 c.
74
Meyer and ZUblin
B., 11, 323
34, 487
1! ,,
JJ
11
....
74
Ceresole
B., 15, 1874
44,41
Methylio isonitrosoacetone ....
CH3.CO.CH:N.OCH3
,,
115-116 u. c.
Liquid —15
„
B., 16., 833
Diacetamide ....
NHAc2
215
59-60
Linneman
W. A., 60, 44
vii., 3
J)
59
Gan tier
C. E., 67, 1255
"
II
74-75
Wichelhaus
B., 3, 847
24, 407
3)
H
a. 210
82 ; s. 70
Hofmann
B., 14, 2732
42, 822
Propionyl formamide
CH3.CH2.CO.CO.NH2
3)
116-117
Claisen and Moritz
B., 13, 2121
37, 693; 40, 154
Amidomaleic diamide
C2H(NH2)(CO.NH2)2
C4H702N3
122
Clans and Voeller
B., 14, 152
40, 204
Ethylic oxamate (oxamethane)
NH2.CO.COOEt
C4H703N
220
110
....
iv., 280
). » »
„
„
....
112
Morley and Saint
43, 401
II W >!
„
ii
..i.
114-115
J. p. [2], 10, 196;
12, 434
.. » •>
„
„
116-117
Grimaux
B. S. [2], 21, 153
28, 564
Ethyloxarnic acid
NHEt.CO.COOH
„
....
120
Wallach
A., 184, 58
32, 186
Aoeturic acid (acetylglycin)
NHAc.CH2.COOH
„
....
206
Curtius
B., 16, 757 ; 17,
46, 1307
1667
» !• i,
„
M
• Ml
d. 130
Kraut & Hartmann
A.. 133,105
Succinamic acid
NH2.CO(CH2)2.COOH
„
300
....
A., 134, 136; 162,
175
n-Nitrosobutyric acid
CH3.CH2.CH(NO).COOH
n
151 d.
Wleiigel
B., 15, 1058
42, 944
/3-isomitrosobutyric acid
CH3.C(N.OH).CH2.COOH
„
140 d.
Westenberger
B., 16, 2996
46, 581
Ethylic nitro-acetate
CH2(NO;).COOEt
C4H7O4N
150-160 d.
Liquid
Lewkowitsch
J. p. [2], 20, 159
38, 32
ii ii
„
„
151-152
Liquid
Forcrand
J. p. [2], 19, 487
38, 33
ii ii
„
„
151-152
Liquid
„
C. E., 88, 974
36, 621
(of. B., 15, 1604)
Diglycollamic acid
O.(CH2.CO.NH2)2
,,
....
a. 125
Heintz
A., 128, 141
vi., 645
Amidodiglycollic acid
NH(CH2.COOH)2
„
d. a. 210
,,
A., 132, 276
vi., 644
Ethylic nitroglycollate
N0.2.CH(OH).COOEt
C4H7O5N
180-182
....
Henry
A. C. [4], 28, 424
Allyl carbamide
NH2.CO.NH.C3H5
C4H8ON2
....
85
And reasch
M. G, 5, 33
46, 732
ii ii
„
1)
....
141
Maly
Z. C. [1869], 261
Succinatnide
NH2.CO. (CH2)2.CO. NH2
O TT O N"
1") 200
D'Arcet
A. 16 215
A.f\
^4 8^2 2
MM
v. , 4ul
eniq) <b 1 <3
TTpnrv
OR 1OO Q.JI
4-fi ooe
Vy. J-V., AV/w, t7-iO
Ethyl oxamide
NH2.CO.CO.NHEt
B
202-203
Wallach
A., 184,65
32, 186
Dimethyl oxamide
NHMe.CO.CO.NHMe
,,
208
Maly & And reasch
M. C. [3], 107
42,633
ii i
„
„
••••
209-210
Henry
C. E., 100, 943
48, 887
51 11
11
it
....
212
Eichter
E. K. T.
1. 11
„
„
209-210
Wallach and West
B,, 9, 266
30, 185
,1 11
,,
)(
210
Wallach & Schulze
B., 14, 422
40,572 •
Aceturamide ....
NHAc.CH. .CO.NH
m'
p . .
B. 17 1674
4-fi 1 ^A7
Acetylmethyl carbamide
NHMe.CO.NHAc
180
Hofmann
B , 14, 2727
42, 822
Ethylmethylacetoximic acid
HON : CMe.CMe : NOH
"
sb. 215
Schramm
B., 16,179
44,573
COMPOUNDS CONTAINING FOUR ELEMENTS.
447
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
1
C4H4(NH.OH)2
C4H802N2
....
173
Ciamician and
G. I., 14, 156
48, 246
Dennstedt
Amidosuccinuric acid
NH2.CO.CH2.CH(NH.CO.
C4H802N3
137-138 d.
Guareschi
B., 10, 1747
34, 138
NH2).COOH
Ethylazaurolic acid
ON.CHMe.N^.CHMe.NO
C4H802N4
....
142 d.
Meyer & Constam
B., 14, 1457
40, 896
3-nitrosocreatinine .... „.
....
„
195
Marcker
A., 133, 310
vi., 503
«- „
....
„
210 d.
„
A., 133, 306
„
Butylpseudonitrol
CH3.CH2.C(NO)(NO2).CH3
C4HS03N2
58
Meyer and Locher
B., 7, 1509 ; A.,
28, 1183 ; 29,
180, 135
904
Ethylic allophanate
NH2.CO.NH.COOEt
„
190-191
Kichter
B. K. T.
Lacturamic acid
NH2.CO.NH.CHMe.COOH
,,
....
155 d.
Urech
A., 165, 99
vii., 723 ; 26,
380
Dinitrobutane
CH3.CH2.CH2.CH(NO.i)2
C4H804N2
190 d.
Liquid
Ziiblin
B., 10, 2085
34, 284
„
„
„
197 p. d.
Chancel
C. B., 96, 1466
44, 915
„
CH3.CH2.C(N02)2.CH3
n
199 c. ; p. d.
Liquid
Meyer
B., 9, 701
30, 288
„
C4H8(N02)2
„
95-96
Beilstein and Kur-
B., 14, 1621
40, 1021
batow
Iso-diiiitrobutaue
CHMe2.CH(NO2)2
H
d.
Liquid
Ziiblin
B., 10, 2087
34, 284
Ethylene allophanate
NH2.CO.NH.COO.C2H4.OH
,,
100
Baeyer
A., 114, 160
i., 134
Diamidosuccinic acid
[.CH(NHj).COOH]2"
„
151 u. c.
Glaus and Helpen-
B., 14, 627
40, 578
stein
,. „
„
„
....
151
Glaus
B., 15, 1849
» »
„
„
d. w. m. a. 200
Lehrfeld
B., 14, 1817
42, 163
Isopropylformamide
H.CO.NHPr/3
C4HaON
220
A., 149, 158
Ethylacetamide
CH3.CO.NHEt
• „
200
Liquid
Wurtz
C. B., 36, 180
i.'., 552
„
„
„
SOS
„
J., 7, 566
„
„
203-204
Liunemann
W. A., 60, 44
vii., 4
„
a
„
205
Wallach and Hoff-
32, 188
mann
Butyramide
CH3.CH2.CH2.CO.NH.,
„
....
115
Chancel
C. B., 18, 8J9
i., 690
216
A. 52, 294
Isobutyramide
CHMe2.CO.NH2
„
216-220
100-102
Letts
B., 5, 672
25, 1020
„
„
„
....
124-5
Munde
B., 7, 1372 ; A.,
28, 247 ; 30,
180, 340
68
„
„
„
....
128-129
Hofmann
B., 15, 982
Ethylacetimide
NH : CMe.OEt
„
97
Liquid
Pinner
B., 16, 1654
44, 1090
Isobutyl aldoxime
„
139
Liquid
Petraczek
B., 15, 2785
44, 5C9
Ethylmethylacetoxime
CEtMe : N.OH
„
152-153
Liquid f. m.
Janny
B., 15, 2779
44, 580
Butylic nitrite
CH3.CH,,CH2.CH2.O.NO
C4H9O.,N
76
Bertoni and Truffi
G. I., 14, 23
46, 1110
Isobutylic nitrite
CHMe2.CH2.O.NO
„
66-70
„
„
„
,, „
J)
„
67
Chapman & Smith
J., 22, 153
Butylic nitrite
CMe3.O.NO
„
76-78
Liquid
Tscherniak
A., 180, 159
29, 902
Nitrobutaue ....
(CH3)3.C.NOj
110-130
T ' 'fl
A. 180 155
Nitroisobutane
CHMe2.CH2.NO2
»
137-140
Liquid
Demole
B., 7, 710; A.,
vii., 897 ; 27,
175, 142
984 ; 28, 561
Nitrobutane
CH3.CH2.CH(N02).CH3
D
abt. 140
Liquid
Meyer and Locher
A., 180, 134
29, 904
n
CH3.CH2.CH2.CH2.NO2
„
151-152 c.
Liquid
Zubliu
B., 10, 2083
34, 284
Propylic carbamate
NH2.COOPr«
„
....
50
Roemer
B., 6, 1102
27, 39
» ..
„
„
194-196
51-53
Cahours
C. B., 76, 1383
26, 872 ; vii.,
1014
Ethylic methylcarbamate ....
NHMe.COOEt
170
....
Schreiuer
J.p. [2], 21, 124
38,312
Amidoisobutyric acid
Me2C(NH2).COOH
„
....
sb. 220
Tieniannand Fried-
B., 14, 1972
lander
Ethylamidoacetic acid
NHEt.CH2.COOH
„
• <•*
a. 160 d.
Heintz
A., 129, 33; 132, 1
vi., 643
a-Methamidopropionic acid ....
CH3.CH(NHMe).COOH
„
brown 180
260 d.
Lindenberg
J.p. [2], 12, 244
29, 701
Ethylglycollamide
CH2(OEt).CO.NHa
„
225
b. 100
Heintz
A., 129, 42
Glycolethylamide
CH2(OH).CO.NHEt
„
250
Liquid
„
A., 129, 29
vi., 647
Guanoliu
C4H9O. N
1 \A 1 1 PL
J.p. [2], 17, 238
...»
+H20
1 L*± — i LO
100
"'.
Butylic nitrate
C4H9.O.NO2
C4H903N
a. 130
Wurtz
J., 7, 575
Isobutylic nitrate
CHMe2.CH2.O.NO2
„
123
Chapman & Smith
Z. C. [1869], 433
22, 153
Base from creatiuine
C4H9O4N
....
152
Marcker
A., 133, 314
vi., 503
448
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
?
....
C4H1UON3
170-172
Linneitiann
vi., 63
Diethylnitrosamine
NEt2.NO
„
176-9 c.
Geuther & Kreuz
A., 127, 43
iv., 114
hager
n
„
177
Knecht
B., 10, 978
32, 569
Methylethylcarbamide
....
„
266-268
52-53
Wurtz
R. [1862], 199 .
iii., 1003
„
„
75
Schreiner
I.p. [2], 22, 300
40,88
„
„
105
„
J.p. [2], 22, 359
„
Diamidosuccinamide
NH2.CO.(CH.NH2)2.CO.NH_,
C4H1002N4
160
Glaus and Helpen-
B., 14, 626
40, 578
steiu
Ethylene dicarbamide
C2H4(NH.CO.NH2)2
„
cf. A., 119,
192
Volhard
P. R., 11, 268
ii., 595
349
Ethylic methanedicarboxyl-
CH(CO.NH2)2.COOEt
C4H1004N2
....
190-191
Amato
G. I., 1, 690
vii.. 9
amide carboxylate
Butaldehyde ammonia
CH3. CH2.CH2.COH +NH3
C4HHON
+ 5H,,0
30-31
Lipp
A., 211, 356
42, 709
Dimethylethj lalkine
....
n
130-134
Ladenburg
B., 14, 2408
42, 166
Acid ammonium acetate
CH3. COONH4 + C2H4O2
C4HU04N
....
76
....
....
i., 13
Furfuronitril ....
C4H3O.CN
C5H3ON
146-148
Liquid
Wallach
B., 14, 752
40, 715
147 (757-8)
Ciamician & Denn-
B., 14, 1058
40, 801
stedt
Nitropyromucic acid
C4H2O(N02).COOH
C5H3O6N
183
Klinkhardt
J.p. [2], 25, 51
42, 499
„ „
„
„
184
Priebs
B., 18, 1363
48, 971
Sarcine
C5H4ON4
n. f. 150
Strecker
A.
v., 196
Suceinocyanimide
c2H4 : (co)j : N.CN
C5H402N2
....
138
Holler
J.p. [2], 22, 207
40, 259
Nitrocarbopyrrolic acid
....
C5H404N2
144-146
Ciamician & Danesi
G. I., 12, 28
42, 875
Hydroxypyridine (chelamide)
C5H4N.OH
C5H5ON
95-96
Lerch
M. G, 5, 367
48,46
„
M
„
107
Kbnig and Geigy
....
5)
a- „
IJ
„
123-5
Fischer & Renouf
B., 17, 764
46, 1050
p- „ .... ....
,,
,,
....
124-5
„
B., 17, 1896
46, 1370
„
„
,,
148
Ost
J.p. [2], 29, 57
48,50
„ (pyridone)
„
»j
350
14S-5
Haitinger & Lieben
M. C., 6, 279
48, 966
» ,.
„
„
+ H20
66-67
„
„
„
Ally lie cyanocarbonate
CN.COOC3H5
CiHsO-jN
135
Liquid
Wagner & Tolleus
B., 5, 1045
26, 381
Pyromucamide
C4H3O.CO.NH2
„
100
A., 116, 282
„
„
„
130-132
Schwanert
C. R., 22, 856
iv., 764
„ —
„
n
....
140-142
Wallach
B., 14, 751
40, 714
•n
„
M
143-143
Ciamician & Denn-
B., 14, 1058
40, 801
stedt
Citraconimide
„
cf. B., 15,
109-110
,,
G. I., 12, 500
44,313
1343
0-Pyrrolic acid
C4H4N.COOH
„
....
161-162 p. d.
Ciamician
M. G, 1, 626;
42, 212
B., 14, 1055
a~ j» »
„
H
sb. 190
191-5 d.
„
„
„
Pyrocomenamic acid
C4H4N.COOH
d. w. m. 250
Ost
J.p. [2], 27, 270
44, 792
Furfuraldoxinie
O.CH:CH.CH:C.CH:N.OH
201-208 s.d.
89
Odernheimer
R, 16, 2989
46, 585
i i
Dihydroxypyridine
C5H3N(OH)2
255 d.
KSnigs and Geigy
B., 17, 1836
46, 1369
Allylalcohol dicyanide
C3H5.(CN)2.OH
C5H6ON2
150-151
Tollens & Wagner
B., 5, 621, 1045
25, 1093; vii., 48
Dipyromucamide
j)
173
Schwanert
A., 116, 272
iv., 765
„
176-5
M. C., 1, 289
Pyrrolcarbamide (tetrolcar-
C4H4:N.CO.NH,2
jj
....
165-166
Ciamician & Mag-
B., 18, 416
48, 809
bamide)
nag hi
.. »
„
11
cf. B., 15,
167
Ciamician & Denn-
G. I. [1882], 84
42, 6(6
944
stedt
>' )5
„
167-168
„
B., 15, 2580
44, 350
Amidohydroxypyridine
NH2.C5NH3.OH+H20
sb. a. 214
214
Krippendorff
J.p. [2], 32, 153
48, 1243
Diacetyl cyanamide ....
CN.NAc2
C5H602N3
d. 75
Mertens
J.p. [2], 17, 14
34, 397
Succinocyaminic acid
COOH.C2H4.CO.NH.CN
C.H,OiN,
....
128
Holler
J.p. [2], 22, 193
40, 259
Dimethyl parabanic acid
CO.NMe.CO.CO.NMe
L |
105
Andreasch
B., 14, 1451
40, 897
(cholestrophane)
»
»
„
....
145
Haly and Hinte-
R, 14, 725
40, 747
regger
» i.
..
„
275-277
145-5
Henschutkin
A., 1 78, 201
29, 379
COMPOUNDS CONTAINING FOUR ELEMENTS.
449
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Fr. dimethyluric acid
cf. A. C. J., 2, 305
C6H603N,
160
Mabery and Hill
B., 13, 740
40, 39
Malylureio acid
NH.CO.NH.CO.CH2.CH.
C5H6O4N2
215-220 d.
Grimaux
C. E., 80, 828
28, 7.r.2
1 1
COOH
Isobutyryl cyanide
CHMe2.CO.CN
C5H7ON
117-120
Moritz
39,13
Butyryl „
CH3.CH2.CH2.CO.CN
"
133-137
»
39,16
Furfurylamine
O.CH.CH : CH.C.CH,.NH2
„
145-146(761)
Liquid
Ciamician and
B., 14, 1476
40, 898
i 1
Dennstedt
Ethylic cyanacetate ....
NC.CH2.COOEt
C5H7O2N
207
....
Van t'Hoff
B., 7, 1383
28, 251
Methyl succinimide
CO.(CH2)2.CO.NMe
1)
234
55-60
Menschutkin
A., 178, 201
29, 380
11 11 ••••
M
934
66-5
„
A., 182, 92
30, 626
Pyrotartriiuide
OO.CHMe.CH2.CO.NH
1)
280 d.
66
Arppe
A., 87, 231
iv., 775
Glutarimide
CO.(CH2)3.C'O.NH
n
151-152
Bernheimer
G. I. [1882], 281
42, 1190
Acetonyl carbaminate
CMe2.O.CO.NH.CO
C5H;03N
75-5-76 c.
Urech
B., 13, 485
38, 545
1 1
11 11
11
„
73
11
B., 11, 468
34, 488
Glutiminic acid
„
180
Schiitzenberger
R, &, 643
Dimethylcyanuric acid
Me2HC3N3O3
C6H703Na
222
Hofmann
B., 14, 2728
42, 822
Malylureid
NH.CO.NH.CO.CH.CH.,.
230-235 d.
Grimaux
A. C. [5], 11, 400
"
COOH
Ethylhydantoi'n
CHEt.CO.NH.CO.NH
CjHsOjNo
b. 100
Heintz
A., 133, 65
vi., 702
i i
Acetonyl carbamide ....
CMe..CO.NH.CO.NH
i>
175
Urech
A., 164, 264
vii., 17; 26, (il
1 " i
Mesaconamide
CSH4(CO.NH2)2
„
176-5
Strecker
B., 15, 1641
42, 1281
Citraconamide
„
„
191 d.
11
B., 15, 1640
„
192
Dimethylic amidocyanurate
(C3N3)(OMe).,NH2
)I
212
Hofmann and
B., 3. 273
vii., 40!)
Olshausen
Diacetyl carbamide
CO(NHAc)2
CiH.Oj.N.
melts
Schmidt
J. p. [2], 5, 64
vii., 208
Dimethylglyoxyl carbamide
CH(OH).CO.NMe.CO.NMe
„
....
b. 100
Andreasch.
M. C., 3, 436
42, 1055
Methylallanto'in
C5H803N4
....
225 d.
Hill
B., 9, 1091
30, 50!)
Ethylic oxalurate
NH2.CO.NH.CO.COOEt
C6H804N2
cf. B., 4, 645
160-170 d.
Henry
C. E., 73, 195
24, 823
ii »
„
„
....
177 -17 S d.
Salomon,
B., 9, 374
30, 75
Succinocarbamic acid
NH2.CO.NH.CO.(CH2)2.
„
203-204
Pike
C. N., 28, 173
27, 49
COOH
11 n
„
„
....
203-205
„
B., 6, 1104
Isobutylic isocyanate
CHMe2.CH.3NCO
C5H9ON
110
Brauuer
B., 12, 1877
Butylic cyanate
CMe3.NCO
„
85-5 c.
Liquid
„
B., 12, 1875
38, 228
Hydroxyisovaleronitril
CHMe2.CH(OH).CN
ti
136 d.
1. -17
Lipp
A., 205, 26
40, 86
Ethylic diamidocyanurate ....
C3N(NH2)2.OEt
C5H9ON5
190-200
Hofmann and
B., 3, 275
vii., 410
Olshausen
Nitroamylene
C6H9.N02
C5H902N
160-170 d.
Haitinger
M. C., 2, 290
40, 1115
„
11
11
69-73 (14)
11
„
„
Nitrosoethyl acetone
CH3.CO.CH(NO)Et
„
....
53-55
Meyer and ZUbtin
B., 11,323
34, 488
11 11
"
"
183-187 c.
53-55
»
B., 11, 695
34, 660
Etliylic isointroso-acetone ....
CH3.CO.CH : N.OEt
„
130
Ceresole-
B., 16, 834
Methylic isonitroso-methyl-
CH3.CO.CMe I N.OMe
„
125 u.c.
„
11
acetone
Methyl diacetamide
NMeAc2
„
102
Liquid
Hofmann
B., 14, 2731
42, 822
0)
„
82-83
Brandes
Z. C. [1866], 459
vi., 829
Butyryl formamide ....
CH3.CH2.CH2.CO.CO.NH,
„
105-106
Moritz
39,16
Isobutyryl „
CHMe2.CO.CO.NHs
,,
....
125-126
„
39, 13
vi., 13
Levulinamide
C4H7O.CO.NH2
„
107
Wolff
A., 229, 249
48, 1124
Caffoline
CH(OH).NMe.C'O.N : C.
C5H9O2N,
cf. B., 15, 29
194-196
Fischer
B., 14, 1907
43, 217
NHMe
Ethylic acetylcarbamate
NHAc.COOEt
C5H9O3N
77-78
McCreath
B., 8, 1182
11 11
,,
,,
77-78
Kretschmar
C. C. [1876], 233
31, 614
n 11 ••••
77-78
Salomon
J. p. [2], 9, 299
27, 790
-
3 M
450
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc,
Alethylic aceturate
. NHAc.CH2.COOMe
C6H903N
254 (712)
5845
Curtius
B. 17, 1672
46, 1307
Ethylic methoxamate
. NHMe.CO.COOEt
»
242-243
s. 8-10
Wallach
A., 184, 68
32, 186
»« 11
»
JT
....
s.b. 0
Wallach and West
B., 9, 265
30, 185
„ a-nitrosopropionate
CH3.CH(NO).COOEt
)»
233 c. ; p.d.
94
Meyer and Ziiblin
B., 11, 693
34, 65!)
!) °- !!
»
»)
....
95
Meyer and Janny
B., 15, 1528
a-Isonitrosovaleric acid
CH3.(CH2)2.C(N.OH).COOH
))
143-144-5 d
Furth
B., 16, 2181
46, 42
y~ i! »
CH3.C(N.OH).(CH,)2.COOH
»
95-96
Miiller
B., 16, 1618
44, 112!)
Dimethyloxaluramide
NH2.CO.CO.NMe.CO.NHM
C5H903N3
225 d.
Menschutkin
A., 178, 203
29, 379
Niti-ovaleric acid
C4H8(NO.,)COOH
C5H9O4N
m.a. 100
cryst.
Dessaignea
A., 69, 274
v., 97!)
Glutamic acid
C3H5(NH2)(COOH),,
»»
135-140 p.d
Ritthausen
.1. p. [2]
vi., 637
i> >i
»»
IJ
....
188-190
Schulz and Urich
Lw. 20, 193; B.,
34,84
8,86
,, ,, "•• •••
)»
11
188-194
Urich and Barbier
B., 16, 314
„ ,,
)1
V
192
Richter
R. K. T., 74
,, „
»
3T
....
202-20V-5
Schulze & Bosshart
B., 16, 314
Ethyltt /3-nitropropionate ....
CH2(NO2).OH2.COOEt
5)
161-165
Liquid
Lewkowitsch
J. p. [2], 20, 167
33, Z3
„ nitrolactate
C5H905N
178
Henry
B., 3, 532
Nitrosopiperidine
C6H10N.NO
C,,H10ON2
218
Liquid
Schotten
B., 15, 425
42, 983
„
n
»
240 pd.
Liquid
Wertheim
A., 127, 81
vi., 947
Ethylacetyl carbamide
CO(N2H2EtAc)
C5H1002N2
120
....
J. p. [2], 21, 31
Butyryl carbamide
NH2.CO.NH.CO.C3H7
»5
176
A., 94, 101
i., 753
Ethylmethyl oxamide
NHMe.CO.CO.NHEt
)»
155-157
Wallach and West
B., 9, 263
30, 184
»i « ••••
»
V
155-157
Wallach
A., 184, 67, 70
32, 186
Dimethyl malonamide
CH,(CO.NHMe)2
))
....
123-125
Henry
C. R., 100, 943
48, 887
it »i
i»
J»
....
128
Freund
B., 17, 134
46, 728
11 11
CMe2(CONH2)2
)>
196-198, a.f.
Thome
39, 545
20«-210
Pyrotartaramide
NH2.CO.CHMe.CH2.CO.NH2
»
175
Henry
C. R., 100, 943
48, 886
Methylpropylacetoximic acid
HO.N : CMe.CEt '. N.OH
»»
170
Sehramiu
B., 16, 181
44,590
Propylic allophanate
NH2.CO.NH.COOPr»
C5H1U0SN3
150-160
Cahours
C. R., 76, 1383
26, 872
Acetonyl uramic acid
NH2.CO.NH.CMe2.COOH
»
160, d.
Urech
A., 164, 274
vii., 18; 26,62
Glycerylic allophanate
C3H5(OH)2(O.C2H3N202)
05H1005N2
160
Baeyer
A., 114, 160
i., 134
Diethylformamide
H.CO.NEt2
C5HUON
175-178
Liquid —20
Linnemann
W. A., 60, 44
vi., 619
„
7)
„
175-178
....
Wallach
B., 14, 744
Isobutylformamide
H.CO.NH.CH2.CHMe2
)>
135
Schmidt & Sacht-
A., 193, 102
36, 139
leben
Isovaleramide
CHMe2.CH2.CO.NH2
»»
....
100
Dessaignes and
A., 68, 333
v., 974
Chautard
ji
)J
ji
....
126
Hofmanu
B., 15, 983
„
»
1)
230-232
1S6-12S
Letts
B., 5, 673
vii., 1196
Methylisopropylacetoxime ....
CHMe3.CMe : N.OH
»
157-158
....
'fiigeli
B., 16, 2984
46, 611
Isoamylaldoxime
CHMe2.CH2.CH : N.OH
»
160-162
3etraczek
B., 16, 829
Isoamylic nitrite
CHMe2.CH2.CH.j.O.NO
CSHH02N
91
lieckher
J., 1, 699
iv., 75
>i )i
»
J)
92
tertoni and Truffi
G. I., 14, 23
46, 1110
Aruylic nitrite
CsH^.O.NO
»J
94-95
lilger
G.J.C. [1874], 352
D ji
»»
1)
96
.
Jalard
A. C. [3J 12, 318
iv., 75
1» 11 •••• •«••
-»)
))
97-98
._
Chapman
G. J. G, 1867
)> »!
»)
)1
98-99
....
vi., 870
» 11
»
)T
99
Guthrie
J., 11, 403
11 11 .... ....
»
J1
96-100
Haisch
C. C. [1872], 352
25, 1092
11 11
CH3.(CH2)3.CH2.O.NO
T»
97
Jertoni and Trutfi
G. I., 14, 23
46, 1110
Nitropentane ...
C5HU.N02
JT
150-160
VIeyer and Stxiber
B., 5, 204 ; A.,
25, 474; vii.,
171, 43
897
Ethylic dimethyl carbamate
NMe2.COOEt
n
39-140
Schreiner
J. p. [2], 20, 125
38, 312
„ ethylcarbamate
NHEt.COOEt
»)
74-175
Wurtz
C. R., 37, 182
i., 751
11 » ••••
»
)»
75-5
Schreiiier
J. p. [2], 20, 125
38, 312
11 11 ••••
>J
»
112-5
»»
J. p. [2], 22, 353
40, 88
Isobutylic carbamate
NHs.COO.CH2.CHMe,
»
20G-207
55
Vlylius
B., 5, 973
26, 266
a-ethylamidopropionic acid ....
C2H3Et(NH2).COOH
M
w. m.
)uvillier
C. R., 99, 1120
48, 373
o-amidoisovaleric acid
CHMe2.CH(NH2).COOH
»?
w. m.
ustin
B. S. [2], 37, 3
42, 589
#- „ „
(CH3)2.C(NHS).CH.,.COOH
H
215
Bredt
B., 15, 2321
3- „ 11
»
»
....
217
jiideke
A., 198, 53
COMPOUNDS CONTAINING FOUR ELEMENTS.
451
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Laetoethylamide
CH3.CH(OH).CO.NHEt
C5HU02N
200
48
Wurtz and Friedel
A. V. [3], 63, 110
ill., 453
Ethyl lactamide
CH3.CH(OEt).CO.NH2
)*
219
62-63
Wurtz
A. C. [3], 69, 175
iii., 452
a-methoxybutyrumide
CH,.CH2.CH(MeO).CONH.,
»;
77-78
Duvillier
C. R., 88, 598
36, 523
<i-hydroxyisovaleramide
CHMe2.CH(OH).CO.NH2
»
104
Lipp
A., 205, 27
40, 86
•y-hydroxyvaleramide
CH3.CH(OH.(CH2)2.CO.NH.,
3J
50
Neugebauer
A., 227, 97
48, 651
Base from putrefaction
....
J)
156
Salkowski
B., 16, 1193
44, 925
Diethylnitrosocarbamide ....
NHEt.CO.NEt.NO
QH.^^.,
5
Fischer
B., 9, 111
29, 912
Isoamylic nitrate
CHMe.!.CH,.CH,i.O.N02
OiH1103N
137
....
Rieckher
J. p. Ph., 14, 1
iv., 108
„ ,,
11
|1
147-148
Chapman & Smith
vi., 868
)> n
11
»
148
....
Hofmann
A. C. [3], 23, 374
iv., 108
Tetramethylcarbamide
OO.(NMe2),
CsH^ONj
175-177
Liquid
Michler & Escherich
B., 12, 1164
36, 935
Diethylcarbaniide
CO(NHEt)2
>1
IOC
Limpricht& Habich
A., 109, 105
» ....
)1
»>
107
Hofrnann
Z. G-
vi., 1051
,, .... ....
»
I)
....
107-5-110
Zotta
A., 179, 101
29, 569
»i
)J
I)
263 c.
112-5
Wurtz
R. [1862], 1 99
11., 564
Dimethylpropylalkine
C^.-jON
124-5-126-5
Ladenburg
B., 14, 2407
42, 165
Hydroxyisoamylamine
C6H10(OH).NH,
J)
157-159
Badziszewski and
B., 17, 839
46, 1190
Schramm
)> ....
t)
»
160
As., 7, 90
Hydroxypropylethylamiiie ....
C3H6(OH).NHEt
»
160
Liebermann & Paal
B., 16, 533
44, 910
Diethylsemicarbazide
Unsymmetiical
C6H13ON3
149
A., 199, 312
Dimethylpropylglycoline ....
CH2(OH).CH(OH).C'H.2.
C6H13OaN
216-217
Liquid
Both
B., 15, 1153
42, 1195
Taurobetain .
NMe2
C H O N
240
Z. P. C. 7 35
Bidimethylamidoearbanude
OO(NH.NMe2)s
^'V^M^V1
C5H14ON4
220-
Renouf
B., 13, 2172
40, 152
Ammonium glutarate
COO(NH,)(CH2)3.COO(NH.,)
CSHU04N2
150
....
Bernheimer
G. I. [1882], 281
42, 1190
Dinitrodihydroxyquinone
C'(OH)2(NO2)2:Oj
C6H203N2
d.w.m. 170
Nietzki
B., 10, 2147
34, 426
(nitranilic acid)
!! >!
M
»
+ xII20
a. 100 +
i)
))
»
Tetranitrodihydroxy benzene
C6(OH)2(N02)<
C9H2010N4
166
Henriques
A., 215, 335
44, 329
Nitrophenylene oxide
C6H3(N02):0
C»H,(NO),:O,=54.1
C6H30SN
C H O N
150
232
Etard
A., 124, 250
A. C. (5), 22, 273
v., 161
40, 583
Trinitrobenzeue
6 3\ /2 •~'2~~~"«^« *•
C6H3(N02)3=?
vg AJ. 3 v.' ^ J. '
CsHaO.N3
106-108
Henriques
A., 215, 356
»» ••• ••"
)) H
TJ
119
Salkowski & Eehs
B., 7, 373
27, 801
>»
=1.3.5
)1
121-122
Hepp
B., 9, 403
30,76
,, .«..» ..."
>J )»
>J
121-122
M
B., 13, 2346
)) ""
» >»
>J
121-122
»
A., 215, 344
44,316
,, ....
11 Jl
J)
121-122 u.c.
Claus and Becker
B., 16, 1597
44, 1093
>»
= »
» (0
145
Rinne and Zincke
B., 7, 871
27, 1163
Trinitrophenol
OH.(N02)3=?
C,,H307N:1
90-104
Zehenter
M. C., 6, 523
48, 1235
„
„ =1.3.4.6
>J
....
96 u.c.
Henriqu«s
A., 215, 331
44, 328
n
=1.2.16
J)
117-118
»
A., 215, 332
»
,, (picric acid)
=1.2.4.6
)J
120
Faust
B., 6, 132
26, 635
n 1> »
)» »»
n
120
Henking
Z. C. [2], 8, 523
25, 483
>j v u
>J »
V
121-121-5
Thorner
B., 12, 1632
» » »
)) 1)
»»
121-194
Mills
P. R. [1881], 205
i> » i)
)> *>
>)
....
122-5
Korner
Z. C. [2], 2, 662
vi., 910
5f U >!
» ?>
»».
121-122
Hepp
G. J. C., 1880
vii., 929
» 11 11
)> »>
»
122-5
Post
B., 7, 331
27,800
„
» =1
»
cf. B., 10, 524
174
Bantlin
B., 8, 22
28, 640
Trinitroresorcinol (stypliuic
(OH)2.(NO2)3=1.3.4.5.6 or
C.H308N:l
....
175-5
Stenhouse
P. R., 19, 410 ;
24, 358 ; vi;.,
acid)
1.3.2.4.6
C. N., 22, 98 ;
1043
A
23, 193
11 11
J> »
>»
....
174-5
Merz and Zetter
B., 12, 2035
38, 113
11 11
J» I»
)*
....
175
Griess
B., 7, 1224
11 11
»> »)
»
...»
175-5
Typke
B., 16, 553
Trinitrophloroglucinol
(OH)3.(N02)3=1.3.5.2.4.G
C6H309N3
....
158
Benedikt
B., 11, 1376
36, 58
„
»» >»
JJ
159-160
Benedikt & Hazura
M. C., 5, 667
48, 554
m-nitrodiazobenzol imide
NOj.C'6H3.N : N.NH
C6H402N4
....
52
Griess
P. T. [1864], (3),
iv., 449, 484
P- ,,
)>
?j
....
71
»
708
)>
»
3 M 2
452
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Aziiuidouitrobeuzene
C6Ha(NO2).N.NHN
CflH402N4
cf. A., 115, 25
211
Hofmanu
P. R., 10, 496
iv., 484
i i
Dinitrobenzene
C6H4(NCg2=1.3
C6H404N2
84
Friedburg
C. N., 47, 52
44, 535
v ••••
1» 11
n
297 c.
Mayer and Staidler
B., 17, 2649
48, 141
77
11 11
i)
84-5
Rommier
B. S. [2], 18, 70
26, 1002
JT .... ...
It JJ
j»
85
Petrieff
B., 6, 557
26, 1028
77 .... ...
11 11
11
87
Eudnew
B., 4, 410
vii., 908
j,
Jl J)
11
87
Salkowski
A., 174, 276 ; B.,
vii., 80, 908 ;
5,873
26, 280
It ....
11 )1
j»
87
Petersen
B., 6, 368
26, 1133
IT
» JJ
T1
87-5
Salkowski & Eehs
B., 7, 372
27,801
)1 .... ....
JJ 1?
Jl
89-1
Schiff
A., 223, 247
46, 1089
11 .... ....
JJ JJ
J)
89712
Mills
P. R. [1881], 205
)T
Jl JJ
11
89-8
Korner
G. I., 4, 305
29, 207
»T .... ....
JJ »T
II
....
89-90
Hlibiier, Babcock
B., 12, 1345
36, 928
and Sohaumann
„
Jl Jl
11
90
Henriques
A., 215, 379
44, 327
1» .... ....
)» 11
»!
90-91
Hepp
B., 13, 2347
f* .... ....
='
11
b. 100
....
i., 544
17
= 1.2
11
117
Laubenheimer
B., 9, 1328
»i ...• ..-•
J? V
11
117-118
Rinne and Zinck6
B., 7, 1372
28, 255
»»
1) 1)
*!
117-9
Korner
G. I., 4, 305
20, 208
IT .... ....
= 1.4
I)
170
Henriques
A., 215, 379
44, 327
>f --. ....
)I 1»
Jl
171
Hepp
B. S. [2], 30, 4
36,51
JT
») )>
11
171-172
Rinne and Zhick6
B., 7, 870
27, 1163
T1 .... ....
11 " »
31
171-172
Henriques
A., 215, 379
44, 327
11
V 1)
11
172
Korner
G. I., 4, 305
29, 208
Niti-oetheiiylnitrofurfurane
NO2.C4H2O.CH : CH.N02
C6H405N2
143-144
Priebs
B., 18, 1362
48, 971
Dniitropheiiol
HO.(NOS)2=1.2.6
11
61-62
Schneider
Z. C. [2], 7, 452
25, 241
Jl »>
))
61-843
Mills
P. R. [1881], 205
11 .... ....
» )>
11
63
Hiibner, Babcock
B., 12, 1346
36, 928
and Schaumann
•» .... ....
»> »
11
63-9
Korner
G. I., 4, 305
29, 229
n
)' »)
. 11
63-6'^
Hiibner & Schneide
A., 167, 105
vii., 909, 929
" 11 11
11
....
64
Faust
B., 6, 132
26, 634
„
» »)
11
64
Hiibner & Schneide
Z. C. [2], 8, 523
25, 483
•i
11 ))
51
64
Post
B., 7, 331
27, 800
IT
= 1-4.5. (?)
11
102-103
Andreae
J. p. [2], 21, 318
38, 467
11 .... ....
=1.3.5
11
....
104
Cahours
A. C. [3], 25, 22
iv., 398
11 ....
1) »T
l|
104
Laurent
A. 0. [3], 3, 212
24, 222
11 ....
» 11
11
104
Bantlin
B., 8, 22
28, 640
11 •". ....
Jl Jl
11
104
»
B., 11,2103
36, 238
V
51 »!
11
105
Bolley
Z. G [2], 7, 45
24, 222
'1 • •*•
„ =1.2.4
15
110-111
Wallach & Kiepen-
B., 14, 2618
heuer
11
j> 11
11
....
111-621
Mills
P. R. [1881], 2005
11 .... ....
M ^
I)
....
112; 113
Bohn & Heumann
B., 15, 3038
44, 584
IT
1) 11
11
....
113
Hemilian
B., 8, 768
29, 918
** «... ....
15 11
11
....
112-114
Guareschi and
B., 18, 1176
vii., 929
Daccomo
n ....
11 11
11
113-114
Hepp
B., 13, 2347
IT .... ....
Jl 11
11
113-114
Siibner & Schneider
Z. C. [2], 8, 523
25, 483
IT ....
11 It
11
113-114
Bohn & Heumann
B., 17, 272
46, 1014
J»
11 »
11
114
Wellgerodt
B., 9, 979
11 .... ....
" 11
>»
114
Engelhardt and
Z. C. [2], 6, 232
vii., 147, 90S
Latschmoff
11
1J M
1»
114
Faust
B., 6, 132
26, 634
11
1' V
!»
114
u
A. P. [3], 3., 103
27, 158
11 ....
" . "
11
114
Post
B., 7, 331
27, 800
51 •>••
*1 '1
11
114
Salkowski
A., 174, 257
28, 367
11
•1 51
)1
114
Slertens
B., 10, 995
32, 605
COMPOUNDS CONTAINING FOUE ELEMENTS.
453
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Dinitrophenol
HO.(NO,)2 = 1.2.4
C6HANS
114
Hiibner, Babcock
B., 12, 1346
36, 928
and Schaumann
„
)1 11
11
114
Hiibner
A., 210, 393
42,507
)1 •••• "••
= 1.3.4
)1
....
134
Bantlin
B., 11, 2104
36, 238
,)
11 )1
11
141
n
B., 8, 22
28, 640
„
= 1.2.3
11
144
»
B., 11, 2104
36, 238
Dinitroquinol
(OH)2.(NO2)2 =1.4.5.?
C6H,06N2
135-136 d.
Nietzki
B., 11, 471
34, 499
Dinitroresorcinol
„ =1.3.4.6
,,
cf. B. 16, 668
142
Benedikt and Hub
M. C., 2, 323
40, 1133
,, ,,
11 ii
n
cf. B.I 6, 110
142-5
Fevre
C. R., 96, 790
44, 733
51 V •"• •"•
=1.3.4.5
)i
cf. B. 16, 668
210
Benedikt and Hub
M. C., 2, 330
40, 1135
,, ,,
" 11
n
212-5
Typke
B., 16, 552
44, 917
11 1) "•• ••"
11 11
n
....
214-5
Schiaparelli & Abel
G. I., 13, 257 ;
46, 175
B., 16, 872
Trinitraiiiliue (picramide) ....
NH2.(NO,)3 =1.2.4.6
C.H406N4
179-180
Clemm
Z. C. [1870], 444
» 51
11 11
11
187
Salkowski
A., 174, 260
28, 366
)) »1
>» »»
J»
1SS
Pisati
A., 92, 327
11 1?
>» )1
»1
188
Liebermann and
B., 8, 378
Palm
11 11
>1 )1
1}
188
Mertens
B., 11, 843
? base
C6H5ON
156
Proskauer and SeL
B., 9, 1264
31, 68
Nitrobenzene...,
C6HS.N02
C6H502N
205 (760) ;
Kahlbaum
B., 17, 1261
121-2 (75);
116-2 (50) ;
102-5 (25) ;
98-1 (20) ;
93-0 (15) ;
87-0 (10) ;
79-1 (5) ;
68-2 (0)
v
»»
If
205 (730)
Stadeler
G.J.C.[1865],40
jl
1»
209-4 (745-4)
....
Briihl
A., 200, 188
38, 296
"
210
Konovaloff
C. R., 95 1284
44, 553
H
H
3
Schiff
A., 223, 247
46, 1089
11
•1
213
3
Mitscherlich
P. A., 31, 625
i., 543
11
„
219-220
3
Kopp
A., 98, 369 ; 137
M
"
169
H
?>
220
....
Ramsay
35, 472
"
|1
._
....
3
Schmidt & Schultz
B., 12, 486
36, 631
Nitrosophenol
OH.NO =1.4
?i
120-130 d.
Baeyer and Caro
A., 188, 360; B.,
vii., 911; 28,
7, 811, 965
84
a-Pyridine carboxylic acid
N.COOH =1.2
M
133-9 ;
Skraup
W. A., 82, 748
40, 744, 745
(picolinic acid)
134-5-136
j» 11
» >»
11
....
134-5-136
Weidel
B., 12, 1992
38, 268
'i »i
It V
11
134-135
Hantasch
B., 18, 1748
11 n
11 11
11
....
135-7-136
Skraup & Cobenzl
M. C., 4, 436
44, 1016
°~ » »'
11 «1
1)
137
Goldschmidt and
B., 16, 2979
46,61
Cons tarn
«- » ,1
15 11
n
....
140
Skraup
W. A., 82, 748
40, 745
#- » 11
= 1.3
11
....
225
Hoozewerff & Dorp
A., 207, 226
42,311
(nicotic acid)
#- 11
)! 51
ii
225-226
11
B., 16, 426
0- »
11 IT
11
225-227 u.c.
Laiblin
B., 10, 2137
34, 432
^ ' ») »
J* 11
11
228
Fischer
B., 15, 63
42, 627
#• >i ii
11 11
M
238-229
Weidel
B., 12, 2004
38, 268
0- „
11 U
11
229
Pechmann & Welsh
47, 152
0- 11 .1
1» »)
11
229-230
Coninck
C. R., 92, 413
40, 444
0- ii 11
V 1}
1>
229-5-230
Skraup
W. A., 82, 748
40, 744
0- .,
'» >1
11
230-231
Coninck
C. R., 92, 413
40, 443
i
11 ii
„ =?
1'
a. 250
Gerichten
B., 14, 315
40, 445
y- i. -I
„ =1.4
1»
a. 287
Bottinger
B., 14, 69
(isonicotie acid)
y~ 11 ii
11 11
!>
....
298-299
Eichter
R. K. T., 97
454
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
•y-Pyridine carboxylic acid
(isonicotic acid
y~ 11 11
y~ 11 11
y~ 11 i>
y- .. »
*' » .>.
y~ 11 M
7- » »
Nitrojihenol
(4th)
»> .-. ••-. J,
J1
)» .... ....
),
I»
IT .... ....
N.COOH=1.4
)) »
JT 11
T) ))
)» »»
ir )T
» Vt
» J)
OH.N02= ?
» )I
» »1
„ = 1.2
IT )1
V )>
>» »
J» »
» J»
M »
»» 11
)) )»
)» JT
Jl )?
!»• »»
» »
» >»
)» l>
5> »
n »
jr »»
» v
» j>
„ =1.3
)» »^
» )>
V =?
» !>
„ =1.4
>1 )»
» )J
?J »)
>5 »>
» J»
» »
» J>
>» )»
>» >*
» )J
)) »)
>» )»
)) »J
)) )>
» t»
» »>
?5 IV
C6H602N
T^
J»
rt
»
»
i)
jj
06H503N
^
»
ii
))
»
5)
)J
Ji
))
)»
J)
»
)»
J»
»
Jl
JJ
J»
»
»
)>
«
)»
1>
)>
)>
11
T1
I>
11
11
11
11
11
11
11
11
11
11
1>
11
11
11
11
«>
B., 12, 2332
205-207
216
314
214
194 (70)
302-5
303
305
305
306
307
309-5
310
—7 to+2
31
34-35
42
44-392
44-8
44-8
46
45
45
45
45
45
45; 46
45
45
45
45
45
45
45
45-2
46
96-96
95-96
96
105-106
108
108
abt. 110
110
110
110
110
110
10
10
10-111
11-455
14
14
14
14
14
14
14
Skraup
Ladenburg am
Schroeder
Ladenburg
Skraup
Behrmann & Hof
man 11
Weidel and Russo
Weidel
Guldschmidt anc
Constam
Post
Fittica
11
Hofmaun
Mills
Laubenheimer
Fittica
Fritsche
Armstrong
Walker and Zincke
Faust
Petersen
Post & Brackebuscl
Korner
Post
Hiibner
Augustiii and Post
Goldstein
Natanson
Armstrong & Pre-
vost
Armstrong& Brown
Schiff
Armstrong
Fittig and Bantliu
Korner
Bantlin
Fittica
11
Eichter
Fritsche
Walker and Zincke
Post
Faust
Petersen
Post & Brackebnsch
Hiibner
Armstrong
Korner
Mills
Schiff
Wagner
Schmidt and Cook
Fittig
Baeyer and Caro
Korner
Basse
W. A., 8-2, 748
B., 17, 1122
B., 17, 772
A., 201, 291
B., 17, 2697
ftT. C., 3, 865
M. G, 1, 41
B., 16, 2980
B., 6, 399
J. p. [2], 24, 54
B., 13, 714
A., 103, 347
P. R. [1881], 205
B., 9, 1820
G..I.C. [1876], 383
P. A. B., 16, 11
24, 175
B., 5, 116
B., 6, 132
B., 6, 368
B., 7, 164, 165
G. I., 4, 310
B., 7, 331
B., 7, 462; 8,
1221; A., 195, 1
B., 8, 1557
B. 8. [2], 30, 434
B., 13, 416
B., 7, 922
B., 7, 923
A., 223, 247
28, 520
B., 7, 180
G. I., 4, 305
B., 11, 2100
B., 13, 711, 1537
J. p. [2], 24, 13
B., 4, 460
J. p., 75, 257
B., 5, 116
B., 5, 853
B., 6, 132
B., 6, 368
B., 7, 163, 331
B., 7, 462
B., 7, 925, 926
G. I., 4, 305
P. R. [1881], 205
A., 223, 247
B., 7, 77
C. L., 3, 41
B., 7, 280
B., 7, 965
G. L, 4, 305
B., 10, 2188
40, 744
46, 1048
43, 1196
38, 410
48, 139
44, 484 .
46,61
26, 904
42,51
40,47
iv., 394
31, 594
iv., 394
25, 868
26, 418
26, 634
26, 1133
27, 475
27, 476 ; 29,
234 ; vii., 92!)
27, 800
27, 801 ; 29,
594 ; 36, 382
29, 386
36, 148
38, 463
27, 1164
11
46, 1089
vii., 908 ; 27,
583
29, 234
36, 237
40, 47
42, 51
vii., 907
iv., 396
25, 418
26, 173
26, 634
26, 1133
27, 475, 800
27, 802
25,868;27,1165
29, 234
46, 1089
vii., 925, 929
vii., 907
27, 696
28, 84
29, 234
34. 416
»,
»
J) .... ....
„ ....
» .... ....
(5th)
»> "» •"• »
j) ....
j, ....
COMPOUNDS CONTAINING FOUR ELEMENTS.
455
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Gh. Soc.
Nitrophenol . ....
OH.NOg— 1.4
C6H6O,N
114
Hiibuer
B.,8,1221;A.195,1
29,594; 38,381
114
B., 13, 416
38, 463
115
Post and Mehrtens
B., 8, 1552
115
Au^ustiu and Post
B., 8, 1557
29, 386
Nitrosoresorcinol
Nitroethenylfurfurane
/3- Hydroxypicolinic acid ...
y- » i>
a- „ „
Hydroxynieotinic acid
u i)
)) M
Nitrosonitranilide
Nitrocatechol
(OH)2.NO=1.3.2
C4H,O.CH:CH.NO,
N.COOH.OH=1.2.<
JI V
55 . )»
= 1.3.6
J) »
» ))
C(1H4.NOj.NH(NO)= 1 . 2
(OH)2.NO,=1.2.3.
—1.2.4
>»
11
)J
)J
fj
)J
»
))
C6H603N3
C6H604N
1
d. 112-148
74-75
250
258
267
301-302 d.
302 d.
SOS
126
86
157
Fdvre
Priebs
Ost
Bellmanu
Ost
Konigs and Geigy
Feer and Konigs
Pechmaini & Welsh
Plagemann
Weselsky and Bene-
dikt
Benedikt
B., 16, 1101
B., 18, 1362
J. p. [2], 27, 291
J. p. [2], 29, 1
J. p. [2], 27, 289
B., 17, 589
B., 18, 2399
47, 150
B., 15, 486
M. C., 3, 386
B., 11, 362
48, 971
44, 795
46, 840
44, 795
46, 1195
42, 973
42, 1200
34, 575
lax
M C 3 387
42 1200
Nitroresorcinol
=1.3.2
H
....
85
88
dikt
Weselsky
M. C., 1, 894
W A 82 1219
40 726
— 134
115
dikt
M C 1 894- A
26 1007 • vil
115
Schiaparelli&Abell
164, 1
G I 13 257
1043
46 174
—1.3,5
d w ni 148
Fevre
C. E 96 790
44, 733
Citrazinic acid
Diuitraniline ... . ..
N.(OH)2.COOH=1,2.6.4
NH2 (NO,),— 1 2 6
»
C«HCO,N
n.d. 275
d.w.m.a.300
137'8
Behrmanu and
Hofmann
B., 17, 2689
G I 4 305
48, 139
29 212
138
B, 7 371
27, 801
138
A 174 273
28 367- vil. 909
— 124
174
Staedel
B 14 899 • A
40 724 • 44 864
175
217, 182
Z C [2] 7 202
24 712
175
Z C [2] 6 444
vii 145
175
A 174 263
vii QfIS
176
B 10 1708
34 142
177
Z C [2] 6 233
vii 1 47
182
Latschiuoff
B 12 1345
182 183
Willgerodt
B 9 978
30 40 J
185
Gottlieb
A 85 26
iv 448
Nitropyrogallol
Aiuidodiuitrophenol (picra-
mic acid)
»j i)
•»» »
» H
» »1
»» ?»
Dinitropyrryl methylketone
u )» »
Apotheobroraine
Dinitroamido-resorciuol
Trinitrodiamidobenzene
Hydroxymethylpurine
Diacetyl dicyanide ....
ji IT •••• ••••
,, ,,
Nitraiuline
(OH)3.NO2=1.2.3.?
OH.NH,.(NO,)S=1.2.4.6
W »
») M
» »»
= 1.4.2.6
NH2.(NO2)2^consecutive
Me.CO.C4NH2(NO2)2
»1
(OH)2.NH2.(NO.,).!=1.3.(?)3
(NH2)2.(NO2)3=1.3.2.4.6
C5N4H2Me.OH
(CH3CO.CN),
M
n
NHyNO.,— 1.2
C.HAN
C,H,0§N,
3)
J)
)1
M
»>
»i
!1
» (?)
G.H.O.N,
C.H.O.N,
C6H6ON4
C6H60,N3
T»
»
+H80
208-209
210 c.
170
205 d.
165
165
167
169-170
170 p.d.
202
114
106-107
185
190
very liigli
233
69
69
69
38
Girard
Dabney
Hiibner
Stuckenber-g
Dabney
Henriques
Ciamician & Silber
»
Maly & Audreasch
Nolting and Collin
Fischer
Hiibner
Kleemann
Petersen
M. O., 1, 882
C. E., 36, 421
A. C. J., 5, 20
A., 210, 392
B., 10, 382
A. C. J., 5, 20
A., 215, 334
B., 18, 1464
u
M. C., 3, 108
M. C., 2, 326
B., 17,260
B., 17, 333
A., 120, 336
B., 18, 257
A., 124, 315
B 6 368
iv., 406
46, 308
42,507
82,474
46, 308
44, 329
48, 993
))
42, 633
46, 1004
46, 996
vi., 23
48, 505
26, 1133
»i «... . .. ....
)» n
M
64
65
Salkowski
A., 174, 278
B 18 1494
vii., 908
25, 418
86
Walker and Zincke
B. 5 114
456
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Nitraiiilinc
„
,,
» .... .... ..
n
»
,,
NH2.N02 =1.2
jj jj
j» ?»
)» »
jj JJ
jj v
j) jj
jj *j
>* j»
= 1.3
JJ 5J
?J J»
JJ 7?
)» JJ>
>J ><
U )>
J> J*
?»• »
» J*
j> *>•
i> *>
)v ;>
»»• »
„ =K*
M M
» »
)» I»
Jl )J
»» '»
» )>
>' T»
>> •»
)». 1>
)>. 17
)> Ji-
lt J)
» )>•
)>• )J
?
J> '
CjH^CO.NH.CN).,.
C4H3O(CONH2)j
OH.NH2.N02 =1.2.6
= 1.2.4
» »
» i)
= 1.4.?
>; )i
Me.CO.C4NH3.NO2
»J
C5H3MeO3N4
(OH)2.N02.NH2 =1.3.(?)3
(NO^CNH^?
=(?)s.l.4
NH2(OH).CCH2.OH,(NO,)3
C.H602N2
»
>J
))
)>
n
jj
»
j>
)>
jj
jj
jj
n
jj
»
)>
jj
)j
u
)>
»
j>
11
j>
u
j>
)j
jj
»
)»
j>
jj
)i
»
u
n
u
jj
C6H602N4
C6H603Na
JJ
J)
>I
I>
T»
J>
H
)J
C6H603N4
C6H,04'N2
C6H604N4
C6HAN4
C6H608N4
285
cf. A, 205, 85
+ xH20
+H2O
66
67
70-71
71
71
71
71-5
71-5
77-5 (?)
99 (?)
107
108
108
108
108
108
109-0
110
110
110
111
112; 114
116
140
141
141
141
14S-9
146
146
146
146
146
146
146
146
148
155
175
212-213 p.d.
104-105
n.f. 240
110-111
133-134
142-143
80-90
2U6
183
156
196-197
797
a. 360
170
210-211
294
99-5 c.
100
Zincke
Stover
Rhine and Zincke
Hubner
j)
Smith
Korner
Laubenheimer
Mixter
Salkowski
Levinstein
Arppe
Griess
Walker and Zincke
Petersen
Hiibner and Mears
Korner
Hofmann and Mus-
pratt
Lermontoff
Gabriel
Losanitsch
Hubner
Mixter
Salkowski
Arppe
Griess
Biedermaun
Korner
Saiidmeyer
Walker and Zincke
Petersen
Salkowski
Fittig
Rinne and Zincke
Stover
Hiibner
Rhalis
Hiibner
»
Jafie
Moller
Klinkhardt
Stuckenberg
Barbaglia
Hubner
v
Ciamician & Silber
»
»
Hill
Benediktand Hubl
Norton and Elliott
Ledoux
Bassett
Lessen
B., 7, 1374
B., 7, 1315
B., 7, 1374
B., 9, 775
A., 208, 301
A. C. J., 6, 172
G. I., 4, 305
B., 11, 1156
A. C. J., 5, 282
A., 174, 257
D. P., 256, 471
A., 90, 147 ;
A., 93, 157
18, 857
B., 5, 116
B., 6, 368
B., 9, 775
G. I., 4, 305
A., 57, 204
B., 5j 235
B., 11, 2261
B., 15, 470
A., 208, 278
A. C. J., 1, 239
A., 174, 257
A^ 90, 147 ;
A., 93, 157
18,857
B., 7, 541
G. I., 4, 305
B., 18, 1492
B., 5, 115
B., 6, 368
B., 7, 42
B., 7, 280
B., 7,871
B., 7, 1315
A., 208, 278
A., 198, 99
A., 208, 278
B., 10, 1708
B., 7, 1671; 8,811
J. p. [2], 22, 220
J. p. [2], 25, 48
B., 10, 387
B., 7, 1259
A., 75, 68; 205, 72
j>
A., 210, 382
u
B., 18, 1465
B., 18, 413
&, 18, 1458
B., 9, 371
M. C., 2, 324
B., 11, 327
B., 7, 1532
Z. C. [1871], 701
Z. C. [2]
28, 255
28, 271
28, 255
30, 303
40, 1131
48, 524
29, 210
34, 975
46, 666
28, 367
48, 1127
iv., 446 ; vii.,
143, 944
vi., 921
25, 418
26, 1133
30, 309
29, 210
iv., 446
vii., 658 ; 25,
503
36, 324
42, 955
40, 1130, 1131
40, 1130
28, 367
iv., 446
vi., 921
27, 808
29, 210
vii., 143
25, 418 ; vii.,
944
26, 1133
27, 467
27, 696
27, 1163
28, 271
40, 1130
38, 119
40, 1131
34, 142
28, 479
40, 259
42, 498
32, 475
28, 273
42,506
j>
48, 993
48, 810
48, 993
30, 75
40, 1133
34, 417
25, 99
vi., 723
>» "• ••-•
» •—
„
>* — *. .... ....
jj- ••-••• ••••• •••«
»j ••"• •-•*
Urocaninic acid
Succinocyamide
Dehydromucamide
Aiuidonitrophenol
,,
,,
^
„
)»
/3-Nitropyrryl methyl ketone
Cl~ M JJ U
<*- J> » JJ
Methylurio acid
Nitroanridoresoreinol
Dinitrodiamidobenzeue
jj
Eulyte
Hydroxylamine picrate
COMPOUNDS CONTAINING FOUR ELEMENTS.
457
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Nitrodulcitan(cf. J., 1860, 522)
Amidophenol (4th)
„
C6H4.OH.NH2 = ?
=1.2
„ —1.3
C6H6012N4
CGH;ON
....
120-130
150; 151
170
d.
Fittica
Bantlin
B. S., 22, 179
B., 13, 713, 1536
A, 103, 352
B., 11, 2101
40,47
11 ~~1 4
184 d
Richter
R. K T., 101
Methoxypyridine
Methyl hydroxypyridine ....
Acetylpyrroline
C5H4MeON
CH : CH.CAc.NH.CH
i i
J)
190-5-191
177-178
89
Liquid
Haitinger & Lieben
11
Ciamician & Denn-
M. C., 6, 279
G. I., 13, 455
48, 966
11
46, 290
11
Pseudoacetyl pyrroline
CH : CAc.CH.NH.CH
i i
»
181-182 c.
220
Liquid
90
stedt
Ciamician & Silber
Ciamician & Denn-
B., 18, 881
G. I., 13, 455
48,808
46, 290
11 i)
CH : CH.CH.NAoCH
> i
90
stedt
Schiff
B., 10, 1501
34, 216
Methylic a-carbopyrrolate ....
11 11 ••••
a-Methyl carbopyrrolic acid
P~ 1} 11 »!
Nitrodiamidobenzene
11
C4H4N.COOMe
C4H3MeN.COOH
(NH2),.NO2 =1.2.4
=1.3.?
= 1.4.6
C6H;03N3
M
JI
....
73
73
135
142-4
169-5
137
161
195
195
Ciamician & Silber
Ciamician & Mag-
naghi
Bell
Ciamician
11
Ladenburg
Barbaglia
Ladenburg
Ledoux
B., 17, 1152;
G. I., 14, 162
B., 18, 1832
B., 10, 1866
B., 14, 1056
B., 17, 149
B., 7, 1259
B., 17, 148
B., 7, 1533
46, 1044 ; 48,
246
36, 525
46, 738
28, 273
46, 738
Hypocaffe'ine ....
COO.CH.NMe.CO.N \ C.NMe
C H ON
181
Fischer
B., 14, 643, 1906
40, 614
1 1
0733
183
A 215 253
44 356
Pyrrylmethyl acetoxime
From Cyanomethine
Anhydro-diacetyl acetamidil
Methyl succinylcarbamide ....
NH : C4H3 CMe : N.OH
CO.C2H4.CO.NH.CO.NMe
i i
JJ
WW
145-146
194
253
147-148
Ciamician & Denn-
stedt
Meyer
Pinner
Menschutkin
B., 17, 432, 2945
J. p, [2], 27, 154
B., 17, 175
A., 178, 209
46, 1044
44, 654
46, 723
29, 380
Ethylbarbituric acid
CO.CHEt.CO.NH.CO.NH
1 _l
„
190
Conrad & Guthzeit
B., 15, 2846
44, 314
Dimethylbarbituric acid
CO.CH2.CO.NMe.CO. NMe
| |
„
123
Mulder
B., 12, 467
,,
CO.CMe2.CO.NH.CO.NH
i j
„
w. m. 200
Conrad & Guthzeit
B., 14, 1643
40, 1033
11 11 "••
Dimethylalloxan
11
CO.NMe.CO.NMe.CO.C(OH),,
C,H805N2
viscous 105
265
A. a. 105
Thorne
Maly & Andreasch
39, 546
M. C., 3, 93
42,631
Ammonium picramate ,„.
Dulcitol hexnitrate (nitro-
dulcite)
11 1» »!
Mannitol hexnitrate (nitro-
mannite)
Isovaleryl cyanide
Hydroxypicoline
Isobutylic cyanocarbonate ....
„ paracyauocarbonate
Ethyl succinimide
C6H2.ONH4.NH2.(NO2)a
C6H3(O.N02)6
)1
»
n
NC.COO.CH2.CHMes
CO.CH2.CH2.O.NEt
i " )
C6H805N4
C6H8018N6
It
C6H9ON
C6H90,N
( „ ).
n
145-150
155
146
232-234
165
68-72
86-5
108
112-113
Liquid
158
1. -12
Girard
Bechamp
Richter
Sokoloff
Etard
Weddige
11
Landsberg
C. R., 36, 421
C. R., 51, 257
B. S., 22, 179
R. K. T., 103
B., 12, 698
A., 131, 74
C. R., 92, 460
J. p. [2], 10, 20.1
J. p. [2], 10, 215
A., 215, 172
iv., 407
il., 351
36, 778
40, 1046
28, 448
28, 449
44,477
11 M
11 11
Dimethyl succinimide
11
CO.CH2.CMe2.CO.NH
»
234
234
sb. 60
20-24
S6
105-107
Menschutkin
Pinner
A, 178, 201
A., 182, 90
B., 14, 1076
29, 380
30, 626
40, 797
Ethylic acetcyanacetate
CHAc(CN).COOEt
NAc3
C6H903N
....
26
78 79
Hallard and Held
Wiehelhaus
C. R., 95, 235
B , 3, 848
42, 1280
24 407 ; vii., 3
3 N
458
ORGANIC COMPOUNDS.
Name,
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Trimethylic cyanurate
....
C6H903N3
100-170
133
Hofmann and Ols
P. K, 18, 493
vii., 409
hauseu
.1 11
....
w
....
132
Hofmann
B., 3, 271, 765
24, 136
11 »
....
„
274
175-176
Wurtz
A. C. [3], 42, 62
ii., 293
11 .,
....
11
175
Hofmann
B., 3, 272, 765
24, 136
ii i.
„
175
„
P. E. S., 18, 433
vii., 409
Ethylie diazosuocinamate
NH2.CO.CN2.CH2.COOEt
a
110-112 d.
Curtius and Koch
B., 18, 1298
48, 886
Hydrocaffuric acid
NHMe.C : N.CO.NMe.CH.
....
245
Fischer
B., 14, 1910
42, 217
i i
CO.^
11 )i
„
„
240-248
„
A., 215, 253
44, 356
Pseudodiazo-acetam ide
(C2H3ON3)3
C6H903N9
170 d.
Curtius
B., 18, 1290
48, 884
Ethylie aeetoxamate
NHAc.CO.COOEt
C6H9O4N
54
Kretzschmar ant
J. p. [2], 9, 299
27, 790
Salomon
11 i.
„
„
54
Kretzschmar
C. C. [1876], 233
31, 614
„ nitroso-aeeto^acetate
Ac.CH(NO).COOEt
(1
52-54
Meyer and Zublin
B., 11, 320
34, 487
... imidosuccinate
COOH.CH.NH.CH.COOEt
„
100
Lehrfeld
B., 14, 1822
42, 164
Caffiiric acid
C6H904N3
210-220 d.
Fischer
B., 14, 1909
42, 217
Ethylie oximidosuccinate ..
COOH.C2H2(N.OH).COOEt
C6H906N
110-111 d.
Ebert
A., 229, 45
48, 1122
Amidotriglycollic acid
N(CH2.COOH).,
C6H906N
a. 190, d.
Heintz
A., 122, 269
vi., 646
Citramic acid
C3H60(CO.NH2)(COOH)2
„
138
Behrmann ant
B., 17, 2687
48, 138
Hofmann
Xyloidin
C6H9(NO2\
CflH907N
b. 180
v., 1060
Nitroisodulcitol
C6H90UN3
b. 100
..>.
A., 127, 364
Mannitol pentanitrate
(C6H8(OH)(O.N02)5
C6H9016N5
77-79
J. [1864], 583
Diethyl carbamine cyanide ...
NC.CO.NEtj
C6H10ON2
219-220
Liquid
Wallach
B., 14, 737
40, 717
Ethylie ethyl cyanamido-
N(CN)Et.COOEt
C6H1002N2
abt. 213
Liquid
Bassler
J. p. [2], 16, 160
34,215
carbonate
Sarcosine anhydride
NMe.CH2.CO,NMe.CH,,CO
„
350
149-150
Mylius
B., 17, 287
46, 994
Dimethyl allantoin
C6H1003N
225
Cloez
I. D., Paris, 1866
vi., 520
Ethylie amidomaleamate
NH^CO.CH :C(NH2).COOE
CfiH1003N2
62 u.c.
Claus and Voeller
B., 14, 152
40, 254
„ imidosuccinamate ...
NH2.CO.CH.NH.CH.COOE
118
Lehrfeld
B., 14, 1821
42, 163
| |
„ a-|8-diisomtrasobuty-
CH3.C(N.OH).C(N.OH).
C6H1004N2
....
140 d.
Ceresole & Kockerl
E, 17, 821
46, 1121
rate
COOEt
„ dioarboxylamide car-
CH(CQNH2)2COOEt
B
190-191
Amato
G. I. ?, 690
25, 401
boxylate
Citrodiamic acid
C3H60(CO.NH2)rCOOH
C6H1005N3
158
Behrmaun and
B,, 17, 2685
48, 138
Hofmauu
Dinitrohexylic acid
CH3.C(N02)2.CMe2.COOH
C6H1006N2
215
Kachler
A., 191, 144, 155
34, 513
Tetranitrodulcitol
C6H10(NQ2)406
C0H10014N4
130-140
Bechamp
C. E., 51, 257
ii., 351
Amylic cyanate
CHPr^Me.O.CN
C6HnON
100-120
Liquid
Wurtz
C. E.,
vi., 114
Isoamylic „
CVHpACN
abt. 100
„
A. C. [3], 42, 43
ii., 195
» '-
„
„
134-135
Liquid
Custer
B., 12, 1329
36, 913
» >'
....
„
200
....
Hofmann and
B., 3, 275
Olshausen
Ethoxybutyronitril
Me.CH(OEt),CH2.CN
v
173
Pinner
B., 12, 2053
38,99
11
)J
173-174
Einne
B., 6, 389
Ally] acetoxime
C6H10:N.OH
187-5 c.
Liquid
Nageli
B., 16, 496
14, 728
Mesityloxime....
J,
180-190 p.d.
Liquid
B., 16, 495
Ethyldiacetamide
NEtAc3
C6HU0,N
185-192
Wurtz
A. C. [2], 42, 55
Ethylie amidoaceto-acetate....
cf. Z.C. 1871, 246
90
J. [1863], 325
Ethylie paramido-aoeto-aoe-
tate
....
"
212-214
30-Sl
Duisberg
B., la, 1386
42, 1193
» 11
f. A., 213, 172
25-28
Preclit
B., 11, 1194
34, 971
Ammonium ethylene dirne-
a. 63
Geuther
J. [1875], 302
34, 97X
thylene carbonate
Nitrosopropylacetone
Isonitrosoisopropylacetone ....
Me.CO.CH(NO).Pr»
Me.CO.C(N.OH).PrP
» '
49-5
5
['read well
Westenbergtr
B., 14, 2159
B., 16, 2992
44, 572
46, 581
Acfcaneine ....
....
C6HnO2N3
10-112
Tischer
A., 215, 253
4i, 356
Ethylie acetamidoacetate ....
NHAc.CH2. COOEt
C6HU03N
260 (712)
8
Curtius
B., 16, 753; 17,
44, 1087; 46,
1673
1307
COMPOUNDS CONTAINING FOUR ELEMENTS.
459
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
|
Authority.
I
Reference.
Watts' Diet.
& J. Gh. Soc.
Isobutylic oxamate
NH2.CO.COOBu3
C6Hn03N
....
89-90
Wallach and Lieb-
B., 13, 507
38, 557
mann
,, „
)»
J>
....
00
Geuther
J. [1863], 324
vi., 601
Ethylic ethyloxamate
NHEt.CO.COOEt
11
244-246 u.c.
Liquid
Wallach
B., 8, 762
28, 1187
)j »
»
»)
244-246
Liquid
Wallach and West
A., 184, 60
32, 186
„ dimethyloxamate ....
NMe2.CO.COOEt
»1
240-250
....
A., 217, 137
u » ••••
'»
')
242-%45
....
Ladenburg
B., 14, 2130
» ji
M
J1
250-260
....
Hofmann
J. [1862], 329
iv., 281
Diethyloxaniic acid
NEt2.CO.COOH
))
a. 80
Heintz
A., 127, 53
40, 718
j) >»
II
J)
....
99-101
Wallach
B., 14, 743
)J
Methyl snccinuraiuide
NH2.CO.CHj.CH2.CO.NH.
C6HU03N3
205-207
Menschutkin
A., 178, 210
39, 380
CO.NHMe
Diethylic carboxylocarba-
NH(COOEt)3
C6Hn04N
226 (760) ;
49-50
Wurtz &Henninger
C. R., 100, 1419
48,969
mate
144^146(20;
Ethylamidodiglycollic acid ....
NH(CH2.COOH)(CHEt.
»
200-220
Liquid
Heintz
A., 145, 214
vi., 646
COOH)
Nitrohexylic acid
CH3.C(N02).CMe2.COOH
)»
....
116;ar.lll-5
Kachler
A., 191, 159
34, 514
Citramide .. .... ....
C6HSO4(NH2)3
aHnO.N,
brown a. 200
210-215
Behrmann and
B., 17, 2685
48, 138
O^^o 4\ ^^2/a
^6 11^4* 3
Hofmanu
Diglycollamic diuramide ....
(NH2.CO.NH.CO.CH4!)2NH
C8Hn04N6
195-200
Mulder
B., 6, 1016
27,48
Oximido-ether
HN : C(OEt).C(OEt) : NH
C0H1202N2
170
25
Pinner and Klein
B., 11, 1482
3S, 47
Propionylethylcarbamide ...
NHEt.CO.NH.C3H5O
U
....
100
Hofmann
B., 15, 754
42, 1052
Isovaleryl carbamide
NH2.CO.NH(C5H9O)
»
....
191
....
A., 94, 102
i., 753
Di-(acetamido)-ethylidene ....
CH3.CH(NHAc)2
»)
169
Tawildarow
B., 5, 477
26,58;vii.,3,32
laodiethyloxamide
NEt.,.CO.CO.NH2
»J
266-268 u.c.
126-127
Wallach
B., 14, 735
40, 717
Dimethylsuccinamide
NHMe.CO.(CH2)3.CO.
»1
....
175
Wallach&Kamenski
B., 14, 170
40, 285
NHMe
» ....
J»
)1
175
Henry
C. R., 100, 943
48, 887
j, ...
NH2.CO.(CHMe)2.CO.NH2
)1
....
n.f. 260
....
J. p. [2], 26, 359
NFT CO.(CH2)4.CO.NH2
220
Henry
C. R., 100, 943
J)
H
Diisonitroso-acetonyl acetone
HON : CMe.(CH2)2.CMe :
))
134-135
Paal
B., 18, 59
48, 505
NOH
Methylpropylglyoxirue
Me.C(NOH) C(NOH).Pr«
))
168
Schramm
B., 16, 2185
46,52
Ethylazaurolic acid
C6H1AN4(?)
142
Meyer & Constam
A,, 214, 328
44, 40
Triaceto-diamide
N2H3Ac3
C6H1203N2
212-217
Gautier
A., 150, 189
vi., 524
Sarcosiue anhydride
(NHMe.CH2.CO)2O
»J
143-146
Traube
B., 15, 2112
44, 192
Oxalyl diethylnitrosohydra-
....
C6H1304N6
144-145 d.
A., 199, 298
zine
Acetyl diethylarnide
NEt2Ac
C6HUON
185-186
Wallach
A., 214, 235
44, 49
Capro-amide ....
CH3.(CH2)4.CO.NH2
120
Hofmaun
B,, 15, 983
C5H,,.CO.NH3
255
Henry
B., 2, 495
Isocaproamide
CHMe2.CH,i.CH2.CO.NH2
Jt
J)
100
Hofmann
J * ^"*f
B., 15, 983
Oaproamide ....
CHMePr«.CO.NH2
95
Kelbe and Warth
B., 15, 311
42, 711
>V
Methyl butylacetoxime
CMe3.CMe : N.OH
1)
....
74-75
Janny
B., 15, 2780
44,580
Piperyl-semicarbazide
C5H10N.NH.CO.NH2
C6H13ON,,
136
Knorr
A., 221, 297
46, 468
Isoamylic carbaraate
NH2.COO(C5HU)
C6HaOJi
220
66
....
A., 71, 106
i., 750
Ethylic propylcarbamate ....
NHPr°COOEt
>J
186
Schreiner
J. p. [2], 20, 125
38, 312
Methylaniidovaleric acid
CH Me2.CH(NHMe).COOH
»J
w.m.a. 120
Duvillier
A. C. [5], 21, 433
40, 713
a-amidocaproic acid (Leucine)
CH3.(CH2)3.CH(NH2).COOH
))
170
Schwanert
A., 102, 221
iii., 581
u »
n
»)
w. m. 170
Mulder
J. p., 16, 290
j»
Amidocaproic acid
C^^NHjJ.COOH
11
210
Kohler
A., 134, 36
vi., 782
,, „
»1
»»
w. m. 210
Nencki
J. p. [2], 15, 390.
32, 596
a-ethoxybutyramide
Cn3.CH2.CH(OEt).CO.NH2
»»
68-70
A. C. [5], 17, 542
0- „
CH,.CH(OEt).CH3.CO.NH2
»»
...."
71
Pinner
B., 12, 2057
38,99
a-hydroxycaproamide
C4H9.CH(OH).CO.NH3
M
140-142
J. R., 12, 367
Hexylnitrous acid .... .' ....
C6H13.N02(2)
„ (?)
212(763)p.d.
Liquid
Chancel
C. R., 100, 601
48. 647
Trimethyl a-propiobeta'ine ...
NMe,.CHMe.CO.O
i i
)1
begins 210
....
Bruhl
B., 9, 40
29, 699
Diethylglvoxylaniide
CH(OEt)2.CO.NH2
CeH.AN
MM
76-5
....
Z. C. [1870], 168
„
»»
IT
81-82
Pinner and Klein
B., 11, 1477
36,47
Isoamylcarbamide
NH,,.CO.NH(CH2)3CHMe2
C6H14ON3
88-91
Ouster
B., 12, 1330
36, 913
Amyl carbamide
NH2.CO.NH.CH2.C4H9
}1
120
Wurtz
B. S. [2], 7, 141
vi., 1116
„
3 M 2
460
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point;
Authority.
Reference.
Wa Its' Diet.
& J. Ch. Soc.
Amyl carbamide
NH2.CO.NH.CHMe.C3H7
C6H14ONS
cf. A, 139, 328
151
Wurtz
B. S. [2], 7, 141
vi., 1116
Nitrosodipropylamine
O : N.NPr2»
»
200-205
Siersch
A., 144, 144
vi., 9C5
?
....
C6H1405N2
....
152
Ehrenberg
J. p., 32, 97
48, 1192
Aceto-ethyl-nitrate .... ' ««
....
C6HU07N2
84-86
....
Nadler
A., 116, 173
Hydroxypropylpropylauiine
NHPr«.C3H6.OH
C6H15ON
174-177
30
Liebermann & Paal
B., 16, 532
44, 910
Trietliylalkamine
cf. a, 14, 1878
)»
161
Liquid
Ladeiiburg
C. R 93, 338
40, 1158
Diacetonalkamine
....
||
174-175
**>•
Heintz
A., 183, 293
31, 592
Ammonium pseudodiazoacet-
(C2H3ON3)3.2NH3
C6H1603NU
....
155 d.
Curtius
B., 18, 1290
48, 884
amide
Acid ammonium propionate
(Et.COONH4+Et.COOH)
C6H1504N
45
Sestini
Z. C. [2], 7, 34
24, 235 ; vii. ,
1010
Trinitrobenzoic acid
COOH.(NO2)3=1 .2.4.6(?)
C7H308N3
....
190
Tiemann & Judson
B., 3, 224
vii., 166
Triuitrohydroxybenzoic acid
COOH.OH.(NOj)s=1.3.(?)3
C7H309N3
+H20
105
Schardinger
B., 8, 1491
29, 584
Nitrobenzonitril
CN.N02=1.2
C,H402NS
....
109
Hiibner
B., 10, 1713
34, 140
„
n »
)»
....
109
Sandmeyer
B., 18, 1495
it
» ;>
J)
....
109
Barthlein
B., 10, 1713
„
>j )»
)»
109-110
Gabriel and Meyer
B., 14, 2338
,,
„ =1.3
J)
cf.A.,149,297
115
Engler
Z. C. [2], 4, 613
vi., 526
j> -«••
» J»
))
....
115
Sandmeyer
B.j 18, 1494
„
M ))
H
....
115
Frioke
B., 7, 1321
jj
J) »
1»
115-117
Gabriel
B., 16, 522
44, 916
j)
)> »
I)
....
117
Scbopf
B., 18, 1063
48, 896
j> .... ...
» »»
j)
....
117-118
.».*
A., 146, 336
j>
„ =1.4
)J
cf.A.,149,298
139
Engler
Z. C. [2], 4, 613
vi., 526
„
J) »
»
....
146
Sandmeyer
B., 18, 1493
» ••••
») »J
j>
147
Bruyn
E. T,, 2, 238
48, 658
,j ....
» »
»I
....
147
Fricke
B., 7, 1322
28, 272
Nitrohydroxybenzonitril
OH.CN.N02=1.3.?
C7H4O3N2
182-183
Smith
J. p. [2], 16, 228
34, 72
Dinitrobenzoic acid
COOH.(NO2)2=1.3.4
C7H40,N3
161 u. c.
Glaus & Halberstadt
B., 13, 816
38, 647
jj jj
=1.2.5
)»
177
Griesa
B., 7, 1224
28, 263
;, ,J
=1.2.4
»
179
Michler
B., 7, 422; A.,
27, 695; 28, 644
175, 150
)) JJ
11 )1
»>
179
Griess
B., 7, 1225
28, 263
), ,,
J' »J
I)
....
179
Tienian and Judson
A., 173, 145, 176;
28, 757; vii.,
B., 3, 223
165
» 1,
5» )i
»
....
179
Hiibner& Stromeyer
B., 13, 461
)) JJ
»' ')
))
....
179
Hiibner
A., 222, 67
» »
I> )>
)>
....
181
Glaus & Halberstadt
B., 13, 816
» Jl
=1.2.6
)»
202
Griess
B., 7, 1225
28, 263
5> JJ
=1.3.5
»»
....
201
Staedel
A.., 217, 194
44,865
J, „
>» »
)>
....
202
Tienian and Judson
B., 3, 224
vii., 165
JJ jj
>» »
)»
....
202
Beilstein and Kur-
B., 13, 355
38, 471
batow
J> JJ
» »
»»
203-204
Staedel
B., 14, 902
40, 725
» »
i» »>
))
....
203-204
Gattermann
B., 18, 1485
I) ))
v »
»»
204
Michler
A., 175, 152
28, 644
») JJ
»» u
))
....
204-205
Mure tow
Z. C. [2], 6, 641
vii., 165
» ))
v )»
)>
....
•204-205
Hiibner
B., 10, 1703
34, 148
» ))
'> »
11
205
jj
A., 222, 67
46, 314
Methylene dinitrocatechol ....
CH2:02:C6H2(N02)2=1.2.(?)2
»J
cf. A., 199, 75
101 u.c.
Jobst and Hesse
B., 11, 1034
34,733
Dinitrosalicylic acid
COOH.OH.(N02)2=1.2.(?)2
C7H407N2
157-158
....
A,, 69, 230 ; 78, 8
» »
=1.2.(?)8
))
165
Salkowski
A., 173, 43
28, 71
» D
„ =1.2.3.5
1)
173
Hiibner
A., 195, 47
36, 382
j» » ....
" i)
||
173
Hiibner & Babcock
B., 12, 1345
Dinitrobydroxybenzoic acid
=1.4.3.5.(2)
n
235 d.
Salkowski
B., 4, 225
24, 556
» »
» !I
)»
....
235-237
jj
A., 163, 36
25, 716
Phenylic isocyanate (carbanil)
PLN : co
C7H6ON
163
Liquid
Hofmann
P. E., 19, 108;
24, 139; vii.,
B., 3, 655
407
» » ij
»»
jj
163 c.
....
Weith
B., 9, 821
30, 639
" » >i
)»
jj
160-165
Eichter
E. K. T., 139
» » jj
j>
jj
166 (769)
Hofmann
B., 18, 765
48, 774
> » i>
ji
»
178-180
Liquid
jj
A., 74, 9
ii., 196
COMPOUNDS CONTAINING FOUR ELEMENTS.
461
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Hydroxybenzonitril .... ' ....
OH.CN=1.3
C7HSON
....
8*
Griess
B., 8, 859
28, 1261
,,
j) »
51
82
Smith
J. p. [2], 16, 221
34, 72
» •••• ••••
„ =1.4
H
....
112-113
Klepl
J. p., 28, 193
46,447
jj
JJ JJ
)J
....
113
Hartmann
J. p. [2], 16, 55
32, 896
,,
„ =1-2
»»
195
....
B. S., 13, 26
„
JJ »»
( „ V
....
280-285
Grimaux
B. S. [2], 13, 25
vi., 1012
Methenylamidophenol
C6H4.N : CH.O=1.2
)J
182-5
30-5
Ladenburg
B., 10, 1124
32, 752
1 1
Anthranil
C6H4.NH.CO or C6H4.N : C.
)I
210-215 d.
L. — 18
Friedlander and
B., 15, 2105
44, 188
i iii
OH=1.2
Henriques
Nitrosoindazole
....
C;H5ON3
....
73
Fischer and Fafel
A., 227, 303
48, 541
Salicylimide ....
C6H..CO.NH.O=1.2
C,H,O,N
n.f. 200
Lirnpricht
A., 98, 261
v., 167
i i
V7 5 z^1
Oxycarbanil ....
CO : N.C6H4.OH=1.2
136-138
Grenvik
B. S, [2], 25, 177
31, 473
Diazobenzoimide
C6H4.N2.NH.O.CO=1.2
C7HAN3
I
145
Griess
Z. C, [2], 3, 165
vi., 259
1 1
,,
=1.3
I)
160
»
Z. C. [2], 3, 164
vi., 258
jj
=1.4
))
185
D
JJ
vi., 259
Benzoyl nitrite
C6H5.CO.N02
C7HS0,N
Liquid
Lippmann and
B., 9, 1464
31, 315
Hawliczek
Nitrobenzaldehyde
COH.N02=1.2
)»
....
43-5-44-5
Gabriel and Meyer
B., 14, 829
40, 730
jj .... •••..
JJ JJ
?)
....
46
Bertagnini
A., 79, 260
I., 570
jj ....
JJ 11
3»
....
46
Friedlander and
B., 14, 2803
42, 840
Henriques
jj .... ....
„ =1.3
n
....
56-57
Gabriel,
B., 15, 838
48, 1070
„
JJ Jl
»
....
58
Lippmann and
B., 9, 1463
31, 315
Hawliczek
,, ....
» =1-4
jj
....
93
Fischer and Greiff
B., 13, 670
38, 640
,,
JJ JJ
jj
104
Friedlander
B., 14, 2577
„ ..,.
» ))
jj
....
106
Fischer
B., 14, 2525
40, 393
Nitrophenylene carbamide ....
NO2.C,H3.NH.CO.NH
C.H503N3
n.f. 300
Hager
B., 17, 2625
48, 150
i i
Nitrobenzoic acid
COOH.N02=?(4th)
C7H5O4N
....
125
Fittica
B., 8, 252
88, 766
» »
JJ JJ
JJ
127
Fischer
A., 127, 140
i., 555
,, „ ....
JJ )>
JJ
....
127
Wilbrandt & Beil-
A., 128, 257
iv., 61
stein
,, >,
» )J
JJ
127
Tiemann & Judson
B., 3, 224
vii., 165
,, ,, .... ....
»J )»
JJ
....
127
Radziszeweki
B., 5, 332
85, 1097
,j ,j .... ....
)) »
JJ
....
127 ; 128.
Fittica
B., 8, 710, 741 ;
28, 1195 ; 30,
9, 788; 10, 481,
412; 38,483,
163.0 ; J. p. [2],
34, 65; 36,
13, 184
151
jj >j •••• *•«
» >»
JJ
....
127
Bodewig
B., 12, 1983
38, 251
» »i •••• ....
» JJ
JJ
....
128
Mills
[2], 4, 363
vi., 314
» jj ••••
JJ 1}
JJ
....
128-130
Fittica
B., 9, 794
30, 411
„ „ .... ....
=1.3
JJ
....
135
»
B., 10, 484; 11,
32, 483; 34,
1210 ; J. p.
981 ; 36, 152
[2], 13, 184
,, 1)
» 1»
»
MM
135-136
»
B., 9, 789
30, 412
JJ JJ
»> W
JJ
....
136
>»
J. p. [2], 13, 184
36, 151
,, „
)1 )»
JJ
....
136
Bodewig
B., 12, 1983
38, 251
JJ J) "« ••••
)» »»
JJ
....
138
Sandmeyer
B., 18, 1494
j, ,, ....
)J 1)
.,,,
...«
138-140
Mouuet, Eeverding,
B., 12, 444
36,625
and Nolting
J) J»
JJ »
JJ
....
139 u.c.
Wiudmann
B., 8, 392
28, 893
,, ,,
)> >>
JJ
....
140
Plascuda & Zincke
B., 7, 985
88,70
JJ ))
)) JJ
JJ
....
140
Fittica
B., 8, 252 ; 710,
28, 766, 1195
741
„ ,,
»' »J
JJ
....
140
Griess
B., 8, 526
28, 892
„ „
J> »)
JJ
....
uo
Hubner
B., 10, 1699
34, 150
:> » • •••
» »
JJ
....
140;r,s.ll7;
Windmann
A., 193, 212
36, 154
of. (slow)
135 ; af.
(quick) 141
V '
462
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Nitrobenzoic acid
COOH.N02=1.3
C7H604N
....
140 ; 142
Salkowski
B., 10, 1258
» jj .... ....
» ,,
jj
....
140
Schiff
B., 11, 1782;
36, 157, 321
G. I., 8, 294
„ „
„ „
,,
....
140-141
Windmann
B., 10, 1159
32, 783
,J jy .... ...
» jj
„
....
140-141
Monnet & Nolting
G. I. C., 1879
J) yy .... ...
„ „
„
141
Beilstein and
A., 163, 134
vii., 165 ; 25,
Kuhlberg
709
„ „
» >.
„
....
141
Naumann
B., 8, 526
28, 892
„ „
» »
„
....
141
Thompson
B., 14, 1186
,, „ .... ...
jj j»
„
....
141
Hubner
A., 195, 1
36, 381
„ „
)> >j
„
....
141
Bodewig
B., 12, 1983
38, 251
„ „ ....
JJ >J
„
....
141-142
McHugh
B., 7, 1267
28, 270
„ „
» »
„
....
141-5
Ladenburg
B., 8, 536
28, 887
„ ,
» ,,
„
141-5
Lellmann and
A., 228, 239
48, 974
Wurthner
„ „
„ „
„
....
142
Hubner
B., 10, 1697
34, 150
„ „
„ „
„
....
142
„
A., 222, 67
46, 314
„ „
» .,
„
....
142
Fittica
B., 9, 788; 10,
30, 412 ; 32,
481 ; 11, 1207;
483 ; 34, 981 ;
J. p. [2], 13, 184
36, 152
„ „
JJ JJ
„
142
Bodewig
B., 12, 1983
38, 251
„ .,
JJ »
„
....
141-142
Conrad
J. p. [2], 15, 241
32, 485
„ „
M >J
„
141-142
Naumann
A., 133, 205
vi., 314
„ „
=1.2
„
....
140-141
Salkowski
B., 5, 722
25, 1024 ; vii.,
947
„ „
„ „
„
141
Windmann
A., 195, 202
36, 154
„ »
» ,>
jj
....
141-143
Bedson
37, 93
„ „
» „
„
....
143
Windmann
B., 8, 393
28, 893
„ „
1? »>
„
....
145
Claisen & Shadwell
G. J. C., 1879
„ „
>. j>
„
....
145
Griess
J. p. [2], 6, 384
26, 637
„ ,,
ii „
„
....
145
Monnet and Nolting
G. J. G, 1879
„ „
>» »
,,
145
Baeyerand Drewsen
B., 15, 2860
J, „
» »
„
....
145-147
Gabriel and Meyer
B., 10, 828
„ „
« »
• „
146 u. c.
Engler
B., 18, 2239
»» » *"* *•*•
... ,,
„
....
146
Noyes
B., 16, 53
), ,7
... „
„
146-147
Liebermann
B., 10, 1038
»» n
0 »
,,
....
146-5
Ulausand Mallmann
B., 11, 760
>' »
.» >.
„
....
147
Kumpf
B., 17, 1074
46, 1004
» „
.. „
„
....
llfl
Windmann
A., 193, 210, 221
36, 154
»
„
....
147-148
Friedlauder and
B., 14, 1920
Ostermeier
„ ,
*. »
,,
149
Windmann
B., 10, 1159
32, 783
„ „ mixture
J-i 1.
„
172-174
Wilbrandt and
A., 128, 265
Beilstein
» » n
». »
jj
172-174
Hubner and Bie-
A., 147, 268
dermann
w »> u
). >J
„
173-175
Faust
J. [1869], 651
» J. jj
JJ JJ
„
178-179
Fittica
B., 8, 254
28, 766
JJ JJ JJ
JJ J.
„
179
Liebermann
B., 10, 863
„ „ .... ....
= 1.4
„
....
230
Eadziszewski
Z. C. [2], 5, 35S
vi., 1102
» JJ
» jj
„
230
Bedson
37, 91
1! »
» j.
jj
233
232-235
234
Griess
Ladenburg
Claus
B., 8, 529
B., 8, 536
B., 15, 2332
28, 893
28,' 887
"
"
....
234
233-237
Hassenpflug
TjtidGiiljii i" ^
B., 8, 712
B. 8 536
28, 1188
JJ J,
9J
232-240
236
Monnetand Nolting
G. J. G, 1879
28, 887
36, 154
,J „
.. »
„
238
Erlenmeyer
B., 8, 535
28, 887
» »
JJ jj
„
238
Micliaeland Norton
G. J. G, 1877
Jl J) .... ...
Jj i)
J.
238
Windmann
B., 8, 393
28, 893
COMPOUNDS CONTAINING FOUR, ELEMENTS.
463
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Nitrobenzoic acid
COOH.N02=1.4
C7H504N
238
Wiudmann
B., 10, 1159
32, 783
,, j) *••• •••
» j>
?)
238
Eennie
41, 223
?, ,,
» »)
)*
238
Windinann
A., 193, 226
36, 154
„ „
)> D
)J
238
Spica
G. I., 8, 406
36, 631
,, „
>» n
3J
238
Maxwell
B., 12, 1766
38, 120
„ ,,
j) )>
I)
236-240
Mills
[2], 4, 363
vi., 314
,, ,,
)j ?>
))
240
Wilbrand&Beilsteii
A., 126, 255
iv., 61
,, ,, —
»i i»
)1
240
Fischer
B., 8, 526
28, 893
» „
)5 )I
)»
240 u. c.
Claus and Witt
B., 18, 1674
„ „
J> )?
H
240
Stuart
47, 158
„ ,,
H )»
j)
240
Noyes
B., 16, 53
Nitrohydroxybenzaldehyde...
COH.OH.NO2=1.2. ?
))
105-107
Mazzara
G. I., 6, 460
31, 597
,, ....
=1.2.7
55
123-125
jj
)>
)»
,,
= 1.3.?
)J
125
Tiemann & Ludwig
B., 15, 3052
44, 586
») ...
„ =1.3.2. or 6
1»
128
Ludwig
C. C., 1884, 35
48, 664
i, ....
»1 M
»I
128
Tiemann & Ludwig
B., 15, 2053, 3052
44, 189
»
=1.3.4
1)
138
»
11
1)
,, ....
J» »
1)
138
Ludwig
C. C. [1884], 35
48,664
»» ....
=1.3.5
)1
166
»
»
»
„
)1 T»
n
166
Tiemann & Ludwig
B., 15, 2054, 3052
44, 189, 586
» ••••
= 1.4. ?
jj
139-140 s.
Herzfeld
B., 10, 1269
34, 65
»
» »>
)>
140
Mazzara
G. I., 7, 285
32, 781
Methylene nitrocatechol
NO,.C6.H3.O.CH2.O=?.1.2
»
cf. A. 199, 73
148 u. c.
Jobst and Hesse
B., 11, 1034
34, 733
" i
Nitrotoluquinone
C6H2Me.(N02):02
»
237
Etard
C. R., 84, 614;
32, 476; 40,
A. C. [5], 22, 275
583
Pyridine dicarboxylic acid ....
N.(COOH)2=?
i)
....
abt. 210
Dewar
C. N., 23, 38
24, 145
»» M >i
=1.2.3
»
S22-225
Furth
M. C., 2, 416
42, 231
(quinolic acid)
»> 5j )i
» »
)>
•<•>
222-225
Hoogewerff & Dorp
B., 12, 747; 13,65
36, 731
i? i) 11
') 11
v
Brown 295
226 d.
Ladenburg & Both
B., 18, 52
48, 558
»» J> 51
Jl ))
»>
d.lOO=njco-
228 - 230
Hoogewerff & Dorp
R. T., 1, 1, 107 ;
44, 90
tic acid; in
(slow); 180
B., 16, 426
cap.tube=
d. (quick) ;
brown 175
a. f. 228
Pyridine dicarboxylic acid
=1.2.4
»
Impure, cf.B
219
Waage
M. C., 4, 708
46, 173
(lutidinic acid)
18, 1745
55 » »»
>» 1)
»
)J
219
Weidel and Pick
M. C., 5, 656
48, 55
n »» »
)» »
»»
n
219
Hantzsch
B., 18, 1745
i* » *»
)J )>
)»
>»
219-5
Weidel and Herzig
M. G, 1, 20
5» 51 »5
» 1»
>i
)»
220
Furth
M. G, 2, 416
42,231
» » )>
» 1>
»
234-235-5
Bottinger
B., 14, 68
M
»» 11 )i
»» J)
)»
235
Ladenburg & Roth
B., 18, 916
48, 816
Pyridine dicarboxylic acid
=1.2.6
))
236
Furth
M. G, 2, 416
42,231
(isocinchomeronic acid)
5j 11 11
>1 1)
»»
236-237
Epstein
B., 18, 1745
5* >i n
» »
»
237-5
Ramsay and Dobbie
B., 11, 326
33, 103
i) ji »)
)1 »
u
237-5 d.
Ramsay
P. M. [5], 4, 244
36, 267
11 i» j»
)J )1
j»
241
Dewar
36, 947
Pyridine dicarboxylic acid ....
= ?
5)
d. 241-245
Ramsay
P. M. [5], 6, 24
JI
11 11 »
» J»
It
d. 244-245
H
P, M. [5], 6, 21
)1
11 j) 11
=1.3.4
1)
cf.A.,173,96
249-250 p.d.
Weidel & Schmidt
B., 12, 1148
36, 947
(cinchona eronic acid)
»
» 11 11
)» ))
*»
250 d.
Hoogewerff & Dorp
B,, 13, 61; A., 204,
38, 405, 896
84
11 11 »
» 1)
)»
250 d.
»
B., 14, 646, 974
40, 611
11 u ij
)t IT
)'
249-251
Furth
M. G, 2, 416
42, 231
" 11 11
)1 »
1»
251-252
Ramsay and Dobbie
33, 103
)i » j»
» )»
5*
258
Furth
M. C., 2, 416
42,231
» ») »j
>' )»
»
258
Michael
B., 18, 2029
» ;» ?)
)) I)
„
258-359 d.
Skraup
W. A., 81, 337
40, 290
Pyridine dicarboxylic acid ....
= ?
)J
....
263
Furth
M. G, 2, 427
42, 231
464
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts1 Diet.
& J. Ch. Soc.
Pyridine dicarboxylic acid ....
N.(COOH)2=?
C7H604N
266-268
Gerichten
B., 13, 1637
40, 110
Acid from diquiiioline
....
ii
....
96 u. c.
Glaus
B., 14, 1942
42, 215
Nitre-salicylic acid +H2O ....
COOH.OH.N02=1.2.3
C7H506N
....
123
Hasse
B., 10, 2187
ii n 11
11 11
)>
cf. 28, 263
124
Hall
B., 7, 1320
vii., 1066
» 11 ii
11 n
))
....
125
Hiibner and Hall
B., 8, 1216
29, 593
ii n 11
11 11
1)
....
125
HUbner
A., 195, 31
36, 381
») n ii
ii n
»
125
Schiff and Masino
G. L, 9, 318
38, 121
ii 11 11
11 11
»
....
131
HUbner
B., 10, 1699
34, 150
ii 11 n
11 »
)i
131
Griess
B., 11, 1733
36, 247
ii i>
11 "
>»
143
Hasse
B., 10, 2187
•» 11
11 i»
)»
....
144
HUbner
A., 195, 31
36, 381
» ii ....
11 11
5)
....
144
Schiff and Masino
G. I., 9, 318
38, 121
>! 11
11 11
M
....
144-145
HUbner and Hall
B., 8, 1216
29, 593
,) ,, ....
11 11
»
....
145
HUbner
B., 10, 1698
34, 150
11 11 .... ....
=1.2.?
)J
218
Hall
B., 7, 1321
28, 263
,| „ .... ...
=1.2.5
T>
228
11
>i
vii., 1066
„ ,,
»» »>
))
228
HUbner
B.,8, 1217
29, 593
,. „
I> »
I)
....
228
Hasse
B., 10, 2189
34, 416
I) J).
» »
M
228
Griess
B., 11, 1731
36, 246, 247
„ ,, .... ....
-M f>
))
228
HUbner
A., 195, 9
36, 380
)! ,1
. )' »
))
....
228
Miigge
B., 12, 1347
36, 928
,, „
-)) »
))
....
228
Babcock
B., 12, 1345
»
„ „
-» »
»i
228
Schiff and Masino
G. I,, 9, 318
38, 121
II 11 .... ....
-»» M
»
228
Mandt
B., 10, 1701
11 II •"•
l> 1)
)i
228
HUbner
B., 10, 1698
34, 150
Nitrohydroxybenzoic acid ....
=1.3.6
)»
169
Griess
B., 11, 1733
36, 247
>« >!
=1,3,2
))
178
11
B., 11, 1734
11
ii ii
= 1.3.4
»
230
ii
B., 5, 856
26, 178
ii n
=1.3.5
-W
....
d.w.m.
HUbner and Grube
B., 10, 1704
ii i
=1.4.5
»)
....
178
Gruber
B., 12, 520
36, 644
11 >
» ))
51
185
Griess
B., 5, 856
26, 178
11 !•! «•••
J) )>
V
186-187
Hasse
B., 10, 2188
34, 416
Hydroxyquinolic acid
N.(COOH)2.OH=1.2.3.6
J>
....
d.w.m. 254
Konigs & Korner
B., 16, 2159
46,85
n n
)» )1
)»
d.w.m. 250
Feer and Konigs
B., 18, 2399
Dinitrobenzamide
(CO.NH2).(N02)2=1.3.5
C7H606N3
....
777
Z. C. [1870], 642
11
» )»
)J
183
Voit
A., 99, 105
i., 541
Trinitrotoluene
Me.(NO2)3=?
C^AN,
Mixture (?)
78-85 ; 78-88
Mills
P. M. [4], 1, 17
29, 393
11 •>•» ••«•
)> J»
»
11
78-853
ii
P. E. [1881], 205
11
=1.3.(?)2
^»
ii
76-82
Beilstein and Kuhl-
Z. C. [2], 5
vii., 1166
berg
"- „
=1.2.4.6
)»
....
80-54
Mills
P. M. [4], 1, 17
29, 393
"- 11
>» »1
)1
80-532
)J
P. R. [1881], 205
o- n
» I»
J»
....
81
Stadel
A., 225, 384
48, 142
o- 11
» J>
»)
....
82
Wilbrand
A., 128, 178
v., 858
"• „
>» 1>
H
82
Hepp
B. S. [2], 30, 4
36,51
y- 11
= ?
»»
....
104
.
A., 215, 366
0- ,,
» M
j>
112
A., 215, 370
Dinitroamidobetizoic acid ....
COOH.NH2.(NO:!)2=1.2.3.5
»»
256
Salkowski
A., 173, 45
28, 71
»» ii
»! 11
»)
....
256
11
B., 4, 872
ii »
„ =1.4.3.5
>j
....
258
Stadel
B., 14, 900
40, 724
(chrysanisic acid)
>» »
11 11
»»
258-259
Salkowski
B., 4, 871
»» » ••••
» 11
»>
$59
11
A., 163, 1
25, 714
i) »»
11 11
»»
....
259-260
Friederici
B., 11, 1977
vii., 336
Isonitrosomeconic acid
C4HO(OH)(COOH)2(C:NOH)
C7H607N
+H20
d. 190
Odernheimer
B., 17, 2083
46, 1302
Trin itroanisol
OMe.(NO2)3=1.2.4.6
C7H507N3
....
58-60
Cahours
A., 69, 238
i., 306
,, ....
)1 I!
-J»
....
64
Post and Merteus
B., 8, 1552
Me.OH.(N02)3=1.2.3.4.5
))
....
102
Noling and Collin
B., 17, 271
46, 1007
„ =1.3.2.4.6
»
....
a. 100
Duclos
A., 109, 135
Ii., 108
ii ii
)?
104
Liebermann & Dorp
B., 4, 655
i.
II )!
15
....
106
Nolting and Salis
B., 15, 1862
11 •!
»
....
106
Wurster and Riedel
B., 12, 17,99
COMPOUNDS CONTAINING FOUR ELEMENTS.
465
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch, Soc.
Trinitrocresol
Me. OH.(NOa)3=l. 3.2.4.6
C7H607N3
106
Emmerling and 0,;
B., 9, 1095
30, 523
penheim
106
jNoltin^ and Salis
B., 14, 988
40, 725
Trinitro-orcinol
jj jj
Me.(OH)2.(NO2)3=1.3.5.2.4.6
C7HAN3
162
Stenhouse
P. R, 19, 410
24, 358
„
» »
jj
....
162-5
Stenhouse & Groves
31, 549
vii., 879-
,, .... ...
j) jj
jj
163-5
Merz and Zetter
B., 12, 2038
38, lia
Trinitromethyl nicraniline ...
C6H2(N02)3(NMe-.N02)
C7HS0SN6
cf. 38, 108
127
Eomburgh
B. T., 2, 304
48, 660
Phenylene carbamide
C6H4:N.CO.NH2=1.2(?)
C7HKON2
....
12&-130
Bendix
B., 11, 2264
36, 314
jj jj
c6H4 : (NH)2 : 00=1.2
))
....
SOB
Rudolph
B., 12, 1296
36, 922
jj u
=1.3
1,
d.w.m. 300
Michler and Zim-
B., 14, 2177
42, 182
mermann
j> jj
=1.4
J)
....
n.f. 320
Lellmann and
A., 228, 199
48, 978
Wiirthner
Hydrazine benzoic anhydride
C6H,.CO.NH.NH=1.2
JJ
cf.B.,13, 681
242 d.
Fischer and Benou
A., 212, 333
42, 1069
i i
Nitrosoformanilide
C6H5.N(NO).COH
CZH602N2
....
39
Fischer
B., 1.0, 959
32, 607
NitrosoDi ethyl nitrobenzene
N02.(CH2.NO)=1.2
C7H603N2
95
Gabriel
B., 15, 3060
j» j>
)» JJ
)5
96-97
Gabriel and Meyer
B., 14, 828, 2333
40, 730
>» u
=1.3
)J
....
115-118
Gabriel
B., 15, 838
42, 1070
» ^
JJ 'J
JJ
cf. B., 16, 522
118-119
»
B., 15, 3060
Nitrobenzamide
N02.CONH2=1.3
»
....
100
....
....
1., 541
j> •••*
JJ >J
JJ
140
Salkowski
B., 5, 724
25, 1024
jj ....
>J Jli
JJr
140-14%
Beilstein,
A., 132, 147
vi., 258
» ....
=1.2
)>.
167
A., 163, 138
M ....
» jj
)1
.....
Iff
Hiibner
B., 10, 1713
34, 140
,r
=1.4
»
197-198-
Beilstein.
A., 132, 143
vi., 258
Formonitranilide
N02.(NH.COH)=1.2
J)
....
122
HUbneB
A., 209, 369
42, 181
Nitrobenzaldoxime ....
NO2.(CH : NOH)=1.4
w
128-5
Herzberg
C. C., 1884, 35
48,662
Dinitrotoluene
Me.(NO2)2=1.2.6
C;H6OtN2
...
Liquid
Cunerth,
A., 172, 222
jj
)) JJ
JJ
....
Liquid
Bernthsen
B., 15, 3016
)* ....
)J JV
J1
....
60
Staedel
A., 225, 384
48, 142
jj .... ....
1) J^
J1
...
60-61
j>
A., 217, 206
44,866
jj ..I. ...
=1.3.4
J>.
60
Beilstein and Kuhl-
A., 155,25; Z. C.
vii., 1166
berg
[2], 5, 280, 521
,, ....
=1.2.4
»
69-17-69-6
Mills
P. M. [4], 50, 18 ;
29, 393
P.R [1881], 205
jj
» »
5»
s. 70
Kosenstiehl
A. C. [4], 27, 433
26, 274
1) »>.
J1
70
Neville & Winther
37, 441
j,
J) 5J
JJ.
70
Tilden
45, 416
)) n-
JJ.
70-5
Schiff
A., 223, 247
46, 1089
„,
»j »»•
JJ
70-5
Limpricht
B., 18, 1400
jj.
» »
»»
....
70-5
Beilstein and Kuhl-
Z. C. [2], 5, 280,
vii., 1166
berg
52-1 ; A., 155, 13
)V ....
)» ^>
>»
300
71
i., 575
JJ .... ....
» ».
J1
71
Buckney
B., H, 1452
34, 863
11 .... .1*.
» )?
J)
71
Gabriel and Meyer
B., 14, 824
40, 730
,,
= '
JJ
74
Heckmann
A., 220, 128
46, 178
JJ ••••
=1,3.5
JJ
90-91
Staedel
A., 217, 182
44,864
,,
)) »
JJ
....
91
j»
jj
44, 865
H .... ....
r» »
J)
91-92
»
B., 14, 901
40, 725
JJ
» )J
))
92-93
j*
A., 217., 189
44, 865
>,
» »
)J
92-4
Neville & Winther
B., 15, 2985
41, 416
1)
= »
1J
99
Stebbings
C. N., 41, 117
38, 715
Nitrosalicylamide
CONH2.OHJST02=1.2.3
11
145-146
Hiibner
A., 195, 35
36, 382
j)
=1.2.5
)?
225
jj
A., 195, 15
36, 381
Amidonitrobenzoic acid
COOH.NH2.N02=1.3.2
?)
melts d.
Griess
B., 2, 435
M ))
= 1..3.4
)5
w. m.
jj
B., 2, 435 ; 5, 198
51 14 ••••
=1.3.0
J»t
....
Solid
jj
B., 5, 198
K 1J.
=1.2.3
Jl
204
Hiibner & Goltsche
B., 10, 1699
34, 150
>» 11
JJ ))
JJ
204
Griess
B., 11, 1732
38, 247
)• »J
,. ,,
)?
204
Hiibner
A., 195, 37
36, 382
.JJ JJ
JJ JJ
)>
205
jj
B , 8, 1217
29, 593
3 o
466
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Amidonitrobenzoic acid
»» «
i) 'j
Dinitroso-orcinol
Nitrobenzyl nitrate
Dinitrobenzyl alcohol
Dinitranisoil ....
COOH.NH2.NO2=1.3.5
=1.2.5
)3 »
»> 3»
=1.4.5
Me.(OH)2.(NO)2=l. 3.5.2.?
(CH2.O.NO2).NO2=1.4
(CH3.O.NOs).(NOs)j=1.4?
OMe (NO2)2— 1 3 4
C7H604N3
JJ
3)
35
33
33
)3
+H20
cf.B.,14,903
15, 1136; A.
217, 208
208
208
263
263d.
265-270 p. d
270 d.
270
284
d.w.m. 110
70-71
71
71
70
Hiibner
Griess
HUbner
Rhalis
Steuhouse & Groves
Staedel
Beilstein and Kuhl-
berg
Bautlin
B., 10, 1703
A., 222, 67
B., 10, 1698
A., 195, 21
B., 11, 1730
B., 8, 1220
A., 198, 112
A., 173, 54
31, 548
A., 217, 208
B., 14, 903
Z. C. [2], 3, 467 ;
A., 147, 351
B 11 2105
34, 148
46, 315
34, 150
36, 381
36, 246
29, 594
38, 119
44, 866
40, 724
vi., 335
36, 238
—1.2.4
85-86
Kekul6
K. L., 3, 77
86
Cahours
A. C [3]
i., 306
„ .... ...* ...
J) ))
"
86-87
86-87
Salkowski & Eehs
Salkowski
B., 7, 371
A , 174 263
27, 801
28, 367
» »
86-87
Willgerodt
B 12 763
36, 717
"
88
Post and Mertens
B., 8, 1552
88
Kbrner
A 69, 236
—1.2.5
96
Henriques
A., 215, 321
44, 327
a. 360
96
Bantlin
B, 11, 2105
36, 238
=1.2.6
"
115-8
116
Korner
Salkowski & Eehs
G. I., 4, 305
B., 7, 371
29, 230
27, 801
116
Salkowski
A 174 273
28, 367
118
Post and Mertens
B., 8, 1552
vii., 909
—1.2.3
118
Bantlin
B 11, 2105
36, 238
Dinitrocresol
Me.OH.(NO.,)2— 1.2.3.5
82
Staedel
B., 14, 899
40, 723
82'5
Limpricht
B., 18, 2179
48, 1233
j» )*
83
TTofmanrt & "Miller
B 14 568
40, 593
85
Neville & Winther
B., 15, 2992
41, 422
85 86
Staedel
A, 217 158
„
"
85-5
85-86
Armstrong & Field
Nolting and Kohn
B., 6, 974
B, 17 371
46, 1003
85-8
Neville & Winther
B., 13, 1946
37, 631
86
Nolting and Salis
B , 14 987
40, 725
86
B 15 1860 1865
» l»
"
86
TTirsn.h
B 18 1513
J» »
86
73
Piccard
Nolting and Salis
B., 8, 685
B 15 1858
28, 1022
44, 59
„ —1.4.3.5
79-80
Nevile & Winther
B , 13 1948
37, 631
"
82
Wichelhaus
B 7 177
27, 721
» »
'
82
Armstrong & Field
B 6 974
83
B 7 1024
83'5
W"agner
B 7 536
» "
84
Martius & Wichel-
B 2 206 • Z C
vi., 508
84
haus
[2], 5, 440
A 173 205
vii., 932
84
Limpricht
B, 7 719
27, 991
33 »
"
84
84
Piccard
Staedel
B., 8, 685
B 14 899
28, 1022
40 723 724
" "
"
84
B 14 986
84
C N 29 282
vii 932
"
85
Staedel
A 217 53 167
44, 862
M
85
J [1866] 360
vi., 508
— 7
"
109 110
B 2 206 • Z C
109 110
haus
[2], 5, 440
B 7 177
27 721
"
no
B 8 686
28 1022
COMPOUNDS CONTAINING FOUR ELEMENTS.
467
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitroamidosalicylic acid
Methyklinitroquiuol
Methyldinitrocatechol
Dinitro-orcinol
,, .... ....
Trinitrotoluidine
Formauilide
n .... ....
„
Benzanride
CO2H.OH.NH2.NO2=1.2.3.5
OMe.OH.(NO2)2=1.4.(2)2
„ =1.2.3.5
Me.(OH)2.(N02),=1.3.5.2.?
1! !>
Me.NH2.(NO.,)3=1.3.2.4.6
C6H5.NH.COH
)>
)»
C6H5.CO.NH»
C7H605N2
C7H606N2
»»
H
i)
j»
C7H.ON
»
))
286-290
220
102
122-123
109-110
164-5
136
46
46
46
115
Babcock
Weselsky& Benedikt
Herzig
Leeds
Stenhouse & Groves-
Nb'lting and Salia
Tobias
Wallach & WUsten
Gerhardt
B., 12, 1345
M. C., 2, 370
M. C., 3, 822-827
B., 14, 483
A., 188, 358
B., 15, 1865
B., 15, 2444
B., 16, 145
J. P. [3], 9, 409
40, 1139
44, 464, 470
40, 584
31, 549
44,59
28,66
ii., 682
i., 538
115
Liebig and Wohler
24, 366
115
G. I., 3, 398
87, 261
125
Hermann & Koch-
B., 15, 1116
,, . ». ....
M
5>
125
125
lin
Friedburg
Guareschi
Z. C. [2], 7, 65
G. I., 3, 398
34, 366
87, 261
128
Schiff and Tarsinari
B., 10, 1785
ISO
Ciamician & Mag-
B., 18, 1829
48, 1143
Benzylaldoxime (cf. B., 16,
824)
„ (polymer) ....
Amidobenzaldehyde
„
»
?
Phenylcarbamic acid
Phenylic carbamate
Phenylnitromethane
Benzhydroxamic acid
Nitrotoluene
„ (impure)
ji .... .... ...
C6H5.CH : N.OH
NH2.COH=1.2
» u
„ =1.3
Probably 2(C7H7ON)
NHPh.COOH
NH2.COOPh
Ph.CH2.NO2
C6H5.0(OH):N.OH
Me.NO2=1.2
)J »J
» )J
„ — t
J1
II
)»
»
)1
C7H702N
))
H
)»
)>
r
))
a. 200 p.d.
225-227
Same as 1.3
219-220
%22-2%3
220-225
161-5
abt. 37
39-40
Solid
230 d.
132
141
Liquid
124-125
Liquid— 20
Liquid
Liquid
naghi
Petraczek
n
Gabriel
Friedlander
Tiemann & Ludwig
Pinner
Kempf
Gabriel
Lessen
Beilstein andKuhl-
berg
Kosenstiehl
Beilstein andKuhl-
berg
Wilson
B., 15, 2785
j»
B., 15, 2004
B., 15, 2572
B., 15, 2044
B., 17, 2005
J. P. [2], 1, 405 ;
B., 2, 741
B., 18, 1254
A., 161,347; B.,
16, 874
Z. C. [2], 7, 99
A. C. [4], 27, 433
Z. C. [2], 5, 521
44, 569
J)
44, 62
44,332
46, 1324
I., 752
vii., 252
24, 341
48, 903
25, 415; vii.,
155
24, 563; vii.,
1166, 1178
26, 274
vi., 285; 26,
272
vi., 486
223
Tollens and Fittig
A., 131, 304
„
>» )>
)J
225
225-230
Liquid
Deville
A. C. [3], 3, 175
M
i., 574
j» •••• •••• •••
» .... .... ...
» =i-a
» »
»
51
227
228
230-281
s. low temp.
16
Beilstein andKuhl-
berg
Monnet & Nolting
Beilstein and Kuhl-
Z. C. [2], 6, 102
B., 12, 443
Z. 0. [2], 5, 521
vi., 1103
vii., 1166
—1.4
51-31
berg
Mills
P. M. [4], 50, 17
89, 393
51-407
P. E. [1881], 205
237-238
52
Rosentieh)
A. C. [4], 27, 433
26, 274
QQQ
54
Kekulo
Z. C. [2], 3, 225
vi., 284
238
54
Jaworsky
J. [1865], 542
v., 858
54
Armstrong
25, 868
235-236
54
Beilstein and Kuhl-
Z. C. [2], 5, 521
vii., 1166
54
berg
Limprioht
B., 18, 1401
236
54
Pellizzari
G. I., 14, 481
48, 770
„ (cf. G.I., 14, 181
Hydroxybenzamide ....
„
,,
Hydroxybenzaldoxiine
)»
(CO.NH2).OH=1.2
= 1.4
=1.3
(CH:NOH).OH=1.2
!' !I
U
))
T)
J>
»)
»
270.d.
d.
54
132
162
167 u.c.
57
57 u.o.
Schifif
Hartmaun
Schulerud
Tiemann and Kees
Lach
A., 223, 247
A., 98, 258
J. p. [2], 16, 51
J. p. [2], 22, 290
B., 18, 1663
B., 16, 1783
46, 1089
v., 150
32, 895
40, 42
44, 1104
3o 2
468
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Hydroxybenzaldoxime
(CH I NOH).OH=1.4
C7H7OjN
65
Lach
B., 16, 1785
44, 1104
Amidobenzoic acid (Anthra-
COOH.NH2=1.2
JJ
143-144
Grothe
J. p. [2], 18, 324
36, 378
nilio acid)
>» »»
» )>
J1
....
143-144
Hesemann and
A., 222, 166
46, 600
Kochler
» u
»1 J»
)»
....
142-145
Hiibner & Meeker
Z. C. [2], 3, 564
vi., 317
)T »J
» )>
))
....
142-145
Hubner and Peter-
A., 149, 133
»
maim
)> »
»J ?5
))
143-144
Jackson
B., 14, 885
40, 735
» »
)J )»
)»
....
144
Hubner
A., 222, 67
46, 315
r> »
J) )J
»
144
Hiibner and Peter-
Z. C. [2], 4, 205
vi., 319
mann
» »
J) >)
J)
144
Petersen
B., 6, 368
26, 1133
» »
J) >»
)J
144
Bedson and King
37, 756
» »)
J> »J
)1
145
Windmann
A., 193, 233
36, 155
i» »
»> )»
?»
....
145
Greiff
B., 13, 289
38, 648
)? »>
»J ;i
)»
145
Skraup
W. A., 82, 748
40, 744
»' »j
">i n
II
....
150-4
Kopp
G. J. C. [1856]
» »
"»; ?»
»)
150
Berthelot
)»
» (4th ?)
= »
u
....
154
Fittica
B., 8, 742
28, 1195
" » )»
!» •>
»
....
154-156
»
B., 9, 790
30, 412
)» » JJ
n j>
'»
....
156-158
D
B., 9, 791
3?
J» 1? »»
n ))
•u
....
154-160
j»
J. p. .[2], 13, 184
36, 151
J» J»
„ =1,3
j)
...
165
Conrad
J. p. .[21 15, 241
32, 485
)' »
» »
U
....
170
Fittica
J. p. [2], 13, 184
36, 152
,j ,,
»» »>
>i
172
Salkowaki
B., 5, 724
vii., 947 ; 26,
1024
» »J
)» I?
)»
....
172
Wachendorff
B., 11, 703
34, 674
„ ,j
»i )>
»j
172
Longuinine
C. B., 86, 1329
34, 768
)) » *"• ••••
» }j
»
....
172-5
Hubner
A., 222, 67
46, 315
,} „
*» >»
»»
172-174
Hiibner & Bieder-
Z. C. [1868]
vii., 317
mann
,, ,, ....
» »)
)»
.1..
173
Petersen
B., 6, 368
26, 1133
It ,, .... ....
» »
5)
173
Gabriel
B., 11, 2262
36, 324
j) ty .... ....
J) T»
•J)
....
173 ; 174
Hubner
B., 10, 1699 ; A.,
34, 150; 36,
195, 1
381
,, „ ....
>' »
)»
....
172-174
Griess
B., 8, 529
28, 893
»» j) .... ....
>5 -)>
))
173-175
Faust
A., 150, 56
vii., 978
,, ,,
•J> 'T»
I>
....
173-174
Hubner & Eaveill
B., 10, 1707
34, 149
,, jj .... ....
» »
)J
....
174
Fittica
B., 8, 741
28, 1195
,5 n •••• ••••
)) 1)
»>
....
174
Raveill
A., 222, 166
46, 600
» n
M 11
»1
....
174
Windmann
A., 193, 230
36, 155
)) )j
») ))
i)
....
174
Skraup
W. A., 82, 748
40, 744
,, >}
,, (?)
))
...
178
Fittica
J. p. [2], 13, Ib4
36, 152
)» j,
=1.4
»)
....
184
Griess
B., 8, 529
28, 893
i> j) .... ....
I) »
H
186
Ladeuburg
B., 6, 130
26, 642
i» »
»1 »
jj
186
Skraup
W. A., 82, 748
40, 744
» )j •••• ••••
» M
»
186-187
Windmann
A., 193, 233
36, ] 55
» jj
)J J>
))
186-187
Wilbrand and Beil-
A., 128, 264
iv., 352
stein
j> »
» »)
»
187
Petersen
B., 6, 368
26, 1133
u i) •••• ....
'» )»
))
...
197
Fischer
A., 127, 142
iv., 352
/3-Amidohydroxybenzalde-
COH.OH.NH2=1.3.(
)»
82-83
Ludwig
C. C. [1884], 35
48, 664
hyde
°- »
=1.3.?
i)
....
107
j)
»
J)
Nitrosocresol ....
Me.OH.NO=1.2,5
))
134-135 d.
Nolting and Kohn
B., 17, 370
46, 1003
5> »
j)
....
130-140 d.
Goldschmidt and
B., 17, 2063
46, 1327
"
Sch mid
(cf. B., 16, 242)
„ =1.3.6
)»
....
d. 145-150
Wurster & Rideal
B., 12, 1799
38, 109
Acetyl a-pyroline carboxyl ....
C4H3NH.CO.Ac(?)
,, (?)
....
75 d.
Ciamician & Silber
G. I., 14, 162
48, 247
Acetoxypyridine .... „„
C5H4N.OAc
i)
210 u.c.
Liquid
Fischer and Eeuouf
B., 17, 1897
46, 1370
COMPOUNDS CONTAINING FOUR ELEMENTS.
469
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Methylpyridine carboxylic
acid
ii "
jj jj
» (0
Pyridine betaine
Azonitromethylphenyl
Isocliinchomeronamide
Nitrobenzyl alcohol
i) „
,, „
,, ,,
„ „
„ ,i
Nitro-methoxybenzene
)5 )»
»' »
r )»
» jj
n »
)> »
»» »»
»' „
Tl »J
»1 »)
»» »)
»> » '"•
)1 )»
Nitrocresol
N.Me.COOH=?
)> »
„ =1.12 or 3
=»
C5H5N.CH,.CO.O
CjHjOjN
»
»
1)
»)
C.H702N3
C7H703N
»
)?
))
>?
»»
»)
1)
))
»»
)1
»
H
))
)»
»»
»)
•>J
»
>l
)j
»
J5
»1
)»
J)
»
)1
))
»»
))
))
)»
))
»»
J)
))
)>
1)
))
»>
))
))
))
»)
)1
»
))
170-180 (3)
265
265
265
276 (734)
276-5 c.
258 c.
254
258-260
258-260
cf.B., 15,1004
262-264
226-230
+H20
Hex. plates
Needles
+H2O
cf. B. 16, 242
285 p.d.
194-196
211
209-210
269
150 d.
153d.
295-5-297
Liquid
74
91
91
92
93
9
9
37
38
48
48
48
51
52
52
Liquid
33
33-33-5
33
33-33-4
33-5
34
56
56
6.9-5
69-5
69-70
77-77-4
78
90-91
60-62
79-80
82-85
94-95
94-6-95
30-34
106-108
128
129
129
126-127
142
14S-143
70-72
Durkopf
Couinck
Dorp & Hoogewerff
Gerichten
Friese
Grimaux
Friedlimder and
Henriques
Staedel
»
Easier
Beilstein and Kuhl-
berg
Brunck
Post and Mertens
Korner
Miihlhauser
Salkowski
Bantlin
Brunck
Kekule"
Korner
Post and Mertens
Bantlin
Willgerodt
Cahours
Hofmann & Miller
)i
Wagner
Neville & Winther
jj
Nolting and Wild
Nolting and Kohn
Staedel
Orth
Hofmann & Miller
Nolting and Wild
Hirsch
Neville & Winther
Knecht
Neville & Winther
jj
Hirsch
»
Nolting and Kohii
Neville & Winther
•»
Nolting & Collin
Bertoni
Orth
Staedel
Armstrong
Bernthsen
Ullmann
Ciamician and
Dennstedt
B., 18, 929
B. S., 42, 100
B., 14, 646
M. G, 1, 45
B., 15, 1251
B., 8, 1079
J. [1877], 437
B. 8. [2], 8, 433
B., 14, 2804
A., 217, 184
B., 14, 899
B., 16, 2715
A., 147, 343 ;
Z. C. [2], 3, 467
Z. C. [2], 3, 204
B., 8, 1552
G. I., 4, 3C5
A., 174, 278; 207,
237
B., 13, 920
B., 12, 156
B., 11, 2100
Z. C. [2], 3, 205
K. L., 3, 76
G. I., 4, 305
B., 8, 1552
B., 11, 2099
B., 14, 2634
A., 74, 299
B., 14, 571
B., 14, 572
B., 7, 537
B., 15, 2983
B., 18, 1339
B., 17, 357
A., 217, 52
B., 15, 1131
B., 14, 569
B., 18, 1339
B., 18, 1512
B., 15, 2980
B., 15, 299
B., 15, 2986
»
B., 18, 1513
i»
B., 17, 371
B., 15, 2978
D
B., 17, 269
G. I. [1882], 302
B., 15, 1131
A., 217, 52
B., 15, 3019
B., 17, 1962
B., 17, 2949
48, 817
48, 273
40, 611
42, 1110
29,85
vi., 335
48, 840
44, 864
40, 724
46, 310
vi., 335
vi., 910
29, 234
38, 641
36, 238
vi., 910
29, 234
36, 238
42, 396
i., 305
40, 593
»
27, 808
41, 426
n
vii., 931
44, 662
42, 1198
40, 593
41, 422
42, 728
41, 417
)>
48, 892
jj
46, 1003
41, 423
»
46, 1007
42, 1198
)»
44,662
vii., 931
46, 1317
48, 378
C6H5.N:N.CH.,.NOS
N.(CO.NH2)S=1.2.6
(CH2.OH).NO2=1.3
=1.2
=1.4
)» Jt
)J •>»
)» J)
OMe.NO2=1.2
)» )?
» J»
)I )»
.'I »»
„ =1-3
» JJ
» =1-4
» J>
» ))
)) »
» »
'» )»
)» J)
Me.OH.NO2=1.2.5.(2)
=1.4.5
» )J
)» Jl
» )>
»» »
)) ))
=1.3.2
J» >»
= 1.2.3
)» »
» I>
=1.4.6
)» JJ
=1.3.5
)) M
=1.2.5
J) »
» »
)) »>
J» »>
=1.2.4
„ =1.3.6
jj »
j> >»
jj »
= 1.2.6
C4H4N.CO.COOMe
>j
)»
i»
Methylic pyrroline-glyoxa-
late
470
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Acetylic a-carbopyrrolate ...
NH : C4H3.COO.COMe
C7H703N
d.
75
Ciamician & Silbei
B., 17, 1154
46, 1044
Pseudacetyl a-carbopyrrolic
Me.CO.C4H2(COOH)NH
„
186
,,
B., 17, 1157 ;
46, 1045 ; 48,
acid
G. I., 14, 162
247
Methoxynicotic acid
N.OMe.COOH=1.2.5
„
237-238
Pechmanu & Welsh
B., 17, 2395
47, 154; 48, 175
Nitrobenzenylamidoxime ...
NO2.C6H4.C(NH2) I N.OH
C7H703NS
174
Schopf
B., 18, 1064
48, 896
= 1.3
Amidonitrobenzamide
(CONH2).NH2.NO2=1.2.3
„
cf. A., 195, 38
109
Hiibner
B., 8, 1217
29, 593
„
=1.2.5
„
....
140
„
B., 8, 1219
„
„
11 >i
„
....
225
11
B., 10, 1698
34, 150
„
„ =1.2.3or5
„
d. 200-210
Kolbe
J. p. [2], 30, 467
48, 666
Methylnitroquinol
OMe.OH.N02=1.4.?
C,H7O4N
....
83
Weselsky & Bene-
M. C., 2, 370
40, 1139
dikt
Methylnitroresorcinol
=1.3.4
„
cf.M.C., 1,898
95
„
W. A., 82, 1219
40, 727
„
=1.3.6
„
....
144
n
,,
B
/3-Nitroorcin
Me.(OH)j.N02=1.3.5.?
„
115
Weselsky
B., 7, 442
27, 694
a- „
„ =1.3.5.?
120
Gallamide
(CO.NH2).(OH)3=1.3.4.5
"
d 245
243
"
Bio 400
"
11
ociiiit tLnci Jrons
., J-O, "iOO
Dinitromethylaniline
NHMe.(N02)2=1.2.4
C7H7O4N3
....
175
Norton and Allen
B., 18, 1996
48, 1214
„
» »
,,
178
Leymann
B., 15, 1234
42, 1057
Dinitrotoluidine
Me.NH2.(N02)2= ?
„
....
94
Hepp
A., 215, 371
44,317
»
„ =1.4.3.5
11
....
166
Heynemann
A., 158, 335
24, 682
»
3» 11
„
....
166
Beilstein aud Kuhl-
B., 13, 242 ; A.,
vii., 1178; 38,
berg
158, 341
636
»
11 11
„
....
166
Staedel
B., 14, 900
40, 724
.1 11
„
....
167-168
„
A., 217, 187
44, 864
11
.1 .1
„
....
168
Kelbe
B., 8, 877
29, 270
•>
=1.4.2.6
„
166-5-168
Beilstein
B., 13, 244
38, 636
»
» ))
„
cf. A., 21 7, 205
168
Tiemann
B., 3, 219
38, 635
»
<> »
„
168
Staedel
A., 225, 384
48, 142
"
7» -S f '
„
192-193
Hepp
A., 215, 368
44, 317
"
= 1.2.3.5
„
208
Kayser
B., 15, 1133
42, 1203
»
i> 11
„
SOS
Staedel
B., 14, 900
40, 724
»
11 11
„
208
„
A., 217, 153
44, 861
!)
D 11
„
209
n
A., 217, 183
44, 864
Ethylic nitropyromucate
C4H2O(NO2).COOEt
C7H70SN
107
Klinkhardt
J. p. [2], 25, 52
42, 499
Dinitroamidocresol
Me.OH.NH2.(N02)2=1.3.(?)3
C7H706N3
156
Emmerling and
B., 9, 1095
30, 523
Oppenheim
Apocaffe'ine
COO.C.COOH
1 fy 1 1 Q
_,. ,
Bl A ft ^*7 • A
»)
11(1 —±Jfa
T iscner
.. i.1*. DO / i i --
40, 614 ; 44,
NMe.C:N.CO.NMe
1 A t -I » (-
215, 277
Mf^ Q i nA
355
Phenyl carbamide
NH2.CO.NHPh
C7H3ON2
144—145
144-5
Maly & Andreasch
Weith
. L-., o, LOO
B., 9, 821
42, 631
30, 639
» »
D
n
lift
Steiner
B., 8, 519
28, 883
!
NH:CPh.NH.OH
H
76-77
Lessen
B., 17, 1588
46, 1324
Benzenylamidoxime
NH2.CPh : N.OH
„
....
70
Tiemann
B., 17, 128
46, 734
»
»
„
70-80
Tiemann & Kriiger
B., 17, 1685
46, 1325
„ ....
»
„
d. 170
79-80
Kriiger
B., 18, 1053
48, 895
11
„
....
80
Pinner
B., 17, 186
46, 739
Amidobenzaldoxime
NH2.(CH : N.OH)=1.3
„
88
Gabriel
B., 16, 1998
44, 1105
„ ....
=1.4
„
....
124
Gabriel & Herzberg
B., 16, 2001
44, 1104
Nitrosomethylamidobenzene
NH2.(CH.NO)=1.2"
"
124-5
132-133
Herzberg
Gabriel and Meyer
C. C. [1884], 35
B., 14, 2339
48, 662
42, 189
Amidobenzamide
NH2.(CO.NH2)=?
„
....
a. 100
Chancel
A., 62, 274
iv., 294
»
=1.2
,,
300 p.d.
108
Kolbe
J. p. [2], 30, 467
43, G66
»
=1.3
„
+H20
75
Beilstein
A., 132, 142
vi., 258
11
)) ^ f
„
72
Chancel
A., 62, 274
iv., 294
>!
=1.4
)(
178-179
Beilstein
A., 132, 142
vi., 258
Hydroxydimethylpurin
C5H2ON4Me2
C7HSON4
112
Fischer
B., 17, 334
46, 997
Nitromethylaniline
C6H5.NH.CH2.N02
149
Steiner
B., 7, 1245
28, 165
Hydroxyphenyl carbamide ....
HO.C6H4.NH.CO.NH2=1.2
„
154 d.
Kalehoff
B., 16, 375
44, 735
11 ii
,, =1.4
168 d.
B., 16, 376
Hydrazinbenzoie acid
NH2.NH.C6H4.COOH =1.3
„
....
186 d.
Griess
B., 9, 1657
J)
31, 475
COMPOUNDS CONTAINING FOUR ELEMENTS.
471
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Hydrazinbenzoic acid
NH2.NH.C6H4.COOH=1.4
C7H8O2N2
220-225 d.
Fischer and Eenou
A., 212, 337
42, 1070
Diamidobenzoic acid
COOH.(NH2)2=1.3.4
„
210 d.
Griess
B., 5, 856
„ „ .... ' ~-
JJ JJ
„
210-211 d.
A., 137, 57
„ ,
=1.3.5
JJ
195 p.d.
Voit
A., 99, 106
iv., 294
„ „ .... , ._
» „
„
228
Hubner
A., 222, 67
46, 315
„ „ ....
„ „
„
....
239
Griess
A., 154, 325
„ „ .... "_
» >»
„
S40
Merz and Weith
B., 15, 2728
Nitrotoluidine
Me.NH2.N02=1.3.6
„
....
53
Limpricht
B., 18, 1402
48, 974
„
=1.4.6
„
77'5
Beilsteinand Kuhl
Z. C. [2], 5, 280
vi., 1105
berg
„
JJ JJ
»,
....
77-5
Buckney
B., 11, 1452
34, 863
„
'J J)
n
77-5
Mixter
A. C. J., 1, 239
40, 1130
„
)J n
„
....
77-78
Neville & Winther
B., 15, 3016
37,441; 41,422
)J •••• "••
J) ji
„
77-5
Limpricht
B., 18, 1400, 2183
48, 974
„
)i 11
„
77-78
Levinstein
D. P., 256, 471
48, 1127
-„
11 11
„
77-5
Cunerth
A., 172, 223
„
Ji ))
„
78
Bernthsen
B., 15, 3017
44, 579
„
J' j)
„
....
78
Nolting and Collin
B., 17, 263
46, 1012
„
„ =1.2.6
„
....
90
Staedel
A., 225, 384
48, 142
„
)J 1)
„
....
91-5
Bernthsen
B., 15, 3017
44, 579
„
JJ )J
„
94-5
Cunerth
B., 7, 644; A.,
27, 903; 28, 83
172, 223
„
=1.3.5
,,
....
95
Becker
B., 15, 1138
43, 1197
„
J> JJ
»i
98
Staedel
A., 217, 199
44, 865
„
J) JJ
,,
....
98-98-4
Neville & Winther
B., 15, 2985
41, 416
„
=1.2.3
„
....
97
Lellmann & Wiirth
A., 228, 239
48, 974
ner
„
= 1.2.4
„
....
106
Levinstein
D. P., 256, 471
48, 1127
„
JJ 11
n
....
107
Limpricht
B., 18, 1401
48, 974
JJ "••
JI 11
„
107
Nolting and Collin
B., 17, 265
46, 1012
„
1J ))
»
106-108
JJ
B., 17, 269
46, 1007
„
J* JJ
„
....
109
Staedel
A., 225, 384
48, 142
,, ....
=1.4.5
,,
110
Kelbe
B., 8, 876
29, 270
„
» „
„
....
114
Beilstein & Kuhl-
A., 155, 23; Z. C.
vi., 1103
berg
[2], 6, 102
„
» i>
,,
....
114
Graeff
A., 229, 340
48, 1127
„ ....
» i,
.)
....
114
Limpricht
B., 18, 1404
„
11 <>
»)
114
Fried erici
B., 11, 1971
36, 311
„
.> „
n
....
114
Fourmeaux
B. S., 42, 337
48, 400
„
... ,,
„
114
Hubner
A., 208, 313
40, 1131
„
.. »
>t
114
Nolting and Collin
B., 17, 263
46, 1012
„
i>. „
,,
114-115
Neville & Winther
....
41, 426
„
» j.
„
116
Gattermann
B., 18, 1483
vii., 1166
„
„ =1.2.5
„
....
127
Limpricht
B., 18, 1404
„
" n
„
....
127-128
Beilstein and Kuhl-
A., 158, 346
24, 682
berg
-,
» n
„
127-129
Neville & Winther
41, 423
vii., 1178
„
!> .1
„
....
128
„
37, 432
„
.' D
..
....
1S9-5
Lellmann & Wurth-
A., 228, 239
48, 974
ner
„
1» »
»
129-130-5
Ladenburg
B., 11, 1652
36, 233
„
JJ JJ
„
....
130
Nietzki
B., 12, 2237
38, 162
„
=1.3.2
..
....
133
Limpricht
B., 18, 1404
,,
!' .1
»
188-134
Beilstein and Kuhl-
Z. C. [2], 7, 99 ;
24, 563, 683 ;
berg
A., 158, 335
vii., 1178
,,
= 1
»J
....
168
Wagner
B., 7, 1273
vii., 931 ; 88,
256
„
JJ 1)
)>
....
168
Cunerth
B., 7, 643
27, 902
Theobromine ....
f NMe.CO.C.NH\ ]
1 1 II xCHr
I CO.NMe.C . N /" J
C7H802N4
....
w. m. 290
w.m. S90-295
Schmidt & Pressler
Keller
A., 217, 287
G. J. G, 1854
44,872
472
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitranisidine
OMe.NH2.NO2=1.2.3
C7H803N2
•
76
Bantliu
B., 11, 2106
36, 238
= 1.3.4
129
Amidobenzylalcohol
)J
(CH2.OH).NH2=1.2
11
C7H9ON
82
Friedlander and
B., 15, 2110
Henriques
OMe.NH2=1.2
216
Liquid 0
Brunck
Z. C. [2], 3, 205
vi., 910
„ ....
)) 11
11
n
216
Liquid
Korner
G. I., 4, 305
29, 235
226-5 (734)
Miilhauser
A., 207, 239
42, 302
1) IJ
)>
228
R, 13, 920
38, 641
J) 11
= 1.3
)i
251 c.
Liquid
Pfaff
B., 16, 614
)1
=1.4
11
245-S46 c.
s. 51-52
Salkowski
B., 7, 1009
28, 64
»
1)
52
Brunck
Z. C. [21, 3, 205
vi., 910
ir
?' *T
» »
1)
II
....
54
Korner
L Jl 1
G. I., 4, 305
29, 235
55-5-56-5
Lossen
A., 175, 324
28, 770
,y
Me.OH.NH2=1.2.6
11
124-128
Ullmann
B., 17, 1963
46, 1317
c£ B., 7, 1270 ...
=1.4.5
M
51
....
135
Nolting and Kohu
B., 17, 360
46, 901
., .... .... ....
=1.4.6
»
....
138-139 ;
Wallach
B , 15, 2834
44, 329
143-144
=1.3.&
151
Nolting and Kohn
B., 17, 367
46, 902
11
=1.2.4
)I
159-161
Wallach.
B., 15, 2832
44, 329
„ .... ....
11
ji »•
) >'
r
*»t
159-161
Maassen
B., 17, 609
46, 1145
159-161
Nolting and Collin
B., 17, 270
46, 1007
„ .... ....
11 IT
= 1.2.5
)T
99
....
172-173 ;
Nolting and Kohn
B., 17, 365
46, 902
174-175
„ ..» ..«
)J TT
II
....
174-175
»
B., 17, 370
46, 1003
175
Hirsch
B., 18, 1514
48, 892
Pseudacetylmethylpyrroline
11 »'
C4H3Ac : NMe
n
ii
200-202
Liquid
Ciamician and
B., 17, 2952
48, 378
Dennstedt
Aeetylmethylpyrroline
C4H3Me : NAc
n
....
4-6
Weidel and Cia-
B., 13, 78
38, 404
mician
/5-ethoxypyridine
C5H4N.OEt
H
Liquid
Fischer and Eenoui
B., 17, 1897
40, 1370
Pseudolutidostyril
CMe : CH.CMe : CH.CO.NH
l)
303-305
180
Hantzsch
B., 17, 2905
48, 397
i _i
Phenyl semicarbazide
C6H5.NH.NH.CO.NHS
C,H8ON3
....
170
Fischer
A.,190, 113
34, 307
Diamidobenzaniide
(CO.NH2).(NH2)2=1.3.5
»
177
Muretow
Z. C. [2], 6, 642
vii., 130
») —
= »
11
183
Voit
i., 541
Pyromucethylamide ....
C4H3O.CO.NHEt
C7H90,N
258 c.
Liquid
Wallach
B., 14, 752
40, 715
Ethylpyromeconamic acid ....
....
n
160
Meunel
J. p. [2], 32, 176
48, 1204
Salicylaldehyde ammonia ...
....
)!•
....
30
Herzfeld
B., 10, 1271
Ammonium salicylite
C6H4.O(NH4).COH=1.2
II
....
115
Ettling
A., 29, 310 ; 35,
v., 169
244
Tetrene uretbane
C4H4 : N.COOEt
|9
180 (770)
Liquid
Ciamician & Denn-
G. L, 12, 84; B.,
42, 606; 44,
stedt
15, 943, 2579
350
Ethylic a-pyrrolate
C4H4N.COOEt
11
230-232
39
Ciamician and Sil-
G. L, 14, 162;
46, 1044; 48,
ber
BM 17, 1152
246
Ethylcarbopyrrolic acid
C4H3EtN.COOH
11
78
Bell
B., 10, 1864
36, 525
Dimethyl pyrroline carb-
CH:CMe.NH.CMe:C.COOH
11
....
210-213 d.
Knorr
B., 18, 1565
48, 995
i i
oxyhc acid
Nitrodiamidotoluene
Me.(NH2)j.NO2=1.2.4.6
C7H902N3
....
132
Tiemann
B., 3, 218
»
„ =1.2.4.3 or I
11
154
»j
B., 3, 220
,,
» »
11
154
Ladenburg
B., 8, 1211
»
» r>
)1
154
Euhemann
B., 14, 2657
42, 392
Ethylic acetylcyanacetate ....
CHAc(CN).COOEt
C7H9O3N
26
....
C. R., 95, 235
Ammonium salicylate
C6H4.OH.COO(NH4)=1 .2
51
126
Procter
J. Ph. [3], 3, 275
v., 155
Hy poethyltli eobromine
C7H903N3
142
Fischer
A., 215, 308
44, 357
Trihydroxydimethylpurin ...
C6N4Me2(OH)3 ?
C7H903N4?
....
Very high d.
»
B., 17, 337
46, 998
? acid
....
C7H904N
d. 135
84-87
Pinner
B., 14, 1070
40, 797
Nitrotoluidine nitrate
C6H3Me.NO,NHs + HNO3
C7H90SN3
185 d.
Beilstein & Kuhl-
Z. C. [2], 5, 280
vi., 1105
berg
Hydrazineaniso'il
C6H4.OMe.N2H3=1.2
C7H10ON2
43
Reisenegger
A., 221, 314
46, 440
Dimethylcarbopyrrolamide...
04H!!Me,,N.CO.NH2
!!
89-90
Bell
B., 10, 1866
36, 525
Ethylsuccinylcarbamide
CO(CH2),.CO.N.CO.NHEt
C;H1003N,
94-95
Menschutkin
A., 178, 204
29, 379
COMPOUNDS CONTAINING FOUR ELEMENTS.
473
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
-Watts' Diet.
& J. Ch. Soc.
Diethylic cyanamidodicar-
N(CN)(COOEt)2
C7H1004N2
....
32-8
,Bassler
J. p. [2], 16, 134
34, 214
boxylate
Dtacetylmethylglyoxime
CMe(NOAc).CH(NOAc)
»
51
Schramm
B., 16, 2187
46, 52
Nitrodehydropiperylmethyl-
C5H7(NO2)N.GOOMe
)>
....
102-103
Schotten
B., 16, 647
44,811
urethane
Oxy-/3-dimethylurie acid
....
C7H1006N4
173-174
Fischer
B., 17,1781
46, 1309
Hydroxyheptamide
C6H9.(OH)(CO.NH2)
C7Hn02N
87
Demarc,ay
C. B., 86, 1135
34, 662
Isopropylsuccinimide
CO.CH.,.CHPr3.CO.NH
i " i
J)
60
Eoser
A., 220, 271
46, 423
Tyroleucine
>J
....
240 d.
Schiitzenberger
A. C. [5], 16, 289
36, 544
»
....
•1»
....
250
»
C. B., 84, 124
31, 725
Diethylic cyanurate
(CN)3(OEt)2(OH)
C7HU03N3
....
173
Limpricht
A., 74, 208
ii., 293
Methylcaffuric acid ..„
....
C7H,,04N3
....
167
Schmidt& Schilling
A., 228, 141
48, 995
Diethylic nitrosomalonate ....
ON : CH(COOEt)2
C7HU06N
d.
Liquid
Conrad and Bischoff
B., 13, 599
38, 629
„ oxalcarbaminate ....
EtOOC.NH.CO.COOEt
))
....
45
Salomon
J. p. [2], 9, 292
27, 791
Ethylic nitrotartrouate
C7HM07N
45-46
Henry
A. C. [4], 28, 415
Diallyl carbamide
CO.N3H2(C3H5)2
C7H12ON2
....
100
Eichter
B. K. T., 153
Amidoheptamide
....
»
....
251 d.
Demargay
C. B., 86, 1135
34, 662
Diethylic amidocyanurate ....
C3N,(OEt)a.NHa
C7H)203N4
...
97
Hofmann and
B.,3, 274;T.B.S.
vii., 410
Olshausen
18, 493
?
....
C7H,AN3
147
Behrend
B., 16, 3027
46, 583
Ethylsuccinuric acid
NHEt.CO.NH.CO.(CH2)2.
C7H1204N2
....
166'5-167
Menschutkin
A., 178, 206
29, 380
COOH
Dinitroheptylene
C7H12(N02)2
>i
....
182
Morris
41, 176
Methylic cyanurate forma-
(CO)sN3Me3+ NHj.COH
C7H1204N4
....
-175
Gautier
,A., 149, 315
vi., 529
mide
Hexylic isocyanate
€6H13.N • CO
C7H13ON
a.100
Pelouze &'Cahours
J. [1863], 526
C7Hj2 : N.OH
Liquid
Na'geli
T3., 16, 497
'44, 728
Acetylpiperidine
C5H10N.Ac
)t
Jl
fff|
Liquid
Schotten
B., M, 426
)
42, 983
„ ....
J)
»
226-227
Liquid
WaHach
A., 214, 238
Tropigenine .... .... ....
C7Hj2O : NH
161
M^erlin^
B., 15, 290
42, 739
J)
1)
))
cf.B.,16,244
159-161
Pesci
G. I., 12, 285, 329
Diacetone cyanhydrine
CMe2(OH).O.CMe,!.eN
C7H13O2"N
135-152
Urech
A., 164, 260
vii., 15 ; 26,60
Amidotrimethylbutyllactide
Me.C.(O.C : O)CH2.CMe2.NH,
J)
a. 180
Heintz
A., 189, 238,
32, 878
Nitrosoisobutylketone
CH3.CO.CH(NO).Bu/»
»
....
42
Treadwell and
B., 15, 2788
44, 572
Westenburger
Ethylic ?
NHMe.CMe : CH.COOEt or
.))
133(50); 215
Liquid
Kuckert
B., 18, 618
48, 750
NMe : CMe.CH2:eO0Et
(o.p.)
Piperylmethylurethane
CsH10N.COOMe
)»
201
Liquid
Schotten
B., 16, 647
44, 814
Isoamylic oxamate
NH2.CO.COO(C5HU)
C7H1303N
92-93
Wallacli and Lieb-
B., 13, 507
38, 557
mann
Ethylsuccinuramide
NH2.CO.(CH2)2.CO.NH.OO.
C7H130,N3
• ..»
195-196
Menschutkin
A., 178, 208
29, 380
NHEt
Ethylic grutamate
C3H5(NH2)(COOH)(COOEt)
C7H1304N.
MM
164-165
Habermann
A., 179, 253
29, 907
Diethylic guanidodicafbonate
NH: C(NH.€OOEt)s
C7H1304N3
....
162-u.c.
Nencki
B., 7, 1588
28, 755
Nitrobornesite
No. of nitre-groups ?
C7H1308N(?)
„,,
30-35
Girard
C. B., 73, 426
24, 915
Diethyhualonanride ;
CHj(CO.NHEt).2
C7H1402N2
....
149
Wallach and 'Ka-
B., 14, 170
40, 285
menski
Dimethylpyrotartaramide ....
NHMe.CO.CHMe.CHs.CO.
)»
MM
113-115
Henry
C. B., 100, 943
48, 887
NH.Me
laoamylic allophanate
NH2.CO. NH.COO.C6HU
C7H1403N2
a. 100
Schlieper
A., 59, 23
i., 133
<) i)
')
)»
....
162
Hofmann
B., 4, 267
Propiodiacetodiamide
N2H3Ac2(C3H60)
J)
220
68
Gautier
A., 150, 189
vi., 525
Ethylic j3-hydroxyainidoglu-
NH2.CO.CH2.G(OH)(NH.,).
C,-H141D4N2
....
86
Pechmann and
B., 18, 2291
48, 1202
tamate
CH,.COOEt
Stokes
Oxallyldiethylamine
NEt2.C3H50
C7H15ON
160
Liquid
Eeboul
C. B., 97, 1556
46, 577
CEnanthaldoxime
j?
195 c.
50
Westenberger
B., 16, 2992
46, 581
CEnantharaide
C6H13.CO.NH2
)>
250-258
05-2
Chiozza
A., 91, 102
„ .... ....
1)
»»
....
95-2
Hofmann
B., 15, 983
„
»
•»
....
94-95
Mehlis
A., 185, 369
34, 135
Piperethylalkamine
cf. B., 14, 1877
)!
199
Liquid
Ladenburg
C. B., 93, 338
40, 1157
3 P
474
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Hydroxyoenauthamide
CH2(OH).(CH2)5.CO.NH2
C7H1502N
....
147
Helms
B., 8, 1170
29, 375
Methamido-a-caproic acid ...
Me.(CH2)a.CH(NHMe).
„
....
w.m. 110
Duvillier
C. R, 90, 822
38, 543
COOH
1
„
193-197
....
Beilstein and Kur-
B., 13, 2029
batow
Ethylic j3-methamido-/3-hy-
NHMe.CMe(OH).CH2.COO
C7H1503N
....
42-43
Kuckert
B., 18, 618
48, 750
droxybutyric acid
Et
Triethylcarbamide
NHEt.CO.NEt2
C7H,,ON2
223 c.
63
Hofmaun
P. R, 11, 273
ii., 565
„
_
223
63
Michler
B., 8, 1665
29, 702
„
„
n
235
....
Wurtz
E. [1862], 199
ii., 565
Pseudohexylcarbamide
NH2.CO.NH.C6H13
„
220 p A
127
Chydenius
B. S. [2], 7, 481 ;'
vi., 1117
Z. C. [1867], 382
Diisopropylcarbamide
NHPr0.CO.NH.Pr3
„
....
192
Hofmana
B., 15, 756
Nitrosotriacetonamine
....
C7H1602N2
72-73
Heintz
A., 185, 1
32, 428
Trimethylene diethylalkine
....
C7H17ON
189-5
Liquid
Behrend
B., 17, 512
46,1115
Diethylpropylalkine
....
„
158-159
Liquid
Ladenburg
B., 14, 2407
42, 165
Diethylpropylglycoline
NEt2.CH2.CH(OH).CH2.OH
O TT f~~\ XT
v^yJj. i • V 2 -^
233-235
Liquid
Eoth
B., 15, 1151
42, 1195
Tetramethylallylalkine
C3H6(OH)Me4N2
C7H18ONS
170-185
Liquid
Behrend
B., 17,510
46, 1114
Hydroxyallyldiethyldiamine
(NHEt)2.C3H5.OH
„.
185
Liquid
Reboul
C. R, 97, 1488
46, 579
Nitrophthalic anhydride
C6H3(N02):(CO)2: 0=4.2.1
C8H3O5N
....
114
Miller
A., 208, 230
42, 404
Nitrobenzoic cyanide
N02.(CO.CN)=1.2
C8H403NS
....
54
Claisen and Shad-
B^ 12, 351
well
Nitrobenzoyl cyanide
=1.3
„
230-231-5
L-17
Claisen and Thomp-
B., 12, 1943
38, 253
(142-147)
son
Nitroisatin
C6H4.CO.CO.N.NO,=1.2
C8H4O4N2
226-230
BaeyeF
B., 12, 1313
36, 938
i i
K.I.
Nitroisatoic acid
C8H405N2
220-230 d.
Kolbe
J. p. [2], 30, 467
48,666
Dinitrophthalic acid
(COOH)2.(NOJ2= 1.2.3.6
CSH40SN2
MM
200
Merz and Weith
B., 15, 2727
44, 344
» »
„ =1.2.3.5
„
....
227
„
B., 15, 2725
„
» »
» »
a
226
Beilstein and Kur-
B., 13,354; C. C.
38, 478 ; 42, 63
batow
[1881], 359
i. »
=1.2.1?
266
„
B. S. (2), 34, 327
40, 436
Dinitrohydroxy tereph thai ic
(COOH)2.OH.(N02)2=1.4.(?)S
CSH409N2
«.*•
178
Burkhardt
B., 10, 1273
34,73
acid
Benzoyl cyanide
C6H6.CO.CN
C8H5ON
206-208
31
Strecker
A,, 90, 62
i., 568
!> »)
„
M
••••
32-33
Hiibner & Buchka
B., 10, 480
Nitrophenylacetylene
C6H4(N02).C : CH=1.2
C^HjOaN
*•**
80
Miiller
A., 212, 140
42, 844
„
» »
J?
....
81-8S
Baeyer
B., 13, 2259
40,275
„
=1.4
1)
MM
149
Miiller
A., 212, 133
42, 842
»
» »
M
152
Drewsen
A., 212, 150
42,847
Cyanobenzoic acid
COOH.CN=1.3
J}
217
Sandmeyer
B., 18, 1499
18, 981
Phthalimide
CBH. '. (CO) '. NH=1.2
99fi 997 n r>
JVEichael
B., 10, 579
o i \ /a
JJ
...»
__'.) — __ i 1 1 .( .
997
Sandmeyer
B., 18, 1499
48, 981
n
— _ j
A., 215, 181
44, 475
TV J)
"
228-229
Biedermann
B., 10, 1166
99Q
Piutti
G. I., 12, 169
42 1297
"
....
•9V
OOQ
A. C. J., 3, 28
40, 1040
Aiithroxanaldehyde
C6H4.l£o.C.CHO=1.2
51
72-5
Schillinger and
B., 16, 2223
46, 60
Wleugel
Isatin ....
C6H4.CO.C(OH) : N=l 2
QCiTi 9m
•p
B. 15 2094
i 1
"
**""
~
-Daeyer
j
liuhara
A. C. J., 3, 26
40 1040
Anthroxanic acid
C6H4.N.O.C.COOH=1.2
i i
C8H503N
190-191
Shillinger and
B., 16, 2224
46,60
Wleugel
Anthranilcarboxy lie acid (Is-
C6H4.CO.N.COOH=1.2
H
....
®Q() fl
&O\J t*.
Friedlander and
B., 16, 2228
46,61
atoic acid)
i i
Wleugel
» »
„ „
)(
....
230
Kolbe
J. p. [2], 30, 467
48, 665
Phthalyl hydroxylamine ....
N(C8H402).OH
1?
....
230 u.c.
Cohn
A., 205, 295
40, 586
Nitrophthalic aldehyde
(COH)2.NO2=1.2.3 or 4
C8H604N
cf.A.,202,219
135
Beilstein and Kur-
B., 12, 688 ; C. C.
36, 722 ; 42, 63
batow
[1881], 359
COMPOUNDS CONTAINING FOUR ELEMENTS.
475
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrobenzoylformic acid ...
C6H4(CO.COOH).NO2= 1 . 2
C8H5O6N
»..
122-123
Claisen & Thompso
B., 12, 1945
n »
» JJ
ii
+xH20
46-47
,,
ii
11 11
=1.3
«
-..
77-78
«
n
38, 254
Nitroterephthalaldehydicaeid
COH.COOH.NO2=1,4.6
„
....
160
Low
B., 18
48, 799
Nitropiperonal
CH2 ; O2 : C6H2(NO,,)COH
„
....
95-5
Remsen and Fittig
Z. C. [2], 6, 97 ;
vi., 948; 24, 935
=4.3.?.l
A., 159, 134
Nitrophthalie aeid
(COOH)2.NO2=L2.3
C8H6Q6N
....
208-210
Faust
A., 160, 57
25, 75
11 n
» »i
M
208-210
Engelhardt anc
Z. C. [2], 7, 262
vii., 978
Latschinoff
„ „
ii 11
„
of. B. 10, 294
208-210
Guareschi
G. I., 7,24
31, 712
n 11 ....
*i 11
11
....
212
Aguiar
B., 5, 899
26, 175
„ „
11 ii
,i
212
Merz and Weith
B., 15, 2724
44, 344
II M •"• •••
41 11
11
....
212
Beilstein and Kur-
B., 12, 688 ; C. C.
36, 722; 38,
batow
[1881], 359
399 ; 42, 63
11 M .".
11 11
„
213
Diehl and Merz
B., 11, 1667
36, 252
„ „
11 11
11
....
212-220
Graeff
B., 15, 1127
42, 1212
II 11 .."
" 11
„
d. 210
318 s.t.
Miller
A., 208, 237
42, 404
„ „
11 11
„
....
219-220
Claus and May
B., 14, 1330
11 11 •".
=L2.4
JJ
....
135 (?)
Beilstein and Kuhl-
B. S. [2], 31, 200
36, 644
"
berg
11 y> .".
11 11
„
d. 165
160
Miller
B., 11, 393
34, 504
11 II "..
ii ii
„
cf.B.11,1191
161
-ii
A., 208, 229
42, 404
Nitroisophthalic acid
= 1.3?
,,
233-239
Storrs and Fittig
A., 153, 283
vii., 979
11 ii
=1.3.5
M
248-249
M
A., 153, 285
11
«
» »•
JJ
....
248-249
Beyer
J. p. [2], 22, 352
40, 96
II M "•.
fli 11
JJ
249
ji
J. p. [2], 25, 470
42, 1294
11 11 ."*.
=1.3. 1
)J
260
11
J. p. [2], 22, 351
40,96
Nitroterephthalic acid
=1.4.5
JJ
2S9
Fittig
Lehrb., 409
II »!
» 11
)J
270
Burkhardt
B., 10, 145
Nitropiperonylic acid
CH2 : 02: C6H2(N02).COOH
35
....
172 u.c.
Jobst and Hesse
B., 11, 1033 ;
34, 733
=4.3.U
A., 199, 70
Pyridine tricarboxylie acid..,.
N.(COOH)3=1.2.3.4
M
d. 190
n. f. 193
Michael
B., 18, 2028
ii 11 11 ....
„ =1^.4.6or 1.3.4.5
JJ
227 d.
Voigt
A., 228, 29
48, 812
11 ii «
= .?
11
cf. B, 12, 410
243
Fiirth
M. C., 2, 416
42, 230
(Berberonie aeid)
6-Pyridine tricarboxylie aeid
1* ii
11
....
244 u.c. ; d.
Hoogewerff & Dorp
B., 12, 158
36, 541
£** 11 11 11
II M
JJ
....
244 d.
Bottinger
B., 13, 2049
40, 182
a" ii ii ii
11 II
JJ
....
244-250 p.d.
Richter
R. K. T., 181
Trinitrophenylie acetate
OAc.(NO2)3=1.2.4.6
C8H508N3
....
75-76
Tommasi & David
A.,169,167;C.E.
vii., 910 ; 26,
77, 207
1238
Trinitrocresotic acid
C6Me.OH.COOH.<NO2)3
C8H509N3
A., 64, 23
170-180
Liebermann,& Dorp
A., 163, 100
Anhydroformyl amidobenza-
C8H6ON.,
....
209-210
Weddige
J. p. [2], 31, 124
48,661
mide
Carbimidoamidobenzoyl
C6H4.CO.C(:NH).NH
JJ
....
214
Griess
B., 18, 2419
48, 1227
Hydroxycinneline .„
c6H4.N : N.CH: c(OH)=i.2
,,
225
Richter
B., 16, 681
44, 1105
?
....
„
....
139
Salkowski
B., 17, 508
46, 1176
Azoxindole ....
....
11
w.m. 220
Baeyer and Knop
A., 140, 27
vi., 736
Benzenylazoxime carbinol ....
Ph.C:N.O.C(OH):N
C8H602N2
197
Falck
B., 18, 2469
48, 1217
H 1
Benzoylene carbamide
„
a. 350
Griesa
B., 2, 416
Nitrosoisophthalidine
C6H4.C(: N.NO).0:CH2=1.2
#i
....
156
Grsebe
B., 17, 2599
48, 166
1 _ 1
Dihyclroxyquinoxaline
G6H4:[N:c(OH)]2:=?
„
280
Bladiu
B. S., 42, 104
48, 257
}5 ....
=1.2
M
....
n. f. 290
B., 18, 674
48, 786
Cyanamidobenzoie acid
C6H4.COOH.(NH.CN)=1.3
11
d.a. 140
200 d.
Traube
B., 15, 2114
44, 192
n 11
11 =1.2.(?)
11
a. 350
3riess
P. R., 18, 91
vi., 320
Nitro-a-toluic nitril
C6H4.N02.(CH2.CN)=1.2
„ V)
cf.B. 17,505
45
Perkin
B., 16, 341
43, 112
11 11 .... ••>>
» J)
,J
....
84
Salkowski
B., 17, 507
46, 1176
11 ,« ••" «"•
=1.3
J)
....
61
11
B., 17, 504
11
11 11 ....
=1.4
JJ
....
114
Badziszewsky
B., 3, 198
» 11
11 11
JJ
....
116
Gabriel
B., 15, 834
42, 1070
3 P 2
476
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Nitro-a-toluic acid
C6H4.N02.(CH2.CN)=1.4
C8H602N2
116
Gabriel
B., 14, 2342
42, 188
Nitrotoluic nitril
Me.CN.NO2=1.3.?
1)
80
Beilstein& Kreusler
A., 144, 176
1
IsnotCjH/NO^CHj.CN q.v.
1» •
cf. 43, 112
45
Salkowski
B., 17, 505
Nitrosoindoxyl
C6H4.C(OH):C(NO).NH=1.2
})
d. w. m. 200
Baeyer
B., 15, 783
1 1
Azodioxindol ....
H
s.b. 260
300
Baeyer and Knop
A.,. 140, 26
vi., 736
C6H4.NH.CO.CH.N02==1.2
C8H6O,N,
d. 175
Baeyer
B., 12, 1313
36, 938
O DO li
Nitrosodioxindol
....
)5
....
300-310
Baeyer and Knop
A., 140, 20
vi., 735
Methoxynitrobenzonitril ....
OMe.CN.N02=1.4.?
»
cf. B., 2, 668
149-150
Henry
Z. C. [2], 6, 209
vii., 81
» i)
=1.2.3
• )J
....
171
Bruyn
B. T., 2, 205
48, 656
Nitrophenylnitroethylene ....
C6H4(NO2)(CH:CH.NO2)= 1 . 2
C8H6O4N2
....
106
Priebs
A., 225, 319
48, 161
»
= 1.3
)1
122
Friedlander and
A., 229, 233
48, 1138
Lazarus
„
=1-4
1»
cf. B., 16, 851
199
Friedlander and
A., .229, 210
»
Ma'hly
Nitrobenzoylformamide
C6H4(N02)(CO.CO.!NH,)=1.2
»
189
Claisen & Shadwell
B., 12, 352
»
= 1.3
)»
....
151-152
Claisen&Thompson
B., 12, 1944
38, 254
»
» J)
)»
151-152
Thompson
B., 14, 1187
Dinitrotoluic aldehyde
Me.COH.(NO2).!=1.3.2.?
C8H605N2
110-112
Bornemann
B., 17, 1473
46, 1163
Uiuitro-a-toluic acid....
(CH2.COOH)(NO2)2=1.2.4
C8H606NS
cf.B., 2, ,210
160
Eadziszewsky
Z. G. [2], 5, 358
vi., 1102
„ „ ....
» »
1J
160
Gabriel and Meyer
B., 14, 823
40, 729
„ „ ....
» »)
»>
160
Heckmann
A., 220, 128
46, 178
Dinitrotoluic acid
Me.COOH.(NO2)2=1.4.2.6
)J
157-158
Briickner
B., 8, 1678
29, 925
„ „ ....
= 1.2.4.6
J»
206
Jacobsen & Wierss
B., 16, 1959
44, 1121
a-Diuitromethoxybenzalde-
COH.OMe.(NO3)3=1.3.(?)2
^)
110
Tiemann & Ludwig
B., 15, 2056
44, 189
hyde
«- „
?» 51
J>
110
Ludwig
C. C. [1884], 35
48, 664
0-
Jl »1
»
155
>»
»
»)
0-
1) »V
)>
155.
Tiemann & Ludwig
B., 15, 2056
44, 189
Dyslyte (cf. A,, 81, 103) ...
....
C8H606N4
189 c.
Bassett
Z. C. [1871], 701
26, 100
Methylic dinitrosalicylate ....
CO<DMe.OH.(N02)2=1.2.(?).,
C8H607N2
124-125
Cahours
A. C. [3], 25, 6
v., 164
» »
» I!
1>
127^128 !
Salkowski
A., 173, 43
28,71
Dinitranisic acid
COOH.OMe.(N02)2=1.4,(?)2
1>
171-173
»
A., .163, 57
vii., 336; 25,
716
»» 11 .... ••••
=1.4.3.5
1)
....
181-182
Salkowski and
B., 10, 1254
34,72
Eudolph
Nitrosonitrobarbituric acid
....
C8H609N6
+4H20
d. 120
Baeyer
A., ,127, 226
(violantin)
Pentanitrodimethylaniline ....
Ce-NMe^NO^
C8H6010N6
....
127
Michlerand Meyer
B., 12, 1793
38, 108
„
)>
)>
....
127
Michler & Salath6
B., 12, 1790
»»
Phenoxyacetonitril
PhO.CH2.CN
C8H?ON
235-238
Liquid
Fritzsche
J. p. .[2], 20, 278
38, 319
Mandelic nitril
Ph.CH(OH).CN
J1
cf.B., 14, 239
s.— 10
Tiemann & Fried-
B., 14, .1967
42,56
.
lander
j, „
»
)»
170 d.
....
Voelckel
P. A., 62, 444
i., 570
Benzyl isocyanate
Ph.CH,,.N:CO
»)
153
Cannizzaro
G. I., 1, 33
24, 927
>' »
>1
J1
175-200
....
Letts
B., 5, 91
vii., 178, 180
Phenylglycocine anhydride....
Ph.N.CH2.CO
i 1
» •
....
263
Meyer
B., 10, 1967
34, 294
Tolyl isocyanate
C6H4Me.N : CO=1.2
J)
186
....
Girard
B., 6, 445
26, 912
j» v
= 1.4
11
185
Liquid
Hofmann
P. E., 19, 108;
24, 139; vii.,
B., 3, 656
407
Anisonitril (cf. Z.C.[2],6,209)
C6H4.OMe.CN=l,4
») •
253-254 u.c.
56-57
Henry
B., 2, 667
vii., 81
Hydroxy-a-toluic nitril
C6H4(OH).(CH2.CN)=1.3
n
....
52-53
Salkowski
B., 17, 506
46, 1176
H J,
=1.2(7)
is
....
69
Will
Z. C. [2], 7, 89
24, 408; vii.,
832
i! i)
" »
J5
....
69
Will and Lauben-
A., 199, 156
38, 265
heimer
»> 5)
=1.4
IJ
69-70
Salkowski
B., 17, 506
46, 1175
Ethenylamidophenol
C6H4.O.CMe : N=1.2
))
200-201
Liquid
Ladenburg
B., 9, 1524
31, 302
Phthalidine
C6H4.C(:NH).O.CH2=1.2(?)
))
337 c. (730)
150
Grsebe
B., 17, 2598
48, 166
COMPOUNDS CONTAINING FOUR ELEMENTS.
477
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Oxindole
C6H4.CH2.CO.NH or
CSH,ON
120
Baeyer and Knop
A., 140, 29
vi., 736
C6H4.C(OH) : CH.NH=1.2
i i .
^87
Methenylamidocresol
C6H3Me.O.CH : N=1.2.3
»> •
200
38-39
Hofmann Miller
B., 14, 570
40, 593
,,
=1.4.3
)j
45-46
ii
B., 14, 572
ii
„
3) JJ
3)
....
46
Nolting and Kohn
B., 17, 361
Piperpropylalkamine
J>
197
Ladenburg
C. R, 93, 338
40, 1158
? (cf. B. 2, 417 ; 13, 977)
C6H4.NH.C(NH).G(OH) : N
C3H7ON3
....
nf. 280
Bladin
B.,18,673;B.S.,
48, 257, T85
=1.2
42, 104
/3-Benzoyl formamide
Ph.CO.CO.NH2
CSH7O2N
+ H20
64-65
Claisen
B., 10, 1665
34, 151
ft- 11 >!
))
3
....
79-80
>!
B., 12, 633
"- >, »
J3
>J
90-91
11
B., 10, 1664; 12,
34, 151
633
y- 11 »
J)
>J
....
130
)!
B., 10, 1665
11
y- » i.
JJ
JJ
(C8H702N)2
134-135
»
B., 12, 635
36, 649
Phenylnitroethylene
Ph.CH:CH.N02
3>
cf.A.,31,269
56-57
Alexejew
B., 6, 1209
27, 261
ii ....
JJ
))
cf. A., 53, 297
56-5-57
Priebs
B., 16, 25.91
46, 313
„
»
J3
....
57-58
Gabriel
B., 18, 2438
....
JJ
5J
....
58
Erdmann
B., ,17, 413
46, 906
Isophenylnitroethylene
JJ
172-180
Priebs
A:, 225, 319
48, 161
Nitrostyrolene
C6H4(NO2)(CH : CH2)=1.3
— 1 9
J)
—5
19 TVI
Prausnitz
fjlHuODQ
B., 17, 598
B., 16, 2213
46, 1175
11 — ***
— 1 4
JI
ILJ!I — 10 u
29
Basler
B., 16, 3006
46, 604
Amidophenoxy acetic anhy-
11 — *•*
CtlH4.O.CH2.CO.NH=1.2
99
»•
....
143-144
Thate
J. p. [2], 25, 266
42,849
dride-
11 »
» it
jr
143-144
Fritzsche
J. p. [2], 20, 288
38, 320
11 11
Dioxindole
= 1
C6H4.CH(OH).CO.NH or
»j
....
166-167
180 p.d.
Thate
Baeyer -and Iv 11 ni »
J. p. [2], 29, 145
A., 140, 9
46, 1171
vi., 735
i i
JT
C6H4.C(OH):C(OH).NH
=1.2
Nitrophthalene „
...»
)J
280-320
48
Dusart
A. C. [3], 44, 332
iv., 113
Nitroamido-a-toluic nitri] ....
(CHS.CN).NH3.NOJ=1.4,6
C8H702N3
....
117-118
Gabriel
B., 15, 839
42, 1070
Phenylic oxamate
NH2.CO.COOPh
C8H703N
132
Wallach and 'Lieb--
B-i 13, 507
38, 558-
»
mann
Phenyloxamic acid (oxanilic)
NHPh.CO.CO0H
JJ
fr. C6H6
149-150
Klinger
A., 184, 265
31, 710
i) » »
JJ
JJ
fr. ether
150-151
n
ir
>r
Isonitrosophenylacetic acid ...
Ph.C(NOH).COOH
JJ
....
127-128
Miiller
B., 16, 1620
44, 429
Nitroacetophenone
CH3.CO.C6H4.N02=1.2
JJ "
cf. B., 3, 886
Liquid —20
Gevekoht
B^ 16, 2084
44, 191
„
=1.3
»J
jj
80-81
Hiibner & Buchka
B., 10, 1714
34, 147
„ .... ....
=1.4
»
....
80-81
Drewsen
A., 212, 159
42,847
Terephthalamic acid
COOH.(CO.NH2)=1,4
JJ
....
214
Sandmeyer
B., 18, 1498
48, 981
Amidobenzoyl formic acid ....
NH2.(CO.COOH)=1.3
jr
270-280 d.
Claisen &Thompson
B., 12, 1946
38, 254
?
....
jj •
261
Ost
J. p. [2], 27, 270
44, 792
Methylic nitrobenzoate
COOMe.NO2=1.3!
C8H7O4N
279
70
Chancel
A., 72, 275
i., 556
n ii
=1.4
JJ
....
96
Wilbrand and Beil-
A., 128, 263
iv., 61
stein
Nitrophenylacetic acid .
(CHS.COOH).NOS=1.2(?)
JJ '
....
98
Eadziszewsky
B., 3, 648
37, 96
11 i>
= 1.4 (?)
JJ"
mixture (?)
114
)j
B.,2,209; 3,648;
37, 96 ; 38,
Z. C. [2], 5, 358
119 ;vi., 1102
11 11
=1.3
JJ
....
117
Gabriel & Borgmann
B., 16, 2065
44, 1121
n 11 •
JJ »1
JV
....
120
Salkowski
B., 17, 506
46, 1176
n ji
= 1.4(J)
JJ '
ortho-?.
133-136
Forrer
B., 17, 985
46, 1021
i» 11
=1.2
1J
....
137-138
Bedson
B., 13, 574
37, 93
j» 11
JJ JJ
)»
....
141.
Salkowski
B.,. 17, 507
46, 1176
i) ,,
=1.4
)J
....
150-151
Bedson
B., 13, 574
37, 91
11 ii
ii >i
31
....
151
Wittenberg
B. S., 43, 111
48, 661
11 11 ...
>i i>
>J
....
149-152
Gabriel
B., 14, 2342
11 n
» ii
)i
....
151-5-152
Maxwell
B., 12, 1765
37,96; 38,120
Nitroacetoxy benzene
OAc.NO2=1.2
Jj
253 p.d.
40-41
Bottcher
B., 16, 1934
44, 1113
478
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Methylic uitrosophenolcar-
C6H4(NO)(O.COOMe)
C8H7O4N
137
Walker
B., 17, 400
46, 1003
boxylate
Nitrotoluic acid
Me.COOH.NO2=1.2.3
„
....
103 u.c.
Glaus and Mann
B., 18, 1122
48, 888
11 11
=1.2.6
„
145
Fittig and Ramsay
A., 168, 202
27,68
11
145
Jacobseu & Wierss
B., 16, 1958
44, 1121
11 11 "•• •*••
11 11
,,
145
Jacobsen
B., 17, 162-164
46, 745
11 11
11
....
145
Fittig and Bieber
A., 146, 245
145
Weith
B., 6. 420
,, „
=1.2.5
„
....
152
Jacobsen
B., 17, 162-164
46, 745
n 11
=1.3.5
,1
....
167
Thol
B., 18, 361
48, 522
„ „
=1.2.4
„
....
179
Jacobsen & Wierss
B., 16, 1958
44, 1121
11 ii •••• ™-
11 11
„
....
179
Jacobsen
B., 17, 162-164
46,745
;„ =1.3.4
„
182
„
B., 14, 2354
42, 185
„ „
H
n
184-5
Landolph
B., 6, 939
„ „
=1.46
„
....
188-189
Fittig and Ramsay
A., 168, 251
27, 68
,, „ .... ....
ji .»
11
189
Fittiea
A., 175,309
28,59
n „
.11 11
„
.«.
189-190
„
B., 6, 939
26, 1227
„ „ ....
ii ?i
n
...
190
Ahrens
Z. C. [2], 5, 104
vi., 1101
„ „
11 .11
11
190
Gerichten & Rossler
B., 11, 706
j, „ .... ....
„ =1.4.5(?)
„
....
189
Fittiea
A., 172, 303
28, 59
,, M ....
11 11
n
....
ISO
M
B., 7, 927
27, 1166; 34, 672
„ a
=1.3.6
„
....
211
lies and Remsen
B., 11, 1328
36, 53
si 11 •••• ••••
J) J)
„
214
Remsen ,& Kuhara
A. C. J., 3, 424
42, 607
M -51 •"• •"•
M »>
„
.cf. A,, 144, 168
214
Kelbe and Warth
A., 221, 157
46,46
„ „ .... ....
» » \'J
_,,
....
217-218
Ahrens
Z. CJ.2], 5, 105
vi., 1101
.,, „ .... ....
=1.3,2
„
....
S19
Jacobsen
B., 14, 2353
42, 185
„ „
11 11
.M
....
220
Ahrens
Z. C. [2], 5, 105
vi., 1101
Niiromethoxybenzaldehyde
COH.OMe.NO2=1.2.?
„
....
88
Voswinckel
B., 15, 2027
44,190
ji
=1.3.?
„
....
,82-83
Tiemann & Ludwig
B., 15, 2055
41
11 11
....
.82-83
„
B., 15, 3052
11
..=1.3.?
-.
....
98
«
B., 15, 2055
„
J> .11
„
Mixture
98
11
B., 15, 3054
„
=1.3.?
,,
....
104-105
11
B., 15, 3057
„
.11 n
„
«...
107
11
B., 15, 2054
Amidoisophthalic acid „.
(COO^)2.NH2=1.3.5
„
cf. J. p. [2],
a. 300
Storrs and Fittig
A., 153, 289
25, 491
Amidotrephthalic „
,=1.4.5
„
d.w.m.
Burkhardt
B., 10, 145
Aldoxime salicylic „
COO]£.OH.(CHNOH)=1.2.5
„
•*<•
179
Furth
B., 16, 2182
46, 42
„ „ „ ....
=1.2.3
11
....
193
11
„
11
Nitrohydroxytoluic aldehyde
COH.Me.OH.NO2=1.3.6.5
„
....
141
Schotten
B., 11, 788
34, 878
11 M
=1.3.4.5
11
....
152
„
B., 11, 789
„
Methylquinolinic acid
N.Me.(COOH)2=? ; on ox.
„
d. 180-185
Hoogewerff and
B., 14, 645
=.N.(COOH)3=1.2.3.5 or 6
Dorp
11 .M ••••
11 11
11
«...
186 d.
Kbnigs
B., 14, 104
Apophyllic acid
C6H3N(COOMe)(COOH)
,,
205
Anderson
A., 86. 196
5, 257 ; i., 350
11 11 •"• ••••
„
„
•*.*
S41-S42
Gerichten
B., 13, 1636
Nitromandelic acid
NO2.C6H4.CH(OH).COOH
C8H706N
....
120
Beyer
J. p. [2], 31, 382
48, 983
=1.3
Nitrophenoxyacetic acid ....
NO2.C6H4.O.CH2.COOH=?
n
....
153
Fritzsche
J. p. [2], 19, 33
36, 322
)! 11 *<••
=1.2
„
....
156-5
Thate
J. p. [2], 29, 149
46, 1170
ii 11 -
M I)
H
....
156-5
Fritzsche
J. p. [2], 20, 283
38, 319
„ ,
=1.4
„
183
„
J. p. [2], 20, 267
38, 320
Nitromethoxybenzoic acid ....
COOH.OMe,N02=1.2.?
.....
88-89
Cahours
A. C. [3], 10, 345
v., 164
,1 11 -
=1.2.?
w
148-149
Kraut
A., 150, 6; 173, 41
vi., 1005
)! Jl
=1.4,5
„
175-180
Cahours
A.
i., 302
1, 11 -
11 «!
Vi
....
186-187
Richter
R. K. T., 186
)1 11 •»••
'1 11
_-
189
Salkowski and
B., 10, 1255
Rudolph
Nitrohydroxytoluic acid
COOH.Me.OH.NO2=1.3.4.?
,,
....
85
lies and Remsen
B., 11, 463
34, 505
11 11
11 11
„
....
86-87
Mahon
A. C. J., 4, 186
42, 1205
11 ,i
„ =1.4.5.3
tl
186-187
Gerichten& Rossler
B., 11, 706
34,672
11 11
11 »
„
....
187-188
Ahrens
Z. C. [2], 5, 105
vi., 1101
COMPOUNDS CONTAINING FOUR ELEMENTS.
479
Name.
Constitution.
Fornnula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrodihydroxyacetophenone
(OH)2.NO2.Ac=1.3.(?)2
CSH705N
142
Nencki and Silber
J. p. [2], 23, 151
40, 591
Methoxyquinolinic acid
N.OMe.(COOH)2=1.2.5.6
)>
....
140 d.
Feer and Koiiigs
B., 18, 2398
48, 1235
Dinitroacetanilide
NHAc.(NO2)2=1.2.4
»
....
120
Eudnew
Z. C. [2], 7, 202
24, 712
,,
=1.2.6
)J
....
197
Salkowski
B., 10, 1696
Nitroisovauillic acid
COOH.OH.OMe.N02
C8H.O,N
....
172-173
Matsmoto
B., 11, 133
34, 502
=1.3.4.?
Nitrovanillic acid
„ =1.4.3.5
H
....
202
Weselsky and Bene
M. C., 3, 392
42, 1201
dikt
„ „
= 1.4.3.?
»
....
d.w.m. 210
Tiemann and Mats-
B., 9, 944
30, 525
moto
,, ,, ....
» »
))
d.w.m. 210
Matsmoto
B., 11, 133
Methylic diuitroamidoben-
COOMe.NH2.(N02)2
C8H7OaN3
....
144
Salkowski
A., 163, 11
25, 714; vii.,
zoate
=1.4.(?)2
336
>i »
=1.2.(?)2
)J
165
)!
A., 173, 46 -f B.,
28, 71 ; vil.,
4,872.
336
Trinitroethylbenzene
Et.(N03)3=?
))
Liquid
....
....
v., 1058
Triuitroxylene
Me2.(NO2)2=1.2.3.4.?
)J
....
55
Fittig and Bieber
....
vi., 294
(cf.G.I.,10,317)
„ =1.4.2.3.5
»
....
127
Schiff
B., 13, 1408
38, 892
„ .... ....
J» 51
»»
129-5
Fittig
A.r153, 276
24, 554
„
» »
)J
....
137
Glinzer and Fittig
A, 136, 307
v., 857, 1058
,,
1> J»
)>
....
137
Fittig and Ahrens
AV147, 15
vi., 294
,, ....
„ =1.3.2.4.6
H
....
176
Preis & Eaymann
B., 12, 220
36, 623
„ .... ....
I> )>
»>
176
Fittig
A., 148, 5
» .... ....
»• »
»)
....
176-177
Fittig and Ahrens
A., 147, 17
vi., 294
,, ....
» yr
J)
177
Luhmann
A, 144, 276
„
» rr
1>
ne
Grevingk
B., 17, 2424
48, 144
*» .... ..-.
» »j
»
177
Beilstein
A, 133, 45,
v., 1058
,,
=1.3.4.(?)2
)»
....
182
Tilden
....
45, 416
Trinitropetrol
C8H7(N02)3
)I
....
162
Bussenius and
A, 113,, 15L
iv., 382
Eisenstuck,
Ethylic nitrocomenate
C5HOs(NO2XOH).COOEt
C8H707N
....
147
Reibstein
J. p. [2], 24, 279
42,197
Trinitrophenetoil
OEt.(NO2)3=1.2.4.6.
C8H707N3
....
78
WJllgerodt
B., 12, 1278
36, 923
n •••• ""
» »
»
....
78-5
Miiller & Stenhouse
A, 141, 80
19, 236; vi.,
911
Trinitroethylresorcinol „„
OEt.OH.(NO2)3=1.3.2.4.6
C8H708N3
120-5
Stenhouse
19, 238
vi., 893
Trinitrodimethylquinol
((>Me)2.(NO2)3=1.4.2.3.5
)»
....
100-101
Habermann
B., 11, 1038
Trinitrodimethylresorcinol ....
=1.3.4.(?)2
»
123-124 u.c.
Honig
B., 11, 1042
34, 728
Trinitrodimethylcatechol _..
„ =1.2.3.4.?
»
....
144-145 u.c.
Tiemann and Mats-
B., 9, 940
30, 524
motor
ji ....
>< »
J)
....
144-145
Matsmoto-
B., 11, 131
Amidoxindole
C6H3(NH2).CH1.CO.NH
CsHsONj
....
200 d.
Gabriel and. Meyer
B., 14, 832
40, 731
=1.4.5
Nitrosoacetanilide
C6H6.NAc.NO
C8H902N2
....
40-41
Fischer
B., 9, 464
30, 205
Benzoyl carbamide
NH3.CO.NHBe
»J
....
171
Miguel
B. S. [2], 25, 104
30, 73
» , jv •••••
))
1»
cf. A., 92, 404
200
....
Z. C. [1868], 305
i., 753
Phenyl oxamide
NH2.CO.CO.NHPh
»
A., 73, 184
224
Klinger
A, 184, 271
Phenylhydrazine glyoxylic
Ph.N2H::CH.COOH
I)
....
d. 137
Fischer
B., 17, 578
46, 1151
acid
» »•
>»'
•»
d.137
Elbers<
A., 227, 340
48, 535
•Phenylglyoxime
Ph.C( : N.OH).CH : N.OH
)>
152
Schramm.
B., 16, 2186
46, 52
Diformyldiamidobenzene ....
C6H4(NH.CHO)3=1.3
»
....
155
Tobias
B., 15, 2447
44, 326
,, ....
=1.4
)»
....
203-5-204
Wundt
B., 11, 828
34, 668
Formamidobenzamide
NH2.CO.C6H4.NH.CHO= 1.2
)»
123
Weddige
J.. p. [2], 31,, 124
48, 661
Isophthalamide
C6H4(CO.NH2)2=1.3
I)
265
Beyer
J, p. [2], 22, 352
40,96
Terephthalaldoxine ....
CSH4(CH : NOH)2=1.4
t»
....
200
Westenberger
B., 16, 2995
46, 581
Nitrosophenylglycocoll
Ph.N(NO).CH2.COOH
08H803N,
105 d.
Schwebel
B., 11, 1132
34, 795
Nitro-acetanilide
C6H4(N02).NHAc=1.2
»
78
HUbner
B., 9, 775
30, 309
„ „
» »
»
....
92-93
»
A., 209, 352
» »
,, =1.3
j>
141-143
Meyer and Stuber
A., 165, 183
25, 305
» u
» )>
j»
....
143
Levinstein
D. P., 256, 471
48, 1127
,, ,,
= 1.4
»
....
207
Nolting and Collin
B., 17,262
46, 1012
480
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitro-acetauilide
C6H4(NO2).NHAc=1.4
C8H803N,
....
207
Kelbe
B., 16, 1200
44,916
11 ,, ....
J> 1>
))
207
Meyer and Stuber
J. [1875], 344
26, 305
»i - n ••••
)) II
11
207
Rudnew
Z. C. [2J, 7, 202
24, 712
Uraniidobenzoic acid
C6H4(NH.CO.NH2).COOH
»T
....
d. 200
Traube
B., 15, 2117
44, 194
=(1.3
Methyl nitrosomethylnitro-
C,H4.NO2.(CHMe.NO)=1.2
J)
58
Gabriel and Meyer
B., 14, 2337
42, 189
benzeue
11 11
»1 »
)»
58
Gabriel
B., 15, 3058, 3060
11 it
=1.3
)J
63-63-5
ii
B., 15, 3061
44, 582
Nitrophenylniethylacetoxime
C0H4.N02.(CMe:NOH)=1.3
H
....
131-132
n
B., 15, 3063
11
Benzenylamidoxime car-
C6H4.C02H.[C(NH2):NOH]
j)
a. 330
Miiller
B., 18, 2486
48, 1227
boxylic acid
=1.4
Nitro-a-toluamide
C6H4.N02.(CH2.CO.NH2)
))
190-192
Gabriel
B., 14, 2342
=1.4
Nitrotoluamide
(CO.NH2).Me.NO2=1.3.?
»
151
Beilstein and
A., 144, 175
Kreusler
Hydroisophthalajuide
(CO.NH2)2.OH^=1.^.4
)>
....
250
Jacobsen
B., 11, 380
34, 583
Azophenylmethazonic acid ....
C6H5.N2.C2H3N203
C8Ha03N4
164 .d.
Kimich
B., 10, 141
32, 325
/3-pyridine tricarboxylamide
N.(CO.NH2)3=symmetrieal
?1
a. 280
Voigt
A., 228, 29
48, 813
Nitrophenylamidoacetic acid
NO2.[CH(NH2).COOH]=1.3
C8H804N2
172 d.
Plochl and Loe
B., 18, 1180
48, 899
Amidonitro-a-toluic acid
NH2.N02.(CH2.COOH)
J)
143-5-144-5
Gabriel
B., 15, 836, 1992
42, 1070
=1.2.4
» -Q- i! 11
=1.3.4
))
184-186
Gabriel. and Meyer
B., 14, 824
40, 730
Dinitroethylbenzene
Et.(N02)2=?
))
Liquid
....
....
v., 1058
Dinitroxylene
Me2.(NO2)2=1.3.2.4
)'
.,,,
82
Grevingk
B., 17, 2423
48, 144
n .... ....
» =»
5»
abt. 92
Rommier
B. S. [2], 19, 434
26, 887
»i .... ....
„ = 1;3.2.5
»)
92-93
!»
i»
26, 888
„ .... ....
)» >»
>»
9^
Fittig
A., 1,48, 5
,, .... ....
5> 3)
Jl
....
93
Fittig and Abrens
A., 147, 17
vi., 294
„ ....
•>» »
J)
93
Grevingk
B., 1,7, 2422
48, 144
.11 ..... ....
„ =1.4,2^
V)
93
Glinzer andCFittig
A., 136, 308
v., 857
,, .... ...
i) ij
,1J
93
Earner
B., 15, 2303
44, 179
» .... ....
!> )l
n
93
Lellmann
A., 228, 250
48, 973
11 .... ....
11 II
j>
93
Fittig and Ahrens
A., 147, 17
vi., 294
i,
1! II
j»
93
Jannasch
A., 171, 79
27, 468
i,
,)l 1>
is
93
Jannasch & Stiinkel
B., 14, 1146
40, 808
V «... ....
=1.4.2.6
»»
123-5
Glinzer and Fittig
A., 136, 307
v., 1058
» ...» ....
.11 ii
>»
....
123
Fittig and Ahrena
A., 147, 17
vi., 294
)j .... ....
n )i
)>
123-5
Jannasch & Stiiukel
B., U, 1147
40, 808
i.
.11 11
»j
124
Lellmann
A., 228, 250
48, 973
n .... ....
n 11
»
,125
Jannaseh
A., 17-1, 79
27, 468
i, .... ....
„ =1.4.2.5
j»
147-148
Lellmann
A., 228, 250
48, 973
„ (double compound)
of 1.4.2.3 and 1.4.2.6
.ji
99-5
Earner
B., 15, 2302
44, 179
» »i
l> >!
i)
99-99-5
Jannasch & Stiinkel
B., 14, 1146
Ketiae dicarbomc acid
(.CMe.N.:C.COOEt)2
si
200-201
Wleugel
B., 15, 1053
42, 949
Nitropyrryline dimethyl di-
N02.C4NHj.(CO.Me),,
)»
....
149
Ciamiciau & Silber
B., 18, 1468
48, 994
ketone
Diuitrophenetoil
OEt.(NO2)2=1.2.6
CSH805N2
57-58
Salkowski & Rehs
B., 7, 371
27, 801
.11 •••• ....
» i)
»
....
57-58
Salkowski
A., 174, 273
28, 367
,i» .... ....
„ =1.3.5
J»
....
85
Andrew
J. p. [2], 21, 335
38, 467
.v
„ =1.2.4
»)
84
Salkowski
A., 174, 263
vii., 908, 929
11
» )»
»
86
Willgerodt
B., 12, 764
36, 717
11 ....
»' »
J)
cf. A., 74,015
86-87
Beilstein and Kuhl-
A., 156,214
berg
Dinitromethylcresol .... _. „;.
Me.OMe.(NO2)2=-l. 4:3.5
J»
122
Staedel
B., 14, 900
40, 724
)» .... .. .
>! 1)
)j
....
122
D
A., 217, 170
44, 863
Dinitronitrosomethyltolu-
Me.NMe(NO).(NO2)2
C8Ha05N4
125
Gattermanu
B., 18, 1488
48, 976
idine
Dinitro-dimethylresonhnol ....
(OMe)2.(N02)2=1.3.(?)2
08H806N2
67
Honig
B., 11, 1042
34,728
„ catechol ...
=1.2.(?)2
»i
....
a. 100
Merck
A., 95, 200
v., 997
COMPOUNDS CONTAINING FOUR ELEMENTS,
481
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
.Dinitro-dimethylquinol
(OMe)2.(N02)2=1.4.5.?
C8H306N2
169-170
Habermann
B., 11, 1037
34, 728
Dinitroethylquinol ....
OEt.OH.(NO2)2=1.4.(?)2
„
....
71
Weselsky and
M. C., 2, 370
40, 1139
Benedikt
55 .... ....
„ =1.3.(?)2
„
75
Aronheim
B., 12, 32
36, 465
Trinitrod i raethy laniline
C6H2(N02)3.NMe2
C8HB06N4
....
115
Krell
B., 5, 880
26, 279
Trinitromethyltoluidine
C6HMe.NHMe.(N02)3
„
137-138
Gattermann
B., 18, 1488
48, 976
Dinitroethoxydihydroxy-
C6H(OH)2(OEt)(N02)2
QjH8O7N2
cf, A., 215, 155
143d.
Nietzki
B., 11, 1449
34, 867
benzene
C6H5.NHAe
C8H9ON
295 (755)
101
Williams
17, 106
v., 1087
112
Gerhardt
A., 87, 164
vi., 418
112
Seifert
B., 18, 1360
"
112-113
Z. C. [2], 5, 699
vii., 4
11
„
293
112-113
Wallach and Hoff-
A,, 184, 86
32, 187
mann
„
„
51
~ .
113
Wurtz
C. B., 7, 3528
24, 1056
„
11
„
113
Menschutkin
B., 15, 2503
„ (?)
» (v
•)>
....
113
Eossing
B., 17, 3006
114-115
Kelbe
B., 16, 1200
44, 916
a-toluatnide ..„
C6H5.CHj.CO.NH2
^
....
155-156
Bernthsen
A., 184, 290
31, 619
181-184
154-155
Weddige
J. p [21 7 100
26, 1241
155 u.c.
Eeimer
r L J! ' J A'-/v
B., 13, 741
Methylphenylaeetoxime
Ph.CMe : NOH
I
59
Jamy
B., 15, 2781
44,580
Methylbenzaldexime
Ph.CH : N.OMe
„
190-192 u.c.
Liquid
Petraczek
B., 16, 826
Methylformanilide
Ph.NMe.CHO
„
243-244
Liquid
Pinner
B., 16, 1652
44, 1090
C6H4.Me.NH(CHO)= 1 .4
45
Hiiibner
A., 209, 372
55 = ?
50
Eosenstiehl
Z. C. [2], 5, 189
vi., 1108
,,
....
50
Hofma.nn
G. L, 5, 392
29, 601
„ —
„ =1.4
„
52?
Tobias
B., 15, 2446
44, 326
„ .... .... ....
„ ,,
H
....
52-53
Senier
M..
47, 765
JO
2-88
56'J> 57'S
Ladenburff
B., 10 1129
32, 754
n n
....
58
Tobias
B., 15, 2446
44, 326
/ \
211
Ladenburff
B., 10 1129
32, 754
)) 55
Toluamide
Me.(CO.NH2)=1.2
135-136
8pic&
G. I. 5 392
29, 601
n
....
» »
"
~~
138
Weith
B>fi 491
"
)> *i
))
tUft
., A), i -. i
55 =1.4
151
Fischli
B. 12 615
36, 638
Amidoacetophenone
C6H4.NH.,,(COMe)=1.2
"
I.
Liquid
Gevekoht
B., 15, 2085
„
0 »
„
242-252
Liquid
Baeyer and Blom
B., 15, 2154
44, 197
55 ....
I) !)
„
_..
92-93
Engler
B., 11, 933
„
=1.4
„
«..
106
Drewsen
A., 212, 163
Dihydroxindole
jj
....
sf. 67-70
Bischoff
R, 16, 1041
? ..„
C4H3O.C : N.CMe,
M
300-310
142
Tonnies and Staub
B., 17, 857
46, 1130
I 1
Tetrene urethane
C8H,O3N
180 (770)
• «**
....
G. I., 12, 84
Benzylic carbamate
NH2.COO.CH.jPh
„
....
86
Cannizzaro
B., 3, 518
vii., 179
55 ,5 ....
„
„
86
5)
G. I., 1, 33
24, 927
Phenylamidaoetic acid
Ph.CH(NH2).COOH
„
_..
255-256
Miiller
B., 16, 1621
44, 1130
)5 55 ""
„
„
....
256
Tiemann and Fried
B., 13, 383
38, 473
lander
)> 5) •".
„
n
....
256
Tiemann
B., 14, 1969
Phenylglycocine
NHPh.CH2.COOH
n
....
110
Michaelson and
Z. C. [1866], 16
vi., 644
Lippmann
55 .... ....
„
„
....
126-127
P. J. Meyer
B., 8, 1156
29, 372
55 ....
„
n
....
126-127
Schwebel
B., 10, 2046
Glycolphenylamine
CeHs.NH.CO.CH2.OH
„
fr. hot H2O
108
Norton and Tcher-
C. B., 86, 1332
34, 775
niak
55 ....
„
„
fr. cold H2O
98
„
B. S., 30, 104
n
Phenylhydroxyacetamide ....
CH2(OH).CO.NHPh
„
....
65-115
Tommasi
B. S., 22, 6
26, 627
Isonitrosophenylethyl alcohol
Ph.C(NOH).CH2.OH
„
....
70
Meyer and Nageli
B., 16, 1624
44, 1076
Phenoxyacetamide
Ph.O.CH2.CO.NH2
,,
....
101-5
Fritzsche
J. p. [2], 20, 277
38, 319
Pheiiylglycollamide
Ph.CH(OH).CO.NH2
"
131
Zinin
Z. C. [2], 4, 710
vi., 802
5 n
482
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts Diet.
& J. Ch. Soc.
Phenylglycollarnide
Methylic benzhydroxaminate
Methylbenzhydroxamic acid
Cresylic carbamate
Amidophenylacetic acid
jj jj
)! JJ
Am M (lacetoxy benzene
j»
Acetamidophenol
j) ....
Nitroethyl benzene
jj jj
jj jj .... ...
Methoxybenzamide
„ „ (anisamide)
„ (B. 2, 666)
Anisaldoxime
Amidotoluic acid
» jj .... ....
jj jj ....
!! )J
jj jj
JJ JJ
JJ JJ
» JJ
)J J,
)> JJ
Nitroxylene
Ph.CH(OH).CO.NHs
Ph.C(OH) : N.OMe
Ph.C(OMe) : N.OH
NH2.COO.C6H4.Me (?)
NH2.(CH2.COOH) =1.3
=1.4
>! !)
OAc.NH2 =1.2
=1.4
OKNHAc =1.4
=1.2
C6H4Et.N02 =1.2
= J
=1.4
OMe.(CO.NH2) =1.2
=1.4
» u
Me.COOH.NH, =1.3.?
= 1.3.4
=1.3.?
=1.3.2
=1.4.6
=1.2.5
=1.2.6
J» »J
=1.2.4
» »
Me,.NOs =1.2.3
=1.2.4
» »
jj >j
„ =1.2.?
=1.3.2
!) »
=1.3.4
)» »
'J JJ
J) )>
J» »J
„ =1.3.5
„ =1.4.5.(?)
» i)
,, (?)
1) >!
Mes.OH.NO =1.4.3.6
" »
C4H2Ac2NH
C6HS.N:N.C2H4.NO3
C8H903N
)I
JJ
)J
JJ
»
J»
J)
?J
JJ
J)
J1
«
M
1»
)>
1»
JJ
)J
J)
»
)»
J»
n
jj
jj
»)
jj
M
M
jj
JJ
)j
JJ
jj
»
Jj
jj
n
jj
jj
jj
» (?)
»j
5)
)J
»)
>1
»»
C8HAN3
225
MM
cf. R 11, 232
227-228
233
245-246
295
250
256
248 (580)
S58(760)s.d.
225
225 (774)
227-228
237-239
235-245
243-244 c.
245-5 (744)
255 c.
234-237
240
245-246
190
Liquid
64-65
125
148-149
199-200 d.
199-200
150
183
179
201
Liquid
Liquid
Liquid
128-129
Solid
137-138
45
b. 100
132
167
172
164-165
165
191
196
196
191
Liquid
29
29
52-55
2
L. —20
67
70-71
cf. A., 176, 56
Liquid
160-165
163
161-162
45-7
136-137 d.
Tieiuann and Friec
lander
Tiemann & Kriiger
Lessen and Zanni
Kempf
Gabriel & Borgmain
Bedson
Gabriel
Morse
Ladenburg
Beilstein and
Kuhlberg
Tollens and Fittig
Beilstein and
Kuhlberg
Grimaux
Cahours
Henry
Westenberger
Kelbe and Warth
Jacobsen
Beilstein and
Kreusler
Jacobsen
Ahrens
Jacobsen
jj
jj
jj
jj
Noltiug and Forel
j»
Jacobsen
jj
j»
Nolting and Forel
Greviugk
Beilstein and
Kuhlberg
Tawildarow
Wroblewsky
Harmsen
Grevingk
Wroblewsky
Jannasch and
Diekmann
Schaumann
Deumelandt
Beilstein and
Kuhlberg
Oliveri
Goldschmidt and
Schmid
Ciamiciau and
Dennstedt
Maier
Meyer and AmbUhl
B., 14, 1967
B., 17, 1690
A., 182, 226
J. p. [2], 1, 410
B., 16, 2065
B., 14, 2342
B., 11, 232
B , 9, 1524
2. C. [2], 6, 624;
A., 156, 206
A., 131, 310
Z. C. [2], 5, 524;
A., 156, 206
B. S. [2], 13, 26
A. C. [3], 22, 353
Z. C. [2], 6, 209
B., 16, 2994
A., 221, 157
B., 14, 2354
A., 144, 178
B., 14, 2354
Z. 0. [2], 5, 104
B., 17, 164
jj
B., 16, 1959
B., 17, 164
B., 16, 1959
B. S., 42, 332
»
B., 17, 160
j»
B., 10, 1013
B. S., 42, 332
B., 17, 2430
J., 22, 415
Z. C., 13, 418
A., 207, 91
B., 13, 1558
B., 17, 2429
A., 207, 94 ; B.,
10, 1248
A., 171, 83
B., 11, 1537
Z. C. [1866], 21
J., 22, 415
G. I. [1882], 161
B., 18, 569
B., 17, 432, 2953
A., 127, 163
B., 8, 751, 1073
42, 56
46, 1325
24, 3-2
44, 1121
37, 92
vii., 903
u
34, 416
31, 303
vi., 292
iv., 485; v.,
1058
vi., 292
vi., 1002
i., 297
vii., 81
46, 581
46, 47
42, 185
42, 185
vi., 1101
46, 745
j»
44, 1121
46, 745
44, 1121
48, 382
J»
46, 737
jj
32, 601
48, 382
48, 145
40, 433
40, 49
48, 145
34, 55; 40, 433
27, 477
36,51
v., 1058
42, 837
48, 775
46, 1044 ; 48,
379
ii., 155
28, 1202
jj .... .... ...
jj • .. .... ....
Nitrosoxylenol
Dipseudo-acetopyrroline
Hipparin
Azonitroethylbenzene
COMPOUNDS CONTAINING FOUR ELEMENTS.
483
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Dehydracetamide
CH2Ac.C: CH.CfCO.NH,) : C
i i
C8H903N
....
208 '5
Oppenheim and
B., 9, 1100
30, 506
(OH)
Precht
Anishydroxamic acid
OMe.(CO.NH.OH) =1.4
))
156-157
Lessen
A., 175, 271
28, 636
Ethyl nitrophenol
OEt.N02 =1.2
H
267-268 (757)
....
Forster
J.p. [2], 21, 343
,, ,,
» »
»
dbt. %58
Liquid
Groll
J. p. [2], 14, 207
20, 247
„ ,,
=1.3
H
264p.d.(760);
34
Bantlin
B., 11, 2101
38, 238
169 (70)
,, ,,
» =1-4
J)
....
57-58
Fritzsche
J. p., 75, 257
iv., 397
,, ,, ....
)J )»
»
....
58
Hallock
B., 14, 37
40, 595
„ ,,
)) »»
))
283
57-58
Riehter
K. K. T., 190
» »
» 5)
51
....
59
Willgerodt
B., 14, 2637
42, 396
„ ,,
»
J1
....
85-87
....
G. I., 11, 396
Nitro-ethylphenol
....
)?
....
212-215
Suida and Plohn
M. C., 1, 178
Methyl nitrocresol
Me.OMe.NO2 =1.4.6
1)
266-267 u.c.
Liquid
Knecht
B., 15, 300
42, 728
„ „ .... ....
=1.4.5
»
274 p.d.
Liquid
Wagner
B., 7, 1273
vil., 931 ; 28,
256
Ethyl uitrosoresorcinol
OH.OEt.NO =1.3.4
M
d. w. m., 180
Aroriheim
B., 12, 31
36, 465
Amidoaiiisic acid
COOH.OMe.NHj =1.4.5 (?)
)»
....
180
Zinin
A., 92, 327
i., 296
,, „ ....
=1.4.6
))
204
Balbiano
G. I., 14, 234
48, 530
Vanillin aldoxime
(CH I NOH).OMe.OH =1.3.4
))
....
117
Lach
B., 16, 1786
44, 1104
,, „ ....
Nitroxylenol ....
» «
Me2.OH.NO2 =1.3.(7)j
jj
....
121-122
68'5
Tiernann and Kees
Lako
B., 18, 1664
A., 182, 33
48, 1072
30, 634
»
)i »
JT
«
*..*
95
Pfaff
B., 16, 616
44, 802
ft-
=1.4.(?)2
J)
236 d.
Liquid
Oliveri
G. I. [1882], 161
42,837
,, y-
» J)
:»
....
89
M
»)
>t
» «-
„ =1.4.2.5
M
115
»
)i
»
,, o-
» ji
j>
....
122
Goldschmidt and
B., 18, 570
48, 775
Schmid
Methylic pseudacetyl-a-
C4H2AcNH.COOMe
>»
....
113
Ciamician & Silber
B., 17, 1156 ;
46, 1045 ; 48,
carbopyrrolate
G. I., 14, 162
247
Hydroxylutidine carboxylic
....
»
+H20
246
Collie
A., 226, 294
48, 374
acid
Nitro-acetdiamidobenzene ....
NH2.NHAc.NO2 =1.4.7
(VE^N,
....
184
Biedermann and
B., 7, 1531
Ledoux
» » •»••
» »
))
186
Ladenburg
B., 17, 148
46, 738
Nitrodimethylquinol
(OMe)2.NO2 =1.4.5
C8H,04N
....
70-71
Habermann
B., 11, 1037
34, 728
i) »
)) »
))
71-5
Miihlhauser
A., 207, 253
Nitrodimethylcatechol
„ =1.2.3 or 4
J)
cf. A., 108, 61
95-96
Tiemann and
B., 9, 939
30, 52
Matsmoto
» ...
» w
1)
*•••
95-96
Matsmoto
B., 11, 131
Nitroethylquinol
OEt.OH.NO2 =1.4.?
JJ
....
83
Weselsky and
M. C., 2, 370
40, 1J39
Benedikt
Nitroethyl resorcinol
=1.3.4
>J
....
79
)3
W. A., 82, 1219 ;
40, 727
M. Q, 1, 895
„ ,, .... ....
=1.3.6
>»
....
131
i)
i>
»
Ethyldicarbopyrrolic acid ....
C4HjEtN.COOH
»»
....
w. m. 250
Bell
B., 10, 1865
36, 525
Dimetliylpyrroline dicar-
COnH.C : CMe.NH.CMe : C.
i |
»
....
197 d.
Knorr
B., 17, 1639
46, 1368
boxylic acid
COjH
51 »
»
»
...
250-251 d.
u
B., 18, 1564
48, 994
Ethylic comenamate....
C5H(NH2)O.OH.OOOEt
I)
+2H2O
205
Eeibstein
J. p. [2], 24, 284
Ethylcomenamic acid
C,,H(NH2)O.OEt.COOH
If
)»
210 d.
Mennel
J. p. [2], 32, 176
48, 1203
Dinitrodimethylaniline
NMe2.(NH2)2=?
C8H904N3
....
73-5
Schraube
B., 8, 621
,, ....
=1.3.4
»>
....
77
Merz and Weith
B., 10, 763
32, 603
„ ....
» )>
)?
78
Leymann
B., 15, 1234
»
=1.2.4
»
....
87 u. c.
Mertens
B., 10, 995
32, 605
„ ....
)> ))
)5
....
87
Wurster & Sendtner
B., 12, 1803
38, 111
i)
= »
»1
....
240-260 d.
Mertens
B., 10, 995
32, 606
Dinitroethylaniline
NHEt.(NOj)3=1.2.4
»
114
Norton and Allen
B., 18, 1997
Dinitromethyltoluidine
Me.NHMe.(NO2)2=1.4.(?)2
))
129
Thomsen
B., 10, 1584
34, 218
i» ....
» )>
)1
....
129
Gattermann
B., 18, 1487
48, 976
Dinitroamidoethylbenzene ....
Et.NH2.(N02)2=1.4.(?)2
)>
134-135
Paucksch
B., 17, 769
46, 1143
3Q.2
4-81
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dinitroxylidine
Me2.NH8.(NO2)2=?
C8H,04N3
....
105
Krell
B., 5, 879
26, 279
,,
» ' =?
))
....
191-192
Beilstein
A., 133, 45
v., 1059
Ethyl-nitropyrogallol
(OH)a.OEt.NOa=?
ChH906N
139
Weselsky & Bene-
M. 0., 2, 215
42,53
dikt
Allocaffeine
....
C8HAN,
....
198
Fischer
A., 215, 275
44, 355
Ethylpicrazide
C2H6.N2H2.C6H2(NO,,)3
C8H906N6
....
200 d.
D
A., 199, 299
Phenylethenylamidoxime ....
Ph.CH2.C(NH2) : NOH
C9H10ON.,
67
Knudsen
B., 18, 1068
48, 897
Methylbenzenylamidoxime...
NH2.CPh : NOMe
))
a. 230
57
Tiemaun & Kriiger
B., 17, 1689
46, 1325
»
)»
Jl
230 u. c.
57
Kriiger
B., 18, 1056
48, 896
Phenylhydroxyacetamidine....
Ph.CH(OH).C(NH2) I NH
)J
....
100
Beyer
J. p. [2], 31, 382
48, 983
»
n
»
....
110
»
J. p. [2], 28, 190
46, 65
Ethenylanilidoxinie
Ph.NH.CMe : NOH
))
121
Nordmann
B., 17, 2753
48, 239
Acetylphenylhydrazine
Ph.N2H2.CO.CH3
)»
128'5
Fischer
A, 190, 129
34, 309
Phenylglycocinamide
Ph.NH.CH2.CO.NH2
1)
....
133
Meyer
B., 8, 1157
29, 373
Methylphenylcarbam ide
NHj-CO.NMePh
)>
....
82
Gebliardt
B., 17, 2095
46, 1321
Benzylcarbamide
NH2.CO.NH.CH2Ph
IT
....
144
Letts
B., 5, 91
25, 448; vi:.,
181
,,
u
JJ-
....
147-147-5
Cannizzaro
B., 4, 412; G.I.,
vii., 181 ; 24,
1,41
928
Tolylcarbamide
Me.(NH.CO.NH2)=1.3
j>
....
142
Cosack
B., 13, 1089
38, 713
j,
)» »
»
142
D
B., 12, 1450
38, 245
„ ....
= 1.4
)J
172
u
J)
M
j]
» »
j»
cf. A., 126, 157
180
Steiner
B., 8, 519
28, 883
j,
= 1.2
tl
185
Cosack
B., 13, 1089
38, 713
Nitroso-methyltoluidine
Me.NMe(NO)=1.2
»j
Liquid
Monnet & Nolting
B., 11, 2278
» ••"
=1.4
n
....
54
Thomsen
B., 10, 1584
34, 218
Nitroso-dimethylaniline
NO.NMe2=1.4
j>-
85-5
Wurster and Roser
B., 12, 1823
» ....
» »
»
....
92
Baeyer and Caro
B., 7, 810, 963
28, 84
Amidoacetanilide
NH2.NHAc=1.4
»
....
161
Nietzki
B., 17, 344
46, 1016
Amidophenylacetamide
NH2.(CH.j.CO.NH2)=1.4
»
....
169-170
Einhorn
B., 17, 2014
p-Amidotoluamide
(CO.NH2).Me.NH2=?
>»
....
115
Beilstein & Kreuslei
A., 144, 181
?
>.*•
)»
....
90
j»
A., 144, 177
Dipropionyl dicyanide
....
C8H1002N2
208
Liquid — 15
Claisen and Moritz
37, 695
» i)
....
))
210-213
Liquid
?>
B., 13, 2121
40, 154
» j)
....
)J
210-212
59
Bruyn
C. C. [1885], 356
48, 963
Phenylhydroxyethenylami-
Ph.CH(OH).C(NH3) nSTOH
JJ
....
140
Tiemann
B., 17, 126
46,, 734
doxime
»
)»
»
.....
158-159
Gross
B., 18, 1075
48, 898
?
Ph.C( : N.OH).CH2.NH.OH
>»
162-163.
Schramm
B., 16, 2183
46, 51
Phenylhydrazido-acetic acid
Ph.N2H2.CH2.COOH
»»
....
157 d.
Elbers
A., 227, 340
48, 535
Methoxybenzene carbamide
OMe.(NH.CO.NH2) =1.2
7>
146-5
Mulhauser
B., 13, 923 ; A,
38, 642; 42,
207, 244
302
Phenylene dicarbamide
(NH.CO.NH2)j=1.2
JJ
....
290
Lellmann
B., 16, 593
44,798
» n
=1.4
»
d. w. m.
»
»1
r>
Ethylnitrosoamidophenol ....
OH.NEt(NO)=1.2
»•
....
121-5
Ftrster
J. p. [2], 21, 361
38, 465
Nitroethylaniliue
N02.NHEt=1.4
5)
95-95-5
Weller
B., 16, 31
44, 579
», .... ....
J» »
T)
....
96
Noltiug and Collin
B., 17, 267
46, 1613
Nitrodimethylaniline
N02.NMe2=1.4
»
cf.B.,12,.529
160
Schraube
I. D. Strassburg,
1875
>,
» »>
>T
....
162
Leymann
B., 15, 1234
v
j) »•
n>
....
161-163
Wurster & Scheibe
B., 12, 1816, 181S
38, 107
»
>i »i
si
162
Wurster
B., 12, 529
36, 626
»
» »v
>^
162-163.
Weber
B., 8, 714
28, 1200
»
» 1>
»j
....
163
Michler •& Walder
B., 14, 2176
»» ....
5J )»
»i
....
163
Merz and Weith
B., 10, 761
32,603
D ....
» »
)i
....
169
Schraube
B., 8, 621
Amidophenylamido-acetic
NH2.[CH(NH2).COOH]=1.3
»»
....
214
Plochl and Loe
B., 18, 1181
48, 899
acid
Nitro-atnidoethylbenzene ....
Et.NH2.NO2=?
a
....
45-47
Paucksch
B., 17, 770
46, 1143
Nitromethyltoluidine
Me.NHMe.NO2=1.4.5
)>
84-85
Gattermann
B., 18, 1487
48, 976
Nitroxylidine
Me2.NO2.NH2=1.3.5.?
11
....
69
Hofmann
B., 9, 1297
31, 93
»
„ =1.3.5.6
»
....
76
Wroblewsky
B., 10, 1248
34, 55
COMPOUNDS CONTAINING FOUR ELEMENTS.
485
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Nitroxylidine
Me2.N02.NH2=1.3.5.6
C8H1002N2
....
76
Wroblewsky
A., 207, 94
40, 433
j,
„ =1.3.4.2
j>
78
Grevingk
B., 17, 2422
48, 145
„ ....
=1.4.(?)2
»
96
Fittig and Ahrens
A., 147, 22
vi., 1131
„ ....
„ =1.3.4.6
i>
....
123
Grevingk
B., 17, 2422
48, 145
»
!> 11
n
....
123
Nolting and Collin
B., 17, 265
46, 1012
,,
11 IT
»
....
123
Fittig and Ahrens
A., 147, 18
vi., 1131
„ .... ....
= ?
)>
MM
130
Luhmann
A., 144, 274
»
Nitrosomethylphenyl semi-
NMePh.N(NO).CO.NH2
C8H1003N4
77 d.
Fischer
A., 190, 165
34,311
carbazide
Pheuylene dicarbamide
C6H4(NH.CO.NH2)2=1 .2
J)
....
290
Lellmann
B., 16, 593
»
=1.3
)>
....
a. 300
Warder
B., 8, 1180
29, 400
„ „
Caffeine (Them, Methyltheo-
bromine)
=1.4
))
)1
cf. B., 15, 29,
453
d. w. m.
177-8
Lellmann
Mulder
B., 16, 593
P. A., 43, 175
i., 707
NMe.CO.NMe.CH : C.C : N.
i i
CO.NMe
» j) »
))
1)
....
230-5
Biedermann
A. P. [3], 21, 175
46, 185
» » )>
)»
)»
234-235
Strecker
A., 118, 172
Amidoethylene nitrophenol...
C6H4.N02.(O.C2H4.NH2)=1.2
CSH1003N3
72-73
Widdige
J. p. [2], 24, 247
40, 1137
» »
=1.4
JJ
....
108-109
»
J. p. [2], 24, 254
40, 1139
Nitroamidoethoxybenzene ....
OEt.NH2.NO2=1.2.4
))
96-97
Andreae
J. p. [2], 21, 327
38, 466
Hydroxycaffe'ine
CgH»N4Oj.OH
CsH.AN,
....
a. 345-
Fischer
A., 215, 268
44, 355
» •••• "™
j>
))
abt. 350-
>j
B., 14, 640
40, 614
Trimethylurie acid
see B. 17, 1786
»
MM
345-
j>
B., 17, 1783
46, 1309
?
C4H3O.CH.N2O3.CMe2
C3H1004N2
d. 145-150
94
Tonnies and Staub
B., 17, 853
46, 1129
Hydrodinitroazobenzene
C8H10N2(N02)2
C8H1004N4
....
220
Lermontoff
B., 5, 234
25, 503
Dinitrodiamidoethoxy ben-
OEt.(NH2)2.(N02)2=1.4 (J),
C8H1005N4
cf. A., 215, 154
245 u. c.
Nietzki
B., 11, 1448
34, 867
zene
a-(3-diisonitrozobutyric anhy-
external anhydride-
C8HI007N4
....
132-133 d.
Ceresole & Kockert
B., 17, 823
46, 1121
dride
Hydroxyethylene aniline- ....
Ph.NH.C2H4.OH
C9HUON
280
Liquid
Demole
B., 6, 1025
27, 77
Dimethamidophenol
OH.NMe2=1.2
»
....
45
Griess
B., 13, 249
38, 637
Ethamidophenol
OH.NHEt=1.2
1)
....
167-5
Foster
J. p. [2], 21, 356
38, 464
Amidophenetoil
OEt.NH2=1.2
)J
228
Liquid
Groll
J. p. [2], 14, 207
29, 247
>j •"•- ••••
J> »i
)J
329 (756)
L. —21
Foster
J. p. [2], 21, 344
38, 464
,, ....
=1.3
J)
180-205(100)
Liquid
Wagner
J. p. [2], 32, 70
48, 1212
>•» ••"
•i =1-4
)I
253
...»
Hallock
B., 14, 37
40, 595
Hydroxy ethey lene amidoben-
NH2.(C2H<.OH)=1.2
»'
....
89-90
Weddige
J. p. [2], 24, 241
40, 1138
zene
Anisamine „
OMe.(CH,.NHs)=1.4
»»
cf. A., 117, 240
a. 100
Cannizzaro
C. R, 50, 1100
i., 297
Methylanisidine-
OMe.NHMe=1.2
J»
218-220,
....
Miilhauser
A., 207, 247
42, 302
Methoxytoluidine
Me.OMe.NH2=1.2.3
n
223
Liquid
Hofmann & Miller
B., 14, 570
40, 593
„ ....
=1.4.5
>i
....
36-38
»
B., 14, 573
IT
»
=1.4.6
>j
cf.A.,215,.89
47
Knecht
B., 15, 1072
42, 969
n
=1.2.5
JS
....
52-53
Hofmann & Miller
B., 14, 571
40, 593
Amidoxylenol
Me2.OH.NHs=1.3.(?)2
)»
....
161
Pfaff
B., 16, 1137
44, 918
» ....
=1.4.2.5
»
d. 180-
scales
Goldschmidt and
B., 18, 570
48, 775
Schmid
Methylpseudolutidostyril ....
»
CMe.CH.CMe.NMe.eO.GH
i i
w
n
292.
292
abt. 70-
90-92
Hantzsch
j)
B., 17, 1028
B., 17, 2906, 2907
46, 1045
48, 398
>'
Acetyldimethylpyrroline ....
C4H2Me2 1 NAc
»
L. —20
Weidel & Ciamician
B., 13, 79
38, 404
Anhydrodiacety lacetamidil. . .
CMe : N.CMe : CH.CO.NH.
i
C8HnON,
....
185
Pinner
B., 17, 174
46, 723
CMe:.N
Methylphenyl semicarbazide
NMePh.NH.CO.NH2
»
....
133
Fischer
A., 190, 164
34, 311
Hydroxyethylene amido-
NH2.(O.C2H4.OH)=1.2
C8H1102N
....
89-90
Wagner
J, p. [2], 28,. 199
46, 436
pheuol
Amidodimethyl quinol
(OMe)2.NH2=1.4.5
))
270 p.d.
74-75
Magatti
B., 14, 71
40, 595
11 11
JJ
»
80
»
G. I. [1881], 353
42, 175
n 11
»
;»
81
Miilhauser
A., 207, 254
42, 303
» »
»
)i
....
81-82
Bassler
B., 17, 2120
48, 1329
436
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
I
C4H3O.C(NH2).CMe2.O
C8HU02N
215-220 d.
Liquid
Tonnies and Staub
B., 17, 857
46, ] 130
i " i
Nitrodiamidoxylene
Me2,(NH2)2.N02=1.3.(?)3
C8Hn02N3
....
212-213
Fittig and Velguth
A., 148, 7
„
„ „
„
....
215
Bussenius and
A., 113, 160
iv., 382
Eisenstuck
Arnidocaffe'ine
C9H,NA.NHS
C8Hn02N6
....
a. 360
Fischer
A., 215, 265
44, 355
Ethylic methylacetocyanace-
CMeAc(CN).COOEt
C^.AN
90-95(15-20)
Liquid
Held
C. R., 98, 522
46, 728
tate
Triacetylforamidil
....
C8Hn03Ns
>.**
224
Pinner
B., 17, 172
46, 723
Diethylic cyanoraalonate ....
CN.CH(COOEt)2
C8Hn04N
120-130 (25)
Liquid
Haller
C. R., 95, 142
42, 1189
Urethaue furfurol
C4H3O.CH(NH.COOEt)2
N
169
Bischoff
B., 7, 1081
28, 146
Diethylic oxaloxamate
NH(CO.COOEt)2
C8HnO6N
67
Salomon
J. p. [2], 9, 295
27, 791
?
C8HnN2.OH
C8H12ON2
....
150
Riess and Meyer
J. p. [2], 31, 112
48, 646
Diallyloxamide
(CH2:CH.CH2.NHCO)2
C8H1202N2
274 d.
154
Wallach & Strieker
B., 13, 513
38, 547
Amidopheuylurethane
NH2.(NH.COOEt)=1.2
„
....
86
Rudolph
B., 12, 1295
Diethylbarbituric acid
NH.CO.NH.CO.CEt-CO
i i
C8H1203N2
182
Conrad & Guthzeit
B., 15, 2849
44, 314
Phenylguanylguanidine ni-
NH:C(NHPh).NH.C(NH2)
C8H1203N6
+HNO3
208-209
Bamberger
B., 13, 1583
40, 44
trate
:NH
Nitrodehydropiperylurethane
C5H,(NO2)N.COOEt
C8H1204N2
51-5
Schotten
B., 16, 644
44, 814
Trimethylic cyanurate difor-
C AN3Me3 + NH(CHO)2
C8H1205N4
168 (24)
163
Gautier
C. R., 67, 804
vi., 529
mamide
Ethylic nitrotartrate
CO2Et.(CH.O.NO.,)2.C02Et
C8H12010N2
....
45-46
Henry
Z. C.,13,692;B.,
3,533
?
basic
C8HI3ON
175-180
Liquid
Canzoneri and Spica
G. I., 14, 341
48, 747
From aldolammonia ....
„
M
160 (20)
Wurtz
C. R., 88, 940
36, 704
Ethylic acetyl-/S-imidobutyr-
NAcICMe.CH2.COOEt
C8H1302N
225
64-65
Canzoneri and Spica
G. L, 14, 491
48, 750
ate
Mesityloxidehydrocyanicacid
....
C8H1303N
....
171
Simpson
A., 148, 354
a » »
„
....
174
Pinner
B., 14, 1074
40, 796
Ethylic acetamido-a-crotoiiate
NHAc.CMe : CH.COOEt
,,
231
63
Collie
A, 226, 294
48, 374
Acetylacecaffe'ine
....
C3H1303N3
106-107
Fischer
A., 215, 299
44, 356
Diethylic amidomaleate
CO2Et.CH : C(NH2).CO2Et
C8H1304N
....
100
Claus and Voeller
B., 14, 151
40, 254
Tropic acid
CTT ~VT/ f^/"W~\TT \
c-LJ.ii.LN \\~s\J\Jfija
,.
220 d.
Merling
A., 216, 351
» >i
„
„
....
d. 220-240
Merling
B., 15, 292
Diethylfumarainide
C2H2 : (CO.NHEt),
C8H1402N2
•Ml
182-183
Wallach and
B., 14, 170
40, 285
Kamenski
Mesitylamide....
222
Pinner
B., 15, 577
42, 941
Hydroxycaprylonitril
C6H13.CH(OH).CN
C8H"aON
I
L. —16
Erlenmeyer and
A., 177, 106
28, 1011
Sigel
Vinyl diacetonamine
....
H
199-200
Liquid
Heintz
A., 189, 214; 178,
32, 878
326; 191, 122
Diallyethylalkamiue
cf. B. 14, 1879
„
197
Liquid
Ladenburg
C. R., 93, 338
40, 1158
Pelletierine ....
....
„
180
Liquid
Tanret
C. R., 86, 1270
34,740
....
„
195
Liquid
„
C. R., 90, 697;
38, 481
"
B. S., 32, 464,
466; 36, 256
Pseudopelletierine
cf. C9H15ON
„
246
Liquid
„
„
„
Oxyconicei'ne ....
„
210-220
Liquid
Hofmann
B., 18, 125
48, 563
Metatropine ....
....
„
238
L. —30
Ladenburg
A., 217, 127
...
,,
237-239
L. —30
Ladenburg
B., 14, 229
40, 263
Tropiue
....
„
229
«...
„
B., 13, 1552
40,57
....
u
229
....
„
A., 206, 294
40, 447
'
9-)Q
B., 13, 608
38, 674
„
....
"
IMnP
60-61
Pesci
G. I, 1881, 538
42, 740
....
,,
«...
61-2
Kraut
A., 133, 87
v., 896
"
„
62
Ladenburg & Roth
B., 17, 151
46, 761
"
„
....
n
63
Schmidt
B., 13, 372
38, 482
Pseudotropine
....
n
241-243
....
Ladenburg
B., 13, 1552
40,57
>-
....
„
241-243
106
Ladeuburg & Roth
A., 17, 151
46, 761
,, ....
....
241
Ladenburg
B., 206, 304
40, 447
Ethylic imidoethylidiuethyl-
NH : CH.CH^CHEt.COOEt
C8H,AN
59-5
Geuther
J. [1863], 324;
vi., 601
acetate
Z.C. [1871], 247
COMPOUNDS CONTAINING FOUR ELEMENTS.
487
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Diisobutyramide
NH(CO.CHMe2)2
C8H1502N
....
174
Hofmann
B., 15, 982
42, 950
Piperyl urethane
C5H10N.COOEt
„
211
Liquid
Schotten
B., 15, 425
42, 983
Triethoxyacetonitril
(EtO)3C.CN
C3H1603N
159-161-5
Bauer
A., 229, 163
48, 1121
Ethylic diethyloxamate
CO(NEt2).COOEt
„
250-254
cf. B., 3, 776
Hofmann
Z. C. [2], 7, 38
24, 263
» »
„
„
253-254
....
Wallach
B., 14, 741
40, 717
,, )!
„
„
260
Liquid
Hofmann
C. R, 52, 902
iv., 281
Diethylic oxytetramate
C4H3O(OEt)2.NHs
»
....
68-69
Demarcay
B. S. [2], 33, 575
40, 255
Suberamic acid
....
„
....
170
Z. C. [1865], 300
Base fr. crotonaldehyde
....
CSH16ON2
200 (i. v.)
....
Combes
C. R., 96, 1862
44, 1079
150-160
AV"ertheim
A., 123 157; 130
"
269
Triethyloxamide
NHEt.CO.CO.NEt2
C9H160S02
257-259
Liquid
Wallach
B., 14, 741
40, 718
Dipropyloxamide
C2O2 : N2H2Pra
„
....
110
Duvillier & Bensine
C. R, 89, 48
36, 912
„
„
„
....
162
Wallach & Schulze
B., 13, 516 ; 14,
40, 572
422
Dimethyladipamide
NHMe.CO.(CH,)4.CO.NHMe
B
....
151-153
Henry
C. R, 100, 943
48, 887
Isopropyl isobutyryl carba-
NHPw3.CO.NH.CHMe2
„
....
86
Hofmann
B., 15, 756
42, 1053
mide
Propylbutyryl carbamide ....
NHPr«.CO.NH.CO.CH2Et
n
....
99
„
B., 15, 757
Diethylic diamidosucciuate ....
COOEt.(CH.NH2)2.COOEt
C8H1604N2
122 «. c.
Glaus & Helpensteii
B., 14, 624
40, 578
„ i,
„
„
122
Glaus
B., 15, 1849
Ethylidene urethane
CH3.CH(NH.COOEt)2
„
....
125 u. c.
Schmid
J. p. [2], 24, 124
» j>
„
„
182 d.
126
Nencki
B., 7, 160
27, 458
C.H16.CO.NHj
C8H, ON
94
Hofmann
B., 15, 983
42 950
a. 200 d.
110
Felletar
Zf! F21 4 fifi1!
vi., 395
. vy. [_^J, ^, \J\JiJ
Capronimido-ether
C5Hn.C(OEt) : NH
it
168
Liquid
Pinner
B., 17, 178
46, 723
Vinyldiacetonalkamine
CMe2.CH2.CH(OH).CH2Me.
„
....
123
Fischer
B., 17, 1794
46, 1291
NH
j
Piperpropylalkine
C6H10 1 N.C3H6.OH
„
194
Liquid
Ladenburg
B., 14, 1880, 2406
„ ....
„
„
194
....
Laun
B., 17, 680
46, 1054
Conhydrin
C8H160 : NH
„
b. 100 (?)
....
Wertheim
W. A., 22, 113
ii., 1
ae.V'i /79M
1 9fi
WA 4fi 9QQ
•vi d&R
»
11
— '>•> U ^ t Zi\JJ
l£/\J
»
. . >., t'>, _.'.'
VA. j *±OO
99R
19(1
TT f
Bl PI 9^1 r\
tMBnt
±4\J
-tioimann
., ' •'. —•>!•>
„ (cf. J. [1863], 435)
„
„
224-5 (719-8)
120-6
Wertheim
A., 100, 328
Ethylic diethamidoacetate ....
NEt2.CH2.COOEt
C8H1702N
177 c.
Liquid — 10
Kraut
A., 182, 176
30, 625
Ethylic isoamylcarbamate ....
CjHu.NH.COOEt
„
218
Liquid
Custer
B., 12, 1329
Triethylglycocine .... (cf. J.
NEt3.CHa.CO.O
H
210-230 d.
A., 182, 175
Briihl
A., 177, 215
1 1
[1862], 333)
Octylic nitrite
CH3.(CH.j)7.O.NO
„
175-177
Liquid
Eichler
B., 12, 1887
38, 229
Nitrooctane ....
C H NO
OAK 91 n
T « ' »
B19 1Hft1
V**ii7»-wv'>
D
j&u«J — — 1 _
JjiquiQ
1)
. j 1 — j 1OOO
|)
Hydroxycaprylamide
C6H13.CH(OH).CO.NH2
„
....
150
Erlenmeyer & Sigel
B., 7, 1108
28, 144
„
„
„
....
150
„
A., 177, 108
28, 1012
Diethamido-a-butyric acid
CH2Me.CH(NEt,,).COOH
„
....
135
Duvillier
C. R, 100, 860
48, 750
Piperpropylglycoline
HO.CH2.CH(OH).CH2.N :
•
223-227(195)
Cryst.
Roth
B., 15, 1150
42, 1195
Nitrosodibutylamine
N(C4H,)2.NO
C8H19ON2
234-237 c.
Meyer and Forster
B., 10, 132
Nitrosodiisobutylamine
„
„
213-216
b. 0
Ladenburg
B., 12, 949
36, 704
a-ethylene diethyldicarba-
....
C8H19OjN4
of.A.,119,356
124 p. d.
Volhard
P. R, 11, 268
ii., 5G5
mide
ft- !) »
....
„
J)
201
H
„
„
Guanoline
....
C8H1804N6
....
114-115
Nencki
B., 7, 1590
28, 755
„ +H2O
....
„
*..i
100
!,
„
„
Hydroxypropylamylamine ....
CsHn.NH.C3H,.OH
C9H19ON
200
0+
Lieberraann & Paal
B., 16, 533
44, 910
Trinitro-umbelliferone
HO.C6(NO2)3.CH : CH.CO.O
C9H309N,
....
216
Posen
B., 14, 2747
42, 839
i i
Quinoline quinone
N ; O,= l ; 1.4
C9H602N
....
d. 110-120
Fischer and Renouf
B., 17, 1644
46, 1371
Quinisatin ....
v. B. 16 2221
P XT n xr
OKK G)Cf)
T> B TT 11
Ri£ 9991
48 7Q
L/9±l6U3iN
MM
ZOO— ZOU
.Kaeyer oc xlomoiKa
, H>, JU^IiUi
*VJ, 1 ij
Nitrophenylpropiolic acid ...
NO2.(C:C.COOH)=1.2
C9HS04N
....
155-156 d.
Baeyer
B., 13, 2258
40, 275
11 »
.. ,.
„
....
157 d.
Muller
A., 212, 142
42,844
» » -
= 1.4
„
....
181 d.
Miiller
A., 212, 139
42, 843
» -
»
.,
....
198 d.
Drewsen
A., 212, 155
42, 846
488
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Nitrocoumarin
....
C9H5O4N
....
170
Bleibtreu
A., 59, 190
"., 94
/3-dinitroquinoline ....
....
C9HS04N3
....
133-134 u. c
Glaus and Kramer
B., 18, 1248
48, 908
»- „ ... ...
N ; (NCg^a, ; a,/3s
»>
....
149-150
Coste
B., 15, 561
42, 979
°- ..
...*
»
182-183 u. c
Glaus and Kramer
B., 18, 1246
48, 908
Pyridiue tetracarboxyJic acid
N.(COOH)4=1.2.3.4.6
C9H608N
....
227 d.
Fischer and Ta'uber
B., 17, 2927
48, 400
» » »
ii »
.»
+2H30
187
»
»
»
» » »
>» »?
1)
»
1884-
Michael
A., 225, 142;
48, 62
B., 17, 491
m-Toluylene isocyanate
C,H3Me(N:CO),
C9H602N2
....
95
Lussy
B., 8, 291
28, 770
Nitroquinoline
N.N02=a,/32 !
»
....
72
Glaus and Kramer
B., 18, 1246
48, 908
M .... ...
i) — °i ; °i
I)
88'5 c.
Schultz
B., 17, 478
„ ....
)> »
J)
....
88 ; sf, 68
Konigs
B., 12, 450
» ....
J> •»
•)>
....
88-89
»
B., 14, 99
„
.J» -H
1J
89
Coste
B., 16, 674
,,
„ =a, ; fa or Oj
»
....
120-123
Coste and Bodewig
B., 17, 928
46, 1197
M ....
i) =ai ; ft
M
149 u. c.
Glaus and Kramer
B., 18, 1250
48, 908
,, .... ....
» i»
11
....
149-150
•Coste
B., 16, 669
44, 811
V
„ =a, ; «2 or /3,
)J
185-186
Coste and Bodewig
B., 17, 928
46, 1197
Phenylparabanic acid
CO.NPh.CO.NH.CO
i i
C9H608N2
..„
208
Stojentin
J. p., 32, 1
48, 1196
Phthalureiide
C6H4 : (CO.NH)2 ; CO=1.2
d. 185-190
Piutti
A., 214, 23
n
Hydroxycinuoline carboxylic
N : N.C6H4.C(OH) : C.COOH
»
260-265
Richter
B., 16, 680
44, 1105
• j
1 1
acid
=1.2
/3-nitro-carbostyril
....
)»
260
Friedlander and
A., 229, 233
48, 1139
Lazarus
y- i. .•
....
»j
iftt
280
j)
»
i)
°- ,) ,1
....
jj
....
nf. 320
»j
91
»
Nitroso-y-hydroxycarbostyril
C6H4.CO.C(N.OH)C(OH):N
»>
....
208 d.
Baeyer & Homolka
B., 16, 2217
46, 78
=1.2
>' »» »
»» )>
»)
„..
208
»
B., 17, 985
46, 1029
Nitrohydroxyquinoline
N.; OH=n, ; &
?5
....
139-14&
Skraup
M. C., 3, 552
44, 94
»» ....
»» -»
))
....
140-141
»
M. C., 4, 695
46,87
» •»••
,, =5«i ; ^i or as
»)
255 n. c.; p. d.
»
M. C., 3, 564
44, 94
(0 ....
....
»)
....
m.a. 300
Weidel & Hazura
M. C., 3, 774
Nitropolyporic acid
....
C9H604N (?)
230
Stahlschmidt
A., 195, 365
36, 383
p-Nitrophenyl nitre-acrylic
....
C9H606NS
cf. B., 16, 850
196-197
Friedlander and
B., 14, 2577;
42, 402
acid
Mahly
A., 229, 210
Acetoxycyanobenzene
C6H4.CN.OAc=1.4
C9H7ON
265-266
57
Lach
B., 17, 1572
46, 1154
Hydroxyquinoline
N ; OH=a,, ; a,
)>
257-260 (748)
69-70 u. c.
Weidel and Cobenzl
W. A., 82, 986
40, 743
»j
Jl »J
»J
258-2 (752)
73-74
Skraup
M. C., 3, 536
44, 92
n
?» »
•>J
....
75
Wurtz
C. R., 96, 1269
44,923
»i ....
)' )>
»)
258
75
Skraup
B., 15, 893
42, 1111
t»
)) 4»
5»
cf. B., 15, 683
75
Bedall and Fischer
B., 14, 443, 1366
40, 613
M
» »
))
....
75-76
Fischer
B., 15, 1979
44,91
)»
-» >»
5»
....
75-76
»
B., 16, 712
44, 1146
)T ....
» :^ai ; &
)J
....
190
Skraup
B., 15, 893
42, 1111
»» .... ....
-» .»
)?
310-320
191-192
Weidel
M. C., 2, 575
42, 227
It .... ....
»» .»»
n
....
193
Happ
B., 17, 193
46, 758
t» .... ...
»? »
))
a. 360
193
Skraup
M. C., 3, 545
44,913
J*
») »
)»
....
194
»
M. C., 4, 695
46, 87
n
„ =aj ; ^ or a2
•J
224-228
Riemerschmid
B., 16, 722
44, 1147
M .-..
•> »>
»»
....
230
Fischer
B., 15, 1979
44,91
j>
»» »
)>
....
235-238 p. d.
Skraup
M. C., 3, 559
44, 95
M >... ....
)> M
))
238
»
B., 15, 893
42, 1111
„ (carbostyril)
N.OH 5=0,13, ;
JJ
....
196
Tiemann and Op-
B., 13, 2070
40, 171
permann
»' »
)» »J
)J
....
198-199
Friedlander and
B., 14, 1916
42, 201
Ostermeier
» »i
)» )J
)1
....
198-199
Einhorn
B., 17, 2012
46, 1338
Kynurine
....
»>
a. 300 d.
201
Kretscby
M. C., 2, 68
40, 828
+3H20
• •>•
J?
52
»
»
»*
COMPOUNDS CONTAINING FOUR ELEMENTS.
489
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Benzylcyanide carboxylic
(COOH).(CH2.CN)=1.2
C9H7O2N
....
116
Wisliceiius
B., 18, 172
48, 532
acid
Amidophenylpropiolic acid....
NH2.(C;C.COOH)=1.2
»i
cf.B.,16,679
128-130 d.
Baeyer and Bloem
B., 15, 2148
Methylphthalimide
C6H4.COO.C:NMe=1.2
I)
abt. 277
132
Grtebe and Pictet
B., 17, 1174
46, 1019
L 1
Phenylmetliylacetoxinie car-
C6H4.COO.N:CMe=1.2
»
....
157-159
Gabriel
B., 16, 1995
44, 1128
i i
boxyhc anhydride
C6H4.CO,C(OMe) :N=1.2
100-102
Baeyer and CEconi-
B., 15, 2094
44, 201
Ji
midea
11
=1.4
»)
187
Meyer
B., 16, 2266
46, 48
Methylpseudisatin
....
))
134
Fischer and Hess
B., 17, 565
46, 1181
Amidocoumarin
C6H3(NHn).CH:CH.COO
»
168-170
Chiozza & Frapolli
A., 95, 253
ii, 93
i " i
=1.2
Dihydroxyquiuoline (hy-
N.(OH)2=ai.?;?
)»
....
189
Friedlancier and
B., 15, 2684
44, 351
droxycarbostyril)
Weinberg
>i »
» )*
•JJ
....
190-5
Friedlander and
B., 14, 1918
44, 201
Ostermeier
)) !!
„ =1.2.3;
«
....
a. 300
Friedlander and
B., 15, 2681
44, 351
Weinberg
)1 »
„ =1.2.4 ;
»
cf.B.,15,2683
w. m. 320
Baeyer and Bloem
B., 15, 2151
44, 197
Nitrocinnamic aldehyde
N02.(CH:CH.COH)=1.3
C9H7O3N
....
116
Kinkelin
B., 18, 484
48, 791
„ »
=1.2
»
....
127
Baeyer & Drewsen
B., 16, 2207
46, 59
,1 !>
»> »
>»
....
127-137-5
Diehl and Einhoru
B., 18, 2336
>! 11
=1.4
))
....
135
Gohring
B., 18, 372
48, 527
!> »
n ))
n
....
141-14S
Diehl and Einhorn
B., 18, 2337
48, 1222
Indoxylic acid
N.C6H4.C(OH).CH.COOH
M
....
122-123 d.
Baeyer
B., 14, 1743
42, 198
=1.2
Methylisatoic acid
"W
d. 245
Panastovic
J. p. [2], 31, 122
48, 667
?
J»
....
108
Bossing
B., 17, 3002
Nitrobenzenylazoximeme-
NO..(C I N.O.CMe : N)=1.3
i i
C9H703N3
109
Schopf
B., 18, 1067
48, 897
thenyl
Nitrosoindazolacetic acid ....
cryst. fr. ethylic acetate
)1
....
123d.
Fischer and Tafel
A., 227, 303
48, 542
i) »
„ other solvents
J»
....
96
>!
!)
»1
Nitrocinnamic acid
(CH : CH.COOH).N02=1.3
C9H704N
....
196
Stuart
....
47, 157
u »i
» »
I)
cf.B.,11,1782
196-197
Schiff
G. I., 8, 294
36, 157, 321
!> !>
» «
»J
....
196-197
Tiemann and Op-
B., 13, 2060
40, 169
permann
11 11 ••••
=1.2
1)
232
Beilsteinand Kuhl-
A., 163, 129
25, 709
berg
1) 11 ""
,** ->»
»)
....
232
Muller
A., 212, 122
42, 841, 845
11 » **"
»» JJ
)»
237
Tiemann and Op-
B., 13, 2059
40, 169
permann
» »
)J »
»»
....
940.
Baeyer
B., 13, 2257
40,274
„ ' u
M »
V
....
240-5-241-5
Gabriel and Meyer
B., 14, 830
), 1, "••
=1.4
11
....
265
Beilsteinand Kuhl-
Z. C. [2], 7, 489 ;
vii., 300, 348 ;
berg
A., 163, 127
40, 169
11 !> ••••
» »
»
d. a. 270
270
Mitscherlich
A. C. [3], 4, 73
i., 987
,1 11
>» »»
51
....
274 ; 276
Muller
A., 212, 122
42,841, 845
)1 11
)> »
»
....
$86-286
Tiemann and Op-
B., 13, 2059
40, 169
perm ann
»! 11
« »»
M
....
286
Stuart
....
43, 407
>» 11
»» )»
))
....
288
Drewsen
A., 212, 151
43, 408
/3-laetone of nitrophenyllactic
N02. (CH.CH2.CO.O)=1.4
»
.;..
91-9
Easier
B., 16, 3004
46, 604
I 1
acid
/3- )1 1! »
=1.3
»
....
98
Prausnitz
B., 17, 597
46, 1175
o-nitrophenylhydroxyacrylic
....
C9H705N
....
nod.
Baeyer
B., 13, 2262
40, 276
acid
Acetylic nitrobenzoate
COOAc.NO2=1.3
i)
....
130-132
Liebermann
B., 10, 863
32, 617
Nitrobenzoylacetic acid
NO2.(CO.CH2.COOH)=1.4
!»
....
135 d.
Perkin & Bellenot
B., 17, 326
46, 1024
Carbostyrilic acid
CO2H.(NH.CO.CO2H)=1.2
11
+H20
WOd.
FriedLander and
B., 15, 332
Ostermeier
3 R
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Carbostyrilic acid
CO2H.(NH.CO.CO2H)=1.2
Q,H706N
....
200 d.
Hofmann & Konigs
B., 16, 734
Kynuric acid „»,
....
55
+H20
187
Kretschy
M. C., 4, 157
Nitrobenzalmalonic acid
NO,[.CH : C(COOH)2] = 1.4
C9H706N
227
Stuart
....
43, 407
n-Nitro-uvitic acid .... ' .„;
(COOH)2.Me.NO2=1.3.5.2
)»
cf.A.,189,171
226-227
Bottinger
B., 9, 806
30, 414
ft- » »
=1.3.5.4
>J
cf.A.,189.180
249-250
»
B., 9, 807
>»
Picolinetricarboxylic acid ...
N.Me.(COOH)3=1.4.2.3.6
JJ
....
230-232 d.
Besthorn & Fischer
B., 16, 71
» »
» ;>
))
d.236
232
Fischer and Timber
B. 17, 2926
48,400
>j »
j> "
)»
238 d.
Michael
A., 225, 121
48, 62
Acetylchrysanissic acid
COOH.NHAc-CNO,),
C9H707N3
270 d.
Salkowski
B., 10, 1696
=1.4.3.5
Benzenylazoximethenyl
N I CPh.N : CMe.O
C9H3ON2
41
Tiemann & Ki iiger
R, 17, 1697
46, 1326
Ethenylazoximebenzenyl ....
N : CMe.N : CPh.O
))
....
57
Nordmaim
B., 17, 2754
48, 239
i i
Anhydro-acetylamidobenz-
»
228
Weddige
J. p. [2], 31, 124
48, 661
amide
Carbonyl pyrroline
CO(NC4H4)2
)J
abt. 238
62-63
Ciamician and
B., 18, 415
48, 809
Magnaghi
Pyrroyl pyrroline
»)
»
....
62-63
»j
B., 18, 1838
48, 1143
Dipyrrylketone (pyrrone) ....
CO(C4H3.NH)2
»
....
160
)»
B., 18, 419
48, 809
)> »
)5
1»
160
i»
B., 18, 1830
Hydroxytoluquinoxaliue
C6H3Me.N:CH.C(OH):N
)J
241-242; 247
Hinsberg
B., 18, 1232
48, 910
i i
Hydrazine cinnamic anhy-
C6H4.CH : CH.CO.N(NH2)
»
....
127
Fischer
B., 14, 480
40, 598
dride
i i
=1.2
Amidocarbostyril
N.OH.NHa -,=0^.0^ ;
»
....
nf. 320
Friedlander and
A., 229, 233
48, 1139
Lazarus
?
CHO.NH.NPh.C(NH).CN
C9H8ON4
....
192-5-193-5
Bladin
B., 18, 1549
48, 980
Phenylhydantoin
CO.NH.CO.CH2.NMe
09HAN2
191-192
Schwebel
B., 10, 2048.
84, 301
1 1
Benzylidene oxamide
Ph.CH.NH.CO.CO.NH
)J
a. 200 d.
Medicus
A., 157, 51
24, 152
i i
Cyanamidophenylacetic acid
(NH.CN).(CH2.COOH)=1.4
)»
....
134
Traube
B., 15, 2121
44, 193
p-Methylnitroso-oxindole ....
....
»I
....
225-226
Meyer
B., 16, 2268
46,48
Indazolacetic acid
NH.N.C6H4C.CH2.C03H
)»
168-170 d.
Fischer and Tafel
A., 227, 303
48, 542
'- ] i
=1.2
Anhydroamidooxalyltoluidic
« i
C6H3Me.NH.CO.C(OH) : N
)3
....
a. 300 s. d.
Hinsberg
B., 15, 2692
44, 323
acid
Dihydroxytoluquinoxaline ....
C6H3Me:[N:C(OH)]2:
»»
nf. 295
Bladin
B , 18, 671
48, 785
o-nitrophenyl 0-alanine lac-
NO2.C6H4.CH.CH2.CO.NH.
C9H803N3
impure
80
Einhorn
B., 16, 2649
46, 305
tam
1 1
Ni tro-cinnamide
NOj-CCH : CH.CO.NH2)=1.4
)J
155-156
Cahours
A. C. [3], 27, 452
i., 989
Ethoxynitrobenzonitril
CN.NO2.OEt=1.2.6
)»
137
Bruyn
K. T., 2, 205
48, 656
Phenylhydrazinemesoxalic
N2HPh : C(COOH)2
C9H804N2
158-164
Elbers
A., 227, 340
48, 535
acid
>» »
»
))
163-164
Fischer
B., 17, 578
46, 1151
Nitrophenylnitropropylene
NO2.(CH I CMe.NO2)=1.2
»j
76
Priebs
A., 225, 319
48, 162
»
=1.4
j)
...t
114
»
)>
»
Phthaluric acid
»
....
d.a. 150
Piutti
A., 214, 20
Nitroamidocinnamic acid ....
(CH : CH.COOH).N02.NH2
Jj
224-5
Herzberg
C. C. [1884], 35
48, 662
=1.3.4
» i)
!' »
»)
224-5
Gabriel and Herz-
B., 16, 2042
44, 1123
berg
» i)
=1.1.2
I)
....
240
Friedlander and
A., 229, 233
48, 1139
Lazarus
!
» »
=1.1.2
j»
254
»»
D
i
))
310 p.d.
111
Bruyn
E. T., 2, 205
48, 657
Nitrohippuric acid
NO,. (CO.NH.CH2.COjH)
C9H805N2
129
Jaffe
B., 7, 1678
28, 478
=1.4
„ „ •>•• »••.
=1.3
)»
-...
abt. 150
Bertagnini
A., 78, 103
Hi., 161
M jj
» 1!
»
162
Conrad
J. p. [2], 15, 254
32, 485
Allyloxydinitrobenzene
(O.C3H5)(N02)2=1.2.4
J»
46-47
Willgerodt
B., 12, 765
36, 717
COMPOUNDS CONTAINING FOUR ELEMENTS.
491
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitro-oxalyltoluidic acid ....
Me.NO3.(NH.CO.CO2H)
C9H805N2
....
d. w. m. 150
Hinsberg
B., 15, 2691
=1.3.4
Ethylic dinitrobenzoate
COOEt.(NO2)2=1.3.5
C9H806N,,
....
90
Staedel
B., 14, 902
40, 725
J! »
)> J)
J)
91
Beilstein and Kur-
A., 202, 223 ; B.,
38,471
batow
13, 355
JJ »
JJ ))
J)
94
Gattermann
B., 18, 1485
Dinitrohydrociimamic acid
(NO2)3.(CH : CH.CO2H)
JJ
cf.B.,13,1680
126-5
Gabriel and Zim-
B., 12, 600
36, 640
' =1.2.4
mermann
Methylic dinitromethylsali-
CO2Me.OMe.(NO2)2=1.2.(?)2
C9H807N2
....
69
Salkowski
A., 173, 47
28,71
cylate
Ethylic dinitrosalicylate
C02Et.OH.(N02)2=1.2.(?)2
JJ
....
98-99
jj
A., 173, 49
j>
„ n
„ =1.2.3.5
)J
....
99-100
Hiibner
B., 10, 1701
34, 151
Ethylic dinitrohydroxyben-
„ =1.4.3.5
J)
....
84
Salkowski
B., 4, 225
24, 556
zoate
,! n
j» )j
))
....
87
»
B., 4, 653
24, 920
i) ii
» >j
)J
87
j»
A., 163, 44
25, 716
jj »
=1.4.(?)a
JJ
b. 100
Earth
J. p., 100, 366
vi., 901
Dhiitrohydro-p-coumaric
(CH2.CH2.C02H)2.OH.(N02)2
JJ
....
137-5
Stehr
A., 225, 57
46, 1350
acid
=1.4.3.5
Dinitrohydrocoumaric acid
=1.2.(?)2
CCH5.CH : CH.CO.NH2
JJ
C9H9ON
155
141-5
Zwenger
Rossum
As., 5, 118
Z. C. fal 2, 362
vi., 716
vi., 471
Phenyllactimide
Ph.CH2.CH.NH.CO(?)
jj
146-147
Posen
L JJ y
A., 200, 97
38, 322
)j .... ....
Ph.CH.NH.CO.CH2(?)
jj
....
280
Schulze & Barbieri
J. p. [2], 27, 337
44, 1122
,,
))
j»
290
Erlenmeyer & Lipp
A., 219, 179
44, 993
Phenyl a-hydroxypropioni-
Ph.CH2.CH(OH).CN
j)
....
57
jj
jj
44, 992
tril
Hydrocarbostyril
C6H,.N : C(OH).CH,.CH2
i i
jj
160
Buchanan & Glaser
Z. C. [2], 5, 194
vi., 715
=1.2
JJ .... ....
55 JJ
j;
160
Gabriel and Zim-
B., 13, 1682
40, 274
mermann
,,
JJ JJ
5)
163
Friedlander and
B., 15, 1424
Atroxindole .. ....
C6H4.CHMe.CO.NH=1.2
sb. 100
119
Weinberg
Trinius
A., 227, 262
48, 529
Xylylisocyanate
Me2.(N ; CO)=?
Jj
JJ
abt, 200
Liquid
Hofmann
P. E., 19, 108 ;
S4, 139 ; vii.,
B., 3, 657
407
E thenylamidocresol
C6H3Me.O.CMe : N=1.4.5
)J
218-219 u.c.
Liquid
Nolting and Kohn
B., 17, 361
46, 901
(748)
Fr. Methylphthalimide
M
300
120
Grsebe and Pictet
B., 17, 1174
46, 1019
1 (cf. B., 18, 669)
C7H6.NH.C(NH).C(OH) ; N
C9H9ON3
nf. 290
Bladin
B. S., 42, 104
48, 257, 785
1
JJ
JJ
d. 230-240
nf. 290
jj
B., 18, 670
48, 785
Phenylnitropropylene
Ph.CH : CMe.NO2
C9H902N
....
64
Priebs
B., 16, 2591 ; A.,
46, 313; 48,
225, 319
161
a-Amidocinnamic acid
Ph.CH : C(NH2).COOH
jj
d. 240-250
Plochl
B., 17, 1621
46, 1349
Benzimidoacetate
C6H5.C( :NH).OAc
jj
....
116
Pinner and Klein
B., 11, 9
34, 492
Anilido-pyruvic acid
C6H5.N : CMe.COOH
„
....
122 d.
Bottinger
A., 188, 336
34, 33
„ ,, ....
J)
JJ
122
jj
B., 10, 818
32, 596
Cinnamhydroxamic acid
Ph.CH I CH.CO.NH.OH
JJ
110
Eostoski
A., 178, 214
29, 273
Amidociunamic acid
(C2H2.COOH).NH2=1.2
JJ
....
158-159 d.
Tiemaun and Op-
B., 13, 2061
40, 169
permann
„ „ ....
=1.4
))
....
175-176 d.
jj
B., 13, 2066
40, 170
„ „ ....
=1.3
JJ
....
180-181
jj
B., 13, 2064
JJ
Acetamidobenzaldehyde
COH.NHAc=1.2
JJ
....
70-71
Friedlander and
B., 17, 457
46, 1020
Gohring
„
JJ JJ
JJ
....
70-71
Friedlander
B., 15, 2575
44, 332
,, ....
=1.4
11
....
154-5-155
Gabriel and Herz-
B., 16, 2004
44, 1104
berg
Ethoxycarbanil
C6H4.OEt.CON=1.4
JJ
....
219
Kohler
J. p. [2], 29, 257
46, 1159
Methoxymandelic nitril
OMe.[CH(OH).CN]=1.2
JJ
....
71
Voswinkel
B., 15, 2025
44, 190
O T> O
492
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Wa tts' Diet.
& J. Ch. Soc.
Methoxymandelic nitril
OMe.[CH(OH).CN]=1.4
C9H9O2N
....
63
Tieraann and
B., 14, 1976
Kohler
Hydroxydihydro-carbosty ril
C6H4.CH(OH).CH2.C(OH).N
1 1
)»-
....
149
Einhorn
B., 17, 2011, 2013
46, 1338
=1.2
ii
»
»
+ 2H2Q
95-97
11
»
n
»
C6H4.CH2.CH(OH).CO.NH
H
....
197-198
Erlenmeyer and
A., 219, 179
44, 993
i >
=1.4
Lipp
7
310
118
Bruyn
R. T., 2, 205
48, 657
i
124
Nemirowsky
J. p. [2], 31, 173
48, 741
Methylic iaonitrosophenyl-
Ph.C( : NOH).COOMe
)l
C9H-9O3N
138-139
Miiller
B., 16, 2987
46, 584
acetate
_
Benzylic oxamate
NH2.CO.COO.CH2Ph
)I
....
134-135
Wallach and
B., 13, 507
38, 557
Liebmann
Hippurie acid
NHBz.CH2.COOH
)>
240
A., 88, 133
Gossmann
A., 100, 69
iii., 157
,i ii
»1
IJ
....
186-5
Curtius
J. p. [2], 24, 239
40, 1144
!> »
I)
»
187-5
Conrad
J. p. [2], 15, 246
34,674
,, »
»»
»
....
187-5
Baum
Z. P. C., 9, 465
48, 982
,i »
»
J»
188-5
Campani
G. I., 8, 57
34, 674
Malonanilic acid
Ph.NELCO.CHa.OOOH
»
....
133d.
Freund
B., 17, 136
46, 729
11 11
»)
J)
132- d.
Kugheimer
B., 17, 235
)>
11 II
)J
»
....
132
Seifert
B., 18, 1360
Nitrophenylethylketone ....
C6H4(,NO2>.CO.Bt=?
»
Liquid
Barry
B., 6, 1007
27, 74
11
=?
)J
....
100
Morley and Green
....
47, 138
j)
=?
))
....
100
Barry
B., 6, 1007
27, 74
Tolyloxamic acid
Me.(NH.CO.COOH)=1.4
J)
168-170
Klinger
A., 184, 285
31, 712
Acetamidobenzoic acid
COOH.NHAc=1.2
)>
....
179
Friedlander and
B., 15, 2108
Henriques
„ ii
» n
)J
....
170-180
Bedson and King
....
37, 754
11 »
M »:
»
....
179-180
Jackson
B., 14, 885
40, 735
„ 11
U ».
5)
....
184 ; 185
Dobner and Miiller
B., 15, 3077, 3078
11 »
=1.3
)»
begins 260
220-230
Forater
A., 117,165
13,235;iv.,291
„ ii
)» )Ji
»
....
238-240
Aschau
B., 17, 429
i) »
=1.4
*>-
....
250 p. d.
Hofmann
B., 9, 1302
31,90
Nitrosoacetoxytoluene
Me.OAc.NO=1.3.?
)»
....
92
Wurster and Eiedel
B., 12, 1799
38, 109
Quiiiolinic acid
C6H4.NH2.(CH3.CO.COOH)
)*
....
143
Dewar
P. R., 30,. 164
40, 1043
Leucolinic acid
»
)J
163
11
11
»J
Acid fr. lepidine
»)
179-180
Drewsen
B., 16, 1955
44, 1149
Nitrophenylazoacetone
NO2.(N2.CH2.COMe)=1.2
C9H90JN3
123-124
Bamberger
B., 17, 2418
48, 157
Nitro-nitrosotetrahydro-
C9H9N(NO)(N02)
n
....
137-138
Hoffmann and
B., 16, 730
44, 1143
quinoline
Koniga
Methylic nitrophenyl acetate
NO2.(CH2.COOMe)=1.4
C9H904N
....
54
Maxwell
B., 12, 1765
38, 120
11 » »
11 n
»
....
54-65
Bedaon
....
37,91
Nitrobenzylic acetate
II »!
»
78
Beilatein and Kuhl-
A., 147, 341 ;
v., 336
berg
Z. C. [2], 3, 467
11 ii
»r r>
1)
85
Grimaux
B. S. [2], 8, 433
vi., 285
Nitrohydrocinnamic acid ....
(CH2.CH2.CO2H).NO2=1.2
»
113
Gabriel and Zim-
B., 13, 1681
40, 274
mermann
„ 11
ii 11
»I
....
113
Gabriel and Steu-
B., 15, 847
42, 1073
demann
i, 11
=1.3
»
....
117-118
n
B., 15, 846
11
ii 11
=1.4
U
163-164
ii
B., 15, 843
11
i) 11
ii 11
»
....
163-164
Beilsteiuaud Kuhl-
Z. C. [2], 7, 487
vii., 348; 25,
berg
300
11 11
II >!
JJ
....
163-164
11
A., 163, 132
vi., 961
Nitrohydratropic acid
(CHMe.CO2H).N02= 1 .4
»
....
87
Triuius
A., 227, 262
48, 529
>i »
=1.2
»5
....
110
11
ii
)J
Ethylic nitrobenzoate
COOEt.N02=1.2
))
30
Beilatein and Kuhl-
A., 163, 137 ;
vii., 165 ; 26,
berg
Z. C., 7, 616
711
11 11
= ?
)J
mixture
37
Fittica
B., 10, 483
32, 483
>i "
„ =?
))
ii
37-38
11
J. p. [2], 13, 184
36, 151
n 11
= ?
» ,
11
38-39
11
ii
36, 152
COMPOUNDS CONTAINING FOUR ELEMENTS.
493
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Ethylic nitrobeuzoate
COOEt.N02=13
C9H904N
....
40-41
Salkowski
B., 5, 724
vil., 947 ; 25,
1024
j) j>
)» »
»
cf. B., 10, 482
41
Fittica
J. p. [2], 13, 184
36, 152, 153
» " ""
» »
1)
298
42
Chancel
J., 2, 327
i., 556
)» "
» ))
J>
....
43
Schiaparelli and
G. I., 13, 257
46, 174
Abelli
•,•) »
)> >»
I>
296
47
Kichter
E. K. T., 220-
„ ;j- [is"],
=H4
)>
57.
Wilbrand and
A., 128, 262
iv., 61
736)
Beilstein
„ 11
11 11
n
....
57'5
Staedel
A., 217, 211, 212
Ethylic nitrosophenolcar-
C6H4(NO).(O.C02Et)= ? .
»
....
109
Walker
B., 17, 400
46, 1003
boxylate
Nitrophenyllactic aldehyde
NO,,[CH(OH).CH,,COH]
j)
....
d. 100
Gohring
B., 18, 720
48, 792
=1.3
Salicyluric acid
HO.C^O.O.CyH.O.NHj
»
....
160
Bertagnini
A., 97, 251
v.,172
-j
p-hydroxybenzuric acid
jj
....
228 d.
....
Z. P. C., 7, 29
Methylene dioxyphenylamid-
CH2:02:C6H3.CH(NHS).
» •
....
210
Lorenz
B., 14, 794
40, 729
acetic acid
C02H
Nitroethylbenzoic acid
CGOH.Et.NO2=1.4.?
ji
cf. A., 216, 220
155-156
Aschenbrandt
B., 12, 1304
36, 920
Nitroxylylic acid
(CH2.C02H).Me.N02=1.4.?
jj
....
195
....
Z. C. [1867], 13
Acetamidosalicylic acid
COOH.OH.NHAc=1.2.5
»
....
218
Hubner
B., 8, 1215
29, 594
i) "•
» - J>
))
218
11
A., 195, 19i
36, 381
a-Nitromesftylenic acid
COOH.Me2.NO2=al.3.5.6
» •.
....
210-212
Schmitz
A., 193, 16S-.
36, 155
» »
„ =1.3.5.?
»
....
218
Fittig
....
vi., 823
ft- ,» ii
=1.3.5.4
)i
ppd. fr. Ba.
179
Jacobsen
B., 11, 2054.,
36, 248
salt
ft- » »
I) »»•• -
M -
cryst. fr.
223
n
J>
J5
C2H60
ft- ,1 »
)» »
»
ppd. fr. Ba.
175
Schmitz
A., 193, 168
36, 156
salt
ft- ,, I)
n )»
»)
cryst. fr.
214-220;rs.
11
»)
>»
C2H6O
162 ; and
remeltsl68
a-Amido-uvitic acid
Me.(C02H)2.NH2=1.3.5.6
J)
cf. A., 189, 176
240 d.
Bottinger
B., 9, 807
80,415
ft- ,1 11
„ =1.3.5.4
»
cf. A., 189, 181
255 d.
11
B., 9, 808
))
Lutidinedicarboxylic acid ...
C5HNMe2(COOH)j
n
....
245
Michael
A., 225, 121.
48, 62
Nitrophenyl /3-lactic acid ..
N02.[CH(OH).CH2.C02H]
C9H906N
....
105
Prausnitz
B., 17, 598
46, 1175
=1.3
))
» » »
=1.2
)»
....
126
Baeyer & Drewsen
B., 16, 2206
46, 58
» >i »
)» J)
)>
....
126
Einhorn
B., 16, 2214
46, 66
1, I) 11
» »
>J
....
127
Baeyer & Drewsen
B., 15, 2861
44,341
I, 1) II
=1.4
M
....
129-131
Easier
B., 16, 3005
46, 604
), II II
I) »
TJ
....
130-132
11
B., 16, 3006
n
II II 11
)> »
JJ
....
132
Gohring
B., 18, 373
48, 527
Methylic nitranisate
CO2Me.OMe. NO2= 1.-4.6
«
•
abt. 100
Cahours-
A., 56, 315
i., 302
Ethylic nitrohydroxyben-
CO2Et.OH.NO2=1.2.3
»-
.„.
44
Hiibner
B., 8, 1216
29, 593
zoate
ii 11
=1.2.5
»
92-93
11
ii
ii
11 ii
)» »
J)
93
11
A., 195, 14
36, 381
11 'i
=1.4.?
)»
....
K.IOO
Earth.
J. p., 100, 366
vi., 901
Nitroethoxybenzoic acid ....
CO2H.OEt.NO2=1^.5
»
....
161-5
Kraut & Prinzhorn
A., 150, 4
vi., 1006
)! 11
» »>
»
....
163
Perkin
A., 145, 312
^0, 429 ;v., 1009
Nitrohydro-p-coumaric acid
(CH2.CH2.CO2H).OH.N02
)V
....
90-5
Stohr
A., 225, 57
46, 1350
Methoxynitrotoluic acid
C02H.OMe.Me^r02=1.2.4.?
»
...
172-174
Canzoneri
G. I., 10, 516
40, 269
ii "
» )»
»
....
173-175
Patern&& Canzoner
G. I., 9, 455
38, 247
i) 11
») >»
))
....
175
11
G. I., 10, 233
38, 884
Diacetylpyromecazonic acid
C5H3NO(OAc)2
tl
....
153-155
Oat
J.p., 27, 259
44, 791
Dinitro-acetoluide
Me.NHAc.(NO2)2=1.4.3.5
C9H906N3
189-5
Staedel
A., 217, 187
11 ••••
11 11
ii
....
190-5
Beilstein& Kuhlberg
A., 158, 341
vi)., 1178; 84,
fiQO
i)
11 ii
11
....
195
Friederici
B., 11, 1976
DO^
491
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Fr. o-nitro-cinnamic acid
«•««
C9H906N
....
94
Morgan
B., 17, 220
46, 747
Nitroveratric acid
COOH.(OMe)2.N02=1.3.4.2
11
cf. B., 9, 938
100 d.
Merck
A., 108, 59
v., 995
» )j •••• •"
)J ))
JJ
200-202
Matsmoto
B., 11, 134
34, 502
Etbylic dinitrobenzoate
CO2Et.(NO.,)2=1.3.5
C9H906N2
....
90
Staedel
A., 217, 182
44, 865
Diiiitrophenylurethane
(NH.COOEt).(NO2)2=1.2.4
C9H906N3
....
110-111
Hager
B., 17, 2029
48, 150
jj
=»
J)
210
Losanitsch
B., 10, 691
Trinitroisopropylbenzene ...
Prf.(N02)3=?
J)
....
109
Fittig and others
A., 149, 329
Dinitroacetaniside
OMe.NHAc.(N02)2=1.2.(?)2
)5
....
147
Muhlhauser
B., 13, 922
38, 641
jj
1' J!
»)
....
157
;j
A., 207, 243
42, 302
Etbylic dinitroamidoben-
COOEt.NH,.(NO2)2=:1.4.3.5
11
....
abt. 100
Cahours
A. C. [3], 27, 454
i., 957
zoate
J» M
•>5 -M
'Jl
cf. B. 4, 871
114
Salkowski
A., 163, 11
vii., 336
» 11
=1.2.(?)2
JJ
....
135
»
A., 173, 47 ; B.,
28, 71 ; vii.,
4, 872
336
Dinitro-amidohydrocinnamic
(CH2.CH2.CO2H).NH2.(NO.j).!
1)
....
190
Stohr
A., 225, 57
46, 1350
acid
=1.4.3.5
Trinitroethyltoluene
Me.Et.(N02)3=?
JJ
....
92
Glinzer and Fittig
A., 136, 314
v., 857
j) .... ....
„ =1.4.2.3.?
)J
....
92
Jannasch & Dieck-
B., 7, 1515
28, 1189
mann
Trinitropseudocumene
Me3.(NO2)3=1.3.4.2.5.6
JJ
cf. A., 151, 261
185
Fittig
Z. C. [2], 4, 577
vi., 296
>j
jj jj
JJ
....
165
Fittig & Laubinger
u
vi., 297
»
JJ JJ
JJ
185
Engler
B., 18, 2235
Trinitromesitylene
„ =1.3.5.2.4.6
JJ
....
230-232
Fittig
A., 141, 134
vi., 299
jj
j' jj
))
232
u
Z. C. [2], 4, 577
vi., 296
jj .... ....
»j jj
»J
....
532
Kurbatow
B., 16, 966
jj
jj jj
JJ
-..
£32
Engler
B., 18, 2235-7
Trinitroethoxy toluene
Me.OEt.(N02)3=1.3.2.4.6
C9H907N3
....
72
Nolting and Salis
B., 15, 1864
44,59
Dinitrotyrosine
C9H9(N02)2N«3
)»
115
Stadeler
J. [1860], 576
v., 934
Dimethyltrinitro-orcinol ....
Me.(OMe)2.(N02),=1.3.5.
C9H90SN3
....
69-5
.fitenhouse
P. K., 19, 410
vii., 880
.. 2.4.6
Benzene azoaeetone
Ph.Nj.CH2.CO.Me
C9HI0ON2
....
148-149
Kichter & Miinzer
B., 17, 1928
46, 1342
Isonitrosoanil acetone
Ph.N:CMe.CH:NQH
»
....
180
Knorr
B., 17, 1637
46, 1368
Ethoxyphenylcyauamide ....
EtO.(NH.CN)=1.2
JJ
04
Berlinerblau
J. p., 30, 97
48, 148
jj
=1(4
H
....
78
)»
jj
»
Nitrosohydromethyl ketole....
C6H4.CH2.CHMeiN.NO=1.2
jj
54-55
Jackson
B., 14, 884
40, 735
i i
Aniidohydrocarbostyril
C6H4.CH2: CH2.CO.N.NH2
j>
....
143
Fischer and Kuzel
A., 221, 261
46, 441
i i
jj ....
C6H3(NH2).C2H4.CO.NH
>j
211
Gabriel and Zim-
B., 12, 602
36, 640
i i
mermann
=1.4.5
PLenylmethyl oxamide
NHMe.CO.CO.NHPh
C9H10OaN2
171-173
Wallach and West
B., 9, 266
30, 185
jj jj
JJ
Jl
179-181
Wallach
A., 184, 70
32, 187
Phenylmalonamide
NH2.CO.CH2.CO.NHPh
JJ
....
163
Freund
B., 17, 135
46, 728
Hippuramide
Ph.CO.NH.CH2.CO.NH2
JJ
....
183
Curtius
J. p. [2], 26, 145
44, 339
jj .... ....
»J
->J
183
Conrad
J. p. [2], 15, 248
32, 484
Acetylphenylcarbamide
NHPh.CO.NHAc
JJ
«
183
Kiihu
B., 17, 2882
48, 260
jj
JJ
)J
183
McCreath
B., 8, 1181
29, 401
Acetylbenzenyl amidoxime...
NH2.CPh : NOAc
JJ
«...
96
Schulz
B., 18, 1083
48, 897
Phenylbydrazinepyroracemic
Ph.N2H : CMe.COOH
?J
misprint
169 p.d. (?)
Fischer & Jourdan
B., 16, 2242
46, 52
acid
» »
»J
Jj
192
Fischer
B., 17, 578
46, 1151
Nitrosoacetoluide
Me.NAc(NO)=1.4
JJ
80 d.
»
B., 10, 959
32, C07
Tolyloxamide
Me.(NH.CO.COJMH2)=1.3
J-
131
Bladin
B. S., 41, 125
46, 1142
jj ....
=1.4
JJ
236-237
jj
jj
46, 1141
Acetainidobenzamide
NHAc.(CQ.NHj)=1.2
JJ
170-171
Weddige
J. p. [2], 31, 124
48, 601
Acetamidobenzaldoxime
NHAc,(CHjNOH)=1.4
JJ
....
205-206
Herzberg
C. C. [1884], 35
48, 662
Diamidocinnamic acid
(CH : CH.CO2H).(NH2)2
)J
....
167
Gabriel & Herzberg
B., 16, 2043
44, 1123
=1.3.4
>j jj
„ =1.3.5
)J
....
167-168
Herzberg
C. C. [1884], 35
48, 662
Tetrahydronitroso-hydroxy-
N.OH=ai ; /3, or a2
-M
....
solid
Eiemerschmied
B., 16, 723
quinoline
11 )!
» =°i ; «i
)»
...»
67-68
Bedall and Fischer
B., 14, 1369
1
COMPOUNDS CONTAINING FOUR ELEMENTS.
495
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitropropionanilide
NO2.(NH.CO.Et.)=1.2
C9H,AN2
....
63
Smith
A. C. J., 6, 172
48, 524
Nitrophenyl dimethyl ace-
NO2.(CMe.NOMe)=1.3
»
„..
63-64
Gabriel
B., 15, 3063
44, 582
toxime
Salycyloxyacetic diamide ....
(CO.NH2).(O.CH2.CO.NH2)
)J
....
158
Rossing
B., 17, 2997
48, 388
=1.2
Uramidophenylacetic acid ....
(NH.CO.NH2)(CH2.CO2H)
»
174 d.
Traube
B., 15, 2122
44, 193
= 1.4
Amidohippuric acid .... ..„
NH2.(CO.NH.CH2.CO2H)
»
A., 78, 112
192
Schwanert
A., 112, 70-
=13
,, ,,
» )!
3>
....
194
Conrad
J. p. [2], 15, .257,
32, 485
Nitroacetoluide
Me.NHAc.NO2=1.4.5
51
....
92
Beilstein and Kuhl-
A., 155^23,^.
vii., 1166
berg
Z. C. [2], 5, -
,, ....
n »
)T
92
Nblting and Collin
B., 17,, 264
46, 1012
„ ....
» )i
3)
....
94-95
Gattermann
B., 18, 1483
»
=1.3.2
1)
....
101-102
Beilstein and Kuhl-
Z. C. [2], 7,. 99 ;
24, 563, 683 ;
berg
A., 158, 348
vii., 1178
,. ....
=1.3.6
))
....
136
Limpricht
B., 18, 1402
48, 974
,, ....
=1.2.4
»
....
150-151
Nolting and Collin
B., 17, 268
46, 1007
) .... ....
=1.2.6
JJ
....
155-5
Cunerth .
B., 7, 643;, A.,
27, 903; 28,
172, 226
83
>i ....
)) !)
JJ
....
157-5-158
Ullmann
B., 17, 1959
46, 1316
j, ....
=1.2.3
J)
....
158
Lellmann and
A., 228, 239
48, 974
Wurthner
>»
= 1.4.6
»
....
160
Cunerth
A., 172, 229
„ .... ....
=1.2.5
»
....
196-197
Beilstein and Kuhl-
A., 158, 345
24, 682 ; vii.,
berg. .
1178
Azotolylmethazonic acid
06H4Me.(N2C2HilN2O3 )= 1.4
C9H1003N4
....
154
Kimich
B., 10, 143
32, 326
Nitrophenylurethane
N02.(NH.COOEt)=1.2
C9HI004N2
....
58
Eudolph .
B., 12, 1295
36, 921
„
=1.4
))
....
129
Hager
B., 17, 2625
48, 149
Nitrohpenyl |3-anilidopro-
N02.[CH(NH2).CH2.C02H]
I)
120-122
Easier
B., 17, 1501
46, 1173
pionic acid
=1.4
Nitrophenyl /3-alanine
NO2.[CH(OH).CH2.CO.NH2]
)J
.....
166-167
»
B., 17, 1494
46, 1172
=1.4
» :>
,) !!
NO2.CH.CH2.CO.O.NH3
5)
)»
....
197.
220
Einhom
Erlenmeyer and
B., 16, 2646
A., 219, 179
46, 304
44, 993
J =1.4
NO2.[OH2.CH(NH2).CO2H]
=1.4
Lipp
Nitroacetaniside
OMe.NHAc.NO2=1.2.?
>J
143
Mulhauser
A., 207, 242
42, 302
Ethylic nitroamidobenzoate
CO2Et.NH2.NO2=1.2.3
))
....
104
Hubner
A., 195, 40
36, 382
Methylic nitroamido-a-tol-
(CH2.CO2Me).NO2.NH2
))
....
94
Gabriel and Meyer
B., 14, 825
40, 730
uate
=1.2.4
Nitro-amidohydrocinnamic
(CH2.CH2.C02H).NOS.NH2
J)
....
137-139
Gabriel and Zim-
B., 12, 601
36, 640
acid
=1.2.4
mermann
!> ))
=1.3.4
)t
....
145
Gabriel and Steude-
B., 15, 845
42, 1073
mann
!! II
>5 »
1)
....
145
Gabriel
B., 15, 845
44, 195
Nitroethamidobenzoic acid ....
CO2H.NHEt.NO2=1.3.5
)»
....
208
Roll wage
B., 10, 1704
34, 148
Dinitroethyltoluene ...
Me.Et.(N02)2=1.4.(?)2
)>
....
Liquid
Jannasch and
B., 7, 1514
Dieckmann
» .... ....
» )>
»
....
52
»
))
Dinitropseudocumene
Me3.(N02)2=1.3.4.(?)2
J)
isomeric
86
Rommier
B. S. [2], 19, 434
26, 888 ; vii.,
402
»
j> H
n
»>
86
»
»
M
Dinitromesitylene
„ =1.3.5.2.4
»
....
86
Fittig
A., 141, 133
vi., 299
Dinitroethoxy toluene
Me.OEt,(NO2),.=1.2.3.5
C9HI005N2
....
46
Nolting and Salis
B., 15, 987, 1860
44, 59
„
» M
»)
....
51
Kayser
B., 15, 1133
42, 1203
„ ....
» »
1J
cf.A.,217,154
51
Staedel
B., 14, 899
40, 723
,,
„. =1.4.3.5
)»
....
73
Nolting and Salis
B., 15, 1858
,,
ii »
))
cf.A.,217,164
75
Staedel
B., 14, 899
H
„
!! )!
i)
....
75
Kayser
B., 15, 1136
42, 1203
496
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitropseudocumylic nitrate
Dinitropseudoeumenol
Dinitronitrosoethyltoluidine
Trinitroethyltoluidine
Dinitrophenylglycerol
Trimtronitrosotrimethyl di-
amidobenzene
Propionanilide
Me2.NO2.NO3=1.3.4.2.6
Me3.OH.(NO2)2=1.3.4.6.2.5
Me.NEt(NO),(NO2)2=1.4.3.5
Me.NHEt.(NO2)3=1.4.2.3.5
[O.C3H5(OH)2].(N02)2=1.2.4
NMe2.NMe(NO).(NO2)3
= 1.3.(?)3
C6H5.NH.CO.CH2.CH3
U9H1005N2
c9n"0o6N4
i?
C9H1007N2
C<,HI007N6
CjHnON
....
84 d.
110
77-78
115-116
83
132
02
105
Auwers
»
Gatterraann
»
Willgerodt
Wurster & Morley
Sestini
Kelbe
B., 17, 2979
B., 17, 2981
B., 18, 1486
»»
B., 12, 766
B., 12, 1815
Z. C. [2], 7, 35 ;
C., 4, 21
B., 16, 1200
48, 380
48, 381
48, 975
)»
36, 717
38, 111
24, 234; vii.,
1009
44, 916
Methy lace tan ilide
j)
„
„ .... ....
., .... ....
Benzylacetamide
» .... ....
Dimethylbenzamide
Ethylbenzaldoxime ,
Amidophenylethylketone ....
C6H5.NMeAc
»
»
»
C6H6.CH2.NHAc
CeHj-CHj-NHjAc
C6H5.CO.NMe2
C6H5.CH : N.OEt
CfiH4(NH2).Ca.Et
Me.NHAc— 1.3
))
)
»
»5
J?
?)
-JJ
)J
• • ))
»
245
240-250
a. 250
300
255-257 oi.c.
503
99-5
99-5
101
loi-rioa
104
30
57
41-42
207:5-209 u.c.
Liquid
65-5
Norton and Allen
Hofmann
Eeinhardt and
Staedel
Hepp
Hofmann
Strakoach
Rudolph
Hallmaun
Petraczek
Barry
Beilstein and Knhl-
B., 18, 1995
B., 10, 599
B., 16, 29
B., 10, 329
B., 7, 525
B., 5, 697
B., 12, 1297
B., 9, 846
B., 16, 828
B., 6, 1007
A., 156, 83
44,578
27, 807
vii., 182 ; 25,
1027
36, 921
30, 418
27,74
vii., 1176
65-5
Jberg
Wroblewsky
B., 8, 574
28, 886
— 1.2
98
Z. C. [21, 7, 135
24, 564
102
B., 9, 1055
30, 510
>» .... •••• ....
1) »>
«
....
102
105
Klingel
Wroblewsky
B., 17, 1613
Z. C, [2], 7, 135
46, 1343
24, 504
,, .... ....
» JJ
» ))
- J)
»
296
105-106
107
107
Hubner and Wal-
lach
Beilstein and Kuhl-
berg
Thomson
J. [1869], 678
A., 156, 77
B., 10, 1586
37, 438
vii., 1176
34, 218
107
Grete
A., 177, 231
29, 74
107-109
Bedson and King
37, 753
108-109
Kelbe
B., 16, 1200
44, 916
„ —1.4
a. 140
Merz and Weith
Z. C. [2], 5, 699
vii., 4
310-350
145-145-5
v., 871
306
US
Beilstein and Kuhl-
A., 156, 74
vii., 1176
» .... .... i...
» <»
-- »
146
147
berg
Grete
Kelbe
A., 177, 231
B., 16, 1200
29,72
44, 916
307
147
Eichter
K. K. T., 222
148
Glaus
B., 15, 317
Dimethamidobenzaldehyde ....
Toluylacetamide
» ....
» ••" •••
Xylylformamide
Mesitylenamide
COH.NMe2= ?
Me.(CH2.CO.NH8)=1.3
=1.2
= 1.4
Me2.(NH.CHO)=1.3.4
Me2.(CO.NH2)=1.3.5
— 1 3 fi
>1
51
)»
,»)
J»
»
....
73
141
161
184
113-114
133
181 as 179
Bossneck
Radiszewsky and
Wispek
»
»)
Gasiorowski and
Merz
Fittig
Ador and Meier
B., 18, 1520
B., 18, 1282
B., 18, 1281
.))
B., 18, 1011
A., 147, 47
B 12 1970
48, 976
48, 889
)»
I)
48, 773
vi., 824
38 252
— 1 45
M
186
Jacobsen
B., 14, 2112
42, 187
Tetrahydrohydroxyquinoline
»j
Ethylic benzhydroxaminate
u »
» »
N.OH=ai ; /3, or a,
„ =a, ; Oj
HO.CPh: N.OEt (?)
Bz.NH.OEt(?)
jj
)1
C9H",AN
»
»
cf.B., 16,874;
18, 727
»
»
116-117
121-122
Liquid
64-65
67
Riemerschmied
Bedall and Fischer
Tiemann & Kriiger
Waldstein
Pieper
B., 16, 723
B., 14, 1368
B., 18, 736, 1053
A., 181, 385
A., 217, 11
44, 1148
48, 790, 896
30, 526
44, 461
COMPOUNDS CONTAINING FOUR ELEMENTS.
497
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
a-Ethylbenzhydroxamic acid
Bz.NEt.OH(?)
CAAN
cf.B.,16,874;
53-5-54-5
Lessen and Zanui
A., 182, 221
31, 188
18, 727
"- 11 11
„
11
....
Liquid
Eiseler
A., 175, 329
<«- 11 »
11
„
54
Pie per
A., 217, 4
44, 461
a" n 11
„
„
53-5
Gurke
A., 205, 285
40, 585
ft-
„
67
Pieper
A., 217, 5
44, 461
ft- 11 11
....
„
....
67-5-68
Gurke
A., 205, 286
40, 585
Ethylic phenylcarbamate ....
NHPh.OOOEt
„
184-186
Liquid
Schiff
B., 3, 649
11 11 ••••
„
„
237
51
Hofmann
B., 3, 654
11 11
11
„
237-S38 d.
51-5-52
Wilm and Wischin
A., 147, 159
vii., 252
Methylic phenaraidoacetate
NHPh.CH2.COOMe
„
48
Meyer
B., 8, 1157
29, 373
a-Phenamidopropionic acid ....
NHPh.CHMe.COOH
„
....
162
Tiemann & Stephan
B., 15, 2036
44, 199
Phenylmethamidoacetic acid
NHMe.CHPh.COOH
„
....
w.m. 274
Tiemann & Priest
B., 14, 1982
42, 50
Phenyl a-amidopropionic acid
Ph.CH2.CH(NH2).COOH
11
a. 260 d.
Plochl
B., 17, 1624
46, 1349
11 a" 11 11
„
„
....
250 d.
Schulze & Barbieri
B., 14, 1788
42, 189
11 "~ 11 11
11
„
cf.B.,15,1006
sb.w.m.
Erleuraeyer & Lipp
A., 219, 200
42, 972
11 ft- 11 11
Ph.CH(NH2).CH2.COOH
„
cf.B.,15,1006
120-121
Poseii
A., 195, 143
36, 378
a-Amidohydratropic acid ....
CH3.CPh(NH2).COOH
„
w.m. 260
Tiemann
B., 14, 1981
42, 57
a- „ „
CH2(NH2).CHPh.COOH
11
169-170
Merliug
A., 209, 11
40, 1143
ft- 11 11
11
11
169-5
Fittig and Wurster
A., 195, 158
36, 379
a-Phenoxy propoiuam ide
CH3.CH(OPli).CO.NH2
„
....
130
Saarbach
J. p. [2], 21, 152
38, 393
Ethoxyformanilide
OEt.NH(CHO)=1.2
11
292
62
Groll
J. p. [2], 12, 208
29, 247
Methoxyacetanilide
OMe.NHAc=1.2
11
303-305
79
Miilhauser
B., 13, 921
38, 641
11 ••••
11 11
11
303-305
78
11
A., 207, 242
42, 302
11 ••* "•*
11 ;i
11
....
84
Herold
B., 15, 1685
Ethoxybenzamide
OEt.(CO.NH2)=1.2
„
110
Limpricht
A., 98, 264
v., 151
Melilotamide . ....
OH.(CH2.CHn.CO.NH£)=1.2
70
Zwei er
As., 5, 120
vi., 716
n
OH.(CHMe.CO.NH2)
110-111
Hlasiwetz
A., 102, 162
iv., 489
Ethylic amidobenzoate
NH2.COOEt=1.2
a
260
Kolbe
J. p. [2], 30, 467
48, 665
11 11 ••••
=1.4
11
....
95
Muller
B., 18, 2485
Dimethamidobenzoic acid ...
NMe!i.COOH=1.3
11
151
Griess
B., 6, 587
26, 1146
11 .i ».
= 1.4
n
235
Michler
B., 9, 401
30, 68
Ethamidobenzoic acid
NHEt,COOH=1.3
„
112
Griess
B., 5, 1038
26, 281 ; viil.,
167
/3-Amidophenyl propionicacid
NH2.(CH2.CH2.COOH)=1.2
11
d.
Gabriel and Steude-
B., 15, 847
42, 1073
mann
ft-
= 1.3
„
84-85
11
B., 15, 846
„
ft- 11 11 11
=1.4
„
....
131
11
B., 15, 847
,,
ft- D 11 11
11 11
„
....
131
....
Z. C. [1869], 195
vi., 961
tt~ 11 11 11
NH2.(CHMe.COOH)=1.4
11
128
Trinius
A., 227, 262
48, 529
Tolylglycociue
Me.(NH.CH2.COOH)=1.2
„
143
Cosack
B., 13, 1091
88, 713
11 ••" •••-
11 11
„
d. 170
145
Meyer
B., 8, 1159
29, 401
„
11 11
„
140-150
Staats
B., 13, 137
38, 387
)» .... ....
11 i,
11
150
Ehrlich
B., 16, 204
„ ,
= 1.3
„
....
?
11
B., 15, 2011
„
=1.4
11
....
166-168
Schwebel
B., 10, 2047
34, 302
„
11 1)
„
....
166-168
Staats
B., 13, 137
„ (misprintinorig.)
11 11
11
...
168-169
Meyer
B., 14, 1324
Toly Ihydroxy acetamid e
Me.(NH.CO.CH2.OH)
11
+ l£H2O
70-130
Tommasi
27, 628
Tolylamidoacetic acid
Me.[CH(NH2).COOH]=1.3
„
sb. 230
d.
Bornemann
B., 17, 1472
46, 1163
Acetamidocresol
Me.OH.NHAc=1.4.5
11
....
159-160
Noltiug and Kohn
B., 17, 361
46, 901
„
1)
„
....
178
Maassen
B., 17, 609
46, 1145
„
= 1.2.4
11
2%4-Z%5
Wallach
B., 15, 2831
44, 329
„
i, 11
11
224-225
Maassen
B., 17, 609
Nitromesitylene
Me3.NO.,=1.3.5.6
11
240-250
41
Fittig and Storrer
A., 147, 1
vi., 299
(cf. A., 179,
11 .1
11
255
42
Ladenburg
B., 7, 1135
28, 64
169)
„
11 11
„
....
44
Biedermann and
B., 8, 57
28, 569
Ledoux
Nitropseudocumene ....
„ =1.3.4.5
„
....
20
Edler
B., 18, 629
48, 771
„
„ =1.3.4.6 (?)
11
265
71
Z. C. [1867], 12
vi., 297
3 s
498
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Amidomesitylenic acid
Mei.COOH.NH2=1.3.5.6
CsHnO.,N
....
186-187
Schmitz
A., 19.3, 171
36, 156
»> M
11 »
)*
1!)0
Jacobseu
B., 11,2055
» » «••
=1.3.5.2
5)
235
Fittig
A., 147, 50
vi., 823
„ ,,
11 11
)1
....
235
Schmitz
A., 1!)3, 171
36, 156
Collidine carboxylic acid
C5NHMe:i.COOH
•>
....
155
Michael
A., 225, 121
48,62
» » »
11
)1
-f2H20
no
B
»
1J
Nitrosoethylphenyl carb-
....
C9HM02N:l
59-5
Fischer
A., 199, 286
amide
Glycolphenylguanidine
NHPh.C(: NH).NH.CHa.
ft
....
260 d.
Berger
B., 13, 993
38, 802
COjH
Nitropropylazobenzene
CH3.CH2.CH(NO2).N : NPh
))
...
98-99
Meyer
B., 9, 386
30, 93
Nitroethylazotoluene
C6H4Me.N2.C2H4.N02=1.2
))
87-88
Barbieri
B., 9, 388
30, 94
*>
=1.4
H
133
?»
B., 9, 387
j>
Phenylamidolactic acid
Ph.C2H.,(OH)(NH2).CO.,H
C.H.AN
189-190
Plochl
B., 16, 2822
46, 606
Ethoxamidobenzoic acid
NH(OEt).COOH=1.4
)1
187
Ladenburg
B., 6, 130
26, 642
Amidophenyllactic acid
NH:.[CH2.CH(OH).COOH]
»
....
188
Erlenmeyer& Lijip
A., 219, 179
44, 994
=1.4
Ethylic hydroxyphenylcar-
OH.(NH.COOEt)=1.2
5'
85
Grenvik
B. S. [2], 25, 177
31, 473
bamate
7) J)
=1.4
,,
....
120
51
B. S. [2], 25, 179
ji
Tyrosine . .
OH.[CH2.CH(NH.,).CO2H]
cf. B., 16, 854
167-168-
Blendernianii
Z. P. C., 6, 234
44, 878
11
=1.4
Methoxymandelatnide
OMe.[CH(OH).CO.NH2]
)J
159
Tiemann
B., 14, 1977
48,57
=1.4
Methoxyphenylamidoacetic
OMe.[CH(NH2).CO.2H]=1.4
5)
....
w. m. 225
M
B., 14, 1979
acid
Methoxyphenylglycocine ....
OMe.(NH.CH2.CO2H)=1.2
55
141-5
Vater
.1. p. [2], 29, 286
46, 1144
»
=1.4
5>
d. w. in. 200
!»
»
5»
Methamidanisic acid
OMe.NHMe.COOH=?
»
a. 200
(4riess
B., 5, 1042
vii., 79:26,282
Nitroethoxytoluene
Me.OEt.NO.,=1.2.3
J»
....
Liquid
Staedel
A., 217, 50, 153
44,865
,,
=1.4.5
»J
275-2S5
Liquid
»
A., 217, 54, 162
44, 662, 862
,,
11 11
I)
Liquid
Kayser
B., 15, 1134
42, 1203
„
= 1.3.?
TJ
....
54
i)
D
»
»i
;> 11
n
54
Staedel
A., 217, 161
44, 862
,,
„ =1.2.5
»i
71
?>
B., 14, 899
40, 723
,,
11 11
n
71
»)
A., 217, 155
44, 862
„
11 11
?»
71
Kayser
B., 15, 1133
42, 1203
,,
= >•
ji
285
72-73
Ladenburg
B., 8, 1212
Nitromethoxyxylene
Me2.OMe.NO2=1.3(?)2
i)
....
56-57
Pfaff
B., 16, 1136
44, 918
Nitromesitol
MeJ.OH.NO2=l. 3.5.2.4
cf.A., 215, 98
64
Kuecht
B., 15, 1376
42, 1200
Acetylethylpyromeconamic
»
j)
140
Mennel
J. p. [2], 32, 17(i
48, 1204
acid
Phenylhydroxyethenylur-
HO.CHPh C(NOH).NH.
^Hn03N,
127
Gross
B., 18, 2478
48, 1218
amidoxime
CO.NH,
Ethylnitrobenzenylamid-
NO2.[C(NH2) : NOEt]=1.3
55
b. 15(?)
Schopf
B., 18, 1065
48, 896
oxirae
Nitro /3-phenylpropylene
N02.[CH(OH).CH2.CH2.OH ;
C,HnO,N
108-101)
Baeyer & Drewseii
B., 15, 2861
44, 341
glycol
=1.2
Aruidophenylglyceric acid ....
NH2.[CH(OH).CH(OH).
U
218
Morgan
J. [1877], 788 ;
C02H]=1.2
0. N. 36, 269
n-ethylnitro-orcinol
Me.OEt.OH.NO2=1.3.5.?
H
54
Weselsky and Bene-
M. C., 2, 371
40, 1140
dikt
£- „
« >i
T»
103
?>
)!
D
Triraethylpyrroline dicarb-
NMe.Mes.(OOtH)J=1.8JM».4
11
• •••
d. 240-245
Knorr
B., 18, 307
48, 555
oxylic acid
Ethylic amidonitrophenyl-
NH.CO2Et).NH2.NO2=1.2.4
C9HU04N3
162
Hager
B., 17, 2631
48, 150
carbamate
Dinitroethyltoluidine
Me.KHEt.(NO2),=1.4.3.5
»»
126-126-5
Gattermann
B., 18, 1485
48, 975
Dinitrodimethyltoluidine ....
Me.NMe2.(N02)2=1.3(?)2
11
107
Wurster and Riedel
B., 12, 1800
38, 109
,, ....
" !>
;>
....
168
n
11
11
Dinitrocumidine
Me.,.NH2.(N02)2=1.3.4.(?)3
»
78
Engel
B., 18, 2232
48, 1210
Dinitromesidine
„ =1.3.5.2.4.6
?i
193-195
Ladenburg
A., 179, 168
COMPOUNDS CONTAINING FOUR ELEMENTS.
49,1
Name.
Constitution.
Formula. ™£*
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Gh. Soc.
Dinitroraesidine
Me3.NH.,.(NO2),,=.1.3.5.2.4.6
C9HU04N3
193-195
Fittig
A., 141, 138
vi., 300
Nitrobeiizylidenediure'ide ....
NO2 C6H4.CH(NH.CO.NH2)2
C9H,,04N5
200 d.
Schiff
A., 151, 194
Menispermine
C9H12ON(?)
120
Pelletier & Uouerbe
A. C. [2], 54, 178
iii., 880
Ethylphenylcarbamide
NH2.CO.NEtPh
C9H1.,ON3
62
Gebhardt
B., 17, 2095
46, 1321
,*
....
I)
99
B. 8., 4, 203
Phenylethylcarbaraide
NH2.CO.NH.CH2.CH2Ph
Ji
112
Spica
G. I., 9, 555
38, 242
n-phenamidopropionamide ....
NHPh.CHMe.CO.NH2
)7
....
140-141
Tiemann aud Ste-
B., 15, 2035
44, 199
phan
Phenylraethamidoacetamide
Ph.CH(NHMe).CO.NH2
»
155
Tiemann and Piest
B., 14, 1983
Methylphenamidoacetamide
NPhMe.CH2.CO.NH2
))
163
Silberstein
B., 17. 2662
48, 160
Benzylic ethenylamidoxime
NH2.CMe : NO.CH2Ph
V
d. 200
Liquid
Nordmanu
B., 17, 2752
48, 239
Ethylic benzenylainidoxime
NH2.CPh : NOEt
))
65-66
Lessen
B., 18, 1194
•i "
)>
»1
67
Tiemann & Kriiger
B., 18, 732
48, 790
!< "
)T
I?
67
Kriiger
B., 18, 1056
48, 896
Ethyltolylnitrosamine
C6H4Et.NEt(NO)=1.4
1>
?
Gastiger
B. a, 42, 338
48, 381
Tolylaraidoacetamide
Me.(NH.CH2.CO.NH2)=1.4
M
....
162-163 d.
Meyer
B., 8, 1160
29, 402
Nitrosodimethyltoluidine ....
Me.NMe2.NO=1.3.?
>1
92
Wurster and Riedel
B., 12, 1797
38, 109
Acetdiamidotoluene
Me.NH2.NHAc=1.2.4
fl
....
158-159
Tiemann
B., 3, 221
,, .... ....
» »
1)
159-160
Wallach
B., 15, 2826
„
» •' »
159-161
»
B., 15, 2835
Xylyl carbamide
Me,.(NH.CO.NH.)=1.3.4
»)
186
Genz
B., 3, 226
vii., 1210
Phenylhydrazinepropionie
NHPh.NH.CHMe.COOH
C9H1202N2
152-153
Fischer and Jordan
B., 16, 2244
46, 53
acid
>i »
NH2.NPli.CHMe.COOTI
?1
187
Reissert
B., 17, 1455
46, 1152
Ethylic amidophenylcarba-
NH2.(NH.COOEt)=1.4
)1
71-72
Hager
B., 17, 2626
48, 149
mide
>i »
= 1.2
J)
....
86
Rudolph
B., 12, 1295
36, 921
Hydrazine hydrocinnamic
(NH.NH2).(C2H4.C03H)=?
)J
....
146
Fischer and Kuzel
A., 221, 261
46, 441
acid
Acethydrazine anisoil
MeO.(N2H2Ac)=1.2
1)
125
Reisenegger
A., 221, 314
46, 440
Ethoxyphenylcarbamide
EtO.(NH.CO.NH2)=].4
»
....
160
Berlinerblau
J. p., 30, 97
48, 148
Nitrocumidine
Pr.NH2.NO2=?
>1
b. 100
Cahours
C. R., 26, 316
ii., 176
Mtroethyltoluidine
Me.NHEt.NOs= 1.4.5
1?
58-59
Gattermann
B., 18, 1483
48, 975
Nitrodimethyltoluidine
Me.NMe2.NO2=1.3.?
)>
84
Wurster and Riedei
B., 12, 1800
38, 109
Diamidociunamic acid
(CH2.OH2.CO2H).(NH2)2
)'
....
142-144
Gabriel
B., 15, 2291
44, 195
=1.3.4
Nitromesidine
Me3.NH2.NO2=1.3.5.2.4
U
....
74
Biedermanu and
R, 8, 58
28, 569
Ledoux
,, .... ...
» »
11
....
75
Hiibner and Schack
B., 10, 1711
34, 144
„ .... ...
« n
))
73-74
Ladenburg
A., 179, 165
,,
n »
)>
72-73
)»
B., 7, 1134
»
•) »
»T
b. 100
Maule
A., 71, 137
2,110; iii., 930
Nitropseudocumidine
=1.3.4.6.5
»)
46-47
Elder
B., 18, 629
48, 771
»
=1.3.4.(?),
»
cf.A., 151,266
137
Fittig and Lauben- Z. C. [2], 4, 577
vi., 297
heimer
Benzylidenediureide
Ph.CH(NH.CO.NH2)2
C9H1202N4
....
195
Schiff
A., 151, 192
Nitrosoethylphenylsemicar-
Ph.N(NO).NH.CO.NHEt
M
....
86-5 d.
Fischer
A., 190, 111
34, 307
bazide
Tolylene dicarbaraide
Me. (NH.CO.N H2)2= 1. 1 .3
»
220
Strauss
A., 148, 157
vi., 1117
» j»
)) )J
)»
220
Lussy
B., 8, 292
Ethyltheobromine
cf. B., 15, 33
»
a. 270
Philips
B., 9, 1309
31, 93
Diamidoethoxytoluene
Me.OEt.(NH2)2=1.4.3.5
C9H)203N2
Liquid
Kayser
B., 15, 1136
42, 1203
Nitro-nitrosotrimethdiami-
NMe2.NMe(NO).NO2=1.4. ?
C9H1203N4
....
87
Wurster & Schobig
B., 12, 1811
38, 111
dobenzene
Tetramethyluric acid
NMe.CO.C.N'Me.CO
))
distila
218
Fischer
B., 17, 1784
46, 1310
1 II /
CO.NMe.C.NMe
Methylphenylethylalkine ...
NPhMe.C2H4.OH
(;9H13ON
218-219(110
Liquid
Laun
B., 17, 676
46, 1011
Dimethamidomethoxy ben-
OMe.NMe2=1.2
»
210-212
Liquid
Miilhauser
A., 207, 248
42, 302
zene
»
= 1.4
5)
....
48
Griess
B., 13, 249
38, 637
3s 2
500
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc
Hydroxyethyltoluidine
Me.(NH.C2H4.OH)=1.4
C,H13ON
286-288
37
Demi ile
B., 7, 636 ; A.,
27, 903
173, 129
Ethoxytoluidine .... , ...
Me.OEt.NH2=1.2.5
)>
....
Liquid
Staedel
A., 217, 217
44, 866
.,
7> »
»
Liquid
Kayser
B., 15, 1135
42, 1203
„ ....
=1.3.1
J)
....
Liquid
ii
»
ii
11
» )J
H
....
Liquid
Staedel
A., 217, 219
44. 866
., ....
=1.4.5
*?
....
40-41
»
A., 217, 220
11
„
J> »1
»)
....
40-41
Kayser
B., 15, 1135
42, 1203
Amidomesitol
Me3.OH.NH2=1.3.5.2.4
fi
cf. A., 215, 99
cryst.
Knecht
B., 15, 1376
Amidopseudocnmeuol
„ =1.3.4.6.2
•)
164-165
Auwers
B., 17, 2980
„
11 Yl
V)
16f5-167
Liebermann and
B., 17, 886
46, 1147
Kostanecki
Phenyldimethamidocarba-
NHPh.CO.NH.NMej
C9H13ON,
....
108
Eenouf
B., 13, 2172
40, 152
mide
•
o-phenylhydrazinepropion-
NH2.NPh.CHMe.CO.NH2
»)
124
Reissert
B., 17, 1454
46, 1152
amide
Ethylphenylsemicarbazide ....
Ph.NH.CO.NjHjEt
)I
111-112
Fischer
A., 199, 295
11
Ph.N2H.2.CO.NHEt
JJ
....
151
Fischer
A., 190, 109
34,307
Nitrosotrimethdiamidoben-
NMes.NMe(NO)=1.4
»
98-99
Wurster & Schobig
B., 12, 1809
38, 111
zene
Dimethainidophenylcarba-
NMe2.(NH.CO.NH2)=1.4
»
....
179
Binder
B., 12, 536
36, 628
mide
Ethylic dimethylpyi-roline-
C4NH2Me2.COOEt
C9H1302N
290 (731)
117-118
Knorr
B., 18, 1564
48, 995
carboxylate
Nitrodiamidomesitylene
Me3.NO2.(NH2)2=1.3.5.2.4.6
C9H1302NS
....
184
Fittig
A., 141, 139
vi., 300
Ethylic ethylacetocyanace-
CEtAc(CN).COOEt
C9HI303N
105-110
Liquid
Held
C. R., 98, 522
46, 727
tate
(2-15)
Camphoronamic acid
„.
C9H1304N
....
212
Hjelt
B., 13, 798
38, 670
Diamidoethoxy toluene
Me. OEt.(NHj)3= 1.4.3.5
C9H14ON2
75
Staedel
A., 217, 221
44, 866
? -amidiue
C4H3O.C(NHEt) : NEt
n
a. 200
Wallach
B., 14, 753
40, 715
)> 11
J>-
51
240
»
A., 214, 232
44, 88
Diethylcarbopyrrolamide ....
NEt(CO.NHEt)=1.2
>1
269-270
43-44
Bell
B.,10, 1863; 11,
36, 525
1813
Hydroxycyanconiue
....
»
156-157
Meyer
J. p. [2], 22, 267
40, 54
Dihydroxycyanconine
C9H12N2(OH;2
C9H14O2N.,
151
Riess
J. p. [2]. 30, 145
48, 235
Caffeine methhydroxide
C8H10O2N4.MeOH
Q,HuOaN4
....
137-138
Schmidt
B., 16, 2588
46, 339
Ethylic cyanurate
EtO.C:N.C(OEt):N
C9H15ON
29
Mulder
R. T., 1, 191
44, 304
j
.C(OEt) : N
\
Phoronoxime
C9H14:N.OH
^»
218 c.
48
Nageli
B., 16, 496
44, 728
Pseudopelletierine +2H2O ...
cf. C. R., 88, 716
11
246
46
Tanret
B. S., 36, 256
36, 658
Ecgonin
....
C9HI503N
+H20
198
Lossen
A., 133, 365
Triethylic cyauurate
....
C9H1503N3
195
Liquid
Cloez
A., 137, 127
vi., 520
„ „ (normal)
(CN.OEt)3
n
....
28
Ponomareff
B., 15, 514
11 i' 11
11
*)
250 (40-50)
29
Mulder
B.,15,71;16,390
42, 590
11 *i
....
?>
235
95
Hofmann
13, 322
ii., 292
» 11
....
)»
....
95
Mulder
B., 16, 390
11 >i
»)
95
Hofmann
B., 3, 766
24, 136
11 11
)>
253
95
Wurtz
J., 7, 567
1> »
....
j)
276
95
Richter
R. K. T., 227
Amidocamphoronic acid
....
C,H1505N
....
212
Hjelt
B., 13, 799
38, 670
Ammonium anhydrocam-
C9H1805N2(?)
,, (?)
125
Kachler & Spitzer
M. C., 6, 173
48, 807
phoronate
Triglycollamic triuramide ...
(NH.CONH.CO.CH2)3N
C9H1606N7
cf.B.,5,1013
nf. 230
Mulder
B., 6, 1016
27, 48
Nitrosotriacetonamine
....
C9H1602N2
....
72-73
Heintz
A., 185, 6; 187,
233
Amidocamptioronamide
....
C9H1604N2
....
160
Hjelt
B., 13, 797
38, 670
Triacetonamiue
CO : (CH2.CMe2)2 : NH
c9n,7oN
....
34-6
Heintz
A., 178, 305
29, 382
11 ....
»
))
....
39-6
»
A., 174, 144
28, 351
>i
))
J)
+H20
58
ii
A., 178, 305
29, 382
Methylpelletierine
»
215
Liquid
Tanret
C. R., 90, 695
38, 481
-methyltopine
»
243
....
Ladenburg
B., 14 2127, 2404
42, 216
COMPOUNDS CONTAINING FOUR ELEMENTS.
501
Name.
Constitution.
Formula.
""••
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
«-methyltropine .... ..«
C9H,.ON
240-245
....
Merling
B., 14, 1830
42, 216
s- „
C7H10.OH.NMe2
)I
198-205 d.
Ladeuburg
B., 14, 2404
)>
Isonitrosoisobutylketone
C9H1702N
....
42
Lang
B., 18, 1364
Ethylic hydroxypentamate ....
....
C9H17O3N
77-77-5
Demarcay
A. C. [5], 20, 488
Ammonium hydroxycam-
C9H13(NH4)0,
C9Hir06N
....
178,
Kachler
A., 191, 143
34, 513
phorate
Isononylamide
CMe2.(CH2)3.CHMe.CO.NH2
C9H19ON
80-81
Kuhlhem
A., 173, 319
28, 354, 884
,, .... ....
1J
)»
81
»)
A., 176, 308
vii., 898
Pelargonamide
CH3.(CH2)7.CO.NH2
7«
92-93
Schalfejeff
B., 6, 1252
27, 255
.,
J?
?r
99
Hofmann
B., 15, 984
42, 950
,,
C8H17 CO.NH2
Ji
105
Kuhlhem
A., 176, 308
28, 884
Ethyl tenauthaldoxime
....
If
185-18T
Liquid
Westeuberger
B., 16, 2993
46, 581
Triacetonalkamine
.....
j'
....
128-5
Heintz
A., 183, 309
31, 592
Pseudotriacetonalkamine
»
....
180
5>
A., 183, 304
»
Tetraethylcarbamide
NEtj.CO.NEtj.
CJH^ON,,
205
Liquid
Michler
B., 8, 1664
29, 702
)>
H
1)
210-215
Liquid
Wallach
B., 14, 747
Isobuty 1 bu ty Icarbam ide
CMej.NH.CO.NHBu/9
»
....
163
Brauner
B., 12, 1875
38, 228
Dibutylcarbamide
CMe3.NH.CO.NH.CMe3
»
242
)j
»
ij
(Enanthodiure'ide
C6H13.CH(NH.CO.NH2)2
C9H2002N4
166 d.
Schiff
A., 151, 186
Oxalyldiethylhydrazine
CO(NH.NEt2)2
C9H22ON4
204
Fischer
A., 199, 297.
From ethylcarbaiuiue
cf. B. S., 11, 221
C9H2202N4
112
Gautier
C. R., 67, 8041
vi., 529
/3-Tetranitronaphthalene
C10H4(N02)4
C10H=0SN4
200
Lautemann and
Z. C42], 1, 564
vi., 849
Aguiar
/9-
>»
IT
200
Aguiar ,
B.,.?, 376, 904;
25, 700 ; 26,
A., 169, 100
175; vii., 835
a- „
>J
»
259
»-
ii
)!
Tetranitro-a-naphthot
Jambosin
C10H3.OH.(N02)J
C10H409N4
c «HCO N
180
77
Merz.«adj Weith
Gr6X1lj3J'd
B., 15, 2715
P. J. [3], 14,717
44, 344
48, 396
Nitro-j9-naphthoquinone
O.O.NO^W, ; (9
^lO-'-^-s^'a1-1
C10H604N
158
Stenhouse & Groves
A., 194, 203
33, 417
»
» =•,".»;(»)
)J
....
158
Liebermanu
B., 14, 1313
Nitrohydroxynaphthaqui-
C10H4(N02)(OH):02
C10H605N
157 d.
Diehl and Merz
B., 11, 1318
34, 888
none
?-Trinitronaphthalene
ClnH5(N02)s
C10H506N3
b. 100
Marignac
....
iv., 15
?-
»•
)>
....
101-103-
Beilstein and Kuhl-
A., 169, 81
27, 160
berg
a- „
»
)»
122
Aguiar
B., 5, 372, 898
25, 700 ; 26,
174; vii., 834
y- »'
Ji-
))
147
Beilstein»and Kuhl-
A., 169, 97 ; B.,
26, 69, 1138; 27,
berg
5, 480 ; 6, 648
160; vii., 835
y- n
lt
J»
154
Aguias-
B., 5, 903
26, 175
»-
«
)5
181
Staedel
A., 217, 153
44, 863
fl-
T>
)»•
208
Beilstein. and K.uhl-
B., 5, 480
26, 69; vii.,
berg
835
0-
»
»
....
210
Laurent
A., 41, 98
iv., 15
0-
»»
J)
....
210
Staedel
B., 14, 901
40, 724
0-
M
))
210
»
A., 217, 174
44, 863
0-
»»
))
SIS
Beilstein and Kuhl-
A., 169, 96 ; B.,
26, 1138; 27,
berg
6, 648
160
0-
J)
1>
214
Lautemann and
Z. C. [2], 1, 564
vi., 848
Aguiar
0-
J*
)>
....
215
Laurent
Gin. vii. [1], 87
iv., 15
0-
»
»
....
218
Aguiar
B., 5, 375, 905
25, 700; 26, 175
Trinitro-a-naphthol
C10H4.OH.(N02)3
C10H507N3
176
Ekstrand
B., 11, 162
34, 508
„ -"- ,,
))
))
176
Merz and Weith
B., 10, 1232
32, 899
» -«-
»
))
....
177
Diehl and Merz
B., 11, 1662
j. -Q- j>
....
»J
177
Bourcart
B., 12, 679
a-Tetranitronaphthylamine....
C10H3(N03)4.NH3
C10H609N5
....
194
Merz and Weith
B., 15, 2718
44,344
P-
))
?)
202
»
B., 15, £720
»»
Pyridine pentacarboxylic acid
C5N(COOH)5
ClnH6010N
d.w.m. 220
Hantzsch
A., 215, 62
44, 85
n-isonitroso-/3-napthhone
C6H4.CH:CH.C:C.N.O.N
C10H6ON2
77; 78
Goldschmidt
B., 17, 216, 803
46, 735, 1137
J =1.2
502
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Pyrocoll
» .... .... ....
C4H3N.CO.C4H3N.CO
C10H602N2
»
....
267
268-269
Ciamician and
Silber
Weidel and Ciami-
B.,17,106;G. I.,
13, 563
M. C., 1, 281
46, 586, 726
40, 290
)T
cian
y -Diuitrouaphthalene
(N02)2=afl ;
CIOH,04Nt
144
Liebermann
A., 183, 274
31, 609
y-
)> >J
))
144
Liebermann and
B., 9, 334
30,81
Hammerschlag
l.
„ =?
))
....
155-1 CO
Ekstrand
B., 17, 1602
46, 1361
•l-
„ =ft;7
V
161-5
Grsebe and Drews
B., 17, 1172
46, 1036
/3-
„ =(»), ;
»>
167
Beilstein and Kuhl-
A., 169, 86
27, 159
berg
ff-
" M
»1
169
Ekstrand
B., 18, 77
48, 548
/»-
y» 11
?>
....
170
Beilstein and Kur-
A., 202, 224
batow
B-
n -)i
n
....
170
Ekstrand
B., 17, 1602
46, 1361
0-
» w
^i
170
Darmstadter and
Z. C. [2], 1, 555
vi., 848
Wichelhaus
a-
>» »
»
170
Aguiar
B., 5, 372, 904
25, 700; 26,
175 ; vii., 834
e-
»» »
>j
....
170
Liebermann and
A., 183, 225 ; B.,
30, 81 ; 31, 60!)
Hammerschlag
9, 334
3-
TJ «»
u
170
Ladenburg
B., 11, 1650
36, 232
0-
V >»
j>
170
Atterberg
B., 9, 1188
t-
H ')
4t
185
....
....
iv., 15
0- „
„ =(ij.; «5
•»
210
Lautemann and
Z. C. [2], 1, 564
vi., 848
Agniar
a- „
»i -»»
»»
210
Liebermann
A., 183, 225
31, 609
a- „
« »
>:
....
211 ; 212
Beilstein and Kuhl-
A., 133, 225 ;
24, 694; 26, 69;
berg
169, 86 ; Z. C.
27, 159 ; 31,
[2], 7, 211; B.,
600 ; vii., 835
5, 480
a- „
»» v
it
....
214
Aguiar and Bayer
B., 4, 251
24, 356
<i- „
» M
M
214
Liebermann and
B., 9, 334
30,81
Hammerschlag
a- „
»> •»
»>
215
Ladenburg
B., 11, 1651
36, 232
«- „
»> )>
J)
216
Aguiar
B., 5, 372, 897
25, 700; 26, 171
a- „
» ji
)5
....
217
Atterberg
B., 9, 1188
Nitroquinoline carboxylic
N.COOH=a1fli1;
)1
219-220
Dobner and Miller
B., 15, 3076
acid
Dinitro-a-naphtliol (Martius
OH^NOj^a.ajB, ;
C10H606N2
130
Clev-e
B. S. [2], 26, 241
31, 208
yellow)
r> •"• 11 fi
>t r>
>i
....
137-138
Fuchs
B., 8, 629
»i ~°~ 11 ))
»' '•"
1>
137-138
Neville & Wintlier
• •<•
37, 632
)! -<»- »1 11
•?•> ri
»
....
138
Darmstadter and
A., 152, 299
vi., 856
Wichelhaus
11 -|l- 11 )1
»i 7)
)»
138
Liebermann
A., 183, 249;
28, 1023; 31,
B., 8, 689
603
.. -0- 11 ,1
1J IT
1)
....
138
Ebell
B., 8, 564
28, 900
1, •" 11 ,,
JJ JT
»1
138
Martius
Z. C. [1868], 80
» 'ft- 1.
OH.NOs;NOa=A?;31
»
194
Grcebe and Drews
B., 17, 1171
46, 1036
1) )!
11 11
W
195
Wallach and
B., 3, 846
24, 355 ; vii.,
Wichelhaus
841
11 11 ••••
11 11
»
197
Armstrong
B., 15, 203
Trinitro-a-naphthylamine ....
C10H,(NH2XN0.2)3
C10H606N4
....
264 d.
Staedel
B., 14, 901
40, 724
11 •«' 11
)1
1)
240-266
11
A., 217, 173
44, 863
11 -£- i)
I)
»)
cf. A., 217,
d. 266
11
B., 14, 901
40, 724
174
Dinitro-fl-methylumbelli-
ferone
(N02)2.(HO).C6H.CMe : CH.
010H607N2
....
220
Pechmann and
Cohen
B., 17, 2137
46, 1332
C00=(?)2.1.4.5
Cinnanyl cyanide
C6H5.CH:CH.CO.CN
C10H7ON.
114-115
Claisen and Ant-
B., 13, 2124
40, 169
weiler
COMPOUNDS CONTAINING FOUR ELEMENTS.
503
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Nitrosonaphthalene
C10H7.NO
C10H.ON
d. 134
84
Baeyer
B., 7, 1640
28, 452
„
„
„
....
89
„
B., 8, 616
Hydroxycomazone ....
....
C10H7ON3
340-360
Krippendorff
J. p. [2], 32, 153
48, 1243
Phenylmalemimide
CO.CH : CPh.CO.NH
i i
C10H.02N
210-211
Perkin
B., 14, 2547
n-Nitronaphthalene ....
C10H7.N02
11
43
Laurent
A., 78, 31
iv.,14;vii.,834
"' „
„
I'-
56-261
Mills
P. R. [1881], 205
«- »
11
ll
58
Liebermann
A., 183, 234
31, 600
a- .,
11
11
....
58
Liebermann and
B., 7, 245
27, 692
Dittler
«- „
11
11
304
....
Koninck and Mar-
B., 5, 12
26, 303
quart
n- „
,1
>1
303-304
58
Jacobson
B., 14, 1793
«- ,1
11
„
58-5
Beilstein and Kuhl-
A., 169, 81 ; Z. C.
24, 695 ; 27,
berg
[2], 7, 211
159
a- •_ ,1
11
„
58-5-59
Guareschi
G. I., 7, 24
31, 712
"- »
U
„
....
59
„
A., 222, 262
46, 842
"- ..
11
11
61
Aguiarr
B., 5, 371
25, 699 ; vii.,
834
n- „ (cf.G.I.,14,181)
11
n
IBM
61-5
Schiff'
A., 223, 247
46, 1089
Nitrosonaphthol
OH.N02=ftai;
11
cf.B.,15,1817
109-5
Stenhouse &.G roves
A., 189, 146
32, 50
.,
n »
11
cf.B.,17,801
110
ffuchs-
B., 8, 1026
29, 248
n =«A ;
„
cf. B.,8, 689
145-15t)d:.
„
B., 8, 626
28, 1023
r,
11 11
11
....
147-148
Worm s^
B., 15, 1816
11
n 11
11
....
150-152
Ilinski
B., 17, 392
..
ii' 11
11
152
Goldschmidf
B., 17, 215, 801
11 •••• *•••
„ =tt,n2;
11
....
175-185
Cleve
B. S. [2], 26, 241
31, 208
11
11 11
•1
cf. B., 8, 689
175-185
Fuchs
B., 8, 627
28, 1023
„
D ir
„
190 d.
Goldsclimidt and
B;, 17, 2065
48, 168
Schmidts
,|
» ir
„
190
Ilinski .
B., 17, 2590
Quiuoline carboxylic acid ....
N.COOH=a>,31 ;
11
....
756
Dobner iftndl Miller
B., 16, 2473
46, 185
n i, » •».
.> »
11
157
Jacobsen & Reimer,
B., 16,. 2605
46, 336
)j 11 D
„ =n.n,,;
„
....
253-254
Forst-& Bohringer
B., 18,' 520
42,982
(cinchonic)
•i 11 11
,,-
„
250 u.c.
Clans anil Weller
B., 14, 1922
11 11 ?>
i> ,,
11
356 u.c.
Skraup
B., 12, 233
36, 656
11 ji *••
u — fll/-*3 »
„
271-272
Riedel
B., 16, 1613
44, 1152
11 'i •*
.. 11
11
273
Dobner and Miller
B., 18, 1644
11 11 •••
'» 11
»
275
Grsebe and Caro
B., 13, 101
38, 398
»i 11 ••••
11 — "i ! n\
11-
186-187-5
Schlosser & Skraup
M. G, 2, 530
42, 72
11 11
11 11
n
185-186
Coste
B., 15, 196
,1
?> 11
„
187
Skraup
B., 15, 893
42, 1111
i» 11
=«,;/3,
11
....
255-257
Fischer and Loo
B., 17, 1901
46, 1372
11 n
V ~~aj i &2
„
291
Skraup
B., 15, 893
42, 1111
11 n ••••
1. »
u
brown 280
291-292
Schlosser & Skraup
M. C., 2, 526
42, 72
D 11
„ =«, ; (i.
11
....
a. 350
Skraup
B., 15, 893
42, 1111
n i)
., ,,
„
a. ftfiO
Schlosser & Skraup
M. C., 2, 519
42, 71
u 11 ••••
11 11
11
....
a. 360
Bedall and Fischer
B., 14, 2574
Acetylisatin ....
G-H ..CO.CO.N Ac= 1 .2
P TT O V
Qntdfl
B. 11 585
34, 586
i i
1U 7 3^-
DUUJA
Phthalylacetamiile
C6H4 : (CO)2 : CH.CO.NH2
11
200 d.
Gabriel & Michael
B., 10, 1556
34, 230
= 1.2
Nitronaphthol
OH.N02=/3ini ;
11
96
Stenhouse & Groves
A., 189, 153
32, 51 ; 40, 736
11 •••• ••••
D D
)1
100
Dusart
C. R, 52, 1183
iv., 117
„ 1!
v
....
102-103
Jacobsen
B., 14, 1792
11 •••• ••••
„ • =/3,jS.,; (?)
11
103
„
B., 14, 806
40, 736
i^ ....
„ =(»),;
11
....
116
Lellmann
B., 17, 112
46, 752
n
» =nA ;
11
....
127
Fuchs
B., 8, 629
11 n
11
128
Liebermann and
B., 7, 243; A.,
27, 692 ; 31,
Dittler
183, 246
599
11
•i 11
V
....
128
Nolting and Wild
B., 18, 1339
51 .... ....
,i 11
„
....
128
Worms
B., 15, 1815
44,69
504
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrouaphthol
OILNO^S,;
C10H;OaN
...<
128
Liebermann
B., 8, 689
28, 1023
„
„ =a,?
„
151-152
Darmstauter and
B., 3, 944
vii., 841
Nathan
„ ..,.
„ =0,-..,;
„
....
164
Cleve
B. S. [2], 26, 241
31, 208
\
„ „
„
cf. B., 8, 689
16 '4
Liebermann and
B., 7, 243; A.,
27, 692 ; 31,
Dittler
183, 246
599
,,
„ „
„
....
164
Lellmann
B., 17, 113
„
,, „
„
....
164
Audreoni and Bie-
B., 6, 343
28, 1023
dermaim
„
n »
,.
....
164
Worms
B., 15, 1814
„ ....
» »
„
164
Ebell
B., 8, 563
28, 900
«-Hydroxyciuchonic acid ....
N.OH.COOH= ?
,,
•...
254-256 u.c.
Weidel & Cobeuzl
M. C., 1, 857
40, 743
?- .. » (Ky-
)J >»
„
257-258 p.d.
Kretschy
M. C., 2, 58
40, 827
nuric acid)
/3-Hydroxycinchonic acid ....
„ „
»
....
320
Weidel
M. C., 2, 571
42, 226
Xanthoquinic acid ....
„ „
„
a. 30.) p.d.
Skraup
M. G, 2, 587
42, 223
j3-Carbostyrilcarboxylic acid
V — -.Jj'^if^.. j
>»
a. 320
Friedlander and
B., 17, 460
46, 1020
Gohring
Jugloxime
HO.C10H5O : NOH
187-187-5
Bernthsen and
B., 18, 208
48, 547
si
Semper
Phthalylglycocine
C6H4 : (CO), : N.CH2.CO2H
C10H704N
....
191-192
Drechsel
J. p., 27, 418
44, 1126
=1.2
Dinitronaphthylamine
N l±^.\^i^\.)^)»^~^\a^pl j
C10H704N3
....
233
Ebell
B., 8, 564
28, 900; 40,
1132
»
15 1)
M
....
SS5
Liebermann and
A., 183, 274; B.,
30, 81 ; 31, 608
Hammerschlag
9, 333
„
=/»*;/»,
J)
238
Grsebe and Drews
B., 17, 1172
46, 1036
Nitrocinnamylformic acid ....
NO2.(CH : CH.CO.CO2H)
C10H705N
135-136
Baeyer & Drewsen
B., 15, 2862
44, 341
=1.2
Nitrobenzalmalonic acid
NO2.[CH:C(CO2H)2]=1.2
CieH70«N
....
161 d.
Stuart
....
47, 156
,, ,,
= 1.3
D
205 d.
„
....
47, 157
» ,i
=1.4
„
....
227 d.
„
47, 158
Nitrocarboxylcinnamic acid
(CH : CH.CO2H).NO2.CO2H
„
....
287 d.
Low
B., 18, 949
48. 799
=1.2.4
Pieoline tetiacarboxylic acid
05NMe(CO2H)4
C10H708N
....
199 d.
Hantzsch
A., 215, 57
44, 85
Nitroso-fl-amidonaphthalene
CJOH6.NO.NH2
C10H8ON2
150-152
Ilinski
B., 17, 392
46, 1035
Nitronaphthylamine
NH2.NO,=a,; a.
C10H802N2
118-119
Beilsteiu and Kuhl-
A., 169, 87 ; Z. C.
24, 695 ; 27,
berg
[2], 7, 211
160
„
)» "l^l >
»
.„.
123-124
Meldola
47, 520
»
» =ft«i ;
„
cf.A.,211,64
126-127
Jacobsen
B., 14, 1793
' „
» »
„
....
126-127
Wittkampf
B., 17, 395
46, 1036
„
,1 =a. j
„
144
Lellmann
B., 17, 112
46, 751
» =0.01 5
„
....
158-159
Liebermann aud
A., 183, 233 ; B.,
27,692; 31,600
Dittler
7,242
„
» =",«: ;
,,
190
Lellmann
B., 17, 110-113
46, 751
,.
)5 5'
D
191
Liebermann and
A., 183, 233 ; B.,
26, 1232; 27,
Dittler
6, 947 ; 7, 242
692 ; 31, 599
„
)> V
»)
....
191
Cleve
B. S. [2], 26, 241
31, 208
„
„ =1
....
198
Lellmann
B., 17. Ill
46, 751
Diisouitrosonaphthalene di-
C10H6(NOH)2=a101 ;
D
p.d. 140
149
Goldsdmidt and
B., 17, 2067
46, 1359
hydride
Schmid
Nitrosomethoxyquinoline ....
N.OMe.NO= ?
H
80
Bedall and Fischer
B., 14, 2572
42, 413
Nitroquinaldine
N.Me ; NO2=a,^1 ; a, or 0,
„
82
Dbbner and Miller
B., 17, 1702
46, 1373
,,
„ =«i/3,; «,
137
„
B., 17, 1700
M
Nitro-p-toluquinoline
v — - '
116-116-5
Fourneaux
B. S., 42, 337
48, 400
Methylcinnoline carboxylic
• i
CMe I CH.N2.0(.,H3.COOH
1 J
»
230 p.d.
Widmann
B., 17,724
46, 1022
acid
Nitro-amido-a-naphthol
OH.NH2.NO2=ra(!).,
C10H803N2
130
Ebell
B., 8, 564
28, 900
Nitromethylcarboatyril
tJ
181
Feer and Konigs
B., 18, 2397
48, 1235
Nitrophenylsuccinimide
NOJ.C6H4.N.CO.(CH2)2.CO
C10H804N2
....
137
Taylor
A., 209, 374
42, 181
=1.2
COMPOUNDS CONTAINING FOUR ELEMENTS.
505
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrophenylsuceinimide
N02.C6H4.N.CO.(CH,,)2CO
C10H804N2
....
156
Taylor
B., 8, 1225
29, 602
=1.2
„
=1.4
„
....
208
„
B., 8, 1225 ; A..
29, 602; 42,
209, 375
181
Nitroso-amido-j9-methyl um-
fr. CeH2(OH)(NH,).CMe :
.. '
140
Pechmann & Cohen
B., 17, 2138
46, 1332
bel 1 if erone
CH.COO=1.?.4.5
Harminic acid
...»
Jl
darkens 300
345 d.
Fischer & Tauber
B., 18, 403
48, 820
Methylic dinitrocinnamate ....
NO2.[CH I C(NO2).CO2Me]
C10H806N8
127
Friedlander and
A., 229, 210; B.,
48, 1137
=1.4
Miihly
16, 850
II II
....
JJ
....
104
Friedlander
B., 14, 2577
42, 402
Methoxydinitrocinnamic acid
(CH : CH.C02H).OMe.(N02)..
CIOH807N2
192-193
Perkin
....
39, 417
Dinitrodiacetylhydroquinone
(OAc)2.(N02)2=1.4.(?)2
C,0H808N2
...»
94
Hesse
A., 200, 246
38, 317
„
JJ JJ
Jl
cf.A.,215,143
96
Nietzki
B., 11, 470
Ethylic dinitrophthalate
CO2Et.CO2H.(NO2)!!=l. 2.3.5
JJ
cf.A.,202,227
18&-187
Beilstein and Kur-
B., 13,354;B. S.
38, 478 ; 40,
or =1.2.4.6
batow
[2], 34, 327
436
Phenyl a-hydroxycrotono-
Ph.CH : CH.CH(OH).CN
C10H9ON
75
Peine
B., 17, 2113
46, 1344
nitril
11 51
JJ
11
80^81
Pinner
B., 17, 2010
46, 1292
Acetamidophenylacetylene ....
C6H4(NHAc).C!CH=1.2
C6H4.CH2.CAc : N=1.2
«
75
182-183
Baeyer& Landsberg
Baeyer
B., 15, 60
B., 12, 1314
42, 623
36, 938
i i
"
Methoxyquiuoliue (methyl-
N.OMe=a,/31 ;
„
246-247 u.c.
Friedlander and
B., 15, 336
42, 733
carbostyril)
Ostermeier
„
•I =»i; ai
„
265-268 u.c.
Liquid
Skraup
M. C., 3, 544
44,91
-,
M JJ
„
....
Liquid
Bedall and Fischer
B., 14, 2570
48, 412
11 =<"i ; #1 or a2
t*
275(720)p.d.
Liquid
Fischer
B., 15, 1980
44, 91
„
„ =o,; ft
„
....
Liquid
Skraup
M. C., 3, 557
11
Hydroxymethylquinoline ....
N.Me.OH^^fta.,;
„
distils
sax
Knorr
B., 16, 2596
46, 334
,, ....
11 »
„
222
....
D. P., 250, 533
46, 757
(Hy-
„ =a,3,; ii.
„
266-267
74
Dobner and Miller
B., 17, 1706; D.P.,
46, 1374; 48,
droxymethylquinaldine)
256, 134
945
11 11
„ =ii3,; ft
„
....
213
„
„
„
11 •!
„ =a101; /3,oro,(?)
,,
....
230
„
D. P., 256, 134
48, 95
J» 11
„ „
11
cf. 220
S32-23&
„
B., 17, 1709
46, 1375
Hydroxymethylquinoline ....
„ =a,; a,/3,(?)
11
....
92-93
Herzfeld
B., 17, 906
46, 1199
„
11 =ai 5 ftai
„
....
94-96
„
B., 17, 905
11
n
11 11
„
95-96
Fischer & Willmack
B., 17, 441
46, 1051
„
i. 11
„
....
95-96
Herzfeld
B., 17, 1552
46, 1199
ii
11 =«"i! "ift
„
220
„
B., 17, 903
n
ii
11 ^al J aia2
„
....
245-248 p.d.
„
B., 17, 1551
n
ii
„ „
„
....
a. 260
n
B., 17, 903
„
? (base)
....
„
280 d.
....
J. E., 11,322
Ciniiamylforniamide....
Ph.CH :CH.CO.CO.NHa
C10H9OaN
...»
129-130
Claisen & Antweiler
B., 13, 2124
40, 169
Phenyl suceinimide (cf. A.,
Ph.N.CO.(CH2)2.CO
JJ
abt 400
150
Taylor
A., 209, 373
68, 27 ; 162, 166)
Ethylic cyanbenzoate
CN.COOEt=1.4
JJ
54
Muller
B., 18, 2485
48, 1227
Etliylphtlialimide
C6H4.CO.NEt.CO=1.2
| J
JJ
276-278
78-5
Wallach and Ke-
B., 14, 171
40, 285
„
11 M
JJ
cf. A., 215, 194
78-79
menski
Michael
B., 10, 1644
34,70
Acetyl oxindole
C6H4.CHAc.CO.NH=1.2
I |
JJ
126
Suida
B., 12, 1327
36, 937
„ „
JJ
130
„
B., 11, 587
34, 587
Ethy Ipseud isatine
Ethylisatine .... ....
C6H4.CO.CO.NEt=1.2
i i
C6H4.CO.C(OEt) I N = 1.2
JJ
95
Baeyer
Piiiicksch
B., 16, 2194
B. 17 2806
46,75
48, 256
i i
JJ
....
Skatole carboxylic acid
C9H8N.COOH
JJ
161 d.
Salkowski
B., 13, 193
» » ii
„
JJ
....
164
„
B., 13, 2218;
40, 175 ; 48.
Z. P. C., 9, 8
569
?-acid
Ph.N.N I CMe.N : C.CO2H
JJ
Clt)H O N
206
17K 177
Fischer & Jourdan
BLidin
B., 16, 2245
B., 18, 1547
46, 53
48, 980
i 1 \> — itt
3 T
506
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet-
& J. Ch.Soc.
Isonitrosomethyloxyquinizine
C6H4.N.NH.CMe.C(N.OH).
C..HAN,
sb. b. 100
157
Knorr
B., 17, 2042
46, 1378
CO=1.2
|
Phenylmalimide
Ph.N.CO.CH2.CH(OH).CO
C10H903N
....
170
Arppe
A., 96, 109
iii., 798
i i
Isonitrosobenzoylacetone ....
Ph.CO.C(NOH).CO.Me
„
....
'123-5-124
Ceresole
B, 17, 815
46, 1168
Nitrocinnamyl methylketone
N02.(CH I CH.COMe)=1.2
„
....
58-59
Baeyer & Drewsen
B., 15, 2858
44, 341
ii >i
» J1
)J
60
Fischer and Kuzel
B., 16, 36
„ „
=1-4
„
....
110
Baeyer and Becker
B., 16, 1969
44, 1120
Ethylphthalylhydroxylamine
C6H4.CO.N(OEt).CO=1.2
„
270 p.d.
103-104 u.c.
Cohn
A., 205, 295
40, 586
I i
Acetyldioxindole
fr. C6H,.CH(OH).CO.NH
MM
127.
Suida
B., 12, 1327
36, 937
1 1 1 0
Aniido-£-methylumbelli-
— i,Z
C6H2(NH2)(OH).CMe : CH.
247
Pechmann & Cohen
B., 17, 2138
46, 1332
i
ferone
COO=?.1.4.5
i
1
Nitroacetamido-a-toluic nitril
NHAc.NO2.(CH2.CN)=1.2.4
C10H903N3
....
112-113
Gabriel
B., 15, 836
42, 1070
Isomtrosomethyldioxyquini-
C6H4.N.N(OH).CMe.
!t
135
Knorr
B., 17, 2042
46, 1379
i
zine
C(NOH).CO=1.2
Phenyltartarimide
Ph.N.CO.(CH.OH)2.CO
C10H904N
230 d.
Arppe
A., 93, 354
i i
Nitrobenzoylacetone
NO2.(CO.CH2.COMe)=1.2
..
55
Gevekoht
A., 221, 323
46, 445
Methylic nitrocinnamate ....
NO^CH : CH.CO2Me)=1.2
IT
72-73
Beilstein and Kuhl-
A., 163, 131 ;
25, 710
berg
Z. C., 7, 616
,. »
=1.4
„
200
161
Kopp
C. B., 53, 636
i., 988
» i>
ii i»
„
281-286
161
„
J. [1861], 420
Acetylisatic acid
NHAc.(CO.CO2H)=1.2
II
160
Suida
B., 11, 586
34, 586
Nitropropenylbenzoic acid ....
CO2H.NO2.(CMe : CH2)
„
....
154-155
Widmaun
B., 15, 2552
44, 330
=1.3.4
Nitrosobenzylmalonic acid ....
Ph.CH2.ON : C(COjH),
C10H905N
cf. B., 16, 609
120 d.
Conrad and Bischoff
A., 209, 217
42,39
Nitromethoxycinnamic acid
(CH : CH.C02H).OMe.N02
n
....
238
SchnelL
B., 17, 1383
48, 1165
=1.2.5
Acetamidoisophthalic acid ....
(CO2H).NHAc. = 1.3.?
m
....
270-280 d.
Hofmann
B., 9, 1301
31, 90
Nitrophenylazo-acetoacetic
NCv(N2.CHAc.CO2H)=1.2
CIOHy05N3
black 183
185
Bamberger
B., 17, 2417
48, 557
acid
Nitroacetamidonitrocinna-
(CH : CH.N02).NHAc.NOa
„
250-252
Friedlander and
A., 229, 233
48, 1139
mene
=1.4.?
Lazarus
Dinitroacetamidocinnamene
(CH:CH2).NHAc.(N02)2
u
....
211-212
Gabriel & Herzberg
B., 16, 2041
44, 1123
„
-1.4.(?)2
j)
211-212
Herzberg
C. C. [1884], 35
48, 662
Dimethylic nitroisophthalate
(C02Me)2.NO2=1.3.5
C10H906N
....
121-5
Beyer
J. p. [2], 25, 490
42, 1294
Ethylic nitrophthalate
(CO2Et).(CO2H).NO2
„
A., 160, 60
110-5
Miller
A., 208, 244
=1.2.3 or 6
,, ,,
„ =1.2.4 or 5
„
....
127-128
„
A., 208, 234
Lutidine tricarboxylic acid....
C7H6N.(CO2H)3
„
....
212 d.
Hantzsch
A., 215, 52
44,85
Nitromeconin....
159-160
Anderson
A., 98, 47
iii., 863
Methoxycinnamic acid diazo-
(CH:CH.C02H).OMe.
C10H906N3
d. 151-152
Schnell
B., 17, 1385
46, 1165
nitrate
(N:N.N03)=1.2.5
Nitroacetoisovanillic acid ....
CO2H.OAc.OMe.NO2
C10H907N
....
168-169
Matsmoto
B., 11, 133
34, 501
=1.3.4.6
Nitroacetovanillic acid
=1.4.3.?
„
....
181-182 p.d.
Tiemann and Mats-
B., 9, 943
30, 525
moto
» i,
„ „
n
....
181-182 d.
Matsmoto
B., 11, 133
Nitro-opianic acid
C02H.(OMe)2.COH.N02=2
ii
....
166
Prinz
J. p. [2], 24, 357
42,402
„ „ .... ...
=2
„
248-249
Wegscheider
M. C., 4, 262
44, 998
Nitrohemipinic acid
(C02H)2.(OMe)2.NO;j
C10H908N
155
Prinz
J. p. [2], 24, 359
42, 402
=1.2.3.4.?
Benzenylazoximpropenyl ...
Ph.c : N.o.CEt : N
L 1
C10HI0ON2
255
L. 10
Schulz
B., 18, 1085
48,897
COMPOUNDS CONTAINING FOUR ELEMENTS.
507
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Phenylethenylazoxime-
Ph-CH^C : N.O.CMe 1 N
C10HI0ON2
262
Liquid
Knudsen
B., 18, 1071
48, 898
i >
ethenyl
Acetamido-a-toluic nitril ...
NHAc.(CH2.CN)=1.4
)J
....
95-97
Gfebriel
B., 15, 835
42, 1070
Acetamido-a- (or /S-) phenyl-
NHAc.C6H4.C2H2N=1.4
1)
97
Friedlander and
B., 16, 1024
amphinitril
Miihly
Amidomethylcarbostyril
N.OH=a, ft ;
J)
....
103
Feer and Kouigs
B., 18, 2397
48, 1235
Methylhydroxytoluquin-
C6H3Me.N : CMe.C(OH) : N
)J
....
220 p.d.
Hinsberg
B., 17, 322
46, 1053
1 I
oxaline
=1.3.4
Fr. phenylhydrazine
....
)>
....
127
Knorr
B., 16, 2597
46, 302
?
195-197
G. I., 12, 31
Phenylhydroxyethenylazoxi-
HO.CHPh.C : N.O.CMe.N
C10H1003N2
65
Gross
B., 18, 1076
48, 898
I i
methenyl
Tolylhydantom
Me.(N.CO.NH.CO.CH2)=1.2
))
176
Ehrlich
B., 16, 743
44, 1106
i i
it •"• *•"
=1.4
)1
210
Schwebel
B., 11, 1128
34, 798
Ethylindoxylnitrosamiiie ...
C6H4.C(OEt) : CH.N.NO
i i
»)
84-85
Baeyer
B., 15, 781
48, 1102
=1.2
Ethylnitrosoindoxyl
C6H4.C(OEt) : C(NO).NH
5)
....
135
j)
B., 15, 784
=1.2
Ethylisatoxime
C6H4.C(NOEt).C(OH) : N
))
138
Baeyer and Com-
B., 16, 1707
44, 1131
I I
= 1.2
Sl/ULK
Ethylpseudoisatin-/3-oxime ....
C6H4.C(NOH).CO.NEt=1.2
I 1
»
160-162
Baeyer
B., 16, 2196
46,75
Ethoxycyanamidobenzoyl ....
C7H5(CN)NO.OEt
>J
*...
173
Griess
B., 2, 416
m-nitrocuminonitril
CN.Pr.NO2=?
»
....
71
Czumpelik
B., 2, 183
Azobenzene acetacetic acid ..,.
Ph.N2.CHAc.CO3H
C10H1003N2
154-155
Meyer
B., 10, 2076
34, 396
jj jj jj ..-
»
))
154-155
ZUblin
B., 11, 1419
34, 880
Phenyl di-isonitrosopropyl
Ph.CO.(C.NOH)2.CH3 (?)
))
....
115 d.
Ceresole
B., 17, 816
46, 1168
ketone
Phenyl di-isonitrosoethyl-
Me.CO.(C.NOH)2.Ph (?)
*J
....
178-179 d.
j)
))
»J
methyl ketone
Nitrosotetrahydrocinchoninic
....
))
....
137
Weidel
M. C., 3, 73
42,533
acid
Hydantom of tyrosine
5»
275-280 d.
Z. P. C., 6, 254
Ethylic oxalnitraiiilate
N02.(NH.CO.C02Et)=1.2
C10H1006N2
....
112
Hubner
A., 209, 368
42, 180
Ethylic nitrophenylisonitro-
N02.[C(NOH).CO2Et]=1.2
»
....
163
Gabriel and Meyer
B., 14, 826
40, 730
soacetate
j> ii
» jj
)>
....
163-163-5
Gabriel
B., 16, 519
44, 920
Ethylic dinitro-a-toluate
(CH2.CO2Et).(N02)3=1.2.4
C^H^OeN,
35
Gabriel and Meyer
B., 14, 824
Dinitrocuminic acid
C02H.Pr.(N02)3
))
cf. A., 69, 244
220
Lippmann and
B., 12, 79
Strecker
Dinitrodurylic acid
Meb.NO2.CO2H=1.2.4.3.6.5
II
205
Gissmann
A., 216, 207
44,334
Diacetdiamidodinitrobenzene
N2H2Ac2.(NO2)2=?
C10H1006N4
....
245-246
Norton and Elliot
B., 11, 328
34,417
5)
(NHAc2).(N02)2=1.4.(?)3'
))
258
Biedermanu and
B., 7, 1532
Ledoux
Ethylic dinitromethoxy-
CO2Et.OMe.(NO2)2=1.2.(?)2
C10H1007N2
47
Salkowski
A., 173, 50
28,72
benzoate
j» jj
=1.4.(?)3
79
jj
A, 163, 59
Methylic dinitroethoxyben-
CO.,Me.OEt.(NO2)2=1.2.(?)2
»)
80
jj
A., 173, 43 ; B.,
vii., 336
zoate
4,872
28,71
Methylic dinitrohydroxy-
OH.(NO2)2.(CH2.CH2.
»
....
87
Stohr
A., 225, 57
46, 1350
phenylpropionate
CO2Me)=1.2.6.4
Dinitromethoxyphenylpro-
OMe. (NO2)2. (CH2.CH2.COjH)
»
124
jj
J!
jj
pionic acid
=1.2.6.4
Benzoyltrimethyleneoxime ...
Ph.C(NOH).CH.CH2.CH2
C10HnON
86-87
Perkin
B., 17, 1442
44, 1155 ; 47,
! 1
845
Benzoylacetonamine
....
)»
....
143
Fischer and Billow
B., 18, 2134
48, 1237
Mesitylcarbiruide
Me3.(N : CO)=1.3.5.6
»»
218-220
Liquid
Eisenberg
B., 15, 1016
42, 956
Carbomesyl ,
C6H2Me.CH2.CO.NH=1.3.5.6
231-232
Wispek
B., 16, 1580
44, 1096
J)
....
3 T 2
508
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diacetanilide
Ph.NAc3
C10HU02N
....
Ill
Hofmann
B., 3, 771
24, 140 ; vii.,
946
Benzoylacetoxime
Ph.CO.ON : CMe2
M
....
41-42
Janny
B., 16, 172
44, 581
Benzylic iso-nitrosoacetone
CH3.CO.CH : N.O.CH2Ph
j>
45-46
Meyer and Ceresole
B., 15, 3072
44, 572
>» »
»
»
244 u. c.
Ceresole
B., 16, 835
PhenylisonitroetLylmethyl
CH3.CO.CH,,C(NOH).Ph (?)
jj
....
65-5-66
)>
B., 17, 813
46, 1167
ketone
Benzylisonitrosoacetone
Ph.CH2.0(NOH).CO.CH3
»>
....
80-81
»
B., 15, 1876
44, 41
is ,, ••••
I)
))
81
Meyer and Ceresole
B., 15, 3072
44, 572
Anilacetoacetic acid
Ph.N : CMe.CH,.CO3H
»
....
81
Knorr
B., 16, 2595
46, 334
Phenylacetimido-acetate
Ph.CH2.C(OAc.) : NH
»)
129
Luckeubach
B., 17, 1423
46, 1134
Acetamido-acetophenone ...
NHAc.(CO.Me)=1.2
j)
....
76-77
Gevekoht
B., 15, 2086
» »j ••••
» >T
»
76
Baeyer and Bloem
B., 15, 2155
44, 198
Methoxycinnamide .„
OMe.(CH:CH.CO.NH2)=1.4
)»
186
Perkiii
J. [1877], 792
31, 411
n » •••• ••••
=1.2
»
....
191-192
jj
J. [1877], 793
31, 415, 421
Amidopropenylbenzoic acid
COOH.C3H5.NH2=1.4.5
Tl
93-94
Widmann
B., 16, 2573
46, 317
Tetrahydroquinoline car-
N.COOH=ai ; j3, or as
)J
....
146-147
Fischer and Korner
B., 17, 766
46, 1197
boxylic acid
1
....
»J
310 p. d.
66
Bruyn
E. T., 2, 205
48, 657
Dimethylic phenylisonitroso-
Ph.C(NOMe).COsMe
C10HU03N
55-56
Mtiller
B., 16, 2987
46, 584
acetate
.
Ethylic phenylisonitroso-
Ph.C(NOH).CO2Et
J»
112-113
Gabriel
B., 16, 519
44, 920
acetate
Ethylic phenyloxamate
NHPh.CO.CO2Et
»)
cf. B., 4, 600
64-5-65
Klinger
B., 8, 310
28, 1025
»» 1» "••
*»
i>
260-300 p.d.
66-67
M
A., 184, 263
31, 710
Methylic hippurate ....
Ph.CO.NH.CH2.CO2Me
»
60
Jacquemin and
C. E., 45, 1011
iii., 162
Sehlagdenhauffen
»i >»
»?
JJ
d.
80-5
Conrad
J. p. [2], 15. 247
32, 484
,, ,, — ....
'J
>»
....
80-5
Campani & Bizzarri
G. I., 10, 257
38, 870
Benzoylethylcarbamic acid ....
Ph.CO.NEt.CO2H
I)
....
110
Lossner
J. p. [2], 10, 254
28, 641
Benzoyllactamide
CH3.CH(OBz).CO.NH2
»»
....
124
Wisliceuus
A., 133, 281
vi., 772
Phenaceturic acid
Ph.CH2.CO.NH.CH2.CO2H
5»
143
Salkowski
B., 12, 654
36, 662
Acetylphenamido-acetic acid
Ph.NAc.CH2.CO2H
»»
185-186
Giacosa
Z. P. C., 8, 95
46, 1061
Phenylsuccinanaraic acid ....
NHPh.CO. (CH2)2.OO2H
•)
....
148-5
Menschutkin
A., 162, 176
25, 496
Acetoxyacetanilide ....
OAc.NHAc=1.4
„
....
150-151
Ladenburg
B., 9, 1529
31, 305
Acetamido-a-toluic acid
NHAc.(CH2.CO2H)=1.2
))
....
142 d.
Suida
B., 12, 1328
), )» )T
=1.4
V
168-170
Gabriel
B., 15, 841
Malontoluidic acid
Me.(NH.CO.CH2.C02R)=1.4
51
....
156 d.
Eugheimer and
B., 17, 740
46, 1023
Hoffmann
Dimethamidobenzoylformic
NMe2.(CO.CO3H)=1.4
)»
....
187
Michler and Han-
B., 10, 2081
34, 421
acid
hardt
p-toluric acid ....
(C2H2O).NH.C7H7.CO2H
Ifift 1f{>i
Kraut
A., 98, 360
v., 869
Nitro-cuminic aldehyde
COH.Pr3.NO2=1.4.6 "
»
5J
AUVJ — 1 U*J
Liquid
Einhorn and Hess
B., 17, 2019
46, 1352
» »
COH.Pr.N02=1.4.5
)J
....
54
Lippmann and
B., 12, 76
36, 464 ; 38,
Strecker
251
» IT
» »
))
Mil
54
Widmann
B., 15, 167
42, 727
Amidomethoxycinnamic acid
(CH : CH.CX),,H).OMe.NH2
))
189
Schnell
B., 17, 1384
46, 1165
=1.2.5
Hippuryl carbamide
NHBz.CH2.CO.NH.CO.NH.,
C10H1103N3
216 d.
Curtius
B., 16, 757
44, 1088
A midopheny lazoace tacetic
NH2.(N2.CHAc.C02H)=1.2"
)>
157 d.
Bainberger
B., 17, 2420
48, 157
acid
Nitrotolylazoacetone
Me.NO2.(N2.CH2.CO.Me)
»
134-134-5
»»
B., 17, 2421
48, 158
= 1.3.4
Pheuylmalamic acid
NHPh.CO.CH(OH).CH2
C.OH.AN
145
Arppe
A., 96, 106
iii., 798
C02H
Nitro-/9-phenyl lactylmethyl
N02.[CH(OH).CH2.COMe]
J)
58
Baeyer and Becker
B., 16, 1969
44, 1120
ketone
=1.4
» »
=1-2
1>
....
68-69
Baeyer & Drewsen
B., 15, 2857
44, 341
Ethylic nitro-a-toluate
N02.(CH2.CO2Et)=1.4
)»
62-64
Bedson
37, 92
»j i>
»' n
)»
cf. B., 2, 209
64
Radziszewski
Z. C. [2], 5, 358
vi., 1102
» »» »••
>! !>
»»
«««•
65-5-66
Maxwell
B., 12, 1767
38, 120
Acetylhydrindic acid
NHAc.[CH(OH).CO.,H]=1.2
J)
142
Suida
B., 11, 586
34, 586
COMPOUNDS CONTAINING FOUR ELEMENTS.
509
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J.Ch. Soc.
Urethanebenzoic acid
CO2H.(NH.CO2Et)=1.3
C10Hn04N
cf. B.,11, 701
189
Griess
B., 9, 796
30, 413
Dimethylic amidoisophtha-
(CO2Me).,.NH2=].3.5
„
176
Beyer
J. p. [2], 25, 504
42, 1296
late
Ethylic p-nitrotoluate
(CO2Et).Me.NO2=?
„
55
Beilstein & Kreuslei
A., 144, 174
Nitrotolylpropionic acid
Me.NO2.[(CH2)£.CO..H]
„
130-136
Effront
B., 17, 2328
48, 152-
=1,2.5
Propylnitrobenzoic „
CO2H.Pra.NO2=1.4.?
„
....
113
Korner
A., 216, 230
Isopropylnitrobeuzoic acid ....
CO2H.Pr/3.NO2=1.4.5
„
157
Paterno and Fileti
G. I., 5, 383
20, 595
V ))
» ..
„
157-158
Widmann
B., 15, 2548
„ ....
« r>
M
158 u. c.
Lippmanu and
B., 12, 78;
36, 464 ; 38,
Strecker
W. A., 78, 570
251
.. „ ...
n v
„
158
Lippmann & Lange
B., 13, 1661
40, 276
Nitroeugenol
C3H5.OMe.OH.N02= 1.3.4.5
„
43-44
Weselsky & Benedikt
M. C., 3, 388
42, 1201
Nitroxylylacetic acid
Me2.NO2.(CH2.CO2H)
"
....
139
Wispek
B., 16, 1579
44, 1096
Niti odiacetdiamidobenzene ...
(NHAc)2.NO2=1.4.5
C.oH^O^
184
Biedermann and
B., 7, 1533
Ledoux
,1 n
» »
„
186
Ladenburg
B., 17, 148
46, 738
,. „ -
=1.3.2
„
....
246
Barbaglia
B., 7, 1258
28, 273
Dinitromethylhydroquinoline
C9H8NMe(NO2)2
D
148
Feer and Konigs.
B., 18, 2390
48, 1245
Phenyltartaramic acid _
NHPh.CO.(CH.OH)2.C02H
C10HU05N
180 d.
Arppe
A., 93, 355
Ethylic nitromandelate
NO2.[CH(OH).CO2Et]=1.3
„
63
Beyer
J. p. [2], 31, 382
48, 983
Methylic nitrophenyl /3-lac-
NO2.[CH(OH).CH2.CO2Me)
.,
50-51
Einhorn and Praus
B., 17, 1660
46, 1351
tate
=1.2
nitz .
» n „
» »
„
51
Einhorn •
B., J6, 2214
46, 66
» » »
= 1.4
n
....
73-74
Easier
B., 16; 3007.,
46, 604
j» iy w
>r »
„
73-74
Einhorn and Praus
, B., 17, 166L,
46, 1351
nitz .
Ethylic nitranisate
N02.OMe.C02Et=?.1.4
,,
....
98-100
Cahours
A. C. [3], 14, 492
i., 302
Methylic nitrohydro-p-cou-
NO2.OH.(CH2.CH2.CO2Me)
„
64
Stohr
A., 225, 57
46, 1350
marate
=U.4
Nitrohydroxyisopropylben-
NO2.(CMe2 OH).CO2H=5.4. 1
n
....
190-191
Widmann.
B;, 15, 2549
44, 330
zoic acid
Ethoxynitrotoluic acid
CO2Et.Me.OEt.NO2=1.4.2.?
„
....
161-162^
Paterno & Canzoner
G. I., 9, 455
38, 247
Ethylic acetylcomenamate ....
CsH2N.OH.OAc.CO!!Et
„
fr. pyridine
152
Ost
J. p. [2], 29, 57
48, 49
?
NO2.[C(NH2) : N.O.CO2Et]
C10HU06N3
.... .
152-153
Schopff
B., 18, 1066
48, 896
=1.3
Methylic nitro-dimethylpro-
C02Me.(OMe)2.N02=1.3.4.?
C10HuOiN
127-128
Matsmoto .
B., 11, 134
34,502
tocatechuate
Methyh'c nitroveratrate
„ ,,
»-
143-144
11-
B., 11, 132
34, 501
„ dinitro-amidohydro-
NH2.(NO2)2.(CH2.CH2.
C10HUO6N3
102
Stohr
A., 225, 57
46, 1350
cinnamate
CO2Me)=1.2.6.4
Trinitroisocymene
Pr0.Me.(NO2)3=1.3.(?)3 ,
1>-
72-73
Kelbe
A., 210, 54
48,301
Trinitrocymene
Pr«.Me.(NOj)3=1.4.(?), ,
„
119
Fittig and others
A., 145, 142
Trinitroethylxylene
Me2.Et.(NO2)3= ?
„
....
119
Fittig and Ernst
A.,139, 194
v., 1058
>. ,
.. »
IV
119
Eommier
B. S. [2], 19, 434
26, 888
„ „
„ =1.3.5.2.4.6
„
238
Jacobsen
B., 7, 1430
28, 259
Trinitrothymol
Pr«.Me.OH.(NO2)3=1.4
C10Hn07N3
.„.
111
Lallemand
A. C. [3], 49, 153
v., 795
Trinitrodiethoxybenzene
(OEt)2.(N02)3=1.3.(?)3
C.^.O.N,
120-5
Stenhouse
A., 141, 227
I! „
„ =1.4.2.3.5
it-
130
Nietzki
A., 215, 153
44, 466
1! ),
„ „
,,_
...
133
„
B., 11, 1448
34, 867
Phenylallylcarbamide
CO.N2H2Ph(C3H5)
C10H12ON2
....
96-97
Maly
Z. C. [2], 5, 263
vi., 1089
a-phenylhydrazidoisobutyric
Ph.N.CMe2.CO.NH
175
Eeissert
B., 17, 1459
46, 1153
anhydride
1 1
Toluene azoacetone
Me.(Ns.CH2.COMe)=1.4
n-
114-115
Eichter & Miinzer
B., 17, 1928
46, 1342
Tetrahydroquinoline carba-
C,H10N.CO.NH,
„
....
146-5
Hoffmann and
B., 16, 733
44, 1144
mide
Konigs
Methylphenylhydrazinepyro-
Ph.NMe.N : CMe.CO2H
C10H12O2N2
78 ; sf. 70
Fisher and Jourdan
B., 16, 2245
46, 53
racemic acid
Propionylbenzenylainidoxime
NH2.CPh : NO.CO.Et
IT
....
93
Schulz
B., 18, 1084
48, 897
Ethylphenylhydrazinegly-
N2EtPh : CH.CO2H
„
....
121 d.
Elbers
A., 227, 340
48, 535
oxylic acid
510
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Acetylphenylethenylamid-
Ph.CH2.C(NH2) : NOAc
C10H12O2N2
....
124
Kuudsen
B., 18, 1070
48, 897
oxime
Phenylpropionylcarbamide ....
NHPh.CO.NH.C3H5O
n
137
Kiilm
B., 17, 2882
48, 260
Ethylbenzoylcarbauiide
NHEt.CO.NHBz
?)
....
168
Leuckart
J. p. [2], 21, 33
» ••••
H
)»
....
192
Miquel
A. C. [5], 11, 318
32, 870
Ethylphenyloxamide
NHEt.CO.CO.NHPh
n
....
169
Wallach and West
B., 9, 263
30, 184
,, ....
J)
»
of. R, 14, 740
169-170
Wallach
A., 184, 66
32, 186
Phenylsuccinamide ....
NH2.CO.(CH2)2.CO.N HPh
»
....
181
Menschutkin
A., 162, 182
25, 497; vii.,
1103
Methylbenzylacetoximic acid
HON : CMe.C(CH,Ph) : NOH
19
180-181
Schramm
B., 16, 181
44, 590
Isophthalimido methyl ether
C6H4[C(OMe) : NH]2=1.3
„
59-62
Luckenbach
B., 17, 1432
46, 1158
Methy Initrosomethy lace t-
NHAc.(CHMe.NO)=1.2
?!
....
109
Gabriel and Meyer
B., 14, 2340
42, 189
amidobeuzene
Diacetdiamidobenzene
(NHAe)2=1.3
)»
....
189
Kelbe
B., 16, 1200
44, 916
»
» JJ
n
....
191
Barbaglia
B., 7, 1257
28, 273,
»
„ =1.4
»>
a. 295
Ledoux
B., 7, 1531
Xylenedicarboxylamide
(CH2.CO.NH2)2=1.4
>j
a. 290
Klippert
B., 9, 1768
31, 468
Nitrosotetrahydromethoxy-
N.OH=a!; ai
»
80
Bedall and Fischer
B., 14, 2572
quinoline
Nitromethylhydroquinoline
C9H9NMe.NO2
»
...
93-94
Feer and Konigs
B., 18, 2390
48, 1245
Ethylic phenylallophanate ....
NHPh.CO.NH.CO2Et
0IOH120SNS
....
120
Stojentin
J. p., 32, 1
48, 1196
„ benzenylamidoxime
NH2.CPh : N.O.CO2Et
>j
127
Falck
B., 18, 2467
48, 1217
carbonate
Acetylphenylhydroxyethen-
HO.CHPh.C(NH2) : NOAc
»)
....
140 d.
Gross
B., 18, 1076
ylamidoxime
Phenylmethylhydantoic acid
NHPh.CO.NH.CHMe.CO.jH
„
....
170 d.
KUhn
B., 17, 2884
48, 261
Ethylacetonitroanilide
NO2.NEtAc=1.4
))
117-5
Weller
B., 16, 31
44, 579
» ••••
» >!
))
MM
118
Nolting and Collin
B., 17, 267
46, 1013
Ethylic benzenylamidoxime-
C02Et.[C(NH2) : N.OH]=1.4
))
135
Miiller
B., 18, 2486
48, 1227
carboxylate
Urethane benzaniide
(CO:mi2).(NH.CO2Et)=1.3
»
....
157-158
Wachendorff
B., 11, 704
34, 675
Ethylic uramidobeuzoate ...
COsEt.(NH.CO.NH!)=1.3
ij
....
176
Griess
J. p. [2], 4, 293
25,81; vii., 166
Dimethamidophenyloxamic
NMe-2.(NH.CO.C02H)=1.4
))
....
192 d.
Sendtner
B., 12, 531
36, 627
acid
Tolylhydautoic acid
Me.[N(CO.NHs)(CH8.CO2H);
:j
....
d. w. m. 200
Schwebel
B., 11, 1129
34, 798
=1.4
Acetamidonitroethylbenzene
Et.NHAc.NO2=1.4.?
»
-....
45-47
Paucksch
B., 17, 770
46, 1143
Nitroacetoxylidiue
Me2.NHAc.NO2= 1 .3.2.4
»
....
149
Grevingk
B., 17, 2426
48, 145
,,
„ =1.3.4.6
»
....
159-160
»
B., 17, 2425
J>
,1 •...
=1.3.4.?
»>
....
172-173
Hofmann
B., 9, 1297
31,92
„
=1.3.5.?(?)
»
...»
180
Wroblewsky
B., 10, 1248;
34, 55; 40, 433
A., 207, 93
,,
=1.4.(?)2
^»J
....
192
Schaumann
B., 11, 1538
36, 52
Nitrophenylhydroxyacet-
NO2.[CH(OH).C(OEt) : NH;
C10H1204N2
84
Beyer
J. p. [2], 31, 382
48, 983
imidoether
=1.3
Ethylic uitramido-a-toluate...
(CH2.CO2Et).NO2.NH2=1.2.4
• J)
....
100
Gabriel and Meyer
B., 14, 825
40, 730
Dinitrocymene
Pr.Me.(NO2)2=?
JJ
It*.
54
Kraut
A., 92, 71
ii., 297
,, .... ...
j> n
»
cf. J. [1873],
205 or 250 (?
Konunier
B. S. [2], 19, 434
26,888
368
Dinitroisodurene
Me4.(N02)2=1.2.3.5.4.6
n
....
156
Jacobsen
B., 15, 1853
44, 52
„
„ =1.3.4.6.2.5
»
.._,
199; SOS
Jannasch and Fittig
Z. C. [2], 6, 162
vi., 828
?— acid
....
»
240 +d.
Curtius
J. p. [2], 24, 239
40, 1144; 44,
26,197; B., 16,
• 340
756
Dinitroisobutylphenol
Bu0.0H.(N02)2=?
Q10H120SN3
....
93
Studer
B., 14, 1474
40, 898
,, ..«
» i)
>»
cf. A., 21 1,244
93
Liebmann
B., 14, 1843
Nitroacetamidodimethyl-
(OMe)£.NHAc.N02=1.4(?)2
)J
....
164
Baessler
B., 17, 2121
46, 1329
quinol
Dinitrothymol
Pr«Me.QH,(NO2)2=1.4.6.(?)
JJ
cf.B., 10,611
55
Lallemand
A. C. [3], 49, 152
v., 795
a-dinitrodiethoxybenzene ...
(OEt)s.(NOs)s=lA2.?
C10HI206N2
....
130
Nietzki
B., 12, 41 ; A.
36, 464; 44, 466
215, 150
P" 11 •••• » >j
1)
....
176
?)
»
))
COMPOUNDS CONTAINING FOUR ELEMENTS.
.511
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
/3-dinitrodiethoxybenzene ...
Dinitrodiethoxyphenol
Benzyldimethylacetoxime ...
Propylbenzaldoxime
Ethylacetanilide .... ..
„
Methyl propionanilide
Butyranilide ....
(OEt);!.(NO2)2=1.4.2.?
(OEt)2.OH.(N02)2=1.4.2.(?)2
CMe2 1 NO.CHjPh
Ph.CH : NOPr
Ph.NEt.Ac
))
Ph.NMe.C3H5O
Ph.NH.OC.(CH0)2.CH3
C10H1208N2
C10H120-N2
C10HI3ON
»)
I)
)>
)>
190 d.
225-226 u.c.
248-250
cf. A., 87, 166
172
152
Liquid
51-53
54-5
58-5
90
Nietzki
»
Janny
Petraczek
Elsbach
Eeinhardt & Stade
Norton and Allen
Gerhardt
B., 11, 1448
A., 215, 157
B., 16, 175
B., 16, 828
B., 15, 691
B., 16, 30
B., 18, 1998
A. C. [31 37, 329
34, 867
44,466
44, 581
44, 578
iv., 480
92
Kelbe
B., 16, 1200
44, 916
A cetam id oethy Ibenzene
5) •"
j*
1>
„
Acetylmethyltoluide
„
,, ....
T> ••••
,, ....
Cuminaldoxime
Acetoxylide ....
Et.NHAc=1.2
»
=1.4
» >1
>1 »
Me.NMeAc=1.2
» »
=1.3
=1.4
»J >»
Pr.(CH I NOH)=?
Me2.NHAc=1.2.4
1)
•J
B
Jl
i»
»
»
»
)?
J»
))
304-305
315-317
250-251
260
283
110-112
94
94
94-5
55-56
66
81
83
52
99
Paucksch
Beilstein and Kuhl
berg
»
Paucksch
Benz
Reinhardt&Stadel
Monnet & Nolting
»
Claus and Steinberg
Thomsen
Westenberger
Jacobsen
B., 17, 768
A., 156,208;Z.C
[2], 5, 524
?>
B., 17, 768
B., 15, 1649
B., 16, 30
B., 11, 2279
M
B., 18, 914
B., 10,1583
B., 16J 2904
B., 17, 161
46, 1143
46, 1143; vi.,
292, 1131
))
46, 1143
44, 578
36, 310
34, 218
46, 581
46, 737
„ — 1
cf. A., 208, 322
112-113
Genz
Z. C. [21, 6, 216
vi., 1131
„ —1.3.4
123
Tawildarow
B., 2, 553-
vii., 1209
12.7
WVoblewsky
B., 10, 1248
34, 54
127
Schmitz
A., 193, 179
36, 157
a. 320
137
"Wroblewsky
A., 207, 92-
40, 433
127
Kelbe
B., 16, 1200
44, 916
127-128
Hofmann
B., 9, 1295, 1300
31, 90, 92
128
Grevingk
B., 17, 2431
48, 145
„ =1.2.3 (?)
129-130
Staedel
B., 16, 28
131-132
Wroblewsky
B., 12, 1228;
36, 920; 40, 433
134
Nolting and Forel
A., 207, 100
B. S., 42, 332
48, 382
„ —1.3.?
134; 135
„ —1.4.5
138-189
Schaumann
B, 11, 1538
36, 52
,, ....
>. )>•
„ =1.3.5
)'
138-139
144-5
Wroblewsky
A., 207, 91
A., 207, 96 ; B.,
40, 433
34,55; 40,433
„ —1.3.2
174
Grevingk
10, 1249
B., 17, 2431
48, 145
175
Nolting and Forel
B. S., 42, 332
48, 382
Formocumidide
Tetrahydromethoxyquinoline
(thalline)
Tetrahydrohydroxymethyl-
quinoline
Tetrahyd roxy quinald ine
Acetylethenyltriamidoben-
zene
?
Ethylphenylhydroxyaceti-
mide
v
Phenyl amidobutyric acid (?)
Propylic phenylcarbamate ....
Isopropylic phenylcarbamate
Ethylic phenylmethylcarba-
mate
Ethylic phenamidoacetate ....
/3-phenatnidobutyric acid ....
a-phenamidoisobutyric acid
Me3.(NH.CHO)=2
N.OMe=a, ; ft
(NMe).OH=a, ; a,
N.Me.OH=a,/31 ; a,
NHAc.NHC2H3.NH2=?
Ph.CH(OH).C(OEt):NH
NH2.CHPh.(CH2)2.C02H(?)
NHPh.CO2Pr«
NHPh.CO2Pr0
NMePh.C02Et
NHPh.CH2.CO2Et
CH3.CH(NHPh).CH2.CO2H
NHPh.CMe2.COjH
?)
))
»
C10H13ON3
C10H1302N
»
j)
j)
)?
)»
»»
j)
»'
282-283
...4
278-282
+2H20
+5H3O
d. 170
243-244
cf. B., 13, 313
121
42-43
114
Liquid
85-90
144 d.
71-72
72
85-86
57-59
90
Liquid
57-58
127-128
184-185
Senier
Fischer
Db'bner and Miller
Salkowski
Feer and Konigs
Beyer
»
Fittig
Roemer
Gumpert
Gebhardt
Meyer
Balbiano
Tieruann
D. P., 256, 192
B., 16, 715
B., 17, 1707
B., 10, 1693
B., 18, 2392
J. p. [2], 28, 190
J. p. [2], 31, 382
B., 17, 202
B., 6, 1113
J. p. [2], 31, 119
B., 17, 3042
B., 8, 1156
G. I., 10, 137
B., 15, 2042
47, 768
48, 1023
44, 1140
46, 1374
34, 140
48, 1245
46, 65
48, 932
46, 744
27,39
48, 656
48, 384
29, 373
38, 462, 542
44, 199
512
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Acetamidoethoxybenzene ...
OEt.NHAc=1.3
C10H1303N
.»•
96-7 u. c.
Wagner
J. p. [2], 32, 70
48, 1212
Methylic dimethamidoben-
NMes.COaMe=1.3
M
270 u.c.
Liquid
Griess
B., 6, 587
26, 1146; vli.,
zoate
187
Ethylic tolylcarbamate
Me.(NH.COsEt)=1.3
»»
....
L.-47
Cosack
B., 13, 1090
38, 713
11 ,1
=1.2
-»1
....
32
Hofmann
P. R., 19, 108
24, 139
11 11
V )»
•»
....
p
Cosack
B., 12, 1450
38, 245
11 1'
»* »
I)
....
45-46
NevilleandWiuthei
B., 12, 2324
vii., 253
11 11
V )»
I)
....
45-46
Lachmann
B., 12, 1349
36, 935
» >!
=1.4
V
cf..B., 3,^i56
52
Hofmann
P. R., 19, 108
vii., 1180
a-tolylamidopropionic acid ...
Me.(NH.CHMe.CO.,H)=1.2
))
cryst.
Tiemann& Stephan
B., 15, 2039
44, 199
«- ,, -,, »
=1.4
H
....
152
11
B., 15, 2037
11
a-Nitrocymene
Pr«.Me.NO2=1.4.5 or 6
)i
Liquid
Landolph
B., 6, 937
26, 1227
i,
» >i
»»
....
Liquid
Fittica
A., 172, 314
28,59
9- „
„ =1.4.6 or 5
.,
124
Gerichten
B., 11, 1092
34, 787
u ....
>• ii
i?
....
124-5
Landolph
B., 6, 937
26, 1227
v
»! -»
V
....
124-5
Gerichten
B., 10, 1251
34, 49
»>
11 11
11
125
Fittica
A., 172, 315
28, 59, 60
a-Amidocuminic acid
Pr.CO2H.NH2=1.4.5 or 6
n
104
Fileti
G. I., 10, 12
40, 424
» »
11 -)>
„
....
104
Lippmann & Lange
B., 13, 1661; 1876
40, 276
»> 11
11 51
>•
cf. B.,-7, 81
104-4
Paterno and Fileti
G. I., 5, 383
29, 595
0- „
„ =1.4.6 or 5
„
....
129
4)
H
11
11 11
>! !>
i>
129
Fileti
G. I., 10, 12
40, 424
11 11
11 11
„
....
129
Lippmann & Lange
B., 13, 1661, 1876
40, 276
Xylylamidoacetic acid
Me2.(NH.CH2.CO2H) = 1.3. ?
.,
....
132-134
Ehrlich
B., 16, 206
44, 594
Nitrosopropylcresol
Pr».Me.OH.NO2=?. 1.3.2
„
cf.B., 16,243
140 d.
Mazzara
G. I. [1882], 333
42, 1200
Nitrosocarvacrol
=1.4.5.?
»
cf.B., 12,383
153
Paterno & Canzoneri
G. I., 11, 124
40, 595
Nitrosothymol
=1.4:6.?
i»
....
155-156
11
n
n
n
11 11
j)
....
155-156
Schiff
B., 8, 1500
29, 583
,,
11 .11
ji
slow Ht.
155-156
Liebermann
B., 10, 78
„
11 11
.,,
quick Ht.
162-166
11
11
„
» 11
-M
....
160-162
Wi'dmanii
B., 15, 170
42, 728
Nitroaoisopropylcresol
Pr0.Me.OH.NO=?.1.3.?
V
cf. B., 16, V93
165-1 67 d.
Mazzara
G. I., 12, 505
44, 463
Nitrodurene ....
Me4.NO2=l. 2.3.5.6
11
MM
165
Ador and Killiet
B., 12, 332
36, 527
Ethylic lutidinecarboxylate
N.Me2.CO2Et=1.2.4.3
• It
246-247 u.c.
Liquid
Michael
B., 18, 2022
48, 1244
11 11 11
= ?
•M
270-300 (?)
Liquid
Canzoneci and Spica
G. I., 14, 448
48, 751
Methylcarbocollidylium de-
C5HMe3NMe.COO
»
abt. 340
102-103
Hantzsch
B., 17, 1025
46, 1045
i i
nyunde
Dimethamidophenyl oxamide
NMe2.(NH.CO.CO.NH2)=1.4
C10H1302N,
....
257-250
Sendtner
B., 12, 532
36, 627
Reduction of dinitrodiethyl
....
JJ
mi
233
Nietzki
B., 12, 42; A., 215,
36, 464; 44,
quinol
151
466
Isobutoxynitrobenzene
OBu0.NO2=1.2
C10H1303N
285-290 d.
L.— 20
Riess
Z. C. [2], 7, 39 ;
24, 221
B., 3, 780
»i
=1.4
»»
275-280
L.— 20
11
1)
N
Ethylanishydroxamic acid ....
OMe.(CO.NH.OEt)=1.4
JJ
....
32
Eiseler
A., 175, 338
28, 767
Ethylic anishydroxamate ....
OMe.(CO.NEt.OH)
)»
84
Pieper
A., 217, 17
44,462
Ethoxyphenylamidoacetic
OEt.(NH.CH2.CO2H)=1.2
-^
120
Vater
J. p. [2], 29, 286
46, 1144
acid
Acetaraidodimethoxybenzene
(OMe)2.NHAe=1.4.15
- 1»
91
Baessler
B., 17, 2121
46, 1329
Hydroxypropylamidobeuzoic
CO2H.NH2.(CMe.!.OH)
J»
nf. 270
Widmaun
B., 16, 2571
46, 317
acid
=1.3.4
Nitrocarvacrol
Pr«.Me.OH.NO3=1.4.5.?
-^1
....
77-78
Paterno& Canzoneri
B., 12, 383
„ .- ....
" 11
»'
79
»
G. L, 11, 124
40, 595
Nitrothymol
— 1 4 fi ?
o lit lid
T> *•
GT ns7<vi 11
oft ft/tn
11 — i «^.U. t
»»
.MM. I I . •
sr acerno
. X. 1 1 0 / tJJ, 1 •>
**o, O*±U
i,
11 11
•»1
~-
137
Schiif
B., 8, 1501
29, 583
T> + £r/"<
GT 111 OA
Af\ RO^
V 11
•»»
x aicr no oc ^aiizoner]
. 1«J 11, 1 - i
^*v» oyo
1 OQ 1 *>(!
GT in OIQ
00 QQQ
n
11 11
J J
.....
1«3O— iO»
i»
. 1.) ! M, --••'
OO, Oo*3
1 Af\
T * lirtv
Bin fti 9
oo A'7'7
11 .,
»»
14U
1 jl (' 1 H ' 1 '] Hit 1 1 1 )
. j 1 > ' , D 1 Z
*>»i *±t i
Ethylic hydroxylntidine car-
N.Me2.OH.CO2Et=?
)1
140
Collie
A., 226, 294
48, 374
boxylate
Nitrodiethoxy benzene
(OEt)2.N02=1.4.5
C10H1304N
49
Nietzki
B.,12,39; A.,215
36, 464; 44, 466
146
Fr. phthalimide
....
i) .;
90-94
Landsberg
A., 215, 195
44, 476
COMPOUNDS CONTAINING FOUR ELEMENTS.
513
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrocoerulignol
Pr.OMe.OH.NO2=11.2.1
C10H1304N
....
124
Pastronich
M. G, 4, 191
44, 1006
Ethylic ethylcomenamate ....
C5H3EtNO2.CO2Et
„
114-115
Mennel
J. p. [2], 32, 176
48, 1204
Ethylic dimethylpyrroline
N.Me2.CO2H.CO2Et
„
....
a. 200 d.
Knorr
B., 17, 1639
46, 1368
dicarboxylate
=1.2.5.3.4
„ „
!) 1!
jj
....
227 d.
„
B., 18, 1563
48, 994
Dinitrodiethylaniline
NEt2.(NO2)2=1.2.4
C10H1304N3
....
180
Lippmann and
M. C., 4, 788
46, 179
Fleissner
Diethylnitropyrogallol
(OEt)2.OH.N02=?
C10H1305N
....
123
Weselsky and Bene-
M. G, 2, 217
42,54
dikt
Ethylic phenylethenylamid-
Ph.CH2.C(NH2) : NOEt
C10H14ON2
....
58
Knudsen
B., 18, 1072
48, 897
oxime
a-Phenamidoisobutyramide....
NHPh.CMe2CO.NH2
J*
....
137
Tiemann
B., 15, 2042
44, 199
Nitrosodiethylaniline
C6H4.NO.NEt2=1.4
M
....
84
Kopp
B., 8, 622
,, ....
» »
„
....
84
Lippmann and
B., 16, 1422
Fleissner
Acetyldimethdiamidobenzene
NMe2.NHAc=L4
„
335 d.
130
Wurster
B., 12, 525
36, 627
„
„ „
jj
....
131
Witt
....
36,360
Propylphenyl carbamide ....
NH2.CO.NH.C6H4Pr=1.4
l)
143
Francksen
B., 17, 1225
46, 1008
Toluidopropionamide
Me.(NH.CHMe.CO.NH2)
„
125
Tiemann & S tephan
B., 15, 2038
44, 199
=1.2
„
=1.4
i)
....
145
n
B., 15, 2037
„
Pseudocumylcarbamide
Me3.(NH.CO.NH2)=?
t)
„..
d.w.m. 227
Engel
B., 18, 2233
48, 1216
Diazocamphor
C8H14.c7c.N : N.6
«
....
73-74
Schiff
B., 14, 1375
42,527
Diisobutyryl dicyanide
....
C10H1402N3
226-228
L. —15
Moritz
....
39, 14
Dibutyryl dicyanide
....
»j
232-235
....
„
....
39, 17
Ethylic phenyhydroxy-
HO.CHPh.C(NH2) : NOEt
„
....
89
Gross
B., 18, 1079
48, 898
ethenylamidoxime
Nitrodiethylaniline
N02.NEt2=1.4
„
....
76
Lippmann and
B., 16, 1422 ;
44, 868, 1100
Fleissner
M. G, 4, 284
Diamidocuminic acid
CO2H.Pr0.(NH2)2=?
„
....
192
Lippmann
B., 15, 2144
44, 194
Phenylacediamine acetate ....
Ph.CH2.C(: NH).NH2+HAc
„
....
192-193
Bernthsen
B., 8, 1320
29, 607
Fr. juglone
C6H202(NMe2)2
„
....
173-174
Mylius
B., 18, 467
48, 804
Ethoxycaffeme
C8H9N402.OEt
C10H1403N4
....
140
Fischer
B., 14, 640; A.,
40, 614 ; 44,
215, 253
355
Methylphenylpropylalkine ....
NPhMe.C3H6.OH
C10H15ON
262
*«.
Laun
B., 17, 678
46, 1011
Ethylphenylethylalkine
NPhEt.C2H4.OH
„
267-268-5
....
„
B., 17, 677
„
Diethamidophenol
OH.NEt2=1.2
„
218-220
Liquid
Foster
J. p. [2], 21, 367
38, 465
Ethamidoethoxy benzene
OEt.NHEt=1.2
„
234-235(751)
Liquid
„
J. p. [2], 21, 346
38, 464
Dimethamidoethoxybenzene
OEt.NMe2=1.3
jj
247 u.e.
Liquid
Wagner
J. p. [2], 32, 70
48, 1212
n
» »
„
....
Liquid
Baur and Staedel
B., 16, 33
Hydroxypropyltoluidine
Me.(NH.C3H6.OH)=1.4
„
290
74
Morley
B., 15, 179
42, 723
„ ....
» jj
„
293 c. ; s.d.
74
„
B., 16, 82
41, 388
Hydroxyethylmethyltolui-
Me.(NMe.C2H4.OH)= 1 .4
„
290-300
Liquid
Demole
B., 7, 637; A.,
27, 903
dine
173, 133
C,nH,, : N.OH
v. C10H17ON
66 '5
p 1 1 i • i.
B., 17, 1578
46, 1138
*~'10'"'i4 * *
•
240 d.
' i oh iscl !i n i< 1 1 <i 1 1 1 i
B., 18, 1730
48, 1058
J)
Zurrer
Amidocarvacrol
Pr".Me.OH.NH2=1.4.5.2
H
....
304
Paterno and Gan-
B., 12, 384
zoneri
Nitrosohesperidene
....
„
....
70-1 ; 71 c.
Tilden & Shenstone
J. [1877], 428
31, 559
Isonitrosoterpene
from caraway
„
....
71
„
„
31, 560
„
„ bergamot
„
....
71
()
J. [1879], 396
„
Nitrosoterpene
„ oil of juniper
„
....
128-5
„
„
31, 558
„ .... ....
„ „ sage
„
....
129
„
J. [1877], 958
31, 557
:,
....
„
....
129
Goldschmidt and
B., 18, 2223
48, 1210
Zurrer
„ .... ....
....
„
....
129-130
Tilden
J. [1875], 391
28, 516
Nitrosoterebenthene
„
....
128-8 c.
Tilden & Shenstone
....
31, 557
„
from camphor oil
„
....
130
Yoshida
47, 786
Nitroso-australene
....
»
....
129 c.
Tilden & Shenstone
....
31, 556
*t TT
514
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Acetyldimethtriamidoben-
NMe.NHAc.NH2=1.3.4 or
C10H15ON
....
153
Wiirster&Sendtnei
B., 12, 1807
38, 110
zene
1.4.3
„
,, „
„
+H20
82
„
„
„
Camplierimide
CIOH1502N
A., 60, 329
180 s. t.
Ballo
A., 197, 332
Hydrazineaniso'il carbamide
MeO.(NsHj.CO.NH£t)=1.2
G10H1502N3
110
Reisenegger
A., 221, 314
46, 440
Nitrocamphor
. C10H14.OH.N02
C10H1503N
83
Schiff
B., 13, 1403
38, 891
Amidocamphoric anhydride
C8H13(NH2):(CO)2.0
„
sb. 150
208
Wreden
A., 163, 339
26, 896; vii.,
237
Diethylic y-amidoisophtha-
(C02Et)2.NH,=1.3.?
Cl(,H1504N
118
Beyer
J.p. [2], 25, 465
42, 1296
late
Nitro-oxycamphor
«
n
163-164
Ziirrer
B., 18, 2228
„
'
„
169-170
Kachler & Spitzer
B., 15, 2337
44, 215
„
•
„
....
175
S warts
B., 15, 2136
?
C4H3O.C(NH3.C2H302).
„
305-310
153
Tonnies and Staub
B., 17, 856
46, 1130
CMe2.O
i
Ethylic diethylcyanurcar-
C3Et2O3N3.COjEt
C.oHjjO.N,
....
107
Wurtz and Henn-
C. R., 100, 1419
48, 969
boxylate
inger
Methoxycyanconiine
C9H1SN( : NH).OMe
C10H16ON2
225
.....
Meyer
J. p. [2], 126, 353
44, 353
Methylhydroxycyanconiine
C9H13N( : NMe).OH
„
275-276
76-5
„
J. p. [2], 126, 348
„
Dimethoxyhydroxycaffeine ...
C8H9O2N4.OH.(OMe)2
C10H1605N4
....
178-179
Fischer
B., 14, 642
40, 614
Amidocamphor
CMH14.OH.NH2
C10H17ON
246-4
solid
Schiff
B., 13, 1404
38, 892
Carvoxime
C10H16 : NOH
v. C10H15ON
70-71
Goldschmidt and
B., 18, 2220
48, 1210
Ziirrer
Camphoroxime
„
it
249-254
115
Nageli
B., 16, 498
44, 728
Isocamphoroxime
HO.C9H)5:C1NH(?)
„
125
„
B., 17, 806
46, 1190
Acetyl y-coniceme ....
C8H14AcN
„
252-255
Liquid
Hofmann
B., 18, 116
48, 563
Methoxycyanethine ....
C9H14N3.OMe
C1UH17ON3
130
Riess
J. p. [2], 30, 145
48, 235
Ethylic mesitylate
CrH12O.CO2Et
C1UH1703N
290
85
Pinner
B., 15, 578
42, 941
» ,,
)5
J)
....
tO
„
B., 14, 1074
40, 796
Amidocamphoric acid
C3HI3.NH2.(C02H)2
C10H1704N
....
160
Wreden
A., 163, 340
25, 896
Ethylimidodiethyldioxamide
NEt(CO.CO.NHEt)2
C10H1704N3
135-138 d.
Schiff
B., 17, 403
46, 907
Campholenic nitril+hy-
C9Hu,.CN+NH.i.OH
C10H18ON2
....
101
Goldschmidt and
B., 17, 2070
46, 1364
droxylamine
Ziirrer
Acetyl copellidine
C8Hl6AcN
C10H19ON
254
•*..
Diirkopf
B., 18, 924
48, 817
Ethylic diethamidocrotonic
NEt2.CMe I CH.C02Et
CUH1902N
160-163(20)
-liquid
Kuckert
B., 18, 619
48, 750
acid
Ethylic oxyhexinamate
C6HrO(OEt)2.NH2
C10H1803N
....
78-7»
Demarjay
A. C. [5], 20, 490
„ isooxyhexinamate ....
„
„
94-95
„
A. C. [5], 20, 492
„ ethyldiglycollamidate
....
C10H1904N
200-220
.liquid
Heintz
A., 145, 230
Isobutylvaleryl carbamide ...
NHBu/s.CO.NH.C.H^O
C10H2l)O,Ns
....
02
Hofmann
B., 15, 758
42, 1053
Ethylidenepropylurethane ....
CH3.CH(NH.CO2Pr)2
C10H2004N2
15-116
Bischoff
B., 7, 1082
28, 146
Caprinamide ....
C H CO NTT
p TT f\-\J
Q
TT f
B. 15 984
9 !&' " 2
vl0**Jl"PI
MM
O
xioimann
i inn
•p _
A., 79, 243
Triacetouemethylalkamine ....
If
C9H18NOMe
I
U. i\J\J
4
Fischer
B., 16, 1606
44, 1153
Dinaethyloxyconine ....
CsH15Me2ON
I*
25-226
.liquid
Hofmann
B., 18, 119
48, 563
Ethyloxyconine
C8H16EtON
?J
40-242
....
Ladeuburg
B., 14, 2409
42, 166
Alkaloid fr. Lupinus lutens
C10H2102N
69-270
2'5
Schulz
B. S. [1879], 874
38, 416
Tripropoxyacetonitril (?) ....
(PrO)3.CN (2)
C10H2103N(?)
16-219
....
Bauer
A., 229, 163
48, 1121
Diisobutylglyoxylamide
(BuSO)2.CH.CO.NHa
....
2-45
Pinner and Klein
B., 11, 1479
36, 47
Dipiperal ly lal kam ine
....
C10IL3ON2(?)
80-290 p. d.
Liquid
Ladeuburg
C. R., 93, 338
40, 1158
Dioxyisoamylamine
(C6HnO)2NH
49-251
L. —20
Radziszewski and
B., 17, 839
46, 1190
Schramm
Allyl cyanide +ethylalcohol
C4H6N.3C3H60
C10HSS03N
73-174
.liquid
Rintie
B., 6, 389
26, 880; vii., 49
Nitro-a-naphthonitril
C10H6.N03.CN
CnH602N2
1
Welkov
B., 2, 408
vi., 848
)? ~a~ »
„
„
00-130
Graeff
B., 16, 2248
46, 80
» •<*• „
i)
„
....
52-153
B., 16, 2247
n
» -«- „
11
„
....
05
B., 14, 1065
10, 822
11 •<*' »
„
„
....
05
B., 15, 1126
» -°- ,,
„
)}
05
3)
B., 16, 2247
16,80
.. -3- ,,
11
11
mpure)
5-120
B., 16, 2248
„
i
. -
COMPOUNDS CONTAINING FOUR ELEMENTS.
515
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Nitro-/3-naphthonitril
C10H6.NO2.CN
CUH602N2
....
172-173
Graeff
B., 16, 2248
46, 80
?-
11 * 11
))
))
100
)J
B., 14, 1063
40, 822
.9
11 * )l
»
)J
148-149
))
J)
»
Diuitro-a-naphthoic acid
C10H5(N02)2.C02H
C..HAN,
263-265
Ekstrand
B., 17, 1601
46, 1361
1} ~P~ ,, ,,
))
)»
....
226
M
B., 17, 1603
11
a
» "•-* 11 i)
1)
»»
....
248
»
))
11
a-Naphthylisocyanate
C10H7.N : CO
CUH7ON
269-270
Hofraann
P. K., 19, 108 ;
24, 139 ; vii.,
B., 3, 658
407, 844
CjsH^OjNst?)
C11H7O3N(?)
cf. A., 21 0,89
191
Hesse
A., 226, 241
48, 276
Nitro-[>-naplitlioic acid
COjlLNO^a!.?
CnH704N
194
Kuchentneister
B., 3, 740
vii., 838
„ -a- „ „
11 i)
19
....
195-196
Ekstrand
B., 12, 1394
38, 261
11 ~a~ 11 11
11 =«,.? ;
j»
....
"215 u.c.
»
B., 18, 73
48, 548
11 ~a~ 11 11
i, ="i ; "i or «2
»
....
233
D
B., 12, 1395
38, 261
11 "Q" 11 11
i' )>
)i
....
235
Graeff
B., 15, 1126
43, 1212
„ -a- „ ,,
11 ))
;>
.—•
238
n
B., 14, 1066
40, 822
11 ~a~ 11 11
11 11
J'
239 u.c.
Ekstrand
B., 18, 77
48, 548
11 -«- >. i)
11 )!
J)
2W-242
Graeff
B., 16, 2250
48, .81
11 ~U~ 5) )1
11 =fll-?
)j
....
255
3J
B., 16, 2252
)»
11 -P" 11 1)
=/M
)»
200
?J
B., 14, 1064
40, 822
„ -#- „ „
=ft.?
))
....
220
Ekstrand
B., 12, 1395
38, 261
„ -|3- » »
»i ))
))
....
228
Kitchen meister
B., 3, 741
vii., 838
,1 -3- » 11
=P,?
*j
....
269 u.c.
Ekstrand
B., 18, 1205
48, 905
„ -0- ,, »
=/M
J»
....
280
n
B., 12, 1395
38, 261
11 -p~ 11 11
=^i..»
)>
....
288-289 n.c.
» , -
B., 18, 1206
48, 905
1! -P- 11 )>
=ft.?
J)
....
293 u.c.
&
B., 18, 1207
11
11 -P- 1) 1!
» »)
))
....
295
Graeff
B., 16, 2252
43,81
Nitromethyldihyroxynaph-
C10H2Me(NO2)(OH)2 : 02
CUH706N
....
255-260
Thorner
B., 12, 1633
38,47
thaquiuone
Dinitrocitraconanil
....
C,,H706N3
cf. A., 85, 21
120
Kudnew
Z. C. [2], 7, 203
24, 712
Trinitro-a-methoxynaphtha-
CleH4.OMe.(NO2)3
CUH;07N3
128
Staedel
B., 14, 900 ; A.,
40, 724; ,.44,
lene
217, 172
863
„ -s-
J)
J>
213
11
)>
n
Dipyridilcarboxylic acid
C10H7ON2.CO2H
CnH302N2
....
179 .
Skraup
B., 15, 896
42, 1112
11 i>
»»
»
....
182-5-184
Skraup & Vortmam
M. C., 3, 370, 597
44, 88
Tolnquinoxalinedicarboxylic
CcH3Me I (.N : C.C02H)., :
CUH804N3
....
d. 145
Hinsberg
B., 18, 1233
48, 910
acid
Dinitro-8-methylnaphthalene
C10H5Me(N02)2
))
....
206
Schulze
B., 17, 844
46, 1184
a-naphthylformamide
C10H7.NH(CHO)
CUH9ON
....
102 (?)
Zinnin
A., 108, 229
ii., 682
a- „
»
»)
137
Liebermann
A., 211, 42
a- „
11
»
138-5
Tobias
B., 15, 2447
44, 326
P-
11
JJ
120
Cosiner
B., 14, 58
40, 606
0-
11
»1
....
128
Tobias
B., 15, 2447
44, 326
(3-
" —,
5J
129
Liebermann
A., 211, 42
a-naphthoainide
C10H7.CO.NH2
»
....
128?
Eakowski
B., 5, 319
a- 11
»J
5>
....
202
Leone
G. I., 14, 120
46, 1362
«- •>
H
J)
....
204
Liebermann
A., 183, 225
31, 608
a- „
M
)>
204
Bossneck
B., 15, 3065
a- „ (misprint in orig.)
5)
)>
cf. A., 142, 121
204
Hofmann
B., 1, 39
vi., 851
a- ,)
)»
)»
207
11
C. K., 66, 476
3- „
))
))
192
Leone
G. I., 14, 120
46, 1362
a- „
))
»)
192
Liebermann
A., 183, 225
31, 608
P- „
)>
»
192
Vieth
A., 180, 320
30,87
Pseudobenzopyrroline
Ph.CO.C4H3:NH
J)
77-78
Ciamician & Denn-
B., 17, 433, 2956
46, 1044; 48,
stedt
379
Phenylcitraconirnide
Ph.N : C6H4O2
0,^,0^
96
Strecker
B., 15, 1641
42, 1281
D ....
))
11
v.a. 100
96
Gottlieb
A., 77, 278
i., 993
Fr. Anilidopyrotartaric acid
....
)»
....
98
Wechsler
B., 18, 1052
48, 901
Allyl phthnlimide
C6H4:(CO)2:NC3H5=1.2
n
....
70-71
Wallach & Kamensk
B., 14, 171
Hydroxfurfuraniline
C6H4(OH).NC6H4O=1.4
11
180-182 d.
Schiff
A., 201, 358
38, 391
Aniluvitonic acid
....
11
....
241-242
Bottinger
A., 191, 321
Nitro-a-ruethylnaphtkalene ....
Me.NO2=a.?
n
....
Liquid — 15
Schulze
B., 17, 845
46, 1184
„ -ft- n
„ =|3.a
11
81
11
B., 17, 844
11
3u 2
516
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Nitroso-methoxynaphthalene
C10H6.OMe.NO=fta1 ;(?)
C10H902N
....
75
Ilinski
B., 17, 2588
48, 168
11 11
„ =ala2 ;(?)
„
98-100
11
B., 17, 2591
11
Methyl /3-nitroso-a-naphthol
O : C10H, : NOMe(?)
n
....
93
Goldschmidt and
B., 18, 2225
Schmid
11 ft- 11 -o- 11
n
„
95
Fuchs
B., 8, 630
11 "- 11 -»- 11
....
11
....
98-100
Goldschmidt and
B., 18, 2226
Schniid
?
C10H6:02:NMe
„
225
Zincke
B., 12, 1646
38, 49
Methamido-a-naphthaqui-
C10H6(NHMe):02
„
....
232 u.c.
Plimpton
....
37, 640
none
Amido-a-naphthoic acid
C10H,(NH2).C02H
,,
fr. C2H6O
Sll-812 u.c.
Ekstrand
B., 18, 78
48, 548
n ~a~ 11 11
„
11
f r. H2O
198-199
11
11
11
n *o- 11 11
11
„
sb. a. 212
a.s. 196
11
11
11
„ -0- „
„
„
iaomeric
211 u.c.
11
B., 18, 1206
48, 905
n ~P~ n 11
11
„
11
219 u.c.
n
B., 18, 1207
n
11 ~P~ 11 11
11
„
11
232 u.c.
11
B., 18, 1208
11
Acetoxyquinoline
N.OAc=a,; a.
11
abt. 280 u.c.
Liquid —20
Skraup
M. C., 3, 541
44, 93
11 •"• •••
„ =0l ; 03
11
298 u.c.
36-38
11
M. C., 3, 555
11
Quinoline beta'ine
....
„
cf.B.,15,1254
171 d ; u.c.
Rhoussopoulos
B., 15, 2007
44, 96
Hydroxyquinoline methyl-
N.OH.Ac=a1£,/32 ;
„
....
232
Friedlander and
B., 16, 1838
44, 1149
ketone
Gohring
Methylquinoline carboxylic
N.Me.CO8H=a1AA ;
„
....
140
Dobne and Miller
B., 17, 1715
46, 1376
acid
11 11
„ „
„
mm
143-144
n
B., 18, 1641
48, 1079
Lepidine carboxylic acid
„ =0,03/3, ;
„
....
182 d.
Besthorn & Fischer
B., 16, 70
44, 600
11 11 11 ••"
„ =a,/31/32 ;
„
....
234
Friedlander and
B.( 16, 1857
44, 1149
Gohring
Quinaldine carboxylic acid ....
„ =n.j9, ; a,
„
....
151
Dobner and Miller
B., 17, 943
46, 1200
n 11 11 — •
„ =aj3, ; |32
„
brown 240
259 d.
11
B., 17, 939
11 11 11
11 =a A ; Pi °r «j
„
brown 275
285 d.
11
B., 17, 941
Nitrocinnamylacraldehyde ....
NO2.(CH:CH.CH:'CH.
CUH903N
....
153
Einhorn
B., 17, 2027
46, 1345
CHO)=1.2
Acetyl-p-methylpseudisatin
...»
»
....
172
Duisberg
B., 18, 197
48, 544
Phthalylpropionamide
C6H4 : (C0)2 : C2H3.CO.NH2
„
....
193-195
Gabriel and Michael
B., 11, 1014
34, 735
=1.2
Indogenide of pyroracemic
NH.C6H4.CO.C : CMe.CO2H
,,
....
197
Baeyer
B., 16, 2199
46, 76
acid
=1.2
Phthalomethimidylacetic acid
NMe.CO.C6H4.C : CH.CO.H
n
....
212 d.
Gabriel
B., 18, 2453
48, 1228
I I
=1.2
Quininic acid
C9H6N(OMe).CO2H
„
....
280 d.
Skraup
M. C., 2, 592
42, 221
„ „ .... ....
„
11
....
280
Forst & Bohringer
B., 15, 521
42, 982
Ethylic nitrophenylpropiolate
NO2.(CiC.CO2Et)=1.2
CUH904N
....
60-61
Baeyer
B., 13, 2259
40, 275
»
=1.4
a
....
126
Drewsen
A., 212, 156
42, 847
Ethylic isatogenate
3O.C6H4.N.O.C.CO2Et
,,
cf.B.,15,V80
115
Baeyer
B., 14, 1741
42, 198
Nitrocinnamylacrylic acid ....
N02.(CH : CH.CH I CH.
„
....
217-5
Diehl and Einhorn
B., 18, 2331
48, 1223
C02H)=1.2
Succinylamidobenzoic acid ....
C2H4 : (00), : N.C6H4.CO2H
„
....
235
Pellizzari
B., 18, 215
48, 534
=1.3
» »
» »
„
...»
235
Mure tow
B., 5, 330 ; J. R.,
25, 1097 ; vii.,
4,295
1103
Benzylpurpuric acid
Ph.CH,C(NO) : (CO.NH) : CO
CnH904N,
....
226
Conrad & Guthzeit
B., 15, 2849
44, 315
Nitrobenzoyltrimethylene-
CH2.CH2.C(C02H).CO.C6H4.
CUH90SN
....
176
Perkin & Bellenot
B., 18, 960
48, 795
carboxylic acid
NO,=1.4
Nitrophenylparaconic acid ....
NO2.(CH : CH.CH2.CO2H)'
CUH906N
....
171
Bolomonson
B., 18, 2155
48, 1224
=1.3
>i 11
=1.4
M
163
11
11
11
Phenylfurfurazide
Ph.N2H : C5H4O
CUH1()ON2
....
96
Fischer
B., 10, 1332;
32, 887; 34, 31
A., 190, 137
i)
n
11
...»
97-98
11
B., 17, 572
46, 1150
?
Ph.C:N.C(OH).CH.CMe:N
i |
11
....
215-5-216
Pinner
B., 17, 2519
48, 159
COMPOUNDS CONTAINING TOUR ELEMENTS.
517
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Die.
& J. Ch. Soc.
a-naphthyl carbamide
C10H7.NH.CO.NH3
C^ON,
cf. A., 101, 90
d.w.m. 250
Pagliani.
B., 12, 386
/3- „ „
„
„
....
287
Cosiner
B., 14, 62
40, 606
Benzenylazoximepropenyl
O.N : CPh.N : C.(CH_)2.C02H
CnHjoOjNj
....
120
Schulz
B., 18, 2459
48, 1219
carboxylic acid
1 1
Benzenyl barbituric acid ....
Ph.CH2.CH : (CO.NH)2 : CO
„
....
206
Conrad & Guthzeit
B., 15, 2846
44, 314
Diacetylhydrazine benzoic
C6H4.CO.NAc.NAc=1.2
„
....
112
Fischer and Eenouf
A., 212, 336
42, 1069
anhydride
1 1
Hydroxycarboxytoluquin-
HO.C : N.C7H6.N : C.CO.NH
CUH1003N4
brown 250
258
Hinsberg.
B., 18, 1231
48, 909
oxaline ure'ide
1 1
CO.NH2
Nitraniline furfurol
N02.(NH.C5H502)=1.3
CUH1004N2
....
100-120 d.
Schiff
A., 201, 357
Pyrotartaronitranil ....
NO2.(N : CSH6O2)=1:4
„
....
155
Arppe
A., 87, 228; 90, 144
iv., 775
Nitrophenyl /3-acetylalanine
NO2.(CH.CH2.CO.NAc)=1.2
,,.
. •-
172
Einhorn
B., 16, 2648
46, 305
lac tarn
Ethylic nitrosoindoxylata (?)
121
Baeyer
B., 15, 781
Nitrosoethylindoxylic acid (T
....
„
200 d.
„
B., 14, 1743
Toluoquinoxaline oxalate ....
C6H3Me.N:CH.CH:N
..
....
135-136
Hinsberg
B., 17, 321
46, 1053
=1.3.4+C2H2O4
Nitrotolylsuccinimide
Me.NO2.(N:C202:C2H4)
„
....
140
Taylor
B., 8, 1225 ; A.,
29, 602; 42, 181
=1.7.4
209, 379
Ethylic nitrosoindoxanthi-
NH.C6H4.CO.C(OH).C02Et
CUH10O5N2
113d.
Baeyer, 'i
B., 15, 777
42, 1101
nate
I 1
Ethylic dinitrocinnamate ...
N02.j;.CH : C(NO2).C02Et]
CuH10p6N2
...*
?
Friedlandef.. and
A., 229, 233
48,1138
=1.3
Lazarus
„ ,,,
=1.4
»
«...
109-110
Friedlander& Mahly
A., 2g9, 210; B.,
48, 1137
B., 16, 850
•» »
»• n
....
109-110
Friedlander
B., 14, 2576
42, 402.
Ethylic nitroso-nitrobenzoyl-
N02.[CO.CH(NO).CO.jEt]
....
220
Perkin & Bellenot
B., 17, 328
46, 1024
acetate
=1.4
Acetylmethylketole
C6H4.CH:CMe.NAc=1.2
CuHnON
• *..
195-196
Jackson
B., 14,. 880
40, 734
Ethylcarbostyril ,.
C6H4.NEt.CO.CH : CH=li2
„.
250 s.d..
Liquid
Friedlander & Os-
B., 14, 1917
42, 201;
termeier
„ „
>,
„
255-256
Liquid
„
B., 15, 335
42, .738
Ethylpseudocarbostyril
>! »
„
....
53-55
Friedlander and
B., 18, 1530
48, 989
Weinberg
Ethylcarbostyril
C6H4.NH.CO.CEt t CH=1.2
„
....
168
Baeyer & Jackson
B., 13, 121
38,407
Dimethylpseudoquinoxyl ....
OH4.NMe.CMe :CH.CO=1.2
»
....
132
Knorr and Antrick
B., 17, 2877
48, 274
Ethoxyquinoline
N.OEt=0l ; H!
285-287(718)
s. in Winter
Fischer
B., 16, 717
44, 1146
Methoxytoluquinoline
N.Me.OMe=a! ; a,aj
„
225-230
Liquid
Herzfeld
B., 17, 1551
46, 1199
Methoxyquinaldine
„ =0,0, ; a,
„
282
125
Dobner and Miller
B., 17, 1707
46, 1374
Toluene hydroxyquinaldine
N.Me.OH.Me=a,(3,05 ; a,
»-
....
185
Knorr
B., 17, 542
46, 1198
Pyrotataranil
CO.CHMe.CH2.CO.NPh
i j
CnHuOjN
300 p.d.
98
Arppe,
A., 90, 139
iv., 774
„
„
n
104
Chiozza
A., 91, 105
Ethylindolecarboxylic acid....
Ph.NMe.N : CMe.CO2H
„
....
183
Fischer and Hess
B., 17, 566
46, 1181
Tolylsuccinimide
Me.(N.CO.C2H4.CO)=1.2
,,
345
75
Becchi
B., 12, 25
36, 462
„ .... ....
M »
n
S88-340 $38)
75
„
B., 12, 321
36, 527
„
„ „
i$
....
75
Michael
B., 10, 579
,i
=1.4
„
...»
150
Taylor
B., 8, 1225 ; A.,
29, 602; 42, 181
209, 378
„ .... ....
» ..
„
....
150
Sell
A., 126, 164
„ ....
„ „
„
344-345(733)
51
Becchi
B., 12, 321
36, 527
Ethylic amidophenylpropio-
NH2.(C;C.C02Et)=1.2
»j
....
55
Baeyer and Bloem
B., 15, 2148
44, 196
late
Amidocinnamylacrylic acid....
NH2.(CH:CH.CH:CH.
ji
176-5
Diehl and Einhorn
B., 18, 2333
48, 1223
COSH)=1.2
Ethyl-p-methyl pseudisatin....
....
»
109-110
Duisberg
B., 18, 199
48, 545
Ethyloxycarbostyril
....
„
....
73
Friedlander & Os-
B., 14, 1919
42, 202
termeier
518
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Kairocoll (quinoline com-
MM
CuH.AN
66
Fischer
B., 16, 719
44, 1147
pound)
Benzenylazoxime propenyl
O.N : CPh.N : c.(CH2)2.co.
CnHn02N3
....
168
Schulz
B., 18, 2463
48, 1219
carboxylaruide
i i
NHa
Isonitrosoantipyrine
C6H(.N.NMe.CMe.OH
11
explodesSOO
cryst.
Knorr
B., 17, 2039
46, 1378
i
(NO).CO=1.2
„ |
Ethylic nitrosobenzoylace-
HO.N : CBz.CO2Et
C11H1103N
120-121
Perkin
....
47, 244
tate
Itaconanilic acid
11
....
189 d.
Gottlieb
A., 77, 284
Acetamidocinnamic acid
NHAc.(CH:CH.C02H)=1.4
11
....
259-263
Gabriel & Herzberg
B., 16, 2041
44,1123
:i 11
» »
11
259-260
Herzberg
C. C. [1884], 35
48, 662
Ethylic indoxylate .... ' w
KC6H4.C(OH).CH.C02Et
)>
120-121
Baeyer
B., 14, 1742
42, 198
=1.2
Ethylindoxylic acid
N.C6H4.C(OEt).CH.CO2H
1)
160
11
B., 14, 1743
11
i i
=1.2
Nitrosoanilidopyrotartari-
NPb(£fO).CMe.CO.NH.
CuHuO^N.
MM
173
Wechsler
B., 18, 1044
48,900
mide
r
CO.CH2
J
T - 1
Nitroantipyrine
C6H4.N.NMe.CMe.CH
))
270-280
Knorr
B., 17, 2040
46, 1378
L
(NO,).CO=1.2
1
Ethylic nitrosobenzoylacetate
HO.N : CBz.CO2Et
CUHU04N
....
121-122
Baeyer and Perkin
B., 16, 2133
46, 64
Ethylic nitrocinnamate
N03.(CH : CH.CO,Et)=1.2
»J
....
^
Beilstein and Kuhl-
A., 163, 131
25, 709
berg
)> 11
YI -11
»)
...«
42
Mtiller
A., 212, 127
42,841
» 11
11 11
11
....
44
Baeyer
B., 13, 2257
40, 274
» 11
=1.3
11
cf.B.11,1783
78-79
Schiff
G. I., 8, 294
36, 321
11 11
=1.4
.,
....
136
Mitscherlich
....
i., 988
11 11
11 11
»)
137
Miiller
A., 212, 127
42,841
11 11
11 -))
r>
138-5
Beilstein and Kuhl-
A., 163, 128;
vii., 348
berg
Z. C. [2], 7, 489
Diactamidobenzoic acid
NACs.C02H=1.2
11
....
220
Bedson and King
....
37, 757
?
NHMe.CO.C6H4.CO.CH3.
11
145 p.d.
Gabriel
B., 18, 2452
48, 1228
CO2H
Ethylic indoxanthinate
NH.CfH4.CO.C(.OH).CO2Et
i i
11
107
Baeyer
B., 15, 775
42, 1101
=1.2
Acetyl-p-methylisatic acid ....
11
172 d.
Duisberg ,
B., 18, 198
48, 544
Ethylic nitrobenzoylacetate
NO2.(CO.CH2.CO2Et)=1.4
CnH.AN
....
49-50
Perkin & Bellenot
B., 17, 327
46, 1024
Ethylic benzanioxalate
CO2H.(NH.CO.CO2Et)=l .2
11
180-181
Baeyer
B., 15, 777
42, 1101
» i)
=1-3
11
225
Schiff
B., 17, 402
46, 906
Benzamsuccinic acid
C02H.(NH.CO.C2H4.CO;1H)
11
222-233
Pellizzari
B., 18, 215
48, 534
=1.3
11 11
n 11
n
230
....
J. R, 4, 295
» i)
=1.4
»
....
225-226
Michael
B., 10, 578
32, 616
Nitrotolylazoacetoacetic acid
Me.N02.(N2.CHAc.COJH)
CuH.ANs
....
176
Bamberger
B., 17, 2421
48, 157
=1.3.4
-nitro-orcyldiglycollic acid....
• .*
CUHH08N
140
Saarbach
J. p. [2], 21, 170
Benzenylazoximebutenyl ....
Ph,C:N.O.CPr«:N
1 1
CUH12ONS
265
Liquid
Schulz
B., 18, 1085
48,897
Dimethyloxyquinizine
»)
....
113
Knorr
B., 17, 549
46, 1153
1 1
11 ....
C6H4.N.NH.CMe.CHMe.CO
))
....
127-132
Knorr and Blank
B., 17, 2050
46, 1380
' i
=1.2
Tolumethyloxyquinizine
C6H3Me.N.NH.CMe.
i
11
183
Knorr
B., 17, 550
46, 1153
CHMe.CO=1.2.3
1
11
=1.4.5
»J
....
140
11
11
»
COMPOUNDS CONTAINING FOUR ELEMENTS.
519
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Gh. Soc.
Anilidopyrotartarimide
CO.NH.CO.CF2.CMe.NHP
C11H1202N2
150
Wechsler
B., 18, 1040
48, 900
I 1
Ethylquinazol carboxylic aek
CSH6N( : NEt).CO2H
»
....
126
Fischer and Kuze
A., 221, 261
46, 442
» ?' »
v. B., 16, 653
))
....
181
)» »
B., 16, 654
44, 812
Nitrosomethyldiacetamido-
NAc2.(CH2.NO)=1.2
CnH1203N2
....
127-5-128-5
Gabriel and Meyer
B., 14, 2340
42, 189
benzeue
Nitrosoethylamidocinnamic
NEt(NO).(CH : CH.C02H)
J»
....
149 d.
Fischer
B., 14, 482
40, 599
acid
=1.2
» »
» »»
'J
cf.B., 16,654
150d.
Fischer and Kuzel
A., 221, 261
46, 440
Azotoluene acetacetic acid ...
Me. (N2.CHAc.CO2H)= 1 .4
ji
....
180-190 d.
Zublin
B., 11, 1419
34, 880
Quinoline ethylic nitrate ...
C9H-N+Et.O.NO2
)>
....
89 u. c.
Claus and Tosse
B., 16, 1278
44, 1009
Ethylic beuzoylallophanate ..
NHBz.CO.NH.CO2Et
CUH1204N2
163
Kretschmar
B., 8, 104 ; C. C
28,563; 31,615
[1876], 233
Hippuramidoacetic acid
NHBz.CH2.CO.NH.CH2
J>
206-5
Curtius
J. p. [2], 24, 239 ,
40, 1144; 44,
CO2H
26, 175
338
Ethylic amidobenzamoxalate
(CO.NH2).(NH.CO.C02Et)
J)
191-5
Schiff
B., ir, 402
46, 906
=1.3
Benzamsuccinamide
C02H.(NH.CO.C2H4.CO.
»
228-229
Pellizzari
B., 18, 214
48, 533
NH2)=1.3
Ethylic a-nitramidocinna-
N02.NH2.(CH : CH.CO.2Et)
J)
....
158-160
Friedlander and
A., 229, 233
48, 1139
mate
=?.2.1
Lazarus
Nitrophenyl-£-acetylalanine
NO2.(CH.OH0.CO.O.NH2Ac
i " i
CnH,AN2
141-142
Einhorn
B., 16, 2647
46, 305
= 1.4
»
» »
»
146-150
Easier
B., 17, 1496
46, 1173
Pyrotartaronitranilic acid ...
NO.,(NH.C5H602.OH)=1.4
1)
....
150.+
Arppe
A., 87, 228; 90,
iv., 775
145
Ethylic nitrotolyloxamate ...
Me.NO2.(NH.CO.CO2Et)
»»
.».
127-128
Hinsberg
B., 15, 2691
44, 323
=1.3.4
Nitroacetamidohydrocinnamic
NHAc.NO2.(CH2.CH2.CO2H
)»
174
Gabriel and Steu-
B., 15, 844
42, 1073
acid
=1.2.4
deroann.
Ethylic dinitrohydrociimamic
(N02)2.(CH : CH.C02Et)
CnH1206N2
,~.
32
Gabriel and Zirn-
B., 12, 601
36, 640
acid
=1.2.4.(?)
raermann
Methylic nitrophenylmeth-
N02.[CH(OMe).CH(JSI02).
CnH12O.N2
....
117 118
Friedlandaif and
A., 229, 210 ; B.,
48, 1138
oxynitropropionate
CO2Me]=1.4
Mahly -
16, 852
Ethylic dinitroethoxyben-
CO2Et.OEt.(NO2)2=1.2.(?)2
)>
....
49
Salkowski.
A., 173, 51
zoate
>» »
=1.4.(?)2
»
59
»
B., 4, 653; A.,
24,920; 29,716
163, 48
Methylic methoxydinitrohy-
OMe^NO^CEvCH,,.
))
....
53
Stohr
A., 225, 57
46, 1350
drocinnamic acid
CO2Me)=1.2.6.4
Ethoxydinitrohydrocinnamic
OEt.(NO2)2. (CH2.CH2.CO2H)
M
126
»»
»
»
acid
=1.2.6.4
Trinitroethoxyphenylure-
OEt.(NO2)3.(NH.CO2Et)
CUH1209N4
....
211-212 d.
Kohler
J. p. [2], 29, 257
46, 1161
thane
= 1.(?)3.4
Phenylangelamide ....
Ph.C4H6.CO.NH2
C,,H13ON
....
128
Perkin
J. [1877], 790
Acetylhydromethylketole ....
C6H4.CH2.CHMe.NAc=1.2
i i
))
....
55-56
Jackson
B., 14, 883
40, 735
Ethoxytetrahydroquinoline ...
NH.H3.OH=a1ft/3i«2;a,
))
275-276(716)
Liquid
Fischer
B., 16, V18
44, 1146
Acetyltetrahydroquinoline ....
....
)J
295
liiquid
Wischnegradsky
B., 13,2400; B.S.
40, 444
[2], 34, 339
„
....
)>
295
L/iquid
Soifmann & Kouigs
B., 16, 734
44, 1144
Ethyldihydrocarbostyril
C6H4CH2.CHAc.CO.NH
))
87-88 ;a.f. 76
3aeyer and Jackson
B., 13, 120
38,407
=1.2
i»
v. B., 15, 377, 2104
))
....
199
Triedlander and
B., 15, 336, 2103
42,732
Ostermeier
Isonitrosoacetophenone ace-
Ph.CO.(CH2)2.CMe : NOH or
CUH1302N
....
22-123
Paal
B., 16, 2868
46, 599
tone
Me.CO.(CH2)2.CPh: NOH
Ethylic amidocinnamate
NH2.(CH : CH.CO,Et)=1.2
))
....
7-78
Tried lander and
B., 15, 1422
42, 1209
Weinberg
Ethamidocinnamic acid
NHEt.(CH: CH.C02H)=1.2
)»
25
>»
B., 15, 1423
» »
11 »
»
....
25
Fischer and Kuzel
A., 221, 261
6, 440
520
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Isobutylene-m-amidobenzoic
....
CnH1302N
d. 190
145-150
Schiff
A., 210, 118
42,304
acid
Isopropylnitrostyrene
(CH I CH3).N02.Pr/3=1.2.4
M
....
Lf.m.
Einhorn and Hess
B., 17, 2025
46, 1353
Methyltetrahydrocinchonic
- Mf*
1»
....
125
Weidel and Hazura
M. C., 5, 643
48, 562
acid
»» »
• »*
1)
....
169-170-d. .
Weidel
M. C., 3, 66
42, 532
Methyltetrahydroquinoline
N.OO3H=a1;/3, or a3
»
«...
164
Fischer and Korner
B., 17, 766
46, 1197
carboxylic acid
?
«...
H
310 p.d.
122
Bruyn
E. T., 2, 205
48, 657
Ethylic malonanilidate
NHPh.CO.CH2.CO2Et
CUH1303N
....
38-30
Eugheimer and
B., 17, 740
46, 1023
Hoffmann
Ethylic hippurate
NHBz.CH2.CO2Et
)»
MM
44
Stenhouse
A., 31, 148
iii., 162
» „ ....
j»
-«
....
60
.Curtius
B., 17, 1663
46, 1348
?) »» •••• ••••
«
»
....
60'5
»
J. p. [2], 26, 145
44, 339
» ») •"> ••••
i »>
-IJ
....
60-5
.Campani & Bizzarri
G. I., 10, 257
38, 870
» jj .... *..'
«
n
a. 180 p.d.
60-5
Conrad
J. p. [2], 15, 246
32, 484
Pyrotartranilic acid
....
•H
A., 91, k)6
147
Arppe
A., 90, 141; 91,106
Ethylic tolyloxamate
Me.(NH.CO.C02Et)=1.4
))
66-67
Klinger
A., 184, 285
31,712
Tolylsuccinamic acid
Me.[NH.CO,(CH2)2.C02H]
)3
....
91
Bechi
B., 12, 322
36, 528
=1.2
»» » ••"
=1.4
1)
157
»»
)j
i)
Acetamidohydrocinnamicacid
NHAc. (CH2.CHj.CO.jH) =1.4
1)
....
143
Gabriel and Steu-
B., 15, 844
42, 1073
demann
Hippurylamidoacetamide ....
NH;Bz.CH2.CO.NH.CHj.CO.
CU^AN,
....
202
Curtius
J. p. [2], 26, 194
44, 339
NH2
Diazoimidoethoxyphenylure-
N:N.C6H3(OEt).N.C02Et
»)
....
b. 100
Kohler
J. p. [2], 29, 257
46, 1160
thane
i i
Amidotolylazo-acetacetic acid
Me.<NH2.(N2.CHA c.CO2H)
»
162
Bamberger
B., 17, 2421
48, 158
=1.3.4
Diacetdiamidobenzamide ....
(NHAc)2.(CO.NH2)=1.3.5
»
a. 265
Muretow
Z. C. [2], 6, 642
vii., 130
Anilidopyrotartaric acid
C02H.CMe(NHPh).CHj.
CnH13Q4N
101-102
Wechsler
B., 18, 1048
48, 900
C03H
Ethylic nitrohydrociunamate
NQs.(CH2.CH2.CO2Et)=1.2
»
.«.
Liquid
Gabriel and Zim-
B., 13, 1681
mermann
»> »
=1.4
))
....
33-34
Beilsteinand Kuhl-
A.,163,133;Z.C.
26, 300 ; vii.,
berg
[2], 7, 487
348
Nitrotolylisobutyric acid ....
Me.N02.(CH2.CHMe.C02H)
n
....
139
Effront
B., 17, 2326
48, 152
=1.2.5
Ethylic nitromesitylenate ....
CO2Et.Me2.NO2=1.3.5.2
n
....
64-65
Schmitz
A., 193, 167
36, 156
i> »
„ =1.3.5.4
»
....
72
Fittig
A., 147, 50
vi., 823
Methyldicarbocollidylium
v. B., 17, 1024
j»
a. 360
81-82
Hantzsch
B., 17, 1023
46, 1045
dehydride
!) »
JI
»
MM
92
M
»
II
Nitrodiacetdiamidotoluene ....
Me.N02.(NHAc)=(?),,.1.3
•5)
....
n.f. 240
Tiemann
B., 3, 9
» ....
n
~»
*••*
253
Ladenburg
B., 8, 1211
29, 401
Diethylic chelidammate
c(OH) : N.c(co2Et).CH.: c :
CUH1305N
+H20
80-81
Lerch
M. C., 5, 367
48,46
CH.COjEt
Ethylic nitrophenyl-|3-lactate
N02.[CH(OH).CH2.C02Et]
«
....
56
Einhorn & Praus-
B., 17, 1661
46, 1351
=1.3
nitz
» )!
=1.4
)j
....
45-46
»
»
»
)) JI
» »
>j
....
45-46
Easier
B., 16, 3007
46, 604
o-Nitrophenyllactic aldehyde
C6H4(N02)[C2H3(OH).CHO]
)>
125 p. d.
Baeyer & Drewsen
B., 16, 2205
46, 58
+acetic aldehyde
+CH3.CHO
Ethylic ethoxynitrobenzoic
CO2Et.OEt.NO2=1.2.3
»»
of. A., 195, 35
Liquid
Hiibner
B., 8, 1216
29, 593
acid
>' »
„ =l.-2.5
jj
cf. A., 195, 15
98-99
»
B., 8, 1219
Jj
Ethylic nitrohydrocoumarate
OH.N02[(CH2)2.C02Et]
»
....
30
Stohr
A., 225, 57
46, 1350
=1.2.4
Nitrodiethoxybenzaldehyde
(OEt)2.N02.CHO=1.4.?.5
H
129-130
Hantzsch
J. p. [2], 22, 472
40, 167
Methoxyisopropylnitroben-
Prf.OMe.N02.C02H=?
jl
145-146
Paterno & Canzoneri
G. I., 10, 233
38, 884
zoic acid
Dmitroacetpseudocumidide ....
Me3.NHAc.(NOs),=1.3.4.(?)s
CUH1306N3
....
204
Engel
B., 18, 2232
48, 1215
COMPOUNDS CONTAINING FOUR ELEMENTS.
521
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Dinitroacetmesidide
Me3.NHAc.(N02)2
CUHI306N3
cf.A.,179,167
275
Ladenburg
B., 7, 1134
28, 63
—1.3.5.2.4.6
„
»» »
1)
MM
276
Ledoux
I. D. Gott., 1875
Ethylio nitroveratrate
CO2Et.(OMe)2.NO2=1.3.4.?
CnH1306N
99-100
Tiemann and Mats-
B., 9, 941 ; 1],
30, 524
moto
132
Trinitrolaurol (?) „
....
CnHI306N3
»..
84
Fittig and others
A., 145, 150
Ethylic dinitroamidohydro-
NH2. (N02)2.(CH2.CH2.CO2
»
95
Stohr
A., 225, 57
46, 1350
cinnamate
Et)=1.2.6.4
Dimtroethoxyphenylure-
OEt.(N02)2.(NH.C02Et)
C^H^N,
....
141
Kohler
J. p. [2], 29, 257
46, 1161
thane
=1.(?)2.4
Methyltrinitrothymol
Me.Pr«.OMe.(NO2)3
)>
....
92
....
Z. C. [1871], 415
—1.4.5.2.3.6
Diethyltrinitro-orcinol
Me.(OEt)2.(NO2)3=1.3.5.2.4.6
CUH1308N3
....
61-5
Stenhouse
P. R, 19, 410 ;
24, 358; vii.,
Z.G [1871], 229
880
Ethylamidohydrocarbostyril
C6H4.N(NHEt).CO.(CH2)2
CnH14ONs
.to
74
Fischer and Kuzel
A., 221, 261
46, 442
i i
=1.2
Ethylhydrocarbazostyril
C6H4.(CH2)2.CO.NH.NEt
l_ 1
)»
165-5
u
B., 16, 1452
44, 1132
=1.2
Butyrylbenzenylamidoxime
NH2.CPh : NO.CO.Pr*
C^H^N,
MM
94
Schulz
B., 18, 1084
48, 897
Ethylic phenylhydraziuepyro-
Ph.N2H : CMe.CO.,Et
JJ
114-115
Fischer & Jourdan
B., 16, 2243
46,53
racemate
Tolylsuccinamide
Me.(NH.CO.C2H4.CO.NH2)
»
....
148
Bechi
B., 12, 321
36, 527
=1.4
„
=1.2
JJ
....
160
»
»
»
Diacetdiamidotoluene
Me.(NHAc)2=1.2.5
))
....
219-220
Witt
35, 360
i) ••••
5) J>
)>
cf.B.,10,1157
220
Nietzki
B., 12, 2237
,,
=1.2.4
J>
....
221
Tiemann
B., 3, 8
„
>i n
J)
....
222
Koch
A., 153, 132
»
» '>
))
....
223
Kelbe
B., 16, 1200
44, 916
» ....
>! I)
»
....
223
Hell and Schoop
B., 12, 724
36, 715
„
» i>
J)
....
824
Ladenburg
B., 8, 1211
29, 401
Nitroso-ethoxyhydroquino-
N.OEt=ai ; a,
»
....
113
Fischer and Eenouf
B., 17, 759
46, 1049
ILne
Nitrosoetharnidohydrocin-
(NEt.NO).(CH2.CH2.C02H)
C11H1403N2
....
78
Fischer and Kuzel
A., 221, 261 ; B.,
44, 1132 ; 46,
namic acid
=1.2
16, 1451
440
Ethylic amidotolyloxamate....
Me.NH2.(NH.CO.CO2Et)
»
....
168
Tiemann
B., 3, 222
=1.2.4
Nitracetopseudocumidide ....
Me3.NHAc.NO2=1.3.4.(?)2
))
....
131
Engel
B., 18, 2231
48, 1215
„
„ =1.3.4.6.5
»
....
193-194
Edler
B., 18, 629
48, 771
Nitracetomesidide
„ =1.3.5.2.4
3>
....
182
Ledoux
B., 8, 58
28, 569
»
» »
;j
....
188
Ladenburg
B., 7, 1134
28, 63
Ethylic phenylhydroxyethe-
HO.CHPh.C(NH2):N.O.
CUH1404N2
....
106-107
Gross
B., 18, 2480
48, 1218
nylamidoxime carbonate
CO2Et
Nitroethoxyphenylure thane
OEt.N02.(NH.CO2Et)=l.?.4
CUH1406N2
....
71
Kohler
J. p. [2], 29, 257
46, 1159
Diethylbenzamide
C6H5.CO.NEt2
CUH16ON
280-282 c.
Liquid
Hallmann
B., 9, 846
30, 418
Acetylpropylanilide
C6H5.NPr"Ac
)»
254 u. c.
56 u. c.
Glaus and Eoques
B., 16, 913
Isovaleranilde
C6H6.NH.(CH2)2.CHMe2
)J
300
100
Schmidt and
A., 193, 102
36, 139
Sachtleben
(cf. A., 84, 109)
)»
JJ
a. 220
115
Chiozza
A. C. [3], 39, 201
v., 975
» — • —•
>J
)>
....
115
Kelbe
B., 16, 1200
44, 916
Isobutylbenzaldoxime
C6H6.CH:NOBu0
)>
237-239 s.d.;
....
Petraczek
B., 16, 828
u.c.
Acetylethyltoluidide
Me.NEtAc=1.2
»
254-256
Eeinhardt & Staedel
B., 16, 31
44, 578
Formamidoisobutylbenzene
BnB.(NH.CHO)=?
»
310-316
59
Gasiorowski & Merz
B., 18, 1009
48, 773
Acetamidopropylbenzene ....
Pr«.NHAc=1.4
)J
....
87
Louis
B., 16, 108
Acetamidoethyltoluene
Me.Et.NHAc=l.?.2
)1
313-315
105-105-5
Benz
B., 15, 1651
42, 1284
Cymene carboxylamide
Me.Pr«.(CO.NH2)=1.4
)>
cf. B., 8, 442
138-139
Paterno and Spica
G. I., 9, 400
38, 163
Cyanocamphor
C10H14.CN.OH
)»
250 p.d.
127-128
Haller
C. R, 87, 843
36, 329
Acetopseudocumidide
Me3.NHAc=1.3.4.2 or 5
M
....
112
Engel
B., 18, 2230
48, 1215
„ ....
„ =1.3.4.6
)j
....
161
Edler
B., 18, 629
48, 771
» ••••
»> >i
j)
....
161
Nolting and Bau-
B., 18, 1146
48, 893
mann
3 x
522
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Acetomesidide
Me3.NHAc=1.3.5.6
CUH15ON
....
210
Nolting & Baumann
B., 18, 1146
48, 893
„ .... ....
„ „
M
..»•
213-214
Ladenburg
B., 7, 1136
28, 64
„
„ „
„
....
216
Biedermann and
B., 8, 58
28, 569
Ledoux
„ .... ....
„ 1(
j)
....
216-217
Ladenburg
A., 179, 173
Tetrahydro-ethoxyquinoline
N.OEt=o, ; a.
„
275-276(716)
Liquid
Fischer
B., 16, 718
Tetrahydrohydroxyethyl
N. 011=^; /3, or a2
„
....
73
Eiemerschmied
B., 16, 724
44, 1148
quinoline
)! 1)
NEt.OH=ai; a,
„
....
76
Fischer
B., 16, 717
„ „
„ „
„
.«»•
76
Fischer and Eenouf
B., 17, 756
46, 1049
Tetrahydromethoxyquinal-
N.Me.OMe=a!3i; ai
„
270
Liquid
Dobner and Miller
B., 17, 1707
46, 1374
dine
Benzenyleth oximidoethy 1
EtO.CPh : N.OEt
CuH15OaN
238,u.c.;(o.p.)
Liquid
Tiemann & Kriiger
B., 18, 742
48, 790
ether
128 (40)
Ethylic ethylbenzoylhydrox-
NEtBz.OEt
„
244 c. (755)
....
Gurke
A., 205, 273
40, 571
amate
p.d.
Ethylic ethylphenylcarba-
NEtPLCOjEt
„
245-250
....
„
„
„
mate
Isobutylic phenylcarbamate
NHPh.C02Bu?
„
216
80
Mylius
B., 5, 973
26, 266 ; vii.,
946
a-phenamidovaleric acid
CHMes.CH(NHPh).C02H
„
....
a. 110
Duvillier
A. C. (5), 21, 433
40, 713
Cumylic carbamate ....
NH2.CO2.CH2.C6H4Pr
„
v. a. 200
88-89
Spica
G. I., 5, 394
29, 582
Ethylic tolylamidoacetate ....
Me.(NH.CH3.COsEt)=1.2
n
272-278
Liquid — 10
Ehrlich
B., 16, 204
44, 594
II !>
=1.3
ji
....
68
„
B., 15, 2012
44, 54
H » ""
=1.4
M
....
48-49
Meyer
B., 8, 1159
29, 402
Diethamidobenzoic acid
NEt2.C02H=1.3
„
....
90
Griess
B., 5, 1040
26, 281 ; vii.,
167
„ ,,
=1.4
„
....
188
Michler and Grad-
B., 9, 1912
32, 334, 335
iiiann
Cuminamidoacetic acid
C6H4Pr.CH(NH2).C02H(?)
„
....
197 d.
Ploschl
B., 14, 1317
42, 515
Ethylic xylylcarbamate
NH(CsH9).C02Et
H
58
Hofmann
B., 3, 657; P. B.,
24, 139; vii.,
19, 108
253
Acetamidoethoxytoluene ....
Me.OEt.NHAc=1.4.5
„
....
106-5
Kayser
B., 15, 1135
42, 1203
„
„ „
„
....
106-5
Staedel
A., 217, 221
44,866
„
=1.2.5
n
....
108
„
A., 217, 218
„
»
!) ))
„
....
108
Kayser
B., 15, 1135
42, 1203
„ ....
=1.3.?
„
....
114
„
„
„
„
„ „
„
....
114
Staedel
A., 217, 220, 222
44, 866
Methamidothymoquinone ....
Me.Pra.NHMe:O2=1.4.(?)3
„
....
74
Zincke
B., 14, 97
40, 596
Ethylic collidine carboxylate
C5HNMe3.CO2Et
„
256
Liquid
Michael
A., 225, 121
48, 61
Toluidine diacetamide
C6H4Me.N(CH2.CO.NH2)2
CUH1402N3
....
250
Meyer
B., 8, 1163
29, 402
=1.4
Ethylic ethoxyphenylcarba-
OEt.(NH.C02Et)=1.4
CnH1503N
250-270 p.d.
94
Kohler
J. p. [2], 29, 257
46, 1159
mate
Methylic dimethamidoanis-
CO3Me.OMe.NMe,=1.4.?
„
288
Liquid
Griess
B., 6, 588
26, 1146; vii.,
sate
188
Ethylanhydracetdiamido-
C6H3Me.N:CMe.NHEt.N03
CUH,503N8
....
93
Hiibner
A., 210, 328
42, 505
toluene nitrate
i i
Ethylic amidoveratrate
CO2Et.(OMe).2=1.3.4.
C1IHI504N
•i>.
88-89
Matsmoto
B., 11, 135
34, 502
Diethylic ethylcyanurdicar-
C3EtO3N3(CO2Et)2
CuHujC^Nj
....
123
Wurtz and Hennin-
C. B., 100, 1419
48, 969
boxylate
ger
Diethylphenylcarbamide
NHPh.CO.NEt2
CnH16ON2
.in
85
Gebhardt
B., 17, 3039
48, 383
Cuminylcarbamide
C6H4Pr.(CH2.NH.CO.NH2)
„
....
133
Eaab
B., 8, 1151
29, 398
=?
Acetyltrimethdiamidoben-
NMe2.NMeAc=1.4
„
95
Wurster & Schobig
B., 12, 1811
38, 111
zene
ji »
„ „
„
+xH2O
78
„
n
„
Acetyldimethdiamidotoluene
Me.NMe2.NHAc=1.3.4
»)
....
158
Wurster and Eiedel
B., 12, 1801
38, 109
Isocymyl carbamide ^
Me.Pr3.(NH.CO.NH2)=1.3.?
„
«...
176
Kelbe and Warth
A., 221, 157
46,47
Ethylanhydracetdiamido-
C6H3Me.N :CMe.NHEt(OH)
B
93
Hiibner
A., 210, 328
42, 505
toluene hydrate
1 |
.. »
» »
„
+2H20
n
„
i)
COMPOUNDS CONTAINING FOUR ELEMENTS.
523
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Walts' Diet.
& J. Ch. Soc.
Ethylic a-phenylhydrazido-
NHj.NPh.CHMe.CO.Et
CnH1602N2
....
116
Eeissert
B., 17, 1456
46, 1152
propionate
Pilocarpin
J>
159
Blyth
....
33, 317
Ethylic amidoethoxyphenyl
OEt.NH2.(NH.C02Et)=l.?.4
C11H1603N
....
88
Kohler
J. p. [2], 29, 257
46, 1160
carbarn ate
i> »
=1.?.4
))
121
j»
»
46, 1161
Diethoxy-oxydimethylpurin
C5N4Me2O(OEt)3
CnH1603N4
....
126-127
Fischer
B., 17, 337
46, 997
Ethoxyethyltheobromin
C.H6EtN2O4.OEt
CnHJ606N2
....
155
)>
A., 215, 306
44, 357
Furfurol diurethane
C4H3O.CH(NH.CO2Et),
»
....
169
Bischoff
B., 7, 1081
Ethylphenylpropylalkine ....
NPhEt.C3H6.OH
CUH17ON
261-263
....
Laun
B., 17, 678
46, 1011
Acetylcyanethine
C9H13N2.NHAc
CUH17ON3
59
Meyer
J. p. [2], 30, 115
48, 140
Dioxyethene toluidine
C6H4Me.N(02H4.OH)2=1.4
C,,H1703N
338-340
Liquid
Demole
A, 173, 137; B.,
27, 904
7,638
Phoronimide
O.CMeBuP.CH,, .CMe.CO.
CUH1703N
....
205
Pinner
B., 14, 1080
40, 797
NH.CO
Ethoxycyanconiine
C9HI2N(NH).OEt
CUH19ON3
229-231
Liquid
Meyer
J. p. [2], 22, 277
40, 55
Ethylhydroxycyanconiine ....
C9H17N(NEt).OH
»
267-268
43
»
J. p. [2], 26, 350
44, 353
Ethoxyhydroxycyanconiine....
C9H12(OEt)N2.OH
C11H1903N2
....
51
Eiess
J. p. [2], 30, 145
48, 235
?
....
))
...»
a. 320
Pinner
B., 14, 1077
40, 797
Ethoxycyanethine
C9H14N3.OEt
CUH19ON3
300
115
Riess
J. p. [2], 30, 145
48, 235
Borneol urethane
cf. C. R., 94, 869
C11HJ902N
....
115
Haller
C. R., 93, 1511
42, 625
C24HJ804N2(?)
( „ ),(!)
....
b. 100
Sonnenschein
B., 9, 1185
31, 97
>J
....
b. 100
Wormley
A. J., 1870, 42
vii., 552
cf. P.J.T. (3), 521, 561, 601
M
....
b. 100
Holmes
P. J. T. [3], 481
29, 942
C13H1402N(f)
»
....
45 ; af. 38
Gerrard
B., 16, 798
Phoronamide ...
NH2.CO.CMe.CHj.CMe(.O).
C11H2003N2
....
a. 300
Pinner
B., 14, 1079
40, 797
CH2.CMe2.CO.NHs
Valerodiacetonamine
Bu/3.CH.CH2.CO.CH2.
CUH31ON
....
21 ; sf. 15
Antrick
A., 227, 365
48, 502
CMe^NH
i
Menthol urethane ....
CnH^OjN
d. 200
165
Arth
C. R., 94, 872
42, 1213
Conylurethane
C8H16N.CO2Et
»
245
MM
Schotten
B., 15, 1947
44, 220
Ethylic oxyheptinamate
C7H90(OEt)2.NH2
CnF2103N
87
Demarcay
A. C. [5], 20, 494
Isovaleral diurethane
C5H10(NH.C02Et)3
C11H2204N2
...»
126
Bischoff
B., 7, 633, 634
27, 891
Amidocamphoronamide
....
CUH3306N3
MM
144-145
Hjelt
B., 13, 797
38, 670
+C2H60
.
Methylnonylacetoxime
C9H19.CMe:NOH
CnH.sON
cf.B., 17,1575
42
Spiegler
M. C., 5, 241
46, 1115
Diisoamylcarbamide
CO(NH.CH.CH2.CHMe2)2
CnH24ON3
270
37-39
Ouster
B., 12, 1331
36, 913
Tetraethylallylalkine
(NEt2)2.C3H5.OH
CnH26ON3
234-5
Liquid
Berend
B., 17, 511
46, 1114
„
M
»
236-238
Liquid
Reboul
C. R., 97, 1488
46, 578
Euchroicacid (cf . P. A.,52, 610)
....
C12H408N2
+2H20
a. 280 d.
Wohler
A., 37, 273; 66, 49
ii., 602
Hexanitrodiresorcinol
C12(N02)6(OH)4
C1SH4016N6
«•••
d. w. m. 230
Benedikt & Julius
M. C., 5, 177
46, 1140
a-Tetranitrocarbazole
C13H6(N03)4N
C13H6O8N6
cf.B.,15,1760
308 d.
Ciamician & Silber
G. I. [1882], 272
42, 1104
0-
»
»
cf.B., 15, 1760
nf. 320
»
)>
»
y- ,.
»
>j
cf.B.,15,1760
285 d.
»
»
n
Dipicrylamine (aurantia) ....
NH[C6H2(N02)3]3
0,3H6012N7
230 d.
Austen
A. J. S. [3], 13,
32, 759
=1.2.4.6 ; 1.4.(?)3
279
>! »
» »
I)
....
233
Gnehm
B., 7, 1401
)» >j
» i)
»;
....
233-234 d.
»
B., 7, 1400
,, ,)
n »
))
....
234 d.
Mertens
B., 11, 845
34, 725
» »
» )>
))
....
238 d.
Gaehm
B., 9, 1245
» i>
» »
»
....
238 d.
Austen
B., 7, 1250
28, 165; 32, 761
» » ••"
„ =1.2.4.6; 1.3.(?)2
)»
cf.B., 7, 1249
261
»
A. J. S., 13, 279
28, 165; 32, 758
Dinitroazophenylene
C12H604N4
d.a. 131
131
Glaus
B., 8, 40
28, 647
Dinitrodiphenylene oxide ....
....
CI2H,06N2
....
200
Hoffmeister
A., 159, 214
Tetranitrodiphenyl
fr.(.C6H4.N02)=(1.4)3
C12He08N4
140
Losanitsch
B.,4, 405
24, 509; vii., 938
Tetranitrophenyl oxide
0[C6H3(N02)2]2=(1.2.4)3
CI2H609N4
....
195
Willgerodt
B., 13, 887
38, 643
» ••••
C6H4(N02).O.C,H2(N02)3
»
....
172-173
Willgerodt and
B., 17, 1766
46, 1328
=1.2; 1.2.4.6
Huetlin
3x2
524
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Tetranitrophenyl oxide
06H4(NO)2.O.C6H3(N02)3
C12H609N4
153
Willgerodt and
B., 17, 1766
46, 1328
=1.4; 1.2.4.6
Huetlin
Tetranitro-diresorcinol
[.C6H(OH)3(N02)2]2
C13H6013N4
....
268
Benedikt and Hiibl
M. C., 2, 330
40, 1134
a-naphthoyl cyanide
C10H7(CO.CN)=a
C12H7ON
....
101
Boessneck
B., 15, 3065
44, 595
a-phenylpyridine ketone
C6H4.CO.CbNH3=1.3 ; 1.2.6
»
315
140-142
Skraup & Cobenzl
M. C., 4, 436
44, 1015
i 1
Ketone from acridine
C[H.).N:CH.CH:C.CH:CH.CO
n
....
nf. 320
Grsebe and Caro
B., 13, 103
38, 399
L J =1.2.3
Naphthalimide
C10H6.CO.NH.CO
C13H702N
....
a. 280
Behr and Dorp
A., 172, 270
27, 1168
i i
Pyrroline phthalimide «..
C4H3N:C.C6H4.CO.O
240-241
Ciamician and
B., 17, 2958
48, 379
1 1
Dennstedt
Nitroazophenylene
C12H702N3
209-210
Glaus
B., 8, 40
28, 647
Trinitroazobenzene
....
C12H706NS
....
112
Petrieff
Z. C. [2], 6, 564
vii., 1183
„
Ph.N2.C6H2(N02)3
„
....
142
Fischer
A., 190, 133
34, 309
»
C6H4(N02).N2.C6H3(N02)2
„
....
169
Janovsky and Erb
B., 18, 1135
48, 894
=4.1; 1.4.2 or 3
„
„ =4.1 ; 1.4.3 or 2
D
MM
180
„
„
„
Trinitrophenyl oxide
Ph.O.C6H2(N02)3=1.2.4.6
C13H707N3
....
1
Willgerodt
B., 12, 1278
» „
C6H4(N02).O.C6H3(N02)2
n
....
114
Willgerodt and
B., 17, 1765
46, 1328
=1.4; 1.2.4-
Huetlin
„ „
=1.2; 1.2.4
„
....
119
„
„
„
Trinitroazoxybenzene
....
C12H70-N6
cf. B., 6, 557
152
Schmidt
Z. C. [2], 5, 421
vi., 272
Trinitrodioxyazobeuzene
....
C12H708N6
MM
102
Petrieff
B., 6, 558
26, 1028
Tetranitrodiphenylamine ....
NH[C6H3(N02)2]2=(1.2.4)3
j)
180
Hager
B., 17, 2630
48, 150
„
»
„
....
192
Gnehm and Wyss
B., 10, 1320
34, 52
„
C6H4(N02).NH.C6H2(N02)3
„
....
205
Austen
B., 7,1248; A.J.S.
28, 165 ; 32,
=1.3; 1.2.4.6
[3], 13, 279
757
„
=1.4 ; 1.2.4.6
„
....
216
„
„
n
Trinitrotrioxyazobenzene ....
....
C12H709N5
....
52
Petrieff
B., 6, 558
26, 1028
Nitrosocarbazole
C6H4.C6H4.N.NO
C13H8ON,
....
82
Zeidler
A., 191, 306
Hydroxyphenanthroline
„
....
159-160
Coste
B., 16, 675
44,811
fr : CH.CH : CH.cX.cn :
CH.C(OH) : N=1.2.6.5
/3-nitroacridine
....
C12H803N3
154
Grsebe and Caro
A., 158, 275
vii., 26
a- ,,
....
,,
....
214
„
„
vii., 25
Dinitrodiphenyl
(.C6H4.N02)2=1.2 ; 1.4
C12H804N2
....
93-5
Fittig
A., 124, 275
iv., 411
„
H »
D
....
93-5
Schultz
A., 174, 201
28, 150
„
,, »)
„
cf. B., 14, 612
93-5
Schultz & Strasser
A., 207, 350
40, 604, 911
„
=0-4).
„
....
213
Fittig
A., 124, 276
iv., 410
„
„ „
„
....
229-230
Liiddens
B., 8, 871
„
„ „
„
233
Schultz
A., 174, 221
28, 150
„ (cf. A., 207, 350)
„ „
„
S8S
Schultz & Strasser
B., 14, 612
40, 604, 911
Dipyridyl dicarboxylic acid
(.C5NH3.COOH)2=(1.2.6)2
„
214-215
Skraup
M. C., 3, 590
,> ,. »
» i>
„
+ 2H20
217 d.
„
B., 15, 896
42, 1112
), )! !>
» )>
„
....
217 d.
Skraup & Vortmann
M. C., 3, 370
44,88
Dinitroazobenzene
(:N.C6H4.N02)2=(1.3)2
c12H8o4isr4
cf. A., 75, 73
s. 15
Janovsky and Erb
B., 18, 1134
48, 894
„
=(1.4),
„
cf. A., 75, 73
206
„
„
„
„
„ „
»
206
Janovsky
M. C., (3, 157
48, 789
Dinitrophenyl oxide
Ph.O.C6H3(N02)2=?
C12H805N2
....
65
Maikopar
B., 6, 564
26, 1026
„ „ .... ....
=1.2.4
»
....
71
Willgerodt
B., 12, 767
36, 717
„ „
jj
....
135
Hoffmeister
A., 159, 208
vii., 941
Dinitrohydroxydiphenyl
fr. C6H4Ph.OH=1.4
„
....
154
Latschinoff and
B., 6, 195 ; J. R,
26, 750 ; vii.,
Engelhardt
5, 52
938
Dinitrodihydroxydiphenyl ....
[.C6H3(OH).N02]3=(?.1.2)2
C12H806NS
....
w. m. 150
Goldstein
B., 7, 735
27, 1093
„
....
„
....
184
„
J. E., 6, 193
Trinitrodiphenylamine
....
C12H306N4
135
Norton and Allen
B., 18, 1997
48, 1214
„
Ph.NH.C6H3(N02)3=?
„
....
175
Austen
A.J.S.[3],13,279
32, 760
»
» »
„
175
Clemm
B., 3, 126
„ ....
C6H4(N02).C6H3(N02)3
„
181
Austen
A. J. S. [3], 13,
28, 165 ; 32,
=1.4 j 1.2.4
279 ;B., 7, 1250
758
COMPOUNDS CONTAINING FOUR ELEMENTS.
525
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Triuitrodiphenylanrine
C,H4(NOa).C6H3(N02)2
C12H806N4
....
189
Austen
A. J. S. [3], 13,
28, 165 ; 32,
=1.3; 1.2.4
279; B., 7, 1250
758
j>
=1.3;1.(2)2
»
....
194-195
Willgerodt
B., 9, 1179
32, 758
Dinitrodiresorcinol
C12H4(N02)2(OH)4
C12H808N2
d.w.m. 170
Hazura
M. C., 4, 610
44, 1114
Ethenyl ainidonaphthol
C10H6.N : CMe.O
C12H9ON
Liquid
Bottcher
C. C. [1884], 898
48, 659
Azoazoxybenzene
C12H9ON3
....
85
Ziniu
A., 114, 225
i., 480
Nitrodiphenyl
Ph.C6H4.N02=1.2
C12H9O2N
....
37
Luddens
B., 8, 871
28, 1258
n ....
» »
»>
....
37
Schultz & Strasser
B., 14, 613
40, 604
D ••••
» ))
)»
....
37
Schultz and others
A., 207, 352
40, 912
» ....
I) ))
»
320 d.
37
Hiibuer
A., 209, 341
,,
=1.3
)>
....
86
Pfankuch
J. p. [2], 6, 107
» •••• •"
J) »
»J
157 (?)
Schultz
A., 174, 212
» ....
= 1.4
)1
....
113
Osten
B., 7, 171
27, 580
)> .... ....
» »»
>J
340 c.
113
Schultz
B.,7,53; A., 174,
27, 468 ; 28,
210
149; vii., 937
M ""
)> »)
»
....
113
Hiibner
A., 209, 340
» .... ....
» »)
)>
....
113
Schultz & Strasser
B., 14, 613
40, 604
»
» »»
«»
....
113
Luddens
B., 8, 871
a-Naphthylglyoxylamide ....
C10H7.CO.CO.NH2
>1
151
Boessneck
B., 15, 3066
44, 595
Nitroazobenzene
Ph.N2.C6H4.N02=1.4
C12H902N3
cf. A., 75, 73
137
Janovsky
M. C., 6, 157
48, 789
„ ....
» »
J>
....
138
Janovsky and Erb
B., 18, 1133
48, 894
Anilidohydroxyquinone
Oj.OH.NHPl^l.4.5.?
C12H903N
....
d.w.m. 200
Zincke
B., 18, 789
48, 787
Nitrohydroxydiphenyl
fr.Ph.C6H4.OH=1.4
))
....
67
Latschinoff
R, 6,195; J.R.,5,52
26,750;vii.,938
„
C6H4(OH).C6H4.N02
1)
....
138
Schultz & Strasser
B., 14, 614
40, 605
=1.4; 1.2
„
11 »
)>
....
138
Schultz and others
A., 207, 351
ji ""
=(l-4)»
)>
170
»
A., 207, 347
40, 911
„ ....
» J*
M
....
170
Schultz & Strasser
B., 14, 614
40, 605
o-Naphthyloxaruic acid
C10H7.NH.CO.COOH
»I
180 d.
Ballo
B., 6, 247
26, 913; vii., 848
Pyrroline methylbenzoic acid
C4H3N: CH.C6H4.CO2H=1.2
JJ
....
174-184
Ciamicianand Denn
B., 17, 2958
48, 379
stedt
Phenoxynicotinic acid
C5H3N(OPh).CO2.H=U.4
»
....
275-280
Pechmann & Welsh
B., 17, 2394
47, 153; 48, 175
o-Nitroazoxybenzene
....
C12H90SN3
....
49
Zinin
A., 114, 220
i., 480
P- ,,
....
»
....
153
»
A., 114, 221
Nitrobenzeneazophenol
C6H4(OH).N2.C6H4.N02
)J
....
183-184
Meldola
47, 659
=(1.4)2
Nitroso-nitrodiphenylamiue
Ph.N(NO).C6H4.N02= ?
))
....
133-5
Witt
B., 11, 757
33, 205
Nitro-acetonaphthol
C10H6.NO2.OAc=a/3
C12H904N
....
61
Bottcher
B., 16, 1938
44, 1113
Methylic nitro-a-naphthoate.
Ci0H6.NO2.CO2Me=?a
J)
109-110
Graeff
B., 16, 2252
46, 81
1> )> "P" >!
= ?/3
)>
112
D
B., 16, 2254
)»
Dinitro-diphenylamine
Ph.NH.06H3(NO2)2=1.2.4
CI2H904N3
153
Hepp
B. S. [2], 305 ; A.,
36, 51 ; 44, 317
215, 363
)> ....
JJ 1)
))
cf. B., 3, 128
153
Clemm
A. J. S. [3], 13,
32, 760
279; J. p., 108,
320; 109, 175
,, ....
» »
)i
156-157
Willgerodt
B., 9, 978
30, 405
,, ....
NH(C6H4.N02)2=(1.2)2
»
211-5
Witt
B., 11, 759
33, 208
,, ....
» !)
)»
....
219-220
Lellmaim
B., 15, 829
42, 1060
»
=(1.4),
»»
....
814
Witt
B., 11, 759
33, 208
D ••••
J) )>
1>
216
Lellmann
B., 15, 828
42, 1060
Nitrobenzeneazoresorcinol ....
C6H4(N02).N2.C,H3(OH)2
»
powder
Meldola
47, 660
=1.4 ; 4.3.1
Dinitroamidoazobenzene (m-)
C6H4(N02).NS.C6H3(N02).
C12H904N6
MM
175-176
Hallmann
B., 9, 390
30, 93
NH2
(m-)
))
»
A., 121, 272
195-5
Griess
P. T., 3, 678
lv., 461
(P-)
»
II
A., 121, 271
224-5
)»
»
»
Dinitroacetonaphthalide
NHAc.(NO3)2
C12H90SN3
cf. B., 4, 850
247
Liebermann and
B., 9, 333
30,81
=aA"2; or ai! "A
Hammerschlag
,,
» »
)»
....
247
Liebermann
A., 183, 273
31, 608
»
» »
»
....
947
Lellmann
B., 17, 114
46, 752
„
» !!
»)
....
250-5
Hiibner
A., 208, 330
526
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula
Boiling
Point.
Melting
Point.
- Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dinitroacetonaphthalide
NHAc-tNO^
C12H906N3
....
251
Ebell
B., 8, 564
28,900
— aJJ^a.t ; or a, ; a,/:
Phthalylaspartic acid
C6H4 : (00)j : N.CH(CO2H).
C12H90,N
233
Piutti
G. I., 14, 473
48, 796
Trinitrohydrazobenzene
Ph.NH.NH.C6H2(NO2)3
C13H906N6
....
181 d.'
Fischer
A., 190, 132
34, 309
Picric acid + benzene
C6H6+C6H2(OH)(N02)3
C12H90?N3
A., 109, 247
85-90
Fritzsche
J. p., 73, 212
iv., 405
B. S., 7, 30
Trinitro-a-ethoxynaphthalen
C10H4.OEt.(N02)3
„
148
Staedel
B., 14, 900; A
40, 724; 44, 863
217, 170
,, -ft-
„
jj
....
186
u
„
„
Diphenylnitrosamine
Ph3N.NO
C12H10ON3
cf.B.,10,130
66-5
Witt
B., 8, 855; A
29,267; 33,203
190, 174
Azoxybenzene
Ph.N.O.N.Ph
jt
cf. B., 6, 557
36
Zinin
J. p., 36, 93
1., 479
(cf. B., 16, 81)
„
jj
cf.B.,13,52
36
Spring
B., 17, 1217
46, 949
„ (cf. B., 14, 2617
„
jj
....
36
Mitscherlich
A., 9
(cf. B., 15, 865)
„
u
....
36
Glaser
G. J. C., 1867
„
„
jj
....
37
Schmidt & Schultz
B , 12, 486
36, 631
Hydroxyazobenzene
Ph.N2.C6H4.OH
„
....
148
Griess
A., 137, 84
vii., 151
(cf. B., 3, 234)
,,
»
„
....
148
Kimich
B., 8, 1027
„
„
jj
...*
150
Tschorvinsky
B., 6, 560
26, 1027
„
j>
„
....
148-154
Mazzara
G. I., 9, 424
38, 163
»
„
„
....
148-154
Kekule
B., 8, 1027
».
„
„
....
152
Wallach and Kie
B., 14, 2617
penheuer
„
jj
„
....
152-153
Wallach and Belli
B., 13, 526
„
H
,.
....
152-154
„
B., 13, 525
„
Ph.N2.OPh(?)
„
....
154
Scichilone
G. I. [1882], 108
42, 726
Phenylazonitrolic acid
Ph.N2.C6H4.NOH
C13H10ON3
....
134
Janovsky
M. C., 6, 157
48,789
Hydroxydipheuylnitrosamine
C,H4.OH.(NPh.NO)=1.4
C12H1002N2
....
95
Philip and Calm
B., 17, 2433
48, 155
Nitrodiphenylamine
Ph.NH.C6H4.N02=1.4
JJ
A., 132, 167
132
Witt
B., 11, 757
33, 205
,,
» jj
JJ
....
133
Lellmann
B., 15, 827
42, 1059
Hydroxyazoxybenzene
Ph.N.O.N.C6H4.OH
JJ
cf. B., 3, 235
145
Wallach and Kie-
B., 14, 2618
42,394
penheuer
a-Eesorcinolazobenzene
Ph.N3.C6H3(OH)3=?.1.3
JJ
....
161
Typke
B., 10, 1577
34, 219
a- „
j> »
JJ
....
165
Meyer and Kreis
B., 16, 1330
44,982
a- „
» »
JJ
....
166
Baeyer and Ja'ger
B., 8, 151
a- „
» jj
JJ
....
167-168
Wallach & Fischer
B., 15, 2816
f-
„ =?.1.3
JJ
....
215 u.c.
Typke
B., 10, 1577
34,219
ft-
» >!
JJ
....
215
Wallach & Fischer
B., 15, 2819
Azophenol ....
:N.C.H4.OH)S=(1.2)3
„
171
Weselsky & Benedikt
A., 196, 344 ; B.,
34, 498; 36, 718
11, 399
»
» <>
»
....
171
3ohn & Heumann
B., 17, 273
46, 1014
»
=(l-4)3
„
....
204 d.
„
B., 15, 3037
»
» jj
„
....
804 d.
Weselsky&Benedikt
A., 196, 340
36, 718
»
„ „
„
d.
214
Ta'ger
B., 8, 1499
29, 580
Nitroamido-diphenyl
NO.,C,H4.C6H4.NH3
„
....
92-93
Schultz
B., 7, 55; A., 207,
27, 468 ; vii.,
=1.2; 1.4
350
938
>i
» »
j,
....
97-98
„
A., 174, 225
28, 150
»
„ =1.4; 1.2
H
....
38
Schultz and others
A., 207, 348
40, 911
,1
=(1.4),
„
....
60
Fittig
A., 124, 278
v., 411
»
„ n
„
....
98
Schultz
A., 174, 222
8, 150
/3-naphthoic carbamide
C10H7.CO.NH.CO.NH2
B
....
15
Vieth
A., 180, 322
0, 87
Nitroamidoazobenzene
....
C13H1002N4
....
95
Griess
;2], 5, 857
i., 921
n
N02.C6H4.N2.C6H4.NH2
JJ
....
03-205
Bolting and Binder
B. S., 42, 340
8, 385
=1.4; 1.?
»
„ =1.3; 1.4
JJ
....
10
Meldola
5, 113
»
....
jj
45
Griess
'21 5, 857
i., 921
Oxalylphenylallylearbamide
X).NPh.CO.CO.N.C3H,,
Ci2H10O3N2
....
07-108
Maly
. JJ J *
. C. [2], 5, 258
irf., 1089
COMPOUNDS CONTAINING FOUR ELEMENTS.
527
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitroacetonaphthalide
NHAc.N03=aA; (?)
C12H1003N:
115
Lellmann
B., 17, 111
46, 751
»
„ =££(?)
„
A., 211, 41
123-5
Jacobsen
B., 14, 805
40, 736
» ....
=a?
„
....'
142
Lellmann
B., 17, 110
46, 751
„
=a?
n
....
171
Anderoni & Bieder-
B., 6, 342
mann
i)
11 =<ri
11
....
171
Lellmann
B., 17, 109
46, 751
„ (cf.B.,7,242)
=«?
„
isoiueric
171
Liebermann
A., 183, 229
31, 599
„ „
11 =a#
„
11
171
„
A., 183, 230
H
11
=a?
„
....
187
Lellmann
B., 17, 110
46, 751
11
jj (II('L' >
„
....
189
Liebermanu and
B., 7, 245
27, 692
Dittler
11
="?
„
....
190
Liebermann
A., 183, 253
46, 752
11
„ =a?
11
....
194
Lellmann
B., 17, 112
46, 751
Benzoquinone+o-nitraniline
C6H4 : 02+C6H4.NO2.NH2
C13H1004N2
....
94-97
Hebebrand
B., 15, 1976
+P- 11
„
H
....
115-120
ii
11
Diuitrohydrazobenzene
N02.C6H4.NH.NH.C6H4.NO2
C12H1004N4
....
220
Lermontoff
B., 5, 234
Dinitroamidodiphenylamine
NH2.C6H4.NH.C6HS(N02)2
'•
....
172
Leymann
B., 15, 1237
42, 1057
Dinitro-a-ethoxynaphthalene
OEt.(N02)2=a1
C^H.AN,
»•••
88
Martius
Z. C. [2], 4, 82
vi., 857
11 ~P" i>
=0,?; ft
„
....
138
Grsebe and Drews
B., 17, 1172
46, 1036
Trinitroaniline + benzene ....
C6H6+C6H2.NH2.(N03)3
C12H10OjN4
....
108-5
Mertens
B., 11, 843
=1.2.4.6
Trinitrobenzene+ aniline ....
C6H3(N02)3+NH2Ph
„
....
123-124
Hepp
A., 215, 356;
36, 51; 44, 316
B. S. [2], 30, 4
Pyridine methopicrate
C5NH5+C6H2.OMe.(N02)3
C12H1007N4
+pi2o
34
Ostermayer
B., 18, 592, 599
48, 813
Hydroxydiphenylamine
Ph.NH.C6H4.OH=1.3
CuHuON
....
81-5-82
Merz and Weith
B., 14, 2345
42, 179
11
i) 11
11
340
81-5-82
Calm
B., 16, 2788
46, 591
11
=1.4
n
330
70
11
B., 16, 2801
46, 591
/3-acetonaphthalide
C10N7.NHAc=/3
„
....
132
Liebermann
A., 183, 225
31, 607
„
11 11
„
....
132
Liebermann and
B., 8, 1110
29, 403
Scheiding
(cf. A., 211, 42)
11 »
„
....
132
Cosiner
B., 14, 59
40, 606
(cf.B.,14,2343)
11 »
„
....
132
Calm
B., 15, 611
42,972
„
11 11
„
....
132
Benz
B., 16, 9
a- „ (cf.B.S.,20,20)
11 — -a
„
....
152
Tommasi
C. R, 76, 1267
26, 1040
11
» 11
„
....
156
Jacobson
B., 14, 1793
11
i) 11
n
....
157-158 '
Kelbe
B., 16, 1200
44,916
11 •••• ••••
i> 11
„
....
159
Bother
B., 4, 850
25, 81
11
11 11
„
....
159
Anderoni & Bieder-
B., 6, 342
vii., 845
mann
„
11 11
„
....
159
Liebermaun
A., 183, 229
31, 599
11
11 11
„
....
160
Calm
B., 15, 615
42, 972
a-naphthylacetamide
C10H7.CH2.CO.NH2
„
....
180-181
Boessneck
B., 16, 641
44, 808
Acetonylquinoline
N.(CH2.CO.Me)=a1/3, ;
„
....
76
Fischer and Kuzel
B., 16, 164
44, 588
Amidobenzeneazophenol
NH2.C6H4.N2.C6H4.OH
C13HnON3
....
138-5
Schmidt
Z. C. [1869], 419;
vi., 272
=1.4; 1.?
A., 122, 174
11
=1.3 ; 1.?
„
....
168
Wallach & Schulze
B., 15, 3021
44, 583
11
=(!••*),
N
....
181
Meldola
47, 659
Nitroso-ethoxy naphthalene....
OEt.NO=a/3
C12HUO2N
....
101
Fuchs
B., 8, 630
Aeetamidonaphthol
OH.NHAc=|3a
»
....
225
BSttcher
B., 16, 1938;
44, 1113; 48,
C. C. [1884], 898
659
Dimethamido-a-naphthoqui-
C10H6(NMe2):02(?)
„
....
118
Plimpton
37, 642
none
Ethamido-a-naphthaquinone
C10H6(NHEt):03(?)
„
....
139-140
„
37, 641
H 11 11
C10H6.O.NEt.O
,,
....
140
Zincke
B., 12, 1646
38,49
Amidobenzene azoresorcinol
NH2.C6H4.N2.C6H3(OH)2
C12Hn03N3
...
too high to
Meldola
47, 661
=1.4; 4.3.1
determine
Nitrocinnatnenylvinylme-
NO2.C6H4.CH : CH.CH : CH.
CuHuOjN
...»
73-5
Diehl and Einhorn
B., 18, 2327
48, 1222
thylketone
COMe=1.2
Nitroethoxynaphthalene
OEt.NO2=j3?
"
....
103-104
Wittkampf
B., 17, 394
46, 1036
528
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dimethamidojuglone
C10H4(OH)(NMe2):02=/3,;
C12H,,03N
....
149-150
Mylius
B., 18, 465
48, 803
(3,0,0,
Ethoxyquinoline carboxylic
N.OEt.COOH=a,0,/32 ;
M
133
Friedlander and
B., 17, 460
46, 1020
acid
Gohring
„ ,, »
„ =a,/3,a2 ;
„
....
145-146
Konigs and Korner
B., 16, 2154
46,84
Ethylic hydroxyquinoline
N.OH.COOEt=a,/3,a2 ;
„
....
206-207
„
B., 16, 2155
„
carboxylate
?— acid
....
H
....
148-149
Weltner
B., 18, 794
48, 794
Nitrocinnamylacetone
N02.(CH : CH.CO.CH2Ac)
C12Hn04N
....
112-113
Fischer and Kuzel
B., 16, 36
44,587
=1.2
Nitrobenzoyltetramethylene
(CH2)3.C(C02H).CO.C6H4.
CISHU05N
....
172
Perkin and Bellinoi
B., 18, 957
48, 795
carboxylic acid
N02=1.4
Nitropeucedanin (cf. A., 176,
....
„
....
100 d.
Bothe
J. p., 46, 371
iv., 386
78)
Anilinetrinitraniline
C6H2(N02)3.NH2+Ph.NH2
C,2HU06N5
123-125
Hepp
A., 215, 359
Diamidophenyloxide
C12H12ON2
....
185
Hoffmeister
A., 159, 209
vii., 941
Ethylnaphthylnitrosamine ...
C,0H7.NEt(NO)=/3
„
....
49
Henriques
B., 17, 2669
48, 168
Harmalol
(?)
darkens 180
212 d.
Fischer and Ta'ube]
B. 18 405
48, 821
•
125
Fittica
B 8 711
28, 1195
H
D., 0, ILL
Azoxyaniline
0:N2(C6H4.NH2)2=(1.4)2
C12H12ON4
....
182-184
Mixter
A. J. C., 5, 1
46, 301
Diacetamido-o-toluic nitril ....
NAc2.(CH2CN)=1.4
C12H1202N2
....
152-153
Gabriel
B., 15, 835
42, 1070
? — amide
0,,H,0ON.(CO.NH2)
„
....
264
Weltner
B., 18, 794
48, 794
Acetoxyphenylethenylazox-
AcO.CHPh.C : N.O.CMe : N
C12H1203N2
....
52
Gross
B., 18, 1077
48, 898
imethenyl
Phenylethenylazoximepro-
O.N : C(CH2Ph).N : C.(CH2)2.
H
....
59T60
Knudsen
B., 18, 2484
48, 1218
1 1, 1 ' • J
penylcarboxyhc acid
CO2H
Diacetylterephthalaldoxime
(CH:NAc).(CH:NOAc)=1.4
,»
....
155
Westenberger
B., 16, 2995
46, 581
Methyloxyquinizinacetic acid
1
„
....
178
Knorr and Blank
B., 17, 2052
46, 1380
CO,H).CO=1.2
?
....
C12H1203N3
brown 150
172 d.
Paal
B., 17, 2762
48, 250
Urocaniuic acid
• (>*
C12H1204N4
+4H20
212-213
Jaffe
B., 7, 1671
Trisuccinamide
(C4H402)3N2
C12HI206N2
....
83
Chiozza and Ger-
A., 90, 108
v., 462
hardt
/3-hydroxypyridine oxalate ....
(C5H6NO)2+H2C204
„ (?)
....
175
Fischer and Eenouf
B., 17, 1896
46, 1370
Ethylic dinitrophenylacetace-
C6H3(N02)2.(CHAc.COOEt)
C12H120;N2
....
94
Heckmann
A., 220, 128
46, 178
tate
=4.2.1
Diethylic dinitrophthalate ....
(C02Et)2.(N02)2=1.2.(?)2
C12H1208N2
....
91
Beilstein and Kur-
B. S. [2], 34, 327
40, 436
batow
Aniline phenate
Ph.NH2+C6H5.OH
C13HI3ON
184-5 u.c.
89-5
Dale and Schorlem-
A., 217, 388
43, 186
mer
» >»
»
„
181
30-8
Dyson
43, 466
» i>
it
M
....
32
Hubner
A., 210, 342
Cumostyril
C9H6PrPON
Ifi7 Ifift
,,,. ,
B-I H OOQQ
UJ 4 — 1OO
W K final i H
.j 17, $iZot>
Acetamidopropenylbenzoic
NHAc.C3H6.C02H=1.2.5
C12H1303N
«..
210-212
n
B., 16, 2575
46, 318
acid
Acetyltetrahydrocinchoninic
. j
fr. CCH5(C02H).CH2.CH :
H
....
164-5
Weidel
M. C., 3, 64
42, 531
acid
CH.NH=1.2
Methylcumazonic acid
C6H3(CO2H).CMe2.O.CMe : N
„
218
Widmann
B., 16, 2576
46, 303
=1.2
Cotarnine
....
M
+H20
100
nf\4- V\ i on
....
ii., 89
Nitrosomethylanilidopyrotar-
CO.NMe.CO.CH2.CMe.NPh.
i j
C12H,303N3
not D. IzO
147
Beckett & Wright
Wechsler
28, 576
B., 18, 1044
48, 900
tarimide
NO
Ethylic aeetylphenyloxamate
NAcPh.CO.CO2Et
C12H1304N
....
64-65
Klinger
A., 184, 268
31, 711
» »
n
,,
....
66-67
B., 8, 311
28, 1025
Ethylic nitropropenylbenzo-
ate
N02.C3H6.C02Et=1.2.5
"
....
Liquid
Widmann
B., 15, 2552
COMPOUNDS CONTAINING FOUR ELEMENTS.
529
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
/3-Lactone of isopropylnitro-
Pr/3.NO2.(.CH.CH2.CO.O)
C12H1304N
....
73
Einhorn and Hess
B., 17, 2022
46, 1352.
phenyllactic acid
L _1
=1.3.4
Nitrocumenylacrylic acid ....
Pr/3.NO,,(CH:CH.C02H)
"
....
141
Widmann
B., 17, 2283
48, 56
» Tl !>
=4.2.1
„
pure
156-157
Einhorn and Hess
B., 17, 2018
46, 1351
I, !, I! —
» ,>
„
ordinary
152-153
„
B., 17, 2017
H
Ethylic benzammalonate
C02H.(NH.CO.CH2.C02Et)
„
172-173
Sehiff
B., 17, 403
46,906
= 1.3
Nitro-aceteugenol
C3H5.OMe.OAc.NO2=1.4.3.?
„
....
61
Weselsky and Bene-
M. C., 3, 391
42, 1201
dikt
Ethylic nitrophenylazoacet-
NO2.(.N2.CHAc.CO2Et)=1.2
C12H1305N3
....
92-93
Bamberger
B., 17, 2416
48, 157
acetate
Nitroquinol dipropionate ....
(O.C3H5O)2.NO2=1.4.5
C13HI306N
....
86
Hesse
A., 200, 247
38, 317
Diethylic nitrophthalate
(COOEt)2.NO2=1.2.?
„
a. 300
Liquid
Faust
A., 160, 57
25,76; vii., 978
!> „
=1.2.4
n
33-34
....
A., 208, 234
» „
=1.2.3
„
43
Miller
B., 11, 1191
34, 982
,> „
„ „
„
45
<•••
A., 208, 243
„ nitroisophthalate ...
= 1.3.5
„
83-5
Beyer
J. p. [2], 25, 489
42, 1294
„ »
1» J»
a
83-5
Storrs and Fittig
A., 153, 288
vii., 979'
Nitroacetoxypropylbenzoic
CO2H.(CMe2.OAc).NO2
„
131-133
Widmann
B., 16, 2569
46, 317
acid
=1.4.5
Ethylic diacetylcomenamate
C5H2N(OAc)2.CO2Et
„
fr. pyridine
38
Ost
J. p. [2], 29, 57
48,49
„ nitro-opianate
COH.NO2.(OMe)2.C02Et
C13H1307N
....
96
Prinz
J. p. [2], 24, 358
42, 402
=6.13.2.1
Methylethyloxyquinizine ....
C6H4.N.NH.CMe.CHEt. CO
C18H14ON2
108
Knorr and Blank
B., 17, 2051
46, 1380
i i
=1.2
Toludimethyloxyquinizine ....
C6H3Me.N.NH!cVe.CHMe.
„
96-97
Knorr
B., 17, 550
46, 1153
CO=1.2.3
j
„
=1.4.5
D
137
„
H
Phenyl acetamidine diacetate
Ph.CH2.C(NHAc):NAc
C13H1402N2
172-173
Luckenbach
B., 17, 1425
46, 1134
Methylanilidopyrotartar-
CO.NMe.CO.CH2.CMe.NH
103
Wechsler
B., 18, 1043
48, 900
imide
Ph
Toluidopyrotartarimide
CO.NH.OO.CH2.CMe.NH.
181
B., 18, 1051
48, 901
i i
C6H4Me=1.2
Ethylpseudoisatin-a-ethyl-
C6H4.CO.C(NOEt).NEt=1.2
n
....
99
Baeyer
B., 16, 2193
46,74
oxime
Ethylic azobenzene acetace-
Ph.N2.CHAc.CO2Et
C12H1403N3
i»i
59-5
ZUblin
B., 11, 1418
34, 880
tate
Diacetylphenyloxethenyl
AcO.CHPh.C(NH3) : NOAc
CI3H1404N2
....
113
Gross
B., 18, 1077
48, 898
amidoxime
Diacetylphenyloxethenyl
AcO.CHPh.C(NH).NH.OAc.
JJ
....
149
Tiemann
B., 17, 127
46, 734
oxamidine
Ethylic dinitrocuminate
Pr.(N02)2.CO3Et=?
C12H1406N3
77-5
J. [1858], 271
Deoxyamalic acid
C12H1406N4
260
Fischer and Eeese
A., 221, 336
46, 467
Ethylic nitrophenylnitro-
NO2.[CH(OMe).CH(NO.,).
C12H14O.N2
77
Friedlander and
B., 16, 852 ; A.,
48, 1138
methoxypropionate
CO,Et]=1.4
Mahly
229, 210
Methylic nitrophenylnitro-
NO2.[CH(OEt).CH(NO2).
n
110
ethoxypropionate
CO2Me]=1.4
"
Methylic ethyldinitrohydro-
OEt.(N02)2.(CH2.CH2.COi!
^
....
36
Stohr
A., 225, 57
46, 1350
p-coumarate
Me)=1.2.6.4
Ethylic methyldinitrohydro-
OMe.(NO2)2.(CH2.CH!!.C02
71
p-coumarate
Et)=1.2.6.4
)J
»
Diethylic dinitrosuccinosuc-
C12H1408N2
brown 100
113-114 d.
Ebert
A., 229, 45
48, 1122
cinate
Cumenylacrylamide
a-ethoxy hydromethyl quino-
line
Pr3.(C2H2.CO.NH2)=?
NMe.H3.OEt=a1/31/3sa;j ; a,
C12H16ON
269-270(716)
185-186
Liquid
Perkin
Fischer
J. [1877], 790
B., 16, 718
3t, 399
44, 1147
Hydroeumostyril „
C9HsPr/3ON
"
135
Widmann
B., 17, 2283
3 v
530
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
?
....
C13HI502N
a. 300
78-80
Canzoneri & Spica
G. I., 14, 448
48, 751
Cumenylamidoacrylic acid ...
C9Hn.02H(NH2).CO2H
J)
....
154-155
W id maun
B., 17, 2283
48,56
o-amidocumenylacrylic acid
cjBv><sm&cjafco&
»
165
D
jj
D
m- »
»
>»
165
»
j)
»
Isoamylidene-m-amidoben-
....
)J
130 ; sf. 100
Schiif
A., 210, 119
42, 304
zoic acid
Ethylic dimethamidobenzoyl
NMe2.(CO.CO2Et)=1.4
C12H1503N
...
95
Michler and Hau-
B., 10, 2082
34, 421
formate
hardt
Anliydro-amidophenolethyl
O.C6H4.NH.CMe.CH2.CO2Et
»
107-108
Hantzsch
B., 16, 1950
44, 1111
acetacetate
=1.2
Acetamidocumic acid
Pr/3.NHAc.C02H=1.2.4
))
....
246
Widmaim
B., 16, 2579
46, 303
»»
>! J)
)i
248-250
Fileti
G I., 10, 12
40, 425
Benzoyl horaopiperidic acid
Ph.CO.C6H10O2N
1»
....
94
Schotten
B., 17, 2545
48, 176
Cuminuric acid
....
1)
A., 109, 31
168
Jacobsen
B., 12, 1514
38, 38
Hy drocotarn iue
....
)>
+iH20
50
Hesse
B., 4, 696; As.,
24, 1065; 25,
8, 261, 326
724 ; vii., 877
j)
»>
....
54
Beckett & Wright
29, 466
28, 577
Ethylic urethane benzoate ...
C02Et.(NH.C02Et)=1.3
C12H1604N
100-101
Wachendorff
B., 11, 702
34, 674
Diethylic amidophthalate ...
(CO2Et)2.NH2=1.2.3
)1
Liquid
Miller
A., 208, 246
42, 405
» »
=1.2.4
»J
....
95
IT
A., 208, 237 ; B.,
34, 983
11, 1192
» »
1J )1
)J
crystalline
Baeyer
B., 10, 125, 107!)
„ amidoisophthalate
=1.3.5
J»
....
118
Beyer
J. p. [2], 25, 503
„ amidoterephthalate
„ =1.4.5
J)
?
«...
A., 121, 92
Actetate of amidopropenyl-
C02H. (NH2 + H Ac).C3H5
})
....
160
Widmann
B., 16, 2574
46, 318
benzoic acid
=1.3.4
Acetamidohydroxypropyl-
COsH.(NHAc).(CMe2.OH)
n
nf. 280
51
B., 16, 2572
46, 317
benzoic acid
=1.3.4
Dimethylic collidine dicar-
N.Me3.(C02Me)2=1.2.4.6.3.5
)»
285-287
82
Hantzsch
B., 16, 1947
44, 1082
boxylate
Monethylic collidine dicar-
N.Me3.CO2H.OO2Et
)>
....
157
Michael
A., 225, 121
48,61
boxylate
=1.2.46.3.5
Triacetamidophenol
OII.(NHAc)3=1.2.4.6
C12H1604N3
263 d.
Bamberger
B., 16, 2401
46, 309
Ethylic hydroxyisopropyl
CO2Et.(CMe.2OH).NO2
C12H1606N
96
Widmann
B., 15, 2550
44,330
nitrobenzoate
=1.4.5
Isopropylnitrophenyllactic
[OH(OH).CH5.C0.2H].NOS
)>
119-120
Einhorn and Hess
B., 17, 2024
46, 1353
acid
Pr0=1.2.4
Ethylic nitrodimethamido-
(NH.CO.CO2Et).NMe2.NO2
C12H1505N3
152
Wurster and
B., 12, 1805
38, 110
phenyloxamate
=1.4.6
Sendtner
/3-butyranilbetame oxalate ....
NH2Ph.CHMe,CH2.COO
C12H1606N
....
137-139
Balbiano
B.,13,313;G. I.,
38, 462, 542
+C2H204
10, 137
Aniline citrate
C6H5.NH.O.C6H604(OH)2
C12H1S07N
b. 100
Pebal
A., 82, 91
iv., 427
Ethylic cyanuro-carboxylate
(NCO.C02Et),
C12H1509N3
118-119
Wurtz & Henninger
('. R, 100, 1419
48, 969
Triethoxytrinitrobenzene ....
(OEt)3.(N02)3=1.2.3.4.5.6
»)
93
Weselskyand Bene-
M. G, 2, 218
42,54
dikt
Piperidylphenylcarbamide ....
PhHN.CO.N:C5H10
C12H16OK2
168
Gebhardt
B., 17, 3041
48, 384
Benzoylpiperylhydrazine ...
C5H10N.NHBz
n
195
Knorr
A., 221, 297
46, 467
Picramide+aniline
C6H.,.OH.(NH2)3+NH,1Ph
C12H16ON4
123-125
Hepp
A., 215, 344
44,316
Diethyl terephthalaldoxime
Ispphthalimidethyl ether ....
C6H4(CH:NOEt)2=1.4
C6H4[C(OEt):NH]2=1.3
C12H1602N2
))
d. 120
55
66 ; a. f. 157
Westenberger
Luckenbach
B., 16, 2995
B., 17, 1432
46, 581
46, 1158
Benzamide+anisaldehyde ....
))
180
Schuster
A., 154, 80
vii., 80
Ethylic dimethamidophenyl
(NH.CO.C02Et).NMe2=1.4
C1SH1603N2
117
Sendtner
B., 12, 531
36, 627
oxamate
Acetamide+auisaldehyde ....
Nitroisovaleryl toluide
v. C12H1602N2
Me.N02.NH(C6H90)=1.3.4
»!
)1
A., 154, 80
180
88-89
Schuster
Friederici
Z. C. [2], 6, 681
B., 11, 1973
vii., 3
36, 312
i) M
Benzoylornithin
Diethylic ketindicarboxylate
C6H802.NH2.NH.C7H60
(.CMe.N:C.C02Et)2
»
C12Hi'604N2
315-317 c.
88-89
225-230
85-5
Hiibner
Jaffe
Wleiigel
A., 209, 364
B., 11, 408
B., 15, 1052, 1054
42, 180
34, 585
42, 949
Isopropyl nitrophenylaceta-
[CH(OH).CH2.CO.NH2].
i)
150
Einhorn and Hess
B., 17, 2023
46, 1353
mide
N02.Pr/3=1.2.4
COMPOUNDS CONTAINING FOUR ELEMENTS.
531
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Dipropyl diuitrobenzeiie
Pr«2.(N02)2=1.4.(?)2
C12HI604N2
....
65
Korner
B., 11, 1865; A.,
36, 142 ; 44,
216, 226
322
Ethyl dinitrothymol
Pr«2.Me.OEt=1.4.6
C12H1605N2
52-53
Ladenburg and
B., 10, 1219
34,60
Engelbrecht
Triethoxydinitrobenzene ....
(OEt)3.NO2=1.2.3.4.?
C12H160;N2
73
Weselskyand Bene-
M. C., 2, 217
42, 54
dikt
Pipecoline picrate
C6H13N+C6H2.OH.(N02)3
C^H^N,
136-138
Hesekiel
B., 18, 913
48,812
Tetramethylic azinsuccinate
[.N: C(CO2Me).CH2.CO2Me]2
C12H1608N2
149-150
Curtius and Koch
B., 18, 1301
48, 886
Capronanilide
C6H3.NH(C6HnO)
C12H17ON
....
95
Kelbe
B., 16, 1200
44, 916
Acetamidoisobutylbenzene ....
Bu0.NHAc=?
»)
A., 211, 238
170
Studer
B., 14, 1473
40, 898
i) j)
» "
)>
....
170
Louis
B., 16, 115
Isobutylformotoluide
Me.Bu0.(NH.CHO)=1.3.2
»»
103-105
Effront
B., 17, 2343
48, 154
.,
=1.5.2
))
105-106
11
B., 17, 2332
48, 152
Acetylcymidine
Me.Pr«.NHAc=1.4.5
j)
112
Widmann
B., 15, 169
Acetylisocymidine ....
Me.Pr0.NHAc=1.3.?
»
118
Kelbe and Warth
A., 221, 157
46,47
Acetamidotetramethylbeii-
Me4.NHAc=1.2.3.5.6
»
210-211
Nolting and Bau-
B.,18, 1149;B.S.,
48, 384, 893'
zene
mann
42, 335
Methyltetrahydromethoxy-
NMe.Me.OMe=a1/31 ; Ol
)»
260-262
Liquid
Dobner and Miller
B., 17, 1708
46, 1374
quinaldin
Tetrahydroethoxymethyl-
NMe.OEt=a, ; /3,
»)
269-270
Liquid
Fischer
B., 16, 718
quinoline
(716)
Isobutylic tolylcarbamate ....
C6H4Me.(NH.CO2Bu0)=1.2
C12H1702N
275-280 p. d.
L. —10
Hofmaun & Mylius
B., 5, 974 ; P. E.,
vii., 1180; 26,
19, 108
266
Ethylic a-xylylglycocine
Me2.(NH.CH2.CO2Et)= 1.3.?
))
Liquid
Ehrlich,
B., 16, 206
44, 594
Carvacrol glycollamide
Me.Pr«.(O.CH2.C02H)=1.4.6
)1
67-68
Spica
G. I., 10, 340
38, 889
Thymol „
=1.4.5
n
96-97
11
11
)!
Amido-cumenylpropionic aciJ
Pr.NH2.(C2H4.C02H)=1.3.?
j»
103-105
Widmann
B., 17, 2283
48, 56
Mesitylurethane
Me3.(NH.CO2Et)=1.3.5.6
u
....
61-62
Eisenberg
B., 15, 1016
42, 956
Isobutylethoxynitrobenzene
Bu0.OEt.NO2=?
C12H1703N
300 d.
Liquid
Liebmann
B., 15, 1991
44,59
Diethylic dimethylpyrroline
N.Me2.(CO2Et)3=1.2,5.3.4
C12H1704N
90-91
Knorr
B., 18, 302
48, 555
dicarboxylate
11 »i
11 11
)J
09
11
B., 18, 1560
48, 994
i» ii
„ =1.2.4.3.5
)5
130
11
B., 17, 1638
46, 1368
Dimethylic dihydrocollidine
N.Me3.(CO2Me)2.H2
5»
....
156
Hantzsch
B., 16, 1947
44, 1082
dicarboxylate
—1.2 4 6.3.5.5.6
Oxypropyltoluidine oxalate....
NH(C3H70)(C7H7)+C2H204
C12H1705N
KM
151
Morley
41, 388
Helicinaldoxime
C6HnO5.O.C6H4.CH : NOH
C12H1707N
190
Tiemaiin and Kees
B., 18, 1663
48, 1072
s=LS
Pentanitrolactose
C12H17(N02)50U
C.jH.AiN,
139'2 p.d.
Ge
J. E. [1882], 253
42, 1043
Diruethaniidothymoquinone
Me.Pr«.(NHMe)2:O.,=2
C12H180,N2
203
Zincke
B., 14, 95
40, 596
1
....
C12H1805N2
....
81
Ehrenberg
J. p., 32, 97
48, 1192
Diethyldime thylarnmouium
(O.NMe2Et2).(NO2)3=1.2.4.6
C12H1807N4
285
Meyer and Leceo
B.,8, 241; 10,315
28, 633
picrate
ii ii
V J)
>»
....
285-287
Lossen
A., 181, 374
32, 191
Tetranitrolactose
C12H18(N02)40U
C12H1S0,9N4
80-81
Ge
J. E. [1882], 253
42, 1043
Diethamidoethoxybenzene ....
OEt.NEt2=1.2
C12H19ON
227-228
Liquid
Foster
J. p. [2], 21, 364
38, 465
(754-3)
Camphorethylimide
c8H14:(co)2:NEt
C12H1902N
274-275
43-44
Wallach and Ka-
B., 14, 164 ; A.,
40, 285
menski
214, 249
ii
»i
j;
275-276
49-50
i»
11
11
Cymidine acetate
C6H3Me.Pr.NH2+HAc
)»
....
112
Widmann
B., 15, 169
42, 728
Ethylcyanethine carboxylate
C,,H13N2.NH.C02£t
C12H1902N3
247
easily
Meyer
J. p., 30, 115
48, 140
Triethyldicarbopyrrolamide
C4H3EtN(CO.NHEt)2
»>
229-230
Bell
B., 10, 1864
36, 525
Oxytetrolamide
C12H906(NH2)S
C12H1905N6
B. S., 33, 575
177-177-5
Demanjay
A. C. [5], 20, 479
40, 255
Triuitrolactose
C12H19(N02)30U
C12H19017N3
....
36-86
Ge
J. E. [1882], 253
42, 1043
Oxalylpiperidine
(C5H10N.CO)2
C12H2002N2
a. 350
88-89
Wallach
A., 214, 278
11
»)
J»
a. 360
90
Schotten
B., 15, 426
42, 983
Acrole'in-ammonia
C12H2003N2
....
d. 100
Eedtenbacher
A., 47, 114
i., 57
Diethoxyhydroxycaffei'ne ....
C8H9N402(OEt)2.OH
C12H2005N4
A., 215,274
195-205 d.
Fischer
B., 14, 641
40, 614
Diethylic oxaldiamidopro-
(.CO.NH.CHMe.CO2Et)2
C12H2006N2
sic
125-127
Schiff
B., 18, 490
48, 760
pionate
11 11
))
11
11
152-154
11
n
11
3 v 2
532
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Dextro-campho-urethane ..
C9H15.NH.CO2Et
C13H2102N(?
115
Haller
C. E., 98, 578
46, 755
Lsevo- „
))
)>
....
126-127
11
11
11
Triethylic amidotriglycollatt
N(CH2.C02Et)3
C12H2106N
280-290 p. d
....
Heintz
A., 140, 264
vi., 647
Diacetonamiue anhydride ..
C12H24ON2
....
83
Antrick
A., 227, 365
48, 503
Amylisocaproylcarbamide ..
Me.(CH2)4.NH.CO.NH.CO.
C12H2402N2
....
94
Hofmann
B., 15, 758
42, 1053
(CH2).,Pr0
Amylcaproylcarbamide
Me.(CH2)4.NH.CO.NH.CO.
)»
97
)*
11
»
(CH2)4Me
Diisoamyloxamide
....
^J
B., 13, 516
128-129
Wallach
A., 214, 316
44, 49
Diamyloxamide
(.eO.NH.C6Hn)2
>J
139
Wurtz
A. C. [3], 30, 490
iv., 285
Lauramide
CnH23.CO.NH2
C,-H.«ON
102
Krafft and StaufFei
B., 15, 1729
42, 1273
Pinitrodiphenylene ketone...
fr.(C6H4)2:CO=(1.2)2
^12 .5^ -*•
C13H605N2
...•
290
Schultz
A., 203, 104
38, 814
a-Dinitrodiphenylene ketone
fr.co:(G6H4)2:o
C13H60,N2
....
145-150
Eichter
J. p. [2], 28, 273
46, 325
oxide
0-
»
))
260
11
)»
11
0- 11 11
»J
»
....
S60
Salzmann and
B., 10, 1401 ; 16,
34, 80
Wichelbaus
862
0- i) 11
»
»)
>•*•
262
Perkin
43, 190
Tetranitrobenzophenone
CO:C12H6(N02)4
C13H609N4
MM
225
Staedel
A., 218, 339
44, 991
Tetranitrodiphenylic car-
[C6H3(N02)2]2C03
C13H6OnN4
125-5
Kempf
J. p. [2], 1, 407
24, 342
bonate
Quinone
Fr.o-naphthoquinoline
Cl3HjO.F
....
205-207 d.
Skraup and Cobenzl
M. C., 4, 436
44, 1014
Nitrodiphenylene ketone ....
C6H4.OO.C6H3.N02
C13H708N
217-218
Strasburger
B., 17, 108
46, 754
J =1.2; 1.2.4
11 11 •—
11 11
T)
....
220
Schultz
A., 203, 103
38, 814
Anhydrobenzamidodiuitro-
C6H.,(NO,)0.O.CPh:N
1- - " " p
CuHjO^f.
....
218
Hiibner
A., 210, 394
42, 507
phenol
=(?)rl.a
Diuitrophenylic m-nitroben-
C6H4(N02).C02.C6H3(N02)2
CI3H708N3
....
150
List and Limpricht
A., 90, 201
i., 556
zoate
Phenanthroline carboxylic
O,NH3.CH : C(CO,H).C^NH3
C13H802N2
....
277
Skraup and Fischer
M.-G, 5, 253
48, 393
acid
=1.2.3.4.5.6 ; 5.6.1.2.3.4
Dinitrofluorene
C12H6(N02)2:CH2
C13H804N2
....
199-201
Fittig and Schmitz
A., 193, 140
36, 164
11
))
J»
brown, 200
255-260 d.
Earth and Gold-
B., 11,849
34, 734; vii.,
schmidt
673
*,
))
j»
a, 260 d.
Barbier
A. C. [5], 7, 472
37, 718
? • Di nitrobenzophenone
CO:C12H8(N02)2
C13H805N2
B., 10, 1836
118 (?)
Doer
B., 5, 797
26, 171; vii., 939
11 )1
))
))
»
129
Linnemann
A., 133, 10
iv., 478
»1 11 •".
n
»1
....
129-5
Doer
B., 5, 797
26, 171
0-
)>
»»
148-149
Staedel and Saur
B., 13, 836
38, 646
i) u
))
»
....
148-149
Pratorius
B., 10, 1836 ; A.,
34, 420; 36, 319
194, 349
11 11
»
)1
148-149
Staedel
A., 218, 339
44, 991
"- >,
J)
J>
189
Staedel and Saur
B., 11, 1747
11 » ....
i)
»
189-190
Staedel
A., 218, 339
44, 991
11 I)
»»
))
....
189-190
Pratorius
B., 10, 1836; 11,
34, 420 ; 36,
745; A., 194, 349
242, 319
7- „
1)
>J
....
189-190
Staedel
A., 218; 339
44, 991
» »
»
I»
....
195-196
Pratorius
A., 194, 371
36, 319
>) j)
51
JJ
a. 196
Staedel
B., 11, 745
34, 671
Dinitrodiphenyl carboxylic
* j
C6H4(N02).C6H3(N02).C02H
C13H806N2
....
252
Strasser & Schultz
A., 210, 192
42, 521
acid
=1.4; 1.2.4
Trinitrobenzanilide
C6H,(N02)2.NH.CO.C6H4
C13H807N4
165
Hiibner
B., 10, 1708
34, 142
NO2=1.3.4; 1.3
11 .... ....
,, =1.13; 1.2
))
178
11
11
)1
11 .... ....
,, =1.13; 1.?
))
202
11
11
•»
Tetranitrodiphenylmethane
CH2:c"2H6(N02)4
C13H808N4
212
172
11
Doer
11
B., 5, 795
Ti
26,170;vii.,948
11
Nitrobenzyl picrate
J»
N02.C6H4.CH2.O.C6H,,(NO,,)3
C13HS0,N4
172
108
Staedel
iumpf
V., 218, 339
B., 17, 1077
44, 991
46, 1005
=1.4; 1.2.4.6
1
COMPOUNDS CONTAINING FOUR ELEMENTS.
533
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Tetranitrocarbanilide
CO[NH.C6H3(N02)J2
C13H809N6
....
a. 200
Losauitch
B., 10, 690, 1296
j,
„
„
204
„
B., 11, 1541
Benzenylamidophenol
C6H4.O.CPh:N=1.2
C13H9ON
314-317
103
Ladeuburg
B., 9, 1526
31, 304
„
» !>
„
MM
103
Morse
B., 7, 1319
53 '*'
,, »
»
103
Htibner & Stiiukel
A., 210, 384
42, 506
»
» )J
ji
....
103
Bottcher
B., 16, 630
„
„ »
,,
....
103
Kalckhoff
B., 16, 1828
44, 1110
Diphenyleneacetoxime
06H4.C6H4.C:NOH
M
B., 17, 807
192
Spiegler
M. C., 5, 195
46, 1182
i i
3-hydroxynaphthoquinoline
HO.C10H5 : C3NH3
„
....
w.m. 250 p.d
Gentil
B., 18, 202
48, 561
Nitrofluorene (A. C. [5], 7, 497)
C6H4.OH,,.C6H3.NO2=1.2 ;
C13H902N
....
154
Strasburger
B., 17, 108
46, 754
1.2.4
Carbazolic acid
C12HSN.CO2H
„
....
271-272
Ciamician & Silber
G. I. [1882], 272
42, 1103
Nitroanhydrobenzoyldiami-
C0H3(NO2).NH.CPh : N
C13H90,N3
196
Stover
B., 7, 1317
28, 271
dobenzene
— ?1 2
» D
»
....
196
Hiibner
A., 208, 308
40, 1131
Nitrobenzophenone
C6H4(NO2).COPh =1.3
C13H9O3N
....
93
Becker
B., 15, 2092
44, 203
„
„ ,,
„
94-95
Geigy and Konigs
B., 18, 2401
48, 1236
„
=1.2
„
....
105
„
B., 18, 2403
„
„
=1.4
5)
....
138
Easier
B., 16, 2718
46, 310
Benzoxynitrosobenzene
C(1H4(NO).OBz=1.4
„
168-175 d.
Walker
B., 17, 400
46, 1003
Benzoxynitrobenzene
C6H4(N02).OBz=1.2
C13H904N
55
Schiaparelli
G. I., 11, 65
40, 603
„
i. „
»
58
Hiibner
A., 210, 386
42, 506
,1
=1.4
„
....
142
„
A., 210, 377
„
„
,> ,,
„
....
142
Schiaparelli
G. I., 11, 65
40, 603
Nitro-o-diphenylcarboxylic
C12H8(NO3).C02H
„
....
221-222
Schmiti!
A., 193, 123
36, 164
acid
,, -P-
„
„
252
^Schmidt & Schultz
A., 203, 118
40, 435
!! -P- »
„
„
....
290
a
n
.
Ethylic nitro-|3-naphthoate....
C10H6.NO2.CO2Et
„
....
93 u.c.
Ekstrand
B., 18, 1206
48, 905
» „ -ft- „
„
„
110-lllu.c.
„
B., 18, 1208
„
,1 » -0- „
,,
„
122 u.c.
n
B., 18, 1207
„
Acid fr. /3-naphthoquinoline
....
„
+H20
206
Skraup
B., 15, 896
a-phenylpyridinedicarboxylic
N.CO2H.(C6H4.CO2H)=1.3.2
,,
....
230-235 d.
Skraup & Cobenzl
M. C., 4, 436
44, 1014
acid
m-nitrobenzylidenenitrani-
....
C13H904N3
114
....
J. [1870], 760
line
Dinitrobenzanilide
C6H4(NO2).NH.CO.C6H4.
C13HAN3
187
McHugh
B., 7, 1268 ; 8, 36
28, 271
N02=(1.3)2
Nitrobenzeneazosalicylic acid
C6H4(N02).N2.C6H3(OH).
3)
...
225 d. (?)
Meldola
47, 666
CO2H=1.4 ; 4.1.2
Dinitrobenzamidophenol
fr. C6H4(OH).NHBz=1.2
C13H906N3
173
Morse
B., 7, 1320
28,272;vii.,903
Benzamidodiuitrophenol
OH.NHBz.(NO2)2=1.2.4.6
1)
218-219
Stuckenberg
B., 10, 383
32, 474
„
» >.
„
....
220
Dabney
A. C. J., 5, 20
46, 309
„
» »
„
....
220
Hiibner
A., 210, 388
42, 506
„
V 1!
„
....
222-223 d.
Bottcher
B., 16, 632
»
„ =1.4.2.6
„
....
250
Dabney
A. C. J., 5, 20
46, 309
„ ....
=1.4. (?)2
H
250
B
„ 46, 308
Nitrobeiizamidonitrophenol
OH.N02.NH(CO.C6H4.N02)
jj
....
225
Hiibner
A., 210, 380
42, 506
=1.?.4 ; (1.3)
Benzoxydinitroamidobenzene
OBz.NH2.(N02)2=1.2.(?)2
j.
....
218-219
„
A., 205, 74 ; 210,
42, 507
395
Dinitrophenamidobenzoic
C6H3(N02)2.NH.C6H4.C02H
j-
262-264
Jourdan
B., 18, 1449
48, 988
acid
=4.2.1 ; 1.2
Benzyl picrate
(O.CH2Ph).(NO2)3=1.2.4.6
C13H907N3
....
149
Kumpf
B., 17, 1076
46, 1005
Trinitrobenzylphenol
C6H4(NO,).CH2.C6H2(OH)
148
Eennie
41,36
(NO2)2=1.4 ; 1.4.3.5
0-Dinitrophenylnitrobenzyl
C6H4(N02).CH2.O.C6H3
.
....
137
Kumpf
B., 17, 1077
46, 1005
oxide
(NO2)2=1.4 ; 1.2.6
"- » »
„ =1.4 ; 1.2.4
„
....
198
Staedel
B., 14, 899
40, 723
M 11
"
"
....
201
Kumpf
B., 17, 1077
46, 1005
534
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
a-Dinitrophenylnitrobenzyl
C,H4(N02).CH2.O.C6Ha
C13H90,N.
198
Finkentscher
A., 217, 177-182
oxide
(NO2),=1.4; 1.2.4
Anilidocarbamidophenol
O.C6H4.N : C.NHPh=1.2
i i
013H10ON2
173
Kalckhoff
B., 16, 1826
44, 1110
Hydroxybenzenylphenylene-
NH.C6H4.N : C.C6H4.OH
„
222-5
Hiibner and Men-
B., 13, 463 ; A.,
38, 556
amidiue
=(1.2)2
sching
210, 345
Diamidodiphenylene ketone
fr. (C6H4)2:CO=(1.2)2
3)
....
286
Schultz
A., 203, 95
38, 814
Benzylidenenitranil ine
Ph.CH:N.C6H4.N02=U
C13H1002N2
66
Lazorenco
J. [1870], 760
Nitrobenzylideneaniline
C6H4(NO2).CH : NPh=1.3
„
61
„
B
„
=1.4
jj
93
Fischer
B., 14, 2526
42,393
Nitrobenzanilide
C6H4(N02).CO.NHPh=1.3
C13H1003N2
144
Engler and Volk-
B., 8, 35
28, 643
hausen
„ ....
» »
„
144
Mears
B., 9, 774
30, 309
Benzamidonitrobenzene
C6H4(N02).NHBz=1.2
„
94
Hiibner & Schwartz
B., 10, 1708
34, 142
„
>. »
„
....
94
Hiibner
A., 208, 301
40, 1131
„
»
„
....
94-95
Stover
B., 7, 463, 1315
27, 806
„
„ =1.3
„
....
152
Bell
B., 7, 498
27, 900
„
» 1!
jj
154
Hiibner & Schwartz
B., 10, 1708
34, 142
(cf.
>. »
„
....
155-5
Hiibner
B., 10, 1716
A 90ft 9Q7'\
>., — >' ', —.' i
»
=1.4
„
....
199
Stover
B., 7, 463, 1315
28, 271
(cf.
i> »
„
....
199
Hiibner & Schwartz
B., 10, 1708
34, 142
A., 208, 294)
Phenolazobenzoic acid
C6H4(OH).N2.C6H4.C02H
„
....
220
Griess
B., 14, 2033
42, 48
= 1.?; 1.3
Benzoylnitroatnidophenol ....
OH.NHBz.NO2=1.2.4orl.4.2
C13H1004N-2
200 d.
Post
A., 205, 73
Nitrosalicylanilide
OH.NO2.(CO.NHPh)=1.3.4
„
....
224
Mensching&HUbnp]
B., 13, 462 ; A.,
38, 556
210, 343
Nitrobenzamidophenol
HO.C6H4.NH.CO.C6H4.N02
....
139 d.
Morse
B., 7, 1320
28, 272
Salicylnitranilide
HO.C6H4.CO.NH.C6H4.
..
154
Hiibner
A., 210, 345
NO2=1.2 ; 1.2
„ =1.2; 1.3
„
217-818
Wanstrat
B., 6, 337
26, 907
»
» ,.
„
....
218-219
Bell
C. N., 31, 244
28, 1201
„
=1.2; 1.4.
»
229-230
»
3?
31
HO.C6H4.CO.C6H3(NH,).NO;,
„
115
Haarmann
B., 6, 339
26, 907
=1.2 ; ?.1.4
Dinitrodiphenylmethane
fr. Ph.CH2.C6H4.N02=1.3
94
Becker
B., 15, 2092
44, 203
»
CH.:C12H8(N02)2
„
118
Pratorius
A., 194. 366
36. 319
„
a
„
....
118
Staedel
B., 11, 745
34,671
»
fr. Ph.CH2.C,H4.N02=1.4
„
172
Doer
B., 5, 795
vii.,948;26,170
>!
" »
„
....
175
Easier
B., 16, 2719
46, 310
"
CH2:012HS(N02)2
„
183
Doer
B., 5, 795
26, 170
» ....
I)
31
183
Pratorius
A., 194, 369
36, 319
Eesorcinolazobenzoic acid ....
C6H3(OH)2.N2.CtH4.C02H
13
....
d.
Griess
B., 14, 2034
42, 49
=1.3.?; 1.3
Dinitrotolylphenyl
(3-dinitrophenylbenzyloxide....
fr. Ph.C6H4.Me=1.4
Ph.CH,.O.C8H3(NO,),=1.2.6
CisH;ANn
....
153-157
76
Carnelley
Kumpf
J. [1876], 420
B., 17, 1076
29,23
46, 1005
a~ »
,, =1.2.4
149
Nitrophenylnitrobenzyloxide
C6H4(N02).CH2.O.C6H4(N02)
„
129
"
B., 17, 1077
"
=1.4; 1.2
»
=(1.4),
183
Benzyldinitrophenol....
Dinitrodiphenylcarbamide ....
Ph.CH2.C6H2(OH)(N02)2
CO(NH.C6H4.N02)2=(1.3)2
31
87-88
233
Rennie
Losanitsch
13
41, 222
B., 16, 50
D
44, 583
Benzyldinitroquinol
=2
(O.CH2Ph).OH.(N02)2
31
a. 100
137
Bruckner
Pellezzari
B., 7, 1235
G. I., 13, 501
46, 437
Ethylic dinitro-a-naphthoate
» -0- ,,
CIOH6(N02)2.C02Et
33
143 u.c.
Ek strand
B., 17, 1601
46, 1361
"
31
141 u.c.
„
B., 17, 1603
,i
Formodiphenylamine
H.CO.NPh,
C13HnON
210-220(i.v.)
165 u.c.
73-74
Girard and Willm
B. S., 24, 99 ; B.,
.j
30,99
8, 1195
COMPOUNDS CONTAINING FOUR ELEMENTS.
535
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Formodiphenylamine
H.CO.NPh2
C^H^ON
....
1
Tobias
B., 15, 2866
Diphenylacetoxime
Ph20 : NOH
5>
B., 16, 823
139-5-140
Jaimy
B., 15, 2782
44,580
Beuzanilide ....
C6H-.CO.NHPh
5)
A., 60, 311
160-161
Wallach
A., 184, 79
„
»
51
159
Leuckart
B., 18, 873
48, 773
159
Frankland & Louis
37, 745
J)
5)
159
Pieschel
A., 175, 310
5»
»J
163
Hiibner
A., 208, 291
40, 1130
))
))
Amidobenzophenone
Ph.CO.C6H4.NH2=1.3
51
87
Geigy and Konigs
B., 18, 2401
48, 1236
„
=1.2
11
103
Higgin
41, 134
,, .... ....
» M
))
....
105-106
Geigy and Konigs
B., 18, 2404
48, 1236
„
= 1.4
J)
123
Higgin
41, 133
,, ....
» 71
1)
124
Geigy and Konigs
B., 18, 2404
48, 1236
„
)> )1
)»
194
Doebner
B., 13, 1013;
38, 804
A., 210, 268
,, .... ....
»J »
»
124
Doebner and Weiss
B., 14, 1836
Formamidodiphenyl
Ph.C6H4.NH.COH = 1.4
n
172
Zimmermann
B., 13, 1967
40, 176
Hydroxybenzaldehydeanilide
HO.C6H4.CH:NPh=1.4
ji
190-191
Herzfeld
B., 10, 1272
34,66
Pseudocinnamylpyrroline ....
C4H4N.CO.CH : CHPh
H
141-142
Ciamician & Denu-
B., 17, 2947
48, 378
stedt
Diamidohydracridine ketone
CO.C8H4.NH.CliH2(NH2),,
C13H,,ON3
....
222-223
Jourdan
B., 18, 1452
48, 988
i- . L
=2.1 ; U.2.4
Phenylic phenylcarbamate ....
NHPh.CO2Ph
C^H.AN
122
Hofmann
B., 4, 249
24, 395
>» 15 ""
I)
H
1S2 u. c.
Eckenroth
B., 18, 517
48, 786
» »
»
" (
....
124
Leuckart & Schmidl
B., 18, 2339
vii., 408
1) »» '"•
)>
i)
125
Gumpert
J. p. [2], 31, 119
48, 656
Beuzylnitrobenzene
Ph.CH2.C6H4.NO2=1.3
i)
....
Liquid
Becker
B., 15, 2091
„
=1.4
„
31
Easier
B., 16, 2717
46, 310
Benzoxyamidobenzene
C6H4(OBz).NH2=1.2
jj
unstable
Bottcher
B., 16, 630
„
= 1.4
51
....
153-154
Hiibner
A., 210, 379
42, 505
Formylhydroxydiphenyl-
C6H4.OH.(NPkCOH=1.4
J»
178
Philip and C.'alm
B., 17, 2436
48, 156
amine
Hydroxybenzanilide
HO.C6H4.CO.NHPh=1.2
))
.,..
132
Kupferberg
J. p. [2], 16, 443
34, 320
i) .... ....
>» »
H
134-135
Wanstrat
B., 6, 336
26, 906
„
» »
ji
....
....
Hiibner
A., 210, 342
?» •••• ••••
=1.3
»'
154-155
Kupferberg
J. p. [2], 16, 445
34, 320
i» .... ....
=1.4
,,
....
196-197
»
J. p. [2], 16, 444
I)
Benzamidophenol (?)
CcH4.OH.NHBz=1.2(?)
|4
B., 16, 632
103
Morse
B., 7, 1319
28, 272
„
=1.2
H
165; 167
Bottcher
B., 16, 631 ;
44, 800 ; 48,
C. C. [1884], 898
658
M .... ...
!> I)
1)
767
Hiibner
A., 210, 387
42, 506
1J .... ....
=1.4
>j
....
227-5
n
A, 210, 378
42, 505
/3-nitrotolylphenyl
fr. Ph.C6H4.Me=1.4
))
305-325
Liquid
Carnelley
J. [1876], 419
29, 22
o- „
» »
1)
....
141
j»
)>
n
Uihydroxybenzaldehydeani-
(CH:NPh).(OH)2=1.2.5
1)
needles
Tiemann and Miillei
B., 14, 1987
lide
/3-naphthimidoacetate
C10H7.C(OAc) I NH
)j
150-152
Pinner and Klein
B., 11, 1487
36, 48
Nitrobenzylidenephenylhy-
NHPh.N: CHLCaH^NO^l-S
C^HOtN,
121
Schroeder
B., 17, 2097
46, 1323
drazine
Nitrobenzylphenyl oxide ....
Ph.O.CH2.C6H4.N02=1.4
CUH1IQ,N
91
Kumpf
B., 17, 1077
46, 1005
Nitrophenylbenzyl oxide ....
Ph.CH2.O.C6H4.NO2=1.2
Jl
29
i»
B., 17, 1076
)»
» j»
=1.4
))
....
106
»)
B., 17, 1075
)»
Beuzylnitrophenol ....
OH.N02.CH2Ph=1.2.4
Jl
71 ; 74-75
Eennie
41, 221
Methylic pyrrolinemethyl-
C4H3N : CH.C6H4.CO.iMe
)>
....
104-105
Ciamician & Denn-
B., 17, 2959
48, 37!)
benzoate
stedt
Nitrocarbanilide
NHPh.CO.NH.C6H4.NO2
C13HU03N3
187
Bruckner
B., 7, 1236
28, 166
Amidobenzeneazosalicylic
NH2.C6H4.N,,C6HS(OH).
»
....
219-220 d.
Meldola
47, 667
acid
CO2H
Benzylnitroquinol
OH.(O.CH2Ph).N02=1.4.5
C13HU04N
,,,,
137
Schiff
G. I., 13, 538
46, 433
,, .... ....
„ =1.4.6
3>
156-158 d.
»
>»
»
£ thy lie nitro-a-imphthoate ....
C10H6.NO2.CO2Et=?a
»
acid m.p. 19(i
63
Ekstrand
B., 12, 1394
38, 261
» » ~a~ ?>
i) =?a J
»>
215
68-69
i»
B., 18, 74
48, 548
536
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Ethylic nitro-a-naphthoate ....
C10H6.NOi,C02Et=?a
CuH.AN
icid m.fi. 233
92
Ekstrand
B., 12, 1395
38, 261
)) JJ "a" JJ
i) »
JJ
„ 238
93
Graeff
B., 14, 1066
» „ -a- „
jj jj
))
„ 241
93
jj
B., 16, 2252
46, 81
jj jj ~P~ jj
=?0
J)
„ 220
82
Ekstrand
B., 12, 1395
38, 261
» » ~P" jj
J» )»
J>
„ 280
107
jj
B., 12, 1396
jj
„ „ -£- „
JJ »
JJ
„ 295
109
Graeff
B., 16, 2254
46, 81
Dinitromethyldiphenylaraine
C6H3.NMePh.(N02)3
C13Hn04N3
167 u. c.
Leymann
B., 15, 1235
42, 1057
y-dinitrotolylphenylamine ....
C6H2Me.(NO2)2.NHPh
JJ
142
Hepp
A., 215, 369
44, 317
Dinitrophenyltoluidine
C6H4Me.NH.C6H3(NO2)2
)J
101-102
Leymann
B., 15, 1236
42, 1057
=1.2 ; (1),
„
=1.4 ; 1.2.4
»J
135
Engelhardt and
Z. C. [2], 6, 225
vii., 147'
Latschinoff
jj t
JJ »J
J»
....
136
Willgerodt
B., 9, 980
30, 405
,,
J) JJ
>J
....
137
....
Z. C. [1870], 233
ji
DinitrodipheDylguanidine ....
NH : C(NH.C6H4.NO.,),!
C13HU04N5
190
Briickner
B., 7, 1235
28, 166
Benzylphenylnitrosamine ....
Ph.CH2.NPh.NO
C13H12ON2
58
Antrick
A., 227, 360
48, 543
Benzoylphenylhydrazine
Ph.NH.NH.CO.Ph
»
....
168
Fischer
A., 190, 125
34, 308
Diphenylcarbamide ....
NH2.CO.NPh2
J»
B., 8, 1666
189 u. c.
Michler
B., 9, 397, 715
30,91
,,
CO(CNHPh)2
JJ
....
200-203
Schiff
B., 3, 651
vii., 253
jj ...» «*..
JJ
)J
....
205
Hofmann
A., 57, 266 ; 70,
i., 756
138
,, ....
JJ
JJ
225
Willm & Wischen
[2], 6, 192
vii., 253
J» •"• ••"
5)
JJ
220-235
Eottermimd
A., 175, 257
28, 768
,,
))
J)
....
232-233
jj
jj
1J
JJ ....
))
JJ
....
233-235
Kuhn
B., 18, 1478
JJ •"• •••
JJ
JJ
....
235
jj
B., 18, 1477
,,
JJ
J)
....
235
Steiner
B., 8, 519
28, 883
,,
J)
JJ
....
235
Michler
B., 9, 716
,*
JJ
JJ
....
235
Buff
B., 2, 499
vii., 583
jj
JJ
)J
235
Weith
B., 9, 881
30, 639
))
JJ
1)
260
....
Hentschel
J. p., 27, 498
44, 1108
„ (cf. B., 14, 2444)
)J
JJ
235
Bender
B., 13, 699
jj ....
JJ
JJ
....
235
Hofmann
B., 14, 2735
)) .... ....
JJ
JJ
234-235
....
A.
j) .... ....
JJ
JJ
....
238
....
A.
Amidobenzanilide
Ph.NH.CO.C6H4.NH,=1.3
JJ
....
114
Engler and Volk-
B., 8, 35
28, 643
hausen
,, ....
=1.2
JJ
....
129
Piutti
B., 16, 1321
44, 999
jj .... ....
» jj
)J
....
130 •
Kolbe
J. p. [2], 30, 467
48, 666
Benzdiamidobenzene
C6H4.NH2.NHBz=1.3
JJ
125
Bell
B., 7, 498
27, 900
jj
=1.4
jj
125
Stover
B., 7, 463
27, 806
»
>» »
)J
....
128
Hiibner
A., 208, 295
40, 1130
)» ....
=1.2
JJ
C6H4(NH2)2?
140
Mixter
A. C. J., 6, 26
46, 1327
(?) ....
=1.3
» (?)
....
260
Iliibner
A., 208, 298
Hydroxybenzylidenephenyl-
HO.CCH4.CH I N2HPh=1.2
jj
....
142-143
Kossing
B., 17, 3004
hydrazine
» jj
» >!
>j
142-143
Tiemann and Kees
B., 18, 1660
Methyloxyazobenzene
Ph.N2.O.C6H4Me
jj
53-5-54
Scichilone
G. I. [1882], 108
42, 726
Phenylazocresol (J., 1879,465)
Ph.N2.C6H3Me.OH=?.l .3
jj
....
109
Nolting and Kohn
B., 17, 366
46, 902
,j .... ...
=?.1.4
jj
108-109
Mazzara
G. I., 9, 424
38, 163
jj .... ...
» jj
jj
108-109
Nolting and Kohn
B., 17, 352
46, 901
jj .... ...
" J!
jj
108
Liebermann and
B., 17, 131
46, 736
Kostanecki
jj
„ =?.1.2
jj
138-130
jj
jj
JJ
jj
Phenolazotoluene
HO.C6H4.N5.C6H4Me "
jj
jj
129-130
151
Nolting and Kohn
Kimich
B., 17, 363
B., 8, 1030
46, 902
29, 268
=1.?; 1.4
y-Diamidobenzophenone
CO:C12H8(N02)3
jj
....
131
Staedel
A., 218, 3.39
44, 991
0-
J>
jj
J. p., 46, 509
165
Doer
B., 5, 797
26,171; vii, 939
0-
JJ
jj
165
Stadel
B., 11,744
34, 671
0-
)J
)>
....
165
Pratorius
A., 194, 356
36, 319
«- j,
JJ
jj
....
172
>j
A., 194, 338
36, 242
COMPOUNDS CONTAINING FOUR ELEMENTS.
537
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
a-Diamidobenzophenone
00:C12H8(N02)2
C13H12ON2
....
172
Staedel
A., 218, 339
44, 991
a- ' . „
»
»>
172
Staedel and Saur
B., 11, 1748
Harmin (cf. J., 1854, 525) ....
see B., 18, 405
M
A., 64, 365
256-257 d.
Fischer and Ta'uber
B., 18, 400
48, 820
Nitrobenzylphenylamine ....
Ph.NH.CH2.C6H4.NO2
Cj.H.jOjN.
68
Strakosch
B., 6, 1062
27,80
Salicyl-a-amidoanilide
NH2.C6H4.NH.CO.C6H4.OH
)>
....
143
Bell
C. N., 31, 244;
28, 1201
= 1.3; 1.2
J. [1875], 746
„ -/3- „
=1.4; 1.2
V
158
Jl
)»
»
Eesoi-cinolazotoluene
C6H4Me.N2.C6H3(OH)2
)»
175-176
Wallach & Fischer
B., 15, 2825
= 1.2 ; 2.1.3
„ ....
=1.4; ?.1.3
Jl
183-184
»
B., 15, 2821
,, .... ....
» »)
»?
187
Wallach
B., 15, 26
42, 610
Orcinol azobenzene
Ph.N2.C,H4Me(OH)j=?.1.3.5
>?
....
183
Typke
B., 10, 1579
34, 219
Phenylmethylacetoxypyrimi-
C4N2HPh.Me.OAc
1J
B., 18, 760
40-41
Pinner
B., 18, 762
48, 752
dine
Nitrodiphenylguanidirie
NH : C(NHPh).NH.C6H4.
C13H,202N4
....
131-132
Bruckner
B., 7, 1236
28, 166
NO,
Toluidineazonitrobenzene ....
N02.C6H4.N2.C6H3Me.NH2 "
»
....
198
Nolting and Binder
B. S., 42, 340
48, 385
=4.1 ; 5.1.2
Toluquinone + o-nitraniline
MM
C13H1204N2
37
Hebebrand
B., 15, 1976
Dinitrophendiamidotoluene
NH2.C6H3Me.NH.C6H3
C13H1204N4
184
Leyniann
B., 15, 1237
42, 1057
(N02)2=4.1.2; (?)3
a-Trinitrotolueneaniline
C6H2Me(NO2)3.NH,Ph
C13H,206N4
83-84
Hepp
A., 215, 365
44, 317
Lutidine picrate
(C6NH3Me2).C6H2(N02)8.OH
C13H120?N4
161
Epstein
B., 18, 883
48, 815
j» » •••• ••••
»
M
176-179
Hantzsch
B., 17, 2909
48, 397
«-y- ,» »
»
»
177
Michael
B., 18, 2026
» » )>
1J
)'
179
Ladenburg & Both
B., 18, 1593
» „ ,,
1»
3T
.179
Ladenburg
B., 18, 914
,, ,, » •••• ••••
»>
)»
181
Voges
A., 215, 56
» ii »
»
)1
181
Hantzsch
B., 17, 2903
Methylacet-a-naphthalide ....
C10H7.NMeAc
C13H13ON
90-91
Landshoff
B., 11, 643
34, 587
Methylpseudostyril of phenyl
CPh : CH.CO.NMe.CMe : CH
JJ
112
Hantzsch
B., 17, 2916
48, 398
picoline
i >
• t
?
CO.CH : CMe.NPh.CMe:CH
197
Perkin
B., 18, 684
48, 762
i ' i
V)
Diphenylsemicarbazide
NHPh.CO.NH.NHPh
C13H13ON3
170
Kiihn
B., 17, 2885
48, 261
Amidobenzdiamidobenzene....
NH2.C6H4.NH.CO.CSH4.
))
129
McHugh
B., 7, 1268
NH.,=(1.3)2
p-Toluidineazophenol
NH2.C6H3Me.N2.C6H4.OH
?1
172
Wallach
B., 15, 2827
44, 584
j3-naphthylurethane
C10H7.NH.CO2Et
C13H,AN
73
Cosiner
B., 14, 60
40, 606
°- ji »
)J
1)
....
79
Hofmann
P. B., 19, 108 ;
24, 139; vii.,
B., 3, 653
253
Ethylic methylquinoline car-
CMe: N.C6H4.CH : C.CO2Et
1)
71
Friedlander and
B., 16, 1837
44, 1149
boxylate
Goliring
Aniline salicylate
HO.C6H4.CO2H+NH2Ph
C13H1303N
....
150
Guthrie
P. M. [5], 18, 27
=1.2
Acetamidocinnamenylacrylic
NHAc.CGH4.CH : CH.CH :
»)
....
253 d.
Diehl and Einhorn
B., 18, 2333
48, 1223
acid
CH.CO2H=1.2
Nitroharmalin
C13H13(N02)N20
C13H1303N3
120
Fritzsche
A., 68, 355 ; 72,
iii., 9
306
Methylic coumalanilidic acid
C4N3(NHPh).C02Me .C02H
C13H1304N
....
140 d.
Pechmann & Welsh
B., 17, 2393
47, 152 ; 48,
175
Ethylic acetindoxylate
N.C,H7c(OAc).CH.CO2Et
I>
....
138
Baeyer
B., 14, 1742
42, 198
i i
Etliylic nitrobenzoyltri-
CH2.CH2.C(COsEt).CO.C.iH,.
l',3IIiAN
84
Perkin & Bellenot
B., 18, 959
48, 795
methylene carboxylate
|_ 1
NO2=1.4
Aniline pyrogallate ....
C6H;,(OH)3.CO2H+C(iH5.NH2
n
126-128
Guthrie
P. M. [5], 18, 109
Triacetylgallauiide
(OAc)3.CONH2=l. 2.3.5
C13H,,07N
150
Schiff and Pous
B., 18, 489
48, 796
/3-diamidobenzhydrol
HO.CH : C12H3(NH2)2
C13H14ON2
....
128-129
Staedel
A., 218, 339
44, 991
Harraaline (A., 38, 363 ; 64,
....
»I
....
238 d.
Fischer and Ta'uber
B., 18, 400
48, 820
360)
Carbanilidocyanmethine
Ph.NH.CO.NH.C6H7N2
C13H14ON4
••*)
225
Keller
J. p. [2], 31, 363
48, 961
Ethylic benzenylazoxime-
O.N : CPh.N : C(CH2)2.C02Et
C13H1403N2
255 p.d.
Liquid
Schulz
B., 18, 2462
48, 1219
propenyl-carboxylate
3 z
538
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Acetylanilidopyrotartarimid
fr.Ph.NH.CMe.CO.NH.CO.
i
C13H1403Na
....
235
Wechsler
B., 18, 1041
48, 900
CH2
_j '
?
C13HUO6N5
.„.
235
Stojentin
J. p., 32, 1
48, 1195
Toluidine phenate
C6H4Me.NH2+Ph.OH=1.4
C,3H15ON
31-1
Dyson
43,468
Diallylamidobenzoic acid _
N(C3HS)2.C02H=1.3
C13H1602N
....
90
Griess
B., 5, 1041
26, 281 ; vii.,
168
Mesitylsuccinimide
C6H2Me3.N:(CO)2:C,H4
„
137
Eisenberg
B., 15, 1018
42, 956
=1.3.5.6
Isonitrosotetramethyloxy-
fr.C6HMe3.N.NH.CMe.CH2.
C13H1502N3
....
156
Haller
B., 18, 708
48, 818
i
quinizine
CO=1.2.4.5.6
J
Ethylic ethylind'oxylate
N.C6H4.C(OEt).CH.CO2Et '
C13H1503N
98
Baeyer
B., 14, 1742
48, 198
=1.2
Ethylic acetamidocinnamate
NHAc.(CH : CH.CO2Et)
J)
137
Friedliinder and
B., 15, 1423
42, 1209
=1.2
Weinberg
Ethylcumazonic acid
N : CEt.O.CMe2.C6H3.CO,,H
„
.„.
202
Widmann
B., 16, 2585
46, 304
" J =1.2.5
?— acid
„ (?)
128-129
Weltner
B., 18, 795
48, 794
Ethylic acetyl-p-methylisa-
....
C13H1604N
....
78-79
Duisberg
B., 18, 198
48, 544
tate
„ ethylnitrobenzoyl-
NO2.C6H4.CO.CHEt.CO2Et
C13H1505N
39-40
Perkin & Bellemot
B., 18, 953
48, 794
acetate
=1.4
„ benzamsucciuate ....
CO2H.C6H4.NH.CO.C2H4.
J)
174
Pellizzari
B., 18, 214
48, 533
OO2Et=1.3
Benzdiamidoacetamidoacetie
NHBz.CH2.CO.NH.CH2.CO
C13H15O5N3
172
Curtius
B., 16, 756
44, 1087
acid
NH.CH2.CO2H
Tetramethyloxyquinizhie ....
C6HMe3.N.NH.CMe.CHn.CO
i i
C13H16ON2
.„.
154-155
Haller
B., 18, 707
48, 818
=1.2.4.5.6
Ethylic azotolueneacetacetate
Me.(N3.CHAc.CO2Et)=1.4
C13H1603N2
• •«.
74
ZUbliu
B., 11, 1420
Nitrobenzaldiacetonamine ....
N02.C6H4.CH.CH2.CO.CH2.
„
«.-«
Liquid
Antrick
A., 227, 365
48, 503
L
CMea.NH=1.2
j
„
11 „ =1-3
„
....
Liquid
,,
n
n 11
IT „ =1.4
ir
142'5
,,
yj
Ethylic /3-hippuramidacetic
NHBz.CH2.CO.NH.CH2.C(X
C13H1604N2
117
Curtius
J. p. [2], 26, 194
44, 339
acid
Et
„ nitrophenylethoxy-
NO2.C6H4.CH(OEt).CH(NO2).
C13H1607N2
...»
52
Friedliinder and
A., 229, 210 ; B.,
48, 1138
nitropropionate
COsEt=1.4
Mahly
16, 852
.. ethyldinitrohydro-
OMe.(N02)2.(CH2.CH2.C02
Jl
49
Stohr
A., 225, 57
46, 1350
p-coumarate
Et)=1.2.6.4
Benzald iacetonamine
Pli.CH.NH.CMe2:(CH)2:CO
C13H17ON
230 d.
61-2
Heintz
A., 193, 62
36, 54
11 11
H
62-63
Fischer
B., 16, 2237
46, 54
Diethamidocinnamic acid ....
NEt2.(CH : CH.COaH)=1.2
C13H,r02N
B., 16, 653
124
Fischer and Kuzel
A., 221, 261
46, 440
Acetylethoxyhydroquinoline
N.OEt=0! ; n,
307
Liquid
Fischer and Eenouf
B., 17, 759
46, 10J9
Butylic hippurate
Isobutylic „ (B. S., 34,
NHBz.CH2.CO2Bu«
NHBz.CH2.CO2Bu0
C13H1703N
....
40-41
45-46
Campani & Bizzarri
G. L, 10, 257
38, 870
527)
"
Hydroxypropylcarboxyl-
phenylurethane
C6H3.C02H.(CMe2.OH).
(NH.CO.,Et)
C13H1705N
167 d.
Widmann
B., 17, 1305
46, 1023
Quinanilide .
CM NH(T H O 1
JJ
d. a. 240
174 c.
lesse
A., 110, 312
v., 9
Ethylic acetoacetate+o-di-
amidotoluene
Ethylic p-tolylhydrazine-
C0H,Me ; (NH), : CMe.CH^
CO2Et
82
91-93
jadenbnrg and
Eiigheimer
tnorr
B., 12, 953
B., 17, 550
36, 716
46, 1154
acetoacetate
Diacetamidomesitylene
Mea.(NHAc)2=1.3.5,2.4
,,
a. 300
jadenburg
A., 179, 177; B.,
38, 1036; 29,
Ethylic anilidopyrotartar-
aiuate
NHs.CO.CMe(NHPh).CH,.
C02Et
C13H1903N2
125
Wechsler
8,677
B., 10, 1039
386
48, 900
Benzylidene urethane
Ph.CH(NH.C02EtJ2
C13H1804N2
71
Bischoff
B., 7, 634-635
27, 891
COMPOUNDS CONTAINING FOUR ELEMENTS.
539
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch, Soc.
m-toluylene urethane
C6H3Me(NH.CO2Et),
C13H1S04N2
137
Lussy
B., 7, 1264
28, 274
[sobutylacetarnidotoluene ...
Me.Bu«.NHAc=1.5^
QuHMON
162
Effront
B., 17, 2322
48, 152
Pentainethylacetanilide
C6Me6.NHAc
»
....
213
Hofrnann
B., 18, 1824
48, 1129
Ethoxyhy droethylqu incline
N..OEt=a, ; .a,
1)
266-268(716
33
Fischer and Kenouf
B., 17, 760
46, 1049
(ethylkairine)
Lsocyminyl urethane
Me.Pr.(NH.OG2Et)=1.3.2
C13H1902N
....
229
Kelbe and Warth
A., 221, 157
46,47
Diacetyltrimethtriamidoben -
NMej.NMeAc.NHAc— 1.4.?
CI3H1902N3
184
Wurster& Schobig
B., 12, 1813
38, 111
zene
Nitroisoamylethoxy benzene
OEt.C5Hn.NO2=?
C13H1903N
a. 300 d.
Liquid
Liebmann
B., 15, 1991
Dietkylic trimethylpyrroline
CO2Et.C:CMe.NMe.CMe:C.
C13H1904N
....
72
Knorr
B., 18, 303
48, 555
dicarboxylate
CQ2Et
Diethyl-m -toluylenecarba-
C6H3Me(NH.CO.NHEt)2
C^H^N,
175
Lussy
B., 8, 292
28, 770
mide
Diethoxyhydroxyethyltheo-
C13K,007N2
152
Fischer
A., 215, 307
44, 357
bromine
Cyanallyl-allylalcoholate
C^H^ON
....
95-96
Z. C. [1870], 401
Allylalcohol+allylcyanide ...
03HS.CN+3C8H6.OH
C13H2303N
95-96
Rinne
B., 6, 389
vii., 49
Valerodiacetonamine oxalate
CUH,,ON+U2H204
C^H^O^N
190 d.
Antrick
A., 227, 365
48, 502
CEnanthodiacetonamine
O6H13.CH.CH.,CO.CH,.
C^H^ON
....
29-5
»
j)
48, 503
i *
CMe2.NH
Fr. ethylcarbamine
MM
C13HS503N5
a. 200
Gautier
C. R., 67, 804
vi., 529
Oxalyldipiperidine ....
not C^HsjON,; as in orig.
C13H26ON2
280-290 d.
Ladenburg
B., 14, 1879
Ethylio diisoamylcarbamate
N(C5H11)2.CO2Et
C13H2702N
246-247
L. —20
Ouster
B., 12, 1334
36, 914
Tetranitroanthraflavie acid
C14H4(N02)404
CwHAiN*
....
d.w.m.307'6c
Schardinger
B., 8, 1488
29, 584
Tetranitroisoanthraflavic acid
J>
1)
a. 300
EOmer & Schwarzer
B., 15, 1046
42, 975
o-dinitrophenanthraquinone
C14H6(N02)2:02
C14HcO(iN2
B., 9, 548
280
Groebe
A., 167, 144
»
JJ
•»
290
Kleemann & Wense
B., 18, 2168
;>
1J
,,
....
290
Schultz
A., 203, 108
a-dinitroantliraquiuone
cf. A., 160, 145; 166, 154
A
B., 16, 54
256-260
Schmidt
J. p. [2], 9, 261 ;
19, 211
0-
»»
....
?
Fritzsche
Z. C. [1869], 114
/3-
....
)>
B., 7, 203
280
Schmidt
J. p. [2], 9, 261
27, 581, 987
0-
)»
2
Anderson
A., 122, 302
y- >*
NOi.C6H3:(CO)2:C6H3.N02
i)
a. 300
Bomer
B., 16, 364
44, 737
=3.2.1; 1.2.6
Dinitrohydroxyauthra-
C6H4 ; (CO)2 : C6H(NO2)2.OH
C14H607N2
268-270
Simoii
B., 14, 465; 15,
40, 608
quinone
=2.1; 1.2.4.6.5
692
Diuitroxantliopurpurin
C14H4O2(N02)2(OH)2
C14H608N2
isomeric
249
Plath
B., 9, 1206
31, 87
» ....
»
1J
»>
249-2CO
>i
B., 9, 1205
n
Diuitroniuiijistin
)>
JJ
251
Schunck & Burner
33, 425
o-nitrophenanthraquinone ....
cuH^cNo^q,
C14H704N
....
215-220
Schmidt
B., 12, 1156
36, 941
«-
V
5)
....
257
Anschiitz & Schultz
B., 9, 1404
31, 210
/3-
»
»)
260-266
Schmidt
B., 12, 1157
36, 941
y- »
»
»
....
263d.
»5
B., 12, 1158
;>
?-
1)
•))
281-282
Lachowicz
J. p. [2], 28, 168
46, 82
/3-nitroantkraquinone
....
5>
220
Bcimer
B., 15, 1786
44, 71
a- „ (B 1 2, 1570)
....
))
A., 166, 148
230
Bottger & Petersen
J. p. [2], 6, 367
26, 389
«- :,
.-..
»
230
Claus and Hertel
B., 14, 978
40,737
Nitrodiphenyleneketone car-
fr. CCH4.CO.C' H3.C02H
C14H706N
245-246
Fittig & Liepmann
A., 208, 8
38, 401
boxy lie acid
= 1.2; 1.2.3.
a-Nitroalizarin (A., 201, 353)
fr. C6H4:(CO)2:C6H2(OH)2
C14H.OCN
194-196
Schunck & Rcinier
B., 12, 587
36, 654
=2.1 ; 1.2.3.4
'I- „ (B.S., 26, 67)
>! »
))
230
Rosenstiehl
A. C. [5], 12, 519
34, 231
8- „ (B., 10, 1760)
C6H4:(CO)2:06H(OH)2.N02
))
244
Simon
B., 15, 692
42, 863
=2.1 ; 1.2.3.4.5
a- „
n »
S»
....
244
Schunck & Romer
B., 12, 585
36, 654
?- „
....
)»
282
)»
B., 12, 587
I)
Phenantliraquinone dioxi-
C6H4.C6H4.(^: N O N ' O
CUH8ON2
181
Goldschmidt
B., 16, 2179
46, 62
mide
3 z 2
540
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Benzidine tetracarboxylic
(.C6H3.NH.CO)2
CI4H802NS
283 u.c.
Claus & Hemmaun
B., 16, 1762
44, 1127
anhydrimide
i i
Nitrophenylphthalimide „.
C6H4:(CO)2:N.C6H4.N02
C14H804N2
....
242-243
Gabriel
B., 11, 2261
36, 324
= 1 2; 1.3
Dinitrophenanthrene
„
....
150-160
Groebe
A., 167, 156
26,896; vii., 85
Nitrosonitroanthrone
see original paper
„
263
Liebermann and
B., 14, 470
40, 607
Landshoff
Dinitroanthrone
„
C14H305N2
116d.
11
B., 14, 472
„
Nitroamidoxyanthraquinoue
....
„
240
Bourcart
B., 12, 1419
38, 263
Dinitrobeuzil . ... ...
C14H8O6N2
octohedra
131
Sacrumenny
B., 5, 1100
26, 502
plates
147
J. R, 4, 278
vii., 157
Isodinitrobenzil
....
,,
J. R, 13, 29
205-206 d.
Soloubeff
B. S. [2], 34, 345
40, 422
Nitrobenzoic anhydride
(N02.C6H4.CO)20=(1.2)2
C14H807N2
....
135
Bischoff and Each
B., 17, 2789
48, 263
/3-Dinitro-p-benzoylbenzoic
....
„
211-212
Plascuda & Zincke
B., 7, 985
28, 70
acid
«- „ „
....
„
240
Plascuda
B., 7, 988
28, 75
«-Dinitrodiphenic acid
(.C6H3.N02.C02H)2=(1.4.2)2
C14H308N2
248-249
Hummel
A., 193, 131
36, 165
«- „ (B., 16, 2346)
»i 11
„
250-251
Struve
B., 10, 76
46, 329
(B., 12, 236)
11 11
„
253
Schultz
A., 196, 29
?)
p- „
fr. (.C6H4.COSH)2=(1.2)2 ....
„
297
„
A., 203, 105
38, 814
Tetrauitrobenzyltolueue
„
C14H808N4
160-161
Zincke
B., 5, 685
vii., 183; 25,
1005
Benzoylphenylisonitril
CsH4Bz.NC=1.4
C14H9ON
118-119
Dobner and Weiss
B., 14, 1838
42, 177
11
„ „
„
118-119
Dobner
A., 210, 271
42, 508
Phenanthreneqninonimide ....
C0H4.C6H4.CO.C:NH=(1.2)2
i,
147
Anschiitz & Schultz
B., 10, 23
32, 492
n
11 11
„
....
158-150
Zincke
B., 12, 1642
38,48
„ ..«
» 11
„
....
167
Anschiitz & Schultz
A., 196, 51
36, 539
Benzoylsalicyl nitril
C6H4(OBz).CN=1.2
C14H902N
A., 99, 250
148-149
Henry
Z. C. [2], 6, 53 ;
vi., 1012
B., 2, 491
Phenylphthalimide
ceH4:(co)2:NPh
„
....
305
Dobner
A., 210, 267
11
„
„
205
Laurent&Gerhardt
J., 1847, 605
Benzoylanthranil
C6H,.CO.NBz=1.2
L |
„
a. 360
122-123
Friedliinder and
B., 16, 2229
46,61
Wleiigel
a-Nitrophenanthrene
....
„
73-75
Schmidt
B., 12, 1155
36, 941
"- »
....
»
70-80
Grsebe
A., 167, 155
26, 896; vii., sr,
0- 11
....
„
126-127
Schmidt
B., 12, 1156
36, 941
y-
....
170-171
B., 12, 1157
Isonitrosophenanthrone
n
158
Goldschmidt
B., 16, 2178
46, 62
Isonitrosoantlirone
....
w. m. 200
B., 16, 2180
Nitrosoanthrone
C6H4.CO.C6H4.CH(NO)
i i
„
146
Liebermann and
B., 13, 1586
40, 99
Lindemann
Amidophenanthraquinone ....
CO.C6H4.C6H3(NH2).CO
„
....
200 d.
Anschiitz & Meyer
B., 18, 1943
48, 1068
=2.1 ; 1.4.2
Amidoanthraquinoue
C&H4:(CO)2:C6H3.NH2
„
241
Roemer
B., 15, 1790
44, 72
=2.1 ; 1.2.3
n
=2.1 ; 1.2.?
„
....
250
Claus
B., 15, 1518
V
i. i.
.1
254 u. c.
Claus and Diern-
B., 14, 1334, 1335
42, 523
fellner
11
>,
11
254 u. c.
Claus and Hertel
B., 14, 979
40, 738
11
» »
U
A., 166, 149
250
Bottger & Petersen
B., 12, 1566;
26, 389
J. p. [2], 6, 367
"
=2.1 ; 1.2.4
Jl
....
301
Bourcart
B., 12, 1418
"
» 11
»
302
Perger
B., 12, 1568
38, 49
11
'i 11
"
302
Liebermann
A., 212, 61
42, 860
„ (B. S., 33, 264)
,,
11
302
Liebermann and
B., 15, 229
Pyrophthalone
....
H
a. 260, p. d.
Bollert
Jacobsen & Eeimer
B., 16, 2604
46, 335
Diazobeuzimide
N2:(C,H4.CO),:NH=(1.2)2
CI4H902N3
«.
b. 200
144-145
11
Fischer
n
B., 13, 680
38, 647
COMPOUNDS CONTAINING FOUR ELEMENTS.
541
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& Jf.. Ch. Soc.
Hydroxyphenylphthalimide
G6H4:(CO)2:N.C6H4.OH
C14H903N
....
220
Ladeuburg
B., i>, 1528
31, 305
=0.8),
/3-Amidohydroxyanthraquin-
C6Er4:(CO)2:C6H2(OH).NH
)J
cf.B.,15,1805| sb. 150-153
Perger
J. p. [2], 18, 139
36, 253.
one (alizarinamide)
=2.1 ; 1.2.3.4
"- ;> •>
„ —2.1 ; 1.2.4.3
)»
A., 183, 205
250
Liebermann and
B., 15, 1799
Hagen
"- !. »
» j>
))
250-260
Liebermann and
B., 8, 380
28, 890
Troschke
» »
?
))
....
301
Bourcart
B., 12, 1418
38, 49, 263
Nitrobenzenylazoximeben-
NO,.(C : N.O.CPh : N)=1.3
C14H903N3
160
Schopf
B., 18, 1067
48, 897
zenyl
" 1 1
Nitrobenzil .... ....
C6H4(NO2).COBz=l.?
C,,H0O,,N
110
Xi n in
As., 3, 153
vi., 306
a-Amidoalizarin
VJ14J-*'9%-'4
)>
?
Perkin
J. [1877], 586
J3- „
....
j>
....
a. 300
Schunck & Romer
B., 12, 588
36, 655
Nitrodiphenic acid ....
CO,H.C6H4.C6H3(NO2).CO2H
C14H906N
217
Strasburger
B., 16, 2347
46, 329
=2.1 ; 1.4.2
Dinitro-a-naph thylsuccini-
CloHs(N02)2.N:(00)!!:C.iH4
C14H906N3
250
Hiibner
A., 209, 382
42, 181:
mide
») » »
)»
»»
250
Haneniann
B., 10, 1713
Fr. papaveric acid
....
C14H9O.N
....
245-246-
Goldschmidt
M. C., 6, 372
48, 1081
Trinitrotolylphenylketone ...
C6H3(N02)2.CO.C6H3Me.N02
C14H907N3
165
Plascuda & Zincke
B., 7, 983
28, 69
Hexanitro-p-ditolylamine ...
NH : C12H2Me.2(NO2)6
C14H9012N.
....
258
Lehne
B., 13, 1545
40, 41
Dibenzenylazoxime
N:CPh.N:CPh.O
C14H10ON4
290
108
Tiemann & Kriiger
B., 17, 1695
46, 1326
i i
Anthroxanaldehyde anilide...
O.N.C6H4.C.CH : NPlx
i }
It
40
Schillinger and
B., 16, 2224
46, 60
Wleiigel
Diphenyldicyanate
PhjAOjNj
C14H1D0.,N2
....
175
Hofraann
B., 3, 765 ; 4,
24, 136 ; vii.,
246 ; As., 1, 57
407
Hydroxybenzenylazoxime-
N : CPh.O.N : C.C6H4.OH
J)
163
Schoff
B., 18, 2475
48, 1217
benzenyl
=1.3
Phthalyldiamidobenzene
C6H4:(NH.CO)2:C6H4
J)
....
178
Biedermann
B., 10, 1165
32, 784
= 1.3; 1.2
»
=1.4; 1.2
))
....
182
»
B., 10, 1164
?»
Amidobenzoid
NH.C6H4.CO.NH.C6H4.CO
))
225
Piutti
B., 16, 1321
44, 999,
i ' i
Phenylenamidinetoluic acid
NH.C6H4.N : C.C6H4.CO2H
I)
abt. 300
Stoddard
B., 11, 294; A.
34, 504
| 1
210, 337
= 1.2 ; 1.4
)) u
» >!
))
a. 300
Briickner
A., 205, 118
40, 93
Diamidophenanthraquiuone
[.C»H3(NH2).CO.]3=(1.4.2)2
)>
nf. 310
Anschiitz & Meyer
B., 18, 1942
48, 1068
a-Diamidoanthraquinone ...
MM
)!
236
Bcittger & Petersen
B., 4, 231, 779;
24, 532 ; vii.,
A., 160, 148
92
a- ?,
....
»i
....
236
Claus&Diernfellner
B., 14, 1337
42, 523
a- „
....
»
....
236
Glaus and Hertel
B., 14, 981
0-
,,
nf. 300
Schmidt
J. p. [2], 9, 266
27, 988
»•
NH2.NH2=1.2
»?
a. 130 d.
Perger
J. P. [2], 18, 138
1-
NHS.C6HJ:(CO)S:C6H3.NH3
»
sb.
a. 300
Romer
B., 16, 366
44, 737
=3.2.1; 1.2.6
Ph enyldiazonitrobenzylcyan-
N02.C6H4.[CH(N : NPh).CN]
C14H1002N4
201-202
Perkin
B., 16, 341
43, 111
ide
= 1.4
....
C14H1003N3
....
188
Fried] iiuder&Miihly
A., 229, 210 ;
48, 1137
B., 16, 850
Azobenzoic acid
(:N.C6H4.C02H)=(1.2)2
C14H1004N2
B., 11, 760
237 d.
Griess
B., 10, 1868
34, 149
,, ,1
)) J)
1)
....
237-238
Homolka
B., 17, 1904
»» i, . .. ....
=(1.3),
)J
B., 8, 41
a. 170
Strecker
A., 129, 133
vi., 321
,, i> .... ••••
=(l-i)2
))
a. 130
Bilfinger
A., 135, 154
vi., 321
j) „
» »
»
....
d. w. m.
Glaus
B., 15, 2332
Diuitrostilbene
))
....
180
Marcker
A., 140, 90
vi., 1107
jj •"• ....
:CH.C6H4.N02)2
»
....
a. 280
Strakosch
B., 6, 329
26, 890
Hydro-anthracene diuitrite
C6H4.CHn.C6H4.C(O.NO)2
J)
125 d.
Liebermaim and
B., 14, 468
40, 607
i i
Landshoflf
542
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
? (cf. B., 14, 484)
C14H10-(-N204
C14H1004N2
....
194
Liebermann and
B., 13, 1586
40, 99
Lindenj aim
u-diiiitrodeoxybenzoin
....
CI4H1006N2
112-114
J. E., 13, 23
a- „ (B., 13, 2403)
....
„
114-116
Golubeff
B. S. [2], 34, 345
40, 422
8-
....
n
120
„
B., 11, 1939
36, 150
8-
....
11
124-125
J. E., 13, 23
P- „ (B., 13, 2403)
....
„
....
125-126
Golubeff
B. S. [2], 34, 345
40, 422
y- „ (J. E., 13, 23)
....
„
154-155
Borodin
B. S. [2], 35, 560
40, 813
Dinitrotolylphenylketone ...
N02.C6H4.CO.C6H3Me.N02
„
....
126-127
Plascuda & Zincke
B., 7, 983
28, 69
=1.4; 1.4.3
11
fr. Ph.CO.C6H4Me=1.3
„
145
Senff
A., 220, 225
46, 427
Methylic diuitrodiphenyl-
N02.C6H4.C6H3(NO2).CO2Me
C14H1006N2
....
156
Strasser & Schultz
A., 210, 192
42, 521
carboxylate
=1.4 ; 1.2.4
Dinitro-oxanilide
(.CO.NH.C6H4.N02)2=(1.4)2
C14H1006N4
A., 209, 366
260
Hiibner & Rudolph
B., 8, 473
42, 180
„
=(1.2),
„
a. 300
Hiibner
A., 209, 369
42, 181
Pyridinedicarboxylic acid ....
Polymer
C14H1003N2
96 u. c.
Claus
B., 14, 1942
Tetranitrobenzyltoluene
fr. Ph.CH2.C6H4Me=1.4
C14H1008N4
160-161
Zinck6
B., 5, 685
Acetylcarbazole
CfH4.NAc.C6H4
C14HnON
a. 360 d.
69
Grsebe and Glaser
A., 163, 352
1 1
Benzilimide ....
11
C42H3204N2
130
Laurent
J. p., 35, 461
Imabeuzil .... .... . .
C,H5.C( : NH).CO.C6H5
11
„
140
11
J. p., 27, 312 ; 35,
iii., 245
461
Phthalidanil
Ph.N : CH.C6H4.COH=1.2
11
160
Hessert
B., 10, 1450
34,67
Ph.N.CHj.C H .CO=1.2
1 ftf)
Bl 1 9*}Q
"
"**
i\J\J
"
., 11, _.j.'
/3-naphtho-y-oxyquiualdine ....
see original paper
j,
....
286
Knorr
B., 17, 543
46, 1198
°- 11 -y-
11
„
292
11
B., 17, 545
Amidobeuzenylazoximeben-
N I CPh.O.N : C.C6H4.NH2
C14HnON3
143
SchOff
B., 18, 2473
48, 1217
zenyl
=1.3
Phenylhydrazine+isatine ....
....
....
210-211
Fischer
B., 17, 577
46, 1151
Fr. Benzil
Ph.C< I NOH).COPh
C14HU0,N
130-131
Wittenberg and
B., 16, 503
44, 804
Meyer
Dibenzamide
NHBz,
„
138
Beilstein & Landolt
A., 111,6
vi., 259
11
„
144
Barth and Senhofer
B., 9, 975
30, 418
"
"
148
1 Afi
Fischer & Troschke
B., 13, 708
M
14o
Gum pert
J. p., 30, 87
48, 53
(?) „ +2H20
Benzimidobenzoate NH : CPh.O.CPh : O
' "
99
148-5
Schaffer
Pinner and Klein
A., 169, 111
B., 11, 766
27, 165
34, 864
Nitrodiphenylethylene
CH2 : CPh.C6H4.NO2
11
86
Anschiitz & Bomig
B., 18, 664
48, 768
Piperonalanilide
CH3:o2:c6H3.cH:NPh
„
65
Lorenz
B., 14, 792
40, 729
=4.3.1
Naphthylsuccinimide
c2H4:(co)2:N.o,0H7
J)
....
152
Hiibner and Hane-
B., 10, 1713 ; A.,
42, 181
maim
209, 382
? (B., 8, 1050)
Dibenzhydroxamic acid
NBz2.OH (?)
C14HU03N3
C14H1103N
....
220 d.
140
Lorenz
B., 7, 1097
vii., 155
11 „
»
11
....
145-146
Lessen
A., 162, 357
25, 415
11 „
"
11
153
MUller
B., 16, 1621
44, 1130
11 i,
"
11
....
153
Steiner
A., 178, 226
29, 271
11 ,, ....
1)
„
156-158 d.
Heintz
Z. C. [2], 5, 733
vi., 725
Nitrodeoxybeuzoin
Beuzamidobenzoic acid
HO.CPh : NO.CO.Ph (?)
NHBz.C02H=1.2
11
J. K., 11, 99
140-142
180-181
Eiseler
Golubeff
Friedlander and
A., 175, 324
B., 12, 693
B., 16, 2229
36, 790
46, 62
Wleiigel
n 11 ....
» 11
„
.-..
182
Bruckner
A., 205, 130
40, 94
11 11
Phenylphthalamic acid
Benzoylsalicylamide
Phenylazoindoxyl
= 1.4
OOsH.(CO.NHPh)=1.2
C.H4.C(OH):CH.N.N2.Ph
•>
A., 99, 249
278
192
200
236 d.
11
Gerhardt & Laurent
Gerhardt & Chiozza
Baeyer
A., 205, 128
J. [1847], 606
J. [1856], 502
B., 16, 2190
46, 74
Nitrophenyltolylketone
C6H4Me.(JO.C6H4.N02
„
....
126-127
Plascuda & Ziucku
B., 7, 983
vii., 183, 861
= 1.4; 1.?
» 11
»
127
Zincke
B., 5, 685
25, 1005
COMPOUNDS CONTAINING FOUR ELEMENTS.
543
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Hydroxybenzylideneamido-
HO.C6H4.CH I N.C8H4.C02E
C14HU03N
....
190
Schiff
A., 210, 116
42, 303
benzoic acid
= 1.2; 1.3
Anthracene nitrate
C,4H10+HN03
»}
....
125 d.
Liebermann and
B., 13, 1585
40, 99
Lindemann
Dyestuff .... (M.C., 1, 894)
>1
228
Weselsky and Bene-
W. A. [2], 82, 121
40, 726
dikt
Nitroso-oxanilide
NHPh.(CO)2.NPh.NO
Cl4Hn03N3
86
Fischer
B., 10, 960
32, 607
Acetophenone nitrophenyl-
Bz.CH2.O.C6H4.NO2=1.4
C14Hn04N
144
Mohlau
B., 15, 2498
44, 332
oxide
Benzoylamidosalicylic acid ..
CO2H.OH.NHBz=1.2.3 or
))
....
189
Hiibner
A., 195, 37
)J 5)
=1.2.?
)»
252
Dabney
A. C. J., 5, 20
46, 308
Disalicylamide
(HO.C6H4.CO)2NH=(1.2).!
JJ
....
197-199 d.
Schulerud
J. p. [2], 22, 289
40, 42
Hydroxyphthalanilic acid ...
HO.C6H4.NH.CO.C6 H4.CO2H
»)
223
Ladenburg
B., 9, 1528
31, 305
=(1.2),
Hydroxybenzyleneamido-
HO.C6H4.CH : N.C6H3(OH)
»
....
245 d.
Schiff
A., 210, 117.
42, 303
salicylic acid
CO2H=1.2; 5.2.1
Nitrosoacetophenone nitr-
Bz.CH2.N(NO).C6H4.N03
CuH.AN,
....
135-145
Mohlau
B., 15, 247.4
anilide
=1.4
1
))
254
Salkowski
B., 17, 509.;
46, 117(i
Dinitrobenzoylmethylaniline
fr. NMePhBz
C14Hn05N3
....
136
Hess
B., 18, 687-
48, 783
Acetophenonediuitranilide ..
CH2Bz.NH.C6H3(N02)2
))
171-172
Mohlau
B., 15, 2479
44, 333
=1.2.4
Dinitrobeiizaniidotoluene ..
Me.NHBz.(NOs)2=1.4.3.5
)>
....
186
Kolbe
A., 208, 312 ;
29, 270 ; 40,
B.,,8, 877
1131
,, ...
=1.4.(?)2
)J
203
Cunerth
A., 172, 229
28, 83
Nitrobenzamidonitrotoluene
CcH3Me(N02).NH.CO.C6H4
1)
188-5
Hiibner
B., 10, 1712 ;
34, 144
NO2=U.4; 1.3
A., 210, 336
Benzoic+nitrobenzoic acids...
Ph.C02H +C6H4(NO2).C02H
C14Hn06N
....
136-137
Fittica
B., 9, 795 ; J. p
30, 411 ; 36,
[81 13, 184
153
Trinitrobenzyltolyl oxide ...
C6H2Me(N02)s.O.CH2.C6H4.
C14H1107N8
....
145
Staedel
B., 14, 899 ; A.
40, 724
NO2=1.3.5.6; 1.4
217, 178, 181
)» »
„ =1.2.6.4; 1.4
)»
....
186-5
Fritzsche
A., 224, 137
46, 1337
Trinitro-p-azoxytoluene
CHHU07N5
....
201
Petrieff
Z. C. [2], 6, 264
vi., 286; 26,
B., 6, 557
1027
Dibenzimide oxide
NH : CPh.O.CPh : NH
014H12ON2
....
106
Pinner and Klein
B., 11, 765
34, 804
Methylanilidocarbamido-
phenol
O.C6H4.N I C.NMePh=1.2
i i
»>
a. 360
Liquid
Kalckhoff
B., 16, 1827
44, 1110
Araidobenzylideneamido-
NH2.C6H4.CH : N.C6H4.COH
)»
....
188-189
Friedliinder and
B., 17, 459
46, 1020
benzaldehyde
=(1.2),
Gohring
a-naphtho-oxymethylquini-
....
»)
....
190
Knorr
B., 17, 551
46, 1154
zine
8-
....
»>
....
190
?)
B., 17, 550
)*
Acetophenonenitrosoanilide
Ph.CO.CH2.N(NO)Ph(!)
CI4H1202N2
73
Mohlau
B., 15, 2472
44, 333
Benzoylbenzenylamidoxime
NHrCPh : N.OBz
>»
....
140
Tienmnn & Kriiger , B., 17, 1694
46, 1326
Phenylhydrazinephenylgly-
N2HPh : CPh.CO2H
)»
....
153 d.
Elbers
A., 227, 340
48, 534
oxylic acid
u »
»
J>
....
153d.
Fisclier
B., 17, 578
46, 1151
Phenylbenzoylcarbamide ....
NHPb : CO.NHBz
»r
199
Kiihn
B., 17, 2881
48, 260
/3-diphenylglyoxime
Ph.(C:N.OH)2.Ph
»
206
Goldschmidt B., 16, 2177
46, 62
"- „
)1
))
237
Goldschmidt and B., 16, 1617
44, 1120
Meyer
Diphenyloxamide (oxanilide)
(.CO.NHPh),
jj
320
245
Gerhardt
A., 60, 308
v., 285
» »
)5
•»
B., 14, 740
245
Klinger
A., 184, 261
31, 710
Acetyloxyazobenzene
Ph.N2.O.C6H4Ac(?)
ji
....
84-5
Scichilone
G. I. [1882], 108
42, 726
Acetoxyazobenzene ....
Ph.N2.C6H4.OAc
j»
a. 360 p. d.
84-85
Wallach and Kie-
B., 14, 2617
penheuer
Dinitrobenzyltoluene
....
)»
,,,,
137
Zinck6
B., 5, 684
vii., 183
Hydroxybenzyleneamido-
HO.C6H4.CH:N.C6H4.CO.
n
186
Schiff
A., 218, 185
46, 455
benzamide
NH2=1.2; 1.3
Nitroamidostilbene
NHj.C8H4.CH : CH.C6H4 .NO2
T?
229-230
Strakosch
B., 6, 330
6, 890
Tolylazophenylcarboxylic
CeH4Me.N,C6H4.COjH
)»
b.
237
Klinger
B., 16, 946
acid
544
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Nitrobenzoylmethylaniliue ...
fr. NMePhBz
C14H1203N2
Ill
Hess
B., 18, 687
48, 783
Acetophenonenitranilide
CH2Bz.NH.C6H4.NO2= 1 .4
»
....
167
Mohlau
B., 15, 2475
44, 333
Phenyluramidobenzoic acid..
NHPh.CO.NH.C6H4.CO,,H
n
270 d.
Kiihtt
B., 17, 2883
48, 201
= 1.3
Benzamidonitrotoluene
Me.NHBz.NO2=1.4.5
;j
....
143
Kolbe
A., 208, 311 ; B.,
29, 270; 40,
8, 875
1131
„
=1.2.6
»
MM
145-14S
Cunerth
A., 172, 224
27, 903
,,
») )>
»
....
145-146
Limpricht
B., 7, 643
88,83
»
» »»
»
167-167-5
Bernthseu
B., 15, 3017
44, 579
»
=1.4.2
)>
....
168
Cunerth
A., 172, 228
28,83
,, ...
>» »
»»
171-172
Bernthsen
B., 15, 3017
44, 579
(B., 7, 1504)
») M
i)
172
Bell
C. N., 30, 212
28, 371
„ (A., 217, 200)
=1.3.5
>»
177
Becker
B., 15, 1138
42, 1197
Toluylnitranilide
NO2,C6H4.NH.CO.C6H4Me
))
A., 205, 118
110
Hubner
A., 210, 328
42, 504
=1.2 ; 1.4
Nitrobenzamidotoluene
C6H4Me.NH.CO.C6H4.NO11
162
»
A., 210, 335 ; B.,
34, 144
=1.4; 1.3
10, 1712
Acetamidonitrodiphenyl
NO2.C6H4.C6H4.NHAc
246 or 264
Schmidt & Schultz
A., 207, 351
40, 911
=(1.4),
Diphenyldinitroethane
C2H2Ph2(N02)2
C14H1204N2
.... -
300 d.
Gabriel
B., 18, 2438
48, 1229
Dinitrodibenzyl
(.CH2.C6H4.NO2)2=1.2 ; 1.4
))
74-75
Stelling and Fittig
A., 137, 262
v., 871
„
» »
)J
75
Leppert
B., 9, 15
29, 704
,, ....
=(1.4)2
jl
166-167
Stelling and Fittig
A., 137, 260
v., 871
,» .... ....
J1 JJ
»J
....
178
Leppert
B., 9, 15
29, 704
Diiiitrodiphenylethane
CH3.CH(C6H4.N02),.
»
....
149
Anschiitz & Romig
B., 18, 664
48, 768
Dinitrobenzyltoluene
fr. Ph.CH2.C6H4Me=1.2
))
100
Plascuda & Zincke
B., 7, 986
28,70
» ....
=1.4
J)
137
Zinck6
B., 5, 684
25, 1004
»
=1.3
»
141
Senff
A., 220, 225
46, 427
Hydrazobenzoic acid
(.NH.C6H4.C02H)2=(1.2)2
»)
B., 7, 1612
205
Homolka
B., 17, 1904
46, 1342
Disuccinyldiamidobenzene ...
ccH4[N:(co)2:c2H4]2
JJ
....
a. 360
Biedermaim
B., 9, 1668
31, 474
Diamidodiphenic acid
(.C6H3.NH2.C02H)2=(?.1.2)2
Jl
....
crystalline
Griess
B., 7, 1612
» »
=(1.4.2),
1>
....
170
5,
B., 7, 1610
28, 460
j) ,) ••••
»» n
JJ
B., 12, 236
170 d.
Schultz
A., 196, 25
36, 538, 653
» )>
» n
Jl
....
170-270
,i
B., 12, 236
36, 653
(?)
" ))
T)
v., B., 12, 236
250
Hummel
A., 193, 128
36, 165
m
>' JJ
»*
»,
250-251
Struve
B., 10, 75
32, 902
Dinitroazotoluene
....
C14H1204N4
....
110
Petrieff
B., 6, 556
26, 1027
Dinitrocresylbenzyl oxide ....
(O.CH2Ph).Me.(NO2)2
C14H1206N2
109
Fritzsche
A., 224, 137
46, 1337
= 1.4.2.6
Nitrocresylnitrobenzyl oxide
NO2.C6H4Me.O.CH2.C6H4.
»)
163
»
)>
*,
NO2=2.4.1 ; 1.4
Dinitro-p-azoxytoluene
....
C14H1205N4
-
145
Petrieff
B., 16, 557
26, 1027
Formyldinitropheuyltohiyl-
C6H3(N02)2.NH.C7H6.NH.
»)
157
Leymann
B., 15, 1237
42, 1057
enediamine
COH
Ethylene nitrophenylether ....
C2H4(O.C6H4.N02)2=(1.3)2
C14H1206N2
139
Wagner
J. p. [2], 27, 201
46, 431
» >,
=(1-4),
1»
142-143
Weddige
J. p. [2], 20, 127
38, 316
)! „ ....
» »
))
....
143
Wagner
J. p. [2], 27, 201
46, 434
»I „
» )!
M
162-163
Weddige
J. p. [2], 20, 127
38, 316
J» ,,
" 11
T1
163
Wagner
J. p. [2], 27, 201
46, 434
4th Nitrobenzoic + 4thAmido-
....
1>
....
156-158 ;
Fittica
J. p. [2], 13, 184
36, 153
benzoic acid
158-160
Benzoylmethylanilide
PkNMeBz
C14H13ON
59
Hepp
B., 10, 329
»
J>
»)
....
63
Hess
B., 18, 686
48, 783
Metliylic diphenylacetoxime
CPh2 : NOMe
>»
92
Spiegler
M. C., 5, 203
46, 1156
Acetophenone anilide
Ph.CO.CH2.NHPh
))
....
93
Mohlau
B., 14, 172
40, 262
Amidodeoxybenzoin
....
»
94
Golubeff
B., 6, 1252
27, 273
,,
....
))
J. K, 11,101
95-96
B., 11, 1239
36, 150
Acetyldiphenylamine
NAcPh2
)J
....
99-5
Merz and Weith
B.,5, 284; 6,1511
27, 375
»»
»
Jl
....
101
Wallach
A., 214, 193
44, 49
,»
J)
))
....
103 u. c.
Clans
B., 14, 2366
,,
»
)J
175
Willm and Girard
B., 8, 1196
Phenylacetanilide
Ph.NH.CO.CH2.Ph
JJ
117
Hofmann
B., 13, 1225
38, 885
COMPOUNDS CONTAINING FOUR ELEMENTS.
545
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
j
Reference.
"Watts' Diet.
& J. Ch. Soc.
Toluanilide
(CO.NHPh).Me=1.4
C14H13ON
....
139
Fischli
B., 12, 616
96, 638
jj •••• ••••
u »
51
140-141
BrUckner
A., 205, 132
40, 94
Benzotoluide
NHBz.Me=1.2
H
142-143
u
A., 205, 130
?j
„
=1.4
»)
155
Kelbe
B., 8, 875 ; A.
29, 270; 40,
208, 310
1131
j) •••• ••"
J» J»
V
232
158
Wallach
A., 214, 217
Aeetamidodipbenyl
Pb.C6H4.NHAc=1.4
T)
167
Osteii
A., 209,344; B.
vii., 937; 27,
7, 173
581
Tolylsalicylamide
HO.C6H4.CH ; N.C6H4Me
JJ
v. 232
100
Jaillard
C. R, 60, 1096
v., 872, 874
= 1.2; 1.?
Z.C. [1865], 440
Hydroxybenzylidenetoluide
=(1.4),
))
...,
213
Herzfeld
B., 10, 2196
34, 423
Acetamidoazobenzene
Pk.N2.C6H4.NHAc=1.4
C14H13ON3
....
141
Schultz
B., 17, 463
jj
I! JJ
....
143
Berju
B., 17, 1400;
46, 1148 ; 48,
C. C. [1884], 87
660
Phenoxyaeetanilide
PhO.CH2.CO.NHPh
CI4HJ302N
99
Fritzsche
J. p. [2], 20, 280
38, 319
1
Ph.CN(OH).CHPh.OH
151-152
\V^ttGnb&r£[ and
B., 16, 504
44, 804
11
Meyer .
Phenamidophenylacetic acid
NHPh.CHPh.CO2H
»»
....
164-168
Stockenius
J. [1878], 779
JJ JJ
»
)»
„..
173-175
Tieruann and Piest
B., 15, 2030
44, 198
Nitrodipheuylethane
Ph.CHMe.C6H4.N02
J)
79-80
Anschiitz & Romig
B., 18, 664
48, 768
Benzaiuidomethoxybenzene....
C6H4.OMe.NHBz =1.2
))
....
59-5
Mulhauser
A., 207, 244
42, 302
M •••
=1.4
?!
....
153-154
Lessen
A., 175, 299
28, 636
Methoxybeuzauilide
C6H4.OMe.(CO.NHPh)=1.4
)>
168-169
Leuckart & Scbmid
B., 18, 2339
„ ( A. C. [3], 23, 353)
1» ))
»
....
168-169
Lessen
A., 175, 292
Benzylamidobenzoic acid ...
(NH.CH2Ph).C02H=1.2
)1
176 u. c.
Glaus & Glyckherr
B., 16, 1285
44, 1009
Phenmethamidobenzoic acid
NMePh.CO.,H=U
,,
....
184
Michler & Sarauw
B., 14, 2180
42, 183
Salicyltoluide _
HO.C6H4.CO.NH.C6H4Me
•»»
....
155-156
Wanstrat
B., 6, 337
86, 907
=1.2 ; 1.4
Methoxyhydroxybenzylidene
(CH : NPh).OH.OMe=1.2.5
»
....
59
Tiemann & Miiller
B., 14, 1992
42,53
anilide
Orcylanilide ....
Me.(OH)2.(CH : NPb)=?
125-12C
Tiemann & Helken
B., 12, 1002
36 79H
berg
"'-'j < &\j
/3-uaphthyl-;3-amidobutyric
CH3.CH(NHC10Hr).CHJ.
f)
....
92
Knorr
B., 17, 543
46, 1198
acid
CO3H
Phenyllutidine carboxylic
C5NHPliMe2.C02H
I)
....
189-190
Hantzscli
B., 17, 2913
48, 397
acid
Benzenylphenyluramidoxime
NHPb.CO.NH.CPh: NOH
CJ4H1302N3
....
115
Kriiger
B., 18, 1059
48, 896
j3-diphenylbiuret
....
»>
165
Hofmann
B., 4, 250
24, 395
"- jj
)>
....
210
j>
B., 4, 265
vii., 193
»- i. •
-))
....
210
Peitzscb & Solomon
J. p. [2], 7, 479
27, 365
Phenylbenzocreatine
C02H.(NH.CNH.NHPh)
J>
....
165 d.
Traube
B., 15, 2120
44, 193
= 1.3
Nitrazotoluene
C6H4Me.N2.C6H3Me.N02
C14H1302N3
._.
63
Petrieff
Z. C. [2], 6, 264
vi., 286
,, .... ....
n
)J
....
67
9)
»
»>
jj ••••
= 1.4; 1.4.?
))
76
»
B., 6, 556
26, 1027
Plienolazoacetamidobenzene
HO.C6H4.N2.C6H4.NHAc
»
-..
208
Walkch & Schulze
B., 15, 3021
44, 583
=?; 1.3
Dehydracetanilide
C8H;03.NHPh
CuH13OaN
115
Oppenheim & Precbt
B., 9, 1100
30, 506
Nitrodiphenylmethylcarbinol
H(XCMePh.C6H4.NO2
»)
....
106-107
Auschiitz & Komig
B., 18, 664
48, 768
Nitrobenzyltolyloxide
C6H<Me.O.CH2.C6H4.NO2
»
91
SVitzsche
A., 224, 137
46, 1337
=(1.4)2
jj
=1.4; 1.?
))
....
181
Staedel
A., 217, 153
44, 864
Nitrotolylbenzyloxide
Ph.CH2.O.C6H3Me.NO2
»
....
54
Tritzsche
A., 224, 137
46, 1337
=1.4.2
Ethylic a-naphthyloxamate....
CJOH7.NH.CO.CO2Et
)>
....
106
Ballo
B., 6, 249
vii., 848; 26,
913
Benzylnitrobenzenylamid-
Ph.CH2.O.N : C(NH2).C6H4.
C14H1303N3
58
Schopf
B., 18, 1065
48, 896
oxime
NO2=1.3
Nitroazoxytoluene
C6H4Me.N2O.C6H3Me.NO2
JJ
....
84
Petrieff
B., 6, 557
26, 1027
=1.4; 1.4.2
BenzdiamidonitroLoIueue ....
Me.NHBz.NH2.NO2=1.4.5.3
1)
....
137-139
Kelbe
B., 8, 877
29, 270
i)
>i 11
»
....
138
Jiibuer
A., 208, 317
40, 1132
4 A
546
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts'Dict.
& J. Ch. Soc.
Ethylenephenylnitrophenyl-
PhO.C2H4.O.C6H4.NO2=1.2
C14H1304N
....
86
Weddige
J. p. [2], 24, 245
40, 1137
ether
Isopropylic nitro-|3-naph-
C10H6(N02).C02Pr/i
1>
....
75-76
Graeff
B., 16, 2254
46,81
thoate
Isopropylic nitro-o-naph-
»
»
....
101-5
»
B., 16, 2252
J)
thoate
Phenyldimethylpyrroline di-
CO2H.C : CMe.NPh.CMe : C.
i i
))
....
d. 224
Knorr
B., 18, 307
48, 555
carboxylic acid
CO2H
Dinitrodibenzylamine
NH(CH5.C6H4.NO2)2
C14H1304N3
93
Strakosch
B., 6, 1058
27, 78
»
JJ
))
....
a. 100
u
B., 6, 1059
Dinitroditolylamine
NH(C6H3Me.NO2)2= (1.4. ?)„
)»
191
Lellmann
B., 15, 832
42, 1060
Ethenyldinitrodiamidodi-
CI4H12(N02)2N2+HN03
C14H130-N5
....
d.w.m. 182
Biedermann
B., 7, 540
27, £08
phenyl nitrate
Nitrosodibenzylamiiie
(Ph.CH2)2N.NO
C14H14ON2
52
Rohde
A., 151, 369
Benzylbenzenylamidoxime ....
NH2.CPh : N.O.CH2Ph
»
....
90-5
Kriiger
B., 18, 1056
48, 896
Methyldiphenylcarbamide ....
NHPh.CO.NMePh
»
203-205
104
Gebhardt
B., 17 2093
46, 1321
Phenamidoacetanilide
NHPh.CH2.CO.NHPh
1)
....
110-111
Meyer
B., 8, 1156
29, 372
Phenylbenzylcarbamide
CO : N2H2Ph.CH2Ph
»
....
168
Letts
B., 5, 93
25,449; vii., 181
Methylbenzoylphenylhydra-
Ph.NMe.NHBz
»
153
Tafel
B., 18, 1743
48, 1061
zine
Acetohydrazobenzene
Ph.NH.NAcPh
»
....
159
Stern
B., 17, 380
46, 1015
Acetamidodiphenylamine ....
NHPh.C6H4.NHAc=1.4
U
....
158
Nietzki and Witt
B., 12, 1402
Azoxytoluene
....
))
57
Petrieff
Z. C. [2], 6, 30
vi., 286
»)
....
»
....
59
»j
B., 6, 557
26, 1027
)» .... ....
....
»
70
Melms
B., 3, 551
vii., 1163
„
»
219
Barsilowsky
A., 207, 117
Nitrosoditolylamine
N(C,H1Me),NO=(1.4)2
3)
....
100-101
Lehne
B., 13, 1544
„ ....
» »
»1
....
103
Cosack
B., 13, 1092
38, 714
Acetdiamidodiphenyl
NH2.C6H4.C6H4.NHAc
»
199
Schultz
A., 207, 332
=(l-4)2
Benzdiamidotoluene
C6H3Me.NHBz.NH2=1.4.6
)J
142
Bell
B., 7, 1505
n
=1.4.5
))
193-194
Hiibner
A., 208, 314
40, 1131
Anhydrodiamidobenzotolui-
....
))
232-233
Kelbe
B., 8, 876
29, 270
dine
Tolylazocresol
C6H4Me.N2.C6H3Me.OH
»J
112-113
Nblting and Kohn
B., 17, 354
46, 901
=1.4; U.4
Diamidomethylbenzophenone
NH2.C6H4.CO.C6H.iMe.NH2
|)
....
a. 220 d.
Liebermann
B., 16, 1929
44, 1097
Acetdiamidoazobenzene
NHAe.C6H4.N2.C6H4.NH2
C14HI4ON4
212
Nietzki
B., 17, 345
46, 1016
= 1.4; 1.?
Benzylphenylhydroxy-
HO.CHPh.C(NH2) ; N.O.
C14H1402N2
102-103
Gross
B., 18, 1080
48, 898
ethenylamidoxime
CH2Ph
Phenylhydrazidophenyl-
N2H2Ph.CHPh.C02H
)J
158 d.
Elbers
A., 227, 340
48, 534
acetic acid
Phenylhydrazine vanillin ....
(CH : N2HPh).OMe.OH
)1
105
Tiemann and Kees
B., 18, 1662
48, 1072
=1.3.4
Nitroditolylamine
C6H4Me.NH.C6H3Me.N02
If
....
85
Lellmann
B., 15, 831
42, 1060
=1.4 ; 1.4.7
Orcinoldiazotoluene
C6H4Me.N3.C6H2Me(OH)2
>3
203-206
Scichlone
G. I, 12, 223
42, 1285
Diacetdiamidonaplithalene ....
C10H6(NHAc)2=£
)3
234
Lawson
B., 18, 801, 2423
48, 803
Oxalyldiphenylhydrazine ....
Ph.N2H2.CO.CO.N2H2Ph
C14H14OJST4
277-278
Fischer
A., 190, 131
34, 309
Ethylenediphenyldinitros-
....
»
....
157
Morley
B., 12, 1794
38, 112
amine
Nitrobenzeneazodimethani-
N02.C6H4.N2.C6H4.NMe2
»
157-158
Meldola
45, 120
liue
=1.3 ; 4.1
«
=(1-4),
>J
....
229-230
jj
45, 107
Nitrobenzeneazoamidoxyleiie
N02.C6H4.N2.C6H2Me2.NH2
))
Mixture (?)
141
J3
43, 428
=1.4; 1.3.5.4 and 1.4; 1.2.6.4
Dehydracetoplienylhydrazine
CsH8O3N.NHPh
C14H1403N2
....
207d.;sf.200
Perkin& Bernhardt
B., 17, 1523
46, 1121
Phenyldimethylpyridazindi-
....
C14H1404N2
....
d. 220
Knorr
B., 18, 308
48, 555
carboxylic acid
COMPOUNDS CONTAINING FOUR ELEMENTS.
547
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Ethylenediphenylnitramine
C2H4(NH.C6H4.NO,,)2=(1.3)2
C14H1404N4
....
206 u. c.
Gattermann and
B., 17, 778
46, 1142
Hager
Diuitrodiethoxynaphthalene
OEt.OEt=? ; ?
CHH1408N2
....
228-229
Alen
B. S. [2], 36, 433
42, 410
Trinitrobenzene dimethyl-
C8H3(NO,)3+NMe2Ph
C14H1408N4
B. S., 30, 5
106-108
Hepp
A., 215, 344
36, 51 ; 44,
aniline
=1.3.5
316
Dibenzylhydroxylamine
(Ph.CH,)2N.OH
C14H15ON
....
123
Schramm
B., 16, 2185
46, 51
Methylmethoxydiphenyl-
C6H4.OMe.NPhMe=1.4
„
313
Liquid
Philip and Calm
B., 17, 2431
48, 155
amine
Benztriamidotoluene
Me.(NH,)2.NHBz=1.3.5.4
C14H15ON3
....
182-183
Kelbe
B., 8, 877
29, 270
»
„ „
„
....
183-185
Hubner
A., 208, 318
40, 1132
Diazoorcen-o-toluidine
....
C14H1502N3
..<.
203-206
....
G. I. [1882], 223
Ethylic ethoxycinchonate ....
N.OH.CO2H=1.2.4 ;
C14H1503N
86
Konigs & Korner
B., 16, 2156
46, 85
Diacetamidopropenylbeuzoic
NAc2C3H6.CO2H=1.2.5
C14H]604N
....
215-216
Widmann
B., 16, 2575
46, 318
acid
Ethylic allylnitrobenzoylace-
NO,.C8H4.CO.CH(C3H5).CO2
C14H1505N
....
45-46
Perkin & Bellenot
B., 18, 958
48, 795
tate
Et=1.4
Ethylic nitrobenzoyltetra-
CH,.(CH0),C(CO.Et).CO.
62-63
n
B., 18, 954
„
methylenecarboxylate
1 _ _ |
C6H4.N02=1.4
Diethylic nitrobenzalmalonic
N02.C6H4.CH:C(C02Et)2
C14H1506N
•
53
Stuart
....
47, 158
acid
= 1.2
»» n jj
=1.4
„
....
93
„
....
„
Trinitranilinedimethylaniline
C8Hs.NHa.(NO,)3+Ph.NMe,
C14H1506N5
139-141
Hepp
A., 215, 359
Diethylic nitrobenzoylma-
N02.C6H4.CO.CH(C02Et)2
C14H1607N
54 u. c.
Bischoffand Each
B., 17, 2792
48, 264
lonate
=1.8
» „
„ „
B
d. 100
92
Bischoff
B., 16, 1045
44, 912
Aniline on pyrotartaric acid
....
C14H16ON2
...*
194-195
Bottinger
B., 17, 997
46, 1006
Nitrosodiethylnaphthylamine
CloH6.NO.NEt2
„
....
165
Smith
....
41, 182
Azoxytoluidine
(NH2.C8H3Me)2:N20
C14H18ON4
....
148
Buckney
B., 11, 1453
34, 863
„
„ =(1.3.4, or 1.4.3)2
„
168
Graeff
A., 229, 340
48, 1128
„
.. ,,
„
168
Limpricht
B., 18, 1405
48, 974
Hydroxyazotoluidine
NH2.C6H2Me(OH).N2.C6H3.
»
....
212 d.
„
„
48, 975
Me.NH2
„
„
51
212 d.
Graeff
A., 229, 340
48, 1128
Ethylenediamidophenol
C2H4(O.C6H4.NH2)2=(1.2)2
C14H1602N2
....
127
Weddige
J. p. [2], 20, 127
38, 316
„
» „
„
....
128
Wagner
J. p. [2], 27, 201
46, 434
„ —
=(1.3)a
„
....
135
„
J. p. [2], 27, 209
11
„
=(1-4)*
„
168-172
„
J. p. [2], 27, 206
„
Dihydroxystilbene diamine
(HO.C6H4.CH(NH2).)2
„
....
180-5
Japp and Hooker
....
45, 675
Dibenzylamine nitrate
(Ph.CH,),NH + HNO,
C14H1803N2
186
Limpricht
A., 144, 304
vi., 337
Ethylic methyloxyquinizin-
C8H4.N.NH.CMe.CH(CHa.
1— i
„
....
138
Knorr and Blank
B., 17, 2052
46, 1380
acetate
i
CO2Et).CO=1.2
1
Diphenylguanylguanidine
NPh : C(NHPh).NH.C(NH2):
C14H1603N8
231
Bamberger
B., 13, 1584
40, 44
nitrate
NH+HNX)3
Diacetylmethylbenzylgly-
Me.(C : NOAc)2.CH2Ph
C14H11(04N2
....
80
Schramrn
B., 16, 2188
46, 52
oxime
Aniline oxalate
(.COONH3Ph)3
....
nf. 180
Piria
C., 2, 305
iv., 427
o-Phenylenediimidobutyric
a
176
Knorr
B., 17, 545
46, 1198
acid
Acetylcarbazolin
C12H14NAc
C14H17ON
....
98
Grsebe and Adlers-
A., 202, 25
38, 660
kron
o-acetamido-cumenylacrylic
C9H10(NHAc).C2H2.CO2H
C14H1703N
....
220
Widmann
B., 17, 2283
48, 56
acid
m-
„
....
240
()
n
Ethylic o-nitrocumenylacryl-
C9H10(N02).C2H2.C02Et
C14HI704N
...»
Liquid
n
„
„
ate
» m- »
„
B
58-59
n
H
M
Triethylic /3-pyridinetricarb-
N.(CO2Et)3=1.2.4.6
C14H1706N
cf., 35, 189
127-5
Voigt
A., 228, 29
48, 813
oxylate
4 A
548
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Pentamethyloxyquinizine ...
C6HMe3.N.NMe.CMe.CH, .
C14H18ON2
....
105-106
Haller
B., 18, 708
48, 818
1 L -i
1
CO=1.3.4.6.5
j
a-conicei'ne pierate
C8H16N.C6H2(N02)3.OH
C14H1807N4
225
Hofmann
B., 18, 8, 11
48, 401
Isoamylic hippurate
NHBz.CH2.CO2.(CH2)2.Pr/i
C14H1903N
B., 11, 1247
27-28
Campani and Biz-
G. I., 10, 257
38, 870
zarri
,, ,, .... ...
„
„
28
Oampani
G. I., 8, 57
34, 674
Suberanilic acid
Ph.NH.C3H1202.OH
„
A., 68, 31
128
Laurent & Gerhard
A. C. [3], 24, 185
v., 448
m -aceta.mido-cumeny Ipro-
C9H10(NHAc).C2H4.CO2H
Tt
168
Widmann
B., 17, 2283
48, 56
pionic acid
Diethylic collidine-dicarb-
N.Me3.(C02Et)2=?
C14H1904N
308-310
Liquid
Hantzsch
A., 215, 21
44, 83
oxyfate
.. »
„
„
310
Liquid
„
B., 14, 1638
40, 1029
Glucovanillin aldoxime
C6H3(CH:NOH).OMe.(0.
C14H190SN
....
152
Tiemann and Kees
B., 18, 1664
48, 1072
C6Hn05)=1.3.4
Glucoseacetonitrose ....
C6H-0(OAc)4.N03
C14H19012N
145
Colley
C. R., 76, 436
26, 612
Picramide+dimethylaniline
NMe2Ph+C6H2(OH)(NH2)3
C14HMON4
139-141
Hepp
A., 215, 344
44, 316
Curaiuyldiacetamide
C6H4Pr.CH(NHAc)2
C14H2002N2
....
212
Raab
B., 8, 1150
29, 398
Diethylic phenylenediglyco-
C6H4(NH:CH2.CO4Et)2=1.3
C14H2004N2
73
Zimmermaim
B., 15, 518
42, 957
collate
»
=1.4
„
83
„
B., 16, 515
44,797
„
=1.2
,,
135
B
()
Dinitrotetraethylbenzene ....
Et4.(NO2)2=1.2.3.5.4.6
,,
....
115
Galle
B., 1C, 1745
44, 1092
Anisaldehyde+urethane ...
MeO.C6H4.CH(NH.C02Et)2
C^H^N,
....
171-172
Bischoff
B., 7, 1080
28, 146
=1.4
Diethylic collidinedicarb-
C5NMe3(CO.,Et),!+ HNO3
C14HM07NS
....
92
Hantzsch
A., 215, 21
44, 83
oxylate nitrate
„ hydrocollidinecarb-
C5NH2Me3(CO2Et)2
C14H,uO4N
310 d ; 315
131
B., 14, 1637 ; A.,
40, 1028 ; 44,
oxylate
215,8
82
Camphorethylimidethylimi-
j .
C8H14.CO.NEt.C : NEt
L i
C14H24ON2
284-286
Liquid
Wallach and Ka-
B., 13, 520; 14,
38, 548 ; 40,
dine
menski .
162; A.,214,245
285
Azoxybenzotoluide
0:N2:(C6H4.CO.NH.C6H4
C14H2403N4
....
290
Mixter
A. C. J., 5, 282
46, 666
Me)2
n-Hexyl-n-cenanthylcarb-
C6H13.NH.CO.NH.C7H130
C14H23O2N2
....
97
Hofmann
B., 15, 759
42, 1053
amide
Myristamide ....
C13H27.CO.NH2
C^H^ON
....
102
Reimer and Will
B., 18, 2016
n
„
A., 202, 174
102
Masino
G. L, 10, 72
38, 460
"
„
„
....
104-105
Krafft and Stauffer
B., 15, 1730
42, 1274
Pseudoveratrine
C14H3603N2?
185
Couerbe
A. C. [2], 52, 352
iv., 745
Trinitrofluoranthene
CI5H306N3
nf. 300
Fittig and Gebhard
....
36, 166
Nitrobenzylidene phthalide
O.CO.C6H4.C : CPh.N02=1.2
L 1
C15H904N
....
195 ; sf. 180
Gabriel
B., 18, 1255
48, 903
Phthalamidobenzoie acid ....
C6H4:(CO)2:N.C6H4.C02H
»
....
217
»
B., 11, 2261
36, 324
» ji
=1.2; 1.3
,,
276
„
B., 11, 2262
„
>! „
» >!
))
282
Pellizzari
B., 18, 216
48, 534
Nitromethylauthraquinone ....
C6H4:(CO)2:C6H2Me.OH
JJ
269-270
Romer and Link
B., 16, 697
44, 1139
=2.1 ; 1.2.4.5
Phenylpyridinetetracar-
N.Ph.(C02H)4=1.4.2.3.5.6
C16H908N
205-207
Hantzsch
B., 17, 1517
46, 1194
boxylic acid
Nitrophenylquinoline
C9H6N.CBH4.N02=a1/31 ; 1.3
C15H1002N2
124
Miller & Kinkelin
B., 18, 1903
48, 1144
Quinidinequinoline anilide ....
fr. N ; O2=a, ; 0,0,,
190+
Fischer and Renouf
B., 17, 1644
46, 1371
Diphenylparabanic acid
CO.NPh.CO.NPh.CO
i i
C15H^03N2
204
Hofmann
B., 2, 688
Benzenylazoximebenzenyl-
O.N : CPh.N : C.C6H4.C02H
"
204
151
Stojentin
Schulz
J. p., 32, 1
B., 18, 2464
48, 1196
48, 1219
carboxylic acid
=1.2
Phenylcyanate + isatin
Phthalimidylnitrobenzyl ....
PhCNO+C8H502N
C6H4.CO.N:C.CHPh.NO2
«
180 d.
199
Gumpert
Gabriel
J. p. [2], 31, 119
B., 18, 1261
48, 656
48, 903
Isatamidobenzoic acid
CO.NH.C6H4.C : N.OBz
i j
„
.»t
251-253
Schiff
A., 210, 121
42, 304
Nitrobenzaldehyde indogen-
ide
CO.C,.H4.NH.C : CH.C6H4.
»
....
273
Baeyer
B., 16, 2199
46, 76
J NOj=U; 1.4
COMPOUNDS CONTAINING FOUR ELEMENTS.
549
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dinitrobenzylidenephthalide
O.CO.C6H4.C(NO:i).CHPh.
C15H1006N2
....
110-113
Gabriel
B., 18, 1251
48, 902
1 ' NO2=1.2
Quinoline picrate
....
C15H1007N4
....
203
Goldschmidt and
W. A., 83, 7
40, 824
Schidt
Hydroxyquinoline picrate ....
N.OH=ai; a.
C16HI008N4
....
203-204
Skraup
M. C., 3, 536
44, 92
» »
„ =o,; 32
i)
235-235-5
n.
M. C., 4, 695
46,87
„ „
„ „
11
....
235-236
„
M.C.,2,575; 3,545
Benzaldehyde indogenide ....
CO.C6H4.NH.C:CHPh
n
175-176
Baeyen
B., 16, 2197
46, 75
L 1
Benzalphthimidine
NH.CO.C6H4.C : CHPh=1.2
182-183
Gabriel
B., 18, 2435
48, 1229
i i
Imidodeoxybenzoincarbox-
Cf,H4.CO.N : C.CH2Ph=1.2
182-183
Gabriel & Michael
B., 11, 1682
36, 246
ylic anhydride
i i
Isobenzalphthalimidine
C6H4.CO.NH.CPh rCH
„
....
197
Gabriel
B., 18, 2449
48, 1231
L I
Formanthramine
C14H9.NH.CHO
„
....
242
Bollert
B., 16, 1640
44, 1140
Anthracenecarboxylamide ...
C14H9.(CO.NH2)
n
....
293-295
Bernstein
B., 16, 2611
46, 330
Phenylcarbostyril
N.OPh=a, 3! ;
C15HnON
....
68-69
Friedlander
B., 15, 336
42, 733
Hydroxyphenylquinoline ....
C9H6N.C6H4.OH=a^ 3, ; 1.3
„.
....
156
Miller. & Kinkelin
B., 18, 1908
48, 1145
Lactone of a-benzylphenyl-
C6H4.C02.N : CPh.CH2=1.2
CI6Hn02N
116-117
Gabriel
B., 18, 1259; 2448
48, 903, 1231
acetoxime carboxylic acid.
\ 1
Lactone of 3-benzylphenyl-
„
n
....
137-139
i}
B., 18, 2448
48, 1231
acetoxime carboxylic acid
Benzylpseudisatin
....
11 '
131
Antrick
A., 227, 360
48, 543
Phenylindolecarboxylic acid
...r
rt
....
173-176
Fischer and Hess
B., 17, 568
46, 1181
Tolylphthalimide
06H4:(CO)2:N.C6H4Me
„
....
153
Frohlich
B., 17, 2679
48, 155
=1.2'; 1.3
„
„ =(1.2),
„
....
179
Piutti
G. I, 13, 542
46, 453
„
t) »
„
....
182
Frohlich
B., 17, 2679
48, 155
,.
„ =1.2 ; 1.4
„
....
200 u.c.
Michael
B., 10, 579
32, 616
„
11 11
11
204
Frohlich
B., 17, 2679
48, 155
Amidomethylanthraquinone
P TT * (r*C\\ ' P TT "VToATTT
O6il4 . (OU)2 . U6±l2JleJM Ji.,
„
....
202
Eomer and Link
B., 16, 698
44, 1139
•=2a :• 1.2.4.5
Benzenylazoximebenzenyl-
o.N:cph.N:c.c6H4.co.
C15Hn02N3
....
160
Schulz
B., 18, 2467
48, 1219
carboxylamide
1 ' TLTTT
NH2
Isatamidobenzamide
C6H4.NH.CO.C : N.C,H4.
....
280 d.
Schiff
A., 218, 185
46, 455
i i
CO.NH2=1.2; 1.3
Nitrosofurfurin (B., 11, 1250)
....
C16Hn04N3
112
„
G. L, 8, 76
34, 657
Phthalylamidobenzoic acid ....
C02H.06H4.CO.NH.C6H4
C16H1V<06N
275-277
Michael
B., 10, 579
32, 616
CO2H=I.2; 1.4
Phenylethenylazoximeben-
Ph.CH2.C : N.O.CPh TN
C16H12ON2
82
Knudsan
B., 18, 1071
48, 897
zenyl
i 1
Acetophenonecarboxylic
.....
ii.
102
Roser
B., 18, 804
44, 797
phenylhydrazide
p-Methylisatinphenylimide
CsH4MeNO : NPh
„
239-240
Meyer
B., 16, 2267
46, 48
3-naphtho-diniethyloxyquin-
....
11.
129
Knorr
B., 17, 551
46, 1154
izine
Hydroxyphenyltoluquinoxal-
C7H6.N : CPh.C(OH) : N
11
....
196-197
Hinsberg
B., 18, 1229
48, 909
ine
Benzylnitrosophthalidine ....
C6H4.CO.N(NO).CH.CH2Ph
C15H12O2N2
92-93
Gabriel
B., 18, 1263
48, 903
1- -, _ j__ - 1
Phthalyldiamidotoluen e
C6H4:(CO.NH)2:CsH3Me
„
....
104
Biedermanu
B., 10, 1165
=1.2 ; 1.2.?
11 „
=1.2; 1.3.?
„
....
192
„
B., 10, 1161
32, 783
?
....
„
1 ITT f\
~T~ "5 -^-•3^-'
200
Stojentin
J. p., 32, 1
48, 1196
Fnrfurine (A., 54, 59) ....
....
C16H1203N2
....
m. b., 100
Stenhouse
A., 74, 283
ii., 747
(A., 88, 127) ....
„
....
100
Fownes
P. T. [1845], 253
34,46
11
See orig. paper
....
116
Schiff
B., 10, 1188
11
Furfuramide (A., 54, 56)....
„
B
....
117
„
„
Dibenzoylcarbamide
CO(NHBz)2
„
Solid
Schmidt
J. p. [2], 5, 60
vii., 268
11 i» ....
11
n
....
210
McCreath
B., 7, 1739
28, 465
Nitrobenzalphthalimidinic
N02.CPh : C(NH2).C6H4.
C16H1204N2
147-150
Gabriel
B., 18, 2440
48, 1230
acid
CO2H=1.2
550
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Isatamidobenzoic acid
C6H4.NH.CO.C : N.C6H4.
C16H1204N2
+H20
251-253 d.
Schiff
A., 210, 121
i i
CO2H=1.2 ; 1.3
Diethylic carboxamidoben-
CO(NH.C6H4.CO2Et)2=( 1 .3
C15Hla06N2
160
Wachendorff
B., 11, 701
34, 674
zoate
Methylindole picrate
C9H9N.C6H2(N02)3.OH
C15H1207N3
....
150
Fischer and Hess
B., 17, 563
46, 1181
Benzylphthalidine
C6H4.CO.NH.CH.CH2Ph
C16H13ON
135-137
Gabriel
B., 18, 1262
48, 903
i i
Amidomethylanthranol
CH.C6H4.C(OH).C6H2Me.
11
183
Homer and Link
B., 16, 704
44, 1138
NH,
Acetamidofluorene
C6H4.C6H,(NHAc).CH2
„
187-188
Strasburger
B., 17, 108
46, 754
i " i
=1.2; 1.4.2
Acetyldiphenylacetoxime ...
PhjC : N.OAc
C15H1302N
....
55
Spiegler
M. C., 5, 203
46, 1156
Dibenzoylhydrocyanide
HN : CBz,,
»
....
195
Zinin
Z. C. [2], 4, 710
vi., 329
Acetamidobenzophenone ...
Ph.CO.C6H4.NHAc
„
A., 210, 270
153
Dobner and Weiss
B., 14, 1838
42, 176, 508
Deoxybenzoiincarboxylamide
NH2.CO.CjH4.CO.CH.jPh
„
165-166
Gabriel
B., 18, 2434
48, 1229
=1.2
Nitrocinnamaldehydephenyl-
NO,j.(CH : CH.CH : N2HPh)
C15H1302N3
....
157-5
Diehl and Einhorn
B., 18, 2338
48, 1222
hydrazine
=1.2
>< 11
=].3
„
160
Kinkelin
B., 18/484
48, 791
» 11
=1.4
„
....
180-181
Diehl and Einhorn
B., 18, 2337
48, 1222
Formylbenzylamidobenzoic
C02H.N(COH)(CH2Ph)=1.2
C15H1303N
196 u.c.
C'laus & Glyckherr
B., 16, 1285
44, 1009
acid
Acetylnitrobenzylidene-
NPhAc.N : CH-C^.NOj
C15H1303N3
170
Schroeder
B., 17, 2098
46, 1323
phenylhydrazine
=1.3
Benzanishydroxamic acid ....
NBz(CO.C6H4.OMe).OH
C16H1304N
131-132
Lessen
A., 175, 288
28, 635, 636
=1.4
Anisbenzhydroxamic acid ....
N(CO.C6H4.OMe)Bz.OH
„
....
147-148
„
A., 175, 294
„
=1.4
Methylic salicylatephenyl-
NHPh.C02.C6H4.C02Me
„
....
238
Snape
47, 775
carbamate
=1.2
Nitrophenoxyethylene
N02.C6H4.O.C2H4.O.Bz=1.2
C16H1306N
76-77
Weddige
J. p. [2], 24, 252
benzoate
Pyropapaveric acid
....
„
230
Goldschmidt
M. C., 6, 372
48, 1081
Dinitro-a-dimethamido-
fr. Ph.CO.C6H4.NMe2
C15H1305N3
142
Fischer
A., 206, 90
40, 587
benzophenone
Salicylethylenenitrophenol
HO.C6H4.C02.C2H4.O.C6H4.
C13H1306N
106
Wagner
J. p. [2], 28, 215
46, 436
ether
N02=(1.2)2
11 „
=1.2 ; 1.4
n
131
„
J. p. [2], 28, 221
Ethylenenitrophenoloxy--
N02.C6H4.O.C2H4.O.C6H4.
„
130
Weddige
J. p. [2], 24, 241
40, 1139
benzoic acid
CO2H=1.4; 1.2
,i „
» »
„
132
Wagner
J. p. [2], 28, 220
46, 435
» n
=(1.2),
„
143
Weddige
J. p. [2], 24, 241
40, 1139
., „
» 11
„
142-148
Wagner
J. p. [2], 28, 214
46, 435
>» i>
„ =1.2; 1.4
„
....
205-207
„
I. p. [2], 28, 222
1)
ii ,1
!» =(1-4)2
218
n
J. [2], 28, 225
|J
Acetobenzylidinephenyl- )
hydrazine )
PLCHIN.NPhAc
C15H14ON2
i fr. alcohol
! fr. hot wtr.
115-117 i
119-120 |
Schroeder
B., 17, 2097
46, 1323
CNC1 on benzylalcohol
....
D
....
143
Cannizzaro
G. I., 1, 33
vii., 178; 24,
927
Anhydride of acid C15H1(!O2N2
See orig. paper
164
Plochl
B., 14, 1141
40, 820
Ethylenediphenylcarbamide
CH2.NPh.CO.NPh.CH2
B
209
Michler and Keller
B., 14, 2183
42, 182
i i
Methoxyphenylphenamido-
C6H4.OMe.[CH(NHPh).CN]
B
61
Voswinckel
B., 15, 2026
44, 190
acetonitril
=1.2
Anhydrobenzoylamidoethyl-
See orig. paper
H
149-151
Weddige
J. p. [2], 24, 250
40, 1138
ene-o-amidophenyl ether
Acetylphenylcarbamide
NHPh.CO.NPhAc
C16H14O2N2
115
McCreath
B., 8, 1182
29, 401
Methylphenylhydrazine
N2MePh : CPh.COoH
116 d.
Elbers
A., 227, 340
48, 535
phenylglyoxylic acid
Beuzoylphenylethenylamid-
CH2Ph.C(NH2) : NOBz
n
144
Knudsen
B., 18, 1069
48, 897
oxime
COMPOUNDS CONTAINING FOUR ELEMENTS.
551
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Diphenylliydrazinepyrorace-
NPh2.N : CMe.CO2H
C15H1402N2
....
145
Fischer and Hess
B., 17, 567
48, 1181
mio acid
Methylene dibenzamide
CH2(NH.CO.Ph)2
))
....
212
Hepp and Spiesa
B., 9, 1427
31, 314
CH,(CO.NHPh)2
220
Seifert
B., 18, 1361
48, 984
222-223
Riigheimer
B., 17, 235
46, 729
298
Freund
B., 17, 134
46, 728
Nitrosobenzylamidoaceto-
Ph.CH,,N(NO).C6H4.Ac
))
54-55
Baeyer
B., 17, 972
46, 1021
phenone
=1.2
Phenylazoacetocresol
Ph.N2.C6H3Me.OAc=?.1.4
J)
....
67-68
Nolting and Kohn
B., 17, 353
46, 901
„
=?.1.2
))
....
81-82
»
B., 17, 364
46, 902
Nitrophenylhydroquinoline....
C9H10N.C6H4.NO2=1.2.3;1.3
»)
100-101
Miller & Kinkelin
B., 18, 1906
48, 1145
Benzoylphenylhydroxy-
HO.CHPh.C(NH2) I NOBz
C)BH1403N2
148-149
Gross
B., 18, 1078
48,898
ethenylamidoxime
2
See B., 17, 129
137
Tiemann
B., 17, 127
46, 734
Methylic diphenylallophanate
i)
»)
231
Hofmann
B., 4, 248
24, 394; vii.,
408
?
N2HPh:CH.C6H4.O.CH2.
))
....
105 ; sf. 60
fiossing
B., 17, 2995
48, 388
CO2H=1.2
Toluylnitrotoluide
C,,H3Me.NO,,.NH(CO.
»
....
165-166
Hiibner
A., 210, 331
42,504
C6H4Me)=1.3.4 ; 1.4
j3-benzoylnitroxylidine
Me2.N02.NHBz=?
)»
A., 208, 323
178
)!
B., 10, 1711
34, 143
a- „
=?
)j
A., 208, 320
184-5
D
!»
!»
Carbonyldibenzenylamid-
CX)(O.N :.CPh.NH2)2
C15H1403N4
....
128-129
Falck
B., 18, 2471
48, 1217
oxime
Benzamidoethylenenitro-
NHBz.C2H4.O.C6H4.NO2
C^AN,
....
94-95
Weddige
J. p. [2], 24, 249
40, 1138
phenyl ether
=1.2
Nitrophenyl-/3-lactanilide ....
C6H4.N02.[CH(OH).CH.,.
»1
176-178
Easier
B., 17, 1502
46, 1173
CO.NHPh]=1.4
Dinitroditolylmethane
fr. CH2(C6H4Me)2
»»
....
164 u.c.
Weiler
B., 7, 1183
28, 151
Dinitrodibenzylmetliane
CH2(CH2.C6H4.N02)2
)»
186
Sesemann
I. D. Zurich
28, 74
Dinitrophenylacetdiamido-
C6H3(NO2)2.NH.C6H,Me.
C16H1406N4
....
163-164
Leymann
B., 15, 1237
42, 1057
toluene
NHAc=(?)3; 2.1.4 or 4.1.2
Piuitroditolylcarbamide
CO(NH.C6H3Me.N02)2
)1
...»
233 d.
Perkin
.<•*
37, 699
=(1.4.1),
Tetrahydroquinoline picrate
C^Hn+C^^NO^.OH
C15H1407N4
...*
125
Ostertneyer
C. C., 1884, 970
48, 672
Ethyl diphenylacetoxime ....
CPh2 1 NOEt
C16H15ON
276-279 p.d.
Liquid
Spiegler
M. C., 5, 203
46, 1156
Beuzoylethylaniline
Ph.NEtBz
»
260 (620)
60
Hesse
B., 18, 687
48, 784
Diinethamidobenzophenone
C6H4Bz.NMe2=?
JJ
330-335
38
Fischer
B., 10, 958
32, 606
N
» ii
»
38-39
ij
B., 12, 797
36, 787
11
11 11
JJ
330-340
38-39
»
A., 206, 88
40, 587
l»
=1.4
)1
A., 217, 257
90
Doebner and Weiss
B., 14, 1837
42, 176
11
11 »
»)
A., 210, 270
90
Doebner
B., 13, 2225
40, 165
Benzylaniidoacetophenone ....
Ph.CH2.NH.C6H4 Ac= 1 . 2
»
79-81
Baeyer
B., 17, 971
46, 1021
Acetamidodiphenylmethane
Ph.CH2.C6H4.NHAc=1.3
1)
91
Becker
B., 15, 2092
Acetophenonemethauilide ....
Bz.CH2.NMePh
H
B., 16, 23
119-120
Staedel and Sieper-
B., 14, 984
38, 639
mann
11
11
»
....
120 d.
ii
B., 13, 843
Benzamidoethylbenzene
C6H4Et.NHBz=1.2
»
147
Paucksch
B., 17, 2802
48, 256
11
=1.4
»>
151
11
))
11
Tolylphenylacetamide
C6H4Me.CHPh.CO.NH2=1.4
>»
151
Tanisch
B., 10, 997
32, 618
Acetamidotolyphenyl
Ph.C6H3Me.NHAc(2)
51
• •>.
114-25
Jackson
A. J. S., 13, 449
32, 762
11
)J
»
114-2
!»
B., 8, 970
29, 269
Xylic anilide
Me2.(CO.NHPh)=1.3.4
»)
....
138-5
Ador and Meier
B., 12, 1971
38, 252
Benzamidoxylene
Me2.NHBz=1.3J
))
A., 208, 322
140
Hiibner
B., 10, 1711
34, 143
11 •••• ••"
ii
»
A., 208, 319
192
11
B., 10, 1710
11
Acetmethamidoazobenzene ....
Ph.N:.C6H4.NMeAc
C15H16ON3
...»
139
Berju
B., 17, 1402 ;
46, 1148; 48,
C. C., 1884,871
660
Diphenylurethane
NPhj.COjEt
C15H1502N
B., 5, 284
72 ; af. 66
Merz and Weith
B., 6, 1512
27, 375
11
Ph.C6H4.NH.CO2Et
)»
....
110
Zimmermann
B., 13, 1965
40, 176
Tolylphenamidoacetic acid ....
Me.[CH(NHPh).C02H]=1.3
)J
137-139
Bornemann
B., 17, 1471
46, 1163
Phenyltoluidoacetic acid
C6H4Me.NH.CHPh.C02H
I>
142-144 d.
Stock enius
J., 1878, 781
= 1.2
552
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Pheuyltoluidoacetic acid ..
C6H4Me.NH.CHPh.COiiH
C15H1602N
167-170
Stockeuius
J., 1878, 780
=1.4
Ethoxybenzanilide
C6H4.OEt.(CO.NHPb)=1.4
J)
....
170
Leuckart and
B., 18, 2340
48, 1224
Schmidt
Methylcarbophenyllutidy-
C6(NMe)HPh.OMe.COMe
M
160-161
Hantzsch
B., 17, 2915
48, 398
liumdehydride
Phenylethenylphenylurami-
Ph.CH2.C(NH.CO.NHPh) :
C15H1502N3
123
Knudsen
B., 18, 1074
48, 898
doxime
NOH
p-acetamidotolylazophenol ..
NHAc.C6H3Me.N2.C6H4.OH
)J
252-253
Wallach
B., 15, 2827
44, 584
Amidophenoxyetbyleneben-
NH2.C6H4.O.C2H4.OBz=1.2
C15H1503N
98-100
Weddige
J. p. [2], 24, 253
zoate
1
CO.CH : CMe.NPh.CMe : C.
n
152
Perkin
B., 18, 683
48, 761
i i
C02Me
Phenylhydroxyethenylphen-
HO.CHPh.C(NOH).NH.CO
C1SH1603N3
155
Gross
B., 18, 2478
48, 1218
yluramidoxime
NHPh
E thylenearaidophenyloxy-
NH2.C6H4.O.C2H4.O.C6H4.
C15H1504N
110
Wagner
J. p. [2], 28, 218
46, 436
benzoic acid
C02H=(1.2)2
» »
=1.2 ; 1.4
>»
185
»
J. p. [2], 28, 223
)»
p-Tolyldimethylpyrroline
C02H.C : CMe.N(C6H4Me).
»
d. 250
Knorr
B., 18, 308
48, 555
dicarboxylic acid
i
CMe I C.CO2H
Dinitroditolylguanidiiie
CN3H3(C6H3Me.N02)2
CBH1504N6
197 d.
Perkin
• •••
37, 698
=(1.4),
Ethylic nitroeinnamylaceto-
C6H4(N02)(CH:CH.CO.
C15H1506N
120-5
Fischer and Kuzel
B., 16, 35, 163
44, 587
acetate
CHAc.C02Et)=1.2
Benzylphenylethenylaruid-
CH2Ph.C(NH2) : NO.CH2Ph
C16H16ON2
55
Knudsen
B., 18, 1072
48, 897
oxime
Ethyldiphenylcarbamide ....
NHPh.CO.NEtPh
»
....
91
Gebhardt
B., 17, 2093
46, 1321
Dimethyldiphenylcarbamide
CO(NMePh)2
>J
350
120-121
Michler & Zimmer-
B., 12, 1166
36, 935
mann
Dibenzylcarbamide
NH2.CO.N(CH2Ph)2
)J
B., 9, 81
1S4-125
Paterno and Spica
G. I., 5, 388
29, 602
»
CO(NH.CH,,Ph)2
))
B., 4, 412
166-167
Cannizzaro
G. I., 1, 41
24, 928
»
11
^i
....
167
Letts
B., 5, 93
25, 449; vii.,
181
)j ....
)J
-?5
....
167
Paterno and Spica
G. I., 5, 388
29, 602
p-tolylglycollanilide
C6H4Me.NH.CH2.CO.NHPh
J>
82-83
Meyer
B., 8, 1161
89,402
Tolylanilidoacetamide
Me.[CH(NHPh).CONH2]
»
127-128
Borueniann
B., 17, 1471
46, 1163
=1.3
Benzenyldimethylphenylen-
C6H4.N : CPb.NMe2.OH
»)
152
Hubner
A., 210, 357
42,505
amidine
Phenylglycocintoluide
NHPh.CH2.CO.NH.C6H4Me
J)
....
171-172
Meyer
B., 8, 1158
29, 372
=1.4
Hydroxybenzylideneamido-
HO.C6H4.CH : N.C6H4.NMe2
;)
134
Nuth
B., 18, 573
48, 784
dimethanilide
=1.2; 1.4
Ditolylcarbamide
CO(NH.C6H4Me)2=(1.3)2
J>
B., 13, 1090
217
Cosack
B., 12, 1450
38, 245, 713
»
=(1.2)2
»
B., 6, 444
243
Nevile and Wintber
B., 12, 2325
»
» »
))
....
250
^acbmann
B., 12, 1350
36, 935
»» .... ....
» !!
»
252 u.c.
ierger
B., 12, 1859
38, 245
)' '••• ....
=(1-4),
»)
255
Weith
B., 9, 821
30, 639
)»
» )i
J)
....
256
tfichler
B., 9, 714
>? ....
» !)
»
....
S56
Sarauw
B., 14, 2446
42,507
11
" )>
»
....
257
Will & Bielschowski
B., 15, 1310
» ....
» I)
)»
.„.
263
Sell
A., 126, 161 (?)
») .... ....
= ?
250-260
jandgrebe
B., 10, 1591
34, 217
Phenylazopseudocumol
Ph.N,,C8HMe3.OH=?.5.4.2.1
J)
....
93
Bolting and Bau-
B., 18, 1149
mann
»
» i)
9}
....
93-94
jiebermann and
B., 17, 886
46, 1147
Kostanecki
/3-diamidobenzhydrol acetate
CH(OAc):C12H8(NH2)2
C15H1602N2
220
Staedel
A., 218, 339
44, 991
Ethoxybenzeueazocresol
EtO.C6H4.N2.C6H3Me.OH
j)
03-104
jiebermann and
B., 17, 883
46, 1147
=1.4 ; 11.4
Kostanecki
COMPOUNDS CONTAINING FOUR ELEMENTS.
553
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
I
Reference.
Watts'Dict.
& J. Ch. Soc.
Cumylazoresorcinol
C6H2Me3.N2.C6H3(OH)2
C15H,AN2
....
199
Liebermann and
B., 17, 882
46, 1147
— 1.34.6 • J.1.3
Kostanecki
.... ....
„
....
200 +d.
B., 17, 132
46, 736
120 d.
Plochl
B., 14, 1141
Nitro-compimnd
fr. Ph.N2.NEt.C6H4Me ....
»
55
Nolting and Binder
B. S., 42, 340
48, 386
„ „
j,
„
....
104-105
„
„
„
Dianisyl carbamide
CO(NH.C6H4.OMe)2=(1.2)s
C^H.AN.,
174
Miilhauser
B., 13, 922 ; A.,
38, 642 ; 42,
207, 245
302
„ „
=?
„
232-234 d.
Lessen
A., 175, 295
,, ,,
=1
„
234
Pieschel
A., 175, 312
Parvoline picrate
C9H13N+C6H2(N02)3.OH
C16H,AN4
149
Waage
M. C., 4, 708
46, 172
9-naphthimidoisobutyl ether
C10H-.C(OBu0) : NH
CUHI7ON
38
Pinner and Klein
B., 11, 1486
36, 48
Ammonium nitrophenyl-jS-
C6H4.NO2.[CH(NHPh).CH2.
CUH1704N,
....
150-156
Easier
B., 17, 1502
46, 1173
anilidopropionate
CO2.NH4]=1.4
Paraxanthine
....
C15H,AN9
a. 250
Solomon
B., 16, 197
44, 601
Diamidotolyl carbamide
CO(NH.C6H3Me.NH2)2
C15H18ON4
....
d.w.m.
Perkin
....
37, 700
Benzylammonium benzylcar-
CHjPh.NH.COj.CNHj.CH,
C15H1802N2
».«t
99
Tiemann and Frid-
B., 14, 1970
42, 56
bamate
Ph)
lander
Oinnamodiacetonamine
CHPh : CH.CH.CH2.CO.
i
CISH19ON
+|H20
49
Antriek
A., 227, 365
48, 503
CH2.CMe2.NH
Benzoyltrope'ine
....
C16H1902N
+JH20
37
Ladenburg
B., 13, 1083
38, 715
(A., 217, 96)
„
+2H2O
58
„
„
„
o-Hydroxylbenzoyltrope'ine
C16H1903N
....
57-60
„
B., 13, 106
38, 410
„ (A, 217, 89)
....
„
....
58
„
B., 13, 1083
m- „ (A, 217, 91)
....
D
....
226
„
B., 13, 1081
38, 714
p- „ (A., 217, 93)
....
„
....
227
„
B., 13, 1082
„
p-Hydroxybenzaldiacetoiia-
HO.C6H4.CH.CH2.CO.CH2.
C16H,AN
....
193d.
Antriek
A., 227, 365
48, 503
L
mine oxalate
CMe3.NH+C2H2O4
i
Gluco-coumaraldoxime
C6H4(O.C6HU06)(CH:CH.
ClbH190?N
....
230
Tiemann and Kees
B., 18, 1961
48, 1073
CH:NOH)=1.2
C,-H O N (?'
204'5-205
Roster
A. 165 107
Cinnamylurethane
Ph.CH : CH.CH(NH.CO2Et)2
C15H2AN.,
....
135-143
Bischoff
B., 7, 1079
28, 146
Dinitrolaserpetin
C15H20(N02)A
C16Hj0OgN2
+H20
115
Kulz
A. P. [3], 21, 161
46, 183
Eserin (Physostigmiu)
....
C15H2102N3
....
45
Jobst and Hesse
A., 129, 115
>. >.
....
„
d. 150
69
Vee
J. [1865], 457
Benzoylhomoconiinic acid ....
Ph.CO.C8H,AN
C15H2103N
142-143
Schotten and Baum
B., 17, 2550
48, 176
Perezonoxime
see B., 18, 946
„
....
153-154
Mylius
B., 18, 938
48, 777
Ethylic pseudocumyliziuacet-
C6H2Me3.N.NH.CMe.CH...
C.sHjAN
....
77-78
Haller
B., 18, 707
48, 818
acetate
J
CO2Et=1.2.4.5
Beuzylidene dipropylurethane
Ph.CH(NH.C02Pra)2
C16H2204N2
143
Bischoff
B., 7, 1082
28, 146
Ethylic toluylene diglyeocine
C6H3Me(NH.CH2.C02Et)2
„
....
70
Zimmermann and
B., 16, 516
44, 798
Knyrin
Methylcopellidine picrate ....
C8H16MeN+C6N2(N02)3.OH
C15H2207N4
....
112
Diirkopf
B., 18, 926
n-Octylformanilide ....
CSH17.C6H4.NH(CHO)=1.4
C^HjAN
....
56
Beran
B., 18, 135
48, 523
Alantamide . ....
C14H20(OH).CO.NH2
HO "NT
210 ( 1
TT n
RQ 1 f\A
• • 23 S
jvaiien
j ity 1OO
***j yio
Hydrosantonamide ....
....
CI5H2303N
J. [1876],620
190 d.
Cannizzaro
G. I., 6, 341
31, 471
1
C16H2304N
....
86
Kuckert
B., 18, 620
48, 750
Oxametharie cyanurate
C3O3N3H3(NH2.CO.CO2Et)3
C16Hj4O12N8
....
155-160
Grimaux
B. S. [2], 21, 154
28, 564
Oxypentinamide
C15H,A(NH3)5
C16H2ANS
203-204
Demaryay
A. C. [5], 20, 487
Diisoamylcarbopyrrolamide
C4H3(C5Hn)N.CO.NH
CnHjjONj
77
Bell
B., 10, 1866
36, 525
(C5Hn)
C14H29.CO.NH2
CTT <~W
*D
P T? on QOQ
l IS ATA
lo '31
MM
IjOUlS
\j, 11., oy, .)_.)
in., 414
Tetranitropyrene
C16H608N4
a. 300
Graebe
A., 158, 293
24, 691 ; vii.,
1028
Dinitrodiphenyldiacetylene ....
(.C = C.C6H4.N02)2=(1.2)2
C16H804N8
212 d.
Baeyer
B., 15, 52
42, 619
Dinitropyrene
....
„
A., 158, 292
a. 240
Goldschmidt
M. C., 2, 581
42, 206
Dinitro-a-naphthylene-
fr. C10H0.O.C6H4
C16H805N2
»•>•
235
Arx
B., 13, 1727;
40, 282
phenylene oxide
A., 209, 145
A »
551
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Dinitrostilbenediearbonic
....
C16H807N2
sf. 73
Reimer
B., 14, 1801
anhydride
?
....
(C16H9ON2)n
....
217
Zincke
B., 15, 286
Nitrodiphenyldiacetylene ...
Ph ^C - C^ C H NO — 12
C16H902N
154-155
Baeyer and Lands-
B., 15, 58
42, 622
berg
Cyanbenzylidenephthalide ...
O.CO.C6H4.C : CPh.CN=1.2
„
164-165-5
Gabriel
B., 18, 1264
48, 902
1 I
Nitropyrene
....
„
140-142
Grain
A., 158, 292
24, 690; vii.,
1027
)J "" "*"* *"
....
„
...
148-149
Goldschmidt
M. C., 2, 580
42, 206
149-150-5
Fittig and Gebhard
B., 10, 2143
34, 432
Phenylnaphthylcarbazole-
C6H4.NH.C10H4:02
1)
I
307
Grsebe and Knecht
A., 202, 13
38, 664
quinone
a-tetranitronaphthylphenyl-
C10H3(N02)4.NHPh
C16H908N5
162-5
Merz and Weith
B., 15, 2717
44, 344
amine
/-*" 11
„
1J
....
253
„
B., 15, 2720
11
Nitrosophenylnaphthylcarb-
C6H4.C10H6.N.NO
| I
C16H10ON2
240
Graebe and Knecht
A., 202, 8
azole
C16H10OrN,
275
Zincke
B., 15, 285
Nitroso-|3-naphthoqumone-
I
C16H1003N2
I
245
B
B., 15, 284
42, 735
anilide
Nitro-a-naphthoquinoneani-
N02.C6H4.NH.C10H6 : 02
C16HI004N2
....
a. 270
Baltzer
B., 14, 1905
42, 205
lide
=1.3
„ -a- „
=1.4
„
....
nf. 270
„
B., 14, 1904
„
« -0- 11
C10H4(OH)(N02).O.NPh
| t
»
246-248
Brauns
B., 17, 1134
46, 1038
» -0-
u
253
Korn
B., 17, 908
46, 1186
Azophenylglyoxylic acid
N2(C6H4.COX:02H).!=(1.3)2
C16H1006N2
....
abt. 151
Thompson
B., 16, 1309
44, 998
11 »
„ „
„
+2H2O
134-5-135
„
„
„
Dinitroethoxyanthraquinone
fr. C6H4:(CO)2:C6H3.OEt
C16H1007N2
158
Simon
B., 15, 694
42, 863
=2.1 ; 1.2.4
Azophthalic acid
N2[C6H3.(C02H)2]2=(?.2.1)2
C16H1008N2
brown 220
230-250 d.
Glaus and May
B., 14, 1331
42, 516
Picrate of /3-benzoquinoline
N.CO2H=a,ft ;
C16HI009N4
216 d.
Riedel
B., 16, 1614
44, 1152
carboxylic acid
Fr. Phenaiithraquiiione
MM
C16HHON
..••
241
Japp and Miller
B., 16, 2418
46, 329
+HCN
Diphenylfumarimide
CPh : CPh.CO.NH.CO
i i
C16HnO£N
....
213
Reimer
B., 13, 746
40,48
Fr. Benzylcyanide
C14H10(CN).C02H
a
222
„
B., 14, 1801
42, 170
Oxyquinonimide
see orig. paper
n
173-5-174
Brener and Zinck6
B., 11, 1997
36, 328
a-naphthaquinoneanilide
....
«...
190-191
Plimpton
37, 635
"- »
c10H6:(o2):NPh
„
MM
190-191
Zincke
B., 12, 1645
38, 49
°- ,,
Ph.NH.C10H5:Os
„
A., 211, 82
191
Liebermann
B., 14, 1666
a-
C10Hb(OH).O.NPh=a^1oB ;
„
B., 15, 279
240-S50
Zincke
B., 14, 1494
40, 915
8-
•i
„
B., 15, 690
nf. 240
Liebermann and
A., 211, 75
42, 522
Jacobsen
P~ 11
» »
11
sb.p.d.
a. 240
Liebermann
B., 14, 1314, 1665
Bezoxyquinoline
N.OBz=a,; fll
D
118-120
Bedall and Fischer
B., 14, 1367
„
„ =a,; j3.
,,
....
86-88
Skraup
M. C., 3, 567
44, 94
„
ii »
....
88-89 s.d
„
11
„
,,
11 =ail ft
230-231
,,
M. C., 3, 556
J)
Benzoylhydroxyquinoline ....
N.OH.Bz=a,/31ft;
a. 270
Friedlander and
B., 16, 1839
44, 1149
Gohiing
Deoxyimidoisatin
....
C16Hn02N3
A., 194, 86
209-210 d.
Sommaruga
A., 190, 379
34, 507
Benzoylimidocoumarin
C6H4.CH.NBz.CH.CO.O= 1.2
i- i
C.eH.AN
170-171
Plochl & Wolfrum
B., 18, 1185
48, 898
Hydroxy-a-naphthaquinone-
C10H4(OH)(NHPh):02
210
Plagemann
B., 16, 896
anilide
Anilidojuglone
=3, ; fta,a2
230
Mylius
B., 18, 473
48, 8P4
Acetaniidoanthraquinone ...
C6H4:(CO)2:C6H3.NHAc
B
....
202
Roeuier
B., 15, 1791
44, 72
=2.1 ; 1.2.3
"
,, =2.1; 1.2.4
»
....
257
Perger
B., 12, 1569
38, 49
COMPOUNDS CONTAINING FOUR ELEMENTS.
555
Name.
Acetamidoaiithraquinone ....
Amidoisatin
Nitrobeuzeneazo-a-naphthol
Acetamido-m-hydroxyan-
thraqumone
» -o- »
I)initrophenyl-a-naphthyla-
mine
» -3- u
Nitroethoxyanthraquinone ....
Trinitrobenzene naphthalene
i> »
Naphthalene trinitrophenol
„ (picrate)
Dipyridyl picrate
Trinitroquinol+naphthalene
/3-naphthol picrate
«- „ ))
HNO3 on strychnine....
Isoindileucine
Nitrosophenyl-j3-naphthyl-
amine
$-naphthaquinonephenylhy-
drazine
0-
a-naphtholazobenzene
0-
p~ 1»
Fr. Benzil hydrocyanide
Phenylfurfuraldehydine
Nitrophenyl-i3-naphthyl-
amine
Hydroxynaphthaquinonehy-
drazine
Naphthaquinoneamidoanilide
Naphthaleneazoresorcinol ....
Isatindiamide
NH.C10H6.NH.N.C6H4.NO2
A =«A ; 1.3
Nitrobenzeneazoamido-a-
naphthalene
Constitution.
C6H4 1 (CO).: C6H3.NHAc
=2.1 ; 1.2.4
NO,.C6H4.N2.C10H6.OH
=1.4; <m
=1.3; a/3
=1.4; a/3
see orig. paper
fr. C10H7.NHPh
C6H4 : (CO), : C6H2.OEt.NO,
=2.1; 1.2.5.6
C6H3(N02)3+C10H8
C10H8+C,H2.OH.(NO..)S
= 1.3.4.6
=1.2.3.6
=»
=1.2.4.6
C6H(OH)2(N02)3+C10H8
Ph.CO.C : N.CPLCH : NH
I 1
C10H7.N(NO).C6H5
C,0H6.O.NPh.NH=j31a. ;
Ph.N2.C,,,H6.OH=?a
=?«
C6H4(N:C6H40)2
C10H5(OH)O.N2HPh
i 1
NH2.C6H4.NH.C10H602=1.4
C10H7.N2.C6H3(OH)2=?;?.1.3
(.NH.C6H4.CO.CNH.)2
C10H6:(NH)2:N.C6H4.N02
=a,/3, ; 1.3
=atBt ; 1.4
N02.C6H4.N2.C10H6.NHS
=1.4 ; e.,/3, ;
Formula.
C,«H,,0:<N
C16HU03N3
C16HU04N
C16Hn04N3
C16Hn07N3
C16Hn07N5
C16HU08N3
C16H12ON2
C16H1202N2
C16H1202N4
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
263
Liebermann and
B., 15, 229; A.,
Bollert
212, 61
250-252
Sommaruga
M. C., 1, 579
....
a. Hg. therm.
Meldola
47, 662
....
191-192
»
47, 668
....
249
»
47, 662
....
170
Perger
J. p. [2], 18, 143
36, 254
242
»j
J. p. [2], 18, 145
»»
B., 13, 1853
77
Streiff
A., 209, 155
40, 176
....
192-195
>»
A., 209, 160
....
243
Liebermann and
B., 15, 1796
44,73
Hagen
....
152
Hepp
A., 215, 377
44, 318
152-153
»
B. S. [2], 30, 6
38,51
....
72-73
Henriques
A., 215, 321
44,328
100
)»
u
)>
....
138
Zehenter
M. C., 6, 523
48, 1235
....
149
j>
»
J. [1857], 456
149
Fritzsche
J. p. [1], 73, 212
iv., 405
....
149
Schultz
B., 9, 549
30, 197
J. [1879], 376
149
Goldsohmidt and
W. A., 83, 7
40, 824
Schidt
....
149-5
Skraup and Vort-
M. C., 3, 370
44,88
maun
....
159
Jacobsen
B., 15, 1863
B., 16, 796
155
Marchetti
G. I., 12, 502
44, 345
))
189-190
»
n
)j
a. 300 d.
Schiff
G. I., 8, 82
34, 679
....
191-192
Engler and Hassen-
B., 18, 2241
48, 1223
kamp
.•'**.«
93
Streiff
A., 209, 159
....
138
Zinckfi
B., 16, 1564
44, 1135
....
138
Zincke&Bmdewald
B., 17, 3030
48, 392
166
Typke
B., 10, 1581
175
i»
»
....
193
Liebermann
B., 16, 2858
46, 610
....
206 d.
Zincke& Bindewalc
B., 17, 3027
134
Liebermann
B., 16, 2860
46, 610
134
Zincke& Bindewalc
B., 17, 3032
196
Japp and Miller
B., 16, 2417
46, 329
95-96
Ladenburg and
B., 11, 1655
36, 235
Engelbrecht
....
85
Streiff
A., 209, 160
230 d.
Zincke and Thelen
B., 17, 1810
46, 1360
175-177
Baltzer
B., 14, 1905
42, 205
....
200
Wallach
B., 15, 28
42, 611
....
111 d.
Sommaruga
A., 190, 374
34, 507
A., 194, 86
a. 300 d.
ji
M. G, 1, 578
....
177
Meldola
....
45, 116
....
180
»
MM
n
....
180
j>
....
43, 430
4 B 2
.556
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc
Nitrobenzeneazoamido-a-
NO2.C6H4.Na.C10H6.NH3
C16H1202N4
....
202-203
Meldola
....
45, 114
naphthalene
= 1.3 ; a,a2 ;
„ -a- „
=1.4 ; a.0, ;
„
....
252
„
....
43, 430
J
C6H4.CO.N2Ph I C.CH2.CO2. H
....
160 d.
Roser
B., 18, 803
48, 797
i i
=1.2
Dinitrobeuzene-naphthalene
C10H8+C6H4(N02)2=1.3
C16H1204N2
52-53
Hepp
A., 215, 379
44, 318
„ „
=1.4
„
....
110-115
„
B. S. [2], 30, 6
36, 51
» »
» )!
,,
....
118-119
„
A., 215, 379
44, 318
Trinitroaniline-naphthalene
C10H8+C6H2.NH.(N02)3
C,,H1206N4
168-169
Liebermann and
B., 8, 378
=1.2.4.6
Palm
/3-napthylamine picrate
C10H..NH2+C6H2.OH.(N02)
C16H1207N4
....
195
Liebermann
A., 183, 264
31, 607
p~ » »
„
„
195
Scheiding
B., 8, 1652
29, 713
Quinoline methopicrate
C9H7N+CliH2.OMe.(N02)3
„
....
164
Ostermeyer
B., 18, 594, 599 ;
48, 672
C. C. [1884], 970
,, )>
„
„
....
164-165
Coste
B., 15, 193
|3-methylquinoline picrate ...
C10H9N+C6H2.OH.(N02)3
„
....
187
Dobner and Miller
B., 18, 1642
m-toluquinoline picrate
„
„
....
206-207
Skraup
M. C., 8, 381
42, 1216
Methylic fl-dinitrodiphenate
fr. (.C6H4.CO2Me)3=(1.2).l
C16H1209N2
131-132
Schultz
A., 203, 111
38, 814
„ a- „
see orig. paper
»
....
177-178
„
„
n
Dinitro-a-dibeuzyldicar-
fr. (.CH2.C6H4.C02H)2
„
226
Eeimer
B., 14, 1804
42, 200
boxylic acid
» -ft- >i ii
)(
....
242
M
B
Nitropapaveric acid
...»
C16H1209N2
....
215
Goldschmidt
M. C., 6, 372
48, 1031
C16H13ON
B., 16, 69
238
Fischer & Rudolph
B., 15, 1502
42 1067
Acetylanthrainine
C6H4:(CH)2:C8H3.NHAc
240
Liebermann
A., 212, 61
42,860
„
„
„
240
Liebermann and
B., 15, 228
Bollert
Azophenol-a-naphthylamine
HO.C6H4.N,,C10H6.NH2
C18H13ONb
+3 H,0
170
Weselsky and
B., 12, 229
=1.4
Benedikt
a-naphtholazoamidobenzene
NH2.C6H4.N2.C10H6.OH
„
....
Solid
Meldola
....
47, 662
= 1.4; aa
0-
=1.4 ; 49
u
Powder
„
47, 663
Benzylindolecarboxylic acid
CI6H1302N
....
195
Antrick
A., 227, 360
48, 543
9
C6H4.C6H4.C(CO2H) : C.
183
Tann anrl IVTillAr
Blfi 941 S
Aft OOQ
., 1 u, ^'ij.o
*O> •>-,.!
1 1
CH2.NH2
Ethylnitrosoanthrone
C6H4.CO.C6H4.CEt.NO
n
*«••
135
Liebermann and
B., 14, 475
40, 607
i i
Landshoff
Nitrodiphenylpyrazene
NO,,C6H4.C3N2HMePh=1.4
C16H1302N3
....
Liquid
Knorr and Jodicke
B., 18, 2259
48, 1247
„
=1.2
„
285 (70)
95 ; 105
„
B., 18, 2261
48, 1248
a-benzamidocinnamic acid ....
Ph.CH I C(NHBz).CO2H
C16H1303N
....
131
Plochl
B., 17, 1618
46, 1348
Benzimidoeinnamic acid
Ph.CH.NBz.CH.CXXH
1 {
„
....
225
„
B., 16, 2816
46, 605
Ethylnitroanthrone
C6H4.CO.C,H4.CEt:NOs
5)
....
102
Liebermann and
B., 14, 474
40, 607
Landshoff
Aniidoethoxyanthraquinone
C6H4 : (CO)2 : C6H2.OEt.NK
„
....
182
Liebermann and
B., 15, 1796
44, 73
=2.1 ; 1.2.5.6
Hagen,
Oxyamidohydroisatin
C(OH) : N.c6H4.C(NH2) : c
C16H1303N3
....
d.w.m. 187-
Sommaruga
A., 194, 100
(OH).C6.H4N:C.OH
190
Dihydroisatinamide
M. C., 1, 562
5)
213
5)
A., 194, 88
36, 63
Ethylanthracenehydride
C6H4.C(O.NO)2.C6H4.CEt.
C16H1306N3
....
130 d.
Liebermann and
B., 14, 473; A.,
40, 607 ; 42,
nitrite
O.NO
Landshoff
212, 1
862
Papaveric acid
....
C16H1307N
233
Goldschmidt
M. G, 6, 372
48, 1080
Trinitrobenzamidophenylu r-
N02.C6H4.CO.NH.C6H2
C16H1309N6
....
210
Hager
B., 17, 2628
48, 150
ethane
(N02)2.NH.C02Et
=!•? 1 l-(?)2.4
Hydroisoindileucine ....
Ph.CH(OH).C:N.CPh.
C16H14ON2
....
160
Engler and Hassen-
B., 18, 2243
46, 48
CH : NH L~
kamp
Methylisatintolylimide
C8H4MeNO : N.CGH4Me
„
....
191
Meyer
B., 16, 2268
n
=1.4; 1.2
COMPOUNDS CONTAINING FOUR ELEMENTS.
557
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Methylisatintolylimide
C8H4MeNO : N.C6H4Me
C16H14ON2
....
259
Meyer
B., 16, 2264
46,48
=1.4; 1.4
Lactimide of benzdiamido-
Ph.CH.CH(NHBz).CO.NH
C16H140 N2
....
187
Plochl
B., 17, 1617
46, 1348
hydrocinnamic acid
I |
Phenylaspartic phenylimide
NHPh.C2H3 : (CO), : NPh(?)
„
....
263
Piutti
G. I., 14, 473
48, 796
Ethoxybenzenylazoximeben-
N : CPh.O.N : C.C6H4.OEt
„
....
71
Schoff
B., 18, 2476
48, 1217
zenyl
i i
=1.3
Oxindole
see CSH7ON
„
....
120
Bedson
....
37, 93
Ethylic phenylenamidine-
NH.C6H4.N : C.C6H4.CO2Et
)>
....
242-243
Bruckner
A., 205, 121
40, 93
toluate
i i i - i i
=1.2 ; 1.4
„ „
» »
i»
A., 210, 340
242-243
Stoddard
B., 11, 296
34, 504
NHj on isatin
....
C16H1403N6
....
295-300
Sommaruga
A., 190, 367
34, 507
Benzoylform-'y-amide
O,:(CPh.CO.NH2)2
C18H1404N2
130
Claisen
B., 10, 1665
34, 151
» D
„
„
....
134-135
„
B., 12, 634, 635
36, 649
A cetbenzamidonitro toluene
Me.NO2.NBzAc=1.2.4
„
....
160
Cunerth
A., L72, 221
28, 83
Azophenylacetic acid
N2(C6H4.CH2.CO2H)2=Mix.
„
B., 2, 210
138
Radziszewski
Z. C. [2], 5, 358
vi., 1102
„ „
=(1.4),
„
....
d. w. m. 300
Wittenberg
B. S., 43, 111
48, 661
/3-Azotoluic acid
N2(C6H.,Me.CO2H)2=: (?. 1 .4)2
„
....
182-184
Fittica
B., 7, 1358
28, 265
y- n >i •'••
» »
»
....
w. m.
„
„
„
?
....
„
....
186
Brauns
B., 17, 1134
46, 1038
Azophenoxyacetic acid
N2(C6H4.O.CH2.C02H)2=?
C16H1406N2
....
151-152
Thate
J. p. [2], 25, 267
42, 849
„ „
=(1.2),
„
....
162
„
J. p. [2], 29, 145
46, 1171
Succindiuitranilide
(CH2.CO.NH.C6H4.N02)2
C16H1406N4
260
Hiibner
A., 209, 377
=(1.4),
Dinitrodiacetbenzidine
(.C6H3.NHAc.NO2)2=(1.4.2)2
„
a. 300
Strakosch
B., 5, 237
Azoxyphenoxyacetic acid ....
ON2(CaH4.O.CH2.C02H)2
C16Hl4OrN2
....
186-187
Thate
J. p. [2], 29, 145
46, 1170
=(1.2)2
Trinitrobenzmesidine
fr. C6H2Me3.NHBz
C16H1407N4
....
300
Schack
B., 10, 1711
„
Me3.(NO2)2.(NH.CO.C6H4.
„
....
307
„
„
34, 144
NO2)=1.3.5.2.4.6 ; 1.3
Dibenzylgly collie nitril
(Ph.CH2)C(OH).CN
C16H,,ON
....
113 ; sf. 110
Spiegel
B., 13, 2221
40, 174
a-naphthylamine phenate ...
C10H7.NH2+Ph.OH
„
....
30-1
Dyson
....
43, 468
Aniline-S-naphthate
Ph.NH2+C10H7.OH
„
....
82-4
„
„
Benzoyltetrahydroquinoline
....
»
B., 13, 2400
75
Hoffmann & Konigs
B., 16, 734
44, 1144
Acetophenoneacetanilide ....
Ph.CO.CH2.NAcPh
C16H1602N
....
126-127
Mohlau
B., 15, 2470
44, 333
Phenyl-a-anilidocrotonic acid
Ph.CH : CH.CH(NHP)i).
»
....
154
Peine
B., 17, 2116
46, 1345
Nitroso-p-tolylamido-p-
....
C16H1602N3
t...
a. 220 d.
Duisberg
B., 18, 193
48, 544
methyloxindole
Benzethylbenzhydroxyl-
Ph.CO.O.CPh.NO.Et
C16H16OaN
B., 16, 874
48-49
Pieper
A., 217, 8
44, 461
amine
a-Ethylic dibenzhydroxamate
....
M
....
58
Eiseler
A., 175, 326
28, 766
»- » »
....
„
58
Giirke
A., 205, 280
40, 585
P- » »
„
63
„
A., 205, 281
„
Benzylic hippurate ....
NHBz.CH2.CO2.CH2Ph
M
289-9
85-5-86
Zanna & Guareschi
B., 14, 2242
Diphenylsuccinamic acid
NPh,,CO.C2H4.CO2H
„
....
119
Piutti
G. I, 14, 351
48, 783
Acetylacetoxydiphenylamine
C6H4.OAc.NPhAc=1.4
„
120
Philip and Calm
B., 17, 2437
48, 156
Benzophenoneurethane
C6H4Bz.(NH.C02Et)=1.4
„
189
Dobner and Weiss
B., 14, 1839
42, 177
„
)> J)
„
....
189
Dobner
A, 210, 273
42, 508
Methylic m-diazoamidoben-
C6H4(C02Me).N2.C6H3(NH.!).
C16H1604N3
160
Griess
A., 117, 12
iv., 294
zoic acid
CO2Me
Dianishydroxamic acid
N(CO.C6H4.OMe)2.OH=(1.4)2
C16H1S06N
....
142-143
Lessen
A., 175, 287
28, 636
Nitrobenzonitromesidide ....
Me3.NO2.(NH.CO.C6H4.NO,)
C16HJ605N3
....
207
Hiibner
B., 10, 1711
34, 144
= 1.3.5.2.4; 1.3
a-trinitroazoxypheneto'il
....
C16H1609N5
....
168
Andreae
J. p. [2], 21, 334
38, 467
p~ ,,
u
....
187
„
„
,,
Phenyl-a-anilidocrotonamide
Ph.CH : CH.CH(NHPh).
C16H16ON,
171
Peine
B., 17, 2116
46, 1345
CONH2
p-tolylamido-p-methyloxin-
....
„
166-167
Duisberg
B., 18, 191
48, 544
dole
Diacetylhydrazobenzene
Ph.NAc.NAc.Ph
C16Hle02N2
....
103
Schmidt & Schultz
B., 12, 485
36, 630
I! J! •••• ;i
„
....
105
„
A., 207, 327
40, 909
558
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Ethylpheuylhydrazine-
N3EtPh:CPh.C02H
C16H1602N2
....
109 d.
Elbers
A., 227, 340
48, 534
phenylglyoxylic acid
Ethidine dibenzamide (Hip-
CH3.CH(NHBz)2
I>
185
Schwartz
W. A., 77, 62
36, 650
paraffin)
» » »
J)
)1
....
188
Nencki
B., 7, 159
27, 458
» » )>
M
))
....
200
Schwarz
A., 75, 201
iii., 155
>» » »
»
5)
204
Hepp and Spiess
B., 9, 1425
31, 314
»» »» »
0
>»
....
210
Maier
A., 127, 162
iii., 155
»i » »
>»
J)
....
215
Schwarz
W. A., 77, 62
36, 650
Dibeiizyloxamide
(.CO.NH.UH2Ph)2
»
....
216
Strakosch
B., 5, 694
vii., 182; 25,
1026
Succinanilide .... ....
(.CH2.CO.NHPh)2
A., 68, 27
226-5-227
Menschutkin
A., 162, 187
25 4Q7 • vii
Jl
*"', ^t«7 1 j VIA.,
1183
Diacetdiamidodiphenyl
(.C6H4.NHAc)2=1.2 ; 1.4
J)
....
202
Schmidt & Schultz
B., 11, 1754
36, 252
» » »••'
)» )>
»
....
202
n
B., 12, 489
36, 652
» »
» »
))
202
Schultz and others
A., 207, 356
40, 912
» »
5) »
»
a. 300
Strakosch
B., 5, 237
» »
=(1-4),
))
....
317
Schmidt & Schultz
B., 12, 489
36, 652
»> n
)> »>
»»
....
317
Schultz and others
A., 207, 332
Ditolyloxamide
(.CO.NH.C6H4Me)2=(1.4)2
))
....
263
Hiibner
A., 209, 371
42, 181
»» )j •••»
» )»
»)
....
267-268
Bladin
B. S., 41, 125
46, 1141
»i » >*••
» »
M
300 (60)
269
Willin and Girard
B., 8, 1196
Tolylazo-acetocresol
C6H4Me.N2.C6H3Me.OAc
»
....
91
Nolting and Kohn
B., 17, 354
46, 901
=1.4; ?.1.4
Piperonylidene amidodi-
CH2 : o2 : c6H3.CH : N.c6H4.
»
110
Nuth
B., 18, 575
48, 784
methaniline
NMe2=4.3.1 ; 1.4
Betistenequinoxime
HO.N : c.c14H14.c : N.OH
i i
>»
128-5-129
Bamberger
B., 18, 82
48, 549
?
))
....
187
Gumpert
J. p. [2], 31, 119
48, 656
Biamidohydrindic acid
C16H10N2(OH)2(NH2)S
C16H1602N4
v. C16H1603N4
215-217
Somiuaruga
A., 194, 96
36,63
Ethylic diphenylallophanate
C16H1603N2
....
98
Hofmann
B., 4, 247
24, 393 ; vii.,
408
Diphenylmalamide
NHPh.CO.CH2.CH(OH).
»
175 p.d.
Arppe
A., 96, 107
iii., 797
CO.NHPh
Benzamidophenylurethane ....
NHBz.C6H4.NH.CO2Et=1.4
M
230
Hager
B., 17, 2628
48, 150
p-Toluylnitroxylide
N02.C6H.,Me2.NH.CO.C6H4
))
187
Hiibner
A., 210, 333
42, 504
Me
P- D ,,
" »
»
187
Bruckner
A., 205, 125
40, 94
Benznitromeaidine
Me3.NHBz.NO2=1.3.5.2.4
jj
168-5
Hiibner & Schack
B., 10, 1711
34, 144
Nitrobenzmesidine
Me3.(NH.CO.C6H4.NCg
»
....
205
»)
»
»
=1.3.5.6; 1.3
Diamidohydrindie acid
C16H10N2(OH)2(NH2)2
C18H1608N4
v.C16H1602N4
215-217 d.
Sommaruga
A., 194, 96
36,63
Azoxyacetanilide
0 : N2(C6H4.NHAc)2=(1.4)2
M
275-278
Mixter
A. C. J., 5, 1
46, 301
Glycolphenylcarbamate
C2H4(O.CO.NHPh)2
C16H1604N2
157-5
Snape
47, 773
Tataranilide
[.CH(OH).CO.NHPh]2
»
a. 225
Arppe
A., 96, 106
iii., 798
»
)>
)»
250 d.
»
A., 93, 353
Diphenyltartaramide
[.CPh(OH).CO.NH2]2
»»
browu 150
230 sf. b. 230
Burton
B., 16, 2232
46,63
Ethylenedibeiizamic acid ....
C2H4(NH.C6H4.CO2H)2
||
....
222-225
Schiff and Parenti
A., 226, 243
48, 266
=(1-3),
Diamido-0-dibenzyldicar-
||
280
Reimer
B., 14, 1802
42, 170
boxylic acid
Diuitroazophenetoil
N2(C6H3.OEt.N02)2=(1.2.?)2
C16H1606N4
....
190
Andreae
J. p. [2], 21, 322
38, 466
P- ,, ,,
=?
>»
284-285
J. p. [2], 21, 323
Tetrahydroquinoline metho-
C9HuN+C6H2.OMe. (NO2)3
C16H1607N4
....
125
Ostermeyer
B., 18, 596
)J
picrate
a- + /3-dinitro-p-xylene
2[C6H2Me2(N02)2]
C16H1608N4
....
99-99-5
Januasch and
B., 14, 1146
40, 808
Stiiukel
Acetophenoneethylanilide ....
Ph.NEt.CH2.CO.Ph
C16H17ON
94-95
Waller
B., 16, 26
44. 582
Beiizamidopropylbenzene ....
C6H4.Pr».NHBz=1.4
)j
115
Louis
B., 16, 108
>
Beuzamidoisopropylbenzene
C6H4.Pr?.NHBz=1.4
))
114-115
B., 16, 113
Acetylditolylamine
NAc(C6H4Me)2=(1.3)2
»)
324 (300)
43
Cosack
B., 13, 1092
38, 714
„
=(1-4),
))
....
85
Gerber
B., 6, 446
COMPOUNDS CONTAINING FOUR ELEMENTS.
559
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Benzoyldimethamidotoluene
Me.NMe2.Bz=1.2.2
C16H17ON
350-360
67
Fischer
A., 206, 91
40, 587
p-toluylxylide
C6H3Me2.NH.CO.C6H4Me
„
....
139
Hubner
A., 210, 332
42, 504
P- »
„
„
139
Bruckner
A., 205, 1-24
Benzomesidide
Me3.NHBz=1.3.5.6
M
....
204
Hubner and Schac'
B., 10, 1711
Benzoylpseudocumidine
Me3.Bz.NH2=1.3.4.?.6
n
130
Frohlich
B., 17, 1805
46, 1319
o-Hydroxyhydranthranol-
C14H10(OH).NHEt
H
162
Liebermann & Giese
B., 10, 610
ethylamide
„
„
„
172
Liebermann
A., 212, 18
42, 856
Acetamidoazotoluene
C^Me.N^CiiHjM e.NHAc
C16H17ON3
157
Nolting and Witt
B., 17, 80
46, 742
=1.3; 1.3.6
„
=1.2 ; 1.3.4
„
....
185
Schultz
B., 17, 470
Ethylic phenylanilidoacetate
Ph.CH(NHPh).CO2Et
C16H1702N
83-84
Stockenius
J. [1878], 780
Dibenzylglycollamide
(Ph.CH2)2.C(OH).CO.NH2
„
192-193
Spiegel
B., 14, 1688
40, 1036
Ethylic diphenylglycocine ...
Ph.C6H4.NH.CH2.COjEt
„
95
Zimmermann
B., 13, 1967
40, 176
=1.4
Ethylic phenyllutidinecar-
C5NHPhMe2.CO2Et
„
316-320
Liquid
Hantzsch
B., 17, 2912
48,397
boxylate
Diglyeollanilide
NH(CH2.CO.NHPh)2
C16H1702N3
....
140-5
Meyer
B., 8, 1155
29, 372
Diacetdiamidodiphenylamine
NH(C6H4.NHAc)2=?
H
203 u.c.
Nietzki and Witt
B., 12, 1403
„
=(1.4)2
„
....
239
Nietzki
B., 11, 1099
34,792
Hydroxythymoquinoneani-
Me.Pra.OH.NHPh : O2
C16H1703N
....
134-135
Schulz
B., 16, 902
lide
=1.4.(?)4
Nitrobenzylidenedimeth-
....
C16H1703N3
....
165
Hubner
A., 210, 371
toluylenamidine
Imidodiethylenenitrophenyl
NH(C2H4.O.C6H4.N02)2
C16H17O6N3
191-192
Weddige
J. p. [2], 24, 248
ether
=(1.2)2
Diethoxydinitrodiphenyl-
(OEt)2.(N02)2.NHPh
„
....
133
Nietzki
A., 215, 157
44, 466
amine
=1.4.(?).t
Benzylidenedimethyltoluyl-
....
C16H19ON2
....
144
Hubner
A., 210, 370
enamidine
Tolylglycocinetoluidide
C6H4Me.NH.OH2.CO.NH.
n
....
91-92
Ehrlich
B., 16, 205
44, 594
C6H4Me=(1.2)2
»
=(1.4),
„
136
Meyer
B., 8, 1161
29, 402
Methoxybenzylideneamido-
MeO.C6H4.CH \ N.C6H4.
„
....
139
Nuth
B., 18, 574
48, 784
dimethaniline
NMea=(1.4).,
Acetyltolidine
NH2.C6H3Me.C6H,Me.
H
306 ; 315 c.
Schultz
B., 17, 468
NHAc=1.2.?;?.2.1
Phenylazocarvacrol
Ph.N2.C8HjMePr.OH
„
80-85
Mazzara
G. I., 15, 214
48, 1132
=5.1.42
Phenylazothymol
=? 1.4.3
i)
....
85-90
Mazzara & Posse tto
G. I., 15, 52
48, 894
Paricine „
J. [1852], 536 ; [1879], 793
„
116
Hesse
A., 166, 263
vii., 347
Acetamidobenzeneazodi-
NHAc.C8H4.N!.C6H4.NMe2
C16H18ON4
....
217
Meldola
....
45, 108
methaniline
=(1.4),
Azophenetoil ....
Na(C6H4.OEt)2=(1.3)3
CI6H1302N2
91
Buchstab
J. p. [2], 29, 299
46, 1148
„ (B., 10, 1653)
=(1.8),
„
240
131
Schmitt & Mohlau
J. p. [2], 18, 200
=(1.4),
„
157
Hepp
B., 10, 1653
34,59
(J. p. [2], 19,
» »
„
....
160
Schmitt & Mohlau
J. p. [2], 18, 199
313 ; 21, 320, 333)
Ditoluidoacetic acid
(C6H4Me.NH)2.CH.CO,H
„
239-240
Meyer
B., 16, 925
=(1-2),
Azoxyphenetoil
0:N2(C6H4.OEt)2
CI8H1903N3
....
102
Schmitt & Mohlau
J. p. [2], 18, 200
36, 317
Phenylammonium phenyl-
CO2H.CH2.NPh.CH2.CO3.
C1CH18O4N2
....
99
Meyer
B., 14, 1326
42, 519
amidodiglycollate
NH3Ph
Azodimethylquinol
N2[C6H3(OMe)2]2=(?.1.4)2
„
....
140
Baessler
B., 17, 2124
46, 1330
From Brucine
„
B., 17, 2849
263-264 (?)
Hanssen
B., 18, 778
48, 819
Oxidation of brucine and
....
„
d. 290-291
285
„
B., 18, 1917
strychnine
•
Dinitrotetramethylbenzidine
fr. (.C6H4.NMe2)2=(1.4)2
C16H1904N4
....
188
Michler & Pattinsou
B., 14, 2164
Ethyleneditoluylenenitra-
(N02.C6H3Me.NH)2C2H4
„
....
195
Guttermanu and
B., 17, 779
46, 1142
mine
=(1.3.6)2
Hager
560
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority. Reference.
Watts' Diet.
& J. Ch. Soc.
Iniidodiethylene-o-nitro-
C16H1S06N4
...»
191-192
Weddige
J. p. [2J, 24, 241
40, 1138
phenyl ether
Dinitrohydrazophenetoll ...
(.NH.C6H3.OEt.NO2)2
n
201-202
Andreae
J. p. [2], 21, 325
38, 466
Ethylethoxydiphenylamine
C6H4.OEt.NPhEt=1.4
C16H19ON
318-320
Liquid
Philip and Calm
B., 17, 2434
48, 155
Isobutoxydiphenylamine ...
C6H4.OBu0.NHPh=1.4
„
68
„
B., 17, 2435
48, 156
Dianisamine ....
NH(CH2.C6H4.OMe)2
C16H1903N
A., 117, 240
32-33
Cannizzaro
C. R, 50, 1100
i., 297
G'amphoranil ....
116
Laurent & Gerhard
A., 68, 36
?-acid
I
C16H1904N
....
70-75
A., 134, 324
Benzoylecgonine
C9H14BzO3N
„
188-5-189
Merck
B., 18, 1594
48, 997
„ ....
„
»»
192 (?)
Skraup
M. C., 6, 556
48, 1249
„
„
„
+4H,0
90-92
„
»J
„
Cyanethine carbauilide
C9H13N2.NH.CO.NHPh
C16H20ON4
....
184
Meyer
J. p. [2], 30, 115
48, 140
Dioxydimethaniline
(.O.C6H4.NMe2)2
C16H2002N2
....
90-4
Hanimann and
B., 12, 681
36, 714
Hanhart
Hydrazophenetoll
(.NH.C6H4.OEt)a=(1.2)a
„
.«.
89
Schmitt & Mohlau
J. p. [2], 118, 203
„
=(l-3)2
),
91
Buchstab
J. p. [2], 29, 299
46, 1148
Diamidodiphenetofl
(.C,H,.OEt.NHs)a=?.1.2
„
....
117
Mohlau
J. p. [2], 19, 383
ImidodiethyleHephenyl ether
....
C16H20O4N2
....
197
Weddige
J. p. [2], 24, 241
40, 1137
nitrate
Tetramethoxydiamidodi-
[.C6H2(OMe)2.NH2]2=(1.4.?)2
„
...•
210
Baessler
B., 17, 2127
46, 1330
phenyl
Homatropine (Oxytoluyltro-
..»•
C16H210SN
A., 217,82
95-5-98-5
Ladeuburg
B., 13, 107, 1086,
38, 815
peiu)
1340
Conilinephthamic acid
C8H16 :N.CO.C6H4.C02H=1.2
n
115
Piutti
G. I., 13, 542
46, 453
Hydroxybenzyluric acid
....
C16H2I05N
60-70
Otto
A., 134, 324
vi., 722
Glucocoumarylmethylket-
C6H4(O.C6HU05)(CH:CH.
C16H2107N
173
Tiemann and Kees
B., 18, 1966
48, 1074
oxime
CMe I NOH)=1.2
Diethoxybenzidine
(.C6H3.NH2.OEt)2=(1.4.2)2
C16H2202N2
....
117
Mohlau
J. p. [2], 19, 381
36, 939
Ethylic phenylizinacetosuc-
....
C16H2204N2
....
80
Knorr and Blank
B., 17, 2051
46, 1380
cinate
Methamidoperezone
C9H17.C6H(OH)(NHMe); O2
C^HjAN
....
112-114
Mylius
B., 18, 940
48, 778
Oxyacanthine
B. J., 17, 267
C16H2306N
B., 15, 2745
139
Wacker
J. [1861], 545
Base
C16HJ402N2
..i*
165-170
Bell
B., 11, 1812
Acetyldiisobutylaniline
C6H4BuP.NAcBu3
C16H2SON
a. 300
73-74
Studer
B., 14, 1473, 2187;
40, 898
A., 211, 241
Acetamido-n-octylbenzene ....
C3H17.C6H4.NHAc=1.4
....
93
Beran
B., 18, 135
48, 523
Imidocaprylamide
C6H13.CH.NH.CH(C6H13).
C16H3002N2
....
79-5
Eyleniueyer and
A., 177, 111
28, 1018
CO.NH.CO
i
Sigel
Imidocaprylic acid
NH[CH(C6H13).C02H]2
C16H3104N
210-215 d.
A., 177, 136
28, 1017
Heptyl-n-octoyl carbamide....
C7H15.NH.CO.NH.C8H16O
C16H3202N2
86
Hofmann
B., 15, 760
42, 1053
Palmitamide ....
C15H3l.CO.NH2
C16H33ON
101-5
1 f\ a i f\>j
Carlet
B. S. [1], 1, 175
Bi e -i >7Qr\
iv., 330
Cetylic nitrate (nitroethal) ....
._.
))
iUo— 107
s. 10-12
Krafft and Stauffer
Champion
.j lOj 1 i oU
C. R, 73, 571
42, 1274
24, 1036 ; vii.,
861
Triisoamylcarbamide
C5Hn.NH.CO.N(C5Hu)2
C16H34ON2
260
Liquid
Custer
B., 12, 1331
36, 913
Anthraquinolinequinone
G6H4:(co)2:c6H2.CH:cH.
C17H902N
185
jrsebe
A., 201, 350
CH:N
i
Quinophthalone
subl.
235 u.c.
Traube
B., 15, 298
44, 668
Alizarin blue (B., 11, 1371 ;
c6H4:(co)2:c6H(OH).,N:
c17n"o4N
270
Graebe
A., 201, 336
15, 1783)
CH.CH:CH2=2.1 ; 1.2.3.4.6
« i.
B. S., 28, 62 ; J. [1878], 1192
268-270
Auerbach
35,801
„ „ (amide)
....
C17H1003N2
255
Grsebe
A., 201, 343
Benzenyl-^-amido-a-naphthol
C10H6.O.CPh : N=a, 3, ;
' i
C17HUON
....
122
Worms
B., 15, 1816
44, 69
>, -«- -B- „
„ =ft a, ;
1)
120
B., 15, 1817
„ -«- -ft- „
»
136
Bottcher
B., 16, 1936;
44, 1113; 48,
a-nitroso-0-benzoxynaphtha-
C10H6(NO).OBz=a1 ft ;
C17HU03N
114
Worms
C.C. [1884], 898
B., 15, 1817
659
44, 69
lene
COMPOUNDS CONTAINING FOUR ELEMENTS.
561
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
/S-nitroso-a-beiizoxynaptha-
C10H6(NO).OBz=p>1 ;
C17HU03N
d. 140-150
Fuchs
B., 8, 1022
29, 247
lene
8- ,, -o-
„ „
,,
....
162
Worms
B., 15, 1816
44, 69
a-nitro-8-benzoxynaphtha-
C10H6(NO2).OBz=a8
C17Hn04N
....
142
Bottcher
B., 16, 1935 ;
44, 1113 ; 48,
lene
C. C. [1884], 898
659
Benzamidodinitronaphtha-
C10H5(N02)2.NHBz=(?)2a
C17HU05N3
252
Ebell
A., 208, 329;
28, 900; 40,
lene
B., 8, 564
1132
Fr. 8-naphthaquinone-p-
C17Hn(NH)N02
C17H1203N2
260-265
Zincke
B., 15, 287
42, 735
toluide
8-benzamidonitronaphthalene
C10H6(N02).NHBz=Sla1 ;
C17H1203N2
....
174-176
Ebell and Hiibner
B., 7, 1318; 8, 562;
28, 272, 900;
A., 208, 327
40, 1132
8-
„ „
„
....
174
Worms
B., 15, 1815
44,69
8-
„ „
„
....
175
Lellmann
B., 17, 109
46, 751
»- »
1) ala2 »
„
....
224
Ebell and Hiibner
B., 7, 1318; 8,563;
28, 272, 900;
A., 208, 325
40, 1132
a- „
»l )»
„
....
224
Worms
B., 15, 1814
a- „
» .)
„
....
224
Lellmann
B., 17, 110
46, 751
8-naphthol-m-azobenzoic acid
HO.C10H6.N,,C6H4.C02H
„
....
235
Griess
B., 14, 2035
42, 49
Fr. 8-naphthaquiuone-p-
C17H12(NO)NOS
„
240-245
Zinck6
B., 15, 287
42,735
toluide
Methylisato'id
v. B., 15, 2100
C17H1204N2
....
219 d.
Baeyer and ^Econi-
B., 15, 2094
44, 201
mides
Nitro-8-naphthaquinone
C10H4(N02)(OH).O.NC6H4Me
TJ
240
Brauns
B., 17, 1136
46, 1038
-o-toluide
i i
,. 11 -P- ,.
,,
w
241
„
B., 17, 1136
„
Nitrodicinnamylketone
CO(CH:CH.C6H4.N02)2
C^AN,
....
254
Baeyer and Becker
B., 16, 1970
44, 1120
m-Phenylpyridine picrate ....
C6H4PhN+C6H2(NO,,)3.OH
C17H1207N4
...
161-163-5
Skraup & Cobenzl
M. C., 4, 436
44, 1013
0- „ „
„
„
....
169-172
„
„
44, 1015
P- ,, >,
„
D
d. a. 220
195-196
Hantzsch
B., 17, 1519
46, 1194
Benzamidonaphthalene
C10H7.NHBz=a
C17H13ON
....
156
Ebell and Hiibner
A., 208, 324;
88, 272
B., 7, 1318
»
J> »
„
....
I
Church
C. N., 5, 324
„
)• »
„
....
156
Worms
B., 15, 1814
••**-.
„
.. »
„
161-162
Kiihn
B., 18, 1477
„
=9
„
....
141-143
Cosiner
B., 14, 59
40,606
„ ....
)J IT
„
157
Klopsch
B., 18, 1585
48, 990
a-naphthoic anilide
C10H-(CO.NHPh)=a
JT
160
Hofmaun
B., 1, 42
» w
» »
»)
160
Bossneck
B., 15, 3065
p- „ ,,
» --P
„
....
170 or 190
Vieth
A.. 180, 323
30, 87
8-naplitholadehydeanilide ....
HO.C10H6.CH : NPh
„
90
Rousseau
A. C. [5], 28, 145
46, 180
Phenylquinaldylketone
N.Me.Bz=a,8, ; o,
n
107-108
Geigy and Konigs
B., 18, 2406
48, 1236
o-amidodiphenylmethylpy-
....
C17H13ON3
....
261
Knorr and Blank
B., 18, 2262
48, 1248
razonecarboxylic anhy-
dride
Oxyquinonemethylimide
C16H9(OH).O.NMe
C17HI302N
170
Breuer and Zincke
B., 13, 631
38, 665
1 1
a-naphthylic phenylcarba-
NHPh.CO2.C10H7
)T
177
Leuckart & Schmidt
B., 18, 2340
48, 1224
mate
"- n »
„
„
....
178-5
Snape
....
47, 776
H" ;> »
„
„
....
155
„
TT
P~ ji »
»
JJ
....
230
Leuckart & Schmidt
B., 18, 2340
48, 1224
Benzoxynitrosonaphthalene
C10H6.NO.OBz=a8
»
....
98
Bottcher
B., 16, 634
Benzamidonaphthol
C'i0Hr,.OH.NHBz=a8(2)
158
Ebell
A., 208, 332
„
=8a
„
....
245
Bottcher
B., 16, 1936;
44, 1113; 48,
C. C. [1884], 898
659
Methylnaphthaquinoneani-
Ph.NMe.C10H5:02
„
».i
150-151
Zincke
B., 15, 282
42, 735
lide
a-Naphtliaquiiione toluide ....
C6H4Me.NH.CIOHs : 0,=1.2
„
....
140-142
Elsbach
B., 15, 689
42, 853
°- ,, n
,.
T)
....
190-195(2)
»
»
H
4 c
562
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
o-naphthaquinone toluide ...
C6H4Me.NH.C10H6 ::O,=1.4
C17H,302N
200
Plimpton
37, 639
"- >» »
i> n
„
....
200
Zincko
B., 12, 1646
38,49
n- „ „
» „
It
....
202-208
Elsbach
B., 15, 687, 688
p- „ ,,
=1.2
„
...
240
„
B., 15, 287, 689
P- ,, *, •"
=1.4
„
B., 15, 1969
246
I!
B., 15, 287, 686
Quinolinebenzylbetaine
CTT /TTT C* *~r^TT XT/f TT THiN
g-d4.V^JIL.V^ . V^Jl.l'I^O±l2JL li).
M
83-84 ; r.s
Glaus and Muchall
B., 18, 364
48, 561
110; af
O.CO=1.2
1
190 d.
Benzylquinolineearboxylic
N(CH2Ph).COiH=a1p'2 ;
„
218
Glaus
B., 18, 1310
48, 908
acid
Acetamidomethylanthra-
C6H4 : (CO)2 :C6H2Me.NHA
C17HU0,N
176-177
Romer and Link
B., 16, 699
44, 1139
quiuone
=2:1; 1.2.4.5
Ethylic phthalamidobenzoate
C6H4 :(CO)2: N,C6H4.CO2Et
C17H1304N
....
152
Pellizzari
B., 18, 216
48, 534
=1.2; 1.3
Nitrodiphenylmethylpyra-
NO2.CaH4.CsN2MePh.C02H
C17H1304N3
202
Knorr and Jodicke
B., 18, 2258
48, 1247
zene carboxylic acid
=1.4
» »
=1.2
„
218
„
B., 18, 2260
DinitromesitylphthaJimide
C6F+:(CO)2:N.C6Me3(N02)2
C17H13O6N3
242
Eisenberg
B., 15, 1018
42, 956
=1.2; 2:1.3.5.4.6
•/-trinitrotoluene naphthalene
C10H9.C6H2Me(N02)s.
n
....
88-89
Hepp
A., 215, 378
44, 318
"- » »
„
,r
97-98
„
^
w
ft- » )!
»
M
....
100
-
jt
Trinitrocresol naphthalene ....
C10H8-fC6HMe.OH.(N02)3
C17H1307N3
106
Nolting and Collin
B., 17, 271
46, 1007
=l.2:4.(?)2
n n
„ =1.3.2.4.6
»»-
....
126-127
Kostanecki and
B., 18, 252
48, 531
Niemetowski
„ „
„ ()
,,
126-127
Nolting and Salis
B., 15, 1862
44, 59
(3-methylnaphthalene picrate
eioH7Me+C6H2.OH.(N02)3
>,•
115
Schulze
B., 17, 844
46, 1184
"- >t ,1
„
„,
116
„
B., 17, 845
n
»-
„
n
116-117
Ciamician
B., 11, 272
34, 439 ; 40, 824
'-
„
„
118-2 c.
„
W. A., 82, 346
40, 247
>» »
• n
„
119'
Goldschmidt and
W. A., 83, 7
40, 824
Schidt
Trinotroorcinolnaphthalene
C10Hs.C6Me(OH)2(N02)3
C17H1808N3
120^
Nolting and Salis
B., 15, 1863
Phenylmethylhydroxypyri-
C11H10ON2.C6H2.OH.(N02)3
017H1308N6
....
189
Pinner
B., 18, 761
48, 752
midine picrate
Methylisoindileucine
C16HnMeON2
C17H14ON2
115
Engler and Hassen-
B., 18, 2243
48, 1223
kamp
Benzenea/zomethoxynaph tha -
Ph.N2.C10H6.OMe=a2o1 ;
r)
....
83
Zincke and Binde-
B., 17, 3028
lene
wald
Benzdiamidbnaphthalene
C10H6.NH2.NHBz=aia,, ;
„
B., 7, 245
186-
Ebell and Hiibner
B., 7, 1318; A.,
28, 272 ; 40,
208, 326
1132
, »
,r
186
Lellmann
B., 17, 110
Tolufurfuraldehydine
....
C17H1402N,
115-116
Ladenburg
B., 11, 595
34, 572
»
19
128-5
B., 11, 1658
36, 234
Difurfuro-m-diamidotoluene
C6H3Me(N : C6H40)2
d.w.m. 120
Schiff
A., 201, 360
38, 392
Methoxynaphthaquinone-
C10H5(OMe)O : N2HPh
B
174-175
Zinck6 and Thelen
B., 17, 1812
46, 1360
hydrazine
Isomethyldiphenylpyrazene
....
194 d.
Knorr and Blank
B., 18, 933
48, 810
carboxylic acid
Methyldiphenylpyrazene
C3N2MePh2.C02H
205
B., 18, 313
48, 556
carboxylic acid
Ditolylparabanic acid
CO[.N(C6H4Me).CO.]2=(1.4);
C17H1403N2
l*u
144
Landgrebe
B., 10, 1590
34, 217
J! )>
=(1.2),
..
202-5-203-5
Berger
B., 12, 1856
38, 244
u.c.
Phenylhydrazine-fl-benzoyl-
C,H4.CO.N,Ph:C.(CH,)2.
210
Roser
B., 18, 804
48, 797
propiocarboxylic acid
1 1
CO2H=1.2
Acetylfurfurine
Dinitrotoluene naphthalene
Nitromesitylphthalimide
C10H8+C6H3Me(N02)2
C6H4:(CO)2:N.C6HMe3.N02
C1?H1404N2
chare. 240
250 d.
60-61
210
Schiff
Hepp
Eisenberg
B., 10, 1189
A., 215, 380
B., 15, 1018
34, 46
44, 318
42, 956
=1.2; 4.1.3.5.6
COMPOUNDS CONTAINING FOUR ELEMENTS.
563
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Gh. Soc.
?-picrate
(C11H11N)+C6H3.OH.(N02)3
C17H1407N4(?)
....
170
Beyer
J. p. [2], 31, 47
48, 672
Tetrauitro-a-ditolylpropionio
C17H14010N4
....
223-225 d.
Haiss
B., 15, 1478
42, 1071
acid
Beuzalplithalethimidine
NEt.CO.C6H4.C : CHFh=1.2
C17H15ON
....
75-77 ; sf. 70
Gabriel
B., 18, 2435
48, 1229
Pseudocumylplithalimide ...
C6H4 : (CO)2 : N.C6H2Me3
C17H1502N
a. Hg.
148
Frohlicli
B., 17, 1803
46, 1318
=1.2; 6. 4.3.1
Mesitylphthalimide
„ =1.2; 6.5.3.1
JJ
....
171
Eiseiiberg
B., 15, 1017
42, 956
Phenanthrenequinimidace-
see orig. paper
»
....
130
Japp & Streatfield
B., 16, 282
41, 271, 274
toue
Acetamidomethylanthranol
)»
»
....
170
Romer and Link
B., 16, 706
Oxalylditolylguanidine
NH:C[.N(C6H4Me).CO.]2
CWHU<^NI
188-5
Landgrebe
B., 10, 1589
34, 216
=(1.4)2
»»
=(1.2),
5)
....
206-207-5 u.c.
Berger
B., 12, 1856
38, 244
Amidodiphenylmethylpyra-
NH2.C6H4.CjN2MePh.CO2H
»
251
Knorr and Jodicke
B., 18, 2259
48, 1247
zene carboxylic acid
= 1.4
Phenylcumazonic .acid
N : CPh.O.CMe.j.C.Hj.COjH
i i
C17H1503N
....
219-220
Widmann
B., 16, 2586
46, 304
=1.2.5
Chelerythrin (Sanguinarin)....
....
C17H1604N
160
Richter
R. K. T., 382
Acetyluitrolapachic acid
C15H12O2.NO2.OAc
G17H1506N
B., 16, 802
166-168
Paterno
G. I., 12, 337
44, 211
Acetylsalicylethylene nitro-
NO2.C6H4.O.C2H4.O.CO.
Q,7H1507N
80
Wagner
J. p. [2], 27, 218
phenyl ether
C6H4.OAc=(1.2)2
Diraethamidoquinoline pi-
C9H6N.NMe2+C6H2.OH.
C17H1607N6
....
215
Coste
B., 16, 673
44,811
crate
(N02)3=ai; ft; 1.2.4.6
Citraconanilide
C5H402(NHPh)s
C^-H^O^
B., 14, 2789
175-5
Strecker
B., 15, 1641
42, 1281
Itaconanilide
)»
))
A., 77, 282
185
n
ji
u
Mesaconanilide
)»
»)
....
185-7
j»
>»
»
Diacetamidofluorene
C13H8(NHAc)2
JI
....
d. 250
Schultz
A., 203, 101
38, 814
1 )iacetyloxybenzy lidine
AcO.C6H4.CH: N2AcPh=l,2
Q17H1603N2
....
133
Roasing
B., 17, 3006
48, 389
phenylhydrazine
I )iacetdiamidobenzophenone
))
....
226-5
Staedel& Pratorious
B., 11, 744; A.,
34, 671; 36,
194, 360
319
Benzoylacetylphenylethenyl-
AcO.CHPh.C(NH2) : NOBz
C17H1604N2
165
Gross
B., 18, 1079
amidoxime
Dibenzdiamidopyroracemic
....
»
....
172 d.
Bb'ttinger
B., 14, 1599
40, 1032
acid
Ethylic nitrobenzalphthalimi-
NOj-CPh: C(NH2).C6H4.C02
n
....
154-155
Gabriel
B., 18, 2441
48, 1230
dinate
Et=1.2
? (ortho)
....
>>
....
144
Brauns
B., 17, 1136
46, 1038
? (para)
....
»
....
222
»
n
)>
BenzamsuccinanDide
NHPh.CO.C2H4.CO.NH.
»)
....
252
Pellizzari
B., 18, 214
48, 533
CfiH4.C02H=1.3
Diacetylresorcinolazotoluene
C6H4Me.N2.C6H3(OAc)2
)?
....
74-75
Wallach & Fischer
B., 15, 2825
=1.2; J.1.3
»
=1.4;?.1.3
»
98
»i
B., 15, 2821
Dinitro-a-ditolylpropionic
....
C17H160,N2
1294
Haiss
B., 15, 1476
42, 1071
acid
Ethoxyquinoline picrate
N.OEt=a, ; o,
C17H1609N4
....
180-181
Fischer and Renouf
B, 17, 759
46, 1049
Toluidine-0-naphthol
C6H4Me.NH2. + C10H7.OH
C17H17ON
....
80-5
Dyson
....
43, 468
Acetamidomethylanthracene
C14H10Me.NHAc
n
198
Roemer
B., 16, 1634
44, 1137
dihydride
Deoxybenzo'incarboxyletha-
Ph.CH2.CO.C6H4.CO.NHEt
C17H1702N
139-140
Gabriel
B., 18, 1258,2435
48, 903
mide
=1.2
Acetonebenzilimide
»
176
....
Japp and Miller
47,24
Hydroxylamiue on acetone-
....
017H1703N
....
146
!>
47, 25
benzil
Eugenolphenylcarbamate ....
NHFh.C02.C6H3.OMe.C3H5
)>
....
95-5
Snape
....
47, 777
Benzoylnitrosothymol
Pr«.Me.OBz.NO=1.4.6.?
»»
....
110
Schiff
B., 8, 1501
29, 583
Cumo-salicylamide
>5
J. [1856], 502
200
Field
A., 65, 45
ii., 178
Phthalopseudocumidic acid....
C6H2Me.,.NH.CO.C6H4.C02H
»
....
179 d.
Frohlich
B., 17, 1809
46, 1320
=1.3.4.6; 1.2
Morphothebaine
H | ..-
190-191
Howard
B., 17, 530
46, 1201
4 c 2
364
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Benzethylanishydroxylamine
MeO.C6H4.CO.CPh ! NOEt
C17H1704N
B., 16, 875
64
Pieper
A., 217, 10
44, 4G1
=1.4
a-Ethylic benzanishydroxa-
NBz(CO.C6H4.OMe).OEt
n
69
Eiseler
A., 175, 336
28, 767
mate
=1.4
a- „
IJ »
„
....
74 u. c.
Pieper
A., 217, 2
44, 461
P" >i >i
....
„
89
„
A., 217, 4
„
a-Ethylic anisbeuzhydroxa-
....
„
Liquid
„
A., 217, 7
niate
ft- )> »
„
A., 217, 7
79
Eiseler
A., 175, 337
28, 767
Auisethylbenzhydroxylamine
MeO.C6H4.C (I NOEt).O. UO.
„
B., 16, 875
93-94
Pieper
A., 217,15
Ph
Ethylic phenyllutidinedicar-
C5NPhMe.2.C02Et.CO2H
j>
....
179-180
Hantzsch
B., 17, 2909
48, 397
boxylate
Ethylic ethylenenitrophenol-
N02.C6H4.O.C2H4.O.C6H4.
Cl;H1700N
....
81
Wagner
J. p. [2], 28, 220
46, 435
oxybenzoate
CO3Et=1.4 ; 1.2
» »
=1.2 ; 1.2
J)
100
„
J. p. [2], 28, 212
„
i) »
=1.2 ; 1.4
„
....
103
„
J. p. [2], 28, 222
„
,, >'
=1.4 ; 1.4
It
131
„
J. p. [2], 28, 224
„
Phenylhydrazineacetophen-
see B., 17, 2764
C1?H18ON2
unstable
abt. 105
Paal
B., 17, 2764
48, 250
oneacetone
Ethyleneditolylcarbamide ....
CO[N(C6H4Me).CH2.]2
„
....
228
Michler and Keller
B., 14, 2184
42, 183
=(1.4)a
Dimethyldiphenylmalona-
CH3(CO.NMePh)2
C17H1802N2
....
109
Freund
B., 17, 137
46, 729
mide
Methylenediphenylacetamide
CH2(NH.CO.CH2Ph)2
„
205
Hepp
B., 10, 1650
34, 66
Phthalopseudocumidamide ....
C6H2Me3.NH.CO.C6H4.CO.
„
218
Frohlich
B., 17, 1807
46, 1319
NH2=1.3.4.6 ; 1.2
Nitrobenzisocymidide
Me.PrP.NHBz.NO2=1.3.(?)2
C17H1S03N2
177
Kelbe and Warth
A., 221, 157
46,47
Butylacridine nitrate
C13H8BuN-)-HNO3
„
139
Be rnthsen & Traube
B., 17, 1509
46, 1183
Phenylhydrazinephenylloe-
....
C17H1804N2
140
Weltner
B., 18, 793
48, 794
vulinic acid
?
CO[O.N: C(NH2).CHPh.OH].,
„
131
Gross
B., 18, 2481
48, 1219
Diethamidobenzophenone ....
Ph.CO.C6H4.NEt2=1.4
C17H19ON
78
Dobner
A., 217, 266
44, 861
Benzisocymidide
Me.Pr/3.NHBz=1.3.?
M
165
Kelbe and Warth
A., 221, 157
46,46
Thymotic aldehyde anilide ....
Me.Pr°.OH.(CH I NPh)
„
....
142
Kobek
B., 16, 2098
46, 56
=1.4.3.6
Ethylic phenyltoluidoacetate
C6H4Me.NH.CHPh.CO2Et
C17H1903N
Liquid
Stockenius
J. [1878], 781
=1.2
., »
=1.4
J)
89-90
,,
n
Benzoylcarvoxime
C10H14 : NOBz
„
95
Goldschmidt and
B., 18, 1730, 1732
48, 1058
Ziirrer
Phenylethenylphenylurami-
Ph.CH2.C(NH.CO.NHPh) :
C17H1902N3
148
Knudsen
B., 18, 2482
48, 1218
doxime ethyloxide
N.OEt
Azobenzenediethamidoben-
Ph.N2.C6H3.(NEt2).C02H
„
125
Griess
B., 10, 526
32, 455
zoic acid
=?.1.3
Hydroxythymoquinonetolu-
Me.Pr«.OH.NHPh : O2
C17H1903N
164-165
Schulz
B., 16, 902
ide
=1.4.2.3.5.6
Piperine (J. [1854], 525 ;
....
n
A., 74, 204
100
Pelletier
Gm., 7 492
iv., 658
[1857], 413)
„ (A., 77, 204; 95,107)
....
„
J. [1877], 891
abt. 110
Wackenroder
Br. Arch., 37, 347
u
C13H903.N(C5H10)
„
synthetical
127-128
Eiigheimer
B., 15, 1391
42, 1217
. -I
10O 1&Q'K
Ethylphenylhydroxyethenyl-
HO.CHPh.C(NOEt).NH.
C17H1903N3
DoiuUZcU
±iCo—J.&iJ O
119
Gross
B., 18, 2479
jj
48, 1218
phenyluramidoxime
CO.NHPh
Oxymorphine....
....
C17H1904N
....
245
Schiitzenberger
B. S. [2], 4, 1 76
vi., 841
Colchicin
....
C17H1905N
....
140
Hiibler
C. C. [1865], 536
vi., 482
C17H2306N
»
....
145
1 A li
Hertel
B., 14, 1412
c
• •••
))
....
14o
Eichter
E. K. T., 383
C16H2306N3 or C23H21OnN
„
....
163
Hondes
C. B., 98, 1442
46, 1055
....
)»
+H20
93
Colchicem J. [1864], 451
C17H2106N
+2H2O
150
Hertel
B., 14, 1412
If
»
M. C., 4, 162
155
Oberlin
J. [1856], 519
COMPOUNDS CONTAINING FOUR ELEMENTS.
565
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference!
Watts' Diet.
& J. Ch. Soc.
Diphenyldiethylcarbamide .
NEt2.CO.NPh2
C17H20ON2
....
54
MichJer
B., 9, 711
30, 290
i)
CO(NEtPh)2
»»
....
79
i>
B., 9, 712
)J
Di(phenethyl)carbamide
NH2.CO.N(CH2.CH2Ph),
?)
J. [1879], 44
108-109
Spica
G. I., 9, 555
38, 242
Benzenyldiethylphenylen-
06H,.N : CPh.NEt.OH=?
n
A., 210, 360
132
Hiibner and Simo
B., 12, 1243
36, 923
i i
amidine
»
» )>
5?
....
136
Howe
A. C. J., 5, 418
46, 741
Tetramethdiamidobenzo-
CO(C6H4.NMeo)2
))
152
Michler and Moro
B., 12, 1169
36, 921
phenone
j)
»
n
179 u. c.
Michler
B., 9, 717
30, 298
•>j
»
;>
....
179
Michler& Dupertiu
B., 9, 1900
32, 334
Di(ethylphenyl)carbamide ..
CO(NH.C6H4Et)2=(1.4)2
»
217
Paucksch
B., 17, 2804
48, 256
Cuminylplienylcavbamide ..
NHPh.CO.NH.C6H3MePr
j»
146
Eaab
B., 8, 1151
29, 399
Dixylylcarbamide
CO : N2H.,(C6H.iMe2):,=4.3.1
»
n.f. 250
Genz
B., 3, 226
vil., 1210
Dinitropodocarpinic acid ..
f r. C9H15.C6H2Me.OH. CO2H
C,7H20O7N2
....
203
Oudemanns
A., 170, 229
=1.2.4.3
Nitrosotetramethdiamido-
fr. CH2(C6H4.NMe2)2
C17H21ON3
165
Michler and Moro
B., 12, 1171
36, 921
diphenylmethane
Apoatropine (atropatropeme
CH2:CPh.CO.C8H14NO
C17H2102N
B.; 16, 243
60-62
Pesci
G. I., 11, 538, 547
42,740
C'innamyltropeine
....
»»
A., 217, 100
70
Ladenburg
B., 13, 1085
38, 715
Nitrosodimethylaniline cyan
....
C17H2102N5
221
Lippmanu and
M. C., 6, 537
48, 1213
hydrin
Fleissner
Piperidine piperate
CdHuN.C12H1004
C17H2104N
100
Babo and Keller
J. p., 72, 53
iv., 656
Coca'iu (impure)
....
)J
A., 133, 351
75
Truphene
C. C. [1881], 447
42,75
,, .... .... ..
)>
J. [I860], 36
98
Niemann
A., 114, 213
i., 1060
98
Merck
B., 18, 2265
?
)>
))
...• «
74
Pinner
B., 14, 1077
Diethylic hydrofurfuryllu-
N.C4H30.(CO2Et)3.Me2
C17H,AN
....
164
Schiff and Puliti
B., 16, 1608
44, 1151
tidine dicarboxylate
=1.2.3.5.4.6
Colchice'in
see Cl;H19O6N
»
Nitropodocarpinic acid
see CnH2(lOjN2
J»
205
Oudemanns
A., 170, 226
Tetramethdiamidobenzhydro
HO.CH(C6H4.NMe2)2
C^H^ON,
....
96
Michler and
B., 9, 1900
32, 334
Dupertius
Tetramethdiamidodiphenyl-
CO(NH.C6H4.NMe2)2
C^H^ON,
....
246
Michler and Zim-
B., 14, 2179
42, 182
carbamide
=(1-4),
mermann
i>
» »
!»
262 d.
Binder
B., 12, 536
36, 628
Hyoscyamine ....
C,THrtoON
89
Blyth
33, 316
17 23
90
EEolm & Reichardt
A., 157, 98
24, 149 ; vil.,
»
664
105
Schmidt
i, 14, 157
u
108'5
Ladenburg and
B., 13, 254, 381
38, 482
»
Meyer
J. [1878], 894
OS'S
jadenburg
C. R., 90, 874
38, 561
)>
i., 14, 1870
OS'S
B., 13, 109, 607
38, 411
Atropine (Daturine)
....«
M
»
v. 140 p. d.
90
»)
i., 474
,, }i •••• "*.
....
»i
....
97
Blyth
33, 316
» »
rom diff. sources
)>
....
7-99
'esci
G. I., 10, 495;
40, 293; 42,
11,59
634
„ „
»
i>
....
06-108
»
1)
j»
„ ,,
j)
)»•
....
09-110
j>
)>
H
„ „ •••• •".
....
»
05-108
jadenburg and
B., 13, 381
38, 482
Meyer
„ „ .... —
....
n
....
13-5
jadenburg
B.,12,492;13,104
38, 411
j i» •"* ....
....
»
A., 217
73-5
jadenburg and
B., 13, 380
38, 482
Meyer
,, „ .... ....
'rom diff. sources
j>
12-5-115-5
chmidt
B., 13, 370
38, 481
» »
....
»>
....
15-115-5
»
B., 14, 156
5) 3> ••'• '•••
....
)>
15-5
Ladenburg
B., 12, 942
Paeudoatropine (Atrolactyl-
n
....
19-120
n
A., 217, 87
44, 671
tropeine)
V 1)
)»
ttl
5)
B., 15, 1027
12, 984
Hyoscine
5.. 14. 1870
?
B.. 13. 254. 1554
38, 674
•r»66
ORGANIC COMPOUNDS.
Name,
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Beuzamsebacic acid
OO2H.C6H4.NH.CO.C8H16
C17H2305N
192-193
Pellizzari
B., 18, 216
48, 534
CO2H=1.3
Acetyltolyl-n-octylauiine ...
C8H17.C6H3Me.NHAc
C^ON
....
81
Beran
B., 18, 147
48, 524
Cerebrine (J. p. [2], 24, 325,
C8H1M0liN (?)
C17H3303N(?
....
155-160
Gobley
J. P. [4], 19, 346
27,909
328)
Alkaloid from lupin seed ...
»•*
C,7H34ON2
216
....
Siewert
25, 519
vii., 758
» ,,
....
C17H3602N2
216
....
Beyer
Lw., 14, 161
„
Dioenanthotriure'id
CO(NH.C7H14.NH.CO.NH2)
CI7H3603N6
....
162
Schiff
A., 151, 189
Dinitrochrysoquinone
C18HS(N02)2:02
C18H806N2
....
230
Adler
B., 12, 1893
38, 263
Tetranitrochrysene
C18H8(N02).,
C18H908N4
A., 158, 307
a. 300
Schmidt
J. p. [2], 9, 283
27, 989
Dinitrochrysene
C1SHIO(N02)2
C1SHI004N2
....
a. 300
Schmidt
J. p. [2], 9, 282
„
a-Phenylpyridine ketoue pic-
C12H7ON+C6H2.OH.(N02)3
CI6H1007N3
....
195-199
Skraup & Cobenzl
M. G, 4, 436
44, 1016
rate
Nitrochrysene
C18H,,.N02
(WAN
A., 158, 306
209
Schmidt
•J. p. [2], 9, 281
27, 988
Phthalic quinaldine (qnino-
C6H4.C.CO.C6H4.CO.C.
„
234-235
Jacobsen & Reimei
B., 16, 1083
44, 922
line yellow)
i
CMe:N=(L2)2
Ethenylacetylamidoalizarin
N: CjHa.o.c6H(OAc) : (co)2:
(WAN
....
238-240
Reimer
B., 18, 1666
48, 1068
Trinitrodiphenylbenzene ....
fr. C6H4Ph2=1.4
(WAN,
....
190
Schmidt & Schultz
B., 11, 1755
36, 163
i) „
» »
n
195
„
A., 203, 127
40, 435
Trinitroisodiphenyl benzene
„ =1.2 (?)
„
....
200
„
A., 203, 130
„
Acenaphthene picrate
C12H8+C6H2.OH.(N02)3
(W^jX,
201-202
Behr and Dorp
A., 172, 263
27, 1168
M „ ....
„
„
....
201-202
Blumenthal
B., 7, 1093
Phenanthroline picrate
C12H8N3-fC6H2.OH.(N02)3
C18H1107N6
....
238-240
Skraup-aad-'Vort-
M. C., 3, 570
44,87
mann
?
C6H:02(NO)(NH.C6H4.N02)2
„
245
Zinck6
B., 16, 1557
44, 1117
Diacetyl /3-nitroalizarin
C14H5(N02)(OAc)i:02
C18Hn08N
....
218
Schunck & ROnier
B., 12, 587
36, 654
Diphenylene oxide picrate ....
C6H4.C6H4.0=1.2
(WAN,
94
Goldschmidt and
M. C., 2, 14 ; 3,
48,617
1 (
Herzig
126
Dinitrodiphenyl benzene ....
fr. C6H4Phj.=1.4
C18H1204N2
....
264
Schmidt & Schultz
B., 11, 1755
36, 163
» »
„ „
)J
277
„
A., 203, 125
40, 435
Trinitrotriphenylamine
N(C6H4.N02)8
C18H1206N4
280
Heydrich
B., 18, 2157
48, 1213
Dinitropolyporic acid
*...
C18H,203N2
....
230
Stahlschmidt
A., 195, 369
Acetylphenyluaphthylear-
C10H6.C6H4.NAc
C18H13ON
121
Grsebe and Knecht
A., 202, 7
bazole
1 1
Nitrosonitrophenylazo-
fr. NO2.C6H4.N2.C6H4.NHPh
C18H1303N5
....
127-128
Meldola
45, 119
phenylaniline
=1.3; 1.4
-» >,
„ =(1.4),
....
sf. 161
169-170
„
m
Pulvamic acid
....
C18H1304N
....
220
Spiegel
B., 13, 1633
40,97
Diacetylamidoalizarin
c6H4:(co)2:c6H(OAc)
C18H1306N
....
268-271
Romer
B., 18, 1668
48, 1069
(OH).NHAc
Diphenyl picrate
Phj+C.Hj.OETXNOj),
C18H1307N3
....
94
Goldschmidt and
W. A., 83, 7
40, 824
Schidt
Acenaphthene picrate
„
„
• •••
160
n
h
Nitrosophenylamidoazoben-
Ph.N(NO).C6H4.N2.Ph
C18H14ON4
....
119-5
Witt
B., 12, 261
35, 187
zene
Phenolbidiazobenzene
(Ph.N2.)2C6H3.OH (?)
„
«...
131
Griess
A., 137, 87
37, 572; 42, 726
Benzeneazoacetoxynaphtha-
Ph.N2.Cll)H6.OAc=a2a1 ;
CWAN,
120
Ziuck6
B., 16, 1564
44, 1135
l«ne
» »
» »
M
....
128
Zinck6 & Bindewald
B., 17, 3030
|3-Indogenide of ethylpseud-
NH.C6N4.CO.C:C.C6H4.
n
....
197-198
Baeyer
B., 16, 2200
46,76
isatin
NEtCO
i
Nitroresorcinol on aniline
....
„
....
238-239
Fevre
C. R., 96, 790
44, 734
acetate
Kynurin
(C9H7ON)2 q.v.
)>
....
201
•Schrniedberg and
25, 1028
vii., 716
Schultzein
(.CHj.CrO.N.CPhrN),
GWA'N4
160
Schulz
B., 18, 2463
COMPOUNDS CONTAINING FOUR ELEMENTS.
567
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Dinitrosodiphenyl diamido-
C6H4(.NPh.NO)2=1.3
C18H140,N4
....
102
Calm
B., 16, 2798
46, 592
benzene
Nitrobenzeneazod iphenyl-
NO..C6H4.N2.C6H4.NHPh
))
....
136-137
Meldola
....
46, 116
amine
=1.3 ; 1.4
» »
i, =(l-4)2
15
151
»
43,440
46, 121
Benzenebidiazophenol
C6H4(.N2.C6H4.OH)2=(1.4)3
1)
sf. b. 205
205-207
»
....
47, 660
a-Benzeneazobenzeneazores-
Ph.N2.C6H4.N2.C6H3(OH)2
»
183-184
Wallach & Fischer
B., 15, 2818
orcinol
&- i) »
»)
H
215
!>
)i
a-Bidiazobenzeneresorcinol ...
(Ph.N2.)2C6H.(OH)3
)*
215
Wallach
B., 15, 25
42, 610
a- „
5»
»)
213-215
Wallach & Fischer
B., 15, 2816
0-
)J
»>
220
j>
B., 15, 2817
0-
)»
»j
225
Wallach
B., 15, 25
42,610
y- „
u
»
....
220-222
Liebermann and
B., 17, 880
46, 1147
Kostanecki
Acetoxynaphthaquinonehy-
C10H5(OAc)O : N2HPh
C18H14OaN2
178-179
Zinck6 and Thelen
B., 17, 1812
46, 1360
drazine
Acetylamido-0-naphthaquin-
....
»
....
215
Zinck6
B., 15, 285
oneanilide
Diuitrophenylbenzidine
NH2.C6H4.C8H4.NH.C6H3
C^H^O^
....
245
Willgerodt
B., 9, 981
30, 405
(N02)2=(1.4)2; 1.2.4
» .... ....
„ =»
>»
255.
Austen
A. J. S., 13, 279
32, 762
Acetyl-0-naphthylplienyl-
C10H-.NPhAc
C18H16ON
93
Streiff
A., 209, 157
amine
„ -a- i)
)»
)J
115
»
A., 209, 154
1
,, -o- »
»
»
115
«
B., 13, L852
40, 176
Benzoylmethyl-a-naphthyl-
C10H7.NBzMe
)?
121
Hess
B., 18, 687
48, 784
amine
» -0- »
)>
»
169
»>
B., 18, 688
»
0-uaphthoic toluide
Cl(1H..CO.NH.C6H4.Me=1.4
»
.„.
191
Vieth
A., 180, 324
30,87
Diabzobenzene-0-naphthyl-
C.oHy.NAc.Nj.Pb
C18H15ON3
152-153
Lawson
B., 18, 799
48, 803
acetamide
Methoxy-/3-naphthoic anilide
MeO.C10H6.CO.NHPh
CuHuOjN
....
169
Leuckart & Schmidt
B., 18, 2340
48, 1224
„ -a- i) »
»>•
J)
21&
»
))
))
Ethyl-/3-naphthaquinone
C10H4EtO2.NHPh
I)
....
104
Zincke
B., 14, 1496
40, 916
anilide
» » »
»»
?t
....
104
»
B., 15, 282
42,735
a-naphthaquinone ethylanilide
02 : C10H6.NEtPh=(ia£
It
155
Elsbach
B., 15, 1810
44, 70
0- » »
=afia
J*
....
165.
»
B., 15, 691
42, 853
Methyl-0-naphthaquinone-
....
»
150
Zinck6 and Brauns
B., 15, 197,0
44, 209
toluide
Oxyquinone ethylimide
C16H9(OH).O.NEt
»
....
129-130
Breuer and Zinck6
B., 13, 632.
33, 665
Acetylflavenol
CH : CMe.C6H4.N : C.C6H4.
M
....
128
Besthorn & Fischer
B., 16, 69
44, 600
OAc=(1.2),
Dicinnamhydroxamic acid ....
N(CO.CH : CHPh)3.OH
C^AN
....
152
Rostoski
A., 178, 219
28, 273
Amylic cyanurate
MM
C18H1603N3
200 d.
Hofman and Ols-
P. E., 18, 493
vii., 410
hausen
0- naphthyldimethylpyroline-
NCCwH^MMCO.H),
C18H1604N
d. 260
Knorr
B., 18, 308
48, 555
dicarboxylic acid
=1.2.5.3.4
(3-ethylnaphthalene picrate....
C10H.7Et-|-C6H2.OH.(N02)3
CuH.^N,
....
69
Brunei
B., 17, 1180
46, 1035
1- „ „ ....
)»
n
71
Marchetti
G. I., 11,439
42, 410
a- „ „
)1
;)
08
Carnelutti
B., 13, 1672
40, 280
a- „ „
)J-
»>•
....
98
Fittig and Eemsen
A., 165, 119
40, 824
a- „ „
»
m
....
99
Goldschmidt and
W. A., 83, 7
n
Schidt
Dimethylnaphthalene picrate
CloH6Me2+C6H2.OH.(N02),
H
R, 16, 428
139
Cannizzaro and
G. I., 12, 393
44,80
Carnelutti
»> »
)>
n
139
Giovannozzi
G. I., 11, 147
42, 855
Guaiene picrate
CliH12+C6Hs.OH.(N02)8
)»
123
Botsch
M. C., 1, 609
42, 211
5C8
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Benzeneazo-a-ethoxynaph-
Ph.N2.C10H6.OEt=a1ai, ;
C18H16ON2
....
98-100
Zinck6 and Binde
B., 17, 3028
thalene
wald
Nitrosobenzazo-|3-ethafflido-
Ph.N2.C10H6.NEt.NO(?)
C18H16ON4
....
97
Henriques
B., 17, 2670
48, 168
naphthalene
Acetyl-p-tolyl-p-methylpseu-
see original paper
C18H160SN2
....
121-122
Duisberg
B., 17, 197
48, 544
doimesatin
Ethoxynaphthaquinonehy-
C,0H6(OEt).O.N2HPh
)»
....
172-173
Zincke and Thelen
B., 17, 1812
46, 1360
drazine
Benzoylanilidopyrotartar-
....
C18H1603N2
....
190
Wechsler
B., 18, 1042
48, 900
imide
Nitrophthalic isocymidide ..
fr. C6H4:(COVN.C6H,Me
C18H1604N2
167
Kelbe and Warth
A., 221, 157
46,47
Pr0=1.2; ?.3.1
Ethylic furfurincarboxylate
016Hn(C02Et)03N2
CI8HI605N2
124
Bahrmann
J. p. [2], 27, 318
Dinitrodiethylcarbobenzonio
....
C18H1606N2
....
155-156
Zagoumenny
A., 184, 170
32, 194
acid
Ethylic dinitroazobenzoic
N2(C6H3.NO2.C02Et)2=l.?.3
C18H1608N4
....
104
....
J. E., 6, 197
acid
/3- phe namidoethoxy naphtha-
C10H7.O.C2H4.NHPh
C18H17ON
....
75
Koelle
B., 13, 1955
40, 178
lene
Apocinchene ....
209-210
Koniffs
B., 14, 1855
42, 224
Phthalic isocymidide
C6H4 : (CO)2 : N.C6H3MePr
C18H1702N
145
j" &w
Kelbe and Warth
A., 221, 157
46, 47
=1.2; ?.3.1
Apochinine ....
....
J»
....
246
Comstock & Konig
B., 18, 1227
48, 911
Oxyapociuchene
....
»
217
11
B., 18, 2385
»i
»
267
Konigs
B., 14, 1858
42, 225
Methoxyphenylimidoaceto-
(MeO.C6H4.CH(CN)2)N2H
C18H1702N3
....
123
Voswinckel
B., 15, 2025
44, 190
nitril
=(1.8),
Ethyl-p-tolyl-p-methylpseu-
see original paper
C18HiaON2
....
151-152
Duisberg
B., 18, 199
48, 544
doimesatin
Ethylic azobenzoate
N2(.C6H4.C02Et)2=<1.4)2
C13H1804NS
A., 132, 148
88
Fittica
B., 8, 252
28, 766
11 11
» Jl
»J
....
88
51
J. p. [2J 13, 184
36, 152
„ ,,
=(1.3)2
)>
b. 100
Strecker
A., 129, 139
vi., 321
11 ,,
11 I*
)»
90-92
J. R, 6, 251
»> 11
» »i
J)
97
Fittica
B., 8, 252
28, 766
„ ,, .... ••«•
11 >i
»»
....
99
»
J. p. [2], 13, 184
36, 152
11 11
= ?
I>
....
102
11
)»
11
11 11 ....
=(1.2),
IT
138-139
11
))
11
Diuitrotetramethylbenzidiue
fr. (.C6H4.NMe2)2=(1.4)2
C18H1804N4
....
188
Michler& Pattinson
B., 17, 118
46, 747
Citro-dianilic acid
....
C18H1805N2
153
Pebal
A., 82, 89 ; 98, 89
Dinitrosuccino-p-toluide
fr. (.CH2.CO.NH.C6H4Me)2
C18H1806N4
217
Hiibner
A., 209, 381
42, 181
Aeetylbenzoylpseudocutni-
Me3.Bz.NHAc=1.3.4.l6
C18H1902N
170
Frohlich
B., 17, 2674
48, 154
dine
Oorydalin ....
J. [1859], 570 ; B. J., 7, 220
C18H1904N
A., 64, 369
130
Wicke
A., 137, 274
vi., 497
Ethylic m-diazoamidoben-
....
C18H1904N3
...i
144
Griess
A., 117, 11
iv., 293
zoate
Ethylic benzoate+ethylic
....
C18H1906N
282-285
Liquid
Fittica
B., 10, 488 ; J. p.
32, 483 ; 36,
nitrobenzoate
[2], 13, 184
153
Ethylidene phenylacetamide
Me.CH.(NH.CO.CH2Ph)2
C^H^N,
IIM
227-228
Bernthsen
A., 184, 318
31, 619
Quinol+ aniline
2(Ph.NH2) + C6H4(OH)2
»
»...
89-90
Heberaud
B., 15, 1973
44, 61
=1.4
Succinotoluide
(.CH2.CO.NH.C6H4Me)2
)»
*••«
100
Bechi
B., 12, 323
86, 528
=(1.2)2
ii
=(1-4),
))
A., 126, 165
256
11
11
11
11
» 11
»
....
256
Hiibner
A., 209, 380
42, 181
Oxalylxylide
.CO.NH.C6H3Me2)2=(?.4.1)2
J)
....
w. m. 125
Schaumann
B., 11, 1538
36, 51
11
=(4.3.1)2
))
204
Genz
B., 3, 227
Methylphthalopseudocumid-
C6H2Me3.NH.CO.C6H4.CO.
))
....
215 d.
Frohlich
B., 17, 1808
46, 1319
amide
NHMe=1.3.4.6 ; 1.2
Hydrokynurin
»...
))
100
Kretschy
W. A., 83, 171
40, 829
Diacetyl-?
CHH14Ac2N2
)»
212-216 d.
Kliuger
B., 16, 945
Cinchotenicin ....
....
C18H2003N2
d. 180
153 u. c.
Hesse
B., 11, 1984
Cinclioteuin ....
A., 176, 232 ; As., 7, 349
JJ i
+ 3H2O
197-198 c.
Skraup
A., 197, 378
COMPOUNDS CONTAINING FOUR ELEMENTS.
569
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
C'iuchotenidine
cf. B., 14, 1892
C18H2003N2
+3H20
256 c. ; d.
Skraup and Vort-
A., 197, 237
36, 949
niann
I) !)
....
.„
....
256
Skraup
B., 11, 1519
Ethylene acetamidophenyl
C2H4(O.C6H4.NHAc)2=(1.2)2
C18H2004N2
....
226
Wagner
J. p. [2], 27, 204
46, 435
ether
Diacetamidodihydroxystil-
[HO.C6H4(NHAe).CH : ]2
,,
....
a. 300
Japp and Hodker
45, 680
bene
Nitrocodein .
....
C18H2006N2
A., 77, 358
211-214
Gerichten
A., 210, 105
42, 313
1
C H O N
255
Knapp and Schultz
A., 210, 185
Diacetdiamidotetracetoxy-
C6(OAc)4(NHAc)2
(V^o'oN.
240 p. d.
Nietzki and Benc-
B., 18, 504
48, 780
benzene
kiser
Benzamidoisoamylbenzene ...
C6H4(C5Hu).NHBz
C18H21ON
....
146-149
Merz and Weith
B., 14, 2346
», ..
„
„
....
146-149
Calm
B., 15, 1645
„ „
„
„
....
144-145-5
„
Isobutylbenzamidotoluene ..
Me.Bu0.NHBz=1.3.6
jj
....
168
Effront
B., 17, 2322
48, 152
Methylthymotic aldehyde
Me.Pr«.OMe.(CH:NPh)
„
....
80
Kobek
B., 16, 2100
46, 56
anilide
= 1.4.3.6
Diglycolamidic ditoluide
NH(CH,,CO.NH.C6H4Me)2
C18H2102N3
....
149-5
Meyer
B., 8, 1155
29, 372
=(.1.4),
Codei'n
cf. C. E., 92, 1140, 1228
CJ8H2103N
+H20
150
Robiquet
A., 5, 109
....
„
A., 77, 341
1153
Richter
R.K. T., 394
B. 15 2259
155
Ger. Pharm., 1882
Diethylic phenyldimethyl-
NPh.Me2.(CO2Et)3=1.2.5.3.4
C^O.N
280 (50)
37-38
Knorr
B., 18, 303
48, 555
pyrroline dicarboxylate
Beuzenyldiethyltoluylene-
....
CjsH^ONj
....
152-153
Hiibner
A., 210, 375
amidine
Xylylamidoacetxylide
C6H3Me2.NH.CH2.CO.N H.
„
....
128
Ehrlich
B., 16, 206
44, 594
C6H3Me2=1.3.?;?3.1
Curaylazocumenol
C6H2Me3.N2.C6HMe3.OH
„
....
147-148
Liebermann and
B., 17, 885
46, 1147
—1.3.4.6 ; ?.1.3.4.6
Kostanecki
Diphenylaminephenate
2C6H4(NH2)24-Ph.OH
C^H^ON,
....
113
Griess
P. T., 1864, 667
iv., 433
Bidimethamidophenylox-
(.CO.NH.C6H4.NMe2)2
C18H.!2O2N4
....
nf. 270
Sendtner
B., 12, 533
36, 627
amide
=(1.4),
Tolylammonium tolyldigly-
CO2H.CH2.N(C6H4Me).CH2.
C^H^O^.,
original mis-
168-109
Meyer
B., 14, 1324
42,519
colamidate
C02NH3.C6H4Me=(1.4)2
print
H
„
ji
....
166-168
Schwebel
B., 10, 2047
,(
Diethylic phenyldimethyl-
see orig. paper
j>
....
127
Knorr
B., 18, 305
48, 555
pyridazindicarboxylate
Pheuylarabinosazone
....
C18H22Q4N4
....
157-158
Scheibler
B., 17, 1732
46, 1287
Phenylgalactosazone
....
„
....
170-171
„
n
„
....
„
....
182
Fischer
B., 17, 582
48, 53
Phenylglucosazone
....
„
....
204-205
„
B., 17, 579
„
. ,,
....
„
MM
206
Tiemann and Kees
B., 18, 1660
Diethylic phenylizinsuccino-
NPh.NH.C.CH2.CH(CO2Et).
C18H2205N2
159-160
Knorr and Biilow
B., 17, 2054
46, 1380
succinate
CO.CH2.CH.CO2Et
Nupharin
C^AN,,
....
s. 40-45 ;sf. 65
Griining
A. P. [3], 20, 582;
44,370
B., 16, 969
*
Menispermin ....
....
D
....
120
Pelletier & Couerbe
A., 10, 198
Paramenisperniin
....
'
250
„
A., 10, 200
Diethylic phenylizindiaceto-
NPh.NH.CMe.CH(CO2Et).
C^HsAN,
....
91
Knorr and Biilow
B., 17, 2058
46, 1381
succinate
U -1 CHAc(CO2Et).
Oxyhexinamide
C18H2105(NH2)5
C18H310SN5
....
214-215
Demarcay
A. C. [5], 20, 490
Isoxyhexinamide
„
N
240 d.
„
A. C. [5], 20, 492
Oleamide
C^H^ON
J., 1859, 368
s. 75
Carlet
B. S., 1, 73
iv., 191
H
J., 1855, 532
79-81
Rowney
7,200
,,
Elaidamide
no c\A
J. [1855], 532
Riciuoleamide
C18H3AN
aA—a**
66
Bouis
A. C. [3], 44, 96
Riciuelaidamide
C. G., 1855, 361
JJ
91-93
Rowney
J. [1855], 533
v., 109
Octyluonoxylcarbaraide
....
C19H3602N2
....
97
Hofmann
B., 15, 760
42, 1053
Stearamide
C17H35.CO.NH2
C18H37ON
J., 1859, 367
s. 107-5
Carlet
B. S., 1, 79
v., 412
,,
" i
_
.... .
107
Hofmann
B., 15, 984
4 D
570
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Stearamide
C H CONH
C1SH37ON
109
Kraft't and Stauffer
B., 15, 1730
42, 1274
Amidostearic acid
C17H34(NH2).o6.,H
C13H3702N
....
63
Gautier and Etard
C. R, 97, 263
46,89
Tetranitro-aurin
C19H10(N02)403
C19H10OnN4
140
Ackermann
B., 17, 1626
46, 1339
Furfurenylamidophenanthrol
O^H4.C6H4.C:c'.N:C(04H30).0
C19Hn02N
231
Japp and Wilcock
....
39, 227
1 1
Di(nitrophenylacetylene) di-
Ac.CH(CiC.C6H4.NO2)2
019H120BN2
d.w.m. 165
Baeyer & Landsberg
B., 15, 213
42, 972
methylketone
=(l-2)2
Acridine picrate
C13H9N+C6H2.OH.(NO,)3
C19H1207N4
....
begins 208
Anschiitz
B., 17, 438
46, 908
/3-naphthoquinoline picrate....
»
»
....
251-252
Skraup & Cobenzl
M. C., 4, 436
44, 1011
Phenylhydroxylacridine
OPh.C6H4.N.C6H3.OH
C19H13ON
brown 260
incompletely
Hess and Bernthsen
B., 18, 696
48, 801
=1.2; 1.2.5
275
p-methylquinophthalone
fr.CcH4 :(CO)2:CH.C9H5MeN.
C19H1302N
....
203
Jacobsen & Reimer
B., 16, 2603
46, 335
Benzoyldinitrodiphenylamine
Bz.N(C6H4.N02)2=(1.2)2
U19H13O6N3
not pure
Lellmann
B., 15, 829
42, 1060
„
=(l-4)2
„
A., 132, 167
224
„
B., 15, 828
„
Benzoyldinitroamidodi-
fr.Ph.C6H3.NHBz.N02=1.4.?
„
A., 209, 346
206
Liiddens
B., 8, 873
28, 1258
phenyl
Trinitrotriphenylmethane ....
CH(C6H4.NO,)3(?)
C19H13O6N3
....
203
Hemilian
B., 7, 1206
28, 153
»
J)
„
...»
206-207
Fischer
A., 194,254
36, 384
a-Fluorene picrate
r.C6H4.CH2.C6H4=(1.2)2(?)
C19H1307N3
....
79-80
Fittig and Schmitz
A., 193, 134
37, 717
°- » »
=(1.2), or
H
....
80-82
Grsebe
A., 174, 194
„
1.2; 1.4
/3- „ „ .... ~.
=1.2; 1.3
„
....
80-82
Barbier
A. C. [5], 7, 486 ;
31, 71 ; 26,
or 1.2; 1.4
C. R, 77, 442
1226
p- » „
>! n
„
....
81
Earth and Gold-
G. J. C., 1878
vii., 524
schmidt
y » .1
=(1.3),
„
....
79-80
Carnelley
....
37, 717
?
= ?
n
....
80
Fittig and Schmitz
A., 193, 115
36, 164
Trinitrotriphenylcarbinol ....
HO.C(C6H4.N02)3(?)
„
A., 194, 256
171-172
Fischer
B., 11, 1079
34, 384, 791
Methylphenanthroline
C13H10Na+C6H,,OH.(N02)3
C19H1307NS
i*.*
253
Skraup and Fischer
M. C., 5, 253
48, 393
picrate
Trinitrophenylicorthoformate
CH(O.C6H4.N02)3=(1.2)3
CuHlsO,Nj
....
182
Weddige
J. p. [2], 26, 445
44,340
i,
=(1-4)3
„
232
„
J. p. [2], 26, 446
Benzoxyazobenzene
Ph.N2.C6H4.OBz
C19H140^8
•*•*
136
Tschirvinsky
B., 6, 561
26, 1027 ; vii.,
151
Ethylic phenyleneamidine-
...*
H
242-243
Bruckner
A., 205, 121
p-toluate
» it
J)
242-243
Hiibner
A., 210, 340
Beuzoylnitrodiphenylamine
NPhBz.C6H4.N02=1.3 or 1.4
C19H1403N2
129
Lellmann
B., 15, 826
42, 1059
Nitrobenzamidodiphenyl ....
Ph.C6H4.NH.CO.C6H4.N02
....
142-143
Liiddens
B., 8, 873
28, 1258
=1.4; 1.3
H
" >»
143
A., 209, 346
Trinitrotriphenylguanidine
N02.C6H4.N:C(NH.C6H4.
C^'AN,
....
189
Losanitsch
B., 16, 50
44, 583
N02)1!=(1.3)3
Methylcarbazole picrate
(C6H4)2:NMe+C6H2.OH.
C19H1407N4
141
Grsebe and Alders-
A., 202, 23
38, 660
(N02)3
kron
Diphenylbenzamide ..„
Ph.CO.NPb2
C19H16ON
B., 15, 1288
176
Wallach
A., 214, 193
44, 49
»
H
„
....
176-5-177
Bernthsen
A., 192, 13
34, 788
»
H
H
...
....
Hofmann
A., 132, 166
!>
„
B., 15, 3013
180
Glaus
B., 14, 2368
Benzamidodiphenyl
Ph.C6H4.NHBz=1.4
n
Liiddens
B., 8, 872
28, 1258
"
" j»
„
....
226
Hiibner
A., 209, 345
»
„
230
Zimmermann
B., 13, 1968
40, 176
Nitroisodiphenylbenzenyl-
PhjN.CPhlN.NO
c H"ON
167-169
Bernthsen
A., 192, 18
34,789
amidine
Triphenylcarbamide
NHPh.CO.NPh
C19H16ON2
136 u.c.
Michler
B., 9, 398, 715
Benzoyldiphenylhydrazine ...
Ph2N2HBz
192
Fischer
A., 190, 178
34, 313
Phenoldiazobenzenediazo-
toluene
Ph.N2.C6H3(OH).N2.C6H4
Me(?)
C19H"6ON4
....
110
Griess
B., 9, 628
30, 416
Phenylbidiazomethoxy-
benzene
(Ph.N2.)2Cr.H3.OMe=1.3.4
" .
110
Nolting and Kohn
B., 17, 368
46, 902
COMPOUNDS CONTAINING FOUR ELEMENTS.
571
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Phenylbidiazocresol
(Ph.N2.)2C6H2Me.OH
C19H16ON4
....
114-115
Nolting and Kohn
B., 17, 364
46, 902
=(2)2.1.2
„
=(2)2.1.3
»
....
149
>,
B., 17, 367
ii
Azobenzene-azo-p-cresol
Ph.N2.e6H4.N2.C6H3Me.OH
»
....
160
»
B., 17, 354
46, 901
Auilidoniethoxyquinone
C6H2(OMe)(NHPh).O.NPh
C19H1602N2
•»»•
188-189
Ziuck6
B., 18, 788
48, 787
"1 * J
L J
anilide
Diauilidotoluquinone
C6HMe(NHPh)s:O2
»J
....
232-233
n
B., 16, 1559
44, 1118
ni-Nitrotriphenylguauidine....
fr. Ph.N:C(NHPh}2
CI9H1002N4
....
159
Losanitsch
B., 16, 50
44, 583
a,-Azotolueneresorcmolazo-
06H4Me.N2.C6H2(OH)3.N2Ph
)>
....
189
Wallach
B., 15, 26
48,610
beuzene
"r »
)>
M
.«.
195-196
Wallach and Fischer
B., 15, 2821
0-
»
ii
....
204-206
»)
B., 15, 2822
«•>- i;
»
H
....
a. 200
Wallach
B., 15, 26
42, 610 .
af l>
»>
j>
....
240-241
Wallach and Fischer
B., 15, 2822
a,-Azobenzeneresorcinolazo-
»»
»
....
195-196
»
B., 15, 2823
toluene
0-
n
j»
....
197-198
n
B., 15, 2824
«i- 11
H
»
....
240-241
11
11
Ethylic |3-naphtholazobenzo-
HO.C10H6.NJ.C()H4.C02Et
C19H19O3N2
....
104
Griess
B., 14, 2035
42,49
ate
=1.3
Acetyl ?
..f i
»
190-191
Zinck6
B., 15, 287
42,735
Propylanilido-;3-naphtha-
PrO.C10H5.O.NPk
Ci9H1702N
....
103-104
H
B., 15, 283
quinone
Isopropylanilido-/3-naphtha-
Pr00.C10H6.O.NPh
»
....
99-100
11
11
quinone
1 '
Ethyl toluido-/3-naphthaqui-
EtO.C10H,.O.N.C,H4Me=1.4
»
....
132-133
11
B., 15, 287
none
i i
11 ii
11 »
i>
135-137
Zinck6 and Brauns
B., 15, 1970
44, 209
Nitrodiamidotriphenylme-
N02.C6H4.CH(C6H4.NH2)2
C19Hn02N,
pm
136
Fischer and Ziegler
B., 13, 672
38, 662
thane
=1-3 j 0),
j3-uaphtholazo-p-acetotoluide
HO.C10H6.N2.C6H3Me.NHAc
)J
.*»*
275-276
Wallach
B., 15, 2830
Diacetylamidomethylanthra-
CH.C6H4.C(OAc).C6H2Me.
C19H170SN
170
Rbmer and Link
B., 16, 706
44, 1138
i
nol
NHAc
Cusparin
no
„.. O.TJ.-1, •
GT 1 ^ ^fi**
Aft O-ll
"••
)?
1...
Va
Jvorneroc xJonringer
. -L.j lo, OOO
**O, O-±l
Methylapocinchenic acid ....
1)
....
233-234
Comstock & Konigs
B., 18, 2384
48, 1249
Benzenylisodiphenylamidine
Ph2N.CPh : NH+HNO,
CI9H1703N32
....
115
Bernthsen
A., 192, 1
34, 788
nitrate
Chelidonine
A., 29, 123, 131
J1
130
Will
A., 35, 113
i., 850
Ethylic nitrodiphenylmethyl-
N02.C,H4.C3N2MePh.CO2Et
ClaH1704N3
• ».*
128
Knorr and Jodicke
B., 18, 2258
48, 1247
pyrazene carboxylate
=1.4
5> >1 11
=1.2
»»
MM
146
i,
B., 18, 2260
48, 1248
Diamidotriphenylcarbinol ....
HO.CPh(C6H4.NH2)2
C19H18ON2
A., 217, 241
b. 100
Dobner
B., 15, 234
42, 957
Benzaldehyde-fbenzidine ....
(.C6H4.NH2)2+C6H5.OH
n
....
231-232
Schiflf
B., 11, 832
34, 668
Ethylic isomethyldiphenyl-
see orig. paper
C19H180SN2
110
Knorr and Blank
B., 18, 932
48, 810
pyrazene carboxylate
Ethylic methyldipheuylpyra-
n
n
121-122
n
B., 18, 312
48, 556
zene carboxylate
Acetomorphotheba'ine
C19H1804N
183
Howard
B., 17, 531
46, 1202
Phenylcarbamidol
....
C19H19ON,
a. 200
Lossen
B., 6, 1394
27, 255
Pararosaniline
HO.C(C6H4.NH2)3=(1.4)3
»
A., 194, 274
abt. 180
Grcebe
B., 12, 2142
„ ( A. C. (5), 8, 192)
» »
)>
....
200
Zimmermann and
B., 17, 2936
Muller
Ditamin
cf. A. 203 147
CTT -n "vr
A 1 *7Q f^£t
19Jd19U2JN
brown 130
75 u.c.
J obst and Hesse
A., 1 7o, OD
Dihydrocinchonine
....
C19H20ON2(?)
202-203
Comstock & Konigs
B., 17, 1996
46, 1384
Ditoluyldiaruidopyroracemic
C19H2004N2
145
Bottinger
B., 14, 1600
40, 1033
acid
Ornithuric acid
C4H7(NHBz)2.COsH
J>
B., 11, 406
182
Jaffe
B., 10, 1925
34,584
Diethylic carboxamidoben-
CO(NH.C6H4.CO2Et)2
C1,HtoOiN1
....
160-5
WachendoriF
B., 11, 702
vii., 166
zoate
=(1.3)2
» »
» »
n
....
162
Griess
J. p. [2], 4, 294
25, 81
4 D '2
S72
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Benzpseudocumene urethane
Bebirine
D .... ....
Thebain
Diethylic pheuyllutidine di-
carboxylate
Benzylnitroarbtitin
Apoquinamine
Cinchonidine ....
Me3.Bz.(NH.CO2Et)
=1.3.4.?.6
A., 86, 184; 153, 61; 176,19
J., [1866], 823; [1867], 525
N.Ph.Me2.(CO2Et)2
=1.2:4.6.3.5
B., 114, 413
A.,82,147; 135)333; 207, 310
=Cinchonidine M.C., 2, 345
slowly heated
quickly heated
C6H3Me(OH)2+2Ph.NH2
cf. B., 15, 37.9
Z. C. [1869], 594
N3HPh:CH.C6H4.O.C6H1105
=1.2
N(C6H4Me).Me2.(COEt)2
=1.2.5.3.4
N.Ph.Me2.(CO2Et)2
=1.2.4.6.3.5
(.C6H4.NH2)2+C6H13.COH
CO(NH.C6H4Pr«)2=(l.4)2
CO(NH.C6H2Me3)2=?
„ =(6.5.3.1)2
C19H210,N
»)
J)
»•
C;9H2104N
C19H21O9N
U^H^ONj
)»
)V
5»
')
»'
))
»»
JV
i»
»-
)>
»»
»
))
)V
I»
n
j»
jj
»
)>
ji
j)
C19H2202N2
»
))
C19H2203N2
C.^AN,
C19H2206N4
C19H2206N,.
C19H2303N
»>'
»
C^BL^N
1)
C19HMON2
»
»
»
»
j>
As., 8, 264
+aq.
B., 16, 384
+2 or 1H20
+2H20
+4H20
+H20
105
180-
198
193
12-5
66-67
142-143 d.
114 u.c.
175-
199-200
200-201
201-203
200
205 u.c.
206-5
208 u.c.
210-5 c.
206-207d;u.c
203-205
203-205
205
205-206
206-5 c.
209 u. c.
225 d. ; u. c.
150
165
236
248-252
240-250
260
268-8
82-85
137 u. c.
160 u. c.
177 u. c.
58
240-246 d.
292 d. ; u. c.
118
187
83
118-5
118-5
121
67
156-157
113-115
205
a. 290
a. 300
abt. 124
184
Frohlieh
Maclagan
Planta
Hesse
Schiff and Puliti
Schiff
Hesse
»
»
»
Glaus and, Weller
Hesse
»
»
Skraup and Yort-
mann
Hesse
Glaus and Bock
Glaus and Buchler
Hesse-
n
u
»
»
Schwabs
Hesse
»
)».
Eichter
Skraup
Hebebrand
Hesse
ji
JT
Hofmann
Forst & Bohringer
Skraup
Hesse
Tiemann and Kees
jrimaux
»
Hesse
j»
Cnorr
Schiff and Puliti
Schiff
<Yancksen
ilngel
Sisenberg
Jesse
»
B., 17, 2675
A.,48, 111; 55,10
A., 77, 333
A., 153, 61
B., 16. 1608
G. I., 13, 538
A., 207, 294
A., 205, 197
B., L4, 1891
B., 14, 1889
B., 14, 1924
A., 181, 58
A., ?, 325
A., 181, 58
A., 197, 226
A., 205, 327
B., 13, 2191
B., 11, 1820
A., 205, 203
B., 14, 46, 1890
B., 11, 1820
A., 205, 330
A., 205, 327
J. P. [3], 38, 389
G. J. C. [1880]
D
A., 122, 231
K. K. T.
G. J. C. [1879]
B., 15, 1974
A., 205, 314
A., 205, 323
B., 15, 857
B., 4, 248
B., 15, 1660
A., 199, 352
A., 225, 21 1
B., 18, 1660
C. R, 92, 1140 ;
A. C., [5], 27, 273
C. R, 93, 591 ;
A. C. [5], 27, 273
A., 222, 203
A., 153, 47
B., 18, 304
B., 16, 1607
B., 11, 832
B., 17, 1224
B., 18, 2233
B., 15, 1017
A.., 202, 147
B., 16, 62
48, 154
i., 526
vii., 1152
v., 759
44, 1151
46, 433
40, 924
i., 971
40, 291
42, 228
30, 315
vi., 463
30, 315
36, 948
40, 184
40, 292
42, 228
40, 616
j»
i., 974
))
vi., 463
40, 616
41,66
24, 394; vii.,
408
42, 1307
48, 65
48, 1072
40, 829 ; 44,
358
42, 218 ; 44,
359
46, 614
vi., 480
48, 555
44, 1151
34, 668
46, 1008
48, 1216
42, 956
38, 676
44, 602
>» ....
/3-Cinchonidine
Homocinchonidine
,,
;, ....
„ ....
,,
Apocinchonine
Apocinchonidine'
Cinchonine
v
Toluquinol+aniline
Apoconquinine
Apoquinine ....
Homoquinine (ultraquiuine)
Isoamylic diphenylallopha-
nate
Chitenidine .. .
Chitenine
Dininitrocinchonamine
Phenylhydrazinehelicin
Codethyline
Methooode'ine
)>
Codamine
DiethyKc p-tolyldimethyl-
pyrroline dicarboxylate
Diethylic hydrophenylluti-
dine dicarboxylate
CEnanthol + beuzidine
Dipropylphenyloarbamide ....
Dicumylearbamide
Dimesitylcarbamide ....
Pereirine
Cinchonamine
COMPOUNDS CONTAINING FOUR ELEMENTS.
573
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Cinchonamine
....
C19H24ON2
....
184-185
Hesse
A., 225, 211
48,64
„
„
....
194-195
Arnaud
C. R., 93, 593
42, 229 ; 46,
Hydrocinchonidine
„
225
Forst & Bohringer
B., 14, 1270
40, 1830
„ ....
„
229
„
B., 15, 520
„ (cinchamidine)
cf. B., 14, 1683, 1893
„
....
229-S30 u. c
Hesse
A., 214, 1
44,98
„ (amorphous)
....
11
b. 100
11
„
,,
Hydrocinchonine
J. p. [2], 8, 294
„
256 u. c.
„
B., 15, 855
„
=cinchotin (?)
„
257-258
Skraup
B., 11, 314
34, 434
„
„
....
268
Caventou & Willm
Z. C. [2], 5, 547
vi., 464
Cinchotin
cf. B., 14, 436, 1266 ; 15, 519
268
As., 7, 378
,1 .... ....
cf. B., 11, 311, 1517
„
277-3 c.
Skraup
A., 197, 352
36, 948
Quinamidine ....
C19Ho4O2N2
93 u. c.
HGSSS
A 907 9Q-* 9QQ
40, 925
,\., Bvfj —•'•>• _.'-
Quinamicine
....
„
....
109 u. c.
„
A., 207, 303
„
Conquinamine (quinidamine]
„
121
„
A., 209, 62
40, 1156
» 11
....
„
B., 14, 2248
123
Oudemanns
A., 209, 38
40, 1155
11 ii
....
„
A., 207, 289
its
Hesse
B., 10, 2158
34, 436
Geisospermine
....
11.
+H20
160 d..
„
A., 202, 143
Quinamine
A., 166, 266 ; 182, 163 ; 197,
ji
J. [1874], 874
172
„.
B., 5, 266; 10,
25, 721 ; 34,
48; 199, 333; 207, 288
2158
436; vii., 346
209, 42
Cinchonamine nitrate
C19H24ON2+HNOS.
C^HjAN,,
195
M
A., 225, 211
48, 65
Ethylic benzamsebate
C02H.C6H4.NH.CO.C8H16.
C19H27O5N
....
146
Pellizzari
B., 18, 216
48, 534
COsEt=1.3
Tetranitroxalei'n
see orig. paper
C20H9014N4
MM
diW.m..200
Claus
B., 14, 2569
42, 399
Dinitro-j3-naphthylene oxide
....
C20H1005N2
A., 209, 140
221
Knecht & Unzeitig
B., 13, 1726
40, 281
I. -"- ,! !.
....
„
A., 209, 137
270
„
B., 13, 1725
,,
Tetranitroisodinaph thy 1
C20H,AN4
....
150 d.
Staub and Smith
....
47, 106
Tetranitro-/3-dinaphthylamine
C20HU09N5
285-286
Ris and Weber
B., 17, 198
46, 752
Trinitrodibenzoresorcinol ...
N02.C6H3(O.C6H4.N02)2
CioH11010N3
....
123
Schiaparelli and
G. L, 13, 257 ;
46, 174
=4.3.1 ; (1.3),
A belli
B., 16, 873
Dinitrazoxynaphthalene (?)...
....
C20H1S06N4
...»
199
Liebermann
A., 183, 225
31,600
/3-dinitroisophthalophenone...
e6H2Bz2(N02)2=i.3.(?)2
eMHlso8N3
B., 13, 322
100
Ador
B. S. [2], 33, 56
38,470
a- „
ii i)
„
„
260
„
„
Dibenzoyldinitrophenol
....
C20H12X)7N2
201
Goldstein
B. S. [2], 25, 394
30, 298
Acridylbenzoic acid
C6H4.lIr.CcH4.C.C6H4.C02H
C20H1302N
d. a. 300
Bernthsen &Traube
B., 17, 1511
46, 1183
Dinitro-j3-dinaphthylamine ....
•«*•
C»HU04N,
224-225
Ris and Weber
B.,. 11, 197
46, 752
Nitrodibenzoresorcinol
C6H3(OBz)2.NO2=1.3.4
CjpHjjO.N
B., 16, 87.2
107
Schiaparelli and
G. I., 13, 257
46, 174
Abelli
Phenanthrene picrate
ei4H10+C6H2.OH.(N03)3
CjoH^Nj
....
141
Japp and Wilcock
....
37, 664, 670
n 11
11
„
143
„
....
37, 664
11 11
ii
„
143
Japp
....
37, 410
1. 11
»
„
....
143
Fittig & Ostermeyer
A., 166, 361
26, 892
11 11
11
„
....
143
Limpricht
B., 6, 533
26, 897
»
11
11
143
Hayduck
G. J. C., 1873
vii,, 85
»
11
11
....
144
Gnebe
B., 5, 862
26, 17S.
)) 11
11
„
....
144
Goldschmidt and
W. A., 83, 7
40, 824
Schidt
11 1)
„
D
«...
145
Graebe
A., 167, 131
26, 894
Anthracene picrate
„
».
138 (?)
„
G. J. C., 1869
»! )I
„
„
....
170
Fritzche
A., 109, 249
v., 351
Phthalidanilide
C6H4.CO.NPh.C : NPh=J.2
L |
C20H14ONa
....
152-153
Gerichteiii
B., 13, 420
38, 474
o-benzo}'lbenzoic phenyl-
see orig. paper
180-182
Boser
B., 18, 805
48, 797
hydrazide
Nitroso a-dinaphthylamine....
(C10H7)2N.NO
11
....
260
Calm
B., 15, 615
42,972
i) 11
„
„
260-262 d.
Landshoff
B., 11, 641
34, 587
Phenanthraquinone hydrazine
J)
....
165
Zinck6
B., 16, 1564
44, 1135
Diphenylamine phthale'in ....
(Ph3N),C.C,H4.COO=1.2
C30H14O$N2
238-238-5
Piutti
G. J., 13, 542
46, 451
574
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Kynuremic acid
Z. P. C., 5, 68
C20H1406N2
A., 164, 155
265 d.
Schmidberg and
[2], 10, 1028
vii., 716
Schultzien
Trinitroaniline anthracene ....
C14H10+C6H2.NH2.(N02)3
C20H1406N4
....
165-170
Liebermann & Palm
B., 8, 378
Triphenylguanidine car-
ph.N:c:(NPh)2:co
C^H^ON,,
....
134
Michler and Keller
B., 14, 2181
42, 182
bamide
„ „
„
J)
+H20
141
„
„
„
Benzoylbenzenyltriamido-
NHBz.C6H3.NH.CPh : N
„
+H20
125-214
Ruhemann
B., 14, 2653
42, 391
benzene
=1.3.2 or 4
Dibenzanilide....
C20H,5O2N
136
Hifferm
B., 12, 678
41, 133
2V ^^ la 2
J. [1856], 501
137
^^ OO
Gerhardt
A., 87, 302
29, 272
J1
155
Losanitch
B., 6, 176
26, 758
....
)j
....
160
Higgin
41, 133
„
....
„
....
161
Steiner
A., 178, 235
29, 272
Benzamidobenzophenone ....
Ph.CO.C6H4.NHBz
„
....
150
Higgin
41, 131
ii
„
jj
A., 210, 271
16t
Dobner and Weiss
B., 14, 1438
42, 176
jj ••••
„
n
....
170
Higgin
....
41, 134
Benzamidobenzoxybenzene ....
C6H4.OBz.NHBz=1.2
C20H16ObN
B., 15, 370
176
Hubner
A., 210, 387
42, 506
„
» jj
„
....
182
Kalckhoff
B., 16, 1828
44, 1110
„
=1.4
„
....
231
Ladenburg
B., 9, 1529
31, 305
Diphenylphthalmic acid
NPh2.CO.C6H4.CO2H
„
....
147-148
Piutti
G. I., 13, 542
46, 451
i
„
....
260
Burkhardt
A., 202, 121
38, 657
Diacetyl oxyquinonimide ....
C16H9(OAc).O.NAc
C20H1604N
200-201
Breuer and Zinck6
B., 11, 1998
36, 328
L J
Dibenzdiamidonitrobenzene
(NHBz)2.NO2=1.3.2 or 4
C20H1504N3
222
Ruhemann
B., 14, 2653
42,391
Dibenzdiamidonitrophenol
OH.(NHBz)2.N02=1.2.4J
C20H16O6N3
....
167-170
Post
A., 205, 70
„
=1.2.6.?
„
....
201-202
„
A., 205, 84
Aeetoxydiacetamideanthra-
014H6(OAc)(NAc2):Oa
C20HI5O6N
257
Bourcart
B., 12, 1419
38,263
quinone
Dibenzoylphenylhydrazine ....
C6H5.N2HBz2
C20H16O2N2
177-178
Fischer
A., 190, 128
34,309
jj
„
jj
....
187-188 u.c.
jj
B., 8, 591
28, 1035
Dibenzdiamidobenzene
C6H4(NHBz)2=1.3
,,
....
240
Ruhemann
B., 14, 2652
42,391
a-Diamidodiphenylphthalide
CeH4.CO.O.C(C6H4.NH2)!!
„
....
179-180
Baeyer
A., 202, 66
38, 652
£• j)
„
205
J(
A., 202, 67
Diacetdiamidodiphenyldi-
(,C;C.C6H4.NHAc)3=(1.2)2
„
....
231
Baeyer & Landberg
B., 15, 61
42, 623
acetylene
Diimidophenolphthale'in
C6H4[C(:NH).C6H4.OH]3
„
A., 202, 112
265-266
Baeyer & Burkhardt
B., 11, 1298
34, 866
Phenylazobenzoxytoluene ....
Ph.N2.C6H3Me.OBz=?.1.2
„
....
110-111
Molting and Kohn
B., 17, 354
46, 902
»
„ =?.1.4
„
113
u
B., 17, 364
46, 901
/3-Diamidisophthalophenone
(NH2)2.Bz2=(?)2.1.3
„
p.d. 70
abt. 100
Ador
B. S. [2], 33, 56 ;
38, 471
B., 13, 322
Acetoxybenzenebidiazoben-
(Ph.N2)2C6Hs.OAc=1.3.4
C20H160:!N4
....
116
Nolting and Kohn
B., 17, 369
46, 902
zene
n-Dibenzdiamidophenol
OH.(NHBz)s=?
C20H1603N3
• >..
187-188
Stuckenberg
A., 205, 68
0-
=1.2.6
»
B., 10, 386
209-213
„
A., 205, 82
32, 475
Eesorcinol phenyl carbamate
C6H4(O.CO.NHPh)2=1.3
C20H1S04N2
....
164
Snape
....
47, 772
Catechol „ „
j, =1.2
„
....
165
B
....
n
Quinol „ „
=1.4
„
darkens 200
205-207
„
....
47, 773
Dinitrodibenzylbenzene
C6H4(CH2.C6H4.N02)2
„
146
Easier
B., 16, 2716
46, 310
=i.f; (1.4),
jj
„ =1.?; (1.3)2
u
165
Becker
B., 15, 2092
44, 203
Carbonyltriphenylguanidine
NPh.CO.NPh.C:NPh
C20HI604N4
....
185
Stojentin
J. p., 32, 1
48, 1196
nitrate
+HN03
Ethylcarbazole picrate
(C6H4)2NEt+C6H2.OH.
C20H1607N4
....
97
Grsebe and Adlers-
A., 202, 23
36, 660
(N02)3
kron
Benzyl diphenylacetoxime ....
CPh2:N.O.CH2Ph
C20H17ON
55-56
Spiegler
M. C., 5, 203
46, 1156
Benzoylbenzylanilide
Ph.NBz.CH2Ph
„
....
104
Fleischer
A., 138, 229
i 1
Methylphenylacridium hy-
C6H4.CPh.C6H4.NMe.OH
i i
M
....
108
Bernthsen and
B., 16, 1813
44, 1133
droxide
Bender
?
PhN I C(NHPh).CO.NHPh
C20H17ON3
234-235
Klinger
A., 184, 281
31, 711
/3-Triphenylbiuret
....
C20H1702N3
105
Schiff
B., 3, 651
vii., 253
a- „ .... ....
....
„
147
Hofmann
B., 4, 250
24, 395; vii., 19
COMPOUNDS CONTAINING FOUR ELEMENTS.
575
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Berberine
....
C20H1704N
MM
120
....
....
i., 579
?- Nitrodibenzyloatechol
(O.CH2Ph),NOs=1.2.?
., (')
....
98
Pellizzari
G. I., 13, 501
46, 437
Nitrobenzeneazoxyleneazo-
NO2.C6H4.Ns.C8H2Me,.N,.
C20H,704N5
....
231
Meldola
....
48, 436
resorcinol
C6H3(OH)2 = 1.4; U.S.?;
4.3.1
Berberine hydroxide
C^H.AN
165
Schmidt
B., 16, 2589
46, 340
Diphenyltolylcarbatnide
NPh2.CO.NH.C6H4Me=1.4
C20H1SON2
....
130 u.c.
Michler
B., 9, 713
Anilidomethoxytoluquinone
C6HMe(OMe)(NHPh).O.N
C20H1802N3
131
Zincke
B., 16, 1561
44, 1118
anilide
i i
Ph
Anilidoethoxyquinoneanilide
C6H2(OEt)(NHPh).O.NPh
)>
134
»
B., 18, 788
48, 787
i i
Diphenylphenylenedicarba-
C6H4(NH.CO.NHPh)2=1.3
C20H1802N4
....
very high
Kuhn
B., 18, 1478
48, 979
mide
n-Resorcinolbidiazotoluene ...
(HO)2.C6H2(N2.C8H4Me)2
»)
....
194--1 95
Wallach and Fische
B., 15, 2825
=1.3.(?)2 ; (1.2),
0-
5) 11
)>
?
»
»
0-
„ =1.3.(?)2; (1.4)2
»
....
202-203
»
!»
a- „
» »
)>
....
255-256
»
H
Di-(amido-p-methoxyben-
<VC6H2(C6H3.NH2.OMe)2
C20H1804N2
....
230
Zincke and Hebe-
A., 226, 60
48, 258
zeue) quinone
brand
Isopropyl-jS-naphthaquinone-
• *•*
C20H1902N
137-139
Zincke and Brauns
B., 15, 1970
44, 209
p-toluide
Ethylapocinchenic acid
....
C20H1903N
....
161-162
Comstock & Konigs
B., 18, 2384
48, 1249
ji »
....
»
+H20
124-126
»
1)
)»
Macleyine
....
C20H1908N
....
200-5-201
Eykmann
P. J. T. [3], 13, 87
42, 1112
»
....
)>
205
«
C. C. [1884], 727
48, 404
Protopine
....
n
....
202
Hesse
As., 8,318, B., 4,
24, 1065 ; yii.,
696; Z.C.,7,653
1025
laobutylnaphthalene picrate
C10H7.Bu3+C6H2.OH.(N02),
C20H1907N3
....
96
Wegscheider
M. C., 5, 236
46, 1185
Triphenylethylcarbamide ...
NPh2.CO.NPhEt
C20H20ON2
needles
Michler
B., 9, 712
30,290
Fr. quinolinemethochloride...
....
»
a. 360
72-75
Ostermeyer
B., 18, 594
I
C9NH7Me)2O
»
MM
112
«»
C. C. [1884], 970
48, 672
Base from rosaniline
....
C^HjAN,
MM
176
Liebermann
B., 5, 144
Vii., 1061;
Diacetyl-p-tolylamido-p-
cf. B., 18, 195
C20H2003N2
....
147
Duisberg
B., 18, 193
48, 544
methyloxindole
Aniline phthalate
C6H4(C02H.NH2Ph)2=1.2
C20H2004N2
B., 12> 1067
145-146
Beamer and Clarke
A. C. J., 1, 245
36, 786
Dinitro-a-dipropylcarboben-
....
C20H2006N2
MM
176
Zagoumenny
A., 184, 171
32, 195.
zoic acid
?
....
CVOH2006N4
d. 240
97
Tonnies
R, 13, 1846
Oxycannabine
....
C20H21,07N2
J., 1871, 786
175-176
....
Z, C. [1870], 87
Tetracetamidodihydroxy-
[.C6H4(OH)(NHAc)2.0.1
C20HOT08N4
268
Bamberger
B., 16, 2402
46, 309
phenylquinone
=(1.2.4.6)2
?
=2C10H1006N
^20*^2oOl2^2
J)
252
Prinz
J. p. [2], 24, 361
Ethylapocinchene
C19H16N.OEt
C20H21ON
»
70-71
Comstock & Konigs
B., 18, 2382
48, 1249
Galipeine
....
C20H2103N
!»
115-5
K6rner& Bohringer
G. I., 13, 363
46, 341
Chinine .. . ....
....
CjoH^ON,
+2H20
81-82
Comstock & Konigs
B., 17, 1989
46, 1383
Allylphthalopseudocumida-
C6H2Me3.NH.CO.C6H4.CO.
C^H^O^
...i
179 d.
Frohlich
B., 17, 1808
46, 1319
mide
NH.C3H6
Benzil on propionitril
....
C20H2,,03N2
.1.1
197
Japp and Tresidder
B,, 16, 2652
46, 314
Azocuraic acid
N2(C6H3Pr.C02H)!1
C20H2304N2
....
262
Alexejeflf
J. E. [1882], 198
42.&71
)1 „
»
»
280 d.
»
B. S., 42, 321
48, 390
Diethylic azophenoxyacetate
N2(CcH4.O.CH2.C02Et)2
C20H2206N2
....
110-111
Thate
J. p. [2], 29, 145
46, 1171
=(1.2)2
Diethylic azoxyphenoxy-
ON2(C6H4.O.CH2.C02Et)2
C20H2!!07N2
,.,.
113-114
>i
»
46, 1170
acetate
=(1.2)2
?-glucoside
NH2.CO,,C6H4.N : CH.C6H4.
»
+2H2O
113
Schiflf
A., 218, 185
46, 455
O.CeH.,0^1.3 ; 1.2
Acetylcodeine
C18H20Ac03N
C^H^N
cf. 27, 1031
133
Hesse
A., 222, 203
46, 614
Toluquinol+o-nitraniline ....
C6H3Me(OH)2+C6H4.N02.
C20H2b04N,
....
37
Hebebrand
A., 15, 1976
44,61
NH2
Helicin m-amidobenzoic acid
COH.(GH.OH)4.CH2.O.C6H4.
CMH2309N
tit*
142
Schiff
B., 12, 2033
38, 12C
CH(OH).NHC6H4.C02H
576
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
I
• •<•
C-^ON.,
205
Glaus and Dannen
B., 13, 2187
40, 183
baum
Methylcinchoniue
A., 90, 219; J.p. (2), 3, 151
„
....
74
Glaus and Miiller
B., 13, 2292
Methylcinchonidine
A., 90, 221
„
+H20
75-76 u.c.
Glaus and Dannen
B., 13, 2192
40, 184
baum
Suberanilide
C6H12(CO.NHPh)2
C^H^N,,
183
Laurent & Gerhard
A. C. [3], 24, 18o
v., 449
Toluquinol+ aniline
C6H3Me(OH)2 +(Ph.NH2 )2
„
....
82-85
Heberand
B., 15, 1974
44,61
Quiuol + toluidine
C6H4(OH)3+(C6H4Me.NH2)
j>
....
95-98
-„
»
n
Diacetdiamidodiethyldiphen-
(.C6H3Et.NHAc)2=(?.1.2)2
»
....
307
Schultz
B., 17, 474
46,904
Quinicine
A., 166, 277 ; 178, 244
n
J. [1853], 473
60
Eichter
E. K. T., 413
24, 61 ; 25, 101
Homoquinine (?)
....
„ (?)
+2to2|H20
nf. 100
Hesse
A., 225, 95
46, 1384
Quinidine
160
v 14
Gouquinine (of. B., 10, 3010)
A.,'l 29, 15; 146,362; 207,309
n
+2JH20
168
*«) A1*
Quinine
A., 207, 309; M. C., 2, 612
176'8
HGSSC
A., 135, 328
vl., 983
TJ
177
B.,10, 2153
34, 434
...»
„
+3H20
57
n
„
„
Hydrazocumic acid
(.NH.C6H3Pr.C02H)2
C20H2404N2
....
?
Alexeeff
B. S., 42, 321
48, 390
Tetramethoxydiacetamido-
;.C0H2(OMe)3.NHAc]2
C20H2406N2
....
251
Baessler
B., 17, 2128
46, 1331
diphenyl
=(1.4. ?)3
Phenylhydrazine glucovanil-
C,H3(CH : N2HPh).OMe.
C20H24O7N2
....
195
Tiemann and Kees
B., 18, 1661
48, 1072
lin
(O.C6HU05)=1.3.4
Codamine
....
C20H25O4N
121
Hesse
A., 153, 56
24, 1064
....
„
....
126
„
B., 4, 694; As.,
25, 723; vii.,
"
8,280; Z.C.[2]
369, 723
7, 641
Laudanine
....
11
• ....
165
,,
A., 153, 53
vi., 774
....
„
A., 176, 201
166
..
B., 4, 694; As.,
24, 1064
"
8,272
Methylcinchouamiue
C20H26ON2
139
n
A., 225, 211
48,66
Ginchamidine
=Hydrocinchonidine (?)
ii
A., 214, 1
229
Forst & Bohringer
B., 15, 520
....
„
230 u.c.
Hesse
B., 14, 1684, 1893
40, 1046
Hydroquinidine (Hydrocon-
....
C^HaAN*
B., 15, 1656
166-167
Forst & Bohringer
B., 14, 1955
quinine)
» .>
....
„
....
168 u.c.
Hesse
B., 15, 855
42, 1113
Hydroquinine
....
„
....
168 u.c.
n
B., 15, 856
11
„ ....
....
„
+H20
100
Schutzenberger
A., 108, 347
v., 25
Azodiethoxybenzene
N2[C6H3(OEt)2]2=(?.4.1)2
Cj.H.jAH.,
128
Nietzki
B., 12, 39; As.,
36, 464
215, 149
Sabadilline
....
C20H2605N2
200
Couerbe
A. C. [2], 52, 352
v., 142
Cystine
....
J. [1880], 370
154-5 c.
lusemann & Marine
Z. C. [2], 1, 161 ;
vi., 540
5,677
a-phenylhydrazidoisobutyri-
PhN2H2.CMe2.CO)2NH
C20H27O2N5
117
Heissert
B., 17, 1461
46, 1153
mide
Echitenine
....
C^H^N
a. 120
ETesse
A., 203, 164
40, 448
Codethyline methhydroxide
C19H2303N+Me.OH
n
C. E., 93, 591
132
Jrimaux
A. C. [5], 27, 273
44, 359
Amygdaline
....
C20H27OnN
+3H2O
125-130
ilichter
E. K. T., 414
Tetrethoxydiamidodiphenyl
C6H2(OEt)2.NH2]2=(U.4.?)2
M
A., 215, 148
129
Nietzki
B., 12, 40
36, 464
Oxethenetoluidine oxalate ....
C6H4Me.NH.C2H4.OH
C^H^N*
121-122
)emole
B., 7, 637
27, 903
+H3C204
Hydrosabadilline
165
Couerbe
A. C. [2], 52, 352
v., 142
Ethylene hydrocyanconiine....
C2H4[N(OH).C9H13N]2
C^AJSr,
153-5
Vleyer
J. p. [2], 26, 351
44, 353
Dicamphorilimide
....
160
Schiff
B., 13, 1405
38, 892
Myristanilide
C13H27.CO.NHPh
C^H33ON
A., 202, 174
84
Masino
G. I., 10, 72
38, 460
Achilleine
C^H3gO15N2
100
Eeiclman
A., 58, 27 ; 155,
vii., 21
153
Nitroarachidic acid
G19H38(N02).C02H
G,H ON
B., 11, 2031
"0
^assinari
G. I., 8, 305
36, 307
Nonyldecoxylcarbamide
G9H19.NH.CO.NH.C10H190
^H^oV
01
lufmann
B., 15, 761
42, 1053
Arachamide
C19H39.CO.NH2
G20H41ON
98-99
Gossamann
A., 97, 262
., 353
Amidoarachidic acid
C19H38(NH2).C02H
C20H4102N
B., 11, 2031
?assinari
G. I., 8, 305
36, 307
COMPOUNDS CONTAINING FOUR ELEMENTS.
577
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Alkaloid from lupin seed ....
C20H4AN2(?)
C20H4403N2(?)
261
....
Siewert
Lw., 14, 161
25, 519; vii.,
758
Tetranitro-/3-diuaphtliy line-
CH2[C10H5(N02);];
C21H120SN4
....
150-160
Eichter
B., 13, 1728
40, 282
thane
)J 'J
„
„
....
d.w.m. 260-
Grabowski
B., 7, 1608
270
Benzeuylamidopheuaiithrol....
c6H4.c6H4.c : c.o.CPh : N
C21H13ON
202
Japp and Wilcock
37, 667 ; 39,
L 1
226
Benzoylphthalylauilide
C.H4:(00),:N.CsH4Bz
C21H1303N
A., 210, 267
183
Dobner
B., 13, 1013
38, 804
= 1.2; I.'!
Dinitrobenzilam
C21H1306N3
275-280
Henius
A., 228, 339
48, 1067
Amyhiaphthalene picrate ....
CUH10+C6H3.OH.(NO:)3
C21H1307N3
....
140-141
Paterno
G. I., 22, 337
44, 212
Fluoranthene picrate
„
11
....
110 (?)
Goldschmidt and
W. A., 83, 7
40: 824
Schidt
„
„
?J
A., 193, 146
18S-183
Fittig and Gebhard
B., 10, 2142
34, 432
„
t>
„
....
184
Goldschmidt
B., 10, 2029
34, 155
Anliydro-o-hydroxybenzoyl-
crtH4.cyH4.c:c.N:c(C6H4.
C21H14ON2
««««
270-276 d.
Japp & Streatfield
....
41, 146
diamidophenanthrene
OH).NH
1 1
,. P- »
J)
„
black 300
a. 350 d
„
....
41, 151
Nitrobenzilam
....
C21H1403N2
178-182
Henius
A., 228, 339
48, 1067
Phthalamidobenzauilide
NHPh.CO.C6H4.N : (CO), :
M
....
207-209
Piutti
B., 16, 1322
44, 999
C,H4=1.?;1.2
Diuitrophthalacene
C21H1404N2
d.a. 270-280
Gabriel
B., 17, 1398
46, 1190
Diuitrolophine
....
C21H140.,N4
100
Ekmau
A., 112, 161
/3-naphthoic a-naphtlialide ....
CUH-.CO.NH.C1BH?
C21H,AN
157
Vieth
A., 180, 325
30, 87
u- „ a- „
I)
„
244 c.
Hofmanu
A., 142, 121 ; B.,
vi., 851
1, 42
Oximidophthalacene
C21H14 : NOH
„
....
265-266
Gabriel
B., 17, 1398
46, 1190
Phenylacetoxyacridine
CPh.C6H4.N.(J6H3.OAc
0S1H,AN
173-174
Hess & Bernthsen
B., 18, 697
48, 801
1 .J
Benzamidobeuzenylazoxime-
N!CPh.O.N :C.C6H4.NHBz
C21H,AN3
213
Schoff
B., 18, 2474
48, 1217
benzenyl
=1.3
Triphenylic cyanurate
C3NAPh3
CjiH^O-jNa
214-216;222c.
Schiff
....
vii., 253, 407
„ „
„
B
....
824
Hofniaim and Ols-
B., 3, 275, 765 ;
24, 136 ; vii.,
hausen
P. R., 18, 493
407, 410
„ isocyauurate ...
n
H
....
260
Hofniaim
B., 3, 765 '
„
„ „
„
M
....
264
„
B., 3, 268
-
„ »
„
v
S70
„
B., 18, 765
48, 774
/3-tribenzhydroxylamine
021H,AN
....
100
Steiner
A., 178, 237
29, 271
a-
....
,}
A., 186, 104
100
Lessen
A., 175, 282
28, 635
y- »
....
„
A., 186, 33,
112
Steiner
A., 178, 240
29, 272
107
0- „
....
M
141
Lessen
A., 1452, 360
25, 416; vii.,
155
a- „
....
m
....
141-142
„
A., 175, 282
28, 635
a- „
....
,t
....
142
Steiner
A., 178, 225
29, 271
a- „
....
PJ
A., 186, 106
143-145
Heintz
Z. 0. (2), 5, 733
vi., 725
Nitrobenzoiubenzoate
C21H,AN
....
137
Zinin
A., 104, 119
i., 560
Alizarin blue diacetate
c6H4:(co)2:c6H(OAc)2.
CniH,AN
224-5
Auerbach
....
35, 804
N:CH.CH:CH2=2.1;1.2.
3.4.6
Trinitroamariiie
....
CS,H,AN5
....
b. 100
Bertagnini
A., 79, 276
i., 162
Methanthrene picrate
CJ6H12+C6H2.OH.(N02)3
^iH1507N3
....
117
Oudemanns
J. p. [2], 9,419
Fluoranthene hydride
„
n
....
186
Goldschmidt
M. C., 1, 225
40, 284
a-dinaphthy Icarbamide
OXNH.CV.H.),,
C2,H,AN3
B., 12, 386
270 d.
Pagliani
U. I., 9, 28
36, 723
„
n
„
a. 300 p.d.
Solid
....
iv., 22
p-hydroxyllophine ....
NH.CPh:CPh.N:C.C6H4.OH
L i
„
....
254-255
Japp and Robinson
B., 15, 1269
U, 326
Dibenzeny lam idobenzoic acid
(C7H6.N)AH3.C02H
C^H.AN,
253-5-254-5
Ladenburg
B., 11, 595, 1657
34, 572
Diuitrodicinuanienylviiiyl
CO(<JH I CH.CJH : OH.C6H4.
C-utl^OjNj
....
208-5
Diehl and Eiuhorn
B., 18, 2328
18, 1222
ketoue
NO.,)2=1.2
4 E
57*
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Acetylhydrophenylacridine...
NAc.C6H4.CHPh.C6H4
C21H17ON
128
Bernthseii & Bendei
B., 10, 1816
44, 1134
i i . .
=(1.2)2
Benzoylbenzenyltriamidotol-
N I CPh.NH.C6H.Me.NHBz
G21H17ON3
195-218
Ruhemann
B., 14, 2657
42, 392
i i
uene
=1.2.4.3 or 5
Acetophenonebenzanilide ...
Ph.CO.CH2.NBzPh
C21H1702N
....
145
Mohlau
B., 15, 2471
44, 333
Xanthorocelliu
C2lH1702N,(f)
183
Stenhouse & Grove*
A., 185, 17
31, 719
Ketone
Ph.(CH:CHX..CO.(CH:CH).!
C21H17O3N
136-5
Diehl and Einhoru
B., 18, 2329
48, 1222
CBH4.NO2=1.2
Hydrocyanvosolic acid
HO.C6H3(CH2.C6H4.0.)2
„
d.w.m. 230
Grsebe and Caro
A., 179, 199
29, 590
+HCN
Dibenzdiamidonitrotoluene...
Me.(NHBz)2.NO2=1.2.4.3
C21H17O4N3
245
Ruhemann
B., 14, 2656
42, 392
or 5
Dim'tramarine nitrate
C21H16N2(N02)24-HN02
C21H1707N5
170 u.c.
Glaus and Witt
B., 18, 1672
48, 1063
Methyldibenzoylphenylhydr-
Ph.NBz.NBz.Me
C21H1802N2
145
Tafel
B., 18, 1740
48, 1061
azine
Dibenzoyltolylhydrazine
C6H4Me.N2HBz2
....
188
Fischer
B., 8, 592
28, 1035
Benzylideue dibenzimide ....
„
197
Roth
A., 154, 76
vii., 184
Dibeiizdiamidotolueue
Me.(NHBz)2=1.2.4
3)
....
224
Ruhemann
B., 14, 2656
42, 392
jj
=1.3.4
„
260-261
Hiibner
A., 208, 315
Toly lazobenzoy Icresol
C6H4Me.N2.C6H3Me.OBz
„
....
95
Nolting and Kohn
B., 17, 354
46, 901
=1.4; ?.1.4
a-orcendialdehydedianilide ....
Me.(OH)2.(GH : NPh)2=?
)J
281
Tiemann and Hel-
B., 12, 1004
keuberg
Phenylbidiazoacetyl-o-cresol
(Ph.N2)2C6H2Me.OAc
C21H1S02N4
....
120-121
Nolting and Kohn
B., 17, 364
46, 902
» -P- »
„
J)
....
156-157
„
B., 17, 368
„
Benzoylnitro-p-ditolylamine
NBz(C6H4Me)(C6H3Me.N02)
C21HI803N2
167
Lellmann
B., 15, 831
42, 1060
Hydrosalicylamide ....
....
„
J. [1857], 317
300
Ettliug
A., 35, 261
Hi., 218
Nitramarine nitrate ....
C21H17N2(N02)+HN03
C21H1805N4
sf. 130
d.w.m. 134
Glaus and Witt
B., 18, 1677
48, 1063
Trinitrotribenzylamine
N(CH2.C6H4.N02)3=(1.4)3
C21H1S06N4
163
Strakosch
B., 6, 1058
27,79
Diethylic dinitrobenzoylma-
(N02.C6H4.CO)2C(C02Et)2
C21H18010N2
cf. 44, 912
93
Bischoff and Rach
B., 17, 2789
48, 264
lonate
=(1.2)2
Acetotriphenylmethylamine
CPh3.NHAc
C21H19ON
207-208
Hemilian and Sil-
B., 17, 744
46, 1032
berstein
Benzoylditoluide
}t
125
Gerber
B., 6, 446
Benzamidoazotoluene
C6H4Me.N2.C6H3Me.NHBz
C21H19ON3
....
135
Nolting and Witt
B., 17, 80
46, 742
=1.3; 1.3.6
Auilidomalonylanilide
NH2.C6H4.CH(CO.NHPh),
C21H1902N3
162
Conrad and Bischofi'
A., 209, 231
42, 39
Amarine nitrate
C21H13N2+HN03
C21H1903N3
165 u.c.
Glaus and Witt
B., 18, 1671
48, 1063
Ethyltriphenylcarbamide ....
NPh2.CO.NEtPh
C21H20ON2
B., 9, 712
80
Kaufmann
B., 14, 2185
Benzoylditolylhydraziue
N2HBz(C6H4Me)2=(1.4)2
I)
186-5
Lehne
B., 13, 1547
40, 41
Anilidoethoxytoluquinoue-
C6HMe(OEt)(NHPh).O.NPl,
C21H2002N2
115-116
Zincke
B., 16, 1561
44, 1118
anilide
Diphenyltoluylenedicarba-
C6H3Me(NH.CO.NHPh)2
C21H2002N4
a. 300
KUhn
B., 18, 1478
48, 979
mide
Alstonine (Chlorogenine) ....
....
C21H2004N2
As., 4, 45
195 u.c.
Hesse
A., 205, 363
40, 624
jj jj ....
....
+ 3^H,O
b. 100
Nitropapaverine (As., 8, 292)
C21H20(N02)04
C2,H2U06N2
+ H20
163
B., 4, 695
24, 1065
Diethylic furfurine dicarb-
C15H10OaN2(C02Et)2
C21H20O7N2
124
Bahrmann
J. p., 27, 295
44, 800
oxylate
Aniline lapachate
C15H1303.NH3Ph
C21H21O3N
121-122
Paterno
G. I., 12, 337
44, 21 1
Papaveriue ....
A., 66, 126; 73,50; 92,336
A Q4- 9"^^t * ~\ *7fi 1 QC . A pi
C21H2104N
130
Blyth
....
33, 316
a*j a-±, AOO , I/O, lyo ; AS.,
8,289
"
147
Hesse
vi., 896
Nitroleuco-basa
N02.C6H4.OH(G6H3.NH2.
C21H2104N3
107-108
Fischer
B., 15, 680
42, 833
OMe)2=1.4; 11.2
Rhceagenine ....
CTT /~v XT
TT
....
21H21O6N
....
223
riesse
A., 140, 149; 149,
vi., 996
35
Rliooadtne
i,
....
232 d.
jj
A., 140, 145; 149,
„
35
Diacetylpseudomorphiue
C17H15(OAc)sN03
C21H21O7N
276
A., 222, 234
46, 617
u-amylnaphthalene picrate ....
G10H7.G5H11+C6H2.OH.
C21H2107N3
85-90
Leone
G. I., 12, 209
42, 1210
'
(N02)3
COMPOUNDS CONTAINING FOUR ELEMENTS.
579
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
a-Amyluaphthalene picrate....
CTT f~i TT 1 /~1 TT f"\TT
i/j-Llj. vyx-Lli i ~p \^f -Cln. \J H,
CilH2I07N3
....
85-90
Boux
B. S., 41, 379
46, 1357
?-
»
„
105-110
„
,,
„
a- „ „ ..-
j»
„
- ..
140-141
„
„
51
0- „ » -
„
„
140-141
Leone
G. I., 12, 209
42, 1210
Strychnine
C^HjA-Nj
221
Blyth
33, 316
I
I
284
Glaus and Glassner
B., 14, 773
40, 748
284
Hanssen
B., 18, 1917
"
B., 14, 1000
285 u. c.
Beckurts
C. C. [1884], 812
48, 675
Tribenzylamine nitrate
(Ph.CHs)3N+HNO3
»)
124
Limpricht
A., 144, 304
vi., 337
Nitrocryptopine
C21H22O5N(N02)
C21H22O7N.!
185
Hesse
As. 8, 312 ; Z. C.
25, 723; vii.,
[2], 7, 641
876
NH2.C6H4.CH(C6H3.NH,.
C21H03O.,N.,
182-183
Fischer
B., 15, 681
42, 833
OMe)s=1.4 ; (?.1.2)2
C21H230,N
58
Hesse
A., 153, 47
vi., 807
Diacetylmorphine
».*
cf. 27, 1038
169
A., 222, 203
46, 613
As., 8, 299 ; A., 176, 200
J. [1867], 523
217 d.
B., 4, 696
24, 1065
Glucocoumarphenylhydra-
C6H4(O.C6HU05)(CH:CH.
C21H2306N2
....
130-132
Tiemann and Kees
B., 18, 1961
48, 1073
zine
C:N3HPh)=1.2
Dimethanilinefurfurol
....
C21H24ON2
70
Fischer
B., 10, 1626
34,52
„
....
„
83
„
A., 206, 142
A., 166, 272 ; 178, 252 ; 211,
C H O N
+H,O
156
Hesse
A., 154, 290
vii., 347
280
'
I^ J-i-O'-'
156
Arata
40, 623
156
P. J.T.[3],11,269
40, 108
Acetylcinchonidine
MM
w
42 u. c.
Hesse
A., 205, 319
40, 615
(Enanthylidene m-nitrobenz-
C6H13.CH(NH.CO.C6H4.
C^H^N,
....
170
Medicus
A., 157, 48
amide
N02)2
Dihydroxypropyldicarboxyl-
CO[NH.C6H3(C3H6.OH).
C21H2407N2
....
very high
Widmann
B., 17, 1307
46, 1023
diphenylcarbamide
C02H]2
Porphyrine ....
C21H.4O3N3
A« 4 42
97 u. c.
Hesse
A., 205, 360
40, 624
A'.iilidoperezone
C9H17.C6H(OH)(NHPh) I O2
C21H2503N
Oft) ~*y ~X£i
133-137
Anschiitz
B., 18, 714
48, 777
„
1)
„
....
138-139
Mylius
B., 18, 941
48, 778
Acetylmethocodeine
C19H22AcO3N
C21H25ON
66
Hesse
A., 222, 203
46, 614
Ethylcinchonine
C19H21EtON2
C21H26ON2
.I.p.[2],3,152
49-50
Glaus & Kemperdick
B., 13, 2287
40, 289
Dimethylcinchonine
C,9Hj,,MejON,
J)
....
74
Glaus and Miiller
B., 13, 2292
„
Ethylcinchonidine
CjjHjsONj (?)
„ (>,
....
90-91
Glaus
B., 11, 1821
36, 169
„
....
„
90
Glaus and Dannen-
B., 13, 2190
40, 183
baum
9
CEnanthylidene dibenzamide
C6H,3.CH(NHBz)2
C21H2602N2
....
128
Medicus
A., 157, 46
24, 151
Toluquinol+p-toluidine
C,H3Me(OH)2+(C6H4Me.
»
....
90
Heberand
B., 15, 1974
44, 61
Acetylhydrocinchonidine ....
C19H23AcON2
„
42
Hesse
A., 214, 12
Hypoquebrachine
....
„
80
19
A., 211, 263
42, 743
Acetylcinchonamine
C19H23AcON2
„
....
80-90
n
A., 225, 211
48,65
C,1H.,6O3N2
214-216 u.
B., 13, 2308 ; A.,
40, 294 ; 42,
c. ; p. d.
211, 265
743
Benzoylpheucaprylamine ...
C8H17.C6H4.NHBz=1.4
C21H27ON
....
109
Be ran
B., 18, 109
48, 523
Benzoylphen-n-octylamine ....
» »
„
117
„
B., 18, 136
„
Laudanosine
A., 176, 202 ; As. 8, 321
C21H2704N
89
Hesse
B., 4, 696 ; Z. C.
24, 1065 ; 25,
[2], 7, 641
724
Tetraethdiamidobenzophe-
CO(C,H4.NEt3)j
C21H28ON2
95-96
Michler and Grad-
B., 9, 1914
32, 335
none
mann
Diisobutylphenylcarbamide
CO(NH.C6H4Bu0)2=(1.4)2
„
283-284
Pahl
B., 17, 1240
46, 1010
Dicuniylcarbamide
CO(NH.CIOH13)2
„
122
Baab
B., 10, 53
Ethylcinchonamine
C19H23EtON2
„
....
140
Hesse
A., 225, 211
48, 66
„ .... ....
„
j»
+ H20
75-78
„
„
J)
Nitroaodiethylaniline cyan-
....
C21H2902NS
....
170
Lippmann and
M. C., 6, 537
48, 1213
hydrin
Fleissner
Valeritrine picrate
C16H27N+G6H2.OH.(NCg3
C21H30O.N4
....
129-130
Ljubavin
B., 6, 566
26, 1023
Oxyheptinamide
C21H2705(NH£)S
C21HS706N6
....
250-252 d.
Demarcay
A. C. [5], 20, 493
4 E 2
580
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
B., 14 [1880], 2701
^21 -"-40^2 2
255-261
67-5-68-5
Baumert
Lw., 27, 15
40, 8:32
255-257
67-68
B., 14, 1151,1321
B., 15, 1951
U
68
,,
B., 15, 632, 634
A., 214, 362
C H O N0
215 d.
B., 14, 1882
Tetraisoamylcarbamide
C21H44ON2
240-241
Liquid
Custer
B., 12, 1332
36, 91 :)
Diphthalyldiamidobenzene ...
c6H4[N:(co)2:c6H4],S
C22H1204N2
252
Biedermann
B., 10, 1165
32, 784
=1.3;(1.2)2
„
=1.4 ; (1.2),
If
....
295 d.
„
B., 10, 1164
„
Glycoldinitrate
C2,H12(N03)2
C22H1206N2
....
190
Rousseau
C. R., 95, 232
42, 1300
Diacetenylphenyl picrate ...
C16H10+C6H2.OH(N02)3
C22H1307N3
....
108
G laser
A., 154, 161
Pyrene picrate
„
„
222
Fittig and Gebhard
B., 10, 2143
34, 432
„ „
„
„
222
Goldschmidt and
W. A., 83, 7
40, 824
Schidt
Araido-a-naphtho'id
C10H6.CO.NH.C10H6.CO.NH
C2.,H14O2N2
....
178-179
Ekstrand
B., 18, 75
48, 548
1 1
Dioxiraidophthalacene car-
C21Hn( : N.OH)2.CO2H
C22H1404N2
272-273
Gabriel
B., 17, 1395
46, 1177
boxylic acid
0-0-Dinaphtbylene acetamide
C10H6.C10H6.NAc
C22H15ON
144
Walder
B., 15, 2175
44,209
> i
0-0-Dinaphthylene hydroxy-
C10H6.C10H6.C(OH):C.NH2
)(
....
d. 200
Rousseau
B., 16, 967
amidoethylene
o-Methoxybenzenylamido-
c6H4.c6H4.u:c.N:qc6H4.
C22H1602N
144-5-145-5
Japp & Streatfield
....
41, 154
phenanthrol
/"VTllf \ /-\
UMe).U
Oxyquinone phenylimide ....
C16H9(OH).O.NPh
1 1
»
158-158-5
Breuer and Zincke
B., 13, 632
38, 6fi.i
Naphthaquinonediphenyl-
....
164
Plimpton
....
37, 643
anilide
Benzoylphthalotoluide
C6H3MeBz.N : (CO)2 '. C6H4
C22H1503N
....
202
Fruhlich
B., 17, 2680
48, 355
=1.14 ; 1.2
Nitroazobenzene-azo-0-
N02,C6H4.N2.C6H4.N2.C10H6.
C22H1503N5
217-218
Meldola
....
46, 113
naphthol
OH=1.3 ; 4.1 ; aft
Pseudophenanthrene picrate
C16H12+C6H2.OH.(N02)3
CaTTjjOyN,
147
Zeidler
A., 191, 295
Isoindileueine picrate
C16H,2N20+C6H2.OH.(N02)3
C22H1508N6
+H2O
150
Engler and Hassen-
B., 18, 2242
48, 1223
kamp
0-Naphthaquirione dianilide
NHPh.C10H5.O.NPh=0aa
C22H16ON2
....
179
Meldola
45, 157
I 1
ft- „ „
'> »
„
178-180
Korn
B., 17, 3021
0-
•i »
„
B., 14, 1493
179-180
Zincke
B., 15, 481
42, 967
0- „ „
» »
,,
....
180-181
Fuchs
B., 8, 1024
29, 247
P- n »
ii ».
„
B., 15, 283
180-181
Zincke
B., 14, 1900
0- ,1 „
„ „
„
....
182
Goes
B., 13, 124
38, 399
a-Oxalylnaphthalide
....
»
200
Zinin
A., 108, 229
o-Methoxybenzenyldiamido-
CBH4.C6H4.C:C.N:C(C6H4.
JI
207-208-5
Japp & Streatfield
41, 153
1 1
pnenantnrene
— 1
OMe).NH
/3-Naphtholtetrazobenzene ....
Ph.N2.C6H4.N2.C10H6.OH
C22H16ON4
195
Nietzki
B., 13, 1838
40, 178
Diamidodinaphthoyl
(CO.C10H6.NH2)2
C22H16O2N.,
....
174 u. c.
Rakowski
B., 5, 1021
26, 391 ; vii.,
838
Dinaphthyloxamide
(.CO.NH.C10H7)2
„
....
200
Zinin
A., 108, 22
iv., 285
Azobenzene resorcinolazo-
Ph.N2.C6H2(OH)2.N2.C10H7
C22H1602N4
153-155 ;156
Wallach
B., 15, 28, 29
42,611
naphthalene
a-Naphtholazobenzeneazo-
HO.C10H6.N2.C6H4.N.,.C6H4.
n
powder
Meldola
...»
47, 665
phenol
OH=aa ; (1.4),
0-
=/3a ; (1.4)2
225
^
47, 660
a-Naphtholazobenzeneazores-
HO.C10H6.N2.C,H4.N2.C6H3"
C22H1603N4
d. w. m.
„
....
47, 665
orcinol
(OH)2=aa; 1.4; 4.3.1
' »i
„ =fta ; 1.4 ; 4.3.1
powder
H
....
Dinitrocresolphthalei'n
CO2H.C6H4.CO.C6HMe.OH.
C2!H1608N2
240
Fraude
B., 12, 241 ; A.,
36, 635
(NO2),=1.2 ; ?.1.2.(2)2
202, 163
Acetyl 0-0-dinaphthylamine
(C10H7)2NAc
C22H17ON
114-115
Benz
B., 16, 20
44, 594
" )?
H
„
124-5-125
„
B., 16, 19
H
» «-«- ,.
H
a
217
„
B., 16, 20
yy
COMPOUNDS CONTAINING FOUR ELEMENTS.
581
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. See.
/3-DiazonaphthaIeneacet-/3-
C10H,.N2.NAc.C10H7
C^H^ON,
....
218
Lawson
B., 18, 2422
48, 1238
naphthylamine
Dipseudocinnauiy 1 pyrroline
C4H2NH : (CO.CH : CHPh)2
C22H1702N
....
238-240
C'iamician & Denn-
B., 17, 2954
48, 379
stedt
3-Dibenzanishydroxylamine
....
C22H1705N
....
109-110
Lossen
A., 186, 21
32, 330
a- „
....
11
....
110-110-5
„
„
„
•y-Benzanisbenzhydroxyla-
n
110
,,
A., 186,8
32, 329
mine
a- „
....
„
113-114
n
„
„
8-
....
„
....
124-125
„
/3-Anisdibenzhydroxylamine
....
„
109-5-110-5
n
A., 186, 25
32, 331
o- „
„
137-137-5
„
„
w
Ethylic dibenzoyleomenamatt
C5H2N(OBz)2.COjEt
C22H17Of.N
fr. pyridine
102
Ost
J. p. [2], 29, 57
48, 49
Retisteue picrate
C16H14+C6H3.OH.(N(X)3
C22H17O7N3
94
Wahlforss
Z. C. [2], 5, 73
vi., 994
Ethylanthracene picrate
C14H9Et+C6H2.OH.(NO?)3
„
....
120
Liebermann
A., 212, 1
42, 863
» »
1»
i)
....
120
Liebermann and
B.,.14, 803
Tobias
/3-Naphthylaceto-/3-naphtha-
C10H7.NH.CH2.CO.NH.
C8H..ON,
170
Cosiner
B., 14, 60
40, 606
lide
CIOH7
n-Naphthylammonium
C10H7.NH.CO.C02.(NH3.
C22H18O3N2
154
Ballo
B., 6, 247
26, 913; vii.,
a-Naphthyloxamate
C10H7)
848
?
....
C22H1S04N2
....
143
Haarmann
B., 6, 341
26, 908
Diacetylresorcinolbidiazo-
(Ph^T2)3.C6H2(OAc)2
C22H1804N4
....
137-138
Liebermann and
B., 17, 881
46, 1147
benzene
Kostanecki
„
„
„
....
183-184
Wallach & Fischer
B., 15, 2816
Dibenzamidoethylenenitro-
NBz.,C2H4.O.C6H4.N03=1.2
C^H.AN,
121-122-
Weddige
J. p. [2], 24, 251
40, 1138
phenyloxide
Diethyldiazoresorcinol
....
C23H1806N2
....
202
Weselsky & Bene-
M. C., 1, 889
40, 72G
dikt
Ethylic dinitrosoindoxan-
C22HI808N4
173 il.
Baeyer
B., 15, 782
42, 1102
thydate
Dimethamidodibenzoylben-
C^Bz^NMe,
C23H,80.,N
a. 360
55
Michler & Duper-
B., 9^ 1901
32, 334
zene
tius
Dihydrodimethylanthracene
fr. C6H4 : (CHMe)2 ; C6H4
C22H1907N3
..*•
170.
Angeblis and An-
B., 17, 167
46, 753
picrate
schutz
Phenylanisaldehydine
C^H^OjNii
128-5—129
Ladenburg & Eug-
B., 11, 1660
36, 234
heimer
Diacetyldiphenyldiamido-
C6H4(NAcPh)2=1.3
163.
Calm
B., 16, 2797
46, 591
benzene
.
„
=1.4
191-7
n
B., 16, 2807
Phthalyltoluide
C,H4(CO.NH.C6H4Me)2
„
180
Stiidel
A., 225, 384
48, 142
=(1.8),
Ditoluyldiamidobenzeue
CGH4(NH.CO.C6H4Me)2
n
228
Bruckner
A., 205, 114
40, 93
=1.2 ; (1.4),
»
„
„
228
Hubner
A., 210, 330
42, 504
Benzamide on anisaldehyde....
....
C22H20O3N2
192
Schuster
A., 154, 82
vii., 80
Tetracetyl a-diamidophenan-
CuH6(NHAc)3(OAc}2
C22H2006N2
nf. 300,
Kleemann & Wense
B., 18, 2168
48, 1240
thraquinol
Diuitrostrychnine ....
....
C22H20C6N4
B., 16, 968
d.w.m. 202
Han riot
C. R, 96, 585
44, 670
„
....
j.
....
226
Glaus and Glassner
B., 14, 775
40, 748
Ethylic di-p-nitrobenzoyl-
[.CH(C02Et).CO.C6H4.N02];
C^H^O.oN,
180
Perkin & Bellenot
B., 18, 953
48, 795
succinate
!
NO,.C6H«.0(N3HPh).CH,
CMH2103N5
....
120
Gevekoht
A., 221, 323
46, 445
C(N2HPh).Me=1.2
Azodimethyloxyquinizine ...
OcH4.CO.CHMe.CMe.N.N)2
1 |
C22H32ON2
....
164
Knorr and Blank
B., 17, 2050
46, 13SO
=(1.2),
(Carvacrolbidiazobenzene
(Ph.N2)2C6HMePr«.OH
C22H22ON4
....
126
Mazzara
G. I., 15, 214
48, 1132
=5.3.1.4.2
Tliymolbidiazobenzene
=(?),.1.4.3
„
168
Mazzara and Pos-
G. I., 15, 52
48, 894
setto
582
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Anilidoisobutoxyquiuoiie-
C8Hj(OBu/3)(NHPh).O.NPh
C22H2202N2
....
138
Zincke
B., 18, 788
48, 787
anilide
i " i
Diaiitipyrene
....
CMHM02N4
250
Knorr
B., 17, 2045
46, 1379
NH.C.N.C6H4.CO.CH.CH2.
C22H22O3N4
211-212
Knorr and Billow
B., 17, 2055
46, 1381
Ethylic phenylizitiquinizin-
hydrobenzene carboxylate
1 - 1
C(:N2HPh).CH(C02
Et).CH2
1
Pheneto'ilazoresorcinol
(EtO.C6H4.N2)2:C6H2(OH)2
C22HM04N4
....
165-167
Liebermann anc
B., 17,883
46, 1147
=(1.4)2 ; (?)2.1.3
Kostanecki
p-Toluidine lapachate
C15H1303.(NH3.C6H4Me)
C^HjAN
B., 16, 801
129-5-130
Paterno
G. I., 12, 337
44, 211
o- „ ,,
„
n
„
135
„
„
Diethylic j3-naphthyldi-
N(C10H7).Me2.(C02Et)2
C^H.aO.N
124
Knorr
B., 18, 304
48, 555
niethylpyrroline dicar-
= 1.2.5.3.4
boxylate
Hydrastine
....
„
....
a. 100
Perrins
J. [1862], 382
„ .... ....
....
„
....
132
Power
C. C. [1884], 938
48, 675
„
....
„
135
Mahla
J. [1863], 455
Narcotine (Opianine)
....
Cyi-aOjN
....
155
Blyth
....
33, 316
11 11
....
»
....
170
....
....
iv., 25
,, ,,
....
„
....
176
Hesse
B., 4, 694; A.,
24, 1065; 25,
,
178, 241 ; Z. C.
723; 29,608;
[2], 7, 641
vii., 876
Opionine
MM
„
227
„
A., 228, 299
48, 1074
Dianiidostrychnine
....
C22H2402N4
B., 16, 968
d.w.m. 225
Hanriot
C. R, 96, 585
44,670
Methyltetrahydrocinchonic
(C,H9NMe.CO)2O
C22H2403N2
297-299
Liquid
Weidel and Hazur
M. C., 5, 643
48, 561
anhydride
(744-3)
Fr. Brucine
....
C22H2404N2
....
284
Hanssen
B., 17, 2266
48, 63
Diacetyl diacetoxystilbenedi-
[.CH(NHAc).C«H4.OAc]3
C22H2406N2
....
216-219
Japp and Hooker
....
45, 679, 683
amine
Acetyl quinine
....
C22HM0;iN2
J. [1876], 813
108 u. c.
Hesse
A., 205, 317
40, 615
Phenylhydraziue phenylaceto-
....
C22H2604N2
....
149
Weltner
B., 18, 792
48, 793
succinic acid
Chairamine
....
„
....
233
Hesse
A., 225, 211
48,67
+ H O
140
Concha! ramine
"H
I -i--i-2
120
"
I
"
„
....
+H.O
108-110
H
„
w
+C2H60
M
+ H3O
82-86
n
M
M
Chairamidine ....
+ H O
126-128
48 PS
Conchairamidine
....
J)
114-115
"
U
Cinchonidine ethylcyanide ....
C19H22N2O+EtCN
C22H27ON3
....
140 d.
Glaus and Merck
B., 16, 2746
46, 338
o-Toluidoperezone ....
C9H17.C6H(OH)(NH.
C22H2703N
....
108-110
Auschiitz & Leather
B., 18, 716
48, 777
C6H4Me) : 02
°- »
» i.
Jl
....
135-136
Vlylius
B., 18, 942
48, 778
P- ..
11 M
„
....
132-134
Anschiitz & Leather
B., 18, 716
48, 777
P- „
11 11
....
133-135
Mylius
B., 18, 942
48, 778
Sebacylanilide
C8H16(CO.NHPh)2
C^H^OaN,,
198
Pellizzari
B., 18, 215
48, 534
Aspidospermatine
....
162 u. c.
ilesse
A., 211, 259
Aspidosamine
11
....
100
„
A., 211, 262
Echitaniine (Dita'ine)
B., 11, 2006; 13, 1648, 1841
C22H29O4N2
+4H20
206 d.
A., 203, 150
40, 448
n-Octylbenzamidotoluene ....
C8H17.C6H3Me.NHBz=?.1.2
C'^ON
....
117
Jeran
B., 13, 147
48, 524
Aspidospermine
B., 12, 1560
"^ ~H O AT
^22*"' 3lT^2^ 2
205-206
Fraude
B., 11, 2189
36, 471
»
....
„
....
205-206
Arata
A. S. C. A., 1879
40, 623
»
....
„
....
205-206
Wulfsberg
P.J.T.[3],11,269
40, 108
,;
....
206
lesse
A., 211, 254
42, 742
Phthalylbenzoanilide
C6H4:(CO)2:N.C6H4Bz
C23H1303N
83
)obner
A., 210, 267
Diphthalyldiamidotoluene ....
C6H4:(CO)2:N.]2C6H3Me
CS3H1404N3
....
232-233
Jiedermann
B., 10, 1161
2,783
= (1.2),; 1.3.?
i,
„ =(1.2)2; 1.2.3
i>
270
jadenburg
B., 10, 1125
32, 753
» ?»
"
....
"
Jiedermann
B., 10, 1165
COMPOUNDS CONTAINING FOUR ELEMENTS.
583
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Menaplithoximide (/3-cyano-
C202:N2H(CN)(C10H.)2
C23H1502N3
245
Perkin
A., 98, 244
9, 8 ; iv., 285
dinaphthyloxamide)
Acetauhydro-p-hydroxyben-
....
C23H1602N2
205-210 p.d.
Japp and Streat-
41, 152
zoyldiamidophenanthrene
fleld
/3-naphtholazobenzeueazosali
HO.C10H6.N2.C6H4.N2.C6H3
C23Hld04N4
....
a. 255
Meldola
47, 668
cylic acid
(OH).C02H=0d; 1.4; 4.1.2
Benzoyl /3-iiaphthylphenyl-
Ci0H7.NPhBz
Cani7ON
....
136
Streiff
A., 209, 158
amine
» ft- >»
))
»
....
147-148 u.c.
Claus and Eichter
B., 17, 1591
46, 1358
11 «- i)
>J
JJ
A., 209, 154
152
Streiff
B., 13, 1852
40, 176
Diazobenzene /3-naphthyl-
C,0H7.NBz.N2Ph
C.H.jON,
....
162-163
Lawson
B., 18, 800
48, 803
benzarnide
Oxyquinone-o-toluide
C16H9(OH).O.N.C6H4Me
C2:,H1702N
....
107-108
Breuer and Zincke
B., 13, 632
38, 665
>i -P- i.
)>
JJ
154-155
11
)>
J)
Benzimide (?)
....
CaHM0JNs
....
167
Riehter
R.K.T., 429
p-Acetoxylophine
NH-CPh 1 CPh.N : C.C6H4.O
1)
229
Japp and Robinson
B., 15, 2169
41, 327
Ac
Diethyltetranitroaurin
C19H8Et,(N02)403
CaH.AiN,
105
Ackermann
B., 17, 1626
46, 1340
o-Benzdianishydroxylamine
....
C23H,,06N
....
137-5-138-5
Lessen
A., 186, 30
32, 331
ft-
....
J)
137-5-138-5
»
11
11
Dianisbenzhydroxylaruine ....
....
•
»>
147-5
11
A., 186, 28
11
jS-Anisbenzanishydroxylamiii
....
)»
148-149
1 1
11
M
«- 11
n
152-153
11
11
11
Diacetyl-dj-p-azotolueneres-
C6H4Me.N2.C(iH2(OAc)2.N,,
C23H2004N4
175-176
Wallach & Fischer
B., 15, 2822
orcinolazobeiizeiie
p"h
11 Q2~ 11
»
»
195-196
11
11
„ c^-azobenzeneresor-
)>
11
175-176
11
B., 15, 2823
cinolazotolueue
)! <V »
I)
»
196-197
11
B., 15, 2824
Hexnitrotetramethdiamido-
fr. Ph.CH(C6H4.NMe.,)2
C^H^O^N,
200 d.
Fischer
A., 206, 128
triphenyluiethane
11 11
11
»
206
Ziegler
B., 13, 787
38, 640
Benzoylbeiizopseudocumidide
Me3.Bz.NHBz=l.3.4.?.6.
O^H^O.N
227
Frohlich
B., 17, 1806
46, 1319
Diacetyltriplienylquanidine
Ph.N : C(NPhAc)2
C23H2102N3
131
McCreath
B., 8, 384
28, 885
Toluanisaldehydine
C3H2AN2
....
152-156
Ladenburg and
B., 11, 1660
36, 234
Rugheimer
Pararosatoluidine
C^H^ON
....
150
Klinger & Pitschke
B., 17, 2443
48, 151
Decarbousne'inanilide
C23Hi306N
B., 15, 2241
169-171
Paterno
G.I. [1882], 231
42, 1082
From narce'ine
....
C3»HB08N
....
210
Beckettand Wright
....
29, 472
Anilidoisobutoxytoluquin-
C6HMe(OBu/3)(NHPh).O.N
C23H2402N2
117
Zincke
B., 16, 1561
44, 1118
oneanilide
Ph
Nitrotetramethdiarnidotri-
NO,.C6H4.CH(C6H4.NMeJ)2
CJIaO.N,
152
Fischer
B., 12, 8Q2
36, 788
phenylmethane
=1.3;
11 11
=1.2 ;
)5
155
11
B., 15, 682
42, 834
11 11
» »
It
159-1 GO
Fischer & Schmidt
B., 17, 1890
46, 1315
11 11
=1.4 ;
)>
176-177
Fischer
B., 14, 2526
42, 393
o-Nitromalachite green
N02.C6H4.C(OH)(CaH4.
CaH2503N3
....
163
Fischer & Schmidt
B., 17, 1891
46, 1315
NMe2)2
Lanthopine ....
n TT r> \r
A o Q O*71
r^j. of\f\
TT
AT r;o KQ
*"'
^23±125>J4i>'
AS., o, z/ 1
abt. zuO
riesse
., lOo, Otf
Cryptopine (?)
see C21H2306N
023H2506N
....
175
Smith
P.J.T.[2],8,595,
vi., 514
791
Tetramethdiamidotriphenyl-
Ph.C(OH)(C6H4.NMe2)2 or
C23H26ON2
120; sf. 116
Fischer
B., 12, 791, 1686
38,40
carbinol (malachite or
HO.C6H4.CH(C6H4.NMe2).,
bitter almond oil green)
= 1.2;
11 11
>' 11
)!
A., 206, 130
127-128
11
B., 14, 2522
42, 393
11 11
» 11
t)
B., 11, 1238
132
Dcibner
B., 13, 2222
40, 165
11 11
=1.4;
)J
A., 217, 250
163
Fischer
B., 14, 2523
42, 393
Diacetyllapoconquiuine
c23n.,6o4N2
60
Hesse
A., 205, 337
40, 618
»>
B., 16, 61
110
,,
A., 185, 301
34, 156
Concusconidine
....
>j
124
11
B., 16, 62
44, 602
Concusconine • ....
....
)>
....
206-208
11
A., 225, 211
48, 66
564
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Concuscouine (cf. B., 16, 01)
C23H2604N2
+ H20
144
Hesse
A., 225, 211
44, 002 ; 48, 66
151
Blyth
33, 310
)J
178 u.c.
Claus and Eohre
B., 14, 773
40, 749
JJ
B., 10, 2161
188
Hesse
A., 185, 310
34, 150, 437
Propiouylquinine
C20H23(CO.C2H5)N202
CogH^O-jNg
129 u.c.
,,
A., 205, 358
40, 020
Cinchoniue hydrogen auc-
C19HMON,+C4H,04
CsBHjgOsN.,
+H20
110
,)
A.
vi., 404
cinate
» »
)>
»»
+ liH20
110
,,
A.
„
Quinine ethylcyanide
C2l)H2402N24-EtCN
Cj.H.O.N.
d. 95-100
90
Glaus and Merck
B., 16, 2747
46, 338
NarceVne
A., 86, 182 ; 176, 198
CaHjaOgN
....
92
....
....
iv., 24
B S., 18, 535 ; J. p. (2), 2,457
134
Blyth
33, 316
,, .... .... ...
*•** ""J W) WJ ) Ut £l* \*V) **1 •*•"
,»
»
B., 7, 105
145-2 c.
Hesse
A., 129, 250
vi., 803
Beuzenyldiisoamylphenylen-
....
C23H32ON2
80-100
80-81 quick,
Hubnerand Siniou
B., 12, 1344 ; A.,
36, 923
aiuidine
90-92 slow
210, 304
Nitrate of ditto
C23H31N2(N03)+HN03
C23H3206N4
....
90
,,
n
,,
Succino-octonitro-u-naphth-
[.CH2.CO.NH.C10H3(N02)4]2
C24H12018N2
256
Hubiier
A., 209, 339
42, 182
alide
» »
»
»
....
256
Hahnemann
B., 10, 1713
Ethylic dinitrophthalacon-
C21H9(NO2)2O2.C02Et
C24H1408N2
....
a. 280
Gabriel
B., 17, 1390
46, 1176
carboxylate
o-Diquinolyline picrate
09NH6.C,NH6=meta
C24H1507N6
....
240
Miller & Kinkelin
B., 18, 1912
48, 1145
ft- „ »
., =«i;/32;a1;aj
)1
268
Fischer
M. C., 6, 546
48, 1247
?
C24H15(N02)N206
C24H1508N3
black 265
275-280
Z incke & Hebebrand
A., 226, 60
48, 258
I <odiuitroazodiphenyl
N2(C6H4.C6H4.N02),=?
C24H1604N4
187
Wald
B., 10, 140
32, 341
Dinitroazoxydiphenyl
ON2(C6H4.C6H4.N02)2=(1.4)4
C24H1606N4
....
255
„
B., 10, 138
?,
Bidinitrophenylbenzidine ....
[.C6H4.NH.C6H3(N02)212
C24H1608N6
330
Austen
A. J.S.[3], 13,279
32, 762
=(1.4; 1.2.4)2
» ....
)> 1»
))
a. 330
Willgerodt
B., 9, 982
30, 406
Succiiiotetranitro-a-naphth-
[.CH2.CO.NH.C10H.)(NO2)2].,
C24H16010N6
B., 10, 1713
225
Hubnerand Hahne-
A, 209, 383
42, 182
alide
mann
Azoxydiphenyl
ON2(C6H4.Ph)2=(l.l)2
C24H18ON2
....
205
Zimmermann
B., 13, 1960
40, 175
Tribenzoylmelamine
(CN.NH.CO.C6H5)3
C24H1803N6
275 d.
Gerlich
J. p. [2], 13, 283
Ethylic dioximidophthal-
C,1H11(NOH)2.CO2Et
C24H1804N2
263-264
Gabriel
B., 17, 1394
46, 1177
acenecarboxylate
?
....
C24H1804N4
250
Zincke& Hebebrand
A., 226, 60
48, 258
From piperonal
....
C24H1806N2
172
Lorenz
B., 14, 792
40, 729
,, ,, .... ....
>1
213
>,
B., 14, 791
»
Azobenzene nitronitrolic acid
[N02.C6H4.N2.C6H4.N(OH).]S
C24H1806N8
....
218
Janovsky
B., 18, 1137;
48, 789, 894
=(1.4)3
M. C., 6, 157
Fr. ethylic dinitrophenyl-
....
C24H18016N6
105-5
Heckmanu
A., 220, 128
46, 178
acetoacetate
Cumeiiylamidopkeuanthrol....
c6H4.c6H4.c : C.N :
1
C24H19ON
186
Japp and Wilcock
....
39, 226
C'(C6H4Pr).0
|
Diauilidoquinone anilide
C6H2(NHPh)2.O.NPh
C24H19ON3
....
202-203
Zincke
B., 18, 787
48, 787
Beuzcyanidine
».*
C24H1902N
123-124
Frankland & Louis
....
37, 742
Beuzoylphthalopseudocumide
C6HMe,Bz.N : (CO), : C6H4
C24H,,03N
....
181
Frohlich
B., 17, 1803
46, 1319
=1.3.4.?.6; 1.2
Acetylnaphthaquiuone phe-
1)
172-173
Plimpton
....
37, 645
nylanilide
Phthalyldiphenylasparagine
C6H4:(CO)2:N.C2H4(COSH).
C24H1905N2
180
Piutti
G. I., 14, 473
48, 797
CO.NPh2
,,
I!
?)
+2H20
112
,>
,,
,,
,,
,,
1)
MM
203
,,
V
,,
j3-Naphthaquiuone ditoluide
C6H4Me.NH.ClllH5.O.N.
C24H20ON2
174-176
Meldola
45, 159
l 1
C6H4Me=(1.4)2
0-
J)
)1
....
177
Fuchs
B., 8, 1025
29, 248
B-
))
178
Kronfeld
B., 17, 715
48, 1038
/3-Naphthyl /3-imidobutyro-
C10H7.N: CMe.CH2.CO.NH
>i
•200
Knorr
B., 17, 543
46, 1198
unphthalide
CwH,
COMPOUNDS CONTAINING FOUR ELEMENTS.
58-5
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Resorcinolquinoline ....
....
C^HjAN,
1()2 u.c.
Hock
B., 16, 886
Succino-a-naphthalide
(.CH2.CO.NH.C10H7)2
J)
B., 10, 1713
285
Hiibnerand Hahne-
A., 209, 382
42, 181
niaiin
C-.Hi.nOjN.,
246
Japp and Hooker
46, 685
V14^*IB ** 2
a. 300
45, 684
Benzoylethoxyfurf urine
C15H10O3N2Bz.OEt
C24H2AN2(?)
....
290
D
Bahrmann
J. p. [2], 27, 317
44, 800
Fr. ethylresorcinol
....
C24H2006N2
230
Weselsky&Benedikl
M. C., 1, 893
40, 726
Tetrahydrazoresorufm
....
CJ4H2007N2
....
d. 100
Brunner & Kramer
B., 17, 1862
46, 1334
a-naphtholazobenzeneazodi-
HO.C10H6.N2.C6H4.N2.C6H4.
C24H21ON6
....
d. 200
Meldola
....
45, 110
methaniline
NMe2=/3a;(1.4)2
/3-
=aa;(1.4)2
>?
209-210
»
....
45, 109
Oxalyltri-o-tolylguanidine ....
C6H4Me.N:(NMe.C6H4.CO),,:
(VH.AN.
179
Berger
B., 12, 1858
38, 244
Aniline pyrogallate
C6H3(O.NHPh)3(?)
C24H2103N3(?)
....
126-128
Guthrie
P. M. [5], 18, 109
Benzylcyanurate
C303N3(CH2Ph)3
JJ
B., 3, 518
153
Cannizzaro
G. I., 1, 33
24, 927
„ .... ....
" .
)»
320
157
Letts
B., 5, 93
25,450;vii.,180
Benzoylphthalopseudocu-
C6HMe3Bz.NH.CO.C6H4.
C24H2I04N
....
195 d.
Frohlich
B., 17, 2674
48, 154
midic acid
CO2H=1.3.4.?.6; 1.2
]letene picrate
C18H,3+C6H2.OH.(N02)3
C^HM0TN,
J. [1858], 440
123-124
Ekstrand
A., 185, 80
32, 497
TJsnic anilide .... ....
C17H1705.CO.NHPh
C^H^CKN
170-171
Paterno
G. I. [1882], 231
42, 1082
Glyceride of phenylcarbamic
C3H6(O.CO.NHPh)3
^^24 23V^6J-
C24H2306N3
....
160-180
Tessmer
B., 18, 969
48, 774
acid
*
Tetramethylhydroanthracene
C14H3Me4+C6H2.OH.(N02)3
C24H2307N3
....
165
Anschiitz & Ebmig
B., 18, 665
48, 768
picrate
•
Leuco-phthal green
C14H6Ph(NMes)s.OH(?)
C24H24ON2
235-236
Fischer
A., 206, 108
40, 588
Ethylanilphthalein
C6H4 : (CO)2 : (NPhEt)3=1.2
C24H2402N2
140-5-141-5
Piutti
G. I., 13, 542
46, 450
Dimethylanuinephthale'in ....
C6H4(CO.C6H4.NMe2)2
C24H2402N2
....
188
Fischer
B., 12, 1692
33, 41
j» ••••
»J
))
....
190-191
>»
A., 206, 92
40, 587
Cuminyldibenzamide
C6H4Pr.CH(NHBz)2
»
....
224
Eaab
B., 8, 1150
29, 398
Anishydramide
A., 56, 309 ; 88, 128
C24H24O3N2
120
Cahonrs
A. C. [3], 14,487
i., 299
Triacetamidotriphenylamine
N(C6H4.NHAc)3
C24H2403N4
....
nf. 240
Heydrich
B., 18, 2158
48, 1213
Hydrotrimethylamarine
C21Hl7Me3N20
C24H26ON2
....
158
Claus
B., 15, 2328
44, 203
Dimethaniline phthalin
NMe2.C6H4.CO.C6H4.CH
C24H2602N2
200
Fischer
A., 206, 101
40, 588
(OH).C6H4.NMe2
Ethyldiantipyrine
....
C24H2602N4
240-250
Knorr
B., 17, 2045
46, 1379
Azoethylmethyloxyquiniziue
....
C24H2604N2
....
160
Knorr and Blank
B., 17, 2051
46, 1380
Ethylhydrastine
C22H22Et06N
a4H,,7Or,N
183
Power
C. C. [1884], 938
48, 675
Leuco-base from vanillin
C6H3(OMe)(OH).CH(C6H4.
C24H2802N2
135-136
Fischer & Schmidt
B., 17, 1895
46, 1316
NMe2)2=5.4.1 ; (?)2
Fr. picrorocellin
C24H2803N2
A., 185, 24
154
Stenhouse & Groves
P. R, 25, 67
31, 719
See C11H19O.N
CO,H O N
Ethylic diphenylizinsuccino-
N2HPh : C.CH2.CH(CO2Et).
VNiHFp/#t*S
C^H^N,
205-206
Knorr and Billow
B., 17, 2055
46, 1381
i
succmate
C(:N2HPh).CH2.CH.
CO2Et
Sebacyl di-m-benzamic acid....
C8H16(CO.NH.C6H4.C02H)2
C24H2806N2
....
275
Pellizzari
B., 18, 215
48, 534
Ethylic dihydroxypropyldi-
CO2H.C6H3(CMe2.OH).NH.
C^HjAN,,
....
a. 300 d.
Widmann
B., 17, 1306
46, 1023
carboxyl diphenylallo-
CO.N(C02Et).C6H3(CMe2.
phanate
OH).CO2H
From rosaniline
Of. B., 2, 443
QsH^ON,
MM
130
Wiehelhaus
B., 16, 2007
44, 1098
From chloranil+dimethani-
....
I*
....
190
M
B., 16, 2006
i)
line
Ethylic azocuminate....
N2(C6H3Pr.C02Et)2
c,4H30o4isr2
....
62
Alexejeff
J. E. [1882], 198
42, 971
Concuscouine hydroxide
023H26Me(OH)04N2
C24H3005N2
+5H2O
202
Hesse
A., 225, 211
48, 66
Methylnarceine
C-nHjsMeOgN
C24H3109N
....
175 u.c.
Claus and Kitzfeld
B., 18, 1574
48, 997
Diethylic ethylene diethyldi-
C2H4(NEt.C6H4.CO2Et)2
C24H3204N2
....
98-100
Schiff and Parent!
A., 226, 243
48, 266
benzamate
=(1-3),
Plithalyltrope'ine
....
»
A., 217, 102
70
Ladenburg
B., 13, 108, 1085
38, 411
Thallin tartrate
(C10H13ON;2+C4H606
C*HB0^,
....
100 s. d.
Vulpius
A. P. [3], 22, 840
48, 399
Phenylmaltosazone
....
CMH3209N4
....
190-191
Fischer
B., 17, 583
48, 54
Phenyllactosazone
....
?J
....
200
i)
»
»
Narceine methonitrate
CjaHjsOjN+MeNOa
C34H32012N2
....
168
Claus and Kitzfeld
B., 18, 1572
Dulphinine
...
C24H3502N
....
119
Blyth
....
33, 317
4 F
586
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
or CktH,JOIKNi
0,,H3,O,N
129-130
Michell
P. J. [3], 31, 768
28, 1267
bt^^JS ID 2
24^^37 7
785, 847
/3-Colchicoresin
....
C24H39010N
....
90
Hertel
B., 14, 1412
Stearanilide
C.sH^.CO.NHPh
C24H4!ON
....
93-6
Pebal
A., 91, 152
v., 412
a,H41O,N
B.. 6, 1186
115 ; 130
Hiibner
J. p. [21 19, 308
36, 950
^2441^4
L L JJ J ^^
Benzenylamidochrysole
c,6Hwc:c.o.cph : N
C8,H16ON
....
259-265
Japp and Streatfiek
41, 157
Benzoxybenzenebidiazoben-
(Ph.N2)2.C6H3.OBz= 1 .3.4
c25nlso2N4
....
138-139
Nolting and Kohn
B., 17, 389
46, 902]
zene
Anilidomethoxyquinoneani-
C19H1602N2+C6H2.OH.
C25H190,N6
....
188
Zincke
B., 18, 738
48, 787
lide picrate
(N02)3
Nitrosotriphenylmethylani-
CPh3.NPh.NO
C2SH24ON2
....
156
Elbs
B., 17, 704
46, 1032
line
Tetraphenylcarbamide
CCXNPh^
»>
....
178-180
Girard and Willm
B. S. [2], 25, 248
30,99
„
Jl
»
B., 12, 1166
183
Michler
B., 9, 710
30, 290
Carbamidoazobenzene
CO(NH.C6H4.N,,.Ph),,
C25H20ON6
....
270 d.
Berju
B., 17, 1404; 0.
46, 1149; 48,
C. [18841, 871
660
Carbonitrotetrimidobenzene
C(NH.C6H4.N02)4=(1.3)4
C25H20Q,NR
286
Hiibner
B., 10, 1719
34, 143
„ ....
=(l-4)«
»
a. 300
»>
B., 10, 1718
)J
Dianilidotoluquinone anilide
C6HMe{NHPh),,O.NPh
C55H21ON8
•
....
167
Zincke
B., 16, 1560
44, 1118
Diaeetylamarine
CaH^CjN,
a6H2202N2
.•••
268
Bahrmann
J. p. [2], 27, 298
44, 799
m-nitrodiamidotriphenylme-
N02.C6H4.CH(C6H4JSTH2).,
C^H^O.^
.«.
81
Fischer and Ziegler
B., .13, 671
38, 662
thane+C6H6
+C6H6
Isoamylanthracene picrate ....
fr.C^r^HAH.^rCeH,
C,HB07N,
....
115
Liebermann and
B., 14, 795 ; A,
40, 736; 42,
Tobias
212, 1
862
Triacetylparaleucaniline
C^H^Ac^,
C25H2AN3
.«.
177
Renouf
B., 16, 1303
44, 981
Diglycoltoluylamidotoluide....
C6H4Me.N(CH2.CO.NH.
C26H2703N3
....
251
Meyer
B., 8, 1164
29, 402
C6H4Me)2=(1.4)3
Tetraniethdiamido-o-acetoxy-
AcO.C6H4.CH(C6H4.NMe2)2
C^H^O.N,
..«
144
Fischer
B., 14, 2523
42, 393
triphenylmethane
Tetramethdiamido-p-acetoxy-
n »
»
.....
146
»>
»
))
triphenylmethane
Tribenzylidene tetrure'ide ....
C7H6(NH.CO^TH.C7H6.
C26H2904N8
....
24&
Schiff
A., 151, 193
NH.CO.NH2)2
Acetyltetramethylparaleuc-
NHAc.C6H4.CH(C6H4.
C^H^ON,
....
108
Fischer and German
B., 16, 708
44, 1098
aniline
NMe2)2
Acetylleuco base
....
1)
....
186
Fischer & Schmidt
B., 17, 1892
4e, 1316
Tetramethd iamidotripheny 1-
EtO.CPh(C6H4JSTMe2)2
C.,5H30ON2
A., 206, 132
162
Fischer
B., 12, 1687
38,40
metliane ethoxide
Quinine valerate
C^HM0,NaHt-CiHieQ,
C25H3404N2
+HELO
90
Bonaparte
J. Chim. Med.,
v., 24
18, 680
Naroe'ine ethonitrate
C.gH2,09N+EtN03
C25H34012N2
....
155
Claus and Eitzfeld
B., 18, 1571
48, 996
(Enanthotetrureide
....
C25H5204N8
155
A., 151, 190
a-dinaphthylene oxide picrate
C20H120+2C6H2.OH.(N02).,
C26H1308N3
167
Knecht & Unzeitig
B., 13, 1725
"• ii »
»
»
MM
173-173
Merz and Weith
B., 14, 197
ft- » »
»
»
....
122-122-5
;>
B., 14, 201
ft-
J»
»1
• •••
135
Knecht & Unzeitig
B., 13, 1726
Dinaphthylenamide picrate....
C20HUJN+C6n2.OH.(N02).)
C26H1607N4
217 ; 219 c.
Walder
B., 15, 2174
44, 209
Dibenzoyldinitrodiphenol ....
(.C6H3.NO2.OBz)2
C26H160SN2
J. K., 10, 318
191
Goldstein
B. S. [2], 30, 434
36, 148
Oxyquinonenaphthalide
Ci!H9(OH).O.N.C10H7
C26H1702N
148
Breuer and Zincke
R, 13, 632
38, 665
Dinitrobenzoylbenzoxydi-
fr. BzO.C6H4.NPhBz=V4
C26H1707N3
194-195
Philip and Calm
B., 17, 2438
48, 156
phenylamine
|3-dinaphthol picrate
C20H1402+C6H2.OH.(N02)3
C^H^N,
174
Walder
B., 15, 2170
a-Naphtholazobenzeneazo-a-
C6H4(N2.C10H6.OH)2
C,,HI8OtN4
d.
Meldola
47, 663
naphthol
= 1.4 ; (aa\
«- „ -ft- „
„ =1.4; aa ; a0
>»
....
235-236
,,
47, 665
ft- „ -ft- „
=1.4 ; (a./3)2
TJ
a. 275
47, 664
Nitrobenzeneazo-a-naphtha-
N02.C6H4.N2.C10H6.N2.
C26H1803N6
d. 245
,,
45, 115
leneazo-/3-naphthol
C10H,.OH=1.3 ; aa ; a/3
Acridine nitrite
CMHMN,+NOSH
C36H190SN3
+ 3H2O
150-151
Medicus
B., 17, 196
46, 748
COMPOUNDS CONTAINING FOUR ELEMENTS.
587
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Benzoylbenzoxydiphenyl-
C6H4.OBz.NPhBz=1.4
C:6H1903N
175
Philip and Calm
B., 17, 2473
48, 156
ainine
Azoxybenzanilide
ON2(C6H4.NHBz)2=( 1 . 2)2
C26H2003N4
195
Mixter
A. C. J., 6, 26
46, 1327
»
=(1.3).
)I
272
»
A. C. J., 5, 1
46, 301
„
ON2(C6H4.CO.NHPh)2
>»
....
310
j»
A. C. J., 5, 282
46, 666
Nitrosotriphenylmethyl-
C6H4Me.N(NO).CPh3=1.4
C26H22ON2
....
145-146
Wittich
B., 17, 706
46, 1032
toluidine
Ph2N2H2 1 (CO)2 : Ph2
C^H^OoN.,
146
Erhardt
A. P., 8, 481
34, 317
Diphenyldiphenylenedicarb-
C12H8(NH.CO.NHPh),
26 2. 12 2
CS.H.AN,
....
a. 300
Kiihn
B., 18, 1478
48, 979
amide
Benzoylparaleucaniline
••••
C26H03ON3
....
149
Kenouf
B., 16, 1302
44, 981
Triacetyl leucaniline
....
G)6rL703N3
...
168
D
B., 16, 1303
J>
Ethyltoluidine phthalein ....
C6H4:(CO)2:(NEt.C6H4Me)2
C!6H28ON2
....
90
Piutti
G. L, 13, 542
46, 450
=(l-2)3
Hexamethtriamidodibenzoyl-
N Me2. C6H3(CO.C6H4. NMe2).
C26H2902N3
....
122
Michler
B., 9, 717
30, 299
benzene
»
»
J>
....
122
Michler & Duper-
B., 9, 1900
38, 333
tius
Benzylcinehonine
....
C!6H3002N2
....
117
Glaus and Treupel
B., 13, 2295
40, 290
Acetylpentamethylparaleuc-
NMeAc.CH(C6H4.NMe2)2
C26H31ONS
142-143
Fischer and Korner
B., 16, 2907
46, 607
anilnie
Benzamido-n-caproic anhy-
[C5H10(NHBz).CO]20
C26H3205N2
B. S., 30, 561
85
Destrem
C. E., 86, 484
34,506
dride
Loxoterygine
....
C26H3402N2
....
81
Hesse
A., 211, 278
48,744
Jervine .... ....
C.,6H37O3N
d. a, 200
Will
A., 35, 117
„ (see C30H4603N2) ....
C26H4302N(?)
u
231 ; 237 ;
Wright and Luff
35, 410, 416
239 c.
Solanicine
....
C26H39ON
....
a. 250 p. d.
Zwenger and Kind
A., 123, 344
v., 345
Aconiue
C.CH.OO,,N
abt. 130
Wright and Luff
33, 320
Solauidine
....
26 39^11
C26H4102N
....
a. 200
Zwenger and Kind
A., 118, 142
v., 345
l>iiiitrocholesterin
C26H42(N02)20
C26H4206N2
120-121
Preiss & Raymann
B., 12, 225
36, 634
liubijervine
C.,6H43O2N
236
Wright and Luff
35, 411
(ilycocholic acid
A., 67, 9 ; 157, 286
C^H^N
....
a. 100
Strecker
Handw.b.,2,1192
42, 1220
D 51 •"• •*••
J. p. [2], 10, 267 ; 25, 99
n
132-134
Emich
M. C., 3, 325; 4, 99
5)
Paraglycocholic acid....
A., 65, 12
»
....
183-184
51
M. C., 3, 340
)>
Anhydrotolylketamiue
(NH.C!6H4.N : O.C6H4)2CO
C27H19ON4
A., 210, 340
277
Stoddard
B., 11, 297
34,504
L. _1
=1.2; 1.4
,,
'» i)
)T
....
277
Briickner
A., 205, 121
40,94
Benzoyldi-/3-naphthylamine
(C10H7)2NBz
C27H,9ON
....
173 u. c.
Glaus and Richter
B., 17, 1593
46, 1358
/3-Diazonaphthalene benzoyl-
C10H7.N2.NBz.C10H7
C,.H,,ON3
....
177
Lawson
B., 18, 2422
48, 1238
/3-naphthylaruiue
Di-3-naphthylphenylcarb-
PhHN.CO.N(C10H7)2
C^H^ON,
179
Gebhardt
B., 17, 3039
48, 384
amide
Tribenzoyldiamidophenol ....
fr. OH.(NHBz)2=1.2.6
C^H^O.N,
183-184
Stuckenbnrg
B., 10, 387
38, 475
„
)> )»
»
183-184
Post
A., 205, 83
»
=1.2.4
»»
231-233
Stuckenburg
B., 10, 381
38, 193
,,
11 )>
T»
231-233
Post •
A., 205, 69
Diphenyldibenzoy Iguanid i n e
CN-.HPhjBzj
C27H2102N3
....
102
McCreath
B., 8, 384
28, 885
Pyrogallolphenylcarbamate....
C6H3(O.CO.NHPh)3
C27H2106N,
....
173
Snape
47, 774
Triacetylhydrocyanrosolic
C21H14N(OAc)3
C27H2306N
143
Grcebe and Caro
A., 179, 200 ; B.,
29, 590 ; 34,
acid
11, 1117
794
Diani idomethoxy tripheny 1-
MeO.C6H4.CH(C6H4.NH2)2+
CS7H28ON2
....
65
Mazzara and Pos-
G. L, 15, 57
48, 1141
methane
C6H5Me
setto
Hydroethylsalicylamide
....
C27H3003N2
....
100
Perkin
[2], 5, 418
vi., 1009
o-Nitrotetrethyldiamidotri-
N02.C6H4.CH(C6H4.NEt2)2
C27H3302N3
....
109-110
Fischer & Schmidt
B., 17, 1894
46, 1316
phenylmethane
Picrorocellin
....
C27H3905N3
....
192-194
Stenhouse & Groves
A., 185, 14
31, 718
Hyoglycocholic acid
....
C27H430SN
....
nf. 120
Strecker and Gun-
A., 62, 215
lii., 234
dalach
Cevine
C27H41(OH)206N
C27H4308N
...*
145
Wright and Luff
33, 350
Myristoxine ....
C(C13H27)2:NOH
C27H65ON
B., 17, 1575
51
Spiegler
M. C., 5, 241
46, 1115
Oery lie nitrate
C^H^O-NOj
C27H5603N
'
76
Champion
O.K., 78, 1150
27, 887
4 F 2
588
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Benzenylbenzaniidoalizariii...
c6H4 : (co)2 : c,;H(OBz).o.
C^AN
—
a. 300
Romer
B., 18, 1669
48, 1069
Phenanthrenequiuonimide
C^N
C H ON2
247
Zincke
B., 12, 1643
anhydride
Diphthalyl-o-p-benzidine ...
[.c6H4.N:(CO)2:c6H4],
C28H16O4N2
....
194
Bandrowski
B., 17, 1183
46, 1015
.> -P-P- »
„
„
....
a. 360
J;
B., 17, 1181
„
Jmidohydroxylauthraquiuone
....
C28H1606N2
A., 166, 153
240
Bottger & Petersen
J. p. [2], 6, 367
26, 390
a-phenyleneuaphthylene
C16H100+2[C6H2.OH.(N02)3]
C28H16015N6
A., 209,141
165
Arx
B., 13, 1727
40, 282
oxide picrate
Oxidation of dibenzylamine
....
C^H^OgN,,
...»
142
Claus
B., 15, 2332
44, 20.3
Benzoylanhydrosalicyldiami*
C2lH13BzON2
C^H^OjNs
....
218-220
Japp & Streatfield
....
41, 148
dophenanthrene
2
C14H8Bz3N3
„
....
239-5-240-5
Goloubeff
B. S., 43, 128
48, 661
a-diphenanthreneoxytriimide
....
C^H^ON;,
....
282
Sommaruga
M. C., 1, 149
&- „ „
....
„
....
a. 300
„
M. C., 1, 158
Beuzamil
....
C28H2002N2(?)
....
170
Laurent
R. S., 19, 446
i., 541
1 ' "i
Dinitrosodiphenyldiisoiudole
NPkC(NO).CPh.NPh.C(NO).C
C2SH28O3N4
™
244
Mohlau
B., 15, 2487
44, 342
> i
Ph
HNO2 oft anthramine
(CUH9NH)2N.OH (?)
C^H^ONj
••»»
250
Bollert
B., 16, 1639
44, 1140
0-naphtholazobenzeneazodi-
NHPh.C6H4.N2.C6H4.N2.
C28H21ON6
....
203-204
Meldola
43, 441
pheuylamine
C10H6.OH=1.4; 1.4; aft
Benzil on benzonitril
....
C28H2103N
....
225
Japp and Tresidder
B., 16, 2653
46, 314
Beuzoxybenzamidomethyl-
BzaC6H4.CO,C6H3Me.NHBg
C28H21O^N
192-193
Liebermann
B., 16, 1931
44, 1097
benzophenone
2
....
C^H^ONj
A., 171, 144
254-256 c.
Guareschi
G. I., 4, 22
27, 584
Benzilimide ....
....
C28H2202N2
....
130
Laurent
R. S., 19, 442
i., 546
1
....
C23H2AN.J
106-110
Ladenburg
B., 11,597
Benzil on benzonitril
J)
.....
168
Japp and Tresidder
B., 16, 2653
46, 314
Dibenzdiamidomethylbenzo-
NHBz.C6H4.CO.C6H3Me»
„
226
Liebeimanu
B., 16, 1929
44, 1097
phenone
NHBz
2
....
C28H2204N3
60-70
Lorenz
B., 7, 1098
t
C24H16N404Ac2
C28H220&N4
....
285
Zincke&Hebebrand
A., 226, 60
48, 258
?
(Ph,N)2C.C2Ht.CO.O
C28H24O2N2
»v
234
Piutti
G. I., 14, 351
48, 783
Dibenzoyldihydroxystubene-
[C6H4(OH).CH.NHBz].,
C^H^O^N,
....
a. 300 d.
Japp and Hooker
....
45, 674
diamine
Aniline +succinylsuccinic
....
C28H2703N3(?)
....
210
Kuorr
B., 17, 546
4e, 1198
ether
Aspidospermatine
....
C^H^OjN,
i...
162
Hesse
A., 211, 249
42, 742
'
....
C^H^OaN.,
....
85
Claus
B., 14, 2372
42, 178
Ethylene-a-naphthylurethane
C2H4[N(C10H7).CO!!Et].$
CsjgH^O.N,
156
Reuter
B., 8, 25
28, 649
?
....
C28H30ON-4
186
Claus
B., 14, 2371
42, 178
Diacetylpentamethylpararos-
....
C^H^OaNa
....
223-225.
Fischer and Korner
B., 16, 2906
46, 607
aniliue
Thapsic anilide
C16H2802(NHPh)2
C-jgH.oOjNj
162-163.
Canzoneri
G. L, 13, 514
46, 461
Verine
C28H44(OH)N07
C^K-iAN
MM
95-130
Wright and Luff
...*
33, 355
Yicme ....
....
C28H5102iNn
B., 9, 301
180 d.
Ritthausen
J. p. [2], 2, 336; 7,
374 ; 24, 202
Myristoyltridecylcarbamide
C,3H27.NH.CO.NH.C14HJ70
C^H^OjNii
103
Reimer and Will
B., 18, 2016
48, 1197
NH3 on isobutaldehyde
(C4H8)7ON6H6
C28H62ON6
d. 90
31
Lipp
A., 205, 5; B.,
38, 621 ; 40, 84
13, 904
1
MM
C29H2103N3
168
Haarmaim
B., 6, 341
26, 908
Di(-p-benzamidophenyl)
N(C6H4.NHBz)2.C02Et
C29H2504N3
....
a. 360
Hager
B., 17, 2628
48, 150
urethane
?
CO(C14H13N2)2
C29H26ON4
115-5
Lob
B., 18, 2428
Hydromethylbeuzylamarine
C21H18MeN2O.CH.,Ph
C29H23ON2
208
Claus
B., 15, 2327
44, 203
Benzylidenediantipyrine
Ph.CH(CuHuONa)2
201
Knorr
B., 17, 2040
46, 1378
Quinine+nitrobeuzaldehyde
C22H2402N2+C6H4.N02.CHO
c^H^o'Tsr,
113-118
Mazzara
G. I., 13, 3G7
46, 466
Roccellauilide
Cl7H3002(NHPh)3
55-3
Hesse
A., 117, 342
v., 113
COMPOUNDS CONTAINING FOUR ELEMENTS.
589
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Carnpholuretkauebeiizalde-
Ph.CH(NH.C02.C10H17)2
C29H4204N2
....
185-187
Haller
C. R, 94, 869
42, 1214
hyde
Pseudojervine
....
C29H43O.N
299 d.
Wright and Luff
35, 413
Carbopetrocene picrate
....
C30H1107N3
185
Prunier
A. C. [5], 17, 28
36,447
Phenylparamide
C6(C202 : NPh)3
C30H1506N3
11. f. 300
Hotte
J. p. [2], 32, 238
48, 1220
Dibenzoylindigo
J. p., 91, 382
C30H1804N2
C.R.,56,1050
108
Schwartz
J. [1863], 557
Fr. dinitrazoxynaphthalene...
C20H,AN4 (?)
C30H1908N5(?
199
Liebermann
A., 183, 225
31, 600
j3-naphthaquiuone di-a-naph-
C10H7.NH.CIOH..O.N.C10H7
C30H2l)ON2
246-247
Meldola
45, 160
thalide
1 '
Dihydroxyphenylcyanurate
[C3N3(O.C6H4.OH)2]2
C30H2008N(i
+6H20
a. 360
Birnbaum & Lurie
B., 13, 1620
Picrate of C24H18O4N4
....
C^A.Nj
....
235 d.
Zineke and Hebe-
A., 226, 60
48, 258
brand
Ethylenebenzoylcarboxylic
[.CH2.C(N2Ph).C6H4.CO]a
C^StflJS4
....
236-237
Eoser
B., 18, 804
48, 797
pheny Ihy drazide
1 J
Benzenebidiazoacenapththol
C6H4(N2.C10H6.OAc)2
CMH2204N4
....
223
Meldola
....
47, 664
=1.4 ; (a«)2
.
Ethylene dibenzhydroxamate
C2H4(NBz.OBz)2
C30H2406N2
....
148
Eiseler
A., 175, 342
28, 768
Nitrous acid on furfurin
....
C^H^O^N,
....
94-95
Schitf
B., 10, 1189
34,46
Ethyleneditolyldimethyl-
C2H4[NMe(C6H4Me).0.
CJItfluXtf.
....
196
Hiibner, Tolle, and
A., 224, 331
40, 1318
ammonium picrate
C6H,(N02)3]2
Athenstadt
Aniline usnate
....
CjoH^OjN,
....
142
Paterno
G. I., 7, 189 ; 8,
32, 786; 34, 884
225
Benzylnarceine
C23H28(CH:iPL)09N
C3oH3i09N
....
169 u. c..
Claus and Eitzfeld
B., 18, 1574
48, 997
Quinine eugenate
C20H2402N2.C10H1202
C30H3604N2
110 p. d.
Hesse
A., 135, 325
vi., 984
Emetine
A. C. (2), 4, 172 ; (5), 8, 233
C30H440,N2
C28H4005N2
62-65
Podwyszotzky
P. J. [3], 10, 642
38, 720
A. C. (5), 12, 277 ; Z. C.
)>
....
70
Lefort
J. P. [4], 9, 241
vi., 580
[1869], 414
Jervine
see C26H3703N
C30H1603N2
193-196
Bullock
P. J. [3], 6, 1009
30, 530
Aconitine (?) ....
see C33H43O12N
C30H4707N
80
Planta
A., 74, 259
i., 55
Myricylic nitrate
CS.HH.O.NO,
C30H6103N
61
Champion
C. R, 78, 1150
27, 887
Alizarin blue dibenzoate ....
C17H7N02(OBz).j
C31H1706N
244
Graebe
A., 201, 342
Dibenzoylniorpliiue
C17H17ON(OBz)3
CS1H2706N
186
Polstorff
B., 13, 98
„
II
»
188-190 c.
Wright and Eennie
28, 322
37, 611
?
C.,,H3303N3
263
Knorr
B., 17, 545
46, 1198
Diacetylapopseudacouiue ....
(C27H37N06XOAc)20
C3IH4301()N
• to
b. 100
Wright and Luff
33, 331
Picro-aconitine
....
C31H4601QN
nf. 100
Wright
....
31, 146-
(3-dinitroanthraquinone
C14H602(N02)2.C18H13
C32H1806N2
cf.B., 3, 811
294
Schmidt
J. p, [2], 9, 250
27, 987
chrysene
£-dinaphthalene oxide pic-rate
C10H6)20+[C6H2.OH.(N02)3]2
C32Hl&015N6
135
Walder
B., 15, 2172
44, 209-
P- 11 » II
»
))
cf.B.,14,201
135
Knecht & Unzeitig
B., 13, 1726
40, 281
a~ ii n >i
»
)>
167
»-
B., 13, 1725
»
Q~ )i ii ii
J)
»
it* •
173
Merz and Weith
B., 14, 197, 199
40, 265
Picrate of C26H16
C.,6H16+C6H2.OH.(N02).,
C32H1907N3
....
177-178
Harpe and Dorp
B., 8, 1049
29, 243
a-Naphthyloxide picrate
(C10H.)J0.[C6Hi,OH.(N02).j]2
C32H2001SN6
114-5-115
Merz and Weith
B., 14, 198
40, 264
ft- ii ii
)»
»
....
122-122-5
11
B., 14, 201
)1
a-Dinaphthol picrate
C20H1402.[06H2.OH.(N02)3]2
C35H20016N0
....
145
Walder
B., 15, 2171
44, 209
ft- 11 i)
11
)»
....
174 u.c.
ii
B., 15, 2170
J)
/3-(3-Dinaphthylamine picrate
C32H21014N7
164-165
Benz
B., 16, 20
44, 593
a-°- 11 11
)»
....
168-169
11
B., 16, 20
44, 594
a-3- ii ii
....
V
....
172-173
i>
B., 16, 17
»
Dibenzdiphenyldiamidoben-
C6H4(NBzPh)2=1.3
C32H2402N2
184
Calm
B., 16, 2798
46, 592
zene
ii
= 1.4
If
218-5
ii
B., 16, 2808
11
Phthalylbidiphenylamine ...
C6Hi(CO.NPh3)2=1.2
)>
....
238
Lellmaon.
B., 15, 830
42, 1060
Benzoylimidocinnamic an-
O(CO.CH.NBz.CHPh)2
C32H2406N2
164-165
Plochl
B., 16, 2815
46, 604
hydride
i i
?
O(CO,CH.NBz.CH.C6H4.
C32H2407N2
160
Plochl & Wolfram
B., 18, 1184
48, 898
OH)2
Benzacin ....
....
CfflH27ON3
. ..
150
Frankland and
....
37, 567
Tompkinsi
1
CsgHgsACjNjP,
C32H!806N2
....
225-227
Japp and Hooker
....
45, 678
590
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Erythrolideofphenylcarbamic
C4H6(O.CO.NHPh)4
C32H3008N4
....
215 d; sf. 210
Tessmer
B., 18, 970
48, 774
acid
Hexethyltriamidodibenzoyl-
NEt2.C6H3(CO.C6H4.NEt2)s
C32H4102N3
70
Michler and Grad-
B., 9, 1914
32, 335
benzene
mann
Oxyacanthine
„.
C32H460UN2
139
Wacker
J. [1861], 545
iv., 288
Cevadine (veratrine)
C27H41N06(OH).O.CO.CMe :
C32H4909N
A., 95, 200
205 ; 206 c.
Wright and Luff
33, 344*
C2H4
„ ,, .... ....
„
„
B., 9, 1116
205
Schmidt & Koppen
A., 185, 224
30, 530, 906
.. »
!!
„
205
Schmidt
A. P. [3], 10, 511
34, 517
(C.C. [1872], 229)'
Lycopodine ....
C H O N
114-115
Bodeker
A., 208, 363
40, 1158
a-Dinaphthylmethane picrate
aiH16.[C6H3.OH(N02)3]2
C^H^N,
142-143
Grabowski
B., 7, 1607
28, 456
Dibenzoyltriphenylguanidiue
NPh : C(NPhBz)2
C33H2502N3
185
McCreath
B., 8, 383
28, 885
C26H35NO7(OH)(OBz) : O
C H O N
185-186
Wright and Luff
33, 325
Aconitine (A., 7, 276; 74, 257)
C26H35NO.(OH)3(OBz)
C^H^O^N
....
183-184
....
33, 159, 325
Fr. /3-Naphthaquinonetoluide
....
C34H2204N4
....
260-265
Zincke and Brauns
B., 15, 1972
44, 209
Tetrabenz-5-diamidopheiiol ....
OH.(NBz2)2=1.2.6
C3,H2405N2
A., 205, 83
182
Stuckenberg
B., 10, 387
32, 475
Oxydimorphine
cf. B., 13, 86-91
C34H3606N2
....
245 d.
Schiitzenberger
B. S., 4, 178
Guoscopine
J. [1878], 873
C34H360UN2
....
233d.
Smith
P. J. [3], 9, 82
34, 987
Sabadilline (Cevadilline)
....
C34H53O8N
200
Couerbe
A. C. [2], 52, 352
33, 339
r, »
....
„
200
Weigelin and Dra-
N. J. P., y, 94
„
gendorff
Azurine
....
C35H3203N4
250-5
Ladenburg
B., 11, 598
34, 572
Colchiceine ....
See C17H1905N
C35H420,,N2
155
Oberlin
A. C. [3], 50, 108
i., 1080
Acetylapoaconitine
C26HS507N(OAc)(OBz):0
C35H43012N
....
180-181 c.
Wright and Luff
....
33, 328.
Stearoxime .... .
(C27H35)2C:NOH
C35H71ON
B., 17, 1575
62-63
Spiegler
M. C., 5, 241
46, 1115
Carbopetroceae picrate
C24H8.[C6H2.OH.(N02)3]2
C36H14014N6
C. E., 88, 316
135
Prunier
A. C. [5], 17, 28
36, 446
/3-Naphtholazobenzeneazo-a-
HO.C10H6.N2.C6H4.N2.C-10H6.
C36H2402N6
....
a. 295
Meldola
43, 437
naphthleneazo-/3-naplithol
^J «.GjQHg.0H — pu j 1 .4 j Qd j a/3
....
C3SH28ONS
....
224
Kimich
B., 18, 1028
29, 268
/~1 TT "W" /"2\
/ij\
9*}fi-9T7
Witt and Thomas
43, 115
Dicodethylene (ethyleuedi-
(cl7Hl8N03)2C2H4
C36H1006N2
_ . in — io 1
d.w.m. 200
Grimaux
C. E., 93, 67 ;
40, 1045 ; 44,
morphiue)
A.C. [5], 27, 273| 359
A popseudoaconitine ....
C^H^OnN
+H,O
102-103
Wright
33, 151
Pseudoaconitine
C.,,H37O5N(OH)3.O.CO.
C36H49012N
+H3O
100 +
Wright and Luff
....
33, 336
C6H3(OMe)2
„
„
„
104-105
„
....
33, 159
Lycoctonine
=pseudoacouitine (?)
100-104
Fliickigei-
J. [1870], 837
33, 335
Pentacetylsolanidine
....
C36H6107N
150
Hilger
A., 195, 322
Heptadecylsteary [carbamide
NH(C17H3i).CO.NH(C13H350)
C36H7202N2
112
Hofmann
B., 15, 761
42, 1053
Veratrine
....
C37H53OUN
....
115
Couerbe
A. C. [2], 52, 352
33, 339
C2sH440-N.O.CO.C6H3(OMe)2
.
180 c.
Wright and Luff
33, 353
Dinaphthylenphenylamine
C26H17N.[C6H2.OH.(N02)3]2
C38H23014N7
169 u.c.
Waldev
B., 15, 2177
44, 209
picrate
?
C24H16Bz204N4
C33H2606N4
....
264-5
Zincke and Hebeb-
A., 226, 60
48, 258
rand
Tribenzoylmorphine
C17HJ6Bz303N
C38H3106N
186
Polstorff
B., 13, 98
38, 407
Triphenylrosauiline
J. [1862], 696 ; [1863], 786
100
....
A., 132, 162
Tetramethdiaraidopropyltri-
C26H32N2+C6H2.OH.(N02)3
C3SH38014N8
....
156
Ziegler
B., 13, 786
38,640
phenylmethane picrate
Dihydrodicinchonine
J,p. [2], 8, 293
C38H4602N4
A.5 108, 348
257-258
Skraup
B., 11, 314
•
Acetylapopseudoaconitine ....
C27H3705N( : 0)(OAc).O.CO.
C38H49012N
...'
115
Wright and Luff
33, 170
C6H3(OMe)2
1
C0H3Me(NH.CO.C6H4.N :
C39HS206N4
220 d.
Schiff
A., 218, 185
46, 455
CH.C,H4.OAc),= U.? ;
(1.3 ; 1.2),
Dihydroxydirnethyldipropyl
Ph.CH[CsH4.N2.C6H2MePr
C39H400SN6
170
Mazzara
G. I., 15, 44
48, 904
diphenyldiazobenzophenyl-
(OH)N]2
metliaue
N.OH=1.4
COMPOUNDS CONTAINING FOUR ELEMENTS.
591
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Benzoylcevadine
C27H41O6N(OBz).O.CO.
C39H63010N
+ 1£H20
170-180
Wright and Luff
....
S3, 351
CMe:C2H4
Diphenyldiisoindole picrate...
C,8H22N2.[C6H.,OH.(N02)3]2
C40H28014NS
127
Mohlau
B., 15, 2487
44, 342
Phthalyldiphenylaminaspar-
c6H,[co.NPh.c2H3 : (CO)., :
C40H3AN4(?
273
Piutti
G. I., 14, 473
48, 797
te'in
NPh]2=1.2
Triphenylamidomethane oxa-
(CPlvNIL^+HiCA
040H3AN2(?
253
Elbs
B., 17, 702
46, 1031
late
Azo-p-toluenephenine
....
C40H3ION6
249-250
Kimich
B., 8, 1032
29, 269
Benzoylapoaconitine.... •
C40H46012N
130
Wright
33, 324
Diacetylcodeuie
C^AcAN,
C40H4608N2
135
Beckett and Wrigh
....
28, 324
Dulcitolide of phenylcarba-
HO.C6Hs(O.CO.NHPh)5
C4,H39OnN6
250
Tessmer
B., 18, 971
48, 774
mic acid
Manitolide „ „
n
»)
....
260d;sf.,25(
«
B., 18, 970
»
(Eoanthohexiire'ide
See A., 151, 190
C41H3t06N12
150
Schiff
A., 151, 190
Benzilam
C42H3202N2
v. C14H9N
113-114
Zincke
B., 16, 891, 892
Bsnzilimule . - .
C.2H,.,O,Nn
v. C,.H,,ON
137-139
B., 16, 890, 891
Itnabenzil
42 32 4 2
^14 ll^-1
v. C,.H,,ON
158-170 d.
!>
B., 16, 891
14'^H
d. 140
))
Henius
A., 228, 339
48, 1067
Dibenzoyldibenzoxystilbene
[C6H4(OBz) : CH.NHBz]2
C42H3206N2
....
246-248
Japp and Hooker
45, 682, 683
diamine
Tetracetyl- ?
....
C42H3AN4
....
190-191
Zincke and Brauns
B., 15, 1971
44, 209
Cinchonamine malate
(C19H24N20).2.C4H60!, (?)
C42HS406N2(!
+H20
160
Arnaud
C. R, 97, 174
46, 88
Solanine (A.C. (2), 31, 109) ....
C43H71016N (?)
C42H75015N
cf. R, 9, 83
200+
Btytn
33, 316
J. [1863], 450 ; [1873], 817
»
....
235
Zwenger and Kind1
A., 26, 232; 118,
v., 346
130
Dinaphthyldiquinonetetrani-
C20Hs(NHPh)2(:NPh)2:02
C^HsAN,
.«.
248-250
Korn
B., 17, 3023
48, 392
lide
Tetrethdiarnidodinaphthoic
NEt2.C10H,,(CO.C10H6.NEt2j,
C44H470,N3
....
130
Smith
....
41, 186
diethamidonapbtbalene
Atisine
....
C46H7406N2
85
Broughton
Medical Press,
31, 146
1874
Veratroidine „
C24H3707N (?)
CMH78016N2
....
129-130
Mitchell
P. J. [3], 5, 768,
28, 1267
785, 847
Narce'ine ethyloxalate
(C23H2909N),,Et2CA
C52H6A2N2
....
174 d.
Glaus and Eitzfeld
B., 18, 1571
48, 996
? ._
—
Ca^^O^N,
150
Weigelin
N. J. P., 37, 94
33, 339
Benzylamarine oxalate
(C28H24N.)2.HA04
Ci3H5004N4
240 u.c.
Claus & Kohtstock
B., 18, 1853
48, 1133
Narceine benzylcarbonate ....
(C23H2909N)2(CH2Ph)2C03
C60H73021N2
135
Clans and Eitzfeld
B., 18, 1573
48, 997
Japaconitine
0[C2,H39OzN(OBz):0]2
C^H^O,^,
181 ; 183 ;
Wright and Luff
....
36, 394-401
185-5 ;.?&£-
186
Homocerebrin „
C^H^O,,^?)
....
b. 155
Parcus
J. p. [2], 24, 326
42, 236
Encephalin „
C1MH206019NH
d. 125
150
»
J. p. [2], 24, 327
Jl
C.HANa
181 u. c.
Hesse
A., 205, 368
40, 624
Anthracene orange
»
225
Bottger
J. p. [2], 2, 130
vii., 86
Colloturine
Composition unknown
)»
....
sb. 234
Hesse
B., 11, 1546
36, 73
Ouscamine „
....
)^
....
218
»
A., 200, 304
38, 329
Loturine
Composition unknown
>»
234 u. c.
>»
B., 11, 1544
36, 73
Methylcodethylene (?)
Probably C13H21NO2(OEt)
)»
132
jrimaux
C. E., 93, 592
42, 218
Oleandrine
B., 14. 2602 ; 16, 254
))
135
begins 56
Bettelii
G I., 6, 310
29, 404
J. [1861], 546
»
70-75
J. [1875], 783
"
Quebrachamine
Composition unknown
n
142
ffesse
A., 211, 265
42, 743
Taxine
J. [1856], 55»
n
80
Vlavine
C. C. [1876], 166
31, 476
....
»»
....
80
VTarm6
B. S., 26, 417
>* *
Acid from Hg fulminate ....
....
))
....
85
Scholvien
J. p. [2], 30, 91
48,39
Usnic acid+aniline
....
»
....
170
Paterno
G. I., 7, 192 ; 8,
32, 787; 34,
225
884
FronjC34H22O6N4
?)
....
212-214
Zincke and Brauns
B., 15, 1973
44,210
! 77-1 %C ; 4'6%N; 12-5% N
)i
...
224
»
B., 15, 1972
j»
592
ORGANIC COMPOUNDS.
(19.) CHOP, CHOAs, CHOSb.
Name.
Constitution,
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Methylphosphinic acid
Me.PO(OH)2
CH60,P
....
105
Hofmann
B., 5,106; 6, 30(
25, 421 ; vii.,
956
Ethylic metaphosphate
EtO.PO,
C2H503P
b. 100
....
Carius
J. [1861], 586
Dimethylphosphinic acid ...
Me2PO(OH)
C2H7O2P
....
76
Hofmann
B., 5, 108
25, 421 ; vii.,
956
Ethylphosphinic acid
Et.PO(OH)2
C3H703P
....
44
n
B., 5, 110
25, 422; vii.,
957
Isopropylphosphinic acid ...
Pr/s.PO(OH;2
C3H903P
....
60-70
5»
B, 6, 304
26, 884 ; vii.,
957
Trimethylic phosphate
PO(OMe)3
C,H904P
197-2
Weger
A., 221, 61
46,11
Hydroxypropylphosphinic
Et.CH(OH).P(OH)2
))
....
158-160
Fossek
M. C, 5, 121
46,834
acid
Diethylphosphinic acid
Et2PO(OH)
04H1102P
....
Liquid — 25
Hofmann
B., 5, 110
25, 422 ; vii.,
957
Isobutylphosphinic acid
Bu0PO(OH)2
C4H.AP
....
100
it
B., 6, 304
26, 884 ; vii.,
957
Dimethylic ethylic phosphate
PO(OMe)2(OEt)
C4HU04P
203-3
....
Weger
A, 221, 61
46,11
Hyd roxy isobu tylphosph inio
Pr.CH(OH).P(OH)2
»
....
168-169
Fossek
M. C., 5, 121, 627
46, 834 ; 48,
acid
504
Isoamylphosphinic acid
C5H11.PO(OH)2
C5H13Q3P
....
160
Hofmann
B, 6, 305
26, 884 ; vii.,
957
Hydroxyamylphosphinic acid
C5H10(OH).P(OH)2
C5H1304P
183-184
Fossek
M. C, 5, 121, 627
46, 834; 48,
504
Phosphenylous acid
Ph.P(OH)2
C,H702P
A., 181, 303
70
Michaelis & Ananofl
B, 7, 1689
28, 467
Phosphenylic acid (phenyl-
Ph.PO(OH)2
C8H708P
A, 181, 321
158
Michaelis
B., 6, 819 ; A,
27, 169 ; 44,
phosphinic acid)
218, 85
735
5» J,
)1
»
158
,,
B, 7, 1070, 1689
28, 171
»» »
)»
>?
158
Schroder
B., 12, 564
Phenylphosphoric acid
PhO.PO(OH)2
C,H704P
G. I., 11, 65
97-98
Jacobsen
B, 8, 1521
29, 596
Diaeetonylphosphinic acid ....
Pr/s.CHAc.PO(OH)2
C6H1304P
+H20
63
Michaelis
B., 18, 902
48, 747
!) »
))
»
B
63-64
,1
B, 17, 1275
46, 991
Triethylphosphinic oxide ....
Et3PO
C.HnOP
240-245
A, 104, 18
Wichelhaus
B., 1, 80
11 „
» (As, 7, 1)
))
240 c.
44
Hofmann
13, 295
iv., 612
» n
»
)1
240
52-9
Pebal
A., 120, 194
!)
n i!
„ (A., 137, 119)
»)
242-8-243 u.c.
a. 51-9
Crafts and Silva
Z. C. [1871], 359
24, 633; vii.,
954
Diethylic ethylphosphite
Et.PO(OEt)2
C6H1503P
188
....
Zimmermann
A., 175, 8
28, 440
»> ,, «...
)»
»»
191
Kail ton
7, 216
iv., 534
„ (J-, 1876,
n
»
188-191
A., 92, 348
Williamson
J,, 7, 563
206)
n rt
j»
»»
192
....
Wichelhaus
As., 6, 269
Triethylic phosphate
PO(OEt)3
C16H1604P
200
Liquid —18
Carius
A., 119, 289
vii., 1120
„ „
J>
5>
214
A, 69, 193 ;
Zimmermaun
A., 175, 1 ; B.,
27, 655 ; 28,
91, 376
7,290
441
)! yi
>1
»J
215
....
Carius
A, 112, 190
vi., 592
,» ,»
>»
»
215
A., 137, 121
Limpricht
J., 18, 471
Carboxylphenyl phosphoric
O2P.O.C6H4.CO,H=1.2
C7HAP
....
145
Anschiitz
A., 228, 308
48, 1062
oxide
Belizophosphinic acid
(HO)2PO.C6H4.C02H=1.4
C7H705P
A., 212, 231
a. 300
Michaelis & Panek
B., 14, 405
40, 604
Tolylphosphinous acid
C6H4Me.P02H2=1.2
C7H902P
....
Liquid
?>
A., 212, 223
42, 960
>, jj
=1.4
J»
....
104
,»
B., 13, 655
38, 641
,, ,, ....
" 1>
>»
104-105
„
A, 212, 218
42, 960
Tolylphosphinic acid
C6H4Me.PO(OH)2=1.2
C7H903P
....
141
,5
A., 212, 232
42, 963
j, »
=1.4
J)
188
»»
B., 13, 655
38, 641
» )>
" >,
»»
189
51
A, 212, 224
42, 962
Cresylic phosphate
PO(OH)2(O.C6H4Me)=1.4
C7H9O4P
116
Rapp
A., 224, 156
46, 1338
Xylylphosphinous acid
C6H3Me2.P02H2
C8HU03P
97-98
Michaelis & Panek
A, 212, 237
42, 964
COMPOUNDS CONTAINING FOUR ELEMENTS.
593
•
Name.
Constitution,
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Dimethylic phosphenylate ....
Ph.PO(OMe)2
cyEiuOjp
247 u.c.
Liquid
Michaelis and Ben-
A., 181, 325 ; B.
29, 598
zinger
8, 1311
Xylylphosphinic acid
C6H3Me2.PO(OH)2
u
186-187
Michaelis & Panek
A., 212, 238
42, 964
Diiuethylphosphobenzoic acid
C6H4.CO2H.PMe2O=1.4
C9Hn03P
243
Michaelis &Czimati
B., 15, 2020
44, 56
Naphthylphosphinous acid ...
C10H7.PO2H.2
C10H9O2P
125-126
Kelbe
B., 11, 1500
36,68
Naphthylphosphinic acid ...
C10H7.PO(OH)2
C10H903P
190
D
B., 9, 1052
30, 525
Diethylphenylphosphine
Et2PhPO
C10H15OP
a. 360
55-56
Ananoff & Michaelis
B., 8, 496 ; A.,
28, 1204
oxide
181, 354
Diethylic phoaphenylite
Ph.P(OEt)2
C^AP
235
Liquid
K6hler& Michaelis
B., 10, 817
32, 449
„ phosphenylate
Ph.PO(OEt)2
CIOH1503P
267 u.c.
Liquid
Michaelis and Ben-
A., 181, 335 ; B.
29, 598
zinger
8, 1311
Turpentine phosphorous acid
CuH.APC
....
50 d.
Kohler & Schimpf
D. P., 199, 510
vii., 959
Diethylic tolylphosphinite ...
C6H4Me.P(OEt),=1.4
C10H1702P
280
Liquid
Michaelis & Panek
A., 212, 222
42, 961
Diphenylphosphinic acid
Ph2PO.OH
C.AAP
B., 11, 885
174
Michaelis & Graeff
B., 8, 1305
29, 596
!> »
»
n
B., 12, 564
190
Michaelis
B., 10, 628
32, 453
» »
J
5?
B., 15, 801
190
Kohler & Michaelis
B., 10, 813
32, 451
Phenylphosphenylic acid
Ph.PO(OH)(OPh)
C12HU03P
....
57
Michaelis and Kam-
B., 8, 1309; A.,
29, 598 ; 44,
merer
181, 336
735
Diphenylphosphoric acid ...
PO(OH)(OPh)2
C12HH04P
A., 143, 193
Liquid
Jacobsen
B., 8, 1235, 1522
29, 596
PC15 on methylene diphenyl
(C13H90)P03 "
CI3H904P
....
255-256
Bichler
J. p. [2], 28, 273
46, 324
oxide
Diphenylmethylphosphine
Ph2MePO
C13H13OP
a. 360
no
Michaelis & Soden
A., 229, 334
48, 1135
oxide
ji u
))
»
• *••
111-112
Michaelis & Coste
B., 18, 2117
Diphenylethylphosphine
Ph2EtPO
C14H15OP
a. 360
121
Michaelis & Soden
A., 229, 334
48, 1135
oxide
Ethylic diphenylphosphinate
Ph2PO.OEt
C14H1502P
....
165
Gotter & Michaelis
B., 11, 888
34, 724
Ethylic phosphate
(EtO)3H.PO.P(OEt)4
Ci4H36O8P2
150-160 d.
Liquid
Geuther
A., 224, 274
46, 1282
Diphenylpropylphosphine
Ph^roPO
C15H17OP
a. 360
Michaelis & Soden
A., 229, 334
48, 1135
oxide
Diphenylisopropylphosphine
Ph2PrfflPO
)>
a. 360
....
»
))
i>
oxide
? acid
....
C16H1703P
....
142
Graebe
B., 7, 1628
28, 457
Triisoamylphosphine oxide ....
(CHMe2.CH2.CH2),PO
C1SH33OP
a. 360
60-65
Hermann
B., 6, 305
26, 884 ; vii.,
955
Diisoamylic isoamylphosphi-
C6HU.PO(OC5HU)2
C^H^P
236
B. S., 18, 151
Eailton
7, 218
iv., 532
nate
» »
»
)>
236
A., 92, 350
Williamson
J., 7, 564
Oxatylic phosphate ....
C16H1503.P03H2
C16H1706P
....
160
Spiegel
B., 13, 2220
40, 173
1 Mpheriylisobutylphosphiue
Ph2Bu0PO
016H19OP
a. 360
Michaelis and Soden
A., 229, 334
48, 1135
oxide
Di pheny li soamy Iphosph ine
Ph2(C6H11)PO
C17H21OP
a. 360
96
n
)!
D
oxide
Phenoxydiphenylphosphine
Ph2P.OPh
C18H15OP
265-270 (62)
Liquid
Michaelis and Coste
B., 18, 2109,2110
48, 1214
Triphenylphosphine oxide ....
Ph3PO
»
a. 360
Michaelis and Soden
B., 17, 922
46, 1180
II 11 I!
))
»)
153-5
Michaelis and Coste
B., 18, 2121
Phenylic diphenylphosphin-
Ph2PO.OPh
C^H^OsP
310 (62) p.d.
135-136
ii
B., 18,2110,2114
48, 1214
ate
Triphenylic phosphite
P(OPh)3
Ci3H1503P
a. 360
Liquid
Noack
A., 218, 85
44, 735
Biphenylic phosphenylate ....
Ph.PO(OPh)2
i)
a. 360
63-5
Vlichaelis and Kam-
A., 181, 338 ; B.,
29, 598; 44,
merer
8, 1308
735
Triphenylic phosphate
PO(OPh)3
C18H1504P
407
B., 15, 640
Andrews
B., 14, 2116
42, 135
11 I!
»
n
410-412 c.
45
Kreysler
B., 18, 1719
)! )>
Jl
»
A., 92, 317
45
Jacobsen
B., 8, 1523
29, 596
Triphenylphosphonium hydr-
C18H1702P
....
148
Michaelis and
B., 15, 803
42, 1062
oxide
Gleichmann
Diphenylbenzylphosphine
(Ph.CH2)Ph2PO
C19H17OP
....
192-193
Vlichaelis and Coate
B., 18,2116,2117
48, 1215
oxide
Dinaphthylphosphinic acid ....
(C10H7)2PO.OH
C20Hi5O2P
• ».•
202-204
Kelbe
B., 11, 1502
36, 68
Tetrahydroxamylidine phos-
(C5H10.OH)4P.OH
C20H4AP
125-126
Girard
A. C. (6), 2, 1
46, 1119
phonium hydroxide
4 o
594
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Tribeuzylphosphine oxide ....
(Ph.CH2),PO
C21H21OP
....
210-212
Letts and Collie
T. E., 30, 181
42, 724
X 11 11
»
H
212
ii
»
42, 725
11 1) 11
»
»i
SIS
Fleissner
B., 13, 1666
40, 264
Tricresylic phosphate
PO(O.C6H4Me)3=(1.4)3
C21H2104P
67-68
Wolkow
Z. C. [1870], 323
11 >i
» )>
))
....
76
Eapp
A., 224, 156
46, 1338
11 i'
» JT
»
....
78
Weber and Heim
B., 15, 640
Stearylglycerolphosphoric
C3H5(OSt)(OH).O.PO(OH)2
C21H4307P (?)
35
Hundeshagen
J. p. [2], 28, 219
46, 282
acid
Trixylylic phosphate
PO(O.C6H3Me2)3=(1.2.?)3
C^H^P
dist.(180-200)
Liquid
Kreysler
B., 18, 1702
48, 1054
,1 11
=(1.3.?),
J)
dist. (200)
Liquid
11
)>
48, 1055
?
C13H13OP ?
025H2202P2(?)
....
154-155
Michaelis and
B., 15, 1963
44,186
Gleichmann
Tetrabenzylphosphonium
(Ph.CH2)4P.OH
C28H29OP
....
190-211
Letts and Collie
T. E., 30, 181
42, 724
hydroxide
/3-Trinaphthylic phosphate ....
PO(O.CIOH7)3
C30H2104P
B., 15, 312
108
Schaffer
A., 152, 290
vi., 856, 859
"- 11 »
n
))
B., 15, 640
145
11
A., 152, 289
JJ
Triisobutylic phosphate
PO(O.C6H,.Bue)3=(1.4)3
C3oH39O4P
a, 400 p.d.
Liquid
Kreysler
B., 18, 1701
48, 1054
Trithymylic phosphate
PO(O.C6H3MePr»),,=(6.4.1)3
M
59
Engelhardt and
Z. a [21 6, 44
vi., 1090
Latschiuoff
ii i)
») ?>
u
....
59
Kreysler
B., 18, 1705
48, 1055
Tricarvacrylic phosphate ....
=(5.4.1 )3
J)
....
71-5-72
Johns
B., 15, 818
ji 11
)» ))
»
dist. in vac.
75
Kreysler
B., 18, 1704
ii
Triisoamylphenylic phosphate
PO(O.C6H4.C5HU)3
C33H4504P
a. 400 p.d.
Liquid
11
B., 18, 1702
48, 1054
Tri(benzylphenylic) phos-
PO(O.C6H4.CH2Ph)3
C39H3304P
J. [1873], 440
93-94
Paterno and Fileti
G. I., 3, 121, 251
27, 372
pliate
/3-Distearyl glycerol phos-
C3H5(OSt)2.O.PO(OH)2
C39H77O8P
60
Hundeshagen
J. p. [2], 28, 219
46, 281
phoric acid
«- 11 1>
J>
J)
....
62-5
ii
,i
n
Arsenmethyl oxide ....
Me.AsO
CH3OAs
....
95
Baeyer
A., 107, 284
1., 402
Cacodylic acid (A., 107, 263)
Me2AsO(OH)
C2H7O2As
B., 12, 22
200; r.s. 90
Bunsen
A., 46, 11
Ethylarsinic acid
EtAsO(OH):,
C2H703As
C.E.,50,1022
abt. 95
Coste
A., 208, 34
Arsenious glyceride
As ! O3 = C3H5
C3H603As
d. 250
50
Schiff
J. [1867], 574
11 11
....
))
....
200; sf. 100
Jackson
C. N., 49, 258
46, 896
Trimethylic arsenite
As(OMe)3
C3H903As
128-129 (760)
B.S., 14, 104
Crafts
J. P. [4], 13, 242
24, 819
„ arsenate
AsO(OMe)3
C3H9O4Aa
213-215 (760)
B.S., 14, 101
11
11
24, 818
ii i)
ii
ii
128-130 (60)
ii
n
11
Arsendiethylic acid
C4HnO2As
....
190
A., 92, 365
i., 398
Cacodyl oxide
O(AsMe2)2
C4Hj2OA82
120
A., 37, 6; 92, 364;
i., 407
107, 283
Phenylarsine oxide
Ph.AsO
C6H6OAs
119-120
Michaelis
B., 10, 624
32, 452
Phenylarsinic acid
Ph.AsO(OH)2
C6H703As
B., 15, 1954
sf. 158
Coste and Michaelis
B., 11, 1884
36, 161
ii ii
n
»
A., 201, 204
168
Michaelis
B., 9, 1568
31, 311
Triethylic arsenite
As(OEt)3
C6H1503As
165-166
B.S., 14, 103
Crafts
J. p. [4], 13, 242
24, 819
i) ii •••• ••••
»
J)
166-168
11
B. S. [2], 8, 206
vi., 221
„ arsenate ...
AsO(OEt)3
C6H1604As
235-238(76")
....
11
,1
vi.. 226
ii ii
j>
)J
148-153 (60)
11
ii
11
ii ii
i)
)>
148-150 (60)
....
11
B. S., 14, 99
Tolylarsene oxide
C6H4Me.AsO=1.2
C7H7OAs
145-146
Coste and Michaelis
B., 11, 1889; A.,
36, 163; 38,
201, 251
397
-ii ii
=1.4
II
156
,i
)>
)»
Tolylarsinic acid
C6H4Me.AsO(OH)2=1.2
C7H9O3As
159-160
11
»
}1
ii i,
= 1.4
JJ
d.w.m. 300
11
')
»
Naphthylarsine oxide
C,0H7.AsO
C10H7OAs
B., 14, 913
245
Michaelis & Schulte
B., 15, 1954
Naphthylai-sinic acid
C10H7.AsO(OH)2
C10H903As
....
197
Kelbe
B., 11, 1503
36, 68
Diphenylarsinic acid
Ph2AsO.OH
C^H^OjAs
B., 12, 564
174
Michaelis and Coste
A., 201, 231 ; B.,
31,311; 38, 397
9, 1569
Dibenzylarsiuic acid
(Ph.CH2)2AsO.OH
C14H15O2As
....
210-5
Michaelis & Patow
B., 18, 43
48, 527
Ditolylarsinic acid
(C6H4Me)2AsO.OH=(1.4)!
5»
• •*•
167
Coste
A., 208, 20
40, 904
Triisoamylic arsenite
As(O.C6Hn)3
C15H3303As
288 (760) p.d.
Crafts
J. P. [4], 13, 242
24, 819
ii ii
»
ii
193-194(60)
ii
B. S., 14, 105
COMPOUNDS CONTAINING FOUR ELEMENTS.
595
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dimetkylic dibeuzarsenate ....
HO.OAs(C6H4.C02Me).,
C16H1506As
MM
a. 280
Coste
A., 208, 23
40, 904
Triphenylarsine oxide
Ph3AsO
ClsH15OAa
....
189
Michaelis
A., 201, 244
„ hydroxide....
Ph3As(OH)2
CI8H17O2As
B., 11, 1888
108
Coste and Michaelis
A., 201, 243
38, 163
Tribenzylarsine oxide
(Ph.CH2)3AsO
C21H21OAa
219-5
Michaelis & Pa'tow
B., 18, 44
48, 527
Diphenylarsine oxide
0(AsPh2)2
C24H20OAs2
A., 201, 230
91-92
Michaelis and Coste
B., 11, 1886
36, 162
Ditolylarsiue oxide ....
0[As(C6H4Me)2]2=(1.4)4
C2SH,,8OAs2
....
98
Coste
A., 208, 20
40, 904
Tritolylstibine oxide
(C6H4Me)3SbO=(1.4)3
C21H21OSb
223-5
Michaelis&Genzkeu
B., 17, 925
46, 1136
„ hydroxide ....
CsH4Me)3Sb(OH)2=(1.4)3
C2lH2ASb
169-5
)*
J)
»
1
(20.) CHSN, CHSP, CHSAs, CHSSb, CHSBi.
Thiocyanic acid
HS.CN
CHSN
85
Artus
v., 505
„
„
„
102
12
Vogel
„
Ammonium thiocyanate
(NH4)S.CN
CH4SN2
....
147
....
v., 506
» »
„
„
....
159
Richter
R. K. T., 12
Thiocarbamide
CS(NH,)2
»
....
149
Reynolds
PI 7, 1
vi., 1117
„
1J
„
149
Volhard
B., 18, 461
„
11
„
151
Baumann
G. J. C., 1873
„
11
i)
....
167
Richter
R. K. T., 12
„
„
„
....
169
Traube
B., 18, 461
48, 739
„
n
„
....
170; af. 149
Pratorius — Seidler
J. p. [2], 21, 129
38, 371
„
„
n
....
172
Glaus
G. J. C., 1875
?
....
„
....
94
Linnemann
A., 120, 86
v., 515
Methylic thiocyanate
MeS.CN
C2H3SN
132-133
....
Cahours
A. C. [3], 18, 261
v., 520
,, >,
„
„
1SS-86
Pierre
C. R., 27, 213
Methylthiocarbimide
Me.N : CS
„
118
j ....
Hofmann
B., 13, 1350
38, 797
„
11
„
119
34 '
„
B., 1, 172
vi., 1056
Thiacetamide
CH3.CS.NH2
C2H5SN
....
107-5-108-5
Bernthsen
B., 10, 38; A.,
32, 887 ; 34,
192, 45
791
„
1)
....
108
Hofmann
B., 11, 340
••«*-
Methylthiocarbamide
NH2.CS.NHMe
C2H6SNS
b. 100
Bernthsen & Klinger
B., 11, 493
Cyanogen sulphide +2NH3
(CN)2S+2NH3
C2H6SN4
94
Linnemann
A., 120, 40
Thiodicyandiamine
u
a. 100
Rathke
B., 11, 965
Guanylic thiocyanate
„
....
118
Volhard
J. p. [2], 9, 6
27, 576
Methylene thiocyanate
CH^SCN),
C3HJ32N2
102
Lermontoff
B., 7, 1282
28, 144
Ethylthiocarbimide
Et.N I CS
C3HSSN
133-2
Liquid
Buff
Z. C. [2], 4, 730
vi., 1055
„
„
„
134
Liquid
Hofmann
B., 1, 206
„
Ethylic thiocyanate
EtS.'CN
„
141-142
Liquid
Meyer and Wurster
B., 6, 965
26, 1224
V )J
„
„
1JJ6&
Liquid
Buff
Z. G. [2], 4, 730
vi., 1055
„ ,,
„
„
146 c.
....
Cahours
A. C. [3], 18, 265
v., 519
Ethylene thiocarbamide
cs:N2H2:c2H4
C3H6SN2
....
194
Hofmann
B., 5, 242
25, 501 ; vii.,
\
492
Ethylic dithiocarbamate
NH2.CS.SEt
C3H7S2N
....
40-41
Chanlaroff
B., 15, 1989
» »
Jl
„
J. [1866], 501
41-42
Conrad & Salomon
J. p. [2], 10, 30
Ethylthiocarbamide
NHj.CS.NHEt
C3H8SN2
....
89
Hofmann
B., 1, 27
>i
11
11
100
s;
Z. C. [1868], 686
vi., 1050
„ ....
„
„
....
106
„
B., 2, 602
Dimethylthiocarbazinic acid
NMe2.NH.CS.SH
C3H8S2N2
....
112
Renouf
B., 13, 2172
40, 152
Propargylic thiocyanate
C3H3.S.CN
C4H3SN
....
Liquid
Henry
B., 6, 729
20, 1123
Ethylene thiocyanate
C2H4(S.CN)2
C4H4S2N2
J. p. [2], 26,
90
Buff
A., 100, 231
v., 520
379
Allylthiocarbimide (mustard
CH2 : CH.CTL.N : CS
C4H5SN
143
....
Dumas and Pelouze
A. C. [2], 53, 182
oil)
11 11
I]
11
148
Liquid
Will
A., 52, 4
v., 516
11 11
„
11
148-2 (760)
Kahlbaum
B., 17, 1261
11 1*
„
„
81-2 (75)
„
„
n 11
H
11
72-2 (50)
„
„
11 11
n
„
57-8 (25)
„
n
I
4 G -2
596
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
j Watts'Dict.
& J. Ch. Soc.
Allylthiocarbimide (mustard
CH8:CH.CH2.N:CS
C4H6SN
53-8 (20)
....
Kahlbauiu
B., 17, 1261
oil)
33 3)
»
»1
48-4 (15)
»
33
33 33
)»
»i
41-5 (10)
33
33
I! 3!
))
))
31-4 (5)
33
3'
1! 1>
»»
)»
14-6 (0)
J3
33
33 33
J)
»)
148-149
....
Gerlich
B., 8, 652
33 »
J)
»
150
....
Billeter
B., 8, 465
33 »
)»
ji
150-4-150-7c
Kopp
A.
Allylic thiocyanate (B., 8, 404
CH2:CH.CH2.S.CN
i>
161
A, 178, 80
Gerlich
B., 8, 652
Propimine thiocyanate
NH : CMe.CH2.S.CN
C4H0SN2
231-232(760)
42
Tscherniac and
A. C. J., 5, 227 ;
44, 568 ; 46,
Norton
C. E., 96, 444
665
33 »
»)
J)
136 (30-40)
....
33
B., 16, 347
Isopropylthiocarbimide
PrP.N : CS
C4H.SN
137-137-5
Liquid
Jahn
B., 15, 1290 ;
M. C., 3, 168
Isopropylio thiocyanate
PrPS.CN
J)
149-151
Liquid
Henry
B., 2, 496
vi., 966
33 3>
J)
)J
152-153
A., 178, 83
Gerlich
B., 8, 651
28, 1019
Propylic thiocyanate
Pr«S.CN
))
163
Liquid
Schmitt
Z. C. [2], 6, 576
vii., 1118
Allylenethiocarbamide (thio-
C3H5.NH.CS.NH2
C4HSSN2
A., 10, 326
70-6
Dumas and Pelouze
A. C. [2], 53, 181
v., 781
sinamine)
33 3)
J. [1854], 599 ; [1855], 656
)»
Z. C., 1869,
74
Wertheim
....
3)
258
Trimethylenethiocarbamide
C3H6.NH.CS.NH
)>
....
198
Lellmann and
A., 228, 199
48, 978
i i
Wurthner
Isopropylic dithiocarbamate
NH2.CS.SPfl3
C4H9S2N
....
97
Gerlich
A., 178, 82
Methylic dimethylthiocarb-
NMe2.CS.SMe
»
B. S., 33, 13
125
Bleunard
C. E., 87, 1040
36, 305
amate
Methylethylthiocarbamide ....
CS:N2H2MeEt
C4H10SN2
J., 1868, 655
54
Hofmann
B, 1, 27
vi., 1051
Isopropylthiocarbamide
NH2.CS.NHPr0
»)
M. C., 3, 168
157
Jahu
B., 15, 1290
Ethylenediamine thiocyanate
C2H4(NH2)2+2HSCN
C4H10S2N4
....
145 p. d.
Hofmann
A., 170, 143 ; B.,
25, 501 ; vii.,
5, 246
491
Diethylamine sulphhydrate
....
C4H13SN
10 (150)
tension
Isambert
C. E., 96, 708
44, 727
Thiophene nitril
C4H3S.CN
C5H3SN
190
Liquid
Meyer and Kreis
B., 16, 2174
46,46
Crotonyl thiocarbimide
C4H7.N:CS
C5H7SN
179
Liquid
Hofmann
B., 7, 516
Thiocyanopropimine thiocy-
(NCS.CH2.CMe : NH)HSCN
C.H7S,N,
d. a. 175
114-115
Tscherniac &Norton
A. C. J., 5, 227 ;
44, 568; 46,
anate
0. E., 96, 494 ;
664
B., 16, 346
Isobutylic thiocyauate
Bu0.S.CN
C5H9SN
174-176
....
Eeimer
B., 3, 757
24, 122; vii.,
223
Butylthiocarbimide
CH3.(CH2)3.N:CS
»>
167
....
Hofmann
B., 7, 512
27, 792
Isobutylthiocarbimide
CHMe2.CH2.N : CS
))
156-159
Simon
P. A., 50, 377
»3
1!
)>
159-160
....
Hofmann
B., 2, 102
vii., 223
?)
33
JJ
160
)3
Z. C. [2], 5, 400
vi., 1056
33
»
1)
161-163
....
33
B., 7, 509
27, 792
33
33
)'
161-163
Eeimer
B., 3, 757
24, 122
Butylthiocarbimide
CH3.CH2.CHMe.N I CS
))
759-5
Liquid
Hofmann
B., 7, 513
27, 792
);
I)
)•
159-160
....
J3
Z. C. [2], 5, 400
vi., 1056
„ (J. R, 11, 179)
CMe3.N:CS
»j
140
10-5
Rudneff
B. S. [2], 33, 300
38, 548
„
)J
»
142
10-5
)3
B., 11, 988
36,41
,,
»
))
14S-5 (733)
10-5
33
B., 12, 1023
36, 713
Crotonylthiocarbamide
NH2.CS.NH.C4H7
C5H10SN2
....
85
Hofmann
B., 7, 516
27, 792
Diethylidene thiocarbamide
CS(N:CHMe)2+NH3
C6HUSN3
....
180
Nencki
B., 7, 162
27, 458
ammonia
Diethylthiocarbamide
CS(NHEt)2
C6H12SN2
J.E.,10, 191
77
Hofmann
Z. C. [1868], 686 ;
vi., 1050
B., 1,26; 2,601
Butylthiocarbamide
NH2.CS.NH.(CH2)3.CH3
33
79
D
B., 7, 512
27, 792
Isobutylthiocarbamide
NH2.CS.NH.CH2~CHMe2
JJ
90
33
Z. C. [2], 5, 400
vi., 1056
»
D
3)
90-91
Reimer
B., 3, 757
24, 122; vii.,
223
33
33
J3
93-5
Hofmann
B., 7, 511
27, 792
Butylthiocarbamide
NH2.CS.NH.CHMeEt
3)
133 ; 134
33
B., 7, 513
33
D
33
J»
....
135
33
Z. C. [2], 5, 400
vi., 1056
COMPOUNDS CONTAINING FOUR ELEMENTS.
597
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Butylthiocarbamide
NH2.CS.NH.CMe3
C6H12SN2
J.K., 11,179
165 d.
Eudneff
B., 12. 1023; B.S.
36, 713; 38,
[2], 33, 300
548
Trimethylenediamine thio-
C3H6(NH3.SCN)2
C5H12S2N4
d. 140
102
Lellmann and
A., 228, 199
48, 978
cyanate
Wurthner
Ethammonium ethylthio-
NHEt.CS.S(NH3Et)
C5H14S2N
J.E., 10,188
103
Hofmann
B., 1, 25, 170
vl., 1049
carbamate
Glyceryl trithiocyanate
C3H5(SCN)3
C6H6S3N3
126
Henry
B., 2, 637
vi., 1057
Amidothiophenol
SH.NH2=1.3
C6H?SN
very high
Liquid
Biedermann
B., 8, 1676
j)
» >J
))
Liquid
Glutz and Schrank
J. p. [2], 2, 223
(B, 12, 2363)
» =1-2
»
234
26
Hofmann
B., 13, 20, 1231
(?)
» =l-4(?)
,, (?)
....
105-106
Schmidt
B., 11, 1168
34, 974
Angelylthiocarbimide
C5H9.N : CS
C6H9SN
190
....
Hofmann
B., 8, 106
28, 564
,,
J>
))
190
....
ji
B., 12, 991
36, 712
Trimethylic thiocyanurate ....
....
C6H9S3N3
....
188
»
B., 13, 1351
38, 798
laoamylic thiocyanate
CHMe2.CH2.CH2.S.CN
C,HUSN
197
J., 1868, 652
Medlock
A., 69, 222
v., 519
» !)
))
1")
195-210
Henry
J., 1, 700
Isoamyl thiocarbimide
CHMe2.CH2.CH2.N : CS
»
183-184
Liquid
Hofmann
B., 1, 173,206
vi., 1056
5! »
5?
)»
182
Buff
Z. C. [2], 4, 730
J)
Amyl ,,(J.E.11,180)
CMe2Et.N : CS
n
166
Liquid — 10
Eudneff
B. S. [2], 33, 300 ;
38, 548
B., 12, 1023
Angelyl thiocarbamide
C6H9.NH.CS.NH2
C6H12SN2
103
Hofmann
B., 8, 106
28, 564
„ >i
»1
5)
103
)?
B., 12, 991
36, 712
Piperidylthiooarbamide
C5H10 : N.CS.NH2
))
92
Gebhardt
B., 17, 3041
48, 384
Thiodiethyloxaraide
NHEt.CS.CS.NHEt
C6H12S2N2
....
54
Wallach & Pirath
B., 12,1064
36, 784
Piperylthiosemicarbazide ....
C5Hi0N.NH.CS.NH2
C6H18SN,
167
Knorr
A., 221, 297
46, 468
Thialdine
J. p. 98, 315 ; B. S. 38, 129
C6H13S2N
A., 103, 93
43
Wohler and Liebig
A., 61, 4
v., 773
B., 11, 1384, 1692
J., 1856, 518
43
Kerr
P. M. [5], 13, 257
Phenylthiocarbimide (Thio-
Ph.N : CS
»
C7H5SN
218-5 (760)
J. B., 10, 184
Kahlbaum
B., 17, 1261
carbanil)
» ."
(Z. G, 1869, 589)
H
134-9 (75)
....
»
))
)) "
V
5»
126-6 (50)
B., 3, 861
;i
?J
1> »
?J
»»
111-6 (25)
B., 9, 1266
ji
))
» "
)»
1?
106-2 (20)
B., 11, 2267
;)
J)
» '>
»)
))
99-4 (15)
B., 12, 1126
»
•J
!) I!
„
51
91-2 (10)
B., 14, 445
?)
)>
» ?»
'J
)»
80-5 (5)
B., 14, 1083
j>
J)
I) »
»
1)
66-1 (0)
B., 15, 985
»
»
)I !'
J)
»}
220
B., 3, 772
Hofmann
P. E., 8, 274, 487
v., 521
» »
)5
))
222
....
»
J., 11, 349
)) »
M
))
222
....
Weith
B., 6, 210
Phenylic thiocyanate
PhS.CN
)7
231 c.
Liquid
Billeter
B., 7, 1753
28, 464
Methenylamidothiophenol ....
C6H4.N : CH.S
Jl
230
Liquid
Hofmann
B., 13, 15, 1224
38, 388
L 1
Phenylthiocarbizine
Ph.N.NH.CS
C7H6SN2
129
Fischer & Besthorn
A., 212, 326
42, 1093
i 1
Amidophenylthiocarbimide....
NH2.C6H4.N : CS=?
)J
MM*
129
Hofmann
B., 12, 1129; 13, 11
38, 388
Phenylenthiocarbamide
C6H4.NH.CS.NH=1.2
1)
brown 260
280 d.
Lellmann
B., 15, 2146 ;
44, 185 ; 46, 49
i i
A., 221, 1
57
» »
»
....
290 d.
5)
B., 15, 2839
44, 324
Thiobenzamide
Ph.CS.NH2
C7H7SN
B., 10, 1240
115-116
Bernthsen
A., 192, 48
34, 789
Thioformanilide
Ph.NH(CSH)
)j
....
134
»
A., 192, 35
34, 790
»
)>
)>
B., 11, 338
137-5
Hofmann
B., 10, 1095
32, 604
„
JJ
»?
137-5
Nicol
B., 15, 211
Dithiocarbanilic acid
Ph.NH.CS2H
C7H7S2N
....
60-70
Eathke
B., 11, 960
Phenylthiocarbamide
NH2.CS.NHPh
C7H3SN2
148-149
Schiff
B., 11, 2167
36, 452
»
»
»
B., 9, 820
153
Gebhardt
B., 17, 3034
48, 383
» ....
»»
J)
J., 1858, 349
154
Clermont
B., 9, 446
Amidothiobenzamide
NH2.(CS.NH2)=1.3
)T
P. B., 10, 599
....
Hofmann
B., 1, 197
» ....
=1.4
)?
170
Engler
A., 149, 302
vi., 527
Amidothiocresol
Me.SH.NH2= 1.2.6
C7H9SN
Liquid
Hesse
B., 14, 489
40, 597
»i .... ....
= 1.3.4
»
Liquid
»
B., 14, 492
„
„ =1.4.6
)»
Liquid
„
B., 14, 492
»
= 1.2.4
j»
....
42
»
B., 14, 488
40, 596
508
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Pheiiylthiosemicarbazide ...
C7H9SN3
....
200-201
Fischer & Besthon
A., 212, 324
42, 1093
Hexylthiocarbimide
CH3.(CH2)5.N : CS
C;H13SN
212 (758)
PYeutzsch
B., 16, 746
44, 1075
»» ••••
CH3.(CH2)3CHMe.N : CS
11
197-198;199
Liquid
Uppenkamp
B., 8, 56
28, 552
Hexylic thiocyanate
J. [1863], 526
11
215-220
....
Pelouze & Cahoura
A. C. [4], 1, 5
v., 520
11 »
CH3.(CH2)3.CHMe.S.CN
Jl
206-207-5 ;
Liquid
Uppenkamp
B., 8, 55
28, 552
210 c.
Piperidylmethylthiocarb-
NHMe.CS.N : 05H10
C7H14SN2
....
125
Gebhardt
B., 17, 3040
48, 384
aniide
Triethylthiocarbamide
NHEt.CS.NEt2
C7H19SN2
205 s.d.
26
Grodzki
B., 14, 2755
43, 823
Diisopropylthiocai-bamide ...
CS(NHPr3)2
11
M. C., 3, 16
161
Jahn
B., 15, 1291
Hexylthiooarbamide ....
CH3.(CH2)5.NH.CS.NH2
11
...
83
Freutzch
B., 16, 746
44, 1075
Resorcinol dithiocyanate
C6H4(S.CN)2=1.3
C8H4S.2N2
....
54
Gabriel
B., 10, 184
32, 325
Benzylthiocarbimide
Ph.CH2.N : CS
C8H7SN
243
Liquid
Hofmann
Z. C. [2], 4, 890 ;
vi., 336, 1056
B., 1, 201
„
»
11
243
Liquid
Henry
Z. C. [2], 6, 207
vii., 180
Benzylic thiocyanate
Ph.CH2.S.CN
)1
256 p.d.
36-38
Henry
B., 2, 638; Z. C.
vi., 1057
[2], 6, 207
,, „ .... ....
I>
11
230-235 d.
41
Barbaglia
B., 5, 689
25, 1017
Tolylthiocarbimide ....
C6H4Me(N:CS)=1.2
))
236
Liquid
Staats
B., 13, 136
38,387
»j ....
1» 11
?1
236
....
Lachmann
I. D. Gottingen,
1879
» •••• •«•
11 »
»)
237
....
Mainzer
B., 15, 1413
,, ....
1> »
11
239
....
Girard
B., 6, 445
26, 912
„ ....
=1.3
11
244 (732-2)
Liquid
Weith and Landol
B., 8, 719
28, 1194
» .... ...
=1.4
»>
237
26
Hofmann
B., 1, 173
vi., 1056
» ....
1) 11
11
237-239
26
Mainzer
B., 15, 1413
42, 1213
» .... ...
»1 1)
11
239
Lachmann
I. D. Gb'ttiugen,
1879
„
Jl ))
»1
....
26
Staats
B., 13, 135
Ethenylamidothiophenol
C6H4.N:C2H3.S
>1
238
Liquid
Hofmann
B., 13, 21, 1236
38, 389
I 1
Methenylamidothiocresol ....
C6H3Me.N : CH.S
)1
255
15
Hesse
B., 14, 492
40, 597
1 I
Methylphenylthiocarbazine....
Ph.N.NMe.CS
C3H3SN2
123
Fischer & Besthorn
A., 212, 330
42, 1095
i 1
Tolylenethiocarbamide
C6H3Me.NH.CS.NH=?.1.3
»)
149
Lussy
B., 8, 293
28, 770
1 1
j» ••••
=1.3.4
^1
284
Lellmann
A., 221, 1
46,49
Thioisophthalamide
C6H4(CS.NH2)2=1.3
C8HSS2N2
....
199-200 d.
Luckenbach
B., 17, 1430
46, 1157
Thioterephthalamide
=1.4
11
263d.
»
B., 17, 1431
Tliiacetaiiilide
Ph.NH.CS.Me
C8H9SN
B., 11, 1595
74-5-76
Leo
B., 10, 2134
34, 409
)j •••• ••"
11
»»
....
75
Hofmann
B., 11, 339
Phenylthiacetamide
Ph.CH2.CS.NH2
1>
....
97-5-98
Bernthseu
A., 184, 293
31, 616
„
11
))
B., 8, 821
98
Colombo and Spica
G. I. [1875], 124
28, 894
5»
11
11
98
Bernthsen
B., 11, 504
Thioformtoluidide
C6H4Me.(NH.CHS)=I.2
11
....
94-96
Seuier
....
47, 764
„ ....
„ =1.4
11
....
173-5
?»
47, 766
Thiotoluamide
C6H4Me.(CS.NH2)=1.4
11
B., 8, 821
168
Dolombo and Spica
G. I. [1875], 124
28, 894
»
» i)
11
B., 8, 441
168
Paterno and Spica
G. I. [1875], 25
28, 643
Methylic phenyldithiocarb-
NHPh.CS.SMe
C8H9S2N
....
87-88
Will
B., 15, 342
amate
?
Ph.CH2.S.C(NH2):NH(?)
C8H10SN2
....
71-72
Jemthsen & Klinger
B., 12, 575
36, 651
Benzylthiocarbamide
Ph.CH2.NH.CS.NH2
11
B., 9, 81
101
'aterno and Spica
G. I., 5, 388
20, 602
Methylphenylthiocarbamide
Ph.NMe.CS.NH2
11
....
107
Gebhardt
B., 17, 2094
46, 1321
»
Ph.NH.CS.NHMe
11
13
i)
B., 17, 3038
48, 383
Tolylthiocarbamide ....
C6H4Me(NH.CS.NH2) =1.3
11
03
Weith and Landolt
B., 8, 720
v .... ....
=1.2
>1
155
Staats
B., 13, 136
38, 387
,1 .... ....
=1.4
11
-...
82
»
B., 13, 136
38, 387
)J ••.. ....
» »
11
B. S., 26, 126
88
Vermont
C. B,, 83, 3107
31, 70
,,
" 11
11
88
Will & Bielschowski
B., 15, 1311
(luanylpheiiyltliiocarbamide
Ph.NH.CS.NH.C(NH2): NH
C8H10SN4 .
B., 14, 2639
75-176
Jamberger
B., 13, 1581
40, 43
COMPOUNDS CONTAINING FOUR ELEMENTS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Phenylenedithiocarbamide ..
.. C6H4(NH.CS.NHS)3=1.3
C8H10S3N4
....
215
Lellmann
B., 15, 2840 ; A.
44, 324; 46, 4! t
221, 1
»
)»
=1.4
I)
....
218
i)
)!
*>
Diethylallylthiocarbamide ..
. Q3Hj.NH.CS.NEt.,
CSH16SN£
55
Gebhardt
B., 17, 3038
48, 3S3
Tolylenedithiocarbimide
. C6H3Me(N:CS)2=?.3.1
C9H6S2N2
B., 7, 1265
Liquid
Lussy
B., 8, 669
28, 1036
»
=?
»
....
60
Gebhardt
B., 17, 3046
Ethylphenylthiocarbimide ..
. C6H4Et(N:CS)=1.2
C9H9SN
240-245
Liquid
Paucksch
B., 17, 2803
48, 256
Propeuylamidothiophenol ..
. C6H4.N : C3H5.S
)J
252
Liquid
Hofmauu
B., 13, 21
38, 389
1 1
Ethylene phenyldithiocarb-
PhN.CS.S.CH2.CH2
C9H9S2N
134
Will
B., 15, 345
42, 723
amate
1 ' 1
Thiocyanuracetic acid
C9H9S6N
....
1.99-5
Claesson
B., 14, 733
40, 715
Ethylisothioformanilide
. Ph.N:CH.SEt
C9H,,SN
230-240
Liquid
Wallach & Wiisten
B., 16, 145
Metliylisothiacetaiiilide
PLNrCMe.SMe
»
244-246
Liquid
Wallach&Bleibtrei
i B., 12, 1061
36, 786
»
>»
»
244-246
Liquid
Wallach
B., 13, 528
38, 557
Thiacetmethylanilide
Ph.NMe.CS.Me
IJ
290 p.d.
58-59
»i
»
))
Thiacettoluide
C6H4Me.(NH.CS.Me)=1.2
))
67-68
n
B., 13, 529
))
,j ...
=1.4
»»
....
127 -5-m
Bernthsen and
B., 11, 1759
36, 147
Trompetter
»
» J)
)»
«...
130-132
Wallach
B., 13, 529
38, 557
Ethylic phenyldithiocarb-
Ph.NH.CSjEt
C9H11S2N
B., 2, 120
56
Hofmann
Z. C. [2], 5, 268
vi., 1050
amate
j»
»
»
B., 15, 570
60
Will
B., 15, 1305
42, 1089
Methylio tolyldithiocarb-
C,H4Me.NH.CS3Me
»J
MM
84
Will&Bielschowski
B., 15, 1310
42, 1090
amate
Tolylthiobiuret
C9H11S2N3
....
158
Tursini
B., 17, 584
46, 1140
Phenylethylthiocarbamide ....
Ph.NH.CS.NHEt
C9H12SN2
97
Hofmann
J. [1868], 655
vi., 1051
I?
)»
)J
• «•*
99-99-5
Weith
B., 8, 1524
29, 574
Phenylethylthiocarbamide ...
NH2.CS.NEtPh
)J
....
113
Gebhardt
B., 17, 2094
46, 1321
Phenyldimethylthioearb-
NHMe.CS.NMePh
•)
«••«
114
u
B., 17, 3037
48, 383
amide
Tolylenedithiocarbamide ....
C6H3Me(NH.CS.NH2)2
C9H12S2N4
«...
216
»
B., 17, 3046
=1.1.3
»
" »
»
....
217
Stiidemann
I. D., Berlin, 1884
)>
" »
))
B., 8, 670
218
Lussy
B., 7, 1266
28, 274
;»
=?.1.3
)J
....
280
Lellmann
A., 221, 1
46, 50
»
=1.1.2
)»
....
290
»
J>
»
)»
=5.1.4
)I
....
d.w.m. high
5»
»
)>
Ethylphenylthiosemicarb-
Ph.NH.CS.N3H,Et
C9H13SN3
t.t.
109-110
Fischer
A., 199, 297
azide
Octylic thiocyanate
C8H17.S.CN (sec.)
C9H,,SN
142
Liquid
Jahn
B., 8, 805
28, 1188
Octylic thiocarbimide
C8H17.N:CS(sec.)
J1
232-232-5
Liquid
i)
M. C., 3, 173
?! *?
» 1»
J)
232-235-5
Liquid
»
B., 15, 1293
» »
» )1
J)
334
Liquid
»»
B., 8, 804
28, 1188
Carboisobutyraldine
....
C9HI8S2N2
....
91
Pfeiffer
B., 5, 701
vii., 228; 25,
1001
Tetrethylthiocarbamide
CS(NEt2)2
C9H20SN2
21(3 u.c.
Liquid
Grodski
B., 14, 2758
42, 823
Dibutylthiocarbaraide
CS(NH.CMe3)2
)>
J.E., 11, 180
162
Eudneff
B. S. [2], 33, 300
38, 548
,,
»»
1>
MM
163
»
B., 12, 1023
36, 713
Octyltliiocarbamide (sec.) ....
C8H17.NH.CS.NH2
J)
114
Jahn
M. G, 3, 173
»»
»J
»)
....
112-5
Eudneff
J. B., 11, 180
,, ....
JJ
))
112-5
Jahn
B., 8, 804
28, 1188
Styrolene thiocyanate
Ph.CH(S.CN).OH2(S.CN)
C10H3S2N2
J. [1880], 404
101-102
Nagel
A., 216, 324
Propylphenylthiocarbimide...
C6H4Pr«.(N:CS)=l.4
C10HUSN
263
Liquid
Francksen
B., 17, 1224
46, 1007
Mesitylthiocarbimide
C6H3Me,.(N:CS)=l. 3.5.6
»
....
64
Eisenberg
B., 15, 1012
42, 956
Tolylethylenedithiocarb-
06H4Me.N.CS.S.C,H4=1.4
i j
C10HnS2N
126
Will and Biel-
B., 15, 1315
amate
schowski
" »
=1.2
1)
....
129
T,
B., 15, 1317
18, 1091
Allylphenylthiocarbamide ....
Ph.NH.CS.NH.C3H,
C10H12SN2
A., 84, 348
95
Zinin
I. p., 57, 173
7., 783
»
)J
)»
98
Weith
B., 8, 1529
Ethylphenyldithioxamide ...
NHEt.CS.CS.NHPh
C10Hi2S2N2
36-37
Wallach
B., 14, 740
10, 718
Xylenic dithiamide
C6H4(Ca3.CS.NH.,)3=1.4
j>
205-206
Klippert
B., 9, 1768
»1, 468
600
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Ethylisothiacetanilide
Ph.N I CMe.SEt
C10H13SN
250 u.c.
Wallach
B., 11, 1592
36, 312
„
H
)»
255-257
....
Wallach and Bleib-
B., 12, 1061
36, 786
treu
Ethylic tolyldithiocarbamate
C,H4Me(NH.CSaEt)=1.2
^10^13^2^
....
72
Will and Biel-
B., 15, 1317
42, 1091
schowski
>i i)
=1.4
»
74
»
B., 15, 1312
ji
Ethyl phenylthiobiuret
....
C10H13S2N3
109
Tursini
B., 17, 585
46, 1141
Tolylethylthiocarbamide
C6H4Me(NH.CS.NHEt)=1.2
C10H14SNS
83-84
Staats
B., 13, 136
38, 387
V) ••••
=1.4
)J
93
!»
11
11
n
» )>
J»
95-96
Weith
B., 8, 1530
29, 575
PropylphenyJthiocarbamide
C6H4Pr»(NH.CS.NH2)=1.4
»
159
Francksen
B., 17, 1223
46, 1007
Mesitylthiocarbamide
Me3.(NH.CS.NH4)=1.3.5.6
))
222
Eisenberg
B., 15, 1013
48, 956
Diallylethylenedithiocarb-
C2H4(NH.CS.NH.C3H6)2
Ci0HlsS2N4
Liquid
Lellmann and
A., 228, 199
48, 978
anjide
Wiirthner
?
[.C(SEt):NEt]2(?)
C10H20S2N2(?)
a. 250
Liquid
Wallach and Pirath
B., 12, 1064
36, 784
Diethylthiuramide disulphide
S2(CS.NEt2)2
<J10H20S4N2
70
Grodzki
B., 14, 2756
42, 823
/3-Naphthylie thiocyanate ....
C10H7.S.CN
CUH7SN
35
Billeter
B., 8, 463
a-Naphthylthiocarbimide ....
C10H..N : CS
»
J. [1858], 350
58
Mainzer
B., 15, 1414
0-
»
»>
62-63
Cosiner
B., 14, 61
40, 606
0-
))
?>
62
Mainzer
B., 15, 1413
Naphthoic thiamide ....
C10H7.CS.NH2
CUH9SN
126
Hofmann
B., 1, 40
/3-Naphthylthiocarbamide ....
C10H7.NH.CS.NH2
CnH10SN2
180
Cosiner
B., 14, 61
40, 60(5
/3-
))
J)
180
Gebhardt
B., 17, 3045
48, 387
a- „
)J
))
B. S.,26, 126
198
Clermon t & Wehrlin
C. E., 73, 347
31, 70
Al lylisothioacetanilide
Ph.N : CMe.S.C3H6
C^H^SN
a. 260 d.
Wallach and Bleib-
B., 12, 1061
36, 786
treu
Isobutylphenylthiocarbimide
C,H4BuP.(N:CS)=1.4
»
266-276
41
Mainzer
B., 16, 2024, et seq.
44, 1107
ii
») ))
))
277
42
Pahl
B., 17, 1236
46, 101(1
G'umylthiocarbimide
C6H3MePr.(N I CS)=?
))
245-270 d.
B., 8, 1152
Eaab
B., 10, 53
Tetramethylbenzene thio-
C6HMe4.(N:CS)=:?
))
65
Hofmann
B., 17, 1916
46, 1320
carbimide
Allyltolylthiocarbamide
Me.(NH.CS.NH.C3H3)=1.4
C11H14SN2
....
97
Maly
Z. C. [2], 5, 258
vi., 1089
)> ...
» »
I»
99
Weith
B., 8, 1528
i) ...
>I )t
7)
J. [1869], 636
100
Jaillard
Z. C. [1865], 441
v., 874
D
)» I)
U
....
112
11
....
vi., 1089
Propylisothiacetanilide
Ph.N : CMe.S.Pr«
C,,H15SN
270-273
....
Wallach and Bleib-
B., 12, 1061
36, 786
treu
Ethylisothiacettoluide
Me.(N:CMe.SEt)=1.2
))
261-262
Liquid
Wallach & Wusten
B., 16, 147
11 ...
=1.4
)»
271-273
Liquid
i>
J!
Ethylic ethylphenyldithio-
NEtPh.CS2Et
CUH15S2N
305-315 p.d.
68-4-68-5 u.c
Bernthsen & Friese
B., 15, 568
42,966
carbamate
Ethyl-p-tolylthiobiuret
CUH1SS2N3
....
134
Tursini
B., 17, 585
46, 1141
Bipiperylthiosemicarbazide...
C6H10:N.CS.NH.N:C6H,0
C11H21SN3
85-5
Knorr
A., 221, 297
46, 468
Piperylthiocarbazide
CStNH.N:C6H10)2
CnH22SN4
181
!»
i>
»)
Carbovaleraldine
....
CnHjjSjNj
....
115-5-117
Schrceder
B., 4 469 ; A.,
24, 707 ; vii.,
168, 237
1196
Thiodiphenylamine
C6H4.NH.C6H4.S
i i
C12H3SN
371 u.c.
180 u.c.
Bernthsen
B., 16, 2898
46, 596
Thiacet-a-naphthalide
C10H7.NH(CS.CH3)
C12HnSN
96
Bernthseu & Trom-
B., 11, 1760
36, 147
petter
Amidodiphenyldisulph-
HS.C6H4.C6H4(NH2).SH
C12HUS2N
153
Gabriel and Dam-
B., 13, 1412
38, 891
hydrate
=1.4; 1.2.4
bergis
Acetothienonephenylhydr-
C4H3S.CMe : N.NHPh
C12H12SN2
96
Peter
B., 17, 2645
48, 142
azine
Thioanilide ....
S(NHPh)
i fin i QP^ ^1
dmit
BQ 1 AAfi
OQ ftf\C)
)>
loU— loo a.
Liquid
OIlHt
.j Oj l^t^D
*«?j OUZ
Diamidopheuylsulphide thio-
S(C6H4.NH2)2
)>
B., 7, 384
105
Merz and Weith
B., 4, 387
24, 567 ; vii..
auiline
1154
» »
»
)»
105-106
Schmidt
B., 11, 1169
Dianridophenyldisulphide ...
S2(C0H4.NH2)2=(1.4)2
C12HJ2S2N2
78-79
)!
B., 11, 1172
34, 975
11
=(1.2)s
}j
93
Hofmann
B., 12, 2364
38, 386
Isobutyltolylthiocarbimide ...
Me.BuS.(N:CS)=1.3.2
C12H15SN
267
44
Effront
B., 17, 2350
48, 154
COMPOUNDS CONTAINING FOUR ELEMENTS.
601
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Isobutyltolylthiocarbimide ...
Me.Bu,3.(N:CS)=1.5.2
C12H15SN
275-280 p.d.
46
Effront
B., 17, 2336
48, 153
Pentamethylbenzenethiocarb
CsMe5.(N I OS)
»
....
86
Hofmann
B., 18, 1827
48, 1129
imide
Allylphenylethylthiocarb-
C3H5.NH.CS.NEtPh
C12H16SN2
26
Gebhardt
B., 17, 3037
48, 383
amide
Piperidylphenylthiocarb-
C5H10 : N.CS.NHPh
»
98
>,
B., 17, 3039
48, 384
amide
Isobutylisothiacetanilide
C6H5.N : CMe.SBufl
C12HI7SN
d.
....
WallachandBleib-
B., 12, 1061
36, 786
treu
Isoamylic phenyldithiocarb-
NHPh.CS2(C5Hu)
C12H17S2N
71
Will
B., 15, 1306
42, 1089
amate
Diethyltolylthiocarbamide ...
C6H4Me.NH.CS.NEt2=1.2
C12H13SN2
102
Gebhardt
B., 17, 3038
48, 383
Pentamethylbenzenethiocarb
C6Me5.NH.CS.NH2
)>
224
Hofmann
B., 18, 1827
48, 1129
amide
Diphenylthioearbirnide
Ph.C6H4.(N : CS)=1.4
C13H9SN
....
58
Zimmermann
B., 13, 1964
40, 176
Diphenylic thiocyanate
Ph.C6H4.S.CN
)>
Impure
84
Gabriel & Deutsoh
B., 13, 389
38, 477
Benzenylamidothiophenol ...
C6H4 1 N.CPh.S=1.2
))
114
Tiemann and Piest
B., 15, 2033
i i
»
» »
»
B., 13, 17
115
Hofmann
B., 12, 2360
38, 386
,»
» ?»
)I
....
115
»
B., 13, 1223, 1237
Anilidophenylthiocarbimide
NHPh.C6H4.N : OS
C13HIOSN3
157
n
B., 12, 1130
36, 806
j»
n
J1
159
»
B., 13, 12
38, 388
Thiobenzanilide
Ph.CS.NHPh
C13HnSN
....
95-97
Leo
B., 10, 2134
34, 409
,, ....
IJ
)»
....
b. 100
n
B., 9, 1216
„
»)
)1
95-5-96-5
Bernthsen
B., 11, 503
»»
»>
J)
98
»
A., 192, 1
34, 789
Methylthiodiphenylamine ...
C6H4.NMe.C6H4.S
»
99-3
j»
B., 16, 2899
46, 596
Diphenylthiocarbamide
CS(NHPh)2
C13H13SN2
A., 207, 139
140
Hofmann
A., 57, 266
i., 756
,,
»
»
B., 12, 773
140
Gnareaehi
G. I., 8, 246
34, 860
„
If
))
A., 68, 39
144
Aschan
B., 17, 428
,,
H
.,
A., 70, 143
144
Weith
B., 6, 210, 967
(Z.C.
»
jj
B., 7, 1304
145
»
B., 8, 1527
29, 575
1869, 584)
,,
»
)J
A., 166, 143
146-5
Guareschi
G. L, 8, 246
34, 860
» ...
»J
)>
B., 12, 1613
153
Bamberger
B., 14, 2638
Diphenylthiosemicarbazide
NHPh.CS.N2H2Ph
C13H13SN3
177
Fischer
A., 190, 122
34, 308
Amidodiphenylthiooarbamide
NHPh.CS.NH.C6H4.NH2
)1
d. 141
Lellmann and
A., 228, 199
48, 977
=1.2
Wiirthner
!>
= 1.3
)>
....
148-153 p.d.
ii
TJ
)1
M
=1.4
»
....
d. 163
)5
»
M
Diphenylthiocarbazide ,_
C13H14SN4
Green 130
150
Fischer
A., 190,119,212,
323
Phenylhydrazinephenylthio-
Ph.NH.NH.CS2N,H4Ph
CI3H16S2N4
....
96-97 p.d.
»
A., 190, 115
34, 307
carbazate
Piperidyltolylthiocarbamide
Me.(NH.CS.N : C5H10)=1.2
013H18SN2
98
Gebhardt
B., 17, 3040
48, 384
»
=1.4
»>
132
)»
)5
»
Diethyltolyleuedithiocarb-
Me.(NH.CS.NHEt)2=1.3.4
Gi3H20S.2N4
149-153
Lellmann
A., 221, 1
46, 50
amide
,,
= 11.3
i?
....
225
Lussy
B., 8, 668
28, 1036
a-Methylpiperidine-a-methyl-
C6H15 : N.CS.SH.NH.C5H9
C-'i3H26S2N2
sb. 100
118
Ladenburg & Roth
B., 18, 48
48, 557
piperylthiocarbamate
Me
Dihexylthiocarbamide
CS[NH.(CH2)5.CH3]2
CMH.SN,
....
40
Frentzel
B., 16, 746
44, 1075
Oxalamidothiophenol
(.C:N.C6H4.S)2
C14H8S2N2
abt. 300
Hofmann
B., 13, 1227
38, 885
?
....
C14H10SN.
90
ji
B., 2, 646
vi., 258
?
014H10S3N2
152
Proskauer and Sell
B., 9, 1265 31,68
?
Ph.CH2.C : N.C6IL,.S
C14HnSN
Liquid
Hofmann
B., 13, 1235 i 38, 887
1
Ph.C : N.C6H,Me.S
H
125
Hesse
B., 14, 493 40, 597
L ' 1
Ht. on thioforniauilide
....
C14HuSNa
....
140
Nicoll
B., 15, 211 ! 42, 958
4 H
002
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
?
NH2.C6H4.C:N3:C(C6H4.
C14H12SN4
....
128-129
Waustrat
B., 6, 033
26, 909
1
NH2).S
1
Thioxanilide
NHPh.CS.CS.NHPh
C14H12S2N2
....
133
Wallach
B., 13, 527
Thiacetdiplieiiylamine
CH3.CS.NPh2
C14HUSN
110-5-111
Bernthsen
A., 192, 39
34, 790
Imidothiobenzobenzylether...
....
)»
....
181
n
A., 197, 351
Ethylthiodiphenylamine
CBH4.NEt.C6H4.S
))
102
j>
B., 16, 2900
46, 596
i i
Tliiobenztoluide
Ph.CS.NH.C6H4M(f
))
128-129
Bernthseii & Trom-
B., 11, 1759
petter
» .... ...
)>
11
....
128-5-129-5
Leo
B., 10, 2134
34, 409
MethyldipheDylthiocarb-
NHPh.CS.NMePh
C14HI4SN2
204-206
87
Gebhardt
B., 17, 2089
46, 1321
amide
Phenyltolylthiocarbamide ...
NHPh.CS.NH.C6H4Me=1.2
))
B., 15, 1419
139
Staats
B., 13, 137
38, 387
„
= 1.4
11
B., 15, 1420
136-137
)J
))
»
„
» J»
)1
....
141
Gebhardt
B., 17, 3035
Thiobenzdiamidotoluene
Me.NH2.(NH.CS.Ph)=?.1.3
)J
197
Bernthsen & Trom-
B., 11, 1760
36, 147
petter
a - Naph thy lally Ithiocarb-
C10H7.NH.CS.NH.C3H5
)J
A., 84, 347
130
Zinin
J. p., 57, 173
v., 783
amide
Base fr. thiocarbanilide
....
»1
....
110
Will
B., 14, 1489
40, 906
Methyldiphenylthiosemicarb-
NMePh.NH.CS.NHPh
C14H15SN3
154
Fischer
A., 190, 166
34, 311
azide
«
Diamidotolyl sulphide
S(C6H3Me.NH2)2=(1.4.?)2
Ci4H16SN2
103-103-5
Merz and Weith
B. 4, 393
vii., 1156
Diallylphenylenedithioearb-
C6H4(NH.CS.NH.C3H6)2
CuH18S2N4
....
158-160 d.
Lellmann & Wiirth-
A., 228, 199
48, 977
atnide
— 1.2
ner
»
=1.3
»
105
Lellmann
A., 221, 1
46, 50
r
= 1.4
»
....
200
»
n
))
Cinnamylamidothiophenol ....
Ph.CH : CH.C : N.C6H4.S
C15HUSN
....
111
Hofmanu
B., 13, 1235
38, 887
L J
Hydrothiodiphenylhydantoiu
Ph.N : C.NPh.(CH2)2.S
C15H14SN2
136
Will
B., 14, 1490
40, 906
1 1
»
»
5)
a. 300 s. d.
)>
B., 15, 343
42, 723
Dibenzylideneammonium
....
C16H14S2N.:
A., 168, 238
100 d.
Quadrat
A., 71, 13
dithiocarbamate
Ethylthiocarbanilide
EtS.C(NHPh):NPh
C15H16SN2
73
Eathke
B., 14, 1777
42, 167
»
»
)1
B., 15, 338
79
Will
B., 14, 1490
40, 906
,,
»
»
B., 15, 1308
157-5 (!)
Bernthsen & Friese
B., 15, 567
Ethyldiphenylthiocarbamide
NHPh.CS.NEtPh
>T
....
89
Gebhardt
B., 17, 2091
46, 1321
Dibenzylthiocarbamide
CS(NH.CHjPh),
?J
....
114
Strakosch
B., 5, 696
25, 1027 ; vii.,
182, 428
»
»
))
114
Paterno and Spica
G. I, 5, 388
29, 602
„
NH2.CS.N(CH2Ph)2
11
B., 9, 82
156-157
j)
11
J)
Phenylethylphenylthiocarb-
NHPh.CS.NH.06H4Et=1..4
n
.*.•
103-104
Mainzer
B., 16, 2021
44, 1106
amide
»
=1.2
*?
148
Paucksch
B., 17, 768
46, 1143
Phenylmethyltolylthiocarb-
NMePh.CS.NH.C6H4Me
»j
....
121
Gebhardt
B., 17, 3035
48, 383
amide
=1.2
»
= 1.4
)»
....
124
ji
B., 17, 2091
46, 1321
Ditolylthiocarbamide
CS(NH.C6H4Me)2=(1.3)2
»
....
122
Weith and Landolt
B., 8, 718
28, 1194
»
=(1-2).
u
216-218
156
Ador and Keilliet
B., 12, 2301
j)
» u
?;
158 u.c.
Bergerd
B., 12, 1854
38, 244
j>
» »
jj
159
Gebhardt
B., 17, 3034
vii., 1116
!)
" »
N
164
Sell
16, 190
v., 872
»
» >;
i;
165 u.c.
Girard
B., 4, 985
25, 720
»
>' »
H
243 sic.
Will & Bielschowski
B., 15, 1317
»
=(1.4)2
i»
176
»
B., 15, 1311
),
» »
»
A., 126, 160
176
Hofmann
B., 7, 1739
28, 466
J.
" »
))
J. [1869], 637
176
Weith
B., 9, 815
Diallyltolylenedithiocarb-
C6H3Me(NH.CS.NH.C3H5)2
C^H^N,
150
Lellmann
A., 221, 1
46, 50
amide
= 1.3.5
„
)' ;j
11
....
150-5
>»
A., 228, 199
48, 977
»>
„ =1.2.3
?)
152
T>
A., 228, 243
n
COMPOUNDS CONTAINING FOUR ELEMENTS.
603
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diallyltolylenedithiocarb-
C6H3Me(NH.CS.NH.C3H5)2
C15H20S2N4
MM
175-5 d.
Lellmaim
A., 228, 199
48, 977
aniide
= 1.2.5
Conylphenylthiocarbamide ....
C8H16 : N.CS.NHPh
C15H22SN2
88
Gebhardt
B., 17, 3041
48, 384
Octylphenylthiocarbamide ....
C8H17.NH.CS.NHPh
C15H24SN2
52-53
Jahn
B., 8, 805
28, 1188
C15H31S2N
41
Bensenhirtz
A., 90, 109
v., 974
,, ....
»
....
41
Schroeder
B., 4, 469
24, 706; vii.,
1195
Succinoamidothiophenol
(.CH2.C:N.C6H4.S)2
CleH13SsN2
....
137
Hofmaun
B., 13, 1231
38, 886
?
CH2Ph.C : Ns:C(CH3Ph).S
C16H14SN2
....
41-42
Bernthsen
A., 184, 310
31, 618
Styrolylic thiocyanate +C6H6
See CIOHSS2N2
C]r,H14S2N2
61-62
Nagel
J. [1880], 404
Phenylimidotolylethylene-
Ph.N : C.N(C6H4Me).C.,H4.S
| 1
C16H16SN2
128
Will & Bielschowsk
B., 15, 1315
thiocarbamate
SBl.4
?
....
)»
....
160
Senier
47, 769
Phenylethyltolylthiocarb-
C6H4Me.NH.CS.NEtPh
C16H18SN2
90
Gebhardt
B., 17, 2091
46, 1321
amide
=1.4
Tolylimidotolylmethylthio-
C6H4Me.N : C(SMe).NH.
»
....
60
Will & Bielschowsk
B., 15, 1316
42, 1090
carbamate
C6H4Me=(1.2)2
j»
=(1.4),
))
....
128
»
B., 15, 1309
))
Mesitylphenylthiocarba mide
C6H2Me3.NH.CS.NHPh
J)
193
Eisenberg
B., 15, 1014
=1.3.5.6
Diphenylethylenedithiocarb-
C2H4(NH.CS.NHPh)2
CI6H18S2N4
....
193d.
Lellmann & Wiirth
A,, 228, 199
48,978
amide
ner
Tetramethylthioaniline
S(C6H4.NMe2)2
C16H20SN2
125
Tursini
B., 17, 587
46, 1141
Thiobenzoyl-a-naphthalide ....
C10H7.NH.CS.Ph
CyHaSN
....
147-5
Bernthsen & Trom-
B., 11, 1760
36, 147
petter
Phenyl-a-naphthylthiocarb-
C10H7.NH.CS.NHPh
C17H14SN2
J. [1858], 350
158-159
Mainzer
B., 15, 1414
42, 1212
ainide
» -ft- »
)»
»)
155-157
»
B., 15, 1417
42, 1213
Tolylimidotolylethylenethio-
C6H4Me.N : C.N(C6H4Me).
C17H18SN2
....
82
Will & Bielscliowsk
B., 15, 1315
carbamate
C.H4.S=1.2; 1.4
»»
=(1.2),
)»
91
»
B., 15, 1317
42, 1091
>j
= (l-4)2
)»
112
)>
B., 15, 1314
J)
Phenylisobutylphenylthio-
NHPh.CS.NH:C6H4BuP=?
C17H20SN2
152
Mainzer
B., 16, 2023
44, 1107
carbaraide
Tolylimidotolylethylthiocarb-
C6H4Me.N : C(SEt).NH.
P
51
Will & Bielscbowsk
B., 15, 1316
42, 1091
amate
C6H4Me=(1.2)2
)»
=(l-4)2
))
87
M
B., 15, 1312
)j
Diethylphenylthiocarbamide
CS(NH.C6H4Et)2=(1.2)2
H
141-142
Paucksch
B., 17, 768
46, 1143
?)
=(1.4),
,,
144-143
j)
JJ
51
11
J» »
))
144
Mainzer
B., 16, 2019
44, 1106
Dixy ly ltli iocarbamide
CS(NH.C6H3Me2)2=(4.3.1)2
»)
152-153
Hofmaun
B., 9, 1296
31, 92
Mesityltolylthiocarbamide ....
C6H2Me3.NH.CS.NH.
))
....
167
Eisenberg
B., 15, 1014
C6H4Me=1.3.5.6 ; 1.2
Diphenyltrimethylenedithio-
C3H6(NH.CS.NHPh)2
C17H20S2N4
115
Lellmann and
A., 228, 199
48, 978
carbamide
Wiirthner
Bidimethamidophenylthio-
CS(NH.C6H4.NMe2)2=(1.4),,
C1.H1BSN4
186-5
Baur
B., 12, 534
36, 628
carbamide
Phenylmethyl-#-naphthyl-
C10H7.NH.CS.NMePh
C18H16SN2
....
127
Gebhardt
B., 17, 2091
46, 1321
thiocarbamide
Tolylnaphthylthiocarbamide
C10H7.NH.CS.NH.C6H4Me
V
....
165-168
Mainzer
B., 15, 1416
42, 1212
=a; 1.2
»i
=« ; 1.4
>1
....
168
D
!»
42, 1213
11
=/3; 1.2
)1
193-194
u
B., 15, 1418
j»
»
=ft; 1.4
)»
....
163-164
i»
B., 15, 1419
)»
Isobutylpheny Itolylthiocarb-
C6H4Me.NH.CS.NH.
C18H22SN,
....
137
»i
B., 16, 2024
44, 1107
aroide
C6H4BuP=1.4; 1.?
Diphenylthiobenzamide
Ph.CS.NPh2
C19H16SN
....
150-151
Bernthsen
A., 192, 37
34, 790
Triphenylthiocarbamide
NHPh.CS.NPh,
O^H^N,
152
Gebhardt
B., 17, 2092
46, 1321
4 H 2
604
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Azobenzenepheiiylthiocarb-
Ph.N.j.C6H4.NH.CS.NHPh
C19H16SN4
...»
179
Berju
B., 17, 1405 ; C.
46, 1149 ; 48,
amide
C. [1884], 871
660
Ethylphenyl-)3-naplithylthio-
C10H7.NH.CS.NH.C6H4Et
C19H18SN2
158-159
Mainzer
B., 1C, 2022
44, 1107
carbamide
Dipropylphenylthiocarbamide
CS(NH.C6H4Pr«)2=(1.4)2
C^H^SN,
....
138
Francksen
B., 17, 1222
46, 1007
Isobutylphenylethylphenyl-
C6H4Et.NH.CS.NH.06H4Bui3
JJ
....
140
Mainzer
B., 16, 2025
44, 1107
thiocarbamide
Dicumylthiocarbamide
CS(NH.C6H2Me3),=?
)J
....
146
Engel
B., 18, 2233
48, 1216
Dimesitylthiocarbamide
=(6.5.3.1)3
JJ
196
Eisenberg
B., 15, 1013
42, 956
Phthalylamidothiophenol ....
C6H4(C : N.C6H4.S)2=1.2 ; ?
C20HJ2S2N2
....
112
Hofmann
B., 13, 1233
38, 886
Triphenylmethylic thiocyanate
OPhj.S.CN
C20H15SN
....
137
Elbs
B., 17, 700
46, 1030
Benzenylisodiplienylamidine
C^HHSN.
151
Bernthsen
A., 192, 1
34, 790
thiooyanate
II >!
....
JJ
203
ii
11
34, 788
Triphenylthiodicyandiamine
NHPh.CS.NPh.C(NHPh) :
C20H1SSN4
....
150
Rathke
B., 12, 774
36, 805
NH
Thiotetrapyridine
....
JJ
B. S., 34, 452
155
Cahours and Etard
C. E., 88, 999
36, 732
Diphenylphenylenedithio-
C6H4(NH.CS.NHPh)2=1.2
C20H18S2N4
d. 170
Cryst.
Lellmann and
A., 228, 199
48, 977
carbamide
Wurthner
11
=1.3
JJ
d. 160-185
161
ii
»i
i)
Thiocuminamide sulphide ....
C6H4Pr.C : N2 : C(C6H4Pr).S
C20H22SN2
....
45
Wanstrat
B., 6, 333
26, 909
> i
Di-(3-naphthiocarbamide
CS(NH.C10H7)2
C21H16SN2
....
193
Gebhardt
B., 17, 3045
» -ft- „
J)
JJ
....
193
Cosiner
B., 14, 61
40, 606
11 -°- i.
JJ
JJ
A., 64, 371
197-198 u. c.
Berger
B., 12, 1860
38, 245
Thiobenzaldine
....
C21H19S,N
....
125
Laurent
A., 38, 323
v., 481
Diphenyltolylene dithiocarb-
C6H3Me(NH.CS.NHPh).,=?
C21H20S2N4
....
167 ; 173
Gebhardt
B., 17, 3046
amide
I' 1!
JJ
JJ
....
172
Studemann
L. D. Berlin, 1884
II 11
=?.1.4
JJ
181 d.
Lellmann and
A., 228, 199
48, 977
Wurthner
II II
= ?.1.3
)»
B., 7, 1265
238
Lussy
B., 8, 670
28, 1036
Isobutylphenyl-0-napthyl-
C10H7.NH.CS.NH.C6H4Bu3
C31H22SN2
152; 160
Mainzer
B., 16, 2026
44, 1107
thiocarbamide
Diisobutylphenylthiocarb-
CS(NH.C6H4Bu0)2=(1.4)2
CMHJSN,
192-5
Pahl
B., 17, 1235
46, 1010
auiide
Dicumylthiocarbamide
CS(NH.C6H3MePr)2=?
Jl
128
Eaab
B., 10, 53
ii
=(?.3.1)2
Ji
....
160
Kelbe and Warth
A., 221, 157
46,47
Ditetramethylbenzenethio-
CS(NH.C6HMe4)2
1J
278
Hofmaun
B., 17, 1916
46, 1320
carbamide
Dibutyltolylthiocarbamide ....
CS(NH.C6H3MeBuP)2=2. 1.3
C23H3:SN2
175
Effront
B., 17, 2344
48, 154
ii •««•
=2.1.5
ii
184
ii
B., 17, 2335
48, 153
Pentamethylbenzenethiocarb-
CS(NH.C6Me5)2
i:
252
Hofmann
B., 18, 1828
48, 1130
amide
Thiosulphaniline
S[C6H3(NH3).S.C,H4.NH2]2
C24H22S:!N4
....
abt. 100
Merz and Weith
B., 4, 392
Thio-a-toluamide sulphide ....
....
C24H27S2N
107-5-108
Bernthsen
A., 184, 302
31, 617
Tetraphenylthiocarbamide ....
CS(NPh2)2
C26H20SN2
....
194-5-195-5
Bernthsen & Friese
B., 15, 1530, 1652
42, 1089
Bidiphenylthiocarbamide ....
CS(NH.C6H4.Ph)2
JJ
228
Zimmermann
B., 13, 1964
40, 176
Thiocarbamidoazobenzene ....
CS(NH.C6H4.N2.Ph)2
C^H^SN,
....
199
Berju
B., 17, 1405 ; C.
46, 1149; 48,
C. [1884], 871
660
Ht. on thiobenzanilide
C27H20S2N2
....
111-5-112-5
Leo
B., 10, 2135
34, 409
Triethylphosphiue sulphide
Et.,PS
06H15SP
94
Cahours & Hofmann
J., 10, 376
iv., 613
Triethylic trithiophosphite ....
P(SEt)3
ceH15S3P
240-280
Liquid
Michaelis
C. N., 25, 57 ; B.,
5,7;B.S.,25,185
„ tetrathiophosphate
PS(SEt)3
C6H16S4P
Liquid — 18
Carius
A., 119, 289
vii., 1120
Triethylphosphine +CS2 ....
Et3P,CS2
C7H15S2P
v. 100
95
Hofmann
As., 1, 32
iv., 614
Diinethylphenylphosphine
Me2PhP,CS2
C9HnS2P
....
97 d. ; 101 s.t.
Czimatis
B., 15, 2017
44,58
+CS2
Dimethyltolylphosphine
Me2(CeH4Me)P,CS2=1.4
CioHis^zP
....
HOd. ; 116
11
B.. 15, 2018
JJ *
+CS,
s.t.
COMPOUNDS CONTAINING FOUR ELEMENTS.
605
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Diethylpheuylphosphine sul -
Et2PhPS
C10H16SP
a. 360
s. ord. temp.
Ananoff
A., 181, 355 ; B.,
28, 1204
phide
8, 497
Dimethylxylylphosphine
Me2(C6H3Me2)P,CS2
CUH15S2P
115 d. ; 121
Czimatis
B., 15, 2018
44,58
+CS.,
s.t.
Tripheriylphosphine sulphide
Ph3PS
C13H16SP
....
150 151
Michaelis and
B., 15, 803
42, 1062
Gleichmann
?
Ph.P.PPh.PPh.S (?)
C18H,,,SP3
....
138
Kohler & Michaelis
B., 10, 811
32, 451
1 1
Triphenylic tetrath-iophos-
PS(SPh)3
C18H15S4P
....
86
Schwarze
J. p. [2], 10, 234
phate
?
Ph4P2S3
C^H^P,
....
192-193
Kohler & Michaelis
B., 10, 816
32, 450
Methylarsine sulphide
MeAsS
CH3SAs
abt. 110
Baeyer
A., 107, 281
i., 402
Cacodyl sulphide
S(AsMe2)2
C4H12SAs3
a. 100
b. 40
Bunsen
....
i., 409
„ disulphide ....
S3(AsMe2)2
CjH^SjAs,,
....
50
„
A., 46, 19
„
Phenylarsine sulphide
PhAsS
C6H5SAs
....
152
Schulte
B., 15, 1956
44, 186
Triethylarsine sulphide
Et.,AsS
C6H16SAs
....
100
....
....
i., 399
Phenylarsine sesquisulphide
Ph2As2S3
C12H10S3As2
....
130
Schulte
B., 15, 1959
44, 186
Triphenylarsine sulphide ....
Ph3AsS
C^H^SAs
....
162
Coste and Michaelis
A., 201, 244
Tetramethylstibine sesqui-
S3(SbMes)2
C4H12S3Sb2
....
b. 100
Landolt
J. [1861], 571
sulphide
Triethylstibine sulphide
Et3SbS
C6H16SSb
A., 97, 333
a. 100
Lowig & Schweizer
J. [1850], 474
i., 344
Triethylic trithiobisinuthite
Bi(SEt),
C.HlsS3Bi
....
79
Claesson
J. p. [2], 15, 193
32, 295
(21.) CHSeN, CHSeP, CHNP, CHNAs.
Ammonium seleniocyauate ....
(NH4)Se.CN
CH4SeNj
d. 170
Verneuil
C. B., 99, 1154
48, 376
Seleniocarbamide
CSe(NH2)2
»
C.R,99,1154
abt. 200 d.
»>
B. S., 41, 599
48, 50, 376
Methylene seleniocyanate ....
CH2(Se.CN)!!
C3H2Se.iN2
....
132
Proskauer
B., 7, 1279
28, 144
Ethylene seleniocyauate
CH2(Se.CN).CH2(Se.CN)
C4H4Se2N,,
128
?j
B., 7, 1280
»
Allylic seleniocyanate
CH2 : CH.CH2(Se.CN)
C4H5SeN
150-184
....
Wohler
A., 109, 125
v., 221
Benzylic seleniocyanate
Ph.CH,(Se.CN)
C8H;SeN
71-5
Jackson
B., 8, 321
28, 1025
Benzyl Seleniocarbamide
NH2.Se.NH.CH2Ph
p.HuSeN,
J. [1877], 351
70 p. d.
Spica
G. I., 7, 90
32, 189
Dibenzyl Seleniocarbamide ....
NH2.Se.N(CH2Ph)3
C15H16SeN2
darkens 150
d. 216
,,
G. I., 7, 90 ; J.
»
[1877], 351
Trimethylphosphine selenide
Me3PSe
C3H9SeP
84
Hofmann and
iv., 609
Cahours
Triethyl phosphine selenide
EtaPSe
C6H16SeP
112
)»
J. 10, 377
iv,, 613
Triphenyl phosphiue seleuide
Ph3PSe
C18H15SeP
183
Michaelis & Soden
A., 229, 334
48, 1134
Ethylcyanophosphine
Et.PH.CN
C3H6NP
49-50
Darmstadter and
C. R, 70, 404;
vi., 933 ; vii.,
Henniger
B., 3, 179
405
Phosphorus anilidonitride ....
P3N3(NHPh)6
C36H36N9P3
....
268
Hofmann
B., 17, 1910
48, 16
„ toluidonitride ....
P3N8(NH.C6H4Me)6=(1.4)(i
C42H4SN9P3
243
»
B., 17, 1912
)»
Cacodylic cyanide
Me2As.CN
C3H6NAs
140
33
Bunsen
A., 37, 25
i., 406
60C
ORGANIC COMPOUNDS.
(22.) MISCELLANEOUS COMPOUNDS CONTAINING FOUR ELEMENTS
OTHER THAN HYDROGEN.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Trichloracetyl bromide
CCl3.CO.Br
CsCl,Bi-0
abt. 143
J. p. [2], 20,
Gal
C. E., 76, 1019 ;
26,746;vu., li)
196
J. [1873], 536
Hexaohlortetrabromethyl
....
C4Cl6Br4O
96
Malaguti
A. C. [3], 16, 4-25
ii., 541
oxide
Trichloracetyl iodide
CC13.CO.I
C2C1,IO
abt. 180
J. [1873], 536
Gal
C. R., 76, 1019
26,746;vii.,U)
Trichlorraethylsulphonyl
CC13.S02C1
CC1402S
170
135
Kolbe
A., 54, 148
v., 560
chloride
» ji
n
»
A., Ill, 105;
135
Rathke
B., 3, 860
24, 345
B.S.,37,390;
Gilb. Ann.
48, 161
Dichlordinitromethane
CC12(NO,)2
CC1204N2
a. 100
A., 38, 16
Marignac
R. S., 5, 375
iii., 1006
Ohloropicrin ....
CC13.NO2
CC13OJST
lll-91c.(751)
A., 106, 144
Thorpe
37, 198
112
A., 101, 212
Hofniann
A., -139, 111
vi., 445
„ (A., 109, 282) ....
)J
I)
112-8(743)
J. [1872], 298
Cossa
G. I., 2, 181
25,889;vii.,328
120
A., 66, 241
Stenhouse
J., 1, 540
i., 923
Trichloracetyl cyanide
CC13.CO.CN
C3C1,ON
117-119
Liquid
Hofferichter
J. p. [2], 20, 196
38, 35
V »>
»
»
121-122
Claessen and Ant-
B., 13, 1936
40, 153
weiller
)) » ••"
....
( „ ).
140
Hofferichter
J. p. [2], 20, 198
38, 35
PC15 on perchlorpyrocoll
....
C5C17ON
146-147-5
Ciamician & Danes!
G. I., 12, 28
42, 875
Nitropeutachlorbenzene
C6C15.N02
C6C1502N
328 p.d.
146
Juugfleisch
A. C. [4], 15, 186;
vii., 147
J. [1868], 353
Perchlorpyrocoll
....
C10C1602N2
320 d.
Ciamician & Danesi
G. I., 12, 31
42, 875
PC15 on perchlorpyrocoll
C10C110ON2
195-197
ji
G. I., 12, 28
)»
Tribromthiophensulphonic
(C4SBrs.SO,).,O
C3Br606S4
....
115-116
Rosenberg
B., 18, 1775
48, 1051
anhydride
Bromnitroform
CBr(NO3)3
CBr06N3
12
Schischkoff
A., 119, 247
iv., 110
Bromopicrin ....
CBr,.NO.,
CBr.,O2N
a. 100
A., 155, 253
Stenhouse
P. M (4), 8, 36 •
i., 923
A., 91, 307
v
JJ
»j
A., 180, 122
10-25
Bolas and Groves
(2), 8, 153
vii., 212
Nitrodibromace ton i tri 1
CBr2(NO,).CN
C2Br.,O2tf2
130-135 d.
50
Kekul6
A., 105, 281
iv., Ill
Dinitrotetrabrombenzene ....
Br4.(NO2)2— 1.2 3546
C.Br.O.No
J. [1879], 394
227-228
Richter
B, 8 1427
29, 390
Nitrodiiodoacetonitril
CI2(N02).CN
C2I202N2
d. 170
86 p.d.
Sell & Biedermann
B., 5, 89
25, 413
Thionylcyanide
SO(CN)2
CjOSN.
70
Gaulie
A., 143, 264
Phosphorus thiocyanate
P(S : CN)3
P&N.P
260-270
Liquid —20
Miquel
A. C. (5), 11,289,
32, 872
349
G07
IV.-COMPOUNDS CONTAINING FIVE ELEMENTS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Amidobenzoic acid+HF
C6H4(NH2.HF).CO2H =1.3
C-H8FO,N
....
175
Paterno & Oliveri
G. I. [1^82], 85
42, 614
f! » »
= 1.2
>j
....
abt. 200 d.
»
JJ
jj
;i » "
=1.4
?»
210-211
»
V
jj
Fluohippuric acid
C6H4F.(CO.NH.CH2.CO2H)
C9H8F03N
....
121-5
Coppola
G. L, 13, 521
46, 446
= 1.2
„ ,,
= 1.3
J)
....
152
)»
jj
)»
)> »
=1.4
))
161-161-5
)>
jj
JJ
Clilorbromiodethane
CH2I.CHBrCl+3(CHBrI.
C2H3ClBrI
193-195 p.d.
Liquid
Henry
C. R, 98, 680
46, 830
CH.2C1)
Chlorbromal
CClBr,,.COH
C2HClBr2O
148-149
Liquid
Jacobsen and
B., 15, eoi
42, 938
Neuraeister
Chlordibromacetic acid ....
CClBr2.CO2H
C2HClBr.,O2
232-234 p.d.
89
Neumeister
B., 15, 603
43, 944
Bromchloral
CCLBr.COH
C2HCl2BrO
126
Liquid
Jacobseu and
B., 15, 600
42, 938
Neumeister
Bromdichloracetio acid ....
CCl,Br.C02H
C2HCLBrO2
215 s.d.
64
Neumeister
B., 15, 602
42, 943
Chloracetyl bromide
CH2Cl.COBr
C2H2ClBrO
127
....
Wilde
A., 130, 372
vi., 21
.1! "
J1
)»
134
....
Gal
B. S., 5, 172
jj
Bromacetyl chloride
CH2Br.COCl
I)
127
Liquid
Geuther
A., 132, 171
vi., 22
!) »
JJ
H
127
Wilde
J., 17, 319
Chlorbromacetic acid
CHClBr.C02H
C2H2ClBrO3
201
Liquid
Ceeh and Steiner
B., 8, 1174
29, 37.3
Ohlorbromal hydrate
CClBrj.CH(OH)2
CsHsClBrsO2
....
51-52
Jacobsen and
B., 15, 601
42, 938
Neumeister
Brornchloral „
CCl2Br.CH(OH)2
C2H3Cl2BrO2
....
51
jj
B., 15, 600
jj
a-Chlordibromacrylie acid
CBr2 1 C01.CO.H
C3HClBr.;02
....
104
Mabery & Lloyd
A. C. J., 6, 157
48, 510
8- jj • »
CBrCi:CBr.CO2H
»>
....
99
»
5J
48, 511
|3-Bromdichloracrylic „
CBrCl : CC1.CO2H
C3H012BrO2
....
75-78
Mabery and
A. C. J., 6, 165
48, 507
Nicholson
/3-Bromtetrachlorpropionic
CBrClj.CCl5.COjH
CjHCljBrOj
....
225 d.
Mabery
A. C. J., 6, 155
48, 508
acid
Chlorbromaorylic acid
....
C3H2ClBrO2
70
Hill
B., 12, 660
36, 616
» jj
....
»1
....
70
Mabery & Lloyd
A. C. J., 3, 124
40, 1126
Tribromchloracetone
....
C3H2ClBr3O
abt. 50
Glaus & Lindhorst
B., 13, 1210
38, 862
„
....
M
+ 4H20
55
Grimaux & Adam
B. S. [2], 33, 257
38, 457
Chlortribrompropionic acid
C2HClBr3.C02H
C3H2ClBr3O2
abt. 98
Mabery & Lloyd
A. C. J., 3, 124
40, 1126
» >!
»
»
102-103
Mabery & Webei
A. C. J., 4, 104
42, 1047
a-Dibromdichloracetone ....
....
C3H3Cl2Br2O
140-141
....
B. S., 32, 14
0-
....
1)
....
Liquid
Conrad & Guthzeit
B., 16, 1552
44, 1083
3-
CH2Cl.CO.CClBr2(?)
»J
Liquid — 10
Carius
B., 3, 394
vii., 14
P-
....
)J
+4H20
49-50-5
j)
B., 3, 395
jj
ft-
....
'1
n
55-56
....
B. S., 32, 14
8-
....
1)
?>
56
Conrad & Guthzeit
B., 16, 1552
44, 1083
a-Dibromdichlorpropionic
C3H2C]2BrA
....
94-95
Hill and Mabery
B., 14, 1679; 16,80;
40, 1029 ; 44,
acid
A. C. J., 4, 263
309
P- jj jj
CBr2Cl.CHCl.C02H
»
....
100
Mabery and
A. C. J., 6, 165
48, 507
Nicholson
y- jj »
id. with /3- (?)
u
....
118-120
Hill and Mabery
B., 14, 1679; 16,80;
40, 1029 ; 44,
A. C. J., 4, 263
309
Chlordibrompropionic acid
C2H2ClBr2.CO!!H
CjHjClBivOj
80
Mabery & Weber
A. C. J., 4, 104
42, 1047
Bromchloracetone
CHsBr.CO.CH,Cl
C,H4ClBrO
176-188
34-35-5
Theegarten
B., 6, 1212
vii., 320
,, ....
J)
J1
177-180
34-35-5
jj
B., 6, 1277
27, 242, 245
Chlorbrompropionic acid ...
CH2Cl.CHBr.COjH
C3H4ClBr02
215
37
Henry
B., 7, 757
27, 978
11 ') •••
JJ
))
210-215 p.d.
37
»
B., 7, 758
27, 980
Chlorbromhydrin
CH,Cl.CHBr.CHj.OH
C3H6ClBrO
197 u.c.
n
B., 7, 757
27, 978
„
J»
»
197
jj
J. p. [2], 10, 185
28, 346
jj
JJ
»
197
....
As., 1, 225
ii., 898
608
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Chloi bromhydrin
CH2Br.CHCl.CPIj.OH
C3H6ClBrO
197
....
Henry
B., 7, 758
,,
CH2Br.CH(OH).CH2Cl
1)
195-197
Liquid
j>
B., 3, 352
,,
»
)J
197
Reboul
J., 13, 458
„
»
)J
190-105
Grimaux & Adam
B. S. [2], 33, 257
38, 457
,,
?
JJ
185-197
....
Henry
Z. C., 13, 604
Chlortribromcrotonic alde-
CBr,Cl.CH : CBr.CH(OH)2
C4H2ClBr30
110 d.
78
Pinner
B., 8, 1324
29, 553
hyde hydrate
or CBraCl.CBr:CH.CH(OH)j
Chlortribroracrotonic acid
Acid from above
C4H2ClBr30;!
....
140
»
>!
jj
Dibromsuccinyl dichloride
COCl.CJH1Brs.COCl
C4H2Cl2Br2O2
218-220 d.
A., 117, 130
Kekul6
As., 2, 86
v., 462
?
....
C4H2Cl4Br4O
....
60
....
Z. C. [1869], 394
?
....
C4H4Cl2Br20
66 d.
Demargay
B. S. [2], 33, 524
38, 626
?
A.C.(5), 20, 464
Jl
67-67-5
»
C. B., 88, 126
36, 458
Ethylic chlordibromacetate
CClBr2.CO2Et
C4H6ClBr202
203
Liquid
Neumeister
B., 15, 604
42, 944
Chlordibrombutyric acid ....
C3H4ClBr2.CO2H
JJ
A., 164, 105
92
Sarnow
B., 5, 470
25, 690
Ethylic bromdichloracetate
CCl2Br.CO2Et
C4H5Cl2Br02
188-189
Liquid
Neumeister
B., 15, 603
42, 944
Trichlordibromethyloxide
CCl2Br.CClBr.O.Et
C4H5Cl3Br2O
....
17
Busch
B., 11, 446
34, 487
?
....
M
135 (40)
ord. temp. ;
Paterno & Pisati
G. I., 2, 333
26, 159 ; vii., 2
s.f.m.
Ethylic chlorbromacetate....
CHClBr.C02Et
C4H6ClBr02
160-163 p.d.
Liquid
Cech and Steiner
B., 8, 1174
29, 373
< Jhlorethylic broruacetate....
CH2Br.CO2.CH2.CH2Cl
»J
213-215 u.c.
Liquid
Henry
C. B., 97, 1308
46, 421
Dichlordibrombutyralde-
CH2Cl.CHBr.CClBr.CH
C4H6Cl2Br202
72
Natterer
M. C., 4, 539
44, 965
hyde hydrate
(OH),
Chlorbromal alcoholate ...
CClBr2.CH(OH)(OEt)
C4H,ClBr2O2
46
Jacobsen and
B., 15, 601
42, 938
Neumeister
Bromchloral alcoholate .
CCl2Br.CH(OH)(OEt)
C4H7Cl2Br02
43
)>
B., 15, 600
»
Trichlorethylidene tri-
CBrs.CH.CO2.CH(CCl3).O
C5H2Cl3Br303
A., 193, 54
132-135
Wallach and
B., 10, 2129
34, 404
bromlactate
i .J
Eeinecke
Tibromethylidene trichlor-
CCl3.CH.COs.CH(CBr,).O
»
jj
149-150
>!
>!
))
lactate
i i
Bromchloralide
....
C6H2Cl4Br03
....
122
Jacobsen and
B., 15, 600
42,938
Neumeister
y3- trich lorace todibrom pro-
CCl3.CO.(CHBr)2.CO2H
C5H3Cl3Br203
97-5
Kekul6 and
A., 223, 170
46, 1122
pionic acid
Strecker
Chlordibromhydroxy-
C4H5ClBr2(OH).CO2H
C5H7ClBr203
....
169
Pinner & Klein
B., 11, 1497
36, 43
valeric acid
Glycerolacetochlorbrom-
CH2Br.CH(OAc).CH2Cl
C5H8aBr02
220or228(?)
A. C. [3], 52, 462
i., 26
hydrin
Dibromchlorpropykthyl-
CHClBr.CHBr.CHj.OEt
C5H9ClBr2O
220 d.
Friedel & Silva
C. B., 75, 81 ;
25, 805; vii.,
oxide
J. [1872], 324
1020
Glycerolethylchlorbrom-
CH2Cl.CH(OEt).CH2Br
C5H10ClBrO
186-188
....
....
A., 119, 239
ii., 883
hydrin
M
C3H6BrCl.OEt
M
200 p.d.
....
Henry
B., 7, 1113
28, 143
Chlordibromresorcinol
C6HClBr2.OCl.OBr=(?)3.1.3
C6HCl2Br3O2
....
175
Benedikt
M. C., 4, 227
chlorobromide
Trichlorresorcinol dibrom-
C6HCl3(OBr)2=(?)3.1.3
C6HCl3Br202
d. 130
»
M. C. 4, 225
44, 984
ide
Fr. chloranilic acid
,,,.
C6HCl3Br3O
As., 8, 17
79-5
Stenhouse
PI 8, 6
vi., 989
Chlorbromquinone
CsH2ClBr:02=(?)2.1.4
C6H2ClBrO2
A., 210, 160
172
Schulz
B., 15, 656
Dichlordibromquinol
(OH)2.Cl2.Br2=1.4.2.5.3.6
C6H2Cl2Br2O2
....
230
Levy
B., 18, 2.369
48, 1210
»
=1.4.5.(?)3
»»
brown 220
230 u.c.
Krause
B., 12, 54
36, 462
Trichlorphenol bromide ....
C6H,,Cl3.OBr
C6H5Cl3BrO
99
Benedikt
M. C., 4, 235
44, 986
Trichlorbromquinol
(OH)2.Cl3.Br=1.4.2.5.6.3
C6H2Cl3BrO2
As., 6, 2f9
229
Levy and Schulz
A., 210, 161
42, 510
a-Chlordibroruresorcinol ....
(OH)2.Cl.Br2=1.4.5.(2)2
C6H3ClBr2O2
86
Benedikt
M. C., 4, 227
0-
= 1.4.5.(?)2
»
105
Eeinhard
J. p. [2], 17, 326
34, 726
Dichlorbromresorcinol
(OH)2.CL,Br=1.4.5.(?)2
C6H3Cl2BrO,
100
,,
J. p. [2], 17, 330
);
Chlorbromquinol
(OH)2.Cl.Br=1.4.5.?
C6H4ClBr02"
171-172
Schulz
B., 15, 656
!
C6HsCl2Br.OH
C6H9Cl2BrO
160-170 (20)
Natterer
M. C. 5, 567
48, 498
Brorabenzoyl chloride
C6H4Br.COGl=1.3
C7H4ClBrO
239
Liquid
Hubner
Z. C., 14, 301
24, 1055
Chlorbrombenzoic acid ...
C6H3ClBr.CO2H
C7H4CiBrO2
sb. a. 160
|
Claus
B., 5, 657
Chlorbromsalicylic acid ....
C02H.OH.Cl.Br=1.2.(?)2
C7H4ClBrO3
151
Clans and Pfeiffei
B., 5, 656
25,1014;vii.,16;i
Broraterephthalicdichloride (COCl)2.Br=1.4.5
CsH3Cl2Br02
304-5-305 -5 c
Liquid
Fischli
B., 12, 620
36, 639
1
COMPOUNDS CONTAINING FIVE ELEMENTS.
609
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Phenylchlorbrompropionic
C2H2ClBrPh.C02H
09H8ClBrO2
....
179-180
....
A., 147, 92
acid
Diacetyldichlordibrom-
(OAc)2.a3.Br,=1.4.2.5.3.6
C10H,Cl3Br204
265
Levy
B., 18, 2369
48, 1210
quinol
»
„ =1.4.2.6.3.5
»J
....
269-270
»)
»
»
Diacetylchlorbromq uinol ....
(OAc)2.Cl.Br=1.4.2.?
C10H8ClBr04
145-146
Schulz
B., 15, 656
a-Chlorbrorncamphor
....
C10H14ClBrO
....
95-96
Cazeneuve
C. E., 100, 802
48, 668
|3-
....
))
....
50
?)
C. E., 100, 859
48, 806
Dichlordibromdipheno-
[.C6HClBr(OCl).0.]2
C12H3Cl4Br2O4
a. 200 d.
Benedikt
M. C., 4, 228
44, 984
quinone dichloride
Dichlord ibromtetrahydr-
[.C6HClBr(OH)2]3
C13H6Cl3BrA
265 d.
)j
M. C., 4, 229
44, 985
oxydiphenyl
Brom-o-cresolphthalem
C6H4(COCl).CO.C6H2MeB r.
C15HloaBr03
....
208; 208-210
Fraude
B., 12, 240; A.,
36, 635
chloride
OH
202, 162
Diazotribrombenzene
C6H2Br3.NBr.NBrCl
C,H2ClBrsN2
d. 100
J. p. [2], 27, 114
chlorod ibromide
Tribromdichloraniline
NH2.Cl3.Brs=1.3.5.2.4.6
C6H3Cl3Br3N
A., 215, 122
219-5
Langer
B., 15, 1332
42, 1059
Trichlordibromaniline
NH2 C13 Brn— 1 2 4 6.3.5
C'6H3Cl3Br.,N'
A., 215, 119
238'5
B., 15, 1330
»
Tetrachlorbromaniline
NH2.Cl4.Br= 1.2.3. 4.6.5
C6H3Cl4BrN
A., 215, 118
227
»
B., 15, 1328
42, 1058
Tribromehloraniline
NH3.Cl.Br3=1.3.(?)3
C,H,ClBr3N
A., 215, 112
123-5
»j
B., 15, 10d5
Dibromchloraniline
NH3.Cl.Br3=1.2.(?)3
C6H4ClBrsN
A., 215, 115
95
j)
))
i)
=1.4.2.6
H
....
?
....
A., 53, 38
Dichlorbromaniline
NH2.Clj.Br=1.2.6.4
C,H4ClaBrN
....
93-5
Fittig&Buchner
A., 188, 22
34,51
Chlorbromaniline
NH2.a.Br=1.2.4
C6H6ClBrN
69-69-5
»
A., 188, 14
34, 50
j» •"• •••'
)) »
»)
69-69-5
Fittig
B., 8, 15
28, 643
Chlorbromoxalethyline
C6H8ClBrN3:Br3
C6H3ClBr3N3
132-133
Wallach
A., 214, 289
44, 49
dibromide
>i »
11
1»
..,,
132-133
Wallach and Op-
B., 10, 1196
34,55
penheim
„ hydi-obromide
C6H8ClBrN2-|-HBr
C,H9ClBr3N2
....
112-5-113-5
n
J»
34, 55
»» 51
»»
»
112-113
Wallach
A., 214, 289
44, 49
Isocyano-p-bromphenyl-
C7H4Cl2BrN
255-256
Liquid
Dennstedt
B., 13, 232
38, 634
chloride
Brombeiizylamine+HCl ....
Br.(CHs.NH,Cl)=1.2
C-H,ClBrN
208
Jackson & White
B., 13, 1219
38, 879
)> »
=1.4
»
....
260 d.
J ackson&Lowery
A. C. J., 3, 247
42, 170
Chlorbeuzylamine+HBr....
CL(CH,NH,Br)=1.4
n
MM
225-230 d.
Jackson & Field
A. G. J., 2, 85
40, 805
Bromtoluidine-f-HGl
Me.Br.(NH3Cl)= 1.3.4
»
.».
221 d.
Wroblewsky
A., 168, 147
27, 51
Dibromtetrahydroquino-
....
C9H10ClBr2N
162 d.
Hoffmann and
B., 16, 737
44, 1145
line+HCl
Ko'nigs
» »
....
>»
74-75 u.c.
Glaus and Istel
B., 15, 823
42,1111
Dibromdibenzylamine
NH2a(CH2.C,H4Br).=(1.2),
C14H14ClBr3N
...*
166
Jackson & White
B., 13, 1219
38, 879
+HC1
» »
=(l-4)2
)J
283
Jackson&Lowery
A. C. J., 3, 247
42, 171
(i-Dichlordibenzylamiue
NH2Br(CH3.C6H4Cl)2=(1.4)2
C14H14Cl2BrN
283-290
Berlin
A., 151, 133
vi., 338
+HBr
"• » »
»» •»
»J
....
280-290
Jackson & Field
«...
40, 805
^ I! I)
ij
))
• -••
224
Berlin
A., 151, 133
vi., 338
y- „ »
= 1
J»
....
210-212
D
)i
)»
8- » »
= ?
J>
198-199
j»
»»
)1
Chlorbenzylquinoline di-
CI6H14ClBr2N
....
91-92 u.c.
Glaus
B., 18, 1306
48, 908
bromide
Brombenzylquinoline di-
....
C16H14Cl2BrN
80 u.c.
»
I>
))
chloride
Phosphenyldichlordibrom-
Ph.PCl2Br3
C6H6Cl3Br3P
A., 181, 298
208
Miehaelis
B., 6, 817
27, 168
ide
4 i
610
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
&-J. Ch. Soc.
Glycerolchloriodhydrin ....
C3H6C1I(OH)
C3H6C1IO
226
J., 13, 458
Reboul
As., 1, 226
,,
C2H3C1I.CH2.OH
»»
....
Liquid
Henry
B., 3, 351
Methylallylchloriodhydrin
C,H3ClI.CH.i.OMe
C4H8C1IO
195-196
....
Silva
B., 8, 1470
Trimetliyl sulphine dichlor
Me3SICl2
C3H9C1SIS
MM
103-104 p.d.
Masson & Dobbin
47, 60
iodide
Chloriodopyridine + HC1
q,NH5ClI + HC1
C5H6C12IN
....
178
Ostermeyer
C. C. [1884], 937
48, 673
Chloriodopicoline
....
C6H6C1IN
....
111
....
J. p. [2], 27, 279
Pyridine methcchloride
C5NH6.MeCl.ClI
C6H8C12IN
....
81-82
Ostermeyer
B., 18, 593
48, 814
chloriodide
Chloroxalethyline metho-
C6H9ClN2.MeI
C7H12C1IN2
A., 214, 262
203
Wallach
B., 13, 515; 14,
iodide
737; A., 184, 45
Chloriodoquinoline
....
C9H7C1IN
158
Ostermeyer
C. C. [1884], 937
48, 673
+HC1
....
C9H8C12IN
118
)»
)1
»
Chloriodoquinoline dichlor-
....
C9H8C14IN
180
»
J)
•
ide + HC1
Chlorquinoline methiodide
(N.Cl=a, ; ftora2)4MeI
C10H9C1IN
....
231-232
Coste & Bodewig
B., 17, 927
46, 1197
Quinoline methiodide chlor-
NMeI.Cl.1 =ai/3202 ;
C10H10C1I2N
102
Ostermeyer
B., 18, 600
iodide
Quinoline methochloride
NMeCLCl.I =a&n.2 ;
C10H10C12IN
....
112
>!
B., 18, 594, 598 ;
48, 673
chloriodide
C.C. [1884], 937
Dimethamidohydroquino-
C9H10N.NMe2 + MeCl + C1I
C12H19C12IN2
....
127
»
B., 18, 597
48, 814
line methochloride chlor-
iodide
y-Dichlordibenzylamine
NH31(CH2.C6H4C1)2
C14H14CUN
....
187
Berlin
A., 151, 133
vi., 338
+ HI
0-
JI
»
....
215
j)
»
vi., 337
*- »
J»
»
....
216-218
»
j)
vi., 338
Diquinoline methochloride
ClsH12Ns.2MeC1.2ClI
C20H13C14I2N2
....
238
Ostermeyer
B., 18, 598
48, 814
chloriodide
Trichlormethylsulphonic
CC18.S02.OH +H2O
CHC1303S
160 p.d.
130
Kolbe
A., 54, 174
v., 558
acid
» >!
»
))
Z. C. [1869],
1S5
Eichter
B, K. T., 12
82
Dichlorrnethylsulphonic
CHC12.S02.OH
CH2CL,O3S
A., 148, 94
a. 140
Kolbe
A., 54, 164
v., 557
acid
Methylsulphonyl chloride
CH3.S02.C1
CH3C102S
150-153
u
A., 54, 164; 114,
v., 556
142.
» »
»
)»
160
Liquid
Nishack
A., 218, 283
44, 972
Methylic chlorosulphate ....
Cl.SO2.OMe
CH3C103S
80(6)
• •••
Behrend
J. p. [2], 15, 32
32, 289
Sulphochloracetyl chloride
C1.CO.CHC1.S02C1
C2HC13O3S
130- 135 (645)
Liquid
Siemens
B., 6, 660
26, 1022
1
....
C2H2Cl2OaS
150
....
Kammerer and
A., 131, 165
v., 476
Carius
Chloral sulphhydrate
CC13.CH(OH)(SH)
C2H3C13OS
123
77
Byasson
C. E., 74, 1290
25, 612 ; vii.,
312
Eichlorethylsulphonyl
C2H3CL.S02C1
C2H3C1302S
130-140
James
J. p. [2], 30, 316
48, 365
chloride
Chlorethylsulphouyl chlor-
CH2C1.CH2.S02C1
C2H4C12O2S
125-127 (30)
....
Konigs
B., 7, 1163
28, 140
ide
» !)
»
»
200
....
....
A., 122, 37
» »
»»
))
200-205
James
J. p. [2], 26, 383
43, 42
Ethylenedisulphonyl chlor-
SO2C1.CH2.CH2.S02C1
C2H4C1204S2
91
Koiiigs
B., 7, 1163
28, 140
ide
Ethoxythionyl chloride ....
Eto.so.a
C2H5C102S
122
Liquid
Michaelis and
B., 7, 1074
J)
Wagner
Ethylsulphonyl chloride ....
Et.S02Cl
»
171
»
>»
))
» „
))
5>
371
J. [1852], 434
Gerhardt and
C. E., 35, 691
v., 554
Chancel
COMPOUNDS CONTAINING FIVE ELEMENTS.
fill
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Ethylsulphonyl chloride ..
Et.S02Cl
C2H5C10.!S
171
Liquid
Otto
B., 15, 122
42, 831
« »»
J)
»
171
....
Strecker
J. [1870], 727
>! »
)I
?)
^77-5 c.
B., 15, 447
Carius
A., 114, 142
Ethylic chlorosulphate ...
Cl.SO2.OEt
C2H5C1O3S
80-82 (i.v.)
Liquid
Purgold
Z. C. [2], 4, 669
vi., 595
51 »J
J1
)J
80-96 (d.p.)
....
»
B., 6, 502
26, 1216
u »*
»»
»
93-95 (100)
....
Miiller
B., 6, 228
,, »i
)»
J)
130
Kuhlmann
A., 33, 108
ii., 529
!) !!
)J
»
154
....
Baumstark
Z. C. [1867], 566
vi., 602
V »
;>
1)
151-158
....
J. p. (2), 15, 30
19, 250
Ethylic chlorthioforraate...
Cl.CO.SEt
C3H5C10S
136
Salomon
J. p. (2), 7, 252
26, 1223
Thiophentrisulphonyl
C4SH(S02C1)3
C4HC1306S4
....
79-80
Rosenberg
B., 18, 1777
48, 1051
chloride
a-Thiophendisulphonyl
C4SH2(S02C1)2
C4H2C12O4S3
70
Jaekel
....
48, 766
chloride
o
P- » 5)
)I
1*
brown 140
148-149 d.
Langer
B., 18, 555
»
3- „
»
»
....
148-149
Rosenberg
B., 18, 1775, 177
a-Thiophensulphonyl
S.SO,C1=1.2
C4H3C1O2S2
....
Liquid
Meyer and Krei
B., 16, 2173
46, 45
chloride
°- i> »
Jl »*
5»
a. 200 d.
Liquid
Weitz
B., 17, 798
46, 1130
£- 11 )>
,. =1.3
»
boils withou
28(?)
i>
»
)>
d.
0- » »
» )1
1?
....
43
Langer
B., 17, 1568
46, 1133
3- „
» »
)»
43-44
Rosenberg
B., 18, 1777
Dichloralsulphhydrate ...
S[CH(OH).CC13]2
C4H4C1G0,,S
B., 5, 154
127-128 d.
Wyss
B., 7, 211
27, 460
)» •"
>»
)J
....
128
Paterno and
G. I., 3, 333 ; B.
27, 459
Oglialoro
7,80
Ethylic dichlorthiacetate ...
CHCl2.CO.SEt
C4H6C12OS
177-178
Liquid
Meyer
B., 14, 1507
40, 890
Chlorsulphethylic ether ...
....
J»
71-72
....
A., 32, 31
ii., 541
Ethylic chlorthiacetate ...
CH2Cl.CO.SEt
C4H,C10S
166-167
Liquid
Meyer
B., 14, 1508
40, 891
?
CCl3.CH(OH).S.CH(OH).Me
C4H7C13O,,S
....
96-97
Michael
B., 9, 1267
31, 188
Isobutylsulphonyl chloride
BuP.SOjCl
C4H9C1O2S
189-191 u.c.
Liquid
Pauly
B., 10, 942
a-Thiophenic chloride
S.COC1=1.2
C5H3C10S
206 c.
Liquid
Peter
B., 18, 543
48, 767
0- „ „
„ =1.3
»»
190 u.c.
Liquid
Nahnsen
B., 17, 2195
48,52
ft- „ „
JI 5»
)»
206 c.
Liquid
Peter
B., 18, 542
Chlorbenzenesulphonyl
CfH4Cl.SO2Cl=1.3
C6H4C1202S
....
Liquid
Limpricht
B., 8, 1071
29,82
chloride
» )»
»» J>
»J
....
Liquid
Kieselinsky
A., 180, 110
29, 931
» »
= 1.2
1)
....
S8-5
Limpricht
B., 10, 320
32, 193
» »
>1 )I
»
....
28-5
Bahlmann
A., 184, 357
32, 610
» ' v
1» »
)1
28-29
Albert
B., 14, 1437
40, 902
V >1
=1.4
»
50
Otto & Brunner
J. [1867], 632
vi., 274
»1 ' »
J» *1
J)
51
Nolting
B., 8, 819
29, 928
!) !!
»» «
)»
....
53
Goslich
A., 180, 107
29, 930
1) »
»» 1)
)J
....
55
Beckurts & Otto
B., 11, 2064
36, 229
Dichlorbenzenesulphonic
C6H3C12.S03H=1.4.?
C6H4CL03S
A., 182, 94
a. 100
Z. C. [1868], 226
acid
Benzenedisulphonyl
C6H4(S02C1)2=1.3
CeH.as.O.S,
B., 9, 584
63
Korner and
G. I., 6, 133
31,81
chloride
Monselise
« H
>» 1»
))
63
Heinzelmann
A., 188, 157
32, 771
>1 )>
= 1.2
))
....
105
Limpricht
B., 9, 553
V »
=1.4
J»
B., 9, 584
131
Korner and
G. I., 6, 133
31, 81
Monselise
Chlor-/3-acetothienone
C4SH3.(CO.CH.,C1)=1.3
C6H5C10S
295 o.
47
Peter
B., 18, 540
48, 765
Benzenesulphonyl chloride
C6H6.S02C1
C6H5C102S
246
Liquid
Heumann and
B., 15, 1118
Kochlin
)» »
»>
»»
246-247 d.
B., 5, 876
Richter
R. K. T., 117
(A., 136, 157)
Benzenesulphonyl chloride
)>
tl
234
A., 87, 299
Gerhardt and
C. R., 35, 690
v., 564
(A., 145, 321)
Chancel
t
Chlorbenzenesulphinic acid
C6H4C1.S02H
N
A,, 145, 323
88-89
Otto & Brumrner
A., 143, 191
vi., 276
4 I 2
(512
OKGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Chlorphenolsulphonic acid
OH.C1.SO3H=1.4.6
C6H6C104S
+H20
75-76
Petersen and
A., 157, 133
vii., 919
Predari
Sulphamylcarbonyl
CiHu.S.COCl
C6HUC1OS
190-195
Liquid
Schone
J. p. (2), 30, 41C
48, 512
chloride
Isoamylic trichlormethyl-
cab.so2.oc6H11
C6HUC1303S
d. 150
....
....
A., 113,38
sulphonate
Benzoylsulphonyl dichlor-
C6H4(S02Cl)(COa)=1.3
C7H4C1203S
abt. 300
....
Kammerer and
A., 131, 159
vi., 323
ide
Carius
Sulphonylchloride of chlor-
CO2H.C1.S02C1 or COC1.C1.
C7H4C1204S
....
140-150
Collen and Bot-
A., 191, 32 ;B., 9,
31, 82 ; 36, 155
benzoic acid
SO3H=1.4.?
tinger
1250
Toluenetrisulphonyl chlor-
C6H2Me(SO2Cl)3
C7H6C1306S3
....
153
Claesson
B., 14, 309
40, 429
ide
Chlorbenzylsulphonyl
C1.(CH2.S02C1)=1.4
C7H6C12O2S
....
85-5
Jackson & White
A. C. J., 2, 159 ;
38, 879; 40, 807
chloride
B., 13, 1218
a-Toluenedisulphonylchlor
Me.(SO2Cl)2=1.2.4
C7H6C1204S2
....
51-52
Blomstrand and
B., 5, 1086
26, 505; vii.,
ide
Hakansson
1171
°- 11 11
11 11
ii
....
52
Gnehm & Forrer
B., 10, 543
32, 612
a- „ „
11 11
„
....
52
Gnehm
B., 10, 1276
32, 893
a- i, 11
n 11
„
....
52
Fahlberg
A. C. J., 2, 181
40, 816
'" n 11
=1
„
....
86-5
Kornatzki
A., 221, 191
46, 70
£*' 11 ji
„ =?
D
....
94
Blomstrand and
B., 5, 1086
26, 505; vii.,
Hakansson
1171
P-
JJ JJ
„
....
94
Limpricht
B., 18, 2180
y- 11 11
=1.3.5
JJ
....
132
„
B., 18, 2177
48, 1233
Benzylsulphonyl chloride
Ph.CH2.S03Cl
C7H7C102S
92
„
B., 6, 534
26, 1040; vii.,
186
11 11
„
11
92-93
Otto and Liiders
B., 13, 1286
38, 812
Toluenesulphonyl chloride
Me.S02Cl=1.2
11
L.f.m.
Beckurts
B., 10, 944
32, 775
» i:
11 11
,,
Liquid
Miiller
B., 12, 1348
11 11
11 !•
„
Liquid
Limpricht
B., 7, 1394
28, 368
11 11
11 11
„
....
Liquid
Pagel
A., 176, 291
28, 898
11 11
!> 11
„
Liquid
Hiibner and Post
A., 169, 29
11 11
» 11
>•)
....
Liquid
Jenssen
A., 172, 236
28, 77
11 11
„ =1.3
„
....
L— 10
Hiibner and Post
A., 169, 50
27,60;vii.,1170
i> 11
11 11
„
....
Liquid
Pagel
A., 176, 298
11 11
i> 11
„
Liquid
MiilJer
B., 12, 1349
11 11
11 11
„
....
Liquid
Pechmann
A., 173, 202
i. 11
„ =1.4
„
250 d.
68
Otto and others
Z. C. [2], 4, 623
v.,860; vi.,290
11 11
11 ,>
„
....
69
Beckurts
B., 10, 944
32, 774
11 11
11 »
.,
....
69
Miiller
B., 12, 1348
vii., 1167
n 11
n 11
11
70
Otto and Grubeu
A., 145, 10
vi., 288
n 11
11 11
11
79
Heumann and
B., 15, 1118
Koch! in
Methoxybenzenesulphonyl
OMe.S02Cl=1.9
C7H7C1O3S
....
55
Haitinger
M. C., 4, 175
44, 990
chloride
Chlorbenzylsulphonic acid
C1.(CH2.S03H)=1.4
„
A., 165, 372
108 d.
Jackson & White
B., 13, 1217;
38, 879; 40, 806
A. C. J., 2, 158
Phenylmercaptan + chloral
C2HCl30+Ph.SH
C8H7C13OS
....
52-53
Baumann
B., 18, 886
48, 749
Ethoxybenzenedisulphonyl
C6H4.OEt.(S02Cl)2
C8H8C12O6S2
106-108
Zander
A., 198, 27
40, 124
chloride
Diacetylchloralsulphhydr-
S[CH(OAc).CClJ,
C8H8C1604S
....
78
Wyss
B., 7, 211
27, 460
ate
Phenylsulphonethyl chlor-
Ph.SO2.C2H4Cl
C8H9C1O2S
....
55-56
Otto and Dam-
J. p. [2], 30, 171
48, 263
ide
kohler
Ethylic chlorbeuzenesulph
C,H4CLSOjEt
„
....
123
Otto & Brummer
A., 143, 191
vi., 276
inite
Xylenesulphonyl chloride
Me2.SO2Cl=1.3.2
„
....
LO
Jacobsen
B., 11, 22
34, 411
11 !»
=1.4.5
24-26
11
11 11
=1.3.4
i,
....
32
Limpricht
B., 18,2174,2188
11 11
i> 11
11
....
Sit
Jacobsen
B., 11, 20
34, 411
11 11
„ =1.2.4
»
....
51-52
»
B., 10,1012; 11, 23
32, 601
COMPOUNDS CONTAINING FIVE ELEMENTS.
013
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
i
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Ethoxyehlorbenzeuesulph-
OEt.Cl.SO3H=1.4i?
C8H9C104S
260
Petersen and
A., 157, 147
24, 243
onic acid
Predari
?
....
C8H12C112O17S3
....
92
Grabowski
B., 6, 1071
27, 46
Ethylic chlorbenzoate
C02Et.Cl.S03H or C02H.C1.
C9H9C105S
130-150
Collen and Bot-
B., 9, 1251
31,82
sulphonic acid (?)
SO3Et=1.4.?
tinger
Tolylsulphonethyl chloride
C6H4Me.S02.C2H4Cl=1.4
CgHnClOjS
....
78
Otto and Dam-
J. p. [2], 30, 321
48, 538
kohler
Mesitylenesulphonyl chlor-
Me3.SO,Cl=l.3.5.6
n
....
57
Holtmeyer
Z. C. [1867], 686
vi., 301
ide
Pseudocumenesulphonj'l
=1.3.4?
?>
....
61
Kadloff
B., 11, 32
34, 414
chloride
Dichlornaphthalene-o-
C10H5ClJ.SO2a
CIOHSC1302S
145
Widmann
B., 12, 2229
38, 168
sulphonyl chloride
Dichlornaphthalene-/3-
1}
)I
• XI
133
11
B., 12, 961
36, 722, 723
sulphonyl chloride
Chlornaphthalenesulph-
01.80201=0,02 ;
C10HeCl202S
B., 16, 570
95
Arnell
B. S., 39, 62
onyl chloride
?-Naphthalenedisulphonyl
C10H6(SO.,C1)2= ?
C10H6C1204S2
....
125
Armstrong
B., 15, 204
chloride
«- •> »
» )»
»>
B., 16, 5VO
157-158
Alen
B. S., 39, 63
°- II !)
» »
Jl
157-158
Ebert and Merz
B., 9, 597
30, 408
a- ,i i.
»» ))
J)
....
159
11
B.,8, 917
29, 262
»- " »
» 1»
»)
....
162
Armstrong
B., 15, 204
L
* i) j)
V »1
)J
....
183
11
B., 15, 205
8-
)» 5»
l>
B., 16, 570
226
Alen
B. S., 39, 63
0-
V ii
JJ
....
096
Ebert and Merz
B., 9, 597
30, 408
ft- ii 11
» IJ
»
227
11
B., 8, 917
29, 262
a-Naphthalenesulphonyl
CIOH7.SO2C1
C10H7C102S
...»
65
Kimberley
A., 114, 132
v., 561
chloride
°- 11 11
j»
»>
A., 183, 225
66
Liebermann
Z. C. [1869], 711
31, 608
ft- 11 >l
>»
»>
»
76
11
11
7)
Tetrachloride of naphtha-
S02C1.C14= ?
C10H7C1!,O,:S
Liquid
Widmann
B., 12, 2229
lene-a-sulphonyl chloride
Tetrachloride of naphtha-
11 =0i ; "i^i^s
11
....
131
»
B., 12, 960
36, 723
lene-/3-sulphonyl chloride
?
....
C10H9C115016S3
70 d.
Grabowski
B., 6, 1070
27,46
Metanetholsulphonyl chlor-
C^HnO.SOjCl
C10H11C108S
182-183
Perrenoud
A., 187, 75
32, 481
ide
Cymenesulphonyl chloride
Me.Pr«.S02Cl=1.2.?
C10H13C10:S
....
syrupy
Glaus and Stusser
B.,13,898;G.L,
38, 632 ; 40,
12, 543
632 ; 44, 460
1! I)
=1.3.?
>J
MM
175
11
ii
)|
Isocymenesulphonyl chlor-
Me.Pn8.S02Cl=1.3.?
n
B., 16, 792
Liquid
Spica
G. I., 12, 543
ide
Chlordiamylsulphone
CSHU.S02.C6H10C1
C10H21C10aS
330
Liquid
Spring and Wius-
B., 17, 538
46, 1127
singer
Tetrachlordihydroxy-
S02(CSH2CLOH)2
clsH6a4o4s
288-289
Ananheim
A., 172, 38; B.,
27, 796; vii.,
sulphobenzide
9, 1150
886
Dichlorsulphobenzide
S02(C6H4C1)2=(1.3)S
C,,H3CL02S
a. 350
Liquid
Otto and Gruber
A., 149, 180
vi., 277
11
=(1.4),
>t
....
140-141
Otto
A., 145, 28
n
„
11 i»
)>
147
Beckurts and Otto
B., 11, 2064
11 ••••
'i 11
H
152
Gericke
A., 98, 389 ; 100,
207
Chlorphenyldisulphoxide....
S202(C6H4C1)2
c12H8a2o2s2
136-138
Otto
A., 145, 323
vi., 920
Diphenyldisulphonyl chlor-
(.C6H4.S02C1)2=(1.4)2
Ci2H8Cl2O4S3
....
203d.
Gabriel and
B., 13, 390, 1411
38, 477
ide
Deutsch
Chlorsulphobenzide
Ph.SO2.C6H4a
C13H9C1O2S
93
Beckurts and Otto
B., 11, 2067
36, 243
Dipheiiylsulphonyl chloride
Ph.C6H4.S02Cl=1.4
n
115 a. c.
Gabriel and
B., 13, 386
38, 476
Deutsch
BenzophenonedisulphoDyl
CO(C6H4.SO,C1)2(?)
C13H8C1206S2
121-5
Beckmann
B., 8, 993
29, 583
chloride
11 11
11
»
....
134
ji
B., 6, 1113
27, 157
614
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Dichloride of benzophen-
CC12(C6H4.S02C1),,
C13H8C1404S2
128-129
Beckmann
B., 8, 993
29, 583
onedisulphonyl chloride
Authraquinone sulphonyl
c6H4 : (CO)j : c6H3.so2ci
C14H7C104S
193
McHoul
B., 13, 692
40,51
cliloride
=2.1 ; 1.2.4
Chlorbenzylsulphone
S02(CH2.C6H4C1)2= ?
^1 4 •"- 12^2^2^
149
....
A., 165, 375
i» ....
=(1-4),
)»
165
Jackson and
B., 13, 1218 ;
38, 879 ; 40,
White
A. C. J., 2, 158
807
» ....
»» »
»
A., 165, 375
167
Vogt and Hen-
A. C. [4], 25, 129
25, 1096
ninger
„ ....
= »
n
....
185
D
A., 165, 375
Chlorbenzyldisulphoxide ....
S202(CH2.C6H4C1)2=(1.4)2
C14H]2C1202S2
120
Jackson and
B., 13, 1218 ;
38, 879; 40,
White
A. C. J., 2, 169
808
Retenedisulphonyl chloride
C18H16(S02C1)2
Cj8H16CL04S2
....
175
Ekstrand
A., 185, 91 ; B.,
32, 498; 34,
10, 1725
155
Nitrochlormethane
OHjOLNO,
CH-CIO^N
98
Mixture (?)
Preibisch
J. p. [2], 8, 309
27, 462
„ ....
»
)»
122-123
Liquid
Tscherniak
B., 8, 609
Isuretine hydrochloride ....
HO.NH.CH:NH+HC1
CHbClON2
....
abt. 60
Lessen and
Z. C. [2], 7, 594
25, 500 ; vii.
Schifferdecker
708
Methylhydroxylamine
....
CH6C1ON
....
148 u.c.
Petraczek
B., 16, 827
+HC1
» »
....
»)
....
149
Lossen
A., 182, 225
Trichloracetchloramide ....
CC13.CO.NHC1
C,HC14ON
A., 60, 261
121
Steiner
B., 15, 1607
Trichloracetamide
CCl3.CO.NHa
CSH3C13ON
240
135
....
A., 56, 286; 60,261
i.,6
.,
»
11
238-239 (746)
136
Bisshopinck
B., 6, 734
26,1129; vii., 4
,,
If
)>
....
138
Steiner
B., 15, 1607
(A., 184, 23)
>'
n
....
139
Beckurts and Otto
B., 14, 590
Chlorglyoxime
HO.N : COI.CH : N.OH
C2H3C1O2N2
....
151
Nageli
B., 16, 500
44, 728
Dichleracetamide
CHCL.CO.NHj
C2H3C12ON
2SS-8S4 (745)
96
Bisshopinck
B., 6, 734
26,1129; vii., 4
,,
))
>!
233
96
Geuther
J. [1864], 317
»»
»j
V
A., 184, 28
96-97
Otto and Beckurts
B., 14, 1618
40, 1030
,,
)»
»»
230
98
Pinner and Fuchs
B., 10, 1066
Acetoehloramide
CH3.CO.NHC1
C2H4C1ON
....
107-108
Steiner
B., 15, 1609
,, ....
J»
»»
110
Hofmann
B., 15, 410
Chloracetaiuide
CH2C1.CO.NHS
)>
224-225 (743)
116
Bisshopinck
B., 6, 734
26, 1129; vii., 4
p.d.
(A., 102, 110;
J»
)1
....
119-5
Menschutkin and
Z. C. [2], 7, 5
24, 150; vii., 4
184, 30)
Jemolojew
Ethyleneglycol chloronitr-
CH2C1.CH2.O.NOS
C2H4C103N
149-150
Liquid
Henry
A.C. [4], 27,243;
ate
B., 3, 530
Chloral ammonia
Ca3.CH(OH).NH3
C2H4C13ON
A., 157, 114
62-64
Schiff
B., 10, 168
32,308
Etheny lamidoxime + HC1
HO.N : CMe.NH2+HCl
C2H7aONs
....
140
Nordmann
B., 17, 2747
48, 238
Ethylhydroxylamine+HCl
....
C2H8C10N
«...
128
Giirke
A., 205, 273
40, 571
Dichlornitroallylene
....
C3HC12O2N
160-180
MM
Pinner
B., 8, 961
Chloralhydrocyanide
CC13.CH(OH).
C3H2C13ON
begins 120
58-59
Hagemann
B., 5, 152
25, 494; vii.,
p.d. ; chief
310
140-145 d.
,> ....
99.
»
....
60-61
Pinner & Bischoft'
A., 179, 77
29, 554
»
»
))
215-220 p.d.
....
Pinner and Fuchs
B., 10, 1059
32, 584
» ....
H
»>
61-62
Wallach
B., 6, 115
26, 627
Trichlornitropropylene (?)
or Trichlornitropropane (?)
C3H2a302N
190-195
Solid
Pinnef
B., 8, 960
29,57
?
Ca3.C(OH).CO.NH
)»
218
Claisen and
B., 13, 1937
i i
Antweiler
Dichlormethoxyacetonitril
MeO.CClj.CN
C^^ON
148-149 (732)
Bauer
A., 229, 163
48, 1120
Dichloracrylamide
CC12 : CH.CO.NH2
JJ
A., 193, 25
112-113
Wallach and
B., 10, 569
32, 591
Huniius
Dichlornitropropylene
....
C3H3C1AN
155-162
....
Pinner
A., 179, 55
29, 549
» ....
M
162
))
B., 8, 961
29,57
Trichloracetylcarbamide ....
CC13.CO.NH.CO.NH2
C3H3C1302N2
A., 157, 246
150 d.
Meldola and
J. [18741 798
27, 405
Tommasi
Nitrosochloracetone
Z.C. [1870], 529
C3H4aO,,N
....
110
Barbaglia
B., 6, 321
26, 878
COMPOUNDS CONTAINING FIVE ELEMENTS.
615
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
a-Chlorallylic nitrate(B., 15,
CH2 : CC1.CH2.O.N02
C3H4C1O,,N
140
Liquid
Eomburgh
It. T., 1, 233;
44, 450
3086 ; C. E., 95, 849)
B., 16, 393
Trichlorlactamide
CC13.CH(OH).CO.NH2
C3H4C1302N
95-96
Pinner and Fuchs
B., 10, 1061
32, 584
Trichlornitropropane
or Trichlornitropropylene (?)
„
190-195
Solid
Pinner
A., 179, 54
29, 57
Isotrichlorglyceramide ....
CCl3.C(OH)2.CO.NH.i
C3H4C1303N
B., 13, 1937
126-127
Claesen and
J. p. [2], 20, 195
40, 153
Antweiler
Chloracetylcarbamide
CH3C1.CO.NH.CO.NH2
C3HSC102N2
d. 160
....
....
J. [1873], 747
Chlormalonamide .... ...
CHC1(CO.NH2)2
„
d. 175
170
Conrad & Bischoff
A., 209, 231
42,39
u-Dichlorpropionamide ...
CH3.CC12.CO.NH2
C3H5C12ON
A., 132, 184
110
Otto
B. S. [1865], 293
iv., 729
a- „
„
„
115-116
Backunts and Otto
B., 9, 1593
31, 298
a- „
„
D
116
Klimenko
B., 3, 467
vii., 1012, 1033
a- „
„
„
....
116-117
Beckurts and Otto
B., 11, 388
34, 488
Glycerol dichlornitrin
C3H5C12(O.N02)
C3H5C12O3N
180-190 p.d.
Liquid
Henry
A., 155, 168
vii., 320
Ethylic cyanate+HCl
EtO.CN+HCl
C3H6C1ON
95
A., 109, 107
Habich and Lim-
A., 105, 395
ii., 196
pricht
Chlorformodimethamide ....
Cl.CO.NMe2
„
165
Liquid
Michler and Es-
B., 12, 1163
36, 934
cherich
o-Chlorpropiouamide
CH3.CHC1.CO.NH2
„
«•••
80
Backunts & Otto
B., 9, 1592
31, 298
Chlorethylic carbamate ....
NH..COOC2H4C1
C3H6C102N
....
76
Nemirowsky
J. p. [2], 31, 173
48, 741
Propyleneglycolchloronitr-
CH3.CHC1.CH3.O.NO, (?)
C3H6C103N
157-158
....
Henry
A. C. [4], 27, 257
afce
Acetoxime hydrochloride
HO.N:CMe2+HCl
C3H8C1ON
....
98-101
Janny
B., 15, 2778
44, 581
DichlormaleJmide (or fum-
c2ci2:(CO)3:NH
C4HC13O2N
179
Ciamician&Silber
B., 16, 2393
46, 293
arimide)
Tetrachlorsucciuimide
CO.CCl2-CCl2.CO.NH
C4HC14O2N
...
200
....
....
v., 462
Tetrachlorcyaupropionic
C2C14(CN).C02H
n
200
A. C. [3], 16, 72
acid
Chlormaleimide (or fumar-
c2Hci : (co)2 : NH
C4H2C102N
131
Ciamician& Silber
B., 16, 2395
46, 293
imide)
Tetrachlorcyanpropion-
C3C14(CN).CO.NH.,
C4H2C14ON2
....
86-87
....
A. C. [3], 16, 72
amide
Pentachlorethylic oxamate
NH2.CO.COO.C2CJ5
C4H2C1503N
a. 200
134
Malaguti
A., 37, 69; 56, 284
iv., 280
1
B., 8, 1328
C4H3C1204N
....
154
Cech
B., 9, 1255
31, 67
Chloral +HCN+HCNO ....
B., 9, 1253
C4H3C1J02N2
v. 100
80
M
B.,8, 1175 ;C. E.,
29, 376; 30, 184
82, 989
Trichlorcrotonaniide
C3H2C13.CO.NH2
C4H4C13ON
B., 3, 788
96
J udson
Z. C. [2], 7, 40
24,233;vi:.,398
Chloraldichloracetamide ....
CC13.CH(OH).NH.CO.CHCL
C4H4C15O2N
....
105
Schiff & Speciale
G. I., 9, 335
38, 103
Ethoxydichloracetonitril ....
EtO.CCl^CN
C4H5C12ON
160-161
Liquid
Bauer
A., 229, 163
48, lli!0
Chlorcrotonamide
CH3.C2HC1.CO.NH8
C4H6C1ON
230-240
107
Saruow
B.,4,734;A.,164,
24, 1047
103
„
„
„
sb. 78
112
Pinner and Klein
B., 11, 1488
36, 41
]
C4H6C1O2N
19f>
S tiC 11 ll OUSG
A., 33, 92
ii., 282
CH2a.CH.CH2.NH.CO.O
j»
i — ' '
106
Thomsen
B., 11, 2136
i i
Erythroldichlordinitrate ....
C4H6C12(O.NO,,)2
C4H6C1AN2
60
Champion
C. E., 73, 114;
24,812;vii.,471
Z. C. [1871], 349
Trichloracetethylamide ....
CCl3.CO.NHEt
C4H6C13ON
229-230
74
Wallach and Ka-
B., 13, 517 ; A.,
38, 547
meuski
214, 225
Chloralacetamide
CCl3.CH(OH).NHAc
C4H6C1302N
....
156
Schiff
B., 10, 169
32, 308
„
„
»»
....
156-157
Wallach
B., 5, 255
25, 61 1
„
H
„
158
Jacobsen
A., 157, 245
vii., 311
1
NHEt.CjClyOH
C4H7C12ON
._
P h
B., 10, 880
32, 586
Dichloracetethylamide
CHCl2.CO.NHEt
„
225-227
57
Wallach and Ka-
B., 13, 517 ; A.,
38, 547
menski
214, 223
Butyrochloralammonia ....
C3H4C13.CH(OH).NH2
C4H8C13ON
62
Schiff iS Tassinari
B., 10, 1781
Ethylic amidoacetate
NH3Cl.CH2.C02Et
C4H10C1O2N
137
Kraut
A., 177, 267
29,61
+HC1
,,
„
,,
....
144
Curtiua
B., 16, 754
44, 1087
Glycolylmethylguanidine
....
C4H13C1203N3
b. 100
....
....
vii., 583
a-Trichlorcarbopyrrolic acid
C4HC13N.C02H
CACLAN
+H2O
d. 150
G. I., 12, 28
Hydroxydichlorpyridine ....
G^NHjClrOH
CaH3C!2ON
....
178
Konigs andGeigy
B., 17, 1835
46, 1363
C.16
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
PCI6 on glutazin
....
C5H3C13ON2
....
282
Pechmaim and
B., 18, 2291
48, 1202
Stokes
Chloral + cyanic acid ....
O.CH(CC13).O.C.O.
C5H3C16O3N
....
167-1 70 p.d.
Bischoff
B., 5, 87
25,407;vil.,310
CH(CCl:t).NH
I
Chlor. deriv. of C5H5O2N....
CjH^CLON
144-145
Ciamician and
G. I., 12, 500
44, 313
Demisted t
PC16 on glutaziu
....
C6H4C1AN2
241-5
Pechmann and
B., 18, 2290
48, 1202
Stokes
Chloralcyanacetyl ....
CC'l3.CH(OAc).CN
CSH4C1302N
208 d.
31
Pinner & Fuchs
B., 10, 1059
32, 584
Chlorcarbethamide (?)
....
C6H4C1.02N3
260
138-140
B. J., 26, 759
Dihydroxypyridine+HCl
C5NH3(OH)2+HC1
C5H6C1O2N
begins d. 140
207
KonigsandGeigy
B., 17, 1837
46, 1369
Butyrochloralhydrocyanide
CCl3.(CHi)j.CH(OH).CN
C5H6C13ON
230 d.
101-102
Pinner & Klein
B., 11, 1488
36, 41
11
n
11
101-102
Pinner and Bis-
A., 179, 97
29, 556
choff
Acetyltrichlorlactamide ...
CCl3.CH(OAc).CO.NH2
C6H6C1303N
....
94-95
Pinner & Fuchs
B., 10, 1060
32, 584
Chloralcarbamide
CO[NH.CH(OH).CC1.,]2
C5H6C1603N2
190
....
A., 157, 246
Chlorimidoangelic acid ...
Me.C'Cl : CH.C(NH>CONH2
C5H7C1ON2
....
113
Pinner & Klein
B., 11, 1494
36, 42
S-chlorcrotonylcarbamide
NH3.CO.NH.C4H6C1O
H
216 d.
1!
B., 11, 1489
36, 41
Dichlorpropoxyacetonitril
PrO.CCl2.CN
C6H-C12ON
182-184
....
Bauer
A., 229, 163
48, 1121
Trichlorhydroxyvaleramide
C4H5C13(OH).CO.NH2
C5H8U1302N
96
Pinner & Klein
B., 11, 1491
36,41
11
)>
1»
119
11
11
)J
Chloralurethane
CCl3.CH(OH).NH.CO2Et
C5H8C1303N
103d.
Bischoff
B., 7, 631
27, 890
Dichloramylic nitrite
O,H9C12.O.NO
C5H9C12O2N
90 d.
....
Guthrie
J., 11, 404
Diethylcarbamic chloride
NEt2.COCl
C5H10C10N
190-195
Liquid
Wallach
B., 14, 747 ; A.,
40, 719
214, 275
Chloraltrimethylamine
CCl3.CH(OMe).NMes
C5H10C13ON
46-48
Meyer and Bulk
B., 4, 967
25, 247
Diammonium chlorcarb-
....
C5H12C1705N3
....
35-37
....
B. J., 26, 759
ethamate
Nitrodichlorquinone
a2.NO2:O2=1.3.4.5.2
C6HC12O4N
....
219-220
Guareschi and
B., 18, 1171,
48, 891
Daccomo
1174
Dinitrotrichlorbenzene ....
C13.(NO2)2=?
C6HC1304N2
335 p.d.
103-5
Juugfleisch
A. C. [4], 15,
vii., 146
186; J., 21, 352
Trichlorquinonechlorimide
C6HC13.O.NC1
C6HC14ON
118
....
J. P. [2], 23, 438 ;
i 1
24, 429
Nitrotetrachlorbenzene ....
C14.N02=1.3.4.5.6
C6HC1402N
....
20-22 ;£Z-;?2
Beilstein and
B., 9, 579; 10, 273;
30, 294; 31,
Kurbatow
A., 192, 238
707
,!
„ =1.2.3.4.5
»
....
64-5
11
»
»
i>
» = »
1)
abt. 300
75-78
Lesimple
B. S. [2], 6, 161
vi., 269
,, ....
„ =1.2.4.5.6
J?
....
98
Beilstein and
B., 10, 272 ; A.,
31, 707
Kurbatow
192, 236
11
»
J>
304 d.
99
Jungfleisch
J., 21, 353
vii., 147
Trinitrochlorbenzen e
C1.(N03)3=1.2.4.6
C6H3C106N3
....
82-5-83
Austen
[3], 13, 279
32, 756
„ (J.[1879],394)
» »
»
A., 92, 326
83
Jungfleisch
J. p. [2], 1, 150
vii., 146, 909
Dinitrodichlorbenzene
C12.(N02)2=1.3.(?)2
C6H2C12O4N2
J. [1875], 323
103
Korner
Z. C. [1870], 375 ;
29, 219 ; vii.,
G. I., 4, 305
914
11
„ =1.4.2.3 or 5
»
318 p.d.
101
Jungfleisch
J. [1868], 348
vii., 146
11
ii ii
Jj
....
101
Engelhardt and
Z. C. [1870], 234
vii., 914
Latchinoff
„ (J. [1879], 394)
ii 11
))
J. [1875], 325
101-5
Korner
G. I., 4, 305
29, 209, 219
)»
=1.4.2.6
5)
312 p.d.
....
Jungfleisch
J., 21, 348
vii., 146
))
ii 11
)1
....
104
Jourdau
B., 18, 1454
)»
11 11
))
312 p.d.
w 4
Engelhardt and
Z. C. [1870], 234
vii., 146, 914
4-
Latchinoff
„ (J. [1879], 394)
11 ii
))
J. [1875], 324
104-9
Korner
<3. I. 4, 305
23, 209, 219
Nitrotrichlorbenzene
C13.NO2=1.2.3.4
C6H2C13O2N
....
55-56
Beilstein and
B., 9, 1688 ; 10,
31, 474, 707;
Kurbatow
272; 11,1979;
36, 310
A., 192, 235
„ (A., 137, 123)
„ =1.2.4.5
11
58
11
11
j)
„ Z.C. [1867], 122
» 11
11
288
57
Jungfleisch
J., 21, 351
vii., 146
COMPOUNDS CONTAINING FIVE ELEMENTS.
617
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrotrichlorbenzene
C13.NO2=1.3.5.6
C6H2C1302N
....
68
Beilstein and
B, 10, 271; 11,
31, 706 ; 36,
Kurbatow
1980; A., 192,
309
233
»
„ =1.2.4.3
»
....
88-89
,>
A., 192, 232
»
» ='
)J
273
b. 100
Lesimple
B. S. [2], 6, 161
vi., 269
Nitrotrichlorpheuol
OH.C13.NO2=1. 2.4.6.5
C6H2C1303N
....
69
Daccomo
B., 18, 1164,1173
48, 889, 891
Dinitroehlorbenzene (8) ...
C1.(NO2)2=1.3.4
C6H3C104N2
....
Liquid
Laubenheimer
B., 9, 765
30, 294
(«) -
1) 11
»
B., 15, 697
36-3
n
B., 9, 762
30, 294
O) -
11 »I
H
„
37-1
?,
B., 9, 763
42, 953
(?) -
11 H
J»
,,
38-8
,,
»»
30, 294
....
1) 1»
>i
....
38-39
,,
B., 8, 1623
29, 577
n
11 )»
»
38
Beilsteiu and
B., 11, 2057
36, 231
Kurbatow
„ (J. [1877], 425)
„ =1.2.6 (?)
i»
315 (762)
43
Jungfleisch
J. [1868], 346
vii., 145
,,
„ =1.2.4
>»
....
50
Engelhardt and
B., 3, 98 ; Z. C.
vii., 908
Latchinoff
[1870], 232, 274
„ ...
»» H
i>
315 p.d.
50
Jungfleisch
J. [1868], 345
vii., 145
j, *..
V 1)
»>
....
50
Beilstein and
B., 11, 1939,2056
36, 144, 230
Kurbatow
„
>! »»
»>
....
53
>,
B., 10, 1992
34, 139
,,(J. [1877], 425)
11 11
»>
53-4
Korner
G. I., 4, 305
29, 211
Dinitrochlorphenol
OH.C1.(N02)2=1.4.5.6
C6H3C106N2
69
Petersen
A., 157, 165
24, 250
»» ••••
» »
1>
70
Engelhardt and
Z. C. [2], 6, 234
24, 247 ; vii.,
Latchinoff
146, 914
„
„ =1.4.2.6
»
....
79-80
Smith and Pierce
B., 13, 35
38, 392
is )»
11
....
80
Engelhardt
Z. C. [2], 6, 234
vii., 146
„ ....
11 D
))
J. [1879], 512
80-5
Armstrong
B., 6, 649
25, 93; 28, 520;
29, 476
,,(Z.C. [1867], 207)
» >i
»»
J. [1875], 339
80-5 ; 81
Armstrong and
25, 865
27, 804
others
,,(Z.C. [1866], 705)
11 )1
»
....
81
Dubois
B., 6, 369
vii., 914
„ ....
11 ))
»»
....
81
Petersen and
A., 157, 156
24, 242 ; vii.,
Predari
919-929
,, .... ....
11 11
»j
....
81
Faust and Saame
As., 7, 195
vii., 912
„ ....
1) 51
„
81
Faust
B., 6, 135
26, 635
11 .... ....
11 )>
n
....
81
Post
B., 7, 335
„
„ =1.2.4.3 or 5
j»
80-81
Petersen
A., 157, 161
24, 249
r •*••
11 »
»»
....
81
Muller
A. P. [3], 3, 103
27, 159
,,
=1.4.(?)2
»»
....
87
Armstrong
28, 364
„
=1.3.2.4 (?)
»»
....
103
Griess
A., 109, 286
iv., 400
„
11 »)
n
....
103
Stenhouse
[2], 5, 435
vi., 914; 28,
364
;.
1» »
ii
....
103
Petersen
A., 157, 171
24, 251
„
)» »J
»»
103
Armstrong
26, 16
j, ....
=1.2.4.6
„
....
110
Post
B., 7, 335
27, 800
,,(Z.C.[1871],591)
» J>
ii
....
110-111
Armstrong '
24, 1113, 1120 ;
vii., 909, 920,
25, 13, 15 ; 26,
923
66 ; 28, 364
„ «...
J> »»
ii
....
110-111
Armstrong and
....
25, 864, 865
Brown
,,
» ))
M
111
Armstrong and
B., 7, 405
27, 804
Prevost
' „
J) )>
)J
....
110-111
Faust
B., 6, 133
26, 635
» .... ....
» »)
)>
....
111
Faust and Saame
Z. C. [2], 5, 451 ;
24, 246; 26,
As., 7, 196
1132 ; vi., 914
,, ...»
JI »
11
....
111
Muller
A. P. [3], 3, 103
27, 157, 158
,,(Z.C.[1871],339)
» )J
)!
....
111
Faust and Muller
A., 173, 312 ; B.,
26, 66 ; 28, 156
5,779
„ (A., 109, 286)
>» ?»
»»
B., 6, 369
111
Petersen
A., 157, 171
24, 250
.»
= '
II
....
114
»
A., 157, 171, 182
25, 95, 864
* ,5
» !,
M
....
114
Petersen and
A., 157, 161
24, 244, 250;
Predari
t
vii., 914
4 K
618
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dinitrochlorphenol
OH.C1.(NO,)S= ?
C6H3C105N2
....
114
Faust
A., 173, 318
28, 364
,, .... ...
)» »
))
....
114
Peters
A., 176, 186
28, 762
Nitrodichlorbenzene
CI3.NOa=1.3.4
C6H3C120SN
J.[1875],323
32-2
Korner
G. I., 4, 305
29, 219
(A., 182, 97)
)) »
n
....
S3
Beilstein & Kur-
B., 7, 1760; 8,
38, 451, 1037 ;
batow
693 ; 9, 634
30, 309, 631
.,
„ =1.2.4
»»
....
43
....
A., 176, 41
(A., 182, 94)
» ))
»
....
«
Beilstein & Kur-
B., 7, 1759; 9,
28, 450 ; 30,
batow
580, 1688 ; 11,
294,631; 31,
1861, 1978
474 ; 36, 143,
310
„ =1.4.6
,,
see
B4-5
Jungfleisch
J. [1868], 348
vii., 145
1, .... ...
» ))
)«
....
54-5
Laubenheinier
B., 7, 1601 ; 8, 224
S3, 648, 759
„ (J. [1875], 324)
» H
H
54-6
Korner
G. I., 4, 305
29, 209, 219
,, .... ...
>J 1)
')
54-5
Jourdan
B., 18, 1454
„
V )>
»»
54-5
Beilstein & Kur-
B., 7, 1761 ; B.,
28, 451; 36, 231
batow
11, 2056
(B., 10, 1993)
» )J
))
....
55
>i
A., 182, 103
30, 631; 34, 139
„ (J. [1877], 424)
>» »»
)»
55
Lesimple
B. S. [2], 4, 226
vi., 269
„ (B., 8, 143)
„ =1.3.5
)i
abt. 240 p.d.
47-5 (?)
Witt
B., 7, 1604
28, 759
„ (J. [1875], 323)
» »
)»
65'4
Korner
G. I., 4, 305
29, 220
„ .... ....
» »
M
....
65
Witt
B., 8, 144
....
„
„ =1.3.2
»
....
71
Beilstein & Kur-
B. S. [2], 30, 25 ;
34, 974; 36,
batow
B., 11, 1861
143
Dichlorpyridine carboxylic
N.C12.CO2H= ?
»
....
180 d.
Ost
J. p. [2], 27, 282
44, 794
acid
» »
=1.(?)2.4
»
....
210
Behrmann and
B., 17, 2695
48, 139
Hofmann
Nitrodichlorphenol
OH.Cl2.NOj=1.2.3.4
C6H8C1203N
....
95
Armstrong
MM
25,96
(Z. C.
11 11-
11
95
Petersen
A., 157, 171
24, 251
[1871], 679)
„ (id. with
= ?
n
106
i)
A., 157, 163 ; B.,
25,95; 26, 1132;
1.2.4.6)
6, 370
vii., 913
» »»
" 11
11
....
106
Petersen & Predari
A., 157, 154
24, 244 ; 28, 364
(B.,2,52)
=1.2.4.6
»»
....
121 ; 121-5
Armstrong
[4 10, 93
vii., 921; 26, 66
„ (Z.C.[1871],
» ))
M
....
121 ; 121-5
Armstrong and
25, 865, 872
vii., 923
520, 678)
Brown
),
» W
!,-
....
121
Armstrong and
B., 7, 405
27, 804
Prevost
i,
5V »>
»
....
121
Armstrong and
29, 476
Harrow
»
5» »
W
....
121
Post
B., 7, 334
27, 800
V "•• ••••
J» !>•
>J-
121-5
Faust
Z. C. [2], 7, 338
25, 62
Jl .... ....
» )»
J>.
....
121-122
Fischer
Z. C. [2], 4, 386
26,1132;vii.,913
.) ....
»>• )V
11-
121-122
Armstrong
24, 1119, 1120
vii., 912
» .... ....
»»• M
n
121-122
Petersen
A., 157, 164
24, 251
»
J»- IV
i*
....
122
11
B., 6, 370
....
11
» »
i,
122
Faust and Saame
A., 130, 195
24, 246
„ (As., 7,
)) )>
11
....
125 d.
Seifert
Z. C. [2], 5, 449
vi., 913 ; 25, 62
185, 195)
j» •••• ....
=1.(?)2.3
51
....
121-122
MUller
A. P. [3], 3, 103
27, 159
1)
>i i)
>!
....
122
Faust and MUller
A., 173, 303
28, 156
»»
11 11
Jl
....
122
Armstrong
....
28, 364
j> .... ...
=1.2.6.4
11
....
125
11
24,1112, 1116
vii., 912, 929
,,
!' 11
11
125
Seifert
As., 7, 198
24, 246
„ (Z.C. [18711
11 >!
11
....
125
Armstrong and
B., 7, 926
25, 865
518)
Brown
,,
» 11
11
....
125
Post
B., 7, 332
27, 800
„
» 11
11
125
Faust
B., 6, 132
26, 635
„
„ =1.2.3 or 5. ?
125
Muller
A. P. [3], 3, 103
27, 159
Dichlor-a-hydroxypicolinic
acid
CsNHCla(OH).C02H
11
....
282 d.
Ost
L J> 7
J. p. [2], 27, 288
44, 795
COMPOUNDS CONTAINING FIVE ELEMENTS.
619
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dinitrodichloraniline
NH2.C1,.(N02)2= 1.3.4.2(0-6
C6H3CI204N3
....
127-128
Beilstein anc
B., 11, 1979 ;
36, 310
Kurbatow
A., 196, 227
Nitrotrichloraniline
NH2.C13.N02=1.3. 4.6.2
C6H3CI302N2
A., 196, 235
124
i»
B., 11, 1980
)»
,,
=1.0)3.3
)»
A., 215, 110
98
Langer
B., 15, 1063
Quinonechlorimide
O.C6H4.NC1=1.4
C8H4C10N
....
84-7-85
Hirsch
B., 13, 1903
40, 164
L 1
„
I) ))
»)
d. 110-115
87-88
»»
B., 18, 1514
48, 892
i»
....
H
....
?
Schmitt
J. p. [2], 19, 316
Nitrochlorbenzene....
C1.NO2=1.2
C6H4C102N
243
8. 15
Sokoloff
J., 19, 552
„ (Z. 0. [1866],
11 11
»
243
15
Jungfleisch
J. [1868], 344
88, 363
621 ; [1870], 231)
„ (B.S.[2],30,25)
11 J)
Tt
24$
32-5
Beilstein anc
B., 9, 635 ; A.
30, 309, 632;
Kurbatow
182, 107
34, 974
(«) .».
„ =1.3
)1
abt. 230
23-7
Laubenheimer
B., 9, 766
30, 295
(ft -.
11 »
H
....
44-2
M
»
Vii., 138
,, ....
» 11
j)
227; 235-6 c.
44-2 ; 44'4 e
»
B., 8, 1622
29, 577
(7407)
„ (J. [1863], 424)
D >i
11
....
45
»
B., 7, 1765
28, 452
„ (J. [1866], 457)
» M
H
....
45
Griess
PI 5, 857
vi., 921
„ (B., 13, 1071)
11 )>
i»
46
Richter
B., 4, 463
24, 688
„ (B., 8, 1417)
JJ »
)>
233
46
Beilstein and
B., 7, 1398, 1761
28, 364, 451 ;
Kurbatow
A., 182, 102
30, 631
„ (J. [1875], 317)
» 11
)?
....
47-9
Korner
G. I., 4, 305
29, 215
„ (J. [1868], 343)
„ =1.4
»)
•
75
Glutz
A., 143, 181
vi., 274
)> .... ...
»i »i
D
....
78
Eiche
A., 121, 358
iv., 416
„
11 »)
)i
....
82
Engelhardt and
Z. C., 13, 231
vii., 907
Latchinoff
„ (J. [1866], 457)
T> 1>
l»
....
83
Griess
[2], 5, 857
vi., 921
,,
« 11
»1
243 (761)
S3
Jungfleisch
A. C. [4], 15, 222
vii., 138, 144
„ ....
V M
n
....
83
Laubenheimer
B., 9, 1827
31, 594
jj
V 51
i*
....
83
Hofmann and
B., 5, 916
26, 168
Geyger
-i
11 ;>
»
....
83
Beilstein and
A., 182, 105 ;
28, 362 ; 30,
Kurbatow
B., 7, 1396
631
11
»» ji
ji
83
Willgerodt
B., 15, 1003
M
»» )i
•»
....
80-3; 83-3
Korner
G. L, 4, 305
29, 220, 221
j»
J> >*
»»
84
Eichter
B., 4, 463
24, 688
Chlorpicolinic acid
N.C1.CO2H=?
)»
sb. 100
168
Ost
J. p. [2], 27, 284
44, 794
Chlornicotic acid
=1.2.5
i)
....
199 d.
Pechmann and
B., 17, 2392
47, 151; 48,
Welsh
175
Nitrochlorphenol
OH.C1.NO2=?
C6H4C10,N
....
Liquid
Beilstein and
B., 7, 488
27, 806
Kurbatow
,1
„ =1.3.6
11
....
38-9 ; a.f. 327
Laubenheimer
B., 9, 769, 1826
30, 295 ; 31, 594
,,
)> »
11
38-9 ; a.f. 32'7
Uhlemann
B., 11, 1162
34, 978
v
=?
1i
43
Beilstein and
B., 7, 488
27, 806
Kurbatow
V •••• .»«
=1.2.6
11
70
Faust and Miiller
B., 5, 778; A.,
26, 65; 28, 156;
173, 307
vii., 906-929
» »
11
70
Miiller
A. P. [3], 3, 103
27, 158
,,
» J)
1)
70
Faust
B., 6, 133
26, 634
,J
V »
11
70
Post
B., 7, 333
27, 800
1)
=1.4.6
V
....
86
Petersen
A., 157, 171
24, 249
)1 •". ....
'> i)
1>
86-87
Miiller
A. P. [3], 3, 103
27, 159
J>
V V
M
86
Post
B., 7, 333
27, 800
»J
» »»
»
86
Laubenheimer
B., 7, 1601
28, 760
» .... ....
» J
»»
....
86-5 ; 87
Beilstein and
B., 7, 487, 1396
27, 806; 28,
Kurbatow
363 ; vii., 905
„ (J. [1879], 512)
>1 )>
»»
....
86-5
Armstrong and
....
25, 865
Brown
,>
1' .)
>;
86-87
Faust and Saame
Z. C. [21 5, 450 ;
24, 244; vi.,
As., 7, 190
912; vii., 912
,,
I! ))
»
86-87
Faust
B., 6, 135
26, 635
4 K 2
620
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& Of. Ch. Soc.
Nitrochlorphenol
OH.C1.NO2=1.4.6
C6H4C103N
86-87
Faust and Miiller
A., 173, 317
vii., 929
„
=1.2.4
»J
109
Armstrong and
....
25, 865
Brown
„
»» *»
1»
....
109-110
Armstrong
....
25, 14
„
« »
J)
110
Faust
B., 6, 133
26, 635
>»
J> )»
)>
....
110
Post
B., 7, 333
27, 800
,,
» »
»)
110-111
Miiller
A. P. [3], 3, 103
27, 158
»
J> )>
J»
....
111
Faust
Z.C.[2],7,339,591
25, 63
» .... ...
91 )»
)>
....
111
Faust and MUllei
A., 173, 309
vii., 906, 92!J
Chlor-y-hydroxypicolinic
N.CO2H.OH.C1=1.2.(I)2
*»
224
Bellmann
J. p. [2], 29, 1
46, 840, 841
acid
Chlor-j3-hydroxypicolinic
>» )>
»
257 d.
Ost
J. p. [2], 27, 290
44, 795
acid
Dinitrochloraniline
NHS.CL(N03)3=1.4.2.6
06H4C1O4N3
J. [1875], 352
1447
Korner
G. I., 4, 305
29, 230
Dichlorhydroxymethyl-
C^MeClj-OH
C6H4C12ON4
274
Fischer
B., 17, 331
46, 996
puriu
Nitrodich'.oraniline
NH2.C13.N02=1. 2.5.6
C6H4CI202N2
J. [1875], 352
66-4
Korner
G. I., 4, 305
29, 209
»
» »
)»
....
67-68
Beilstein and
B., 11, 1978; A.,
36, 309
Kurbatow
196, 222
„ (A., 196, 228)
=1.3.5.6
»)
....
79
»
B. S. [2], 30,25;
34, 974 ; 36,
B., 11, 1979
310
„ (A., 196, 226)
„ =1.4.5.6
i)
....
95-96
!»
B., 11, 1979
36, 310
„ (A., 215, 111)
= 1.2.4.6
)>
-...
99
Langer
B., 15, 1064
.,
» »
:)
100
Witt
B., 7, 1603
28, 759
„
» »
))
....
100
)1
B., 8, 820
29, 935
„
I! »
»
100
Beilstein and
B., 11, 1979; A.,
36, 310
Kurbatow
196, 230
„ ....
=1.2.5.4
j»
153
»
j»
36, 309
(B., 9, 1688)
„ =1.2.3.6
»>
....
162-163
)»
»
31, 474; 36, 310
„
„ =1.3.5.4
H
....
170-171
»
B. S. [2], 30, 25 ;
34, 974; 36, 310
B., 11, 1979
„
» »
»
175
•»
A., 196, 228
>» ....
=1.3.4.6
)J
171
)>
B., 9, 580
30, 294
„ (A., 196, 226)
5» »
»>
....
175
ji
B., 11, 1978
36, 309
„ (A, 196, 230)
= 1.2.6.4
»>
....
188
)?
B., 11, 1979
„ ....
>i »
»
188
Witt
B., 7, 1604; B.,
36, 310
8,144
Amidotriclilorphenol
OH.C13.NH2=1.2.4.6.3
C6H4C13ON
....
95
Daccomo
B., 18, 1166
48, 890
»
=1.(?)3.4
)»
....
159
....
J. p. [2], 23, 438;
24, 426
»
„ =?.1.2.3.?
>»
....
I
Hirsch
B., 13, 1908
Nitrochloraniline
NH2.C1.N02=?
CACIO.N,
....
89
Jungfleisch
A. C. [4], 15, 186
vii., 145
„ .... ....
=1.2.4
>»
....
104-105
Beilstein and
A., 182, 108
30, 632
Kurbatow
„
=1.4.6
)J
....
113-5
Laubeuheimer
B., 8, 225 ; J.
28, 648
and Korner
[1875], 351
„ .... ....
)> »>
J)
....
115
Beilstein and
B., 7, 1761 ; 9,
28, 451 ; 30,
Kurbatow
633; A., 182,99
308, 631
„ (J. [1875], 351)
» n
»»
116-4
Korner
G. I., 4, 305
29, 209, 219
„
=1.2.5
J|
....
117—118
Beilstein & Kur-
B., 8,693; 9,633;
28, 1037 ; 30,
batow
A., 182, 101
308, 631
» .... ....
=1.3.6
)J
123-5 n.c.
Laubenheimer
B., 9, 1827
31, 594
,,
I> )»
J*
123-124
»
B., 11, 1158
34, 976
»
5) i»
))
....
123-2
Korner
G. I., 4, 305
29, 220
» .... ....
» »
>»
....
123-5
[Jhlemann
B., 11, 1162
34, 978
,, .... ....
') )>
124-135
Beilstein & Kur-
A., 182, 105 ; B.,
28 J037 ; 30,
batow
8, 693 ; 9, 634
309, 631
)) •"• "••
„ =1.3.4
)1
....
156-157
i»
»
30, 309, 632
Nitroamidochlorphenol ....
OH.C1.NH2.N02=1.2.6.4
C6H5C103N2
....
140
Armstrong
25, 14
vii., 914, 929
»
» >!
5»
...»
158; 100
»
....
25, 97
(Z.C. [1871], 339)
COMPOUNDS CONTAINING FIVE ELEMENTS.
621
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Nitroamidochlorphenol
OH.C1.NH2.NO2=1.2.6.4
C6H6C1O3N2
160
Griess
A., 109, 291
iv., 407
(A., 173, 315)
„
jj u
„
160
Armstrong
Amidodichlorphenol
OH.C12.NH2=1.2.6.4
C6H5C12ON
165-166
Siefert
As., 7, 202
vi., 913
jj
= 1.2.4.6
„
1
„
As., 7, 189
„
= 1.(2)2.4
)J
175
Jasger
B., 8, 896
28, 1260
Nitrodiamidochlorbenzene
C1.(NH2)2.N0.2=1.3.5.4
C6H6C102N3
192-194
....
A., 192, 233
Amidodichlorphenol + HCi
OH. C12.NH3C1=1. 2.6.4 or 4
C,H6CI3ON
b. 230
Siefert
As., 7, 202
vi., 914
Amidophenol+HCl
OH.NH3Cl=4th
C6H8C1ON
mixture ?
w.m. 230 p.c
Fittica
B., 13, 1536
40, 47
Tetrahydrochlorpicolinic
C5NH7C1.CO2H
C6H8C102N
....
265-270 d.
Ost
J. p. [2], 27, 283
44, 794
acid
Acetylepichlorhydrin
CH2Cl.CH.CH2.NAc.CO2
I I
C6H8C1O3N
79
Thomsen
B., 11, 2137
36, 217
Ethylic chlormaleamate ...
NH2.CO.C2HCl.CO2Et
5J
....
102 u.c.
Claus & Voeller
B., 14, 151
40, 254
Nitrate of chloroxy-base...
C6H7C10N2+HNO3
C6H8C104N3
133
Keller
J. p. [2], 31, 363
48, 961
Tetranitrodichlord ulcitol
C6HSC12(O.N02)4
C6H8C12012N4
....
108
A. C. [4], 27, 192
Tetranitrodichlormaunitol
„
3J
145
Borchardat
B. S. [2], 19, 199 ;
26, 747 ; vii.,
A. C. [5], 6, 126
774
Crotonic-chloralacetamide
CCl3.C2H2.CH(OH).NHAe
C6H8C13O2N
170
Pinner
A., 179, 21
29, 549
Chloraldiacetamide
CCl3.CH(OAc).NHAc
C6H3C1:!O3N
117-118
Schiff
B., 10, 170
32. 308
Dichlorisobutoxyaceto-
Bu0O.CCl2.CN
C6H9C12ON
195-197
Liquid
Bauer
A., 229, 163
48, 1121
nitril
Chlordiethoxyacetouitril ..
(EtOX.CCl.CN
C6H10C102N
159-5-161-5
*.*•
jj
^
Butyrochloralacetamide ..
CCl3.C2H4.CH(OH).NHAc
C6H10C1302N
A., 179, 40
158
Schiff & Tassinari
B., 10, 1785
Ethylic dichlorethoxamate
NHEt.CCl2.CO2Et
C6HUC1202N
....
50+
Wallach
A., 184, 76
32, 187
Nitrotrich lorbenzoic acid ...
CO2H.C13.NO2=1.2.4.6.3
C7H,C13O4N
....
220
Beilsteiu
A., 152, 239
Nitrochlorbenzonitril
CN.C1.NO2=1.2.3 or 5
C7H3C1O2N2
105-106
Henry
B., 2, 493
Dinitrochlorbenzoic acid ....
CO2H.C1.(NO2)2=1.2.3.5
C7H3C106N2
238
Wilkens & Rack
A., 222, 166
46, 602
Dinitrochlorsalicylic acid....
CO2H.OH.C1.(NO2)2
C7H3C1O7N2
78
Hasse
B., 10, 2191
34, 416
=1.2.5.(?)2
|3-Pyridinedicarboxyl
N.(CO.C1)2= ?
C7H3C12O2N
269-270
49
Ramsay
P. M. [5], 6, 24 ;
36, 267
chloride
J. [1878], 439
a~ jj i)
=1.2.6
„
284
60-5
Epstein
B., 18, 1746
°- jj »
»J J»
„
284
60-5-61
Ramsay
P. M. [5], 4, 244
jj
(J. [1877], 437)
y-Pyridiuedicarboxyl
JJ -— '
„
265
88-89
H
P. M. [5], 621
jj
chloride (J. [1878], 439)
Nitrodichlorbenzaldehyde
COH.C12.N02=1.2.4(?).6
C7H3C1203N
>•••
136-138
Gnehm
B., 17, 753
46, 1028
Dinitrotrichlortoluene
Me.CI3.(NO2)2— 1.2.3 4.5 6
C,H Cl O N
141
•jpp] JCT
Bl ft 499
48 77f>
V^7J~1-3V/13\_»4J.1 2
....
i^ i
.) * \ '!. — —
^°j / 1 \j
»
„ =1.2.4.5.3.6
„
....
225
Schultz
A., 187, 280
j>
jj jj
fl
....
227
Seelig
B., 18, 422
48, 770
Nitrobenzoyl chloride
COa.N02=1.2
C7H4C103N
....
s.f.m.
Claisen and
B., 12, 351
Shadwell
,j
„ =1.3
„
65-268
Liquid
Cahoura
A. C. [3], 23, 339
i., 568
j, j.
jj »
„
....
29
lichardson
B., 12, 351
„ »
jj jj
jj
84 (50-55)
33
Claisen and
B., 12, 1943
38, 253
Thompson
j. jj
jj jj
„
275-278 p. d.
35
McHugh
B., 7, 1268
28, 270
Nitrochlorbenzaldehyde ....
COH.C1.NO2=1.3.2 or 4
„
60
Hiiller
D. P., 255, 356
48, «50
Nitrochlorbenzoic acid ....
CO2H.C1.NO2=?
C7H4C104N
118
jimpricht and
A., 102, 261
i., 557
Uslar
jj jj
„ =1.3.6 or 2
„
....
136
Hiibner
Z. C. [2], 2, 614
vi., 316
jj u
j> jj
„
....
136
Hiibuer & Weiss
B., 6, 175
jj u
= 1.3.4
„
....
136-137
....
A., 185, 275
jj jj
» JJ
„
....
137
Hiibner
A., 222, 67
46, 315
u u
=1.3.5
„
....
147
jj
B., 10, 1703 ; A.,
34, 148 ; 46,
222, 67
315
jj u
„ =1.2.3 or 5
JJ
....
164-165
Z. C. [2], 2, 614
vi., 316
jj jj
=1.4.5
„
178-180
Z. C. [2], 2, 615
jj
jj jj
JJ JJ
jj
....
179-180
Hiibner & Raveill
A., 222, 166
16, 601
jj u
=2
„
205
Otto
A., 122, 129
v.,60
jj »j ••••
„ =1.3.2 or 6
»
225-230
Hiibner
Z. C. [2], 2, 614
«., 316
622
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Nitrochlorbenzoic acid
CO2H.C1.NO2=1.3.2 or 6
C7H4C104N
....
235
Hubner
A., 222, 67
46, 315
Nitrochlorsalicylic acid ....
CO2H.OH.C1.NCX,=1.2.5 (V)
C7H4C106N
162-163
Smith and Pierce
B., 13, 35
38, 392
n i
"=»
1)
....
151
Rogers
I. D., Gottingen,
1875
Trichlorbenzamide
(OO.NH2).C13=1.2.4.6
CrH4Cl3ON
167-5
Beilstein and
A., 152, 238
vi., 313
Kuhlberg
,, ....
„ =1.3.4.5
»
....
176
Salkowski
A., 163, 32
25, 715 ; vii.,
130, 164
Nitrotrichlortoluene
Me.Cl3.NO2=1.2.3.4.?
C7H4C1302N
....
58
Schultz
A., 187, 277
i)
ii »
»1
GO
Seelig
B., 18, 422
48, 770
»»
= 1.2.4.5.?
11
....
88-5
Beilsteiu
A., 152, 240
»»
1) 1»
11
....
92
Seelig
B., 18, 422
48, 770
Amidotrichlorbenzoic acid
CO2H.C13.NH2=1.2.4.6.3
11
....
210
Beilstein
A., 152, 240
Trichloralhydrocyanide ....
3(CC13.CHO)+HCN
C7H4C1903N
A., 173, 297
123
Cecil
B., 9, 1020
Nitrochlorsalicylainide
(CO.NH2).OH.C1.NO3
C7H5C1O4N2
....
192
Smith
B., 11, 1227
=1.2.5.?
„
« »
»
....
199
Smith and Pierce
B., 13, 35
38, 392
Dinitrochlormethoxybenz-
OMe.Cl.(N02)2=1.4.2.3
C7H5C106N2
J. [1875], 339
65-4
Korner
G. L, 4, 305
29, 230
ene
Dichlorbenzamide
(CO.NH2).C12=1.3.4
C7H5C12ON
....
133
Beilstein
A., 152, 228
vi., 312
,,
=1.2 4 (J)
11
....
155
»>
A., 179, 290 ; B.,
28, 1194 ; 29
8,815
587
4, .... ....
=1.2.6
)>
166
Schultz
A., 187, 273
32, 782
Amidodichlorbenzaldehyde
COH.C12.NH2=1.(?)2.2
11
77-78
Gnehm
B., 17, 754
46, 1028
Nitrobenzylidene dichloride
C6H<.N02.CHC12=1.4
C7H5C1202N
46
Zimmerman n and
B., 18, 997
48, 771
Miiller
»> "
=1.3
1)
....
65
Widmann
B., 13, 676
38, 635
Nitrodichlortoluene
Me.Cl2.N02=
')
274 p.d.
s.— 14
Wroblewsky
A., 168, 212 ; Z.
27, 56 ; vii.,
C. [2], 6, 164
1167
Dichlorsalicylamide
(CO.NH2).OH.C12=1.2.3.5
»>
209
Smith
B., 11, 1226
Amidonitrotrichlortoluene
Me.Cl3.NH2.NO2=1.2.4.5.(;)3
C7HSC13O2N2
....
191
Seelig
B., 18, 423
48, 770
»»
=1.2.3.4.(02
»
....
192
»j
»
)!
?
....
CyH.Cl.OjN
d.
123-124
Wallach
B., 6, 118
26, 627 ; vii.,
310
Phenylic cyanate hydro-
PhO.CN+HCl
C7H6C1ON
45
Hentschel
B., 18, 1178
48, 888
chloride
Chlorbenzamide ....
(CO.NH2).C1=1.3
11
....
122
Limpricht and
A., 102, 263
i., 540
Uslar
,,
=1.2
11
....
139
Kekule
A., 117, 154
vi., 258
„
=1.4
u
170
Emmerling
B., 8, 882
28, 1261
Nitrobenzyl chloride
C6H4.N02.CH2C1=1.3
C7H6C102N
....
45-47
Gabriel and
B., 16, 2064
44, 1121
Borgmann
n »*
„ . =1.2
11
B., 8, 1102
49
Geigy & Kb'nigs
B., 18, 2402
46, 1004
(B, 17, 1073)
11 11
=1.4
1)
....
71
Wachendorff
B., 8, 1102
U )) •••-
» !)
»
....
71
Beilstein and
A., 139, 337
vi., 285
Geitner
It >? •• •
» »
)>
71-5
Mohr
A., 221, 215
46, 69
11 »
» „
)<
....
72
Strakosch
B., 6, 1059
1> 11
» >!
!>
73
Grimaux
B. S. [2], 8, 433
vi., 285
(A., 185, 271)
Nitrochlortoluene
Me.Cl.N02=1.4.?
)»
243
Liquid — 13
Wroblewsky
A., 168, 203 ;
27, 55; vii.,
Z. C. [2], 6, 683
1105
11
» »
11
253
Liquid — 13
D
tj
»
11
=1.3.?
»
249
Liquid— 20
»
B., 7, 1062
j»
=1.4.5
)1
8-9
Eugelbrecht
B., 7, 797
27, 986
n .... ...
=1.4.6
V
34-35
>»
»>
»
11 .... ...
!> »
))
....
38
Beilstein
A., 158, 336
24, 680
(A., 185, 273)
=1.3.4
*)
....
64-€5
Wachendorff
B., 9, 1346
31, 207
Amidochlorbenzoic acid ...
C02H.C1.NH2=1.3.2 or G
H
145-148
Cunze & Hubner
A., 135, 111
vi., 318
»i u
» »
•l
US
Hubner & Weiss
B., 6, 175
26, 747
)1 5,
„ =1.2.3 or 5
l)
212
....
A., 147, 264
COMPOUNDS CONTAINING FIVE ELEMENTS.
623
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Amidochlorbenzoic acid ....
C02H.C1.NH2=1.4.5
C7H6C102N
212
....
A., 147, 258
;i ))
=1.3.5
)J
....
215-216
Hiibner
B., 10, 1703
34, 148
» 11
» )J
:>
216
11
A., 222, 67
46, 315
Chlorsalicylamide
(CO.NH.2).OH.C1=1.2.5
55
222-223
Smith
B., 11, 1227
Nitrochlormethoxy benzene
OMe.Cl.NO2=1.3.6
C7H6C103N
70-5
Uhlemaim
B., 11, 1162
34, 978
„ (J. [1866], 459)
=1.2.?
11
....
93-94
Fischli
B., 11, 1463
34, 866
Dichloroxydimethylpurin
C5N4Me2OCl2
C7H6C12ON4
183
Fischer
B., 17, 334
46, 996
Aniidodichlormethoxy-
OMe.Cl2.NH,,=l.(?)2.4
0-H7C12ON
....
71-5
Jaeger
B., 8, 897
28, 1260
benzene
Dichlorethoxypyridine ....
C6NH2012.OEt
»>
31
Konigs & Geigy
B., 17, 1835
46, 1369
1
C5H2Cl3N2.OEt
C7H7C13ON2
....
83
Pechmann and
B., 18, 2292
48, 1202
Stokes
Amidochlormethoxybenz-
OMe.Cl.NH.,=l.?.2
C7H8C10N
260
52
Herold
B., 15, 1685
42, 1287
ene
Pyridinebetaine+HCl ....
C5H6N.CH2.CO.O+HC1
C7H8a02N
sf. 190
202-205 d.
Gerichten
B., 15, 1252
42, 1110
L 1
Butyroehloralcyanacetyl ....
CCl3.C2H4.CH(OAc).CN
C7H9C1302N
240-252 p.d.
Liquid
Pinner & Klein
B., 11, 1490
36, 41
Benzenylamidoxime
Ph.C(:NOH).NH2+HCl
C7H9C10N2
....
185
Falck
B., 18, 2467
48, 1217
+ HC1
Nitrotoluidine+HCl
Me.NH3Cl.NO2=1.4.6
C-HjClOjN,
220 d.
Beilstein
Z. C. [2], 5, 280
vi., 1105
Chlortoluidiue nitrate
Me.Cl.(NH3NO3)=1.4.?
C7H9C1O3N2
....
165 d.
Wroblewsky
A., 168, 147
87,55
)! 11
>» )»
)»
....
169 d.
n
Z. C. [2], 6, 683
vi., 1105
11 11 •"•
=1.4.?
)»
....
179 d.
11
A., 168, 147
27, 55
» n
=1.3.4
1)
....
189
n
11
27,54
Ammonium dichlorcresol....
Me.ONH4.Cl2=1.4.(?)2 C7H9C13ON
....
125
Glaus & Eiemaun
B., 16, 600
44, 1112
Trichloracetoxyvaleramide
CCl3.C3H6(OAc).CO.NH2
C7H10C13O3N
phys. isom.
96
Pinner & Klein
B., 11, 1491
36,42
11
)>
)»
n
119
n
11
)»
Crotonchloralurethane
CC13.C2H2.CH(OH).NH.
1»
....
123-125
Bischoff
B., 7, 633
27, 891
C02Et
Propoxyethoxychloraceto-
PrO.CCl(OEt).CN
C7Hi2ClO,,N
182-184
....
Bauer
A., 229, 163
48, 1121
nitril
a-Pyridinetricarbonyl
....
C8H2C1303N
205-206 (40)
....
....
A., 201, 320
chloride
Isatin chloride
C6H4.CO.CCi:N=1.2
I 1
C8H4aON
....
180 d.
Baeyer
B., 11, 1296; 12,
456
Uiiiitropheuyltrichloracet-
CCl3.CO.NH.C6H3(NOs)j
C^CIAN^
118
MM
Tomassi and
B. S., 21, 399
27, 316
amide
Meldola
Nitrodichloracetophenone
fr.C6H4Ac.NO2=1.2
C8H6C12O3N
73
Gevekoht
A., 221, 323
46, 445
Nitrodichloracetoxybenz-
OAc.Cl2.N02=l.(?)2.2
C8H5C1204N
....
77
....
As., 7, 188
ene
Dinitrodichloracetanilide....
NHAc.Cl2.(N02)2=1.3.4.2.6
C8H5C1ANS
245-246
Beilstein and
A., 196,227; B.,
36, 310
Kurbatow
11, 1979
Nitrotrichloracetanilide ....
NHAc.Cl3.NO2=1.3.4.6.2
C8H5C1303N2
193
11
A., 196, 235 ; B.,
36, 310
11, 1980
Dinitrotrichlorethoxybenz-
om.ci3.($o^=i
C8HSC1306N2
....
100
..„
A., 149, 153
ene
Tetrachloracetanilide
NHAc.Cl4=1.2.3.4.6
C8H5C14ON
....
173-174
Beilstein and
A., 196,236; B.,
36, 143
Kurbatow
11, 1862
N itrochlorcinnamene
C6H4(N02).CH : CHC1=1.2
CsHjCKXN
....
58-59
Lipp
B., 17, 1071
46, 1030
11
C6H4(NO2).CC1 : CH2=1 .4
)»
63-6 i
Drewsen
A., 212, 162
42, 847
Chloramidophenoxyacetic
C1.NH2.(O.CH2.C02H)
J)
....
196-197
Thate
J. p. [2], 29, 145
46, 1171
acid
=?.1.2
11 11
)» )J
||
....
197
»
J. p. [2], 25, 266
42, 849
Nitrodichloracetanilide ....
NHAc.Cl3.N02=1.3.4.6
C8H6C1203N2
...
123-124
Beilstein and
A., 196, 226 ; B.,
36, 310
Kurbatow
11, 1978
„ (B.S.[2],33,25)
„ =1.3.5.6
n
138-139
»)
11
34,974; 36,310
„
„ =1.2.5.4
11
....
145-146
n
n
36, 309
»i
„ =1.3.4.2
11
152-153
11
11
36, 310
11
=1.2.4.6
n
....
188
j»
B., 11, 1979
11
11 11
u.
....
J88
Witt
B., 7, 1603
28, 759
!» ....
=1.2.5.6
1)
....
204-205
Beilstein and
A., 196, 222 ; B.,
36, 309
Kurbatow
11, 1978
624
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrodichloracetanilide ...
NHAc.Cl2.N02=1.2.4.6
C9H6C1208N2
....
210
Beilstein and
B., 11, 1979
Kurbatow
,,
)» )»
V
210
Witt
B., 8, 144
„ (B.S.[2],30,25
=1.3.5.4
»
....
222
Beilstein and
A., 196, 228 ; B.
34, 974; 36, 310
Kurbatow
11, 1979
Di n itrod icli lorxy leue
Me2.Cl2.(NO.2)2=1.4.2.5.3.6
»»
225
Kluge
B., 18, 2098
48, 1209
Trichloracetanilide
Ph.NH.CO.CCl3
CsHjCl-jON
....
80-81
Wallach and
B., 13, 517
Kamenski
„ (B. S., 21, 399)
)»
1»
B., 3, 784
82
Judson
Z. C. [2], 7, 40
vii., 10
?
Ph.NH.CO.Cl3 or C6H,C1,,.
»
....
94
Tommasi and
....
27, 315
NHAc
Meldola
Acettrichloranilide
NHAc.Cl3=t.2.3.4
»
....
120-122
Beilstein and
B., 9, 1688 ; 11,
31, 474; 36, 143
Kurbatow
1862; A., 196, 234
„
„ =1.2.4.5
))
....
184-185
11
11
36, 143
„ (B., 8, 1656)
„ =1.2.4.6
»1
....
204
11
>i
))
»
i) ii
»
....
204
ii
B., 8, 1656
20, 712
Nitrotriehlorethoxybenz-
OEt.Cl3.N02=?
C8H0C1.,03N
53-54
....
A., 149, 152
ene (?)
Nitrochloracetanilide
NHAc.Cl.NOa=1.3.6
C8H7C103N2
....
115
Beilstein and
B.,8, 693; 9,634;
28, 1037 ; 30,
Kurbatow
A., 182, 105
309, 631
11
=1.2.4
51
....
139
11
A., 182, 103
30, 632
(B., 9, 635)
=1.3.4
I)
141-142
11
A., 182, 107
30, 309, 632
)i ....
= 1.2.5
Jl
....
153-154
ii
A., 182, 101; B.,
28, 1037; 30,
8,693; 9,634
308, 631
Dinitrochlorethoxybenzene
OEt.Cl.(NO2)2=1.4.2.6
C8H7C106N2
....
51
Petersen
A., 157, 165
24, 245, 248
»
» 11
n
....
54-55
Petersen and
A., 157, 161
vii., 914, 929
Predari
Dichloracetanilide
Ph.NH.CO.CHCl2
C8H7C12ON
117
Cech
B., 9, 339, 1022
30, 66
,,
»
11
117-118
Pinner & Fuchs
B., 10, 1062
32, 585
„
)J
)i
....
117-118
Cech
B., 10, 1266
Acetdichloranilide
NHAc.Cl2= 1.3.4
„
A., 196, 217
120-5
Beilstein and
B., 8, 694 ; 10,
28, 1037 ; 34,
Kurbatow
2090; 11,1861
299 ; 36, 143
„
= 1.2.5
n
....
132
11
B., 11, 1861
36, 143
„ .... ....
=1.2.4
»
140
Witt
B., 7, 1602 ; J.
28, 759 ; 34,
[1874], 724
298
„
1> 1»
i»
....
140-5
J»
B., 8, 1228
,,
» J»
ll
....
143
Wenghoffer
J. p. [2], 16, 448
34, 298
j» •••• ••••
)) »
j»
A., 182, 95 ;
143
Beilstein and
B., 8, 1655 ; B.,
29, 712 ; 36,
196, 219
Kurbatow
11, 1861
143
„ (B., 11, 1801)
=1.2.3
j*
11
156- 157
n
B., 10, 2091
34, 299
„ ....
= 1.2.6
»
11
175
i»
B. S. [2], 30, 25 ;
34, 974; 36,
B., 11, 1861
143
„
„ =1.3.5
»
11
186-187
i)
B., 11, 1861
36, 143
Phenylnitroethylene di-
Ph.CHCl.CHCl.NO2
C8H7C1202N
....
30
Priebs
A,, 225, 319
48, 161
chloride
Nitrotolylene chloride
(CH2C1)2.NO2=1.4.5
»
....
35
Grimaux
A. C. [4], 26, 331
25, 817
» 11
» J)
»i
45
...»
Z. C. [1871], 598
Nitrodichloretlioxy benzene
OEt.Cl2 NO2=1.(?)2.6
C8H7C12O3N
As., 7, 188
29
Fischer
Z. C. [2], 4, 386
vi., 913
11
=1.(?)*.4
>»
As., 7, 201
35
Seifart
Z. C. [2], 5, 449
11
Benzenylmethoxime chlor-
Ph.CCl : NOMe
C8H8C10N
225 u. c.
Liquid — 10
Kriiger
B., 18, 1057
48, 896
ide
Methylphenylcarbamide
Ph.NMe.CO.Cl
„
280
88
Michler and
B., 12, 1165
36, 935
chloride
Zimmermann
Chloracetanilide
Ph.NH.CO.CH2Cl
>i
....
84
Pinner & Fuchs
B., 10, 1058
32, 585
„ (B.S. [2], 19, 400)
n
:i
....
97
Tommasi
C. E., 76, 885
26, 911
(B., 13, 518)
)»
ii
....
134
Cech
B., 10, 1377
»» .... ....
n
ii
....
134-5
Meyer
B., 8, 1153
29, 372
Acetchloranilide
NHAc.Cl=1.3
ii
....
72-5
Beilstein and
A., 182, 104 ; B.,
28, 1037 ; 30,
Kurbatow
9, 634
309
•,1 .... ....
=1.2
11
B., 8, 693
87-88
11
11
11
„ =1.4
11
....
162
Witt
B., 8, 1226
)l ••" •••• !! ,)
11
162
Wenghoffer
J. p. [2], 16, 448
34, 298
COMPOUNDS CONTAINING FIVE ELEMENTS.
62.5
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority. Reference.
Watts' Diet.
& J.Ch. Soc.
Acetchloranilide
NHAc. 01=1.4
C8H8C10N
....
172-5
Beilstein and
B., 7, 1761 ; A.
28. 451
Kurbatow
182, 98
Chlorphenylacetamide
C6H4C1.(CH2.CONH2)=1.4
Jl
....
175
....
A., 147, 349
?
))
134
....
A., 207, 141
Methamidochlorbenzoic
CO2H.NHMe. Cl=1.2.?
CSH8C102N
178
Coste and Bode-
B., 18,431
48, 793
acid
wig
Nitrochlorethoxy benzene
OEt.Cl.NO2=1.4.6
C8H8C103N
B., 14, 37
61
Hallock
A. C. J., 2, 258
40, 595
i)
» »
J>
As., 7, 193
61-62
Faust and Saame
Z. C. [2], 5, 451
vi., 913
»
=1.2.4
))
B., 14, 37
78
Hallock
A. C. J., 3, 21
40, 595
Chlorcyamic acid
C7H.C1(NO2).CO2H
C8H8C104N
+H20
186
Bellmann
J. p. [2], 29, 1
46, 840
Aniline trichloracetate ....
CClb.C02.NH3Ph
C8H8C1302N
....
145
Beamer and
A. C. J., 1,23;
36, 786
Clarke
B., 12, 1067
Nitrochlorethamidobenzene
NHEt.Cl.NO2=1.3.6
C8H9C102N2
83-84
Laubenheimer
B., 11, 1157
34,976
Ohlorcaffeine(J. [1850], 435)
CSH9C1O2N4
188
Fischer
A., 215, 261
44, 354
Amidodichlorethoxy benz-
OEt.Cl2.NH3=l.(?)3.4
C8H9C13ON
275
46
Jaeger
B., 8, 898
28, 1260
ene
Methyldichlorpseudoluti-
fr. NMe.Me2 : 0=1.2.4.6.6
»
187
Hantzsch
B., 17, 1031
46, 1047
dostyril
Aniline dichloracetate ....
CHCl2.COj.NH.jPh
C8H9C12O2N
122
Beamer & Clarke
A. C. J., 1, 23 ;
36, 786
B., 12, 1067
i) »
»»
JI
125
Cech & Schwebel
B., 10,289; C. C.
32, 179; 34,
[1871], 134
216
Aniline chloracetate
CH2Cl.CO2.NH3Ph
C8H10C1O2N
88
Clarke & Beamer
A. C. J., 1, 23;
36, 786
B., 12, 1067
Lutidine carboxylic acid
N.Me2.CO2H=1.2.4.3
J)
....
166
Michael
B., 18, 2024
48, 1245
+HC1
„ >i »
=?
»
+H30
220 d.
Canzoneri and
G. L, 14, 448
48, 751
Spica
Phenylethenylamidoxime
CH2Ph.C(NH3C]) : NOH
CsHj^ON,
....
155
Knudsen
B., 18, 1069
48, 897
+HC1
Phenylhydroxyacetamidine
Ph.CH(OH).C(NH3Cl) : NH
»
....
213-214
Beyer
J. p. [2], 28, 190
46,65
+HC1
1) »
»
))
....
214
)»
J. p. [2], 31, 382
48, 983
Nitrosodimethaniline
C6H4(NO).NMes=1.4
)»
....
177
Baeyer and Caro
B., 7, 810, 963
28, 84
+HC1
Acetdiamidobenzene + HC1
NH3Cl.NHAc=1.3
)>
280
Wallach&Schulze
B., 15, 3020
44, 583
Diamidodimethoxybenzene
(OMe)2.NH2.NH3Cl=1.4.5.?
C8H,3C102N2
169
Kariof
B., 13, 1676
40, 272
+HC1
Chlordipropoxyacetonitril
(PrO)2CCl.CN
C8H14C1O,,N
199-202
....
Bauer
A., 229, 163
48, 1121
Dichlorethylidene urethane
CHCl2.CH(NH.CO2Et)2
cp^wyo^N,
....
120
Bischoff
B., 5, 81
» »
»)
ji
A., 33, 96
122
• «••
J. p. [2], 24, 120
Chlorethylidene urethane
CH2Cl.CH(NH.C02Et)2
CSH15C1O4N.,
J., p. [2], 24,
147
Bischoff
B., 3, 760; 5, 82;
24, 136 ; 25,
122
7,630
412; vii., 411
Diethylic aspartate+HCl
CO2Et.CH2.CH(NH3Cl).CO2
C8H16C104N
95
Curtius and Koch
B., 18, 1294
48, 885
Et
Tetramidophenetoiil
OEt.(NHs)4=1.2.3.4?
C8H16C12ON4
....
nf. 360
Kohler
J. p. [2], 29, 257
46, 1161
+ 2HC1
Capronimidoether+HCl ....
C6H,,.C(OEt) : NH,C1
C8H18C1ON
....
ord. temp. ;
Pinner
B., 17, 178
46, 723
s.b. 0
Dichlorcarbostyril
N.OH=a,/31 ;
C9H5ClaON
....
249
Friedlauder and
B., 15, 1425
42, 1209
Weinberg
Chlorhydroxyquinoline ...
N.OH.C1=?
C9H6C1ON
180
Friedlander
B., 15, 2685
44, 351
51 ....
,, =ai/31/3; ;
M
241-242
»i
B., 15, 2680
»
,,
» j>
»
241-242
Ostermeier
B., 15, 336
42, 733
»
„ =ai£1a2 ;
j»
246
Baeyer and Btem
B., 15, 2149
44, 196
A chloride of hippuric acid
C9H6C102N
220
40-50
....
A., 112,65
ii., 161
Methylpseudochlorisatin ....
C6H3Cl.CO.CO.NMe=?.1.2
TJ
191
Coste & Bodewig
B., 18, 431
48, 793
Nitrocinnamyl chloride ....
NO2.(CH:CH.COC1)=1.2
C9H6C1O3N
64-5
Fischer & Kuzel
B., 16, 34
Propionyltrichlornitro-
O(.C3H5O).C13.NO2=1.2.4.6.3
C9H6C1304N
65
Guareschi and
B., 18, 1173
48, 891
phenol
Daccomo
4 L
626
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Trichloracetdinitrotoluide
Me.(NO2)2.(NH.CO.CCl3)
C9H6C1306NS
• «>*
141-142 u.c.
Friederici
B., 11, 1975
=1.3.5.4
Acetotrinitrochloranisidin
OMe.NHAc.Cl.(N02)3
C9H7C108N4
....
198
Herold
B., 15, 1686
42, 1287
Dichloracetamidobenzoic
CO2H.(NH.CO.CHC12)=1.2
CjHyCljOaN
....
173
Jackson
B., 14, 887
40, 735
acid
Trichloracetnitrotoluide ..
Me.NO2.(NH.CO.Cla)=1.3.4
C9H7C1,O3N2
A., 209, 363
54-55
Friederici
B., 11, 1972
36, 311
Chloracetamidobenzoic
C02H.(NH.CO.CH2C1)= 1.2
C9H8C1O3N
....
d.200
Jackson
B., 14, 888
40, 735
acid
Formylmethamidochlor-
CO2H.(NMe.COH).Cl
J)
....
201-202
Coate& Bode wig
B., 18, 430
48, 793
benzoic acid
=1.2.4 or 6
Ethylic nitrochlorbeuzoate
CO2Et.Cl.NO2=1.2.3 or 5
C9H8C104N
....
28-29
Hubner
Z. C. [2], 2, 615
11 !)
= 1.4.5
„
....
58
„
Z. C. [2], 2, 615
vi., 316
» 1)
)» J)
„
....
59
Eaveill&Hiibnei
A., 222, 166
46, 601
» »
„ =1.3.2 or 6
„
....
282
Cunze & Hiibuer
A., 135, 113
„
(J. [1865], 332)
Nitrophenylehlorlactic acic
C6H4.N02.(CH2.CH(OH).
C9H8C1O6N
165 ; 16G
Beilstein and
A., 163,142;Z.C.
25, 300; vii.,
CO2H)=1.4
Kuhlberg
[2], 7, 487
348
1! !)
=1.2
„
....
119-120
Baeyer
B., 13, 2261
40, 275
Ethylic nitrochlorsalicylate
CO2Et.OH.Cl.NO2=1.2.5.?
„
....
89
Smith and Pierce
B., 13, 35
38, 392
Acetdinitrochloranisidine
OMe.NHAc.Cl.(NO2)2
C9H8C1O6N3
....
165
Herold
B., 15, 1686
42, 1287
Benzylidenechloral-
Ph.CH :N.CH(OH).CC13
C9H8a3ON
«...
130
Schiff
B., 11, 2166
36, 452
ammonia
Trichloracettoluide
C6H4Me.NH.CO.CCl3=1.4
()
B., 3, 784
102
Judson
Z. C. [2], 7, 40
vii, 10
Acetotrichlortoluide
Me.NHAc.013=1.3.4.(?)2
„
190-191
....
A., 187, 279
Chloralbenzamide
Ph.CO.NH.CH(OH).CCl3
C9H8C13O2N
146
Pinner and Klein
B., 11, 11
„
„
»
....
150-151
....
A,, 157, 245
„ (J. [1879], 552)
i)
„
....
150-151
Wallach
B., 5, 255
vii., 130, 311
Acetnitrochloranisidine ....
OMe.NHAc.Cl.NO2=] .2.(?)2
C9H9C1O4N2
185
Herold
B., 15, 1686
42, 1287
Dinitrochlormesityleue ....
Me3.Cl.(NO2)2=1.3.5.2.4.6
„
....
176
Fittigand Hooge-
Z. C. [2], 5, 168
vi., 299
werff
,,
» »
n
....
178-179
....
A., 150, 325
Dichloracettoluide
C6H4Me.NH.CO.CH012=1.4
C9H9C12ON
....
153
Cech
B., 10, 879
32, 586
Benzenylethoxime chloride
Ph.CC! : N.OEt
C9H10C1ON
230 u.c. (o.p.)
Liquid — 10
Tiemann and
B., 18, 733
48, 790
Kriiger
<> »
„
„
125 (45)
....
„
ii
„
» „
„
„
230 u.c.
L. f.m.
Kriiger
B., 18, 1057
48, 896
>. »
»
„
232; 239 c.
Lossen
B., 18, 1194
Phenylethylamidocarb-
NEtPh.CO.Cl
....
52 u.c.
Michler
B., 9, 399
30, 92
onyl chloride
Chloracettoluide
C6H4Me.NH.CO.CH2Cl=1.4
n
16V5
Meyer
B., 8, 1154
29, 372
„ (B. S., 19, 400)
„ „
„
sb. 110
162
Tommasi
B., 6, 569 ; C. B.,
26, 911
76, 885
Acetchlortoluide
Me.NHAc.Cl=1.4.5
n
«•«•
99
Wroblewsky
Z. C. [2], 5, 322 ;
27, 54 ; vi.
A., 168, 196
1104
„
=1.3.4
„
....
130-131
Engelbrecht
B., 7, 798
27, 986
„ ....
=1.2.4
n
MM
139-140
„
B., 7, 797
J)
Chlorethylic phenylcarb-
NHPh.CO2.C2H1Cl
C9H10C102N
i...
51
Nemirowsky
J. p. [2], 31, 173
48, 741
amate
Acetchloranisidine
OMe.NHAc. 01=1.2.?
„
326
150
Herold
B., 15, 1686
42, 1287
Nitrochlormesitylene
Me3.Cl.NO2=1.3.5.2.4
„
A., 150, 324
56-57
Fittigand Hooge-
Z. C. [2], 5, 168
vi.,'299
weiff
Ethoxychloroxydimethyl-
C5N4Me2OCl.OEt
CjHuClOjN,
....
160
Fischer
B., 17, 335
46, 997
purin
Trichlorhydroxycyanconine
C9H10C13N2.OH
C.H.jCa.ON,
132
Eiess
J. p. [2], 30, 145
48, 236
Ethylbenzimide + HCl ...
Ph.C(OEt) : NH,C1
C9H12C10N
d.w.m. 118-
Pinner
B., 16, 1655
44, 1090
120
Ethylic amidobenzoate
C6H4.NH3Cl.C02Et=1.2
C9H12C1O2N
....
170
Kolbe
J. p. [2], 30, 467
48, 665
+HC1
/3-lutidinebetain + HCl ...
....
»
....
162-5
....
C. E., 95, 300
COMPOUNDS CONTAINING FIVE ELEMENTS.
627
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Benzylic ethenylamid-
Ph.CH2.O.N : CMe.NH3Cl
C9H13C10N2
....
163
Nordmann
B., 17, 2752
48, 239
oxime+HCl
?
....
C9H14C1604N2
151-152
....
....
iv., 736
?
....
C9H15C15O4N2
166-168
....
....
»
?
....
C9H16C1503N3
....
110-5
Otto
A., 116, 195
ii., 532
Oxallyltrimethammonhim
O.CH2.CH.CH2.NEt3Cl
C9H20C1ON
....
Liquid — 20
Eeboul
C. K., 93, 423
40, 1122
chloride
L 1
?
....
C9H28C1805N4
....
163-164
....
....
iv., 736
Trinitro-a-dichlornaphth-
C12 ; C12
C10H3C1206N3
....
178
Widmaun
B. S. [2], 28, 509 ;
32, 900 ; 38, 47
alene
B., 12, 1714
» ~€~ i)
C1;C1
»
....
198-200
Alen
B. S. [2], 36, 433
42, 410
„ -«-
C12 ; C12
11
200-201
»
»
42, 409
Nitro-8-tetrachlornaphth-
C12 ; C12
C10H3C1402N
....
154-155
Atterberg and
B., 10, 1843
34, 322
alene
Widmann
Dinitro-|3-dichlornaphth-
012=0,0., ;
c10H4aAN2
....
158
Widmann
B. S. [2], 28, 510 ;
32, 900 ; 38, 47
alene
B., 12, 1714
„ -3-
C1;C1
»
....
245-246
Alen
B. S. [2], 36, 433
42, 409
» -y- »
( L.-^fij ; a .
»»
246
Widmann
B. S. [2], 28, 505
32, 900
» >» »
i> »>
)i
....
246
Atterberg
B., 9, 1730
31, 466
11 "e~ »
C1;C1
)»
B., 15, 320
252-253
A16n
B. S. [2], 36, 433
42, 409
a-Dinitrochlornaphthalene
«i "j ; "i
C10H5C104N2
....
104-106
Faust and Saame
A., 160, 68 ; Z. C.
25,65; vi., 846
[2], 5, 705
»- »
1»
»J
106
Atterberg
B., 9, 927, 1187
30, 516 ; 31, 85
0-
a, a, ; a2
»)
180
H
B., 9, 928
30, 516
Dichlormalei'c phenylimide
c2a2:(CO)2:NPh
C10H6a202N
....
201
Kauder
J. p. [2], 31, 1
48, 652
Nitro-5-dichlornaphth-
C1.C1 ; NO2=a,a2 ; QI
»
92
Widmann
B. S., 28, 509 ;
32, 900 ; 38, 47
alene
B., 12, 1714
„ -8-
Cl ; C1.NO2
»»
....
95
Alen
B. S. [2], 36, 433
42, 409
„ -«- !)
Cl ; a.N02=|3 ; ? ? or ? ; /3 ?
1»
....
113-5-114
»
»
»
I) -V- "
one Cl=j3
»»
....
119
Cleve
B. S. [2], 29, 499
34, 736
„ -«- »
Cl ; Cl.NO,=/3 ; 1 1 or ? ; 0 ?
»5
....
139-139-5
Alen
B. S. [2], 36, 433
42, 409
,. -8- „
a ; C1.NO2
»
....
141-5-142
»
n
»
» -y- »
Cl ; Cl.N02=a, ; a2 1
»
....
142
Atterberg
B., 9, 928
30, 516
,, -y- >»
» )»
J»
....
142
Widmann
B. S. [2], 28, 505
32, 900
Nitrochlornaphthalene ....
Cl.N02=a,a2
C10H6C102N
....
85
Atterberg
B., 9, 927, 1187
30, 516 ; 31, 85
»
» »»
I)
85
Cleve
B. S. [2], 26, 241
31, 208
Chlorquinolinecarboxylic
N.OH.C02H=a1|3l32 ;
))
....
200 p. d.
Friedlander and
B., 17, 460
46, 1020
acid
Gohring
Methoxycinnamic acid di-
C6H3(CH : CH.CO2H).OMe
C10H,C103N2
....
d. 102
Schnell
B., 17, 1385
46, 1165
azochloride
(N : NC1)=1.2.5
Hydro xycomazine+2HCl
C10H6N3.OH+2HC1
C10H9C12ON3
....
265
Krippendorff
J. p. [2], 32, 153
48, 1243
Hydroxyquinoline metho-
C9NH6(OH)MeCl + H2O
C10H10C10N
....
210
Ostermeyer
C. C. [1884], 970
48, 672
chloride.
Ethylic phenylimidochlor-
Ph.N : CaCOjEt
C10H10C102N
....
91
Klinger
A., 184, 275 ;
28, 1025; 31, 711
acetate
B., 8, 312
Chlorbenzylmalonamide ....
Ph.CH2.Ca(CO.NH2)2
C10HHC1(XN2
d. 210-220
abt. 80
Bischoff & Emmert
B., 15, 1113
Dinitrochlorcymene
Me.Pr«.a.(NOa)s=1.4.5.(?),
C10HnC104N2
....
100-101
Ladenburg and
B., 10, 1221
34,60
Engelbrecht
>i
=1.4.6.(?)2
H
108-109
Gerichten
B., 11, 1091
34, 787
Ethylic phenamidodichlor-
Ph.NH.Ca2.C02Et
C10H:nCl202N
....
71
Klinger
B., 8, 311
28, 1025
acetate
»» »»
n
»
108-110(i.v.)
71-72
n
A., 184, 273
31, 711
Nitrocymylene chloride ....
C6H3Pr.NO,.CHCl2
IT
••••
s.— 10 to— 20
Widmann
B., 15, 167
42, 727
Acetochloroxylide
Me2.Cl.NHAc=1.4.2.5
C10H12C10N
....
171
Kluge
B., 18, 2098
48, 1208
Thymoquinonechlorimide
C10H12C102N
d. 160-170
Liquid — 21
Andressen
J. p. [2], 23, 169
40, 590
Dimethamidophenyltri-
NMe2.C6H4.CH(OH).Ca3
C10H12C13ON
....
111 p.d.
Boesaneck
B., 18, 1517
48, 976
chlormethylcarbinol
Nitrophenylhydroxyacet-
N02.C6H4.CH(OH).C(OEt) :
C10H13C104N2
....
129
Beyer
J. p. [2], 31, 382
48, 983
imidoethev + HC1
NH2C1=1.3
Phenylacetimidoethylether
Ph.CH2.C(OEt) : NHSC1
C10K14C1ON
....
85 d. ; sf. 60
Luckenback
B., 17, 1422
48, 1134
+ HC1
C-28
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Amidochlorthymol
Me.Pr«.OH.Cl.NH2
C10H14C10N
....
100-5
Andressen
J. p. [2], 23, 175,
40, 590
=1.4.5.(?)2
180
Mandelicimidoether + HO
Ph.CH(OH).C(OEt): NH2C1
C10H14C102N
120
Beyer
J. p. [2], 31, 382
48, 982
» »
„
,,
121
„
J. p. [2], 28, 190
46,65
Araidochlorhydroeugenol
C3H6Cl.OMe.OH.NH2
„
97
Weselsky and
M. C., 3, 390
42, 1201
=1.3.4.5
Benedikt
Nitrochlorcamphor ( + ) ...
C10HHC1(NO,)0
C10HJ4C103N
d. b. 200
83
Cazeneuve
B., 17, [3], 141 ;
46, 1041
C. E., 98, 306
„
„
„
93-94
Schiff and Puliti
B., 16, 888
(— ) ...
„
„
d. a. 100
05
Cazeneuve
C. E., 96, 589 ;
44, 667
B., 16, 972
„
,,
)»
110
Schiff and Puliti
B., 16, 889
Terpene (fr. bergamot)
C10H16(NO)C1
C10H16C10N
J. [1875], 390
98
Tilden and Shen-
J. [1877], 427
31, 560
nitrosochloride
stone
Hesperidene nitrosochloride
n
103
„ „
J. [1877], 428
31, 558
Australene nitrosochloride
;J
....
103
„ ,,
„
31, 556
Hydrochlorcarvoxime
„
d. 162-5
132-5
Goldschmidt and
B., 18, 1731, 1732
48, 1058
ZUrrer
Carvenenitrosylchloride
C10HI6(HNO,).NOC1
C10H17C104N2
....
114-115
Meissen
G. I., 13, 99
44, 1140
nitrate
Amidohydroxycamphor
C10H14(OH)(NH3C1)0
C10H1SC102N
250
Kachler and
M. C., 4, 643
44, 1008
+HC1
Spitzer
Methamidochlor-a-naphth-
C10H4Cl(NHMe) : O2
CnHgClOjN
....
150
Plagemann
B., 15, 485
42,973
aquinoue
Ethoxychlorquinoline
N.OEt.a=a,/3,3J ;
CnH10C10N
269
Liquid
Friedlander
B., 15, 2684
„
„ =a1/31a2 ;
„
270
43
„
„
Crotonie-chloralbenzamide
CCl3.C2H2.CH(OH).NHBz
CnH10Cl302N
....
150
Pinner
A., 179, 21
29, 549
Quinoline+chloral+H2O
CC13.CH.O.NC9H7.H2O
66
Ehoussopoulos
B., 16, 882
1 1
Butyrochloralbenzamide ....
CCl3.C2H4.CH(OH).NHBz
CiiH12Cl,02N
....
132-133
Schiff &Tassiuari
B., 10, 1785
34, 23
Ethylic tolamidodichlor-
Me.(NH.CCl2.CO2Et)=1.4
cl.Hl.ClAN
59-60
Klinger
A., 184, 287
31, 712
acetate
Diethamidobenzoyl chloride
C6H4.NEt2.COCl
C.jH^ClON
....
70
Smith
41, 185
COC12 on diethamido-
)J
...
225 d.
„
....
„
naphthalene
Trichlorethyliden-ethoxy -
CCl3.CH(OEt).NH.C6H4Me
CnH14Cl3ON
••>.
76-77
Wallach
B., 5, 254; A.,
25, 611 ; 28,
toluidine
= 1.4
173, 280
350 ; vii.,
311, 1179
Isobutoxybenzamidine +
Ph.C(OBu0) : NH2C1
CnH16C10N
135 d.
Pinner and Klein
B., 10, 1892
HC1
E thylhydrazinhydro-
NH3Cl.NEt.C6H4.(CH2)2.
CnH17C102N2
146
Fischer & Kuzel
B., 16, 1453
44, 1132
cinnamic acid+HCl
CO2H=1.2
Amidoethoxyphenyl-
OEt.NH3Cl.(NH.CO2Et)
CnH17ClO3N2
....
155-156
Kohler
J. p. [2], 29, 257
46, 1160
ure thane +HC1
=1.1.4
Dimethoxybenzenetrimeth-
(OMe)2.(NMe3Cl)=1.4.5
CnHI9C102N
172
Baessler
B., 17, 2122
46, 1330
ammonium chloride
Diainidoethoxyphenyl-
OEt. (NHj).,. (NH.CO.jEt)
CnH18C103N3
238
Kohler
J. p. [2], 29, 257
46, 1161
urethane +.HC1
= !.(?) .4
Chlorisovaleral-diurethane
C4H8Cl.CH(NH.CO2Et)2
C11H21C104N2
130
Bischoff
B., 7, 634
27, 891
Triamidoethoxyphenyl-
OEt.(NH3Cl)3.(NH.C02Et)
233
Kohler
J. p. [2], 29, 257
46, 1161
urethane+3HCl
=1 ('0 4
Dinitrodichlordiphenyl ....
....
C12H6C1204N2
140
A., 207, 340
Tetrachlorazoxybenzene ....
ON2(C6H3a2)2=(1.2.5)2
C12H6C14ON2
141
Laubenheimer
B., 7, 1601
28, 759
»
" ,,
„
141-5
„
B., 8, 1627
n
=(1.3.5),
„
171-172
Beilstein and
A., 197, 84 ; B.,
36, 231
Kurbatow 11. 2057
Nitrochlorquinoneanilide ...
Cl.N02.NHPh : 02
C15H7C104N2
206-208
Guareschi and
B., 18, 1172
48, 891
=1.(4 or 6).3.2.5
Daccomo
Nitrodichlorazobenzene
C6H4C1.N2.C6H3C1.N02
C12H7C1202N3
210
Calm and Heu-
B., 13, 1184
38, 880
=4.1; 1.4.?
niann
Nitrodichlorazoxy benzene
C6H4C1.N2O.C6H3C1.NO2
C12H7C1203N3
133-134
ji )i
B., 13, 1185
=4.1 ; 1.4.?
COMPOUNDS CONTAINING FIVE ELEMENTS.
629
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrodichlorazoxy benzene
C6H4Cl.N2O.C6H3Cl.NOi!
C12H7C1203N3
134
Heumanu
B., 5, 912
26, 168; vii.,
=4.1 ; 1.4.?
150
Trichlorazophenol
fr. N2(C6H4.OH)2=(1.2)2
C12H7C1302N2
....
235
Bohn and Heu-
B., 17, 275
46, 1015
mann
Nitrosonitrochlordiphenyl-
Cl.N02.(NPh.NO)=1.3.2 or
C12H8a03N3
....
110-5u.c.
Laubenlieimer
B., 9, 772
30, 295
amine
1.2.3
Dichlorazoxybenzene
ON2(C6H4C1)2=(1.3)2
C12H8a3ON2
sb. 180
97
»!
B., 8, 1624
20, 578
»
» »
)J
....
114-115
Schultz
B., 17, 465
46, 903
,,
=(1.4),
M
....
155
Hofmann and
B., 5, 916
(Z. C. [1866], 269)
Geyger
»
1> ))
»
....
155-156
Heumann
B., 5, 912
26, 167 ; vii.,
150
,» ....
» )»
))
156
Willgerodt
B., 14, 2635
42, 396
» ....
» V
J)
....
156
»
B., 15, 1004
Dichlorazophenol
N2(C6H3C1.0H)2
C12H8C1202N2
86
Schmidt & Ben-
J. p. [2], 8, 1
27, 260; vii.,
newitz
904
fl-Dichlorquiuone-m-nitr-
C6H2C1202+C6H4.NH2.NO2
C12H8C1304N2
....
112
Niemeyer
A., 228, 322
48, 1066
aniline
Nitrochlordiphenylamiue
a.N02.NHPh=1.3.?or 1.?.3
C12H9C1O2N2
108-5 u. c.
Laubenheimer
B., 9, 772
30, 295
/3-Dichlorquinone aniline....
C6H201202+Ph.NH2
CI2H9C12O2N
....
154
Niemeyer
A., 228, 322
48, 1066
°- » »
»»
J)
180
>i
»
»
Tetrachlorquinolaniline ....
C6Cl4(OH)2+Ph.NH2
C12H9C1402N
115
»)
»
n
Chloracet-a-uaphthalide ....
C10H7.NH.CO.CH2C1
C12H10C1ON
161
Tommasi
C. R, 76, 1267 ;
26, 1040 ; vii.,
B. S., 20, 20
845
Acetchlor-a-naphthalide ....
C1()H6Cl.NHAc
1)
....
184
Seidler
B., 11, 1201
34, 983
Dimethamido-ehlor-a-
C,0H4Cl(NMe2):02
C12H10C102N
....
85
Plagemann
B., 15, 487
42, 974
naphthaquinone
Ethamido-chlor-a-naphth-
C10H4Cl(NHEt) : 02
)1
....
110
)>
B., 15, 485
»
aquinone
Nitrochlorphenamido-
C6H3C1(NO2).NH.C6H4.NH2
C12H10C102N3
....
150-151
Laubenheimer
B., 11, 1158
34, 976
aniline
= 1.4.5 ; 1.3
Dinitrochlorphenolaniline
C6H2C1(NO2)2.OH +Ph.NHs
C12H10C105N3
137
Smith and Pierce
B., 13, 36
38, 392
Trichlorquinolaniline
C6HCl3(OH)2+Ph.NH2
C12H10C180,N
....
60
Niemeyer
A., 228, 322
48, 1066
Dimethamidophenyltri-
NMe2.C6H4.CH(OAc).CClj
CI2H14C1302N
84-85
Boessneck
B., 18, 1518
•'*
chlormethylcarbinol
acetate
Ethylic collidinedicarb-
C6NMe3(C02Et)(C02H)
C13H16C104N
...<
178 d.
Michael
A., 225, 121
48,61
oxylate+HCl
+HC1
Isophthalimidoethylether
C6H4[C(OEt) : NH2C1]2=1.3
CI2H18C1202N2
....
a.270;sf.255
Luckenbach
B., 17, 1431
46, 1158
+ 2HC1
Ethylic aspartate+£HCl....
(C02H.CH2.CH(NH2).C02
0,^.3010^2
....
199
Curtius and Koch
B., 18, 1294
48, 885
Et)2.HCl
Nitrobenzqxytrichlor-
(O.CO.C6H4.N02).C13.N02
C13H6C1306N2
d. 245
106-1
Daccomo
B., 18, 1165
48, 890
nitrobenzene
=1.2.4.6.5 ; 1.2
j>
„ =1.2.4.6.5 ; 1.3
)>
d. 290
146-3 c.
>j
»
»»
Nitrobenzoxytrichlornitro-
(O.CO.C6H4.N02).C13
C13H6C1304N
....
131-132
»
j>
u
benzene
=1.2.4.6; 1.3
Dinitrochlordiphenylamine
C6H2a(N02);!.NH.C6H4.
0,^010^,
254-256
Jourdan
B., 18, 1454
48, 989
carboxylic acid
CO2H=4.6.2.1 ; 1.2
» V »
C6H3(N02)2.NH.C6H3C1.
))
280-282
M
B., 18, 1450
48, 988
C02H=4.2.1 ; 1.4.2
Dinitrodichlorcarbanilide
....
C13H8C1206N4
208-210
B. S., 32, 170
Nitrochlorbenzanilide
(CO.NHPh).Cl.NO2=1.4.3
013H9C103N2
131
Baveill & Hiibner
A., 222, 166
46, 601
Chlorbenznitranilide
C6H4C1.CO.NH.C6H4.NO2
n
180
Wilkena& Rack
»
46, 602
=1.2; 1.4
Dichlorbenzanilide
(CO.NHPh).Cl2=1.2.3 or 5
CJ3H9C12ON
240
)»
»
46, 603
Diphenamidocarbonyl-
NPh2.COCl
013H10C10N
85
GLrard and Willrn
B. S. [2], 25, 251
30, 99
chloride
•
\
)»
»
)«
B., 9, 397
85
Michler
B., 8, 1666
Chlorbenzanilide
(CO.NHPh).Cl=1.2
»»
....
114
Wilkena & Back
A., 222, 166
46, 602
„ ....
= 1.4
,•»
....
194
Emmerling
B., 8, 882
28, 1261
630
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diamidochlorhydroacrid-
CO.C,H3C1.NH.C6H2(NH3)2
C13H10C10N3
....
230
Jourdan
B., 18, 1453
48, 989
ineketone
L 1
=2.(4 or 6).l ; 7.1.2.4
Nitrochlorphenyltoluidine
C6H3Cl(N02).NH.C6H4Me
C13HnC102N2
....
124
Laubenheimer
B., 11, 1157
34, 976
=1.4.5 ; 1.4
Chloranisidine picrate
OMe.NH2.Cl=1.2.?
C13HUC108N4
200 d.
Herold
B., 15, 1686
42, 1287
Amidobenzophenone+HC
C6H4Bz.NH3Cl=1.3
C13H12C10N
187
Geigyand Konigs
B., 18, 2401
48, 1236
Diamidochlordiphenyl-
C6H2C1(NH2)2.NH.C6II4.
C13H12C102N3
....
245 d. ; sf.
Jourdan
B., 18, 1455
48, 989
amine carboxylic acid
CO2H=4. 6.2.1 ; 1.2
235
Dinitrodichlordiphenyltri-
....
C14H7C1604N2
....
143
Zeidler
B., 7, 1181
28, 148
chlorethane
Chlorphenylphthalimide ...
c6H4:(co)2:N.c6H4ci
C14H8a02N
....
194-195
Gabriel
B., 11, 2260
36, 323
=1.2 ; 1.4
Chlorbenztrinitrotoluide ...
C6H4Cl.CO.NH.C6HMe
C14H9a07N4
....
239
Schreib
B., 13, 467
38, 557
(NOS)3=1.2 ; 4.1.2.3.?
Chlorbenzdinitrotoluide ....
C6H4Cl.CO.NH.C6H2Me
C14Hloa05N3
....
228
»
B., 13, 466
»
(N02)2=1.2 ; 4.1.3.?
Benzoyltrichlortoluide ....
Me.Cl3.NHBz=l.(?)3.3
C14H10C13ON
....
213
....
A., 187, 279
Chlorbenznitrotoluide
C6H4Cl.CO.NH.C6H3Me.NO
C14H11C103N3
....
139
Schreib
B., 13, 466
38, 557
=1.2; 4.1.3
Benzenylbenzoxime chlor-
Ph.CCl : N.O.CH2Ph
C14H12C10N
....
Liquid
Kruger
B., 18, 1058
48, 896
ide
Chlorbenztx)luide
C6H4Cl.CO.NH.C6H4Me
))
....
131
Schreib
B., 13, 465
38, 557
=1.2; 1.4
Dichlorazoxy toluene
ON2(C6H3Me.Cl)i!=(L2.?)s
C14H12C12ON2
....
128
Hofmann and
B., 5, 919
26, 169
Geyger
Chlorbenzamidotoluide ....
C6H4Cl.CO.NH.C6H3Me.
C^H^CION,
....
153
Schreib
B., 13, 467
38, 557
NH2=1.2 ; 4.1.3
Trichlordimethylaniline
•••*
C14H13C13ON2
....
138-139
....
J. p. [2], 24, 440
amidophenol
Benzylatnidobenzoic acid
CO2H.(NH2Cl.CH2Ph)=1.2
C14H14C102N
....
104-106 n.c.
Glaus & G lyckherr
B., 16, 1285
44, 1010
+HC1
Dinitrobenzylamine + HC1
NH2C1(CH2.C6H4.N02)2
C14H14C104N3
....
173
Strakosch
B., 6, 1059
27,78
» *»
»
»J
212
>i
B., 6, 1057
)»
fi-dichlordibenzylamine
(C6H4C1.CH2)2NH.HN03
C14H14a203N2
178
Berlin
A., 151, 141
vi., 338
nitrate
y~ )» »
5»
»
193
»
»
It
0- i) »
»
•J
204
»
»»
JJ
Diethylic pentachlorcollid-
C8H4Cl6(C02Et)2Cl2N
C14H14C1704N
149-150
Hantzsch
A., 215, 19
44,83
inedicarboxylate dichloride
KCN on chloracetamide ....
....
C14H18C1S05N4
....
120
Schiff & Speciale
G. I., 9, 325
38, 103
Hydrocotarnine ethochlor-
C12H15N03.EtCl
C14H20C103N
100
Beckett & Wright
....
29, 166
ide
Chlorphth alimidy Iben zyl... .
....
C15H10C10N
MM
230-232
Gabriel
B., 18, 1261
48, 903
a-Trichlortetracetdiamido-
Me.Cl3.(NAc2)2=1.2. 4.5.3.6
C16H16C1304N2
MM
220
Seelig
B., 18, 423
48, 770
toluene
?-hydrochloride
NH2ClPh.CH(OH).C6H4.0.
C15H16a04N
....
190-191
Rossing
B., 17, 2993
48, 388
CH2.CO2H=1.2
Ethyleneamidophenoloxy-
NH3C1.C6H4.O.C2H4.O.C8H4.
»J
• •• >
177
Wagner
J. p. [2], 28, 199
46, 436
benzoic acid+HCl
CO2H
0-Naphthimidoisobutyl-
C10H7.C( : NH2Cl).OBu3
C15H18C1ON
....
140 d.
Pinner and Klein
B., 11, 1487
36,48
ether+HCl
Dichlordibenzylamine car-
(C6H4C1.CH2.NH3)2C03
C1SH18C1203N2
114-115
Jackaonand Field
A.C.J., 2, 85
40, 804
bonate
=(1.4)2
Benzylphenyldimethammo-
NPhMe2(CH2Ph)a
C15H20C10N
110
Michler and
B., 10, 2079
34,300
nium chloride
Gradmann
Chlor-a-naphthoquinone-
C10H4C102.NH.C6H4.]SrO
C16H9a03N2
126
Plagemann
B., 15, 486; 16,
nitrosoanilide
=1.4
896
Chlor-a-naphthoquinone-
C10H4C102.NH.C6H4N02
C16H9a04N2
245
»
B., 15, 485
42, 973
nitranilide
=1.3
» »
,, =1.4
))
282
si
)»
)l
Benzochlorquinoline
a,H5ClN.Bz
C16H10C10N
264
Skraup
B., 15, 894
42, 1111
COMPOUNDS CONTAINING FIVE ELEMENTS.
631
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Chlor-u-naphthoquinone-
C10H4ClO2.NHPh
C^H^ClOsN
....
202
Knapp & Schultz
A., 210, 189
42, 511
anilide
,, »
„
„
....
207-208
Plagemann
B., 15, 485
42,973
Trinitrochlorbenzeiie-
C10H8+C6H2C1(N02)3
C16H10C106N3
....
95-96
Liebermann and
RQ O*"Q
j O, o i fj
naphthalene
=1.2.4.6
Palm
Dinitrochlorbenzene-
C10H8+C6H3C1(N02)2=?.1.3
C16HUC104N2
....
78
Willgerodt
B., 11, 603
34, 570
naphthalene
Chlor-a-naphthoquinol-
C10H4Cl(OH)2.NHPh
C16H12C102N
....
170-171
Knapp & Schultz
A., 210, 190
42,511
anilide
?
....
C16H12C1202N2
....
110
Loeb
B., 18, 2427
Trichlorethylidenedibenz-
CCl3.CH(NHBz)2
C16H13C1302N2
257
Hepp and Spiess
B., 9, 1428
31, 314
amide
Dinitroditolyltrichlor-
fr. CCl3.CH(C6H4Me)2
C16H18C1304N2
....
121-122
Fischer
B., 7, 1192
28, 154
ethane
Anilidobutyranilide + HC1
Ph.NH2Cl.CHMe.CH,.CO.
C16H19aON2
....
206-207
Balbiano
B., 13, 313;G.I.,
38, 462, 542
NHPh
10, 137
Imidodiethylenephenyl-
NH2Cl(C2H4.OPh)2
C16H30C10N
....
213
Weddige
J. p. [2], 24, 241
40, 1137
ether+HCl
Chlor-a-naphthoquinone-
C10H4C102.NH.C6H4Me.NO2
C17HnC104N2
....
230
Plagemann
B., 15, 487
42,973
nitrotoluide
=1.2.?
,, i)
=1.4.?
„
....
236-240
„
J)
,,
Chlor-a-naphthoquinone-
C10H4ClO2.NH.C6H4Me=1.2
C17HI2C102N
152
„
B., 15, 487; A.,
„
toluide
210, 191
>, »
=1.4
„
196
„
„
„
Benzoy Ihydroch lorcarvox-
HC1.C10H14 : N.OBz
C^HjoClOjN
....
114-115
Goldschmidt and
B., 18, 2222
48, 1210
ime
Ziirrer
Trichlorcarbazole picrate....
C12H8C13N+C6H2.OH.(N02)3
C18H9C1307N4
....
100
Knecht
A., 202, 27
38, 661
Trichlorquinonedi-m-
C6HC1302(C6H4.NH2.N02)3
C18H13C1S06N4
....
108
Niemeyer
A., 228, 322
48, 1066
nitraniline
a-Dichlorquiuonedi-m-
C6H2a302(C8H4.NH2.N02)2
C18H14Cla06N4
....
110
J?
„
,,
nitraniline
(5th nitropheno))3+HCl
(C6H4.OH.N02)3.HC1
C18H16C109N3
....
110
Fittica
J. p. [2], 24, 1
42,51
/3-Dichlorquinonedianiline
C6H2C1202.(C6H5.NH2)2
C18H16C1202N2
262
Niemeyer
A., 228, 322
48, 1066
Trichlorquinoldianiline ....
C6HC13(OH)2.(C6H6.NH2)2
C18H17C13O2N2
....
67
„
„
H
Dichlorquinoldiauiline
C^^ljCOHJ.XC^.NH,.),
C18H18C1AN3
....
112
„
„
,i
1
....
C18H18C1604N4
190
Otto
....
iv., 737
Chlorquinoldianiline
C6H3C1(OH)2.(C6H6.NH2)2
C18H,9C102N2
....
92
N iemeyer
A., 228, 322
48, 1066
PC16 and POC13 on codeine
....
C18H19C1202N
196-197
Gerichten
A., 210, 110
42, 312
PC15 on codeine
....
C18H20C102N
....
147-148
„
A., 210, 107
J)
Chlorcodeine (A., 77, 368)
....
C19H20C103N
....
178
„
A., 210, 114
42, 313
?
....
C18H2iCl707N4
....
214
Otto
....
iv., 737
1
....
C1SH26C1807N4
157
„
....
n
Fluorenepicrylchloride ....
C13H10+C6H2C1(N02)3
C19H12C106N3
....
69-70
Liebermann and
B., 8, 378
»,
=1.2.4.6
Palm
Benzoyldichlordiphenyl-
NBz(C6H4Cl)!i
C19H13C12ON
....
149
Claus
B., 14, 2369
amine
„
J?
„
....
153-154 u.c.
Claus & Schaare
B., 15, 1286
Methylapocinchene + HC1
C13H16N.OMe+HCl
C19H20C10N
....
198
Comstock and
B., 18, 2381
Koniga
Cinchonidine chloride
....
C19H21C10N2
108-109
5,
B., 17, 1987
46, 1383
Hydrochlorapocinchonine
A., 205, 348
C19H23C1ON2
197
....
J. p. [2], 8, 282
Hydrochlorapocinchon-
A., 205, 346
»
200
J. p. [2], 8, 283
idine
Hydrochlorapochinine
A., 205, 341
C19H23C102N3
....
160
J. p. [2], 8, 285
Dinitroheptachlordi-
fr.C10H6Cl3.C.0H4Cl4(?)
C20H7C1704N2
....
104-106
Faust and Saame
A., 160, 72 ; Z. C.
25, 65 ; vi., 847
naphthalene
[2], 5, 705
Dinaphthoquinonechlor-
o,: c10H5.c10a,o.Nci
C^H^ClOaN
d. 130
85
Hirsch
B., 13, 1910
40, 164
imide
i 1
Phenanthrenepicrylchlor-
C14H10+C6H2C1(N02)3
C20H12C106N3
• *•!
88
Liebermann and
B., 8, 378
ide
=1.2.4.6
Palm
Phenanthrenediiiitrochlor-
C14H10+C6H3C1(NO2)2=1.3.5
C20H18C104N2
44
Willgerodt
B., 11, 604
34, 670
beuzene
-
632
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Acridy Ibenzoic acid + HC1
C18H8N.C6H4.C02H+HC1
C20H14C102N
163
Bernthsen and
B., 17, 1511
46, 1183
Traube
KCN on chloralbenzamide
J. [1879], 552
cjiHci4oy4
131
Schiff and Spe-
G. L, 9, 335
38, 103
ciale
Carbonyltri phenylguan-
NPh.CO.NPh.C : NPh + HCl
C20H16C10N3
190
Stojentin
J. p. [2], 32, 1
48, 1196
idine + HCl
L I
Diacetylchloranilido-
C10H4Cl(OAc)3.NHPh
CjoH.eClO.N
168-169
Knapp & Schultz
A., 210, 164
42, 511
naphthoquinol
Nartine liydrochloride
....
C20H17C106N2
275
Gerichten
B., 14, 314
40, 445
Aldehyde on chloral-
....
C20H20C18ON6
....
121
Schiff and Tas-
B., 10, 1787
34, 23
ammonia
sinari
?-Hydrochloride
C20H,,C10N2
....
112
Ostermeyer
B., 18, 595
48, 814
/3-Dichlorquinoldi-p-tolu-
C6H2Cl2(OH)2(C6H4Me.
C20H22C12O2N 2
....
72
Niemeyer
A., 228, 322
48, 106(i
idine
NH2)2
a- „
J)
0
114
i»
)J
D
Quinidinechloride
....
C20H23C10N2
131-132
Comstock and
B., 18, 1223
48, 910
Konigs
Quininechloride
)»
151
V
B., 17, 1988
46, 1383
Chlorquinoldi-p-toluidine
C6H3Cl(OH)2.(C6H4Me.
C20H23C102N2
90
Niemeyer
A., 228, 322
48, 1060
NH2)2
Cinchonine hydrochloride
C20H25C10N2
....
100
Bouchardat
....
i., 975
J! 1'
A., 135, 326
»»
130
Hesse
A., 122, 226
vi., 464
Homo-cinchonidinemetho-
MM
)}
158 u.c.
Glaus and Block
B., 13, 2192
40, 184
chloride
Quinine perchlorate
C20H2402N2.HC104
C20H25C106N2
+7H20
45
....
MM
v., 21
Benzoylchlorbenzdiam ido-
C6H3Me.NHBz.(NH.CO.
C21H17C102N2
....
178
Schreib
B., 13, 468
38, 557
toluene
C6H4C1)=1.3.4 ; 1.2
Diuitroamarine + HC1
C21H16N2(N02)2.HC1
C21H17C104N4
214 u.c. ; d.
Claus and Witt
B., 18, 1673
Diuitrostrychnine + HCl ....
C21H2002N2(N02)2+HC1
C21H21C106N4
abt. 40
Hanriot
C. B., 96, 585
44, 670
Trichlortribenzy lami ne
....
C21H23C1402N
170-175
Berlin
A., 150, 137
vi., 338
+HC1
Acetylhydrochlorapo-
....
C21H5SC102N2
150
....
A., 205, 353
cinchonidine
Quinine methochloride ...
C20H2402N2.MeCl
C21H27C1O2N2
181-182
Claus&Mallmaun
B., 14, 77
40, 619
Tetranitro-a-dinaphthyldi-
C22H 10C12O8N4
213-214
Grabowski
B., 11, 301
34, 509
chlorethylene
,! 'ft' »
....
»
292-293
n
sj
n
„ -jS-diuaphthyl-
C22HnCl308N4
258
J)
B., 11, 300
>j
trichlorethane
Chlorpyrene picrate
C16H9C1+C6H2.OH.(N02)3
C22H12C10.N3
177-178 d.
Goldschmidt and
M. C., 4, 239
44, 1001
Wegschneider
Dichlorquinone diethoxy-
C6Cl202(NH.C6H4.OEt)2
C22H20C1204N2
abt. 200
Schmidt and
J. p. [2], 24, 426
42, 400
anilide
= ; (i.2),
Andresen
Chloralquinine
C20H24O2N2+CC13.COH
C22H25a303N2
149
Mazzara
G. I., 13, 269
46, 187
Benzoylchlor-(3-naphthyl-
C10H6Cl.NPhBz
C^H^CION
152 u.c.
Claus & Eichter
B., 17, 1592
46, 1358
phenylamine
Diacetylhydrochlorapo-
....
CaH^aO.N,
168
A., 205, 351
conchinine
Diacetylhydrochlorapo-
....
))
184
A., 205, 352
quinine
Dianilidechlorphenyl-
C6HCl(NHPh)2.O.NPh
i i
C24H18aON3
195
Andresen
J. p. [2], 28, 422
46, 431
quinonimide
Hydrodimethylamarine-
C21H,sMe2ON2.MeCl
C^H^CION.;
168
Claus
B., 15, 2328
44, 203
methochloride
Hydrotrimethylamarine
C21H17Me3ON2.HCl
>»
204
j>
))
|)
+HC1
Narce'ine methochloride ..
CjBHjoOaN.MeCl
C24H32C109N
210 u.c.
Claus & Kitzfeld
B., 18, 1572
48, 997
Amylchloranthracene
C14H8Cl.C5Hn+C6H307N3
C25H22C107N3
108
Liebermann
A., 212, 1
42, 863
picrate
Diphenyldiazobenzenecarb
CO(NPh.N:NPh)2.2Ha
C25H22CI2ONS
101 d.
Saraw
B., 14, 2443
42, 507
amide+HCl
Narce'ine ethochloride
C23H.sOsN.EtCl
C»HMC10,N
170
Claus & Ritzfeld
B., 18, 1570
48, 990
COMPOUNDS CONTAINING FIVE ELEMENTS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Dibenzoyldichlorazoxy-
0(.NBz.G6H4Cl)2
C26H18C1203N3
125
Hofmann and
B., 5, 917
26, 169 ; vii.,
benzene
Geyger
151
Cinchonine benzylchloride
C19H22ON2+Ph.CH2Cl
C^H^CION,
C27H31C1ON,,
248
Glaus & Treupel
B., 13, 2295
40, 290
Nitrocholesterylchloride ...
G26H42C102N
....
148-149
Preis & Raymann
B., 12, 225
36, 634
Benzoyldichlordi-/3-naphth
NBz(CloH6Cl)2
C27H17C12ON
203 u.c.
Glaus & Bichter
B., 17, 1594
46, 1358
ylamine
ft
Hydromethylbenzylamar-
C21H13Me(CH2Ph)ON2.HGl
C29H29C10N2
205
Glaus
B., 15, 2327
44, 203
ine+HCl
Narce'ine benzylchloride ...
CsaHogOgN + PkCHsjCl
C30H36G1O9N
....
162 u.c.
Glaus & Eitzfeld
B., 18, 1572
48, 997
Gl on K-nitrocamphor
....
C30H43C120UNS
....
110
Schiff
G. I., 10, 21
40, 439
Ethylenediphenylcarb-
CO(NPh.C2H4.NPh.COCl),,
C31H28C1203N4
....
167
Michler & Keller
B., 14, 2183
42, 182
amide chloride
Benzylcinchoninebenzyl-
C19H21(CH2Ph)ON2+Ph.
C^H^CION,
255 d.
Glaus & Treupel
B., 13, 2296
40, 290
chloride
CH2C1
Ethyleneditolylcarbimide
CO[N(C6H4Me).C3H4.
C35H36C12O3N<
155
Michler & Keller
B., 14, 2184
42, 183
chloride
N(C8H4Me).COCl]2=(1.4)4
?
C32H16Cl207(NPh3)s
C12!JH98C1207N8
....
228
Piutti
G. I., 14, 470
48, 783
Methylphosphinic chloride
Me.POCl2
CH3C12OP
163
32
Hofmann
B., 6, 306
26, 884 ; vii.,
957
Ethoxyphosphorous chlor-
EtO.PClj
C2H6C12OP
117
....
Menschutkin
A., 139, 344
40, 159
ide
» »
„
„
117-Sc. (768-5)
Thorpe
J. [1876], 205
37, 346
Ethylphosphinic chloride....
Et.POCl2
„
170
Eathke
Z. C. [2], 6, 57
vi., 935
,. » ••••
„
„
175
Liquid
Michaelis
B., 13, 2175
40, 159
Dimethylphosphinic chlor-
Me2PO.Cl
C2H6C10P
204
66
Hofmann
B., 6, 307
26, 884 ; vii.,
ide
957
Epichlorhydrin+PCl3 ....
G3H5OC1+PC13
03H5C14OP
133-140(100)
....
Hanriot
B.S.[2],32,552
38, 457
Dihydroxychloralphos-
(CC13.CHO)2PH3
C4H5C1602P
....
143
Girard
A. C. [6], 2, 1
46, 1119
phine
i
1
C4H6C13O.PH3
C4H8C13OP
....
96
„
J)
Isobuty Iphosphinic chloride
Bu0.POCL2
C4H9C12OP
154-156
....
Eathke
Z. C. [2], 6, 57
vi., 935
» „
„
„
154-156
J., 19, 487
Menschutkin
A., 139, 347
1
C^^OP
134-140 (22)
Liquid
Fossek
M. G, 5, 627
48, 504
Isoamylphosphinic chloride
C6HU.POG12
CjHuCljOP
173
Eathke
Z. C. [2], 6, 57
vi., 935
„ »
„
„
173
J., 19, 487
Menschutkin
A., 139, 348
Chlorphenoxyphosphinic
C6H4C1.0.POCL!=1.4
C6H4C1302P
265
Liquid
Kekulo
B., 6, 944
26, 1239 ; vii.,
chloride
918
Phenylphosphinic chloride
Ph.POCl2
c6H5aaop
258
....
Michaelis & Kam-
A., 181, 301 ;
29, 597
merer
B., 8, 1306
» »
JJ
n
260 u.c.
Liquid
Michaelis
B., 6, 818
27, 169
Phenoxyphosphorus
PhO-PCL,
216 p.d.
Liquid
Noack
A., 218, 85
44, 735
dichloride
Phenoxyphosphinic chloride
PhO.POCl2
C8H5C1203P
241-243
Liquid
Jacobsen
B., 8, 1521
29, 596
Chlorpheny Iphosphoric acid
G6H4C1.0.PO(OH)2=1.4
C6H6C104P
....
80-81
iarbaglia&Kekule
B., 5, 877 ; 6, 944
26, 278
Diacetonephosphorous
PCl.O.GMe2.CHAc
i i
C6H10C102P
235
Liquid
Michaelis
B., 17, 1274
46, 991
chloride
» »
„
„
235. </745)
35-36
„
B., 18, 900
48, 747
»
„
„
154 (100)
„
J1
,,
„ trichlor-
PCl3.O.CMe2.CHAc
C8H10C1302P
• •••
115
B., 18, 901
n
ide
i i
1
....
c8H16aop
s. 127-5
Crafts and Silva
24, 637
vii., 954
Chlorcarbonylphenyl phos-
C8H4(O.P02).COC1=1.2
C;H4C104P
181 (11)
80
Anschiitz
A., 228, 308
48, 1062
phoric oxide
Benzophosphinic chloride....
C6H4(POC1,,).COC1=1.4
C7H4C1305P
315
83
Michaelis & Panek
B., 14, 408
40, 604
Chlorcarbonylphenylphos-
C6H4(O.POC12).COC1=1.2
C7H4C1303P
168 (11)
Liquid
Anschiitz
A., 228, 308
48, 1062
phoric dichloride
Trichlortolylphosphinicacid
C6HCl3Me.PO(OH)2=(?)3.1.4
G7H6a3o3p
....
190-5
Michaelis and
B., 8, 1315
29, 393
Lange
Tolylphosphinic chloride ....
C6H4Me.(POCl2)=1.4
C7H7C12OP
284-285
Liquid
Michaelis & Panek
A., 212, 217
42, 960
4 M
634
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
<Jhlor-/3-naphtliolphos-
C10H6C1.0.PO(OH)!!
C10H8C104P
....
205
Claus and Zini-
B., 14, 1483
40, 915
phoric acid
mermann
Diphenoxyphosphorus
(PhO)2PCl
C1SH,0C103P
295 (731)
Liquid
Noack
A., 218, 85
44, 735
chloride
Phenoxyphenylphosphin ic
(PhO)PhPOCl
i)
a. 360
....
Michaelis
....
tj
chloride
Diphenoxyphosphinic
(PhO)2POCl
c^cio,,?
314-316(272)
....
Jacobsen
B., 8, 1522
29, 596
chloride
Phenoxydiphenylbenzyl-
Ph.CH2.PPh2Cl.OPh
C^ELjClOP
si. 194
232-236 p.d.
Michaelis & Coste
B., 18, 2116
48, 1215
phosphonium chloride
a-Distearylglycerolphos-
C,H6(OSt)2.O.POCl2
C^CL^P
....
24
Hundeshagen
J. p. [2], 28, 219
46, 281
phinic chloride
Phosphosantonic chloride....
PO(CI6H1803C1)3
C46H64C13010P
....
198
Cannizzaro and
G. I., 10, 459 ;
40, 286
t
Carnelutti
J. [1880], 895
Arsenic trichloride+ alcohol
AsClI+CsH6.OH
C2H6ClbOAs
148
Liquid
Luynes
C. R, 50, 831
vi., 217
Phenylarsinic chloride (A.,
Ph.AsOCl2
C6H5Cl2OAs
d. 120
100
Michaelis
B., 10, 625
32, 452
201, 202)
Benzoylarsinic chloride ....
Ph.CO.AsOClj
C7H6ClAAs
....
157-158
....
A., 208, 16
Tolylarsinic chloride
C6H4Me(AsOCls)=1.2
C7H7Cl2OAs
....
1
A., 201, 253
» »
=1.4
»>
69
M
Dibenzylarsinedihydroxy-
(Ph.CH2)2AsCl(OH)2
C14H16ClO.,As
128
Michaelis&Patow
B., 18, 43
48, 527
chloride
Tribenzylarsinehydroxy-
(Ph.CH2),AsCl.OH
C21H22ClOAs
....
162-163
»
B., 18, 44
j)
chloride
Diphenyldichlorarsenic
(XAsCLPh,,),
C24H20Cl4OAs2
117
Coste & Michaelis
B., 11, 1886;
36, 162
oxide
A., 201, 230
t
Sba6+CH3.OH
CH4Cl5OSb
d. 130
81
Carleton Williams
B., 9, 1135
30, 465
1
SbCl5+C2H5.OH
C2H6ClsOSb
d. on boiling
66-67
»
)I
30, 463
'1
SbCl6+(C2H5)20
C4H10Cl6OSb
....
68-69
»
»
30, 466
Ethylenechlorthiocyanate
C2H4CL(S.CN)
C3H4aSN
202-203
Liquid— 20
James
J. p. [2], 20, 352;
36,808
26, 378
Thiocyanethylsulphinchlor-
....
C3H6C1S2N
a. 100
....
A., 153, 311
ide
a-Chlorallylthiocyanate (id.
CH2 : CC1.CH2.S.CN(?)
C4H4aSN
180-181
Liquid
Henry
C. R., 95, 849;
44, 173
with following ?)
B., 15, 3085
Chlorallylcarbimide
C3H4C1.N:CS
J>
186
Liquid
»
B., 5, 188
25, 479 ; vli., 50
a-Chlorallylthiocarbamide
CH2 : CC1.CH2.NH,CS.NH2
C4H7C1SN2
....
90-91
j>
j)
vii., 50
«- »
»
J)
90
»T
C. B., 95, 849
44, 174
?
C6H3C1.N : N.S
CCHSC1SN2
....
103-5
Beilstein and
A., 197, 82 ; B.,
36, 231
Kurbatow
11, 2057
Amidochlorphenylmer-
SH.C1.NH2=1.2.4
C6H6C1SN
129 ; 130
Albert
B., 14, 1435, 1438
40, 902
captan
Methenylamidothiophenol
ii • j
C6H4.N:CC1.S=1.2
C7H4C1SN
248
Liquid
Hofmann
B., 12, 1127
chloride
» «
» >!
»
248
24
»
B., 13, 8-9
Chlorphenylthiocarbimide
C,H4C1.(N:CS)=1.3
»
249-250
Liquid
)»
B., 13, 14
38, 388
j»
=1.2
»
249-250
44-45
»i
)J
!»
»
=1.4
)>
....
40
Losauitsch
B., 5, 156
25, 511 ; vii.,
1118
»»
'i »
))
249-250
44-5
Hofmann
B., 13, 13
38, 388
»
» i)
>»
....
45-47
Beilstein and
A., 176, 51 ; B.,
28, 1200
Kurbatow
7, 1490
Phenylthiocarbizine+HCl
C7H6SN3+HC1
C7H7C1SN2
....
240
Fischer and
A., 212, 316
42, 1094
Besthorn
Chlorbenzylic thiocyanate
C6H4C1.(CH2.S.CN)=:.4
C8H6C1SN
....
17
Jackson & Field
A. C. J., 2, 85 ;
40, 804
B., 11, 905
Benzylthiocarbamidine
Ph.CH2.S.C( : NH).NH3C1
C8HuClSNj
166-168
Bernthsen and
B., 12, 574
36, 651
H-HC1
Klinger
i
COMPOUNDS CONTAINING FIVE ELEMENTS.
635
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Azothiodicblordithiophenol
SN2(C6H3C1.SH)2
C12HSC12S3N2
....
147
Beilstein and
B., 11, 2057;
36, 231
Kurbatow
A., 197, 80
Lsophthalimidothioethyl-
C,H4[C(SEt) : NH2C1]2=1.3
O jn tl •, gOloO^-^' 2
yellow 175
190
Luckenbach
B., 17, 1435
46, 1158
ether+HCl
Pichlordiphenylthioearb-
CS(NH.C6H401)2=(1.3)2
C13H10C12SN2
....
121-122
Hofmann
B., 13, 14
38, 388
amide
»
=(l-2)2
V
....
145-146
>»
31
jj
»
=(1.4),
)J
....
166
Losanitsch
B., 5, 156
25, 510; vii.,
944
»
»1 I»
»
....
168
Hofmann
B., 13, 13
38, 388
>i
II »
»»
....
168
Beilstein and
A., 176, 47 ; B.,
28, 1200
Kurbatow
7, 1489
Tolylimidotolylcarbamine-
C6H4Me.NH2Cl.C( : N.C6H4
C18H19aSN2
173
Will and Biel-
B., 15, 1310
thiomethyl+HCl
Me).SMe=(1.4),
schowski
Tolylimidotolylcarbamine-
C6H4Me.NHCl.C( : N.C6H4
C17H19C1SN2
....
219
«
B., 15, 1314
thiethyleue+HCl
Me).S.C,H4=(1.4).
i
Tolylimidotolylcarbamine-
C6H4Me.NH,Cl.C( : N.C6H4
C1TH21C1SN2
....
180
»
B., 15, 312
thioethyl + HCl
Me).SEt=(l.4)s
Tetramethdiamidodipheu-
CS(NH.C.H4.NMe,)s=(1.4)3
C17H24C12SN4
....
71
Baur
B., 12, 534
36, 628
ylthiocarbaruide + 2HC1
Ethylthiophosphorus di-
EtS.PCl2
C2HSC12SP
172-175
Liquid
Michaelis
B., 5, 7 ; C. N.,
vii., 965
chloride
25,57
Phenylthiophosphinic
PLPSClj
CpjOfP
270 d. (o.p.) ;
Liquid
Kohler and
B., 9, 1053 ; 13,
30, 525 ; 38,
chloride
205 (130)
Michaelis
463
558
Diethylthioarsenic chloride
(EtS)2AsCl
C4HloClS2As
150 d.
....
Claesson
B. S. [2], 25, 183
31, 585
Methylic cyanide +PC13 ....
MeCN.PCl3
C2H3C13NP
72
....
Henke
A., 106, 281
ii., 258
Triphenylarsonium chloride
3(Ph.NH2).AsCl3
C18H21Cl3N3As
205-210
90
Schiff
J. p., 89, 226
iv., 474
Triphenylstibonium chlor-
3(Ph.NH2).SbCl3
C18H21Cl3N3Sb
80
Schiff
J. p., 89, 226
iv., 474
ide
Diiodobromacrylic acid ....
CBrI : CI.CO2H
C3HBrI2O3
160
Mabery & Lloyd
A. C. J., 3, 124
40, 1125
» »
CI2 : CBr.CO2H
)>
....
182
Homolka & Stolz
B., 18, 2282
48, 1198
lododibromacrylic acid ....
CBr2:CI.CO2H(?)
C3HBr2I02
139-140
Mabery & Lloyd
A. C. J., 4, 92
42, 1048
» »
CIBr : CBr.CO2H
»»
....
147
Homolka & Stolz
B., 18, 2282
48, 1198
lodobromacrylic acid
CjHBrl.COjH
C3H2BrIO2
....
96
)»
»>
j»
» j) ••••
)»
»)
....
110
Hill
B., 12, 660
36, 616
„ ,,
»
»»
....
110
Mabery & Lloyd
A. C. J., 3, 165
40, 1124
Trimethylsulphinedibrom-
Me3SIBr,
C3H,Br2IS
94-95 p.d.
Dobbin and Mas-
47,57
iodide
son
lododibromtoluidine
Me.NHj.Br2.I=1.2.3.5.4
C7H6Br2IN
64
Wroblewsky
A., 192, 210 ; B.,
30, 510 ; 34,
9, 1055
978
Bromphenyltrimethyl-
C6H4Br.(NMe;r)=1.3
C9H13BrIN
.*••
201
Wurster and
B., 12, 1819
38, 108
ammonium iodide
Scheibe
)> »
=1.4
II
185 d.
»
B., 12, 1819, 1820
»
Brombenzylquinoline di-
C<,H,N.C7H.Br.I2
C16H14BrI2N
....
109-110 u.c.
Claus
B., 18, 1306
48, 908
iodide
Dibrom-a-thiophenic acid
S.CO2H.Br2=1.2.(?)2
C6H2Br202S
209-211
Peter
B., 18, 544
48, 765
?) ~a" » »» •—
» i)
u
identical (?)
212-213
Bonz
B., 18, 2310
48, 1206
„ '«- >, » ••••
>l 1!
u
u
220-221
i»
1)
»
4 M 2
636
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dibrom-3-thiophenic acid
S.C03H.Br,=l.3.(?),
C5H2Br2O2S
identical (?)
220
Bonz
B., 18, 2306
11 -£- ii 11 -
11 11
1J
„
£80
„
B., 18, 2308
48, 1206
Pentabrombenzenesulph-
C6Brs.S03H
C6HBr503S
....
190
....
A., 181, 226; 191,
onic acid
205 ; 197, 306
Tetrabromben zenesulph-
Br4.S03H=6. 4.3.2.1
C6H2Br4O3S
A., 181, 217
melts on Pt.
Keiuker
A., 186, 299
32, 464
ouie acid
„ ,,
„ =5.4.3.2.1
,,
A., 181, 45
168-169
Spiegelberg
A., 197, 292
36, 801
Tribrombenzenesulphonic
Br3.SO3H=1.2.4.5
C6H3Br303S
....
140
Limpricht
A., 191, 188
34, 493
acid
„ „
11 11
„
....
140
Spiegelberg
A., 197, 282
36, 798
(A., 186, 288, 303)
Tribrombenzenesulphonic
11 11
11
+3H20
80
Limpricht
A., 191 188
34, 493
acid
„ „
=1.3.5.4
„
....
145
„
A., 191, 193, 207
ii »•
" T>
„
+H20
100
Beinker
A., 186, 271
32, 461, 466
» 11
11 11
„
„
95
Limpricht
A., 191, 193, 207
34, 493
11 ,.
=1.3.4.5
„
....
?
....
A., 181, 39
» u
„ =1.2.3.5
11
....
?
A., 181, 29
Methylic dibrom-a-thio-
S.CO2Me.Br2=1.2.(?)2
C6H4Br202S
identical (?)
80-5
Bonz
B., 18, 2314
48, 1206
phenate
Methylic dibrom-0-thio-
„ =1.3.(?)2
„
„
80
„
„
M
phenate
Dibrombenzenesulphonic
Br2.SO3H=1.2.4
C6H4Br203S
anhydrous
66-5-67-5
Spiegelberg
A., 197, 263
36, 797
acid
11 ii
11 11
„
+3H2O
67-5-68-5
„
„
,»
11 11
„
„
57-58
Goslich
A., 186,145, 148;
31, 595 ; 32,
B., 9, 1860
460
X 11
= 1.3.5
„
A., 181, 25,
84-86
Schmitt
A,, 120, 129
(M. C., 2, 193)
201
„ acid
=1.3.4
„
anhydrous
110
Limpricht
A, 191, 185, 232
34, 493
11 11
15 »>
.,
+xH2O
80
„
„
11 I!
=1.4.5
„
anhydrous
132
Woelz
A., 168, 81
26, 1142
11 ,,
>• 11
„
„
128
Borns
A., 187, 350
32, 768
11 51
11 11
„
11
128
Limpricht
B., 8, 1072
29,82
11 11
11 11
„
11
124
„
A., 186, 129, 139
32, 460
(B., 10, 1539)
„ acid
11 11
„
+2H2O
117
Hiibner & Wil-
A., 167, 117 ;
24, 1056 ; 26,
liams
Z. C. [2J, 7, 14
1039 ; vii., 154
.. 11
i. 11
„
+3H20
100
Limpricht
B., 8, 1072
29, 82
11 11
11 11
„
„
99
„
A., 186, 134
32, 460
11 .1
11 11
„
„
98
Borns
A., 187, 350
32, 768
11 11
11 11
„
„
97
Bahlmann
A., 186, 312, 321
32, 608
i) >i
=1.2.3
11
?
....
A., 188, 152
Brombenzenesulphonicacid
Br.SO3H=1.2
C6H5Br03S
B., 7, 1352
!
Bichter
B. K. T., 117
11 i.
,, =1.3
„
B., 8, 819
?
„
„
11 11
„ =1.4
H
B., 8, 594
88
„
„
Brombenzoic acid sulph-
C02H.Br.SO2Br=?
C7H4Br204S
....
182-184
Lennep
Z. C. [2], 7, 67
vii., 1114
onylbromide
Thihydrobrombenzoic acid
CO2H.Br.SH=1.3.2 or 6
C7H5BrO2S
192-194
Frerichs
B., 7, 795
„ ....
= 1
„
....
242-243
Lennep
Z. C. [2], 7, 69
24, 371; vii.,
1115
„ -
=1.3.?
„
....
254-256
Upmann and
Z. C. [2], 6, 295
24, 371 ; vii.,
Hiibner
1115, 1155
Brombenzaldehydosulph-
COH.Br.SO2H=1.4.?
C7H6Br03S
....
131
Bottinger
A., 191, 26 ; B.,
31, 468 ; 34,
inic acid
9, 1784
730
Brombenzoic sulphinic acid
CO2H.Br.S02H=1.4.?
C7H6Br04S
slow heat
238-239 d.
„
„
34, 730
11 11
» 11
„
quick heat
245-248 d.
„
„
Toluenesulphonylbroiuide
C6H4Me.S02Br=1.4
C7H7Br02S
95-96
Otto
A., 142, 98
v., 859
Bromphenylthioglycollic
06H4Br.S.CH2.C02H
C8H7BrO2S
....
112
Claesson
B. S. [2], 23, 444
29, 567
acid
Dibromxylenesulphonie
Me2.Br2.SO3H=1.3.4.6.2
08H8Br263S
165 d.
Jacobsen and
B., 11, 1534
36,61
acid
Weinberg
COMPOUNDS CONTAINING FIVE ELEMENTS.
637
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Bromphenylthiohydroxy-
C6H4Br.S.CMe(OH).CO2H
C9H9BrO3S
».*»
114-5
Baumann
B., 18, 263
48, 514
propionic acid
=1.4
Brombenzoic ethylic sulph-
CO2H.Br.SO3Et=1.4.?
C9H9BrO6S
-....
84
Bottinger
A., 191, 19
34, 730
onate
Bromnaphthalenesulph-
Br.S02Br=a1a2 ;
C10H6Br202S
....
114-5
....
B. S. [2], 28, 516
onylbromide
Bromnaphthalenesulphonic
Br.SO3H=?£
C10H7BrO3S
....
62
Darmstadter and
A., 152, 305
vi., 861
acid
Wichelhaus
) »
» =fe
))
B. S., 28, 516
104
»
A., 152, 303
n
» »
„ =0^2 ;
)J
»
137-139
»
»
11
i> )>
» j»
)J
B., 12, 1964
138-139
Otto and Morries
A., 147, 164
Bromcymenesulphonic acid
Me.Pr«.Br.SO3H=1.4.(?)3
C10H13Br03S
....
130-132
Paterno and Can-
G. I., 11, 124
40, 594
zoneri
Broraisocymenesulphonic
Me.Prf.Br.S03H=1.3.(?)s
)J
....
108-109
Kelbe
A., 210, 37
48, 300
acid
Tetrabromoxy s ulphobenz-
B., 9, 1150
C12H6Br404S
....
278-279 d.
A., 172, 41
31, 796
ide
Dibromsulphobenzide
(C6H4Br)2S02=(1.4)2
C12H8Br202S
....
168
Armstrong
Z. C. [2], 7, 321
24, 174
„ ....
I> >»
»
....
168
Nolting
B., 8, 594
» ....
I> '»
J>
172
Beckurts & Otto
B., 11, 2065
36, 229
a-Dibromfluorene sulphonic
fr.C6H4.CH2.C6H4=(1.2)2
C13H8BrAS
....
142
Hodgkinson and
B., 16, 1103
43, 172
acid
1 '
Matthews
Dimethoxydibromsulpho-
(C6H3Br.OMe)2S02
C14H12Br204S
....
166
....
A., 172, 48
benzide ,
Dieth oxy di bromsulpho-
(C6H3Br.OEt)2S02
C16H16Br204S
....
183
....
A., 172, 53
benzide
Sulphotoluylenethylene ....
(C9H1002S)2.Br3
C18H20Br304S2
....
95
A., 143, 219
Diisoarayloxydibrom-
(C6H3Br.OC6Hu)2S02
CaH-.gBrAS
....
100
A., 172, 57
sulphobenzide
Tribromnaphthalenedi-
fr.(c10H7)2:s(:o):cIOH6
C30H17Br3OS
182 u.c.
Ekstrand
B., 17, 2602
48, 170
naphthylsulphoxide
Nitrodibrommethane
CHBr2.NO3
CHBr2O2N
155-160 d.
Liquid
Tscherniak
A., 180, 130; B.,
27, 1152; 29,
7,920
901 ; vii., 894
Nitrobrommethane
CH2Br.NOj
CH2Br02N
143-144
Liquid
51
JJ
D
Nitrodibromethylene
CBr2:CH.NO3
CsHBr2O2N
....
112
Merz and Zetter
B., 12, 2047
38, 114
Tribromacetamide
CBr3.CO.NHj
C2H2Br3ON
119-5-1S1
Guareschi
G. I., 6, 370
31, 458
,,
))
))
119-121
Weidel & Gruber
B., 10, 1149
32, 779
»j ....
»
»
....
120-121
Guareschi
B., 9, 1436
Dinitrobromethane
CH3.CBr(NOs)2
C2H3Br04N2
....
Liquid — 17
Meer
A., 181, 1
30, 186
Acetdibromamide
CH3.CO.NBr2
C2H3Br2ON
....
100
Hofmann
B., 15, 413
Dibromacetamide
CHBr2.CO.NH2
))
....
150-155
Demole
B., 11, 318
„ ,
)»
>»
154
Kessel
B., 11, 2116
„
J)
))
156
Schaffer
B., 4, 369
(A.,122,121)
T»
»
....
156
Steiner
B., 7, 506
27, 886
(B., 9, 1436)
11
I»
156-157
Guareschi
G. I., 6, 370
31, 458
Nitrodibromethane
CH3.CBr2.NOa
C2H3Br202N
162-164 u.c.
Liquid
Meyer&Wurster
B., 6,96; 7, 1313
26, 611
„
....
1J
165
....
....
A., 180, 114
vii., 895
Acetbromamide
CH3.OO.NHBr
C2H4BrON
....
108
Hofmann
B., 15, 408
42,951
„ ....
)3
»
+H20
70-80
n
»?
))
Bromacetamide
CH2Br.CO.NH2
»)
*>*•
165
Kessel
B., 11,2117
Nitrobromethane
CH3.CHBr.NO2
C2H4BrO2N
145-148
Liquid
Meyer& Wurster
B., 6, 95
26,61 l;vii.,895
„ .... ....
....
1)
146-147
....
Tscherniak
A., 180, 126 ; B.,
27, 1152; 29,
7,918
901
Brommtricglycol
C2H4Bi-O3N
164-1G5
Henry
A. C. [4], 27, 243
Bromacetylcyanide
CHjBr.CO.CN
C^BrON
77-79
A., 131, 66
Tribromacety Icarbamide ....
CBr3.CO.NH.CO.NH2
C3H3Br302N2
....
148
A., 130, 149
v., 960
/3-Bromallylic nitrate (B., 5,
CHBr : CH.CHJ.O.NO,
C3H4Br03N
140-150
Liquid
Henry
B. S. [2], 18, 232
452)
Propiondibromamide
CH3.CH2.CO.NBr2
C3H5Br2ON
....
100
Hofmann
B., 15, 754
C38
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Nitrodibrompropane
CH3.CH2.CBr2.N02
C3H6Br202N
184-186
Liquid
Meyer and
A., 180, 118; B.,
27, 982 ; 29,
Tscherniak
7, 716
902; vil., 897
Propionbromaraide
CH3.CH2.CO.NHBr
C3H6BrON
80
Hofinann
B., 15, 753
42, 1052
Isonitrobrorupropane
Me.CBr(NO2).Me
C3H6Br02N
148-150
Liquid
Meyer and
A., 180, 117 ; B.,
27, 982 ; 29,
Tscheniiak
7, 715
902 ; vii., 897
Nitrobrompropane
Me.CH2.CHBr.N02
)I
155-160
Liquid
!!
51
»
»» ••••
»J
JJ
160-165
....
....
A., 181, 19
Dibrommale'imide
C2Br2:(CO)2:NH
C4HBr2O2N
J. [1877], 706
225
Kisielinski
W. A., 74, 561
34,43
„ ....
))
J)
225
Ciamiciau and
G. I., 14, 31 ; B.,
46, 1116 ; 48,
Silber
17,556; 18,1460
993
Brommaleimide (J. [1877],
C2HBr:(CO)2:NH
C4H2BrO2N
150-152
Kisielinski
W. A., 74, 561
34,43
706)
Brommaleinamide „
C2HBr(CO.NH2)2
C4H5BrO2N2
....
168-175
,,
»
34, 44
Dibromdiacetamide
....
C4H5Br2O2N
A., 133, 141
98
A., 142, 69
Amidobromsuccinic acid ....
C.,H2Br(NH2)(CO2H)2
C4H6BrO4N
140 u. c.
Claus
B., 15, 1851
Erythroldinitrodibrom-
C4H~6Br2(O.N02)3"
C4H6Br206N2
....
75
Champion
C. R, 73, 114;
24, 811 ; vii.,
hydrin
Z. C. [1871], 348
471
Bromalacetamide
CBr3.CH(OH).NHAc
C4H6Br3ON
158
Jacobsen and
B., 15, 601
42, 938
Neumeister
„
))
)J
....
160
Schiff and Tas-
B., 10, 1787
34, 23
sinari
Brompropylenecarbamide
C3H6Br : (NH)2 : CO
C4H7BrON2
....
120
Andreasch
M. C., 5, 33
46, 733
Dinitrobrombutane
Me.OH2.CH2.CBr(NO2)2
C4H7BrO4N2
....
Liquid
Zublin
B., 10, 2C86
34, 285
Dinitrobromisobutane
CHMe2.CBr(NO2)2
J)
....
38
»>
B., 10, 2088
?j
NitrodibromiaobutaDe ....
CHMe:.CBr2.N02"
C4H;Br202N
180-185
Liquid
Detnole
A., 175, 149; B.,
27, 984; 28,
7, 792
563; vii., 897
Nitrodibrombutane
Me.CH2.CH2.CBrrN02
JJ
203-204 c
Liquid
Zublin
B., 10, 2085
34, 284
Isobutyrobromamide
CHMej.CO.NHBr
04HsBrON
92
Hoftnann
B., 15, 755
42, 1052
Nitrobromisobutane
CHMej.CHBr.NOj
C4H8Br02N
173-175 c.
Liquid
Zublin
B., 10, 2087 ; A.,
34, 284
175, 148
Nitrobrombutane
Me.CH2.CH5.CHBr.NOj
»
180-181 c.
Liquid
)!
B., 10, 2085
1>
Dibrompropylcarbamide ....
CH2Br.CHBr.CH2.NH.CO.
C4H8Br2ON2
109
Andreasch
M. C., 5, 33
46, 732
NH2
Bromallylcarbamide + HBr
CHBr : CH.CH2.NH.CO.
))
158
»
))
j»
NH3Br
Tribrom a-pyrrolinecarb-
C4NHBr3.C02H
C5H2Br3O2N
d.w.m. 140-
Ciamician and
G. I., 14, 162;
46, 1044 ; 48,
oxylic acid
150
Silber
B., 17, 1154
247
Brompyromucamide
C4HBr.CO.NHs
C5H3BrON
146
Canzoneri and
G. I., 15, 113
48, 1144
Oliver
Bromhydroxypyridine ....
N.OH.Br=1.2.?
»
206
Pechmann and
47, 151
Welsh
Dibromhydroxypyridine ...
N.OH.Br2=1.2.(?)2
C6H3Br2ON
....
206-207
Konigs & Geigy
B., 17, 591
46, 1195
Tribromanhydropyvuril ...
C5H3Br302N4
....
180 d.
A. C. [5], 11, 388
Brom-#-hydroxypyridine...
No. of Br. atoms ?
C6H4BrON
58
Fischer & Renou!
B., 17, 764
46, 1050
Dibromdimethylmalonam-
CBr2(CO.NHMe)2
C6H8Br202N2
....
162
Freund
B., 17, 785
46, 1124
ide
Bromalurethane ....
CBr3.CH(OH).NH.CO2Et
C6H8Br303N
i.i.
132
Bischoff
B., 7, 632
27, 891
Nitrodibromquinone
C6HBr2(N02):02
C6HBr204N
....
244-246 d.
Guaresehi and
B., 18, 1174
48, 891
Daccomo
Dinitrotribrombenzene ...
Br3.(NO2)2=1.2.4.3.5(?)
C6HBr304N2
....
125
Mayer
A., 137, 226
vi., 269
„ (J. [1875], 313
» u
J»
....
135-6
Korner
G. I., 4, 305
.29, 225
„ (J. [1879], 388
» »»
)»
....
135-5
Pauebianco
G. L, 9, 354
38, 105
„ (J. [1875], 313
„ =1.2.3.4.5 or 6
„
....
162-4
Korner
G. I., 4, 305
29, 226 .
»1 ..
„ =1.3.5.2.6
1»
....
187
Jackson
B., 8, 1173
29, 390
„ (J. [1875], 31 7
» »
))
....
192
Korner
G. I., 4, 305
29, 227
»
» »
»)
...i
192
Wurster & Beran
B., 12, 1822
38, 106
Nitrotetrabrombenzene ..
Br4.NO2= 1.3.4.5.6
C6HBr402N
26; 60
Limpricht
A., 191, 202
»
» »
))
....
88
Mayer
A., 137, 228
vi., 269
»
» »
))
....
96
Eichter
B., 8, 1424
29, 390
)> ••
11 >!
))
96
Limpricht
A., 191, 175
34, 495
Diazodibromphenol
C,HjBr!1.Nj.O=(?)s.1.2
C6H3Br2ONj
....
d. 100
Bohmer
J. p. [2], 24, 460
COMPOUNDS CONTAINING FIVE ELEMENTS.
639
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diazodibrompheuol
C6H2Br2.N.!.0=(?)2.1.4
C6H2Br2ON2
....
d. 137
Bohmer
J. p. [2], 24, 453
42, 397
i i
„
=2.6.1.4
Jl
....
d. 142
u
J. p. [2], 27, 108
„
=2.6.1.1
»
....
d. 145
»
J. p. [2], 24, 470
42, 398
„
=2.6.11
)>
....
d. 145
Mohlan
B., 15, 2493
Dinitrodibrombenzene ....
Br2.(NO2)2=1.4.2.6
C6H2Br204N2
....
99-100
Austen
B.,9,918; A.C.J.
30, 513
[1881], 184
„
„ =1.3.(?)2
>»
....
117-4
KSrner
G. I., 4, 388; J.
29, 228 ; vii.,
[1875], 333
916
»>
„ = L2.(?)2
)>
....
120
Austen
B., 8, 1183
29, 389
»
=1.2.4.6(?)
))
•i.i
158
»
»
J!
„
=1.4.2.3(2)
))
159
jj
B., 9, 622
30, 406
Nitrotribrombenzene
Br3.NO2= 1.3.4.6
C6H2Br302N
....
93-S
Korner
G. I., 4, 305
29, 223, 225
(J. [1875], 315)
,,
» »
)>
....
95
Mayer
A., 137, 226
29, 390
,,(J. [1875], 315)
„ =1.2.3.5
1)
....
111-9; 112
Korner
G. I., 4, 305
29, 217, 226
»1 »
„ =1.3.4.5
»
....
119-5
»
»
29, 226
„
„ =1.3.5.6
»
124
Reinke
A., 186, 271
32, 462
„
»» «
J)
124-125
Limpricht
A., 191, 175
34, 494, 496
„
)i 11
)»
....
124-5
Jackson
B., 8, 1172
29, 390
„
11 11
>J
....
124-5
Wurster & Beran
B., 12, 1821
38, 106
„ ....
?i ji
1J
....
125
Limpricht
B., 10, 1540
34, 221
,,(J. [1875], 316)
>» i>
)>
I77u.c. (11)
125-1
Korner
G. I., 4, 305
29, 227
„
„ =1.3.4.2
1>
w. m. 187
j>
)1
29, 226
Nitrotribromphenol
OH.Br3.NO2=1.2.4.6.3
C6H2Br303N
....
85
Linder
B., 18, 614
48, 775
„
15 )>
j>
....
89
Daccomo
B., 18, 1167
48, 890
Pentabrompseudacetylpyr-
C4Br3(CO.CHBr2)NH
C6H2Br6ON
....
200
Ciamician and
G. I., 13, 455
46, 292
roline
Dennstedt
Dinitrobrombenzene
Br.(N02),=l.a4
C6H3BrO4N2
B., 11, 1159
59-4
Korner
G. I., 4, 305; J.
29, 208
(J. [1877], 424)
[1875], 332
„ ....
=1.2.4
»
....
69-5
Andrews
B., 13, 2129
„
»1 11
n
....
70-634
Mills
P. E. [1881], 205
,, ....
)) )»
11
71-5
Spiegelberg
A., 197, 258
36, 796
„ (J. [1870], 523)
» 11
»
72
Kekul6
A., 137, 167
vi., 268
„ (J. [1876], 383)
1> 1»
i)
72
Walker & Zinck6
B., 5, 117
vii., 143, 908
,j
1) 1»
»>
....
72
Zinck6 & Sintenis
B., 5, 791
26, 167
j,
)1 )>
»
72
Austen
B., 7, 1250
28, 165
-,j ....
11 >1
?)
....
75-2
Korner
G. I, 4, 305
29, 211
„
» =»
»
87
Austen
B., 8, 1183
29, 389
Dinitrobromphenol
OH.Br.(NO2)2=1.4.2.6
C6H3BrO6N2
....
71
»
A. C. J., 3, 184 ;
36, 50
A.J.S.[3],16,46
i» ...»
» )>
»
....
75-6
Koruer
G. I., 4, 305
28,521; 29,228;
vii., 916
,.
1» 51
)»
....
76
)>
G. I., 4, 387
vii., 905, 929
„ (J. [1878], 550)
" »
>»
76
Armstrong
28, 521
„
1» )»
J)
....
78
Petersen
A., 157, 171
24, 252
,,
» i)
»»
....
78
Korner
A., 137, 204
28,520; 38,50
„ (J. [1877], 548)
J! »>
5J
....
78
Armstrong
B., 7, 922, 924
25, 865; 27, 1164
„ (J. [1875], 339)
H >J
)»
....
81-4 ; 85-6
Korner
G. I., 4, 305
29, 217, 230
}) ....
=1.3.(?)J
)1
91-5
»
G. I., 4, 387 ; J.
29, 228, 231 ;
[1875], 340
vii., 905, 916,
929
1»
=»
11
....
108-110
Fittica
J. p. [2], 28, 176
46, 55
))
>1 ))
J)
....
110
Laurent
E. S., 6, 65
iv., 399
M
'J )»
T1
110
Petersen
A., 157, 171
24, 252
1»
= 1.2.4.6
||
....
114-115
Norton and Allan
B., 18, 1996
I)
» !>
»»
....
115
Hiibner and
B., 6, 172
26, 751
Brencken
jj
" »
))
....
115
Post
B., 7, 335
37, 80 )
„ (J. [1877], 548)
« !)
n
....
116
Armstrong
28, 520
640
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dinitrobromphenol
OH.Br.(N03)2=1.2.4.6
C6H3Br05N2
117
Armstrong and
B., 6, 650; 7, 922
25,800; 27,1164;
(J. [1876], 448)
others
924
29, 477 ; vii.,
910,921
»
1» >1
»
118
Rennie
...»
41, 224
„ (Z.C.[1868],324
» »)
))
....
118-8
Korner
G. I., 4, 394 ;
29, 228; vii., 91 5
J.[1875], 335,33
Di ni trobroipresorcinol
(OH)2.Br.(N02)2=1.3.(2)3
C6H3Br06N2
192-5
Typke
B., 16, 555
44, 917
ji
»» »
»
B., 15, 1101
193
Fevre
C. R., 96, 790
44, 733
Nitrodibrombenzene
y
Br2.NO2=1.4.5 (?)
C6H3Br.,O8N
Liquid
....
A.C.J.[1881], 18
„
„ =1.2.4
11
296 c.
58
Kiese
A., 164, 179 ;
25, 304; 26, 64;
B., 2, 62
vi., 263
„ (J. [1875], 305
)1 'J
))
57-8 ; 58-6
Korner
G. I., 4, 305
29, 218
,,
1) >1
I)
58
Meyer
B., 7, 1563
vii., 139
,,
„ =1.3.4
»»
60-61
Meyer and Stiiber
B., 4, 960; 5, 52,
25, 304; vii., 139
7, 1562
„ (A., 165, 176)
» )1
)»
....
61
Wurster and
B., 7, 419
27, 691
Grabenjnann
,, ...
»1 »1
)1
....
61
Richter
B., 8, 1423
»1 ...
»> 1)
»»
....
61-6
Korner
G. I., 4, 305 ;
29,217;vii.,916
J. [1875], 306
„ (J. [1875], 307)
„ =1.3.2
»
....
8S'6
»
G. I., 4, 305
29, 218
„ (A., 133, 52)
! „ .=1-4.6
V
....
83-492
Mills
P. R. [1881], 205
„ (A., 137, 168)
« »
n
....
84
Couper
25, 304
vii., 139
„ (B., 5, 632)
)> »
j)
....
84
Riese
A., 164, 176
26, 64
1) ....
>» »
»i
84
Richter
B., 8, 1422
vi., 263
„ (J. [1875], 308)
)) )1
'»
85-4
Korner
G. I., 4, 305
29, 216, 223
„ (J. [1877], 424)
„ =1.3.5
»»
104-5
i)
G. I., 4, 390 ;
29, 218; vii., 915
J. [1875], 307
N i trodibromphenol
OH.Brj.NO2=l.(?)2:3
C6H3Br203N
91
Lindner
B., 18, 613
48, 775
„ (J. [1877], 548)
=1.2".4.6
11
117
Armstrong and
B., 7, 923, 924
27,1164;28,521
Brown
» »
.11 1)
. 1?
....
117-5
i) »
25, 860
vii., 915, 929
»1
» .. »
!»
117
Brunck
Z. C. [2], 3, 203
,,(Z.C. [1868], 323)
»' "
1)
....
117-117-5
Goldstein
B., 11, 1944
36, 148
,,
» ))
i)
....
117-118
Korner
J. [1875], 336
24, 252
»? ••••
)> »J
>J
....
119
»
A., 137, 207 ;
vi., 912
Z. C. [2], 21, 148
M ....
„ =1.2.6.4
»
132 u.c.
Armstrong and
....
25, 860
Brown
„
*> »
»
....
14.1
Brunck
Z. C. [2], 3, 204
vi., 912
i» ....
j> »)
1>
....
141
Armstrong and
25, 875 ; 28, 521
vii., 915, 921,
Brown
929
11
>» »
1)
141
Petersen
A., 157, 182
25, 864
„
» »
)»
?•••
141
Post
B., 7, 331
27,800
n •••
j' j»
))
141
Armstrong and
J. [1876], 448
29, 477
Harrow
ji
» )»
142
Lellmann and
B., 17, 2731
48, 266
Grothmann
(A., 205, 95)
» j>
11
....
144
Post and Bracke-
B., 7, 169
27, 476
busch
Nitrodibrotnresorcinol
(OH)a.Brs.NOa=1.3.4.6.2
C6H3Br204N
....
117
Weselsky and
M. G, 1, 895
40, 727
Benedikt
„
=1.3.(?)3
)1
B., 16, 1101
d.w.m. 138
Fevre
C. R. 96, 790
44, 733
„
= 1.3.(?)3
11
147
Hazura
M. C. 4, 610
44, 1114
„
" )»
J)
....
147
Weselsky
A., 164, 1
25, 1007; vii.,
1043
Nitrosotribromoxindole ....
C6H3Br302N2
sb. 190
162
vi., 736
Nitrotribromaniline
NH2.Br.,.NO2= .?
»
A., 137, 60
?
Griess
P. T. [1864], 709
), ....
=1.(?)2.4.3
»»
....
102-5
NSlting & Collin
B., 17, 266
46, 1013
i, ....
=1.2.4.6.3
i)
....
102-5
Korner
G. I., 4, 305 ;
29, 210
J. [1875], 347
it
=1.2.3.4.6
•»
....
161-4
H
»)
29, 217
COMPOUNDS CONTAINING FIVE ELEMENTS.
641
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrotribromaniline
NH2.Br3.NO,,=1.2.4.6.3
C6H3Br302N2
214-215
Remmers
B., 7, 351
27, 697
Nitrobrombenzene
Br.NO2=1.2
C6H4Br02N
....
36-39
Eichter
B., 4, 461
24, 688
j> ••••
J? »
}1
....
37
j»
B., 4, 55
24, 825
„
» )>
1)
250-251
37-38
Hiibner and
Z. C. [2], 6, 369 ;
25, 418 ; vii.,
Alsberg
A., 156, 316
138, 143
(B, 6, 1545)
» »
JJ
....
37-38
Zincke & Walker
B., 5, 115
vii., 908
»
)I J)
1J
37-38
Zincke and Sin-
B., 5, 791 ; 6, 123
26, 640 ; vii.,
tenis
947
„
» n
))
38
Petersen
B., 6, 373
26, 1133
„
ii n
)!
260-263
39-41-5
Andrews
B., 13, 2128
,,
11 >i
»
....
41
Wurster
A., 173, 145
28, 758
„ .... ....
11 »
»
....
40; 41
Augustin & Post
B., 8, 1557, 1559
29, 386
„ (G. I., 11, 396)
11 »
1»
261 c.
41-41-3
Fittig & Mager
B., 7, 1179
28, 147
„ (J. [1875], 302)
i> »
1J
....
43-1
Korner
G. I., 4, 305
29, 212, 234
„ (J. [1863], 423)
,, =1-3
))
....
56
Griess
P. T. [1864], 712;
iv., 416 ; vii.,
J. [1866], 457
138, 143
j,
1> 11
M
....
56
Richter
B., 4, 462
24, 688, 825
„
» 11
»»
....
56
Petersen
B., 6, 371, 373
26, 1133
„ .... ....
11 »
»
....
55-56
Wurster
B., 6, 1543 ; A.,
27, 369; 28,
173, 145
757
„ ....
>» »
i»
....
56
Wurster and
B., 7, 417
27, 691
Grubenmann
(B., 7, 870)
» )»
»
....
56
Wurster and
B., 7, 905
27, 1163
Nolting
j, .... ...
II »
l)
256-5 c.
56
Fittig & Mager
B., 8, 364
„ (J. [1877], 423)
!» »
ll
....
56
Johnson
B., 10, 1709
34, 142
)» "" ""
I) Jl
»
....
56-4
Korner
G. I., 4, 305 ; J.
29, 208, 212,
[1875], 302
219
„ ....
» =?
l)
mixture
b. 90
Couper
A. C. [3], 53, 309;
i.,543;iv., 416
A., 104, 226
„ (J. [1863], 423)
„ =1.4
»
....
120; 125
Griess
J. [1866], 457
24, 687; vi.,
921
„
1» 11
M
....
125
Zincke & Sintenis
B., 6, 123
26, 640
„
11 1»
»j
....
125
Richter
B., 4, 460 ; 555
24, 825; vii.,
907, 925
„
») I»
11
....
125
Walker & Zincke
B., 5, 114
25, 418
„ ....
11 1»
)»
....
125
Petersen
B., 6, 371, 373
26, 1133
,,
)» »I
)»
....
125
Wurster
B., 6, 1544 ; A.,
27, 370; 28,
173, 145
756
„ (A., 137, 166)
» 11
N
....
125-126
Griess
P. T. [1864], 712
iv., 416; vii.,
138, 143
» ....
» »
n
....
125-5
Korner
G. I., 4, 305 ; J.
29, 209, 212,
[1875], 302, 327
217
»
11 1»
»
....
126
Hofmann and
B., 5, 919
26, 169
Geyger
1)
11 )1
n
....
126
Augustin & Post
B., 8, 1559
29, 386
„ (J. [1876], 370)
11 11
11
255-256
126-127
Fittig & Mager
B., 7, 1175
28, 147
„ (G. I, 11,396)
11 11
i?
....
127
Spiegelberg
A., 197, 257
36, 796
Brompyridinemono-(or di-)
1) 11
C7
H4BrO4N (?)
199 d.
Gerichten
A., 210, 79
42,314
carboxylic acid (?)
Nitrobromphenol
OH.Br.N02=1.3.6
C6H4BrO3N
....
44
Laubenheimer
B., 11, 1160
34,976
i>
=1.4.6
»
....
87-88
Hiibner and
B., 6, 170
26, 751 ; vii.,
Brenken
915, 929
j>
11 )!
n
....
88
Korner
G. I., 4, 305; J.
29, 228; vii.,
[1877], 547
905, 912
ji
» )1
»
....
88
Armstrong and
....
25, 865
Brown
jj ...* ....
» »
»»
88
Post
B., 7, 333
27,800
j)
11 »
j>
....
88
Jaubenheimer
B., 11, 116(
34,976
u ....
» »)
»
....
88
Staedel & Danini
B., 11, 1750
36, 239
„ (Z.C.[1868],323)
» 1)
i)
....
88
Brunck
Z. C. [2], 3, 203
,, ( „ )
=1.2.4
«
....
102
n
Z. C. [2], 3, 204
vi., 912
4 N
642
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Nitrobrompheuol
OH.Br.NO2=1.2.4
C6H4Br03N
....
102
Armstrong and
25, 865
vii., 915, 928
Brown
„
U »
H
102
Post
B., 7, 333
27,800
„ .... ....
=1.13
Ji
....
110
Pfaff
B., 16, 612, 615
,, ....
=1.1.3
»
147
Lindner
B., 18, 612
48, 775
Bromhydroxynicotic acid
N.OH.Br.CO2H=1.3.?.6
T)
296
Pechmann
B., 17, 2399
48, 176
Nitrobrom resorci nol
(OH)s.Br.NO,=1.3.U
C6H4Br04N
....
147
....
A, 104, 7
Dinitrobromaniline
NH2.Br.(NO2)2=1.2.4.6
C,H4BrO4N3
144
Korner
G. I., 4, 394 ; J.
20, 229 ; vii.,
[1875], 350
916
„
= »
»
....
153-154
Leyraann
B., 15, 1235
11
=1.4.(?)2
5)
....
160
Austen
B., 9, 919
30, 513
ii ....
= »
»»
....
165-170
ii
B., 8, 1183
29, 389
„ (J. [1875], 333)
= ?
»
....
178-4
Korner
G. I., 4, 305
29, 231
Nitrodibromaniline
NH2.Br2.N02=?.1.4.?
C6H4Br202N2
75
Austen
B., 9, 622
30, 406
„
=1.2.4.6
)»
123
Remmers
B., 7, 349
27, 697
„
» »
))
....
127-S
Korner
G. I., 4, 394 ; J.
29, 210, 219,
[1875], 347
229; vii., 915
11 ••"
=1.2.6.4
»
....
202-5
n
ii
ii
„
» )i
n
....
202-203
Balbiano
G. I., 14, 9
46, 1172
11 ....
i> ii
)>
....
203-204
Hiibner
B., 10, 1709
34, 142
11
:i J>
H
....
204
Wurster&Nolting
B., 7, 1564
29, 389
11
i> i)
J)
....
soe-sor
Losanitsch
B., 15, 474
42, 955
Nitroethenylnitrofur-
....
C6H4Br206N2
....
110-111
Priebs
B., 18, 1362
48, 971
furanedibromide
Amidotribromphenol
OH.Br3.NH2=l,2.4.6.3
C6H4Br3ON
....
115
Daccomo
B., 18, 1168
48, 891
Tribromacetopyrroline ....
....
J)
....
179
Ciamician and
B., 18, 1765
48, 1078
Silber
Methylic tribrom-a-pyr-
C4NHBr3.CO2Me
C6H4Br3O2N
209-210
B.,17,1153;G.L,
46, 1044; 48,
rolinecarboxylate
14, 162
247
Nitrobromaniline
NH2.Br.N02=1.2.4
C6H6Br02N2
104-6
Meyer and
B., 5, 633 ; 6,
25, 1003; 27,
Wurster
1542
369; vii., 144
ii
» „ »
»
104-5
HUbner & Johnson
B., 10, 1709
(J. [1875],
» II
M
104-5
Korner
G. I., 4, 305
29, 219
305, 350)
(A., 171, 59)
=1.4.2
>»
....
110
HUbner & Ketschy
B., 6, 796
26, 1146
(J. [1875],
1) »
n
111-4
Korner
G. I., 4, 305
29, 217, 220
328, 347)
j,
J) »
n
....
112
Eemmers
B., 7, 347
27, 696
„ (A.., 209, 357)
» »
»
....
112
Wurster&Nolting
B., 7, 906
27, 1164
„ ....
=1.4.5
n
....
131-132
Nolting & Collin
B., 17, 266
46, 1013
,, ....
=1.3.6
»)
....
149-150
"Wurster
B., 6, 1544 ; A.,
27, 370 ; 28,
173, 145
756
„
ii i>
n
....
150
Wurster and
B., 7, 419
27, 691
Grubenrnann
„ (J. [1875], 307,
ii i>
n
....
151-4
Korner
G. I., 4, 305
29, 209, 217
333, 348)
Bromnitrosooxindole
»
nf. 240
....
vi., 736
Amidodibromphenol
OH.Br2.NH2=1.2.4.6
C6H6Br2ON
91-92
Holz
J. p. [2], 32, 65
48, 1211
ii
=l.(%-4
J)
....
178
Bohmer
J. p. [2], 24, 470
42, 398
»
» »
»
....
180
Moblau
B., 16, 2850
46, 594
ii ....
=1.2.6.4
»>
190
Lellmann and
B., 17, 2731
48, 266
Grothmann
Dibrompseudacetylpyr-
C4HBr2Ac:NH
»»
143-144
Ciamician and
G. I., 13, 455
46, 291
roline
Dennstedt
Dibrommethoxypyridine ....
N.OMe.Br2=?
J>
....
192
Hofmann
B., 12, 987
36, 733
»
ii ii
»
192
Lieben and
B., 17, 1507
46, 1196
Haitinger
»
11 »
J>
....
196
11
M. C., 6, 279
48, 966
Amidobromphenol
OH.Br.NH2=1.4.6
C6H6BrON
128
Schiitt
J. p. [2], 32, 61
48, 1211
>i
=1.2.4
n
....
158 u.c.
Holz
J. p. [2J, 32, 65
)>
Brompseudacetylpyrroliue
C.HjBrAc I NH
11
....
118-120
Ciamician and
G. I., 13, 455
46, 291
Deuustedt
COMPOUNDS CONTAINING FIVE ELEMENTS.
643
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Nitrobromdiamidobenzene
(NH2)2.Br.NO2=1.3.5.2
C6H8Br03N8
....
d.w.m. 163 ;
Korner
G. I., 4, 305
29, 227
sf. 163
J. [1875], 353
11
=1.4.2.5
)>
....
nf. 156
11
)1
11
Dimethyldibrombarbituric
CO : (NMe.CO)2 : CBr2
C6H6Br203N3
....
175-180
Mulder
B., 12, 467
36, 619
acid
Nitrate of bromoxy-base ...
C7H7BrON2+HNO3
C6H8Br04N3
....
158 d.
Keller
J. p. [2], 31, 363
48, 961
Tetranitrodibromdulcitol...
C6H4Br2(N02)4(OH)4
C6H8Br3012N4
100
....
A.C. [4], 27, 193
Tetranitrodibrommamiitol
)>
J)
....
148
Bouchardat
A. C. [5], 6, 127
26, 748
B. S. [2], 19, 19
Dibromdipropionamide ...
NH(CO.C2H4Br)2
C6H9Br202N
...
148
....
A., 142, 71
Nitrodibrombenzoic acid ...
CO2H.Br2.NO2=1.3.5.6
C7H3Br2O4N
162
Hiibner and An-
A., 158, 13
24, 365; vli.,
gerstein
162
11 i* •••
„ =1.3.4.6
)>
162
HUbner
B., 10, 1706
34, 149
11 11 —
11 11
)>
....
162
Smith
A., 222, 166
46, 601
11 11 •••
„ =1.3.5.6
J)
233-234
Hesemann anc
)>
46, 600
Kochler
Dinitrotribromtoluene
Me.Br3.(NO2)2=1.2.4.6.3.5
C7H3Br304N2
....
217-220
Neville & Winthe
B., 13, 975
37, 451
Nitrotetrabromtoluene ...
Me.Br4.NO2— 1.2 3456
C7H3Br4O2N
212
i
11
11
11
„ =1.2.3.5.6.4
11
...
213
11
11
11
„ =1.2.3.4.6.5
i)
....
215-216
11
....
11
Bromphenylic cyanate
C6H4Br.(O.CN)=1.4
C7H4BrON
226
39
Dennstedt
B., 13, 228
38, 633
Nitrobrorubenzoic acid ...
CO2H.Br.NO2=1.3.6
C7H4BrO4N
....
139-140
....
A., 143, 234; 149
132
11 )!
11 11
)>
....
140
HUbner & Fried-
A., 158, 29
24, 366 ; vli.,
burg
162
11 11
11 11
)>
140-141
Philipp
vi., 315
11 ii
„ =1.3.5
)>
....
161
Hesemann and
A., 222, 166
46, 599
Kochler
11 51
=1.2.5
))
....
177-178
Burghard
B., 8, 560
28, 892
11 11
« >J
))
....
179-180
Rhalis
A., 198, 109
38, 119
11 11
=1.4.5
»
....
195
HUbner and Only
Z. C. [2], 1, 547 ;
vi., 316
2, 241
11 1!
11 11
»»
....
197-199
Bedson
B., 10, 531
32, 482; 37,97
!> 11
11 11
»
....
199
Hiibner and Only
A., 143, 248
vi., 315
1) 11
11 11
)»
....
199
Burghard
B., 8, 558
28, 892
11 11
11 11
J»
....
199
Raveill & Hubne
B., 10,1707; A.,
46, 601
222, 166
11 11
„ =1.3.2
)>
246-248
Hubuerand Ohly
A., 143, 238
vi., 315
1) 11
11 11
))
....
250
HUbner & Fried-
A., 158, 29
24, 366; vii.,
burg
162
Nitrobromsalicylic acid ....
CO2H.OH.Br.NO2=1.2.5.3
C7H4BrO5N
....
175
Lellmann and
B., 17, 2729
48, 265
Grothmann
11 11
„ =1.2.3.5
)>
222
11
B., 17, 2725
)J
Dinitrodibromtoluene
MeBr2.(NO2)2=1.3.5.2.?
C7H4Br204N2
....
105
Neville &Winther
B., 13, 967
37, 437
11
„ =1.3.5.2.?
?J
157-6-158
11
11
>T
11
„ =1.2.6.3.1
>»
....
161-6-162-2
11
B., 13, 973
37, 446, 451
Nitrotribromtoluene
Me.Br3.NO2=1.2.3.6.?
C7H4Br302N
91-91-4
)!
37, 451
11
„ =1.2.3.5.?
>»
....
95-170 (?)
11
11
11
=1.2.5.6.4
»
105-8-106-8
11
B., 14, 418
39. 86
11
=1.2.3.4.?
)>
106-107
11
37, 451
11
=1.2.3.6.?
?)
215
Wroblewsky
A., 168, 195;
24, 1062; 27,
Z. C. [2], 7, 271
54
Amidotribrombenzoic acid
CO2H.Br3.NH2=1.2.4.6.3
»>
....
169 d.
Beilstein and
Z. C. [2], 1, 505 ;
vi., 317
Geitner
A., 139, 6
)! !•
» 11
jj
170-5
Vollbrecht
B., 10, 1708
Nitrosornethylmtrobrom-
(CH2.NO).Br.NO2=1.4.6
C7H5Br03N2
151-153
Gabriel & Meyer
B., 14, 827
40, 730
benzene
Dinitrobromtoluene
Me.Br.(N02)2=1.3.2.?
C7H6Br04N.,
....
103-104
Grete
A., 177, 258 ;
8, 888; 29,72
B., 8, 567
Dinitrobrommethoxy-
OMe.Br.(NO2)2=1.2.4.6
C7H6Br06N2
47
Balbiano
G. I., 14, 234
8, 530
benzene
4 N 2
644
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diuitrobrommethoxy-
OMe.Br.(NO2)2=1.3.(?)2
C7H6BrO6N2
....
109-4
Korner
G. I., 4, 305 ; J.
29, 231 ; vii.,
beuzene
[1875], 341
916, 929
Dibrombenzamide
(CO.NH2).Br2=1.3.4
C7H6Br2ON
151-152
Burghard
B., 8, 560
28, 892
» .... ....
» »
)>
—
151-5
Beutnagel
A., 222, 166
46, 601
Nitrobenzylidene di-
CHBr2.NO2=1.4
C7H5Br2O2N
A., 185, 268
82-82-5
Wachendorff
B., 9, 1346
31, 207
bromide
»
» »
=1.3
»
A., 185, 279
101-102
»
B., 9, 1347
»>
Nitrodibromtoluene
Me.Br2.NO2=1.2.3.4 or 6
)>
56-5-57-5
Neville &Winther
37, 435
39, 86
(J.[1870],
» »
»
....
59
Wroblewsky
A.,168,188;Z.C.
24, 686; 27, 54;
528; [1871], 450)
(2), 7, 209
vii., 1165
„
=1.2.6.4
»»
....
56-8-57
Neville & Winther
37, 445
39,86
» ....
=1.3.4.5
»»
....
62-63-6
M
B., 13, 974
37, 447 ; 39, 86
(B., 14, 419)
=1.2.5.3
)i
....
69-5-70
)>
»
n
i) ••••
„ =1.2.6.3
»
....
79
Wroblewsky
A.,168, 192;Z.C.
24, 1062; 27,
(2), 7, 271
54; vii., 1165
„
=1.2.4.6 (?)
»
....
78-80
Neville & Winther
....
37, 443, 451
„
»» »
H
....
80-81
»
39,86
»
=1.3.4.2
)>
....
86-6-87-5
H
B., 14, 419
37, 451 ; 39, 86
»
J) )»
»
....
86-87
Wroblewsky
A., 168, 184
27, 53; vii., 1165
(J.[1870],
=1.2.5.4
)>
86-87
»)
A.,168, 147; Z.C.
24, 564; 27,
528; [1871], 450)
(2), 7, 135
53; vii., 1165
„
» »
»i
....
87 ; 88-39
Seville & Winther
B., 13, 974
37, 445, 451
„
» »
»
....
87-89
H
B., 14, 419
39, 86
„ ....
„ =1.2.3.5
»
....
105-4
))
B., 13, 965
37, 434
„
„ =1.3.5.4
n
....
124
Wroblewsky
A.,168, 189; Z.C.
24, 686 ; 27,
(2), 7, 209
54; vii., 1165
„
=1.(?)2.6
»
225-226
Wachendorff
B., 9, 1347
31, 207
i)
„ =1.3.4.6
»»
?
Neville & Winther
B., 14, 417, 419
Amidodibrombenzoic acid
CO2H.Br2.NH2=1.3.5.6
»
196
Hiibner
A., 158, 16 ; Z. C.
24, 365 ; vii.,
(2), 7, 65
162
!) ))
„ =1.3.4.6 or 2
»
225
»
B., 10, 1706
34, 149
(A., 185, 281)
„ acid
» ji
j)
....
225
Greiff
B., 13, 289
38, 648
» »
n »
11
..,.
225
Wachendorff
A., 185, 281
i) »
I! I)
)»
225
Smith
A., 222, 166
46, 602
i) »
„ =1.3.5.6
)j
225
Hessemann and
»
46, 600
KOchler
j> M
„ =1.3.5.4
^j
....
?
....
A., 139, 1
Nitrodibrommethoxy-
OMe.Br2.NO2=1.2.4.6
C7H6Br2O3N
76-7
Kbrner
G. I., 4, 393 ; J.
29, 229 ; vii.,
benzene
[1875], 337
915, 929
)>
. „ =1.2.6.4
>J
122-6
)»
»
))
M
1) »
n
122-123
Balbiano
G. I., 14, 9
46, 1172
J)
)» ))
M
....
126-127
A., 217, 70
Nitrodibromcresol
Me.OH.Br2.N02=1.4.(?)2.6
»
A., 215, 89
83
Knecht
B., 15, 1071
42,969
„
=1.2.(2)2.4
II
....
91-92
Nolting & Collin
B., 17, 270
46, 1007
N itrodibromorcinol
Me.(OH)2.Br2.NO2
C7H6Br2O4N
....
112 d.
Weselsky
B., 7, 444
27, 694
=1.3.5.2.(?)2
Formobromanilide
C6H4Br.(NH.CHO)=1.4
C7H6BrON
119
Dennstedt
B., 13, 234
38, 634
Brombenzamide
C6H4Br.(CO.NH2)=1.3
(}
....
150
Engler
B., 4, 707
24, 924
Nitrobenzylbromide
CH2Br.NO2=1.3
C7H6Br02N
A., 185, 278
57-58
Wachendorff
B., 9, 1347
31, 207
!)
=1.4
»
A., 185, 266
99-100
n
B., 9, 1346
»
Nitrobromtoluene
Me.Br.NO2=1.3.2
»
Liquid
Neville & Winther
B., 13, 1945
37, 630 ; 39, 86
„
=1.3.?
)j
269
s. —20
Wroblewsky
A., 168, 170
27, 53
„
=1.3.?
M
s. 15
Grete
A., 177, 231
29, 72
„
=1.4.5
n
....
Liquid
Wroblewsky
B., 8, 571 ; J.
28, 888; 37,
[1870], 527
442
,, .... ...
>i »
>»
255-256
Liquid —20
)»
A., 168, 177 ;
27,53;vi.,1104;
Z. C. [2], 7, 165
vii., 1167
(B., 6, 799)
i> ,>
»
....
30-6-32
Neville and Win-
37,442
ther
,,
» »
M
....
31-32
n
B., 13, 972
39,86
„
» »
»»
33-34
Beilstein
A., 158, 344
24, 682
COMPOUNDS CONTAINING FIVE ELEMENTS.
645
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrobromtoluene
Me.Br.NO2=1.4.6
C7H6BrO2N
....
42
Eichter
B., 8, 572
„
» »
))
256-257
43
Heynemann
Z. C. [2], 6, 402
vii., 1167
„
» »
)>
256-257
43
Wroblewsky and
B, 8, 571; A,
27, 53; 28, 888;
Kurbatoff
168, 177 ; Z. C.
vi., 1104; vii.,
[2], 7, 165
1167
„
» »
J»
....
44-4-45-2
Neville and Win-
37, 441
39, 86
ther
,, .... ....
j> >»
»1
....
45
Heynemann
A, 158, 340
24, 681
»
» »»
»
....
45-5
Hubner and Eoos
B., 6, 799
27, 165
,j .... ....
=1.3.6
))
....
54-55
Grete
B., 8, 566; A,
28, 887 ; 29, 72
177, 246
»» ....
)) J»
J)
267
55
Wroblewsky
A, 168, 178 ; B.,
27, 53 ; 28, 155
7, 1063
-,, .... »••»
» »»
»>
....
55
Neville and Win-
>•**
39,86
ther
„
=1.2.4
»>
....
74-75
»>
....
i]
M
=1.2.5
n
76-3
>»
B., 14, 419
37, 431 ; 39, 86
„ ....
=1.3.5
j»
....
81-81-8
i»
....
39, 86
,, .... ....
» >»
»
....
81-4-81-8
)>
B., 13, 964
37, 433
„ ....
» i)
)j
269-370
86
Wroblewsky
B., 8, 573; A,
28, 886 ; 84,
192, 203
977
Amidobrombenzoic acid ....
COi!H.Br.NH2= 1.3.2
»
....
171-172
Hubner
A, 143, 244 ; 149
vi., 317
134
!> »
=1.2.5
)>
175-177
Burghard
B., 8, 560
28, 892
!) ))
» >1
H
....
180
Kichter
E. K. T., 159
» »
„ =1.3.6
»>
....
208
Hubner
A, 143, 241 ; 149,
vi., 317
133
» II ••••
=1.3.5
»
....
215
Hesemann , and
A, 222, 166
46, 600
Kb'chler
II »
=1.4.5
H
....
220-221
Burghard
B., 8, 558
28, 892
(B., 10, 1707)
!) »
)» »
H
....
225
Eaveill& Hubner
A, 222, 166
48, 601
Nitrobrommethoxybenzene
OMe.Br.NO2=1.4.6
C7H6Br03N
87
Korner
G. I., 4, 305
29, 217
)i
n n
>»
....
88
Staedel
A, 217, 55
44, 662
»)
u )>
1)
....
88
Staedel & Damm
B., 11, 1750
36, 239
ii
=1.13
1)
....
103-104
Pfaff
B., 16, 614
»
=1.2.4
J»
....
105
Balbiano
G. L, 14, 234
48, 530
»
» »
»
106
Staedel & Damm
B., 13, 838
38, 641
»
» )I
)>
....
106
Staedel
A, 217, 66
44, 662
Methylic bromhydroxy-
N.Br.OH.C02Me=l.?.2.5
»
....
221-222
Pechmann
B., 17, 2398
48, 176
nicotate
Dinitrobromme thamido-
NHMe.Br.(N02)2=1.2.4.6
C7H6Br04N3
....
147
Norton and Allen
B., 18, 1995
48, 1214
benzene
Nitrodibromtoluidine
Me.NH2.Br2.NO2=1.3.2.6.4
C7H6Br202N2
....
124-130
Neville and Win-
B., 13, 973
37, 444 ; 39, 86
ther
Brommethaniline nitrosa-
NMe(NO).Br=1.4
C7H7BrON2
....
74
Wurster and
B., 12, 1816
38, 107
mine
Scheibe
Nitrobromtoluidine
Me.NH2.Br.N02=1.4.3.5
C7H:BrO2N2
63 ; 64-65
Neville and Win-
B., 13, 968
37, 433 ; 39, 86
ther
» ....
» »
»
....
61?B
Wroblewsky
B., 8, 573 ; A,
28, 886; 34,'
192, 203
977
„
„ =1.3.5.6
»
....
87-88
Neville and Win-
B., 13, 1945
37, 630 ; 39, 86
ther
,i
„ =1.3.2or6.4
)»
102-103
5»
B., 13, 972
37, 444
»
=1.2.5.3
»>
....
139
Wroblewsky
A., 192, 207
34, 977
>t
>' »
»
....
143
Neville and Win-
B., 13, 969
37, 433 ; 39, 86
ther
,,
=1.3.6.4
»
....
179-181
»
B., 13, 972
37, 444; 39, 86
„ ....
„ =1.2.3.5
ji
....
180-3-181-3 c.
»
B., 13, 964
37, 432; 39, 86
Bromtheobromin
A., 215, 305 ; 217, 302
C7H7BrO2N4
....
310 s.d.
Fischer
B., 14, 644
40, 614
Dibromanisidine
OMe-NHj-Br^ 1.2.4.6
C7H7Br2ON
....
Liquid low
Staedel and
A, 217, 63 ; B.,
44, 663 ; 38,
temp.
Damm
11, 1750
641
646
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Dibromanisidme
OMe.NH2.Br2=1.4.2.6
C7H7Br2ON
....
Crystalline
Staedel and
A., 217, 63 ; B.,
44, 663; 38,
(B., 13, 838)
Damm
11, 1750
641
Bromanisidine „
OMe.NH2.Br=1.4.2
C7H8BrON
....
Liquid
„
„
„
(36, 239) ...
=1.2.4
„
....
97-98
„
„
„
?
....
C7H3Br2O3N,
....
204-205
Bell
B., 11, 1814
Bromtoluidine nitrate
Me.(NH3N03).Br= 1.4.5
C7H9BrO3N2
....
182
Wroblewsky
A., 168, 147
27, 51
„ ,
„ =1.2.3or5
„
....
183d.
„
A., 168, 147 ; Z.
24, 564; 27, 52
C. [2], 7, 135
Bromhydroxylnitrodehy-
C6H7(N02)N(HOBr).CO2Me
C7H11BrO5N2
130
Boessneck
B., 16, 647
dropiperylmethylure-
thane
Dibromisatin
C6H2Br2.CO.C(OH) : N
C3H3Br202N
....
250
Baeyer and
B., 15, 2098
44, 202
i i
(Econimides
=1.3.?.4
Tibromnitrosooxindole ....
....
C8H3Br302N2
....
162
Baeyer and Knop
A., 140, 36
Bromisatin ....
C6H3Br.C.C(OH) : N=l.?.4
C8H4BrO2N
250
Baeyer and Blom
B., 17, 965
46, 1026
255
Baeyer and
B., 15, 2098
44, 202
J)
(Econimides
Dibromisatoxime
C6H2Br2.C(NOH).C(OH) : N
C8H4Br202N2
....
d.w.m. 255
Baeyer and Corn-
B., 16, 1709
44, 1131
L I
stock
Dibromnitrosodioxindole....
C8H4Br203N2
....
275
Baeyer and Knop
A., 140, 25
vi., 735
Bromindazole carboxylic
NH.N.C6H3Br.C.CO2H
C8H,,Br02N2
d.
Fischer and Taf el
A., 227, 303
48, 542
1 J
acid
?
....
C9H5BrO4N4
....
d. 142
....
A. C. [5], 11, 420
Dibromdioxindole
«...
C8H5Br2O2N
170
Baeyer and Knop
A., 140, 19
Nitrodibromacetophenone
NO2.(CO.CHBr2)=1.3
C3H5Br2O3N
....
59
Engler
B., 18, 2240
48, 1223
„
fr. NO2.(CO.CH2Br)=1.2
JJ
85
Gevekoht
A., 221,323
46, 445
Bromoxindole
....
C8H6BrON
176
Baeyer and Knop
A., 140, 32
vi., 736
Phenylbromnitroethylene
Ph.CBr:CH.N02
C8H6Br02N
....
67
Priebs
A., 225, 319
48, 161
Bromdioxindole
....
„
,
165
Baeyer and Knop
A., 140, 20
Nitrophenylbromethylene
C6H4.NO2.(CBr : CH2)=1.2
J) \ /
6H10Br204N2
255
Morgan
B., 17, 222
46,47
Nitrobromacetophenone ....
NO2.(CO.CH2Br)=1.2
C8H6Br03N
55
Gevekoht
A., 221, 323
46, 445
„
=1.3
5)
....
96
Hannius
B., 10, 2008
34, 147
Nitrobromphenylaceticacid
(CH2.CO2H).Br.N02=1.4.5
C3H6Br04N
112-115
Bedson
B., 10, 530
32, 482
^
» >!
„
113-114
„
...
37,97
I) 1!
» «
„
mixture
130
Radziozewsky
B., 2, 208
!> V
=1.2.?
„
162
Bedson
....
37, 101
!> I)
=1.4.6
M
....
167-169
„
B., 10, 530
32, 482; 37, 99
Nitrobromtoluic acid
C02H.Me.Br.NO2=1.3.(?)2
5)
....
175-176
Fittig and others
A., 147, 34
vi., 1100
» i)
„ =l-4.(?)2
I)
170-180 d.
Landolph
B., 5, 268
25, 473 ; vii.,
1175
!> 1)
=1.4.5.?
H
....
204-205
Fittica
A., 172, 303
28, 59
Bromapophyllic acid
....
....
204-205 d.
Gerichten
A., 210, 91
42,314
Nitrobromanisic acid
CO2H,OMe.Br.NO2=?
CsH6Br05N
....
182
Balbiano
G. I., 14, 234
48, 530
Nitrodibromacetanilide ....
NHAc.Br2.NO2=1.2.4.6
C8H6Br203N2
....
209
Remmers
B., 7, 348
27, 697
Nitrophenylnitroethylene
NO2.(CHBr.CHBr.NO2) =1.2
C3H6Br204N2
90
Priebs
A., 225, 319
48, 161
dibromide
» ..
=1.4
J)
....
102
„
„
„
Tribromamidoacetophen-
(CO.CHBr2).Br.NH2=].3.6
C8H6Br3ON
....
140-145 d.
Baeyer and Blom
B., 17, 967
46, 1027
one
Tribromacetanilide
NHAc.Br3=1.2.4.6
a
232
Remmers
B., 7, 350
27, 697
Nitrotribromethoxybenzene
OEt.Brij.NO2=l.(?)3.3
C8H6Br303N
79
Lindner
B., 18, 614
48, 775
Tribromdiazophenetoil
OEt.(N2.N03).Br3=1.2.(?)3
C3H6Br304N3
....
d.w.m. 92
Mohlau and
J. p. [2], 24, 476
42, 396
nitrate
(Econimides
Bromterephthalamide
(CO.NHs)3.Br=1.4.5
C8H.BrO2N2
270
Fischli
B., 12, 620
36, 639
Nitrobromacetanilide
NHAc.Br.NO2=1.4.6
CsH7BrO3N2
102
Remmers
B., 7, 347
27, 696
„ (A., 209, 356)
» »
B
104
Elubner & Retschy
B., 6, 796
26, 1146
Nitroamidobromphenyl-
(CH2.C02H).Br.NH2.NO3
C8H7BrO4N2
MM
191-192
Gabriel
B., 15, 1994
44, 64
acetic acid
=1.3.4.5
Dibromacetanilide
NHAc.Br2=1.2.4
C3H7Br2ON
....
146
Remmers
B., 7, 348
27, 696
COMPOUNDS CONTAINING FIVE ELEMENTS.
647
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Phenylnitroethylene di-
Ph.CHBr.CHBr.NOo
C8H7Br2O2N
....
86
Erdmann
B., 17, 414
broruide
Nitrostyrolene dibromide
NO2.(CHBr.CH2Br)= 1.2
JJ
....
52 ; si. 50
Einhorn
B., 16, 2214
46,66
j> »
=1.4
JJ
72-73
Basler
B., 16, 300G
46, 604
)» )»
=1.3
JJ
....
78-79
Prausnitz
B., 17, 598
46, 1175
Acetamidodibromphenol ...
OH.Bra.NHAc=1.2.6.4
JJ
173-174
Holz
J. p. [2], 32, 65
48, 1211
i)
=1.4.6.2
JJ
....
186
»»
)J
J)
Nitrodibromxylene
Me2.Br.,.NOj=1.3.(?)3
JJ
....
108
Fittig and others
A., 147, 28
vi., 295
j> •••
=1.4.5.(?)2
JJ
....
111-112
H
J»
)J
Nitrodibromethoxybenzen
OEt.Br2.NO2=1.2.4.6
C8H7Br203N
....
46
Staedel
A., 217, 58
44, 663
»
=1.2.6.4
JJ
....
108
»>
A., 217, 67
JJ
jj
=1.(?)2.3
JJ
....
110
Lindner
B., 18, 613
48, 775
Nitrodibromethoxyphenol
OH.OEt.Br2.NO2=1.3.2.6.4
C3H;Br2O4N
....
69
Weselsky and
M.C., 1, 897
40, 727
Benedikt
Dibromdiazopheneto'il
OEt.(Ns.NOj).Br2=1.2.(?)j,
C8H7Br204N3
....
d. 101-5
Mohlau and
J. p. [2], 24, 476
42, 396
nitrate
CEhmichen
Bromacetanilide
NHAc.Br=1.2
C8H8BrON
J. [1875], 342
99
Korner
G. I., 4, 305
29, 212
(B, 7, 346)
=1.4
JJ
165
Giircke
B., 8, 1115
29,400
„ (J.I 1875], 342]
JJ JJ
JJ
....
165-4
Korner
G. I., 4, 305
29, 212
„
JJ »)
JJ
165-5
Kelbe
R, 16, 1200
44, 916
» .... ...
JJ JJ
JJ
....
167-168
....
A., 209, 355
Bromphenylglycocine
Br. (NH.CHs,CO2H)= 1 .4
C8H8Br02N
....
98
Dennstedt
B., 13, 236
38, 634
Methylic bromphenylcarb-
Br.(NH.C02Me)=1.4
JJ
124
n
B.; 13, 229
38, 633
amate
Acetamidobroinphenol ...
OH.Br.NHAc=1.2.4
JJ
....
157 u.c.
Holz
J. p. [2], 32, 65
48, 1211
„
=1.4.2
JJ
golden
177 u.c.
Schiitt
n
JJ
)>
JJ JJ
JJ
white
179
»
n
J»
Amidobromphenylacetic
(CH2.CO2H).Br.NH2=1.4.5
JJ
....
133-134
Bedaon
B., 10, 1658
34, 70 ; 37, 98
acid
»» ji
=1.3.4
JJ
....
135-136
Gabriel
B., 15, 840
42, 1070
u »
=1.4.6
JJ
....
167 d.
Bedson
B., 10, 1658
34,70; 37,100
» )?
=1.2.?
JJ
....
186
»
JJ
JJ
Bromanisamide
(CO.NH2).OMe.Br=?
JJ
185-5
Crespi
G. I. [1881], 419
42, 192
Nitrobromxylene
Me2.Br.NOs=1.3.4.?
JJ
260-265 p.d.
Liquid
Fittig and others
A., 147, 31
vi., 294
Nitroethanediazobrom-
C6H4Br.N2.C2H4.N02=1.4
C8H8BrO2N3
....
135-138 d.
Hallmann
B., 9, 393
30, 93
benzene
Bromethoxynitrobenzene
N02.(O.C2H4Br)=1.2
C8H8Br03N
38-40
Weddige
J. p. [2], 21, 129
38, 316
»
JJ »J
»
....
43-5
)>
J. p. [2], 24, 246
40, 1137
»
=1.3
»»
39
H
J. p. [2], 24, 255
40, 1139
»
=1.4
JJ
....
62-63
J)
J. p. [21 21, 127
38, 316
»
» »
JJ
....
63-64
1>
J. p. [2], 24, 254
40, 1130
Nitrobromethoxybenzene
OEt.Br.N02= 1.4.6
JJ
....
43
Staedel
A., 217, 57
44, 663
, »
» — i)
JJ
....
47
Hallock
B., 14, 37
40, 595
(A.C.J.,3,20)
»
= 1.2.4
JJ
....
55
»
JJ
71
»
=1.?.3
JJ
....
57
Lindner
B., 18, 612
48, 775
D
=1.2.4
JJ
....
98
Staedel
A., 217, 67
44, 663
»
= »
JJ
138
....
A. C. J., 3, 20
Amidobromanisic acid
CO2H.OMe.Br.NH3
JJ
....
185
Balbiano
a I., 14, 234
48, 530
=1.4.2.3 or 6
Nitrobromethoxyphenol ....
OH.OEt.Br.NO2=1.3.?.4 or 6
C8HsBr04N
....
114
Weselsky and
M. C., 1, 898
40, 727
Benedikt
Amidotribromethoxybenz-
OEt.Brs.NH2=l.(2)3.2
C8H8Br3ON
....
77
Mohlau
J. p. [2], 24, 481
42,396
ene
»
=1.(?)3.3
JJ
crystalline
liindner
B., 18, 614
48, 775
Nitrosobromdimethaniliue
NMe2.Br.NO=1.3.?
C8H9BrON3
....
148
Wurster &Scheibe
B., 12, 1819
38, 108
Diamidobrompheny laceti c
(CH2.C02H).Br.(NH2)2
C8n9BrO.,N2
....
195-200 d.
jlabriel
B., 15, 1995
44, 64
acid
=1.3.4.5
Bromcaffeme (Z. C. [1867],
M. C., 3, 90 ; A., 215, 264
C8H9Br02N4
206
Tischer
B., 14, 639
40, 614
616)
Amidodibromethoxybenz-
OEt.Br2.NH2=l.(?)2.3
C8H9Br2ON
L. b. 0
liindner
B., 18, 613
48, 775
ene
648
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Amidodibromethoxybenz-
OEt.Br2.NH2=1.3.5.6
C9H9Br2ON
....
52-5
Mohlau
J. p. [2], 24, 479
42, 396
ene
»
=1.2.6.4
J)
67
Staedel
A., 217, 71
44, 663
n
=1.2.4.6
»
....
92
»
A., 217, 65
T)
Dibrommethylpseudoluti-
fr. NMe.CO.CH:CMe.CH:C
»
....
173
Hantzsch
B., 17, 1030, 2907
46. 1047
dostyril
i i
-
Me
Amidobromethoxybenzene
OEt.Br.NH2=l.?.3
C8H10BrON
....
Liquid
Lindner
B., 18, 612
48, 775
»
=1.2.4
»
....
Liquid
Staedel
A., 217, 69
44, 663
»
=1.4.2
J»
....
57
»
A., 217, 62
»
Bromhydroxylnitrode-
C5H-(N02)N(HOBr).CO2Et
C8H13Br06N2
....
157
Schotten
B., 16, 646
44, 814
hydropiperylurethane
Bromhydroxylbromde-
CsH7BrN(HOBr).C02Et
C8H13Br203N
MM
140
»
B., 16, 648
44,811
hydropiperylurethane
Dibromethylidenediure-
fr. CH2Br.CH(NH.C02Et)2
C8H14Br204N2
..•.
115-116
Bischoff
B., 5, 86
25,412;vii.,411
thane
Bromethylidenediurethane
CH!!Br.CH(NH.C02Et)2
»
MM
142
»»
B., 5, 85
))
1
....
C9H4Br606N4
....
250 d.
Grimaux
C. R, 80, 828
28, 753
Nitrobromquinoline
N.Br=ai ; ft
C9H6BrO2N2
....
133
Coste
B., 15, 1918
44,91
»
» = »
*J
....
133
»
B., 15, 1919
»
Dibromhydroxyquinoline
N.OH=a, ; a,
C9H5Br2ON
....
193-195
Bedall & Fischer
B., 14, 1367
H
» — j)
J>
....
195-196
....
M. C., 3, 543
Dibromphenylmethyl-
C6H2Br2.CO2.N : CMe
C9H5Br202N
....
223-223-5
Gabriel
B., 16, 1996
44, 1128
acetoxime-o-carboxylic
anhydride
Nitrodibromcinnamic acid
N02.(CBr : CBr.CO2H)=1.4
C9H5Br2O4N
....
179-180
Urewsen
A., 212, 157
42,84
Bromhydroxyquinoline ....
N.OH=a, ; ft
C9H6BrON
....
184-185
Skraup
M. C., 3, 554
44, 94
»
N.OH.Br=a,/3,aj ;
»
266-267
Friedlander
B., 15, 1425, 2682
42, 1209
n
» »
1)
....
266
Baeyer and Blom
B., 15, 2149
44, 196
j»
....
)J
....
272-273 d.
Skraup
M. C., 3, 566
Methylbromisatin
C6H3Br.CO.C(OMe) : N
C9H6Br02N
...»
147
Baeyer & (Ecoiii-
B., 15, 2095
44, 201
1 J
mides
Nitrobromcinnamaldehyde
N02.(C2HBr.COH)=1.3
C9H6Br03N
....
90
Kinkelin
B., 18, 485
48, 791
M
N02.(CBr : CH.COH)= ?
n
....
96-97
Zincke & Hagen
B., 17, 1817
46, 1344
>»
= »
!)
....
136
?> »
B., 17, 1816
i)
Nitrobromcinnamic acid ....
N02.(C2HBr.C02H)=1.4
C9H6Br04N
....
146
Miiller
A., 212, 137
42,842
)> )> •—
=1.4
JJ
....
205
»
A., 212, 135
»
Propionyltribromnitro-
0(C3H60).Br3.N02=?
C9H6Br303N
....
70-71
Guareschi and
B., 18, 1174
48, 891
phenol
Daccomo
Hexabrommalolacturil ....
...»
C9H6Br606N4
250 d.
A. C. [5], 11,406
Bromindazoleacetic acid ....
....
C9H7BrO2N2
....
200 d.
Fischer and Tafel
A., 227, 303
48, 542
Nitrophenyldibrompro-
NO2. (CHBr.CHBr.C02H)
C9H,Br204N
....
180
Baeyer
B., 13, 2258
40, 275
pionic acid
=1.2
» »
=1.4
J>
....
217-218
Drewsen
A., 212, 151
42, 846
p-Bromhydrocarbostyril ....
N.OH=a1^1 ;
C9H8BrON
....
178
Gabriel and Zim-
B., 13, 1683
40, 274
mermann
Acetamidobrombenzoic acid
CO2H.Br.NHAc=1.3.2 or 6
C9H8Br03N
214-215
Jackson
B., 14, 886
40, 735
Nitrophenylbrompropionic
N02.(CHBr.CH2.CO2H)=1.2
C9H8BrO4N
....
139-140
Einhorn
B., 16, 2209
46,65
acid
» !)
=1.4
))
170-172 d.
Easier
B., 16, 3002
46, 603
Ethylic nitrobrombenzoate
CO2Et.Br.NO2=1.3.6 or 2
n
....
55
Hubner and Ohly
A., 143, 238
vi., 315
» »
=1.2.5
i}
....
65-66
Rhalis
A., 198, 111
38, 119
» »
=1.7.4
»
....
70
Hubner and Ohly
A., 143, 250
vi., 316
» »
=1.4.5
)>
74
n
)>
»
» »
„ =1.3.2 or 6
jj
80
A., 143, 241
n
Methylic nitrobromphenyl-
(CHs.C02Me).Br.N02=1.4.5
j>
40-41
Bedson
37, 98
acetate
» »>
=1.4.6
u
66-68
37, 100
Nitrobromhydrocinnamic
(C3H4.CO,,H).Br.N02=1.4.5
B
90-95
Gabriel and Zim-
B., 13, 1684
40, 274
acid
mermann
» n
=1.4.6
»
....
141-142-5
»
B., 13, 1682
»
COMPOUNDS CONTAINING FIVE ELEMENTS.
649
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dibromafflidodihydro-
N.OH.HJ.NHJ=a1/31j32a!; /3,
C9H8Br2ON2
....
179
Gabriel and Zim-
B., 12, 603
36, 640
carbostyril
mermann
Nitrophenylmethoxydi-
N02.[CH(OMe).CBr2.N02]
C9H8Br205N2
....
145-146
Friedlander and
A, 229, 233
48, 1138
bromnitroethane
=1.3
Lazarus
Acetamidotribromtoluene
Me.Br3.NHAc=1.2.3.4.5
C9H8Br3ON
....
171-173
Neville&Winther
B., 13, 975
37, 447 ; 39, 86
»
„ =1.2.3.6.5
11
....
179-181
M
B., 13, 974
H
Bromamidodihydrocarbo-
N.OH.H2.NH2=a1/310.1a3)- /3,
C9H9BrON2
....
218-219
Gabriel and Zim-
B., 12, 603
36, 640
styril
mermann
Acetamidonitrobroni-
Me.Br.NHAc.N02=1.3.4.5
C9H9Br03N2
....
210-5
Wroblewsky
B., 8, 573; A,
28, 886 ; 34,
toluene
192, 202
977
>»
» »
!)
....
210-5
Neville&Winther
....
39,86
Dinitrobrommesitylene ....
Me3.Br.(N02)2=1.3.5.2.4.6
C9H9BrO4N2
....
189-190
Tittig and Storer
A, 147, 8
vi., 299
)!
11 )1
i)
....
194
Sussenguth
A, 215, 248
44, 470
Dinitrobromcumene
* =?
»
....
214-215
Fittig and Storer
A, 147, 14
Acetamidodibromtoluene....
Me.Brj.NHAc=1.2.5.3
C9H9Br;!ON
....
144-145
Neville&Winther
B., 13, 974
37, 448; 39, 86
11
=1.(?)2.3
N
154
Wroblewsky
A, 168, 147
27, 54; vii.,
1177
1!
=1.3.4.5
11
....
162-163
Neville&Winther
B., 13, 975
37, 447; 39, 86
j»
=1.2.4.5
H
—
168-168-6
?»
B., 13, 971
37, 440, 443
»
=1.2.3.5
11
....
204-205
>»
B., 13, 964
37, 434; 39, 86
Phenybiitropropylene di-
Ph.CHBr.CBrMe.N02
C9H9Brj02N
....
77-78-5
Priebs
A, 225, 319
48, 162
bromide
Acetmethamidobrom-
NMeAc.Br=1.4
C9H10BrON
....
99
Wurster and
B., 12, 1818
benzene
Scheibe
Acetamidobromtoluene ....
Me.Br.NHAc=1.4.5
JI
....
113-7-114-6
Neville&Winther
B., 13, 972
37, 443 ; 39, 86
,, ....
=1.3.4
11
....
117-5
n
....
39, 86
i)
ii )>
1)
....
117-5
Wroblewsky
Z. C. [2], 5, 279 ;
27, 51; 34, 977
A, 168, 153 ;
vi., 1104
192 196
ji «...
» »
)>
....
117-5
Grete
A., 177, 231
29, 72
}1 ...
„ =1.3.2 or 6
11
....
156
n
B., 7, 796; 8, 567;
27, 986; 28,
A, 177, 231
888 ; 29, 73
„
i) V
11
....
156-157
Wroblewsky
Z. C. [2], 7, 135 ;
24, 564; 27,51;
A, 168, 147
vii., 1177
»
» »
11
....
156-157
Neville&Winther
....
39, 86
„
=1.3.5
11
167-168
»
B., 13, 964
37,434; 39,86
Ethylic bromphenylcarb-
C6H4Br.NH.C02Et=1.4
C9H10Br02N
...
84-85
Dennstedt
B., 13, 228
38, 633
amate
Amidobromhydrocinnamic
(CH2.CH2.C02H).Br.NH2
»
....
104-105
Gabriel
B., 15, 2292
44, 195
acid
=1.3.4
ii )>
=1.4.5
ji
....
117-119
j)
B., 13, 1684
Nitrobrommesitylene
Me3.Br.NO2=1.3.5.2.4
!)
....
54
Fittig and Storer
A, 147, 7
vi., 299
Acetdiamidodibromtoluene
Me.Br2.NH2.NHAc=(?)3.1.3
C9H10Br.,ON3
....
208 d.
Tiemann
B., 3, 222
Acetdiamidobrom toluene...
Me.Br.NH2.NH Ac=(1)f 1.3
C9HuBrON3
b. 100.
....
A, 153, 134
p-Nitrophenyl-|3-alanine
....
C9HuBr04N2(?)
....
132-135
Easier
B., 17, 1496
46, 1173
+HBr
Dibromtetrahydroquinol-
C9H9Br2N.2HNO3
C,HuBra06N3
189 u.c.
Clans and Istel
B., 15, 823
42, 1111
ine nitrate
Tribromdiethylcarbo-
NEt.Br3.(CO.NHEt)
C9H11BraONa
....
120-121 d.
Bell
B., 11, 1813
pyrrolamide
=1.2.3.4.5
Tribromhydroxycyan-
C9H10Br3N2.OH
)i
....
149
Biess
J. p. [2], 30, 145
48, 236
coniine
?
....
C9H12Br203N2
....
197 d.
Bell
B., 11, 1813
Bromhydroxycyancouiine
....
C9H13BrON2
....
172
Meyer
J. p. [2], 26, 358
44, 353
ji ...
....
11
....
?
Iliess
J. p. [2], 30, 145
48, 235
I
C9H13Br2ON
....
250 d.
Comstock and
B., 17, 1993
46, 1383
Kbnigs
£-Tetranitrobromnaph th-
Br.(N02)4=(?)3;(i)2
010N3Br08N4
....
189-189-5
Merz and Weith
B., 15, 2714
44, 344
alene
«- .,
n n
))
....
245
!)
B., 15, 2719
n
Trinitrobromnaphthalene
MM
C10H4Br06N3
....
184-5
Labhardt
B., 12, 680
Dibrompyrocoll(G.I.,12,29)
....
C10H4Br202N2
....
288-290
Ciamician
G.I., 11, 321,330
4 o
650
ORGANIC COMPOUNDS.
Natue.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Brompyrocoll (G. I., 12, 29
C4HSN I (CO)2 : C4H2BrN
C10H5Br02N2
....
190-192
Ciamician
G. I., 11, 321, 33
42, 234
Dinitrobromnaphthalene .
Br.(N02)2=a,a2; a,
C10H5Br04N2
....
143
Merz and Weith
B., 15, 2711
44, 343
„
,, =0,0,, ; a.2
;,
....
169-5
Labhardt
B., 12, 679
„
„ „
„
....
170-5
Merz and Weitl
B., 15, 2711
44, 343
Nitrodibromnaphthalene.
....
C10H6Br20,N
....
96-5-98
Guareschi
A., 222, 262
46, 842
„ (B., 16, 422
....
„
....
100-105
Canzoneri
G. I., 12, 424
44,67
..
....
„
....
116-5
Jolin
B. S. [2], 28, 515
44, 67
Nitrodibrom-a-naphthol .
....
C10H5Br203N
....
120-125
Biedermann
B., 6, 1120
Nitrobromnaphthalene .
Br.NO2=a1a2 ;
C10H6BrOaN
....
83-84
Guareschi
E. A. T. [2], 35
,.
» »
„
....
85
Jolin
B. S., 28, 515
„ (B., 10, 294
., =»
„
100
Guareschi
G. I., 7, 24
31, 713
» »
.> =?
„
....
122
„
„
M
„ (A., 222, 262
» =ft ; ai °r ft ; ai
„
122-5
„
E. A. T. [2], 35
46, 842
„ (B., 15, 528
.. = '
j>
127-5
„
G. I. [1881], 542
42, 735
»
„ =/3,a2
„
....
131
Meldola
47, 507
»
» =a2^i ;
„
....
131-132
Liebermann ane
B., 8, 1109 ; A.
29, 403; 31,
Scheiding
183, 262
606
Nitrosobrom-j3-naphthol ..
C10H6(NO).Br.OH
C10H6BrO.N
....
61-65
Canzoneri
G. L, 12, 424
44,68
Acetylbromisatin
C6H3Br.CO.CO.NAc
C10H6Br03N
....
170-172
Baeyer and (Eco
B., 15, 2096
44, 201
L 1
nimides
Nitrobrom-a-naphthol ..
OH.Br.NO2=a1/3la2 ;
J)
....
136 d.
Meldola
47, 501
»
„ =a1a,/31 ;
„
....
142
Biedermann
B., 7, 538
27, 802
,.
» »
JJ
....
142
Scheiding
B., 8, 1652
29, 713
Tribromoxylepidine
....
C10H6Br3ON
....
nf. 280
Comstock anc
B., 17, 1992
46, 1383
Konigs
Tribromethylphthalimide
fr. C6H4:(CO)2:NEt=1.2
C10H6Br302N
....
186-189 d.
Michael
B., 10, 1645
34, 70
?
(CO.CBr3).[C( : NH).CO2H]
C10H6Br303N
213 p.d.
Kronfeld
B., 17, 717
46, 715
=1.2
Nitrobromuaphthylamine
Br.NH2.N02=^iaia2
C10H7Br02N2
....
197
Meldola
....
47,500
a
„ =aia2/32 ;
„
....
200
Liebermann and
B., 8, 1109 ; A.,
29, 403 ; 31,
Scheiding
183, 260
606
Diacetoxydinitrobrorn-
(OAc),.Br.(N02)2=1.3.(?)3
C10H7BrOsN2
B., 16, 1101
135
Fevre
C. E., 96, 790
44,733
benzene
Ethyldibromisatin
C6H2Br0.CO.C(OEt):N
C10H7Br202N
«««•
87-89
Baeyer and (Eco-
B., 15, 2099
44, 202
L 1
nimides
=1.3.?.4
/3-Nitroso-a-naphtholdi-
....
J>
144-145
Fuchs
B., 8, 1022
29, 247
bromide
Cinchonic acid dibromide
C9H6Br2N.C02H
M
....
188 u. c.
Claus
B., 18, 1307
48, 908
Carboxy Initroph enyldi-
(CHBr.CHBr.C02H).NO2.
C10H7Br206N
....
d. 220
Low
B., 18, 949
48, 799
brompropionic acid
CO2H=1.2.4
a-Nitronaphthalene tetra-
C10H7.N02+Br4
C10H7Br402N
....
131
Guareschi
A., 222, 262
46, 842
bromide
0- » ,,
n
„
...»
142-143-5
„
„
n
y- » »
„
„
....
172-173
„
Methylbromcarbostyril ....
N.OMe.Br^a^.a., ;
C10HsBrON
....
93 •
Friedlander
B., 15, 1424
42, 1209
Bromoxyquinaldine
N.OH.Me.Br=a,a2/31/32 ;
n
....
258
Knorr & Antrick
B., 17, 2875
48, 274
Ethylbromisatin
C6H3Br.CO.C(OEt) : N
C10H3Br02N
.«••
107-109
Baeyer and (Eco-
B., 15, 2095
44, 201
i i
nimides
Acetamidonitrobrom-
CH2.CN).Br.NHAc.N03
C10H8Br03N3
190-191
Gabriel
B., 15, 1994
44,64
benzylcyanide
=1.3.4.5
Acetylbromisatic acid
C6H3Br.NHAc.(CO.CO2H)
C10HsBr04N
....
178-180
Baeyer
B., 15, 2096
44,201
Dibromisatoethyloxime
C6H2Br2.C(NOEt).C(OH) : N
1 1
C10H8Br202N2
dark 240
252
Baeyer & Com-
B., 16, 1709
44, 1131
Tribromacetamidoaceto-
CO.CHBr2).Br.NHAc
CloH8Br302N
185 d.
stock
Baeyer and Blorn
B., 17, 967
46, 1027
phenone
=1.3.6
Diacetamidotribrombenz-
Bra.NAc2=1.3.5.6
„
....
23
Remmers
B., 7, 350
27, 697
ene
Acetamidobrombenzyl-
CH2.CN).Br.NHAc=1.3.4
CIOH9BrON2
27-129
Gabriel
B., 15, 840, 1993
4,64
cyanide
Bromethylisindazolcarb-
MM
C10H9BrO2N..
10
TischerandTafel
A., 227, 303
8, 543
oxylic acid
COMPOUNDS CONTAINING FIVE ELEMENTS.
651
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Acetamidodib ronmaphth-
Br2.NHAc=/3 ; a^
C10H9Br2ON
....
221
Meldola
47, 514
alene
J5
» =a ; $2ai
))
....
221-222
»
....
47, 511
Etliylic dibromisatate
Br2.NH2.(CO.C02Et)=1.3.4
C10H9Br203N
....
105
Baeyer and CEco-
B., 15, 2099
44,202
nimides
Methylic nitrophenyldi-
N02.(CHBr.CHBr.CO2Me)
C10H9Br204N
— •
98-99
Baeyer
B., 13, 2258
40, 275
brompropionate
=1.2
Acetamidobromcinnamene
(OH : CH2).NHAc.Br=1.4.?
C10H10BrON
....
182-5
Gabriel & Herz-
B.,16,2043;C. C.
44, 1123 ; 48,
berg
[1884], 35
662
1
....
C10H10Br02N
....
125-126
Gabriel
B., 18, 2455
48, 1228
Acetamidobromaceto-
Ac.Br.NHAc=1.3.6
)?
....
160
Baeyer and Blom
B., 17, 965
46, 1026
phenone
Ethylic bromphenylox-
Br.(NH.CO.C02Et)=1.4
C10H10Br03N
....
154-156
Klinger
B., 8, 311 ; A.,
28, 1025 ; 31,
amate
184, 266
710
Acetamidobromphenyl-
(CH2.CO.iH).Br.NHAc
a
164-165
Gabriel
B., 15, 841
acetic acid
=1.3.4
Ethylic nitrobromphenyl-
(CH2.C02Et).Br.N02=1.4.5
G10H10Br04N
....
Liquid
Bedson
....
87,98
acetate
i) »
= ?
))
....
crystalline
11
....
37, 100
Ethylic nitrobromanisate....
CO2Et.OMe.Br.NO2= 1
C10H10Br06N
85
Balbiano
G. I., 14, 234
48, 530
Nitrophenylethoxydi-
N02.C6H4.[CH(OEt).CBr2.
C10H10Br206N2
....
98-99
Friedlander and
A., 229, 233
48, 1138
bromnitroethane
N02]=1.3
Lazarus
Dinitrobromisocymene
Me.Pr0.Br.(N02)2= ?
C10HuBr04N2
55
Kelbe
B., 15, 42
42, 619
Dinitrobromcymene
Me.Pr».Br.(NO2)2=1.4.6.(?)s
)J
97-98
Gerichten
B., 11, 1092
Ethylic bromphenamido-
Br.(NH.CH2.CO2Et)=1.4
C10H12Br02N
....
95-96
Dennstedt
B., 13, 238
38, 635
acetate
Nitrobromcymene
Me.Prf.Br.N02=1.3.6.?
)>
••«*
121
Kelbe
B., 15, 40
42, 619
Nitrotribromcamphor
....
C10H12Br303N
175
S warts
B., 15, 2136
44, 215
Nitro-/3-dibromcamphor ....
C10H13Br203N
124-126
Kachler& Spitzer
M. C., 3, 219
42,865
Nitrobromcamphor
....
C10H14Br03N
....
103
Cazeneuve
B. S. [2], 42, 69
48, 270
„
....
n
104-105
Schiff
G. I., 11, 21 ; B.,
38, 891 ; 40,
13, 1402
438
Brotn-a-naphthoamide
(CO.NH2).Br=ai?
CHH3BION
....
240-241
Hausamann
B., 9, 1518
31, 318
Nitrobrommethoxyuaph-
OMe.Br.N02=a1/3la2
CnH8Br03N
114-115
Meldola
...»
47, 502
thalene
Bromtarconin
A., 210, 84 ; 212, 197
))
235-238 d.
Gerichten
B., 14, 312
32, 535
Acetarnidobromquinoline
N.Br=aj;ft
CnH9BrON2
....
104-105
Coste
B., 15, 1921
44,91
Ethylic nitrodibromcin-
NOj.(CBr : CBr.C02Et)=1.4
CuH9Br204N
«...
85-86
Drewsen
A., 212, 157
42, 847
namate
Methylbromtarconinic acid
B., 15, 1459
CuH10Br03N
dark, 215
223
Gerichten
A., 212, 177
44,91
Ethylic a-nitrobromcin-
NO2. (C2HBr.C02Et) =1.4
CuH10BrO4N
....
63
Muller
A., 212, 132
42, 842
namate
Ethylic j3-nitrobromcin-
>» !)
)»
....
93
))
»
ii
namate
•.
Dibromethylquinazolcarb-
*.»
CuH10Br202N2
....
196
Fischer and
A., 221, 261
46, 442
oxylic acid ,
Kuzel
Bromethylquinazolcarb-
...
C11H11Br02N2
....
173d.
n
»
j)
oxylic acid
Ethylic nitrophenyldi-
N02.(CHBr.CHBr.C02Et)
C^HHETAN
....
71
Muller
A., 212, 130
42, 841
brompropionate
= 1.2
i) »
=1.4
1>
....
110-111
>j
A., 212, 129
»
i) »
» !!
»
...
110-111
Baeyer
B., 13, 2258
40, 275
)» »
» 11
11
113-116
Drewsen
A., 212, 154
42,846
Dibromtetrahydroquino-
C9H!)Br2N.C2H204
)»
....
171 u.c.
Claus and Istel
B., 15, 820
42, 1111
line oxalate
1
C10H9MeBrO2N
CuH12Br02N
114-115
Gabriel
B., 18, 2455
Acetaniidobromhydrociu-
(CH2.CH2.C02H).Br.NHAc
CuH12BrO3N
MM
159-5-160-5
),
B., 15, 2293
44, 195
namic acid
=1.3.4
Bromethoxy hyd roquino-
N.OEt=a!; a,
CnH13Br02N2
86
Fischer and
B., 17, 761
46, 1050
linenitrosamine
Kenouf
Bromethoxyhydroquino-
» >i
CuH14BrON
d. 150
44-5
,,
))
))
line
4 o 2
652
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Trinitrodibromdiphenyl ..
C6H3Br(N02).C6H2Br(N02)2
C12H6Br206N3
....
177
Lellmann
B., 15, 2838
44,343
Trinitrotribromazoxybenz-
ON2:C12H6Bra(N02)3
C12H6Br207N5
....
174
Werigo
A., 165, 192
26, 384; vii.,
ene
150
Tetranitrodibromdiphenyl
NH[C6H2Br(N02)2]2
C12HsBr.,O3Nb
....
167-5
Austen
A. J.S.[3], 13,279
32, 761
amine
.
» »
H
„
....
235
„
„
„
»> »
H
„
240
„
„
„
» »
()
B
242
H
„
» »
„
B
....
235-242
Gnehm
B., 8, 930
29,84
Bromnaphthalimide
C10H5Br:(CO)2:NH
CI2H6BrO2N
a. 265
Blumenthal
B., 7, 1095
Dinitrodibromdiphenyl ...
....
C12H6Br204N2
....
148
....
A., 132, 206; 174,
•
218
Dinitrotribromdiphenyl-
fr. NH(C6H3Br2)2
C12H6Br304N3
....
209-210
Gnehm and
B., 10, 1324
34,53
amine
Wyss
Trinitro-p-bromdiphenyl-
C,,H4(N02).C6H2Br(N02)2
C12H7Br06N4
....
157-5
Austen
B., 9, 920
30, 513
amine
Nitrodibromdiphenyl
C6H4Br.C6H3Br.NO2
C12H7Br2O2N
i.i*
127
Lellmann
B., 15, 2837
44, 343
=4.1 ; 1.4.?
1
Dinitrodibromdiphenyl-
fr. Ph.NH.C6H3(NO2)2
C12H.Br2O4N3
196
Leymann
B., 15, 1236
amine
Nitrobromphenol+dinitro-
(C6H3Br.OH.N03) [C6H2Br.
C12H7Brs08N3
»ii
60-65
Fittica
J. p. [2], 28, 176
46,55
bromphenol
OH.(N05)2]
Tribromresorcinolazo-
Ph.N2.C6Br3(OH)2=(?)4.3.1
C12H7Br3O2N,,
.»•
186
Typke
B., 10, 1578
34, 219
benzene
Tetrabromacetonaphth-
C10H3Br4.NHAc
C12H,Br4ON
....
138
Meldola
43,8
alide
Nitrobromdiphenyl
C6H4Br.C6H4.N02=1.4; 1.2
C12H8Br02N
360
65
Schultz
A., 174, 220
28, 149
„
n »
„
• i.*
65
Schultz & others
A., 207, 351
40, 911
„
=(1.4),
„
a. 360
173
Schultz
B., 7, 54 ; A., 174,
27, 468; 28,
218
149; vii., 938
Nitrobromethenylnaph-
N02.C6Hs.CBr : CH.C.N I
C12H8Br02N3
....
242
Prager
B., 18, 2163
48, 1239
thaleuediamine
1
CMe.NH.C
i
Dinitro-p-bromdiphenyl-
(WBKW
120
Austen
B.,9,920; A.J.S.
30, 513; 32,
Ph.NH.C6H2Br(N02)2
amine
(3), 13, 279
761
» "'• !>
C6H4Br.NH.C,H3(N02)2
„
***•
152-153
Willgerodt
B., 11, 602
34,570
=1.?; 1.2.4
Dibromazoxybenzene
ON2(C6H4Br)2=(1.3)2
C12H9Br2ON2
111-111-5
Gabriel
B., 9, 1405
31, 307
„
=(l-4)2
JJ
....
172
Hofmann and
B., 5, 919
26, 169; vii.,
Geyger
150
»
„ „
H
....
175
Werigo
A., 165, 189
26, 385
Nitrobromacetonaph-
NHAc.N02.Br=n1a201 ;
CI2H9Br03N2
224-225
Meldola
B., 16, 421
43, 9 ; 47, 499
thalide
H
=a1/31a2;
....
229
Biedermann
B., 7, 539
27, 802
It
» »
„
....
232
Lellmann and
B., 8, 1109; A.,
43,9
Scheiding
183, 260
Dibromacetonaphthalide ....
NHAc.Br2=/3(?)2
Cj.HgBr.pN
....
208
Lawson
B., 18, 2425
48, 1239
„
,, =«(?),
5)
225
Meldola
B., 11, 1906
36, 165
Leucodibromquinone-
C6H4(OH).NH.C8H2Br2.OH
C12H9Br2O2N
170
Mo'hlau
B., 16, 2848
46, 594
phenolimide
=1.4; l.(?)a.4
?
C12H9Br202N3
....
150
Werigo
A,, 135, 176
vi., 270
?
....
159
n
A., 135, 178
iv., 412
Bromacetonaphthalide ....
NHAc.Br=/3iai;
C,2H10BrON
134-135
Cosiner
B., 14, 59
40, 606
»
,. =3i«j;
„
....
186-5
Meldola
....
47, 509
»
» =aA;
jj
187
„
....
47, 510
,,
„ ^«jf
j?
190
Biedermann
B., 7, 538
27, 802
»
„ =aa
,, 1 p
192
Prager
B., 18, 2160
"
,, =a,?
>
B., 11, 1906
193
Bother
B., 4, 850
28,81; vii., 845
COMPOUNDS CONTAINING FIVE ELEMENTS.
653
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Bromcotarnine
....
CI2H12Br03N
100 d.
Wright
....
32, 531
Ethylbromtarconinic acid
....
„
....
223-225 d.
A., 212, 182
Dibromethylisatoethyl-
CfH2Br2.C(NOEt).C(OEt):^
C12H12Br20.,N2
....
115-116
Baeyer and Com
B., 16, 1710
44, 1131
oxime
stock
o-Nitrocumenyldibrom-
Pr.NO2.(C2H2Br2.C02H)=3
C12H13Br204N
....
171
Widmann
B., 17, 2282, 2283
48, 56
propionic acid
ni" » »j
„ „
H
....
184
Tribromhydrocotarnine
....
C12H13Br403N
....
190-200
Wright
....
32, 544
+HBr
Bromhydrocotarnine
MM
C12H14Br03N
...*
76 c. ; 78 c.
,(
....
32, 530, 534
+HBr
Isopropylnitrophenylbrom-
PrP.NO2.(CHBr.CH2.CO2H)
C12H14BrO4]Sr
....
127 d.
Einhorn and
B., 17, 2020
46, 1352
propionic acid
=4.2.1
Hess
Nitrobenzoyltribromnitro-
N02.C6H4.C02.C6HBr3.N02
C13H6Br304N
d. 215
129-2 c.
Daccomo
B., 18, 1168
48, 890
phenol
=1.2; 1.2. 4. 6.3
M
„ =1.3; 1.2.4.6.3
„
....
153-8 c.
H
„
JJ
Dibromphenylic nitro-
NO2.C6H4.CO2.C6H3Br2
C13H,Br204N
MM
90-100
List and Lim-
A., 90, 204
i., 556
benzoate
=1.3; (?)3
pricht
a-Dibromphenylpyridine-
....
H
....
204-205
Skraup & Cobenz
M. C., 4, 436
44, 1014
dicarboxylic acid
Benzamidodinitrobrom-
NHBz.Br.(NO2)3=1.4.(?)2
C13H8BrO5N3
195-196
Meinecke
B., 8, 565
28,900
beuzene
Dinitrobrombenzanilide ..
fr. NHBz.Br.NO2=1.4.6
)>
221
Hiibner
B., 10, 1710
34, 142
Beuzamidonitrodibrom-
NHBz.Br2.NO2=l.(2)2.2
C13H8Br2OsN2
....
194-195
)(
I)
benzene
Tetrabromcarbanilide
CO:N2H2(C6H3Br2)2
C13H8Br4ON2
sb. 230-235
Otto
B., 2, 410
Benzamidonitrobrombenz-
NHBz.Br.NO2=1.4.6
C13H9Br03N.,
....
137-138
Meinecke
B., 8, 565
28, 900
ene
•>
»
»
....
137
Hiibner
B., 10, 1710
34, 142
»
=1.2.4
.
160
B., 10, 1709
Benzamidodibrombenzene
NHBz.Br2=?
C13H9Br3ON
134
B., 10, 1710
Dibrompseudocinnamyl-
....
....
225
Ciamician and
B., 17, 2948
48, 378
pyrroline
Dennstedt
Benzyloxynitrodibrom-
benzene
(O.CH2Ph).Br2.NO2=1.2.4.6
(WBrAN
....
64-5 u.c.
Bx>ll and Holz
J. p. [2], 32, 56
48, 1209
„
„ =1.2.6.4
M
93-5
48, 1210
Dinitrodibrommethyldi-
fr. NMePh.C6H3(N02)2
C13H9Br204N3
....
194
Leymann
B., 15, 1236
42, 1057
phenylamine
Brombenzanilide
Br.(CO.NHPh)=1.4
C13H10BrON
197
Hiibner
B., 10, 1707
34, 149
Benzamidobrombenzene ....
Br.NHBz=1.4
202
Meinecke
B., 8, 564
28, 900
Brompseudocinnamylpyr-
....
MM
175-177
Ciamician
B., 17, 2948
48, 378
roline
Benzyloxynitrobrombenz-
(O.CHjPh).Br.N02=1.4.6
CJ3H10Br03N
83'5 u.c.
Roll and Holz
J. p. [2], 32, 56
48, 1209
ene
„
„ =1.2.4
125'5 U.C.
Benzybaitrobromphenol „..
OH.Br.CH2Ph.NO2=1.2.4.6
64-65
Eennie
41, 223, 224
Methylic bromphenoxy-
N.Br.OPh.C02Me=(?)2.1.4
183-5
Pechmann
B., 17, 2399
48, 176
nicotate
Dibromcarbanilide
CO(NH.C(1H4Br)2=(1.4)2
C13H10Br2ON2
w.m. 220-225
Otto
B., 2, 409
„
„
w.m. 225
•Jarauw
B., 15, 45
Hydroxydibrombenzyl-
idenephenylhydrazine
HO.C6H2Br2.CH : N2HPh
D
....
148
flossing
B., 17, 3009
48, 389
Dibromorcinolazobenzene
Ph.N3.C6Me.Br2.(OH)2
C13H10Br202N2
....
183
Typke
B., 10, 1580
34, 219
Benzdiamidobrombenzene
Dibromcarbanilidocyan-
methine
NHBz.Br.NH2= 1.2.4
CI3H11BrON2
C13H12Br2ON4
..»
205
238
liibner
Keller
B., 10, 1709
J. p. [2], 31, 363
34, 142
48, 961
Bromcarbanilidocyan-
methine
Ph.NH.CO.NH.C6H6BrN2
CuH13BrON4
....
90
n
..
,,
Ethylkairine bromide
Dinitrotetrabromanthra-
N.OEt=a, ; a,
C13H18BrON
C14H2Br406N2
....
5
05
Tischer & Renouf
Clausand Hertel
B., 17, 762
B., 14, 981
46, 1050
40, 738
quinone
€54
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dinitrodibromanthra-
....
C14H4Br206N2
....
239
Glaus and Diern-
B., 14, 1337
42, 523
quinone
fellner
Dinitrobromanthraquinone
....
G14H5Br06N2
....
213
»
B., 14, 1333
w
Nitrodibromanthraquinone
....
C14H5Br2O4N
245
ii
B., 14, 980, 1334
H
Nitrobromanthraquinone
....
C14H6Br04N
261
Glaus and Hertel
B., 14, 980
40, 738
Nitroamidodibromanthra-
....
C14H6Br204N3
....
180-183 u.c.
Glaus and Diern-
B., 14, 1337
42, 523
quinone
fellner
Amidodibromanthra-
....
C14H7Br2O2N
169-170
D
B., 14, 1334
D
quinone
Bromphenylphthalimide ...
C6H4:(CO)2:N.C6H4Br
C14H8BrO2N
....
203-204
Gabriel
B., 11, 2261
36, 324
=1.2; 1.4
Nitrobromphenanthrene ...
C6H4.CH : CBr.CfH3.NO2
»
195-196
Anschlitz
B., 11, 1218
34, 984
Di-p-bromdiphenyldicyan-
C14H8Br202N2
....
199
Dennstedt
B., 13, 229
ate
Diazoimidobrombenzoic
N3H(C6H3Br.C02H)2
C14H9Br204N3
147
Hubner
A., 222, 67
46, 316
acid
=(2.3.1),
Acetyltetrabromdiphenyl-
NAc(C6H3Br2)2
C,4H9Br4ON
....
157-158
Gnehm
B., 8, 928
29, 83
amine
Acetylbromcarbazole
C12H7BrN.Ae
C14H10BrON
....
128
Ciamician and
G. I. [1882], 272
42, 1104
•
Silber
Dinitrodibromdibenzyl ....
....
C14H10Br204N2
....
204-205
....
A., 137, 270
v., 871
Dibromapophylline
....
C14H10Br404N2
B., 15, 1251
229 d.
Gerichten
A., 210, 94
4S, 315
Dibromdiphenylbiuret ....
NH(CO.NH.C6H4Br)2
C14HnBr202N3
d. 280
w.m. 240
Dennstedt
B., 13, 230
38, 633
Dibromapophylline +HBr
....
Cu-Bu-BrtOJS,
begins d. 170
170-205
Gerichten
A., 210, 79
42,315
Bromacetamidodiphenyl ....
fr. Ph.C6H4.NHAc=1.4
C14H12BrON
....
247
....
A., 209, 345
Dibrom-p-azoxytoluene ....
....
C14H12Br.|ON2
....
138
Petrieff
B., 6, 557
26, 1027
Bromphenamidoacetbrom-
C6H4Br.NH.CH2.CO.NH.
u
ab. 145
161
Dennstedt
B., 13, 237
38, 635
phenamide
C6H4Br=(1.4)2
Bromazoxytoluene
C6H4Me.N2O.C,H3MeBr
C14HI3BrON2
74
Melms
B., 3, 552
vii., 1163
=1.4; 1.4.?
Diethylic nitrobenzoyl-
NO,.C6H4.CO.CBr(C02Et)2
C14H14Br07N
72
Bischoff & Each
B., 17, 2793
48, 264
brommalonate
=1.2
Diethylic dibromcollidine-
C8H7Br2(C02Et)2.NBr2
C14H17Br404N
....
102
ii
A., 215, 17 ; B.,
44,82
dicarboxylate dibromide
14, 1638
Diethylic dibromhydrocol-
C8H9Br2(C02Et)2.NBr2
C14H19Br404N
MM
88
i)
ii
ii
lidinedicarboxylate di-
bromide
Malontribromanilide
CH2(CO.NH.C6H2Br3)2
CI5H8Br602N2
145-146
Freund
B., 17, 782
46, 1123
=(1.3.5.6)2
Brombenzalphthalimidine
....
(\6H10BrON
«...
210-211
Gabriel
B., 18, 1260, 2435
48, 903
Nitrobromcinnamalde-
C6H4(NO2).CBr:C2H2:N2
C15H12Br02N3
120
Kinkelin
B., 18, 485
48, 791
hydephenylhydrazine
HPh=1.3
)> ii ••••
=1
)>
134
Zincke & Hagen
B., 17, 1817
46, 1344
u ii
=?
»
154
)!
B., 17, 1816
i)
Acetoxydibrombenzyl-
AcO.C6H2Br2.(CH : N2HPh)
C15H12Br202N3
188
Bossing
B., 17, 3008
48, 389
idenephenylhydrazine
=1.(?),2
Brombenzylamine carbon-j
(C6H4Br.CH2.NH3)2C03
C15H18Br203N2
....
95
Jackson & White
B., 13, 1219
38, 879
ate
=(1.2)2
>i 11 ••••
=(l-4)2
))
....
131-133
Jackson and
A. C. J., 3, 247
42, 170
Lowery
Benzeneazo-/3-naphthol
....
C16H9BrON2
....
160-161
Margary
G. I., 13, 438
46, 326
bromide
11 i)
....
»)
167-168
Zincke & Binde-
B., 17, 3032
wald
Nitro-|3-naphthaquinone-p-
O.N(C6H4Br).C10H4(OH).
C16H9Br04N3
....
245-246
Brauns
B., 17, 1136
46, 1038
bromanilide
N02
Brom-a-naphthaquinone-p-
O.N(C6H4Br).C1|0H4Br(OH)
C16H9Br202N
....
238-240
Baltzer
B., 14, 1901
42, 204
bronianilide
Brom-a-naphthaquinone-
anilide
O.NPh.C10H4Br.OH
%
C16H10Br03N
....
165-166
»
B., 14, 1902
42, 205
COMPOUNDS CONTAINING FIVE ELEMENTS.
655.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
a-Naphthaquinone-p-brom
O.N(C6H4Br).C10Hs.OH
C1BH10Br02N
....
266-269
Baltzer
B., 14, 1902
42, 204
anilide
Bromnaphthalene picrate
C10H7Br-fC6H2.OH.(N02)3
C16H10Br07N3
....
133
Wichelhaus
B., 2, 305
vi., 845
i3-Naphthaquinonehydr-
....
C16H10Br2ON2
215-219
Zincke & Binde-
B., 17, 3031
48, 392
azidedibromide
wald
Fr. nitrocinnamic acid
or C8H6BrO2N
C!6H10Br204N2
....
255
Morgan
B., 17, 222
46, 747
Brom-a-naphtholazobenz-
HO.C10H6.N2.C6H4Br
C16HnBrON2
....
185
Margary
G. I., 14, 271
48, 546
ene
=a . ; 1.4
» -°- n »
» »
„
195
„
M
„
Bromhydroxynaphtha-
see B., 17, 1813
C16H11Br02N2
....
196-198
Zincke & Thelen
B., 17, 1813
46, 1360
quinonehydrazine
Methylisatinbromtolyl-
C8H4MeNO.N.C6H3MeBr
C16H13BrON2
....
210
Meyer
B., 16, 2267
46,48
imide
=1.4; 4.1.3
Ethylic dibromdiphenyl-
C6H,Br.NH.CO.N(C6H4Br).
C16H14BrAN2
153
Dennstedt
B., 13, 229
38, 633
allophanate
CO2Et=(1.4)2
Dibromazodimethylquinol
fr. N2[C6H,(OMe)2]2
C16H16Br204N2
220
Baessler
B., 17, 2125
46, 1330
Dibromanisidine oxalate ...
OMe.NH2.Br2=1.2.4.6
C16H16Br406N2
....
147-148
Staedel & Damm
B., 11, 1750 ; A.,
36, 239; 44,
217, 55
663
» n
„ =1.4.2.6
J)
....
195 d.
n
„
„
Diphenyltartaramide
(.CPh(OH).CO.NH2)2+HBr
C16HI7Br04N2
....
185 d.
Burton
B., 16, 2233
46,63
+HBr
Diphenoxydiethylene-
NH2Br(C2H4.OPh)2
C^H^BrON
nf. 216
Weddige
J.p. [2], 24, 241
40, 1137
amine+HBr
Methylbromisato'ide
....
C17H10Br204Ns
....
230-231
Baeyer
B., 15, 2095
44, 201
Brom-a-naphthanilide
C10H6Br.(CONPh)=j31/32 ;
C17H12BrON
194
Miller
B. S., 43, 125
48, 667
Brom-a-tnethylnaphthalene
C10H5BrMe + C6H2(NO,,)3.
C17H12Br07N3
....
105
Scliulze
B., 17, 1528
46,1184
picrate
OH
,. -0- i, 5,
>» »
„
....
113
„
B., 17, 1529
„
Cinchonic acid benzyl-
NBr(CH2Ph).CO2H=a1|32 ;
C17HI4BrO2N
130 u.c.
Claus & Muchall
B., 18, 363
48, 561
bromide
Acetoxydibrombenzyl-
AcO-CsHjEryCH : N2AcPli
C!7H14Br203N2
158
Rossing
B., 17, 3010
48, 389
ideneacetphenylhydrazine
= 1.(?)2.2
Bromethoxyhydroquinoliue
N.OEt=ai; a.
C17H17Br08N4
107-108
Fischer &Renouf
B., 17, 761
46, 1050
picrate
Nitrobromphenol+ dinitro-
2C6H3Br.N02.OH+C6H2Br
CI8H11Br3011N4
....
68-70
Fittica
J. p. [2], 28, 176
46, 55
bromphenol
(N02).OH
Ethylbromisatoi'de
....
C18H12Br204N2
....
244-245
Baeyer
B., 10, 2095
2 (Nitrobrombenzene) +
(NO2)2.Br=1.3.4
C18H12Br208N4
65
Spiegelberg
A., 197, 259
36, 796
benzene
Fr. amidonaphthaquinon-
MM
C13H12Br402N2
....
237
Kronfeld
B., 17, 718
46, 1037
imide
Bromcode'ine
A., 77, 362
CuH^Brt^N
....
161-162
Gerichten
A., 210, 112
42, 312
Benzoyldibromdiphenyl-
NBz(C6H4Br)2=?
C19H13Br2ON
142
Lellmann
B., 15, 830
42, 1060
amine
Brom-o-ethoxyhydroethyl-
C13H18BrON+C6H2.OH.
C19H21Br09N4
...»
174
Fischer&Renouf
B., 17, 762
46, 1050
quinoline picrate
(N02)3
Tetrabromdiiniidophthal-
C6H4(CNH.C,H2Br2.OH).,
C20H12Br.02N2
A., 202, 114
a. 280
Baeyerand Burk-
B., 11, 1299
34, 866
e'in
hardt
Isobutylbromisatoide
....
C20H16Bra04N2
MM
210
Baeyer
B., 15, 2097
44. 202
Bromquinolinemethyloxide
C9H6BrNMe)20
C20H18Br2ON2
146-147
Coste
B., 15, 189
42, 980
Dibenzdiamidobrom-
Me.Br.(NHBz)2=U.2.4
C2lH17Br02N2
214
Kuhemann
B., 14, 2658
toluene
Fr. dibromstrychnine
....
C21H19Br02N2
....
216
Beckurts
B., 18, 1238
48, 911
CEiianthylidenedibrom-
....
C21H2,Br206N4
.„•
170
Medicus
A., 157, 44
24, 151
nitrobenzodiamide
Cinchonine methobromide
C.20H24ON2.MeBr
C21H27BrON2
dark, 245
265-269
21aus and Miiller
B., 13, 2291
40, 289
Quinine methobromide ....
C20H2402N2.MeBr
C2lH27Br02N3
....
124-126
Glaus &Mallmann
B., 14, 76
40, 619
Acetyldinitrodibromfluor-
C22H8Br2O1()N2
....
250
Baeyer
A., 183, 1
31, 204
escei'n
Cinchoninemethylethyl-
C19H,2ON2.MeBr.EtBr
C^oB^ON,
197
Dlaus and Miiller
B., 13, 2294
bromide
656
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Papaverine ethobromide ....
C21H21O4N.EtBr
C23H26Br04N
110-lllu.c.
Claus & Hiietlin
B., 18, 1577
48, 996
Isoamylbromanthraeene
C6H4:C2Br(C5H11):C6H4+
C^HjjBrOjNj
....
110
Liebermann and
B., 14, 795; A.,
40, 737; 42,
picrate
C6H2.(N02)3.OH
Tobias
212,1
863
Narcei'ne ethobromide
C^HjgOaN.EtBr
C25H34Br09N
....
165 u.c.
Claus & Eitzf eld
B., 18, 1570
48, 996
Dibenzdiamidodibromdi-
(.C6H3Br.NHBz)2
C26HlsBr202N2
195;r.m.99;
Lellmann
B., 15,2835,2838
44, 343
phenyl
r.s.125-130;
r.m. 195
Diphthalimidodibromdi-
[C6H4:(CO)2:N]2:(C6H3Br)2
C28H14Br204N2
....
300-301 u.c.
Gabriel
B., 11, 2262
36, 324
phenyl
? -acid ....
C28H17Br304(N02)4
C28H17Br3012N4
....
180
Fleischer
A., 144, 201
vi., 1087
Tetracetyltetrabromdiimi-
C6H4(CNAc.C6H2Br2.OAc)2
C28H20Br406N2
„..
241
Baeyer and Burk-
B., 11, 1299 ; A.,
34, 866
dophenolphthalei'n
hardt
202, 117
Br on k-nitrocamphor
....
C30H43Br2014N3
94-95
Schiff
G. I, 11, 21
40, 438
Diphenyldiisoindolazodi-
For constitution see B., 15,
C40H26Br402N6
....
198
Mb'hlau
B., 15, 2492
44,343
bromphenol
2495
Ethyloxide+antimony tri-
Et20+SbBr3
C4H10Br3OSb
begins 91
Liquid
Nickl6s
C. K., 52, 369
vi., 596
bromide
Bromallylthiocarbimide ....
C3H4Br.N : CS
C4H4BrSN
200
...
Henry
B., 5, 188
vii., 50, 1018
Bromallylthiocarbamide ....
NH2.CS.NH.C3H4Br
C4H7BrSN2
....
110-111
„
„
vii., 50
„
H
„
see next
146
Maly
B. S. [2], 8, 129
v., 782
Allylthiocarbamidedibrom-
NHyCS-NH-CaHsBrj
C4H8Br2SN2
see preceding
146-147
„
Z. C. [1867], 42
ide
Bromphenylthiocarbimide
C6H4Br.(N:CS)=1.4
C7H4BrSN
....
60-61
Weith & Landolt
B., 8, 716
28, 1194
Bromphenylthiocarbizine....
C7H6BrSN2
....
210
Fisher & Besthorn
A., 212, 331
42, 1095
Thioformamidobrombenz-
C6H4Br.(NH.CSH)=1.4
C7H6BrSN
189-190 d.
Dennstedt
B., 13, 236
38, 634
ene
Bromphenylthiocarbamide
NH2.CO.NH.C,H4Br=1.4
C7H7BrSN2
183
„
B., 13, 231
„
Brombenzylthiocyanate ....
Br.(CH,.SCN)=1.2
C8H6BrSN
....
?
....
A. C. J., 2, 316
....
„
=1.4
H
25
Jackson & Lowery
B., 10, 1212
34,64
Bromph eny Idithiourethane
C6H4Br.NH.CSaEt=1.4
C9H10BrS2N
...
89
Dennstedt
B., 13, 232
38, 634
Tliioacetanilide+EtBr ....
Ph.NH.CS.Me+EtBr
C10H14BrSN
....
130
Bernthsen
A., 192, 1
34, 791
Dibromdiphenylthiocarb-
CS:N.,H2(C6H4Br)2=:(1.4)
C13H10Br2SN3
sb. 200
178
Otto
B., 2, 409
arnide
Bro mdiphenylthiocarb-
Br.(NH.CS.NHPh)=1.4
C13HnBrSN2
....
158
Dennstedt
B., 13, 231
38, 634
amide
Methyleneiodophenyl-
Ph.S02.CH2I
C7H7IO2S
64-5
Michael & Palmer
A. C. J., 6, 253
48, 536
sulphone
lodotoluenesulphonic acid
Me.I.S03H=1.2.?
C7H7IO3S
....
L. 0
Mabery & Palmer
A. C. J., 6, 170
48, 539
„ „
=1.4.?
1)
• *••
crystalline
Glassner
B., 8, 561
Tolylsulphonethyliodide ....
C6H4Me.S02.C2H4I=1.4
C9HUI02S
....
100
Otto and Dam-
J. p. [2], 30, 321
48, 538
kOhler
Tetriodoxysulphobenzide....
S02(C8H2L,OH)2
C12H6I404S
B., 9, 1150
260-270 d.
Annaheim
A., 172, 44
27, 796
Diiodoacetamide (A., 117,
CHI2.CO.NH2
C2H3I2ON
yellow 170 ;
201-202 ; sf.
Curtius
B., 18, 1286
48, 884
356)
sb. 185-190
198
Iodoacetamide(Z. C. [1871],
CHjI.CO.NHj
C2H4ION
....
157-158
Henry
C. R, 100, 114
48, 373
5)
/J-Iodopropionamide
CH2I.CH2.CO.NH2
C3H6ION
100-101
B
;)
);
lodosuccinimide
CH2.CH2.CO.NI.CO
C4H4IO2N
d. 100
135 d.
Bunge
As., 7, 128
vi., 1043
Trinitroiodobenzene
C6H2I(N02)8
C6H2I06NS
164
Hepp
A., 215, 361
44, 316
D i nitroiodobenzene
I.(N02)2=1.2.4
C,H3I04N2
J. [1875], 322
88-5
Kbrner
G. I., 4, 305
29, 211
,.
„ =1.2.6
1137
B
„
Dinitroiodophenol
OH.I.(N02)2=1.2.4.6
C6H3I05N2
51
106
Armstrong
B., 6, 651
vii., 916, 929
„
" i>
„
....
106
Post
B., 7, 336
27, 800
(Z. C. [1863], 325)
»
" I!
»
....
108
Weaelsky
A., 174, 111
vii., 917, 929
COMPOUNDS CONTAINING FIVE ELEMENTS.
657
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dinitroiodophenol
OH.I.(NO2)2=1.4.2.6
C6H3I06N2
J. [1875], 340
112-9
Korner
G. I., 4, 305
29, 231
»
»i n
»
....
113
Armstrong
B., 6, 650
vii., 917, 929
»
» j)
)>
113
Post
B., 7, 336
27, 800
Nitrodiiodobenzene
L,NO2=1.3.4
C6H3I202N
J. [1875], 325
168-4
Korner
G. I., 4, 305
29, 222
Nitrodiiodophenol
OH.I2.NO2=1.2.4.6
C6H3I203N
....
98
J!
J. [1867], 617
vi., 915; vii., 929
(cf.vii.,916)
„ =1.2.6.4
»
154-155
Busch
B., 7, 462
27, 802
,, .... ....
» i)
»
A., 174, 108
156-5
Korner
J. [1867], 617
vi., 915; vii., 929
„ (Z.C. [1868], 324)
» )>
>i
A, 205, 91
157-158
Post and Bracke-
B., 7, 168
27, 476; vii., 923
busch
Nitroiodobenzene
I.N02=1.3
C6H4I02N
290
Liquid
Schutzenberger
E. [1862], 144 ;
vi., 269
-
and Segenwald
J. [1862], 251
5, ....
» »
11
....
34
Griess
J. [1866], 457 ;
vi., 921 ; vii.,
Z. C. [1866], 21
138
» .... ....
»» i»
1)
....
35-36
Kichter
B., 4, 553
24, 824
„
)> )>
)1
J. [1879], 388
36
Korner
G. I., 4, 305
29, 234
» .... ....
» =1-2
M
J. [1875], 321
49-4
j»
JJ
29, 211
j, ....
„ =1.4
1)
....
171
KekuM
A, 137, 168
vi., 269
,, .... ....
» 11
)J
....
171-5
Griess
Z.C. [1866], 218,
vi., 921 ; vii.,
J. [1866], 457
138
j, ....
)» »
»»
J. [1875], 320
171-5
Korner
G. I., 4, 305
29, 211
Nitroiodophenol
OH.I.NO2=1.2.6
C6H4I03N
....
66-67
Hiibner & Busch
B., 7, 462
27, 801
,, .... ....
„ =1.?.6
M
....
90-91
»j
»
vii., 917, 929
„
„ =1.2.4
>!
J. [1867], 616
93
Korner
Z. C. [1868], 324
vi., 914
»
)> »
))
....
93
Post
B., 7, 333
27, 800
„ .... ....
„ =1.2(?).6
)>
....
109-110
Armstrong
....
vii., 917, 929
(?)
„ =1.2.4
»
cf. vii., 916
154-155
Hiibner & Busch
B., 7, 462
27, 802; vii.,
916, 929
Nitrodiiodoaniline
NH2.I2.NO2=1.2.4.3
C6H4I202N2
....
145-5
Michael & Norton
B., 11, 113
34, 406
„
=1.2.6.4
)»
....
243-244
»
B., 11, 114
34, 407 ,
Nitroiodoaniline (?)
NH2.I.N02=1.?.3
C6HjI02N2
....
85-95
»
B., 11, 113
))
»
=1.2.4
)»
....
105-5
j)
B., 11, 114
)>
»j •••• ••••
=1.4.6
»
....
122
?j
B., 11, 109
J)
»
=1.3.6
JJ
J. [1875], 353
nf. 220
Korner
G. I., 4, 305
29, 222
Nitroiodobenzoic acid/3- ....
CO2H.I.NO2=1.3.?
C7H4I04N
....
174
Grothe
J. p. [2], 18, 326
36, 377
,, ,, y- -
=1.3.?
n
....
192
»
»
»
» »
„ =1.4.5
n
....
210
Glassner
B., 8, 562
28, 888
,, » «- -
=1.3.?
»
....
220
Cunze & Hiibner
A, 135, 111
vi., 316
„ „ a- ...
11 !>
»
235
Grothe
J. p. [2], 18, 325
36, 377
Nitroiodosalicylic acid
CCXH.OH.I.NO.^l.^?),,
C7H4I05N
....
1
....
A., 174, 108
» »
=1.2.5.3
»
204
Hiibner
B., 12, 1347
36, 928
» »
=1.3.(?)2
»
....
?
....
A., 174, 109
!) »
=1.4.(?)2
i)
..,,
7
....
A, 174, 110
Dinitroiodotoluene
Me.I.(N02)2=1.4.(?)2
C7H5I04N2
137-138
Glassner
B., 8, 561
27, 897
Dinitroiodocresol
OMe.I.(N02)2= ?
C7H6I06N2
75
Heynemann
Z. C. [2], 6, 402
vii., 1178
Nitrobenzyliodide
NO2.CH2I=1.2
C7H6I02N
75
Kumpf
B., 17, 1074
46, 1005
j, ....
„ =1.4
ij
....
127
»
)>
»
Nitroiodotoluene
Me.I.NO2=1.3.?
»
....
Liquid
Beilstein
Z. C. [2], 3, 102
vii., 1166
» ....
=1.4.5
)>
....
55-56
Heynemann
A., 158, 344
24, 682
»
=1.4.6
)1
286 d.
60-5-61
jj
A., 158, 337 ;
24, 681 ; vii.,.
Z. 0. [2], 6, 402
1167
„
=1.3.?
))
....
98-99
Beilstein
Z. C. [2], 3, 102
vii., 1166
i)
=1.2.2
))
....
103-104
Heynemann
A, 158, 347
24, 682
i) ....
=1.3.?
)>
....
108-109
jj
A., 158, 350
a- Amidoiodobenzoic acid ....
C02H.I.NH2=1.3.2 or 6
»
137
Grothe
J. p. [2], 18, 326
36, 377
$- J! » ••••
„ =1.3.6 or 2
»
209 d.
»
J. p. [2], 18, 327
))
lodethoxytrinitrobenzene
(O.C2H4I).(N02)3=1.2.4.6
C8H6I07N3
...
69-5
Andrews
B., 13, 244
38, 619
Acetamidoiodobenzene ....
NHAc.I=1.4
CSHSION
....
181-5
Michael & Norton
B., 11, 108
34, 406
Hydrotropine iodide
....
C8H16ION
....
115
Ladenburg
A., 217, 74
44, 672
Diiodohydroxyquiuoline ....
CsNHJ.j.OH
C9HSI2ON
....
205
Ostermeyer
C. C. [1884], 937
48, 673
lodocarbostyril
N-OKfea^a., ;
C9H6ION
276
Baeyer & Blb'm
B., 15, 2149
44, 196
Etkylic j3-nitroiodobenz-
CO2Et.I.NO2=1.3.6 or 2
C9H3I04N
...i
64
Grothe
J. p. [2], 18, 326
36, 377
oate
4 t
658
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Ethylic a-nitroiodobenz-
CO2Et.I.NO2=1.3.2 or 6
C9H6I04N
84
Grothe
J. p. [2], 18, 325
36, 377
oate
lodohydroxycyanconine ....
C9H12IN2.OH
C9H13ION2
....
157
Eiess
J. p. [2], 30, 145
48, 236
Piperpropylalkine meth-
C8H17ON,MeI
C9H20ION
....
142
Laun
B., 17, 680
46, 1054
iodide
Valerobetame iodide
C8HnO2.NMe3I
C9H20IO2N
....
191 d.
Korner & Menozzi
G. I., 13, 351
46, 425
Nitroiodonaphthalene
I.N02=/31a1 ;
C10H8I02N
....
88-5
Meldola
....
47, 519
11
,. =°,s,;
„
....
108-5
„
....
„
11
„ =0^2 ;
„
....
123
„
....
47, 519, 523
Nitroiodonaphthol
OH.I.NO2=a2a!i32 ;
C10H8I03N
....
145-146
„
....
47, 524
Cinchonic acid diiodide ...
C9H6I2N.CO2H
C10H7I202N
d. 200
242 d.
Glaus
B., 18, 1308
48, 908
Methylphenylethylalkine
NPhMe(C2H4.OH).MeI.I4
C10HI8I6ON
....
87 d.
Laun
B., 17, 677
46, 1011
methoperiodide
Dimethoxybenzenetri-
(OMe)2.NMe3I=1.45
CHH1SI02N
....
202
Baessler
B., 17, 2122
46, 1329
methylammonium iodide
Diiodoazoxybenzene
ON2(C6H4I)2=(1.3)2
C12HSI2ON2
....
crystalline
Gabriel
B., 9, 1410
31, 307
11
=(1.4),
„
....
199-199-5
„
B., 9, 1408
„
Nitroiodacenaphthalide ....
NHAc.I.N02=a2a1/32 ;
C12H9I03N2
....
235-236
Meldola
....
47, 523
lodacenaphthalide
NHAc.I=aiai ;
C12H10ION
196
„
j,
Ethylic collidinecarboxy-
C5HNMe3.C02Et+MeI
C12H18I02N
....
128
Michael
A., 225, 121
48,62
late methiodide
Benzamidodiiodobenzene ....
NHBz.Ia=1.2.4
C,3H9I2ON
181
Rudolph
B., 11, 81
34, 423
Benzamidoiodobenzene ....
NHBz.I=1.2 (?)
C13H10ION
....
180
Hiibner
B., 10, 1717
34, 143
„
„ =1-4 (?)
„
....
210
„
B., 10, 1718
lodophenylphthalimide ....
c6H4:(co)s:N.c8H4i
C14H8I02N
227-228
Gabriel
B., 11, 2261
36, 324
=1.2; 1.4
Harmine methiodide
C13H12ON2.MeI
CI4H16ION2
dark 282
298
Fischer & Ta'ube
B., 18, 402
48, 820
Harmaline methiodide ....
C13H14ON2.MeI
C14H17ION2
...i
260
„
B., 18, 405
48, 821
Diethylic collidinedicarb-
C5NMe3(C02Et)2+HI
C14H20I04N
....
170 d.
Hautzsch
A., 215, 1
44,83
oxylate+HI
+MeI
C6NMe3(C02Et)2 4- Mel
C16H22I04N
....
138
„
A., 215, 25
„
11 11
„
„
d. 160
140
„
B., 17, 1021
46, 1045
Dimethamidobenzophenone
C6H4Bz.NMe3I
C18H19ION
A., 210, 269
181 d.
Dobner & Weiss
B., 14, 1836
48, 176
+MeI
Nitrosodimethaniline tri-
2[C8H4(NO).NMe2]I3
C16H20I302N4
115-5
Dafert
M. C., 4, 496
44, 978
iodide
Campherethylimidethyl-
C18H14.C(NEt).NEt.CO+EtI
C H ION
244-245 d.
Wallach and Ka-
B., 14, 163; A.,
40, 285
i i
imidme ethiodide
menski
214, 246
Ethylicphenyllutidinecarb-
C5NHPhMe2.CO2Et+MeI
C17H2UI02N
sf. 200
205-206 d.
Hantzsch
B., 17, 2914
48, 398
oxylate methiodide
Tolufurfuraldehydine
C17H14O2N2+MeI
C1SH17I02N2
in*
195-5 d.
Ladenburg
B., 11, 1658
36, 234
+MeI
+MeI3
C17H1402N2+MeI3
C18H17I302N2
MM
126-128
„
„
B
+MeI5
C17H1402N2+MeI6
C1SH17I602N2
•«*•
109
„
„
n
Homocinchonidine meth-
C19HaON3+MeI
C.ft.ION,
A., 90, 221
248 d.
Glaus and Bock
B., 13, 2192
40, 184
iodide
Methylcinchonine periodide
....
C20H25I3ON2
....
90-92
Jb'rgensen
J. p. [2], 3, 145
vii., 340
Nitrosodiethaniline tri-
2[C8H4(NO).NEt2]2I3
C20H2SI302N4
....
118
Dafert
M. C., 4, 496
44, 978
iodide
Methylcinchonine meth-
C.oH24ON2.MeI
C2iH27ION2
• ...
201
Glaus and Miiller
B., 13, 2293
40, 289
iodide
Cinchonidine methiodide.. .
„
„
245-255 d.
Glaus and Dan-
B., 13, 2188
40, 183
nenbaum
Homocinchonidine eth-
C19H22ON2.EtI
11
B., 14, 47
261 d.
Glaus
B., 11, 1821
36, 168
iodide
Quinine methiodide
C20H2402N2.MeI
C31H27I02N2
d. 210-215
233-236 d.
Glaus and Mall-
B., 14, 76
40, 619
mann
Methylcinchonine triiodide
C20H24ON2.MeI3
C21H27I3ON2
161-162
Jbrgensen
J. p. [2], 3, 145
vii., 340
Methylquinine „
C20H2402N2.MeI3
C^H^I^N.,
159-160
B
B
M
Methylquinidine „
J)
n
....
164-165
J. p. [2], 3, 153
Papaverine methiodide ...
C21H2104N.MeI
C22H24I04N
....
80 u.c.
Glaus & Huetlin
B., 18, 1577
48, 996
1
COMPOUNDS CONTAINING FIVE ELEMENTS.
659
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Cinchonidine ethiodide ....
C20H24ON2.EtI
C22H29ION2
...»
249 d.
Glaus and Dan-
B., 13, 2188
40, 183
nenbaum
Quinine ethiodide
C20H24O2Nj.EtI
GaHalOiN,
A., 91, 163
210-211 d.
Glaus and Mall-
B., 14, 78
26, 1180
mann
Methylquinine methiodide
C20H23MeO:!]Sr2.MeI
0
....
215-218
i)
B., 14, 80
Cinchonine ethtriiodide ....
C20H24ON2.EtI3
C^H^IjON,
....
141-142
Jb'rgensen
J. p. [2], 3, 152
vii., 340
Quinine „
C20H2402N2.EtI3
v-'22-t*-29-^3^2-^' 2
....
150-151
ii
ii
J)
Cinchonine dimethiodide ..
C20H24ON'2.2MeI
CrfH^ON,
brown 210
235 d.
Glaus and Miiller
B., 13, 2293
40, 289
Quinine dimethiodide
C20H2402N2.2MeI
OsjHjoIjOjNj
brown 140
140-160 d.
Claus& Mallmann
B., 14, 77
Papaverine ethiodide
C21H21O4N.EtI
C23H26I04N
216
Glaus & Hue'tlin
B., 18, 1577
48, 996
Ethylhomocinchonidine
C19H21EtON2.EtI
C.H»IONt
....
236
Glaus
B., 11, 1823
36, 169
ethiodide
Homocinchonidine dieth-
C19H22ON2.2EtI
C.ftAPN,
....
255 d.
»
B., 11, 1824
i)
iodide
Quinine methiodethiodide
C20H24O2N2.MeI.EtI
CjBHjjIjOjNa
MM
157-160 d.
Glaus & Mallmann
B., 14, 77
Quinine ethiodmethiodide
)J
H
206-208 d.
ii
B., 14, 78
Brucine methiodide
C23H2604N2.MeI
C24H29I04N2
....
270
Hanssen
B., 17, 2267
48,64
Tri (nitrosodimethaniline)
3(C,H4.NO.NMe2)Is
C24H30I203N6
123-5
Dafert
M. C., 4, 496
44, 978
diiodide
Narce'ine methiodide
C23H2909N.MeI
C24H32I09N
.**•
173d.
Claus & Eitzfeld
B., 18, 1571
48, 996
Ethylcinchonine ethiodide
C20H23EtON2.EtI
C^H^ION,
....
242 d.
Glaus and Kem-
B., 13, 2288
40, 289
perdick
Ethylcinehonidine ethiod-
n
i)
....
257 d.
Claus and Dan-
B., 13, 2191
40, 183
ide
nenbaum
Cinchonine diethiodide ....
C20H24ON3.2EtI
C34H34I2ON2
....
264 d.
Claus and Kem-
B., 13, 2288
40,289
perdick
Quinine diethiodide
C20H2402N2.2EtI
C21H34I202N3
....
115
Skraup
M. C., 2, 611
42. 219
p-Nitrotetramethdiamido-
C6~H4.NO2.[CH(C6H4.NMe2)2]
Cj.HaJjOjN,
....
220 d.
Fischer
B., 14, 2526
42, 393
triphenyhnethane di-
+2MeI
methiodide
m- » i)
» )»
1)
....
225
Fischer & Ziegler
B., 13, 672
38, 662
Malachite green methiod-
Ph.qOHXCeH^NMe.,),.
C25H32I2ON2
B., 15, 236
171-172 d.
Do'bner
B., 13, 2225 ; A.,
40, 165
ide
2MeI
i
217, 254
Dimethanilinephthalem di-
C6H4(CO.C6H4.NMe2)2.2MeI
C^IO^
....
185 d.
Fischer
A., 206, 95
40, 588
methiodide
Tri(nitrosodiethaniline)
3(C6H4.NO.NEt,)Is
C80H42IAN6
MM
127
Dafert
M. C., 4, 496
44, 978
diiodide
Phenoxydiphenylmethyl-
PMePh2I.OPh
C19H18IOP
s.d. 131
134-136
Michaelis and
B., 18, 2116
48, 1215
phosphonium iodide
Coste
Tetrahydroxyamylidene
(C6H10.OH)4PI
CJLJ.OP
....
119
Girard
A. C. [6], 2, 1 ;
46, 1119
phosphonium iodide
C. E., 94, 215
Benzarseniodide
AsI2.(C6H4.CO2H)
C7H5I2O.,As
153
Coste
A., 208, 13
40, 904
Dibenzarseniodide
AsI.(C6H4.CO!!H)J
C14H10I04As
....
a. 280
ii
A., 208, 24
40, 905
*
Methylthiocarbamide+HI
NH2.CS.NHMe+HI
C2H7ISN.,
b. 100
Bernthsen and
B., 11, 493
34, 569
Klinger
Thiocarbamide -f-Mel
....
»
....
117
1!
B., 11, 493
ii
Allylthiocarbamide+I2 ....
C3H5.NH.CS.NH2+ .s
C4H8I2SN2
....
90 d.
Maly
Z. C. [2], 5, 258
vi., 1088
Me thy Ithiocyanopropim in e
SCN.CH2.CMe : NMe-pHI
C5H9ISN2
157
Tscharniac and
C. B., 96, 494
44, 568
+HI
Norton
Allylthiocarbamide+Etl
C3H5.NH.CS.NH2+EtI
C6H13ISN2
A., 94, 103
72
J. [1869], 259
lodophenylthiocarbimide ....
C,H4I.(N:CS)=1.4
C7H4ISN
65
Losanitsch
B., 5, 158
lodobenzylthiocyanate ....
C6H4I.(CH2.SCN)=1.4
C8H6ISN
40
Mabery and
B.,11,58;A.C.J.,
34, 422
Jackson
2,250
Methenylamidothiophenol
C6H4.N:CH.S+MeI
C3H8ISN
....
210
Hofmann
B., 13, 16
38, 388
+MeI
Thiacetophenamide + Mel
Me.CS.NHPh+MeI
C9H12ISN
139
Bernthsen
A., 192, 1
34, 791
Ethylene phenyldithiocarb-
NPh-CIlSMeJ-CHj-CHj
C10H12IS2N
....
149
Will
B., 15, 346
amate+Mel
4 p 2
660
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Gh. Soc.
Ethylene p-tolyldithiocarb-
N(C6H4Me).CI(SMe).S.C.H4
CUH14IS2N
....
107
Will and Biel-
B., 15, 1318
amate+Mel
schowski
)i 0- „ „
....
)>
....
151
»
»
42, 1091
Diiododiphenylthiocarb-
CS(NH.C6H4I)2=(1.4)2
C13H10I2SN2
....
173
Losanitsch
B., 5, 158
amide
Phenylimidophenylcarb-
NPh : C(NHPh).SEt+HI
C16H17ISN2
....
157-5
Bernthsen and
B., 15, 567
42,966
aminthiethyl + HI
Friese
Thiocyanocarbonic acid ....
SNC.COjH
C2H02SN
43
Henry
J. p. [2], 9, 464
28, 58
Methylio thiocarbamate ....
NH2.CS.OMe
C2HSOSN
43
Salomon
J. p. [2], 8, 115
27, 362, 363
Methylic carbaminethion-
NH2.CO.SMe
)J
....
95-98
Blankeuhom
J. p. [2], 16, 358
34, 215
ate
Dinitrodimethylsulphon-
fr. SO2(NHMe)2
C2H606SN4
d. 160
90
Franchimont
0. C. [1885], 384
48, 970
amide
Ethylsulphonamide
Et.SO2.NH.2
CjHyOjSN
....
58 u.c.
James
J. p. [2], 26, 384
43, 43
Dimethylsulphamic acid ....
NMe2.SO3H
C2H703SN
....
165 d.
Behrend
B., 15, 1613
42, 1282
Isethionamide
HO.CH2.CH2.SO2.NH2
j»
B.. 12, 1605
190-193
Seyberth
B., 7, 392
27, 790 ; 38, 28
Amidoisethionic acid
NH2.CH2.CH2.SO3H
»
....
a. 360
Dittrich
J. p. [2], 18, 63
36, 226
(Taurine)
Dimethylsulphoxide
Me2SO+HNO3
C2H704SN
....
100
Saytzeff
A., 144, 148
vi., 827
nitrate
Dimethylsulphonamide ....
NHMe.SO2.NHMe
C2H8O2SN2
....
78
Franchimont
C. C. [1885], 384
48, 969
»
NMe2.S02.NH2
))
....
96-96-5
Behrend
B., 15, 1611
42, 1282
Ammonium isethionate ....
HO.CH2.CH2.SOSNH4
C2H9O4SN
130
Strecker
....
vii., 705
)i »
»
>»
....
135
Seyberth
B., 7, 391
27, 790
Acetyl thiocyanate
Me.CO.SCN
C3H3OSN
131-132
Liquid
Miquel
C. R, 81, 1209
29, 570
)» )> ••"
))
»
133-133
Liquid
»
A. C. [5], 11, 295
32, 869
Khodaninic acid
HS.CH2.CO.S.CN
CSH3OS2N
B., 12, 1594
168-170
Nencki
J. p. [2], 16, 4
Thiocarbimidacetic acid ....
CS : N.CH2.C02H
C3H302SN
B., 14, 734
b. 100
Volhard
J. p. [2], 9, 6
27, 574
)) !>
»
»
B., 12, 1594
125-126
Claesson
B., 10, 1353
34,39
» »
)I
))
128
Nencki
J. p. [2], 16, 1
32,873
Thiocyanacetic acid
NC.S.CH2.C02H
M
+|H20
149 d.
Claessou
B., 14, 731
Thiocyanuracetic acid
»
or triple
199-5 d.
)»
B., 10, 1346;
polymer
14, 733
Glycolylthiocarbamide
NH.CS.NH.CH2.CO or
i i
C3H4OSN2
B., 8, 1264 ;
200 d.
Richter
E. K. T., 39 ; B.,
(Thiohydantom) (A., 166,
10, 824, 1352,
12, 1593 ; 13,
383 ; 168, 133)
NH : C.S.CH2.CO.NH
1853; 12, 972,
788, 1422 ; M.
1385
C., 1,442; A.,
207, 121
Methylic thioxamate
NH2.CS.C02Me
C3H6O2SN
MM
86
Weddige
J. p. [2], 10, 200
28, 448
Carbaminethioglycollic acid
NH2.CO.S.CH2.CO2H
C3H503SN
....
132-134
Claesson
B., 10, 1350
34,38
ii »
»
»
• •*.
142-143
Nencki
J. p. [2], 17, 69
34, 663
>» »
»
»
MM
143
»
J. p. [2], 16, 11
32,873
Acetylthiocarbamide
NH2.CS.NHAc
C3H6OSN2
....
11 '5 u.c. (sic)
»
B., 6, 599
26, 1130
i, ....
»
)J
165 (sic)
Nencki & Leppert
B., 6, 905
Ethylic thiocarbamate
NH2.CS.OEt
C3H7OSN
A., 75, 128
36
Debus
A., 72, 11
v., 492
(Xauthamide)
» »
5J
»)
A., 82, 262
38
Salomon
J.p. [2], 8, 115
27, 362
Ethylic isothiocarbamate....
NH2.CO.SEt
)J
....
102
Pinner
B., 14, 1083
40, 811
i> u
)J
))
....
108
....
J. p. [2], 7, 257 ;
10, 32 ; 16, 375
Methyltaurine
NHMe.CH2.CH2.S03H
C3H903SN
241-242
Dittrich
J. p. [2], 18, 63
36, 225
Taurocyamine
C2H4(CH4N3).SO2H
C3H9O3SN3
• it.
224-226
»
J. p. [2], 18, 76
36, 226
Taurogly cocy amin e
NH : C(NH2).NH.CH.,CH2.
»
....
260
Engel
B., 8, 1597
S03H
Dinitrothiophene
C4SH2(N02)2
C4H204SN2
290 p.d.
52
Meyer & Stadler
B., 17, 2649
48, 141, 250
„ ....
....
»!
....
75-76
»
B., 17, 2650
J)
,,
)>
78
Stadler
B., 18, 530
48, 764
Nitrothiophene (B., 18,
C4SH3.NO2
C4H3O.,SN
224-225 c.
44
Meyer & Stadler
B., 17, 2649
48, 141
533)
Nitrothienol
C4SH2.OH.N02
C4H3O3SN
....
115-116
Stadler
B., 18, 2319
48, 1205
COMPOUNDS CONTAINING FIVE ELEMENTS.
661
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Nitrothiophenesul phonic
C4SH2.NO.,.SO3H
C4H30SS2N
....
d.
Stadler
B., 18, 534
48, 764
acid
Methylthioparabanic acid
CS.NMe.CO.CO.NH
C4H402SN2
....
105
Andreasch
B., 14, 1448 ;
40, 897
i i
M. C., 2, 278
Nitrothiophenesulphon-
C4SH2.NO2.(SO2.NH2)
C4H4O4S2N2
....
172-173 u.c.
Stadler
B., 18, 536
48, 764
amide
Ethylic thiocyanocarbonate
NC.S.C02Et
C4H502SN
160-210d.
41
Henry
J. p. [2], 9, 464
28, 57
Thiodiglycollimide
....
)»
...*
128
Schulze
Z. C. [1866], 182
v., 777
a-Thiophenesulphonamide
S.(S02.NH2)=1.2
C4H503S2N
....
141
Meyer and Kreis
B., 16, 2173
46, 46
!)
» »
»>
....
142
Langei'
B., 17, 1568
46, 1133
/3-
=1.3
»
....
147-148
»j
B., 18, 562
»
JJ ))
»
....
148
»
B., 17, 1568
46, 1133
Thiophenedisulphonamide
S.(SO2.NH2)2= ?
C4H604S3N2
....
142
»)
B., 18, 561
48, 766
»
»J )»
»
....
213
Jakel
D
))
» »
»
black 240
280 d.
Langer
B., 18, 556
48, 766
Ethylic thioxamate
NH2.CS.C02Et
C4H7O2SN
....
63
Weddige
J. p. [2], 9, 133
27, 567
Methylic carbamiuethio-
NH2.CO.S.CH2.CO2Me
C4H703SN
....
75-80
Claesson
B., 10, 1351
glycollate
Thiodiglycollamic acid ...
....
n
....
125
Schulze
Z. C. [1866], 183
v., 776
Thiocyanopropimine nitrate
SCN.CH2.CNHMe+HN03
C4H703SN4
....
183
Tscherniac and
C. E., 96, 494
44,568
Norton
Ethylic dithioallophanate
NHj.CS.NH.CS.OEt
C4H8OS2N2
170-175 d.
Blankenhorn
B., 10, 446 ; J. p.
32, 424; 34,
[2], 16, 361
215
Ethylic thioallophanate ...
NH2.CO.NH.CS.OEt
C4H8O2SN2
....
180 d.
Peitsch and
J. p. [2], 7, 477
27, 364
Salomon
Dithioglycollamide
(.S.CH2.CO.NH2)2
C4H802S2N2
155
Clae'sson
B., 14,411
40, 581
Sulphonediacetamide
(NH2.CO.CH2)2SO2
C4H8O4SN2
d.w.m. 220
Lov6n
B., 17, 2822
48, 241
Ethylthioglycollamide
EtS.CH2.CO.NH2
C4H9OSN
....
44
Claesson
B. S. [2], 23, 445
29, 568
Ethyltaurine
NHEt.CH2.CH2.SO3H
C4Hn03SN
147
James
....
47, 369
Dimethyltaurine
NMe2.CH2.CH2.S03H
)»
....
d.w.m. 270-
»
47, 371
280
Tetramethylsulphonamide
SO2(NMe2)2
C4H12O2SN2
73
Belirend
B., 14, 722, 1811
40, 717
Ht. on Am. isethionate ...
0[(CH2)2.S02.ONH4];
CJELuOftX,
C2H703SN
196-198
Carl
B., 12, 1605
38, 28
Dimethliydrazine sulphate
(NMe2.NH2)2H2S04
C4H1S04SN4
MM
105
Renouf
B., 13, 2171
40, 152
a-Thiophenamide
S.(CO.NH2)=1.2
C5H6OSN
171-5 /
Peter
B., 18, 543
48, 765
J8- ,,
=1.3
JJ
180 u.c.
Nahnsen
B., 17, 2196
48, 52
Ethylidenerhodanic acid ...
CHMe : C(SH).CO.S.CN
C5H6OS2N
....
147-148
Nencki & Bour-
B., 17, 2279
48,40
quin
Methylacetylenecarboxyl-
CMe:C.CO.S.C(NH2):NH
C5H6OSN2
....
a. 300
Nencki & Silber
J. p. [2], 25, 72
40, 501
thiocarbamide
Dimethylthioparabanic
CS.NMe.CO.CO.NMe
| |
CSH602SN2
....
112-5
Andreasch
B., 14, 1450 ;
40, 897
acid (thiocholestrophane)
M. C., 2, 281
Butyrylthiocyanate
C3H7.CO.S.CN
CSH.OSN
180 d.
Liquid
Miquel
A. C. [5], 11, 295
32, 869
Ethylic thiocyanacetate ...
NC.S.CH2.CO2Et
C6H7OjSN
220 p.d.
J., 18, 347
Heintz
A, 136, 223
j» » •••
»
J>
225
Liquid
Claesson
B., 10, 1349
„ thiocyanuracetate
....
>J
(polymer)3
80-5
Heintz
A, 136, 223
H )> •"
....
»>
B., 10, 1347
81
Claesson
B., 14, 733
Thiacetonuramic acid
SeeB., 11,469
»
B., 6, 1117
152
Urech
B., 11, 467
34, 488
Succinothiocarbamic acid....
NH2.CS.NH.CO.CH2.CHS.
C5H803SN2
....
210-5-211
Pike
C. N., 28, 173;
27, 49
C02H
B., 6, 1105
Ethylic acetyldithiocarb-
NHAc.CS2Et
C6H9OS2N
••*.
122-123
Chanlaroff
B., 15, 1987
44,40
amate
Ethylic ethylthiocarb-
NHEt.CS.OEt
C5HUOSN
204-208
Liquid
Mulder and
J. p., 103, 178
vi., 1049
amate
others
» »
NHEt.CO.SEt
»
204-208
Liquid
j»
D
>)
5J 1>
J»
))
204-208
Liquid
Hofmami
B., 2, 118
Isobutylic thiocarbamate ....
NH2.CS.OBu/s
)J
J. p., 16, 380
36
Mylius
B., 5, 976
26, 266
Allyltaurine
NH(C3H5).C2H4.S03H
C5HU03SN
190-195
James
....
47, 369
Trimethyltaurine ....
NMe2.C2H4.SO3Me
C5H1303SN
nf. b., 300
j>
....
47, 373
Dimethyltaurocyamine ....
Me2(CN.NH2)N.C2H4.S03H
C5H1303SN3
....
245 d.
»
..-
47, 374
Nitro-3-thienylglyoxylic
S.NOj.(CO.C02H)=l.?.3
C6H305SN
92 ; sf. 78
Peter
B., 18, 542
48, 765
acid
662
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Trinitrobenzenesulphonic
C6H2(N02)3.S03H
C6H3O9SN3
....
185
Willgerodt
J. p. [2], 32, 117
48, 1232
acid
11 11
)J
»
+HS0
100
n
11
?J
Dinitrothiophenol
SH.(NO,)2=1.2.4
C6H404SN2
....
272-280
11
B., 9, 978
30, 405
11 ....
1) >»
»
....
275-280
n
B., 10, 1686
34, 141
Dinitro-/3-acetothienone ....
S.Ac.(NOt),=1.3.(?)j
C6H406SN,
166-167 p. d.
Peter
B., 18, 541
48, 765
Dinitrobenzenesulphonic
SO3H.(N02)2=1.2.4
C6H407SN2
....
106-108
Willgerodt and
C. C. [1884], 809
48, 665
acid
Mohl
Nitrothiophenol
SH.NO8=1.4
C6H6O2SN
....
77
Willgerodt
B., 18, 331
48, 519
Isonitrosothienylacetic acid
S.[C(NOH).C02H]=1.3
C6H6O3SN
136 d.
Peter
B., 18, 539
48, 765
Nitroacetothienone
S.Ac.N02=1.3.?
B
....
86
11
B., 17, 2647; 18,
48, 142, 765
541
„
=1.3.1
»
....
122-5
11
B., 17, 2647 ; 18,
11
540
Nitrobenzenesulphonic acid
SO3H.NOS=1.3
C6HS06SN
A,, 177, 66
60-70
Rose
Z. C. [2], 7, 234
25, 1016
Dinitrobenzenesulphon-
(S03.NH2).(NO2)2=1.2.3
C,H506SN3
....
235
Limpricht
B., 9, 554
30, 303
amide
11
» «
11
....
238
Sachse
A., 188, 448
32, 752
Nitroresorcinolsulphonic
(OH)2.N02.S03H=1.3.(?)2
C6H507SN
+ liH20
124-125
Hazura
M. C., 4, 610
44, 1114
acid
Oxalylallylthiocarbamide
NH.CS.N(C3H5).CO.CO
C6H602SN2
....
89-90
Maly
Z. C. [2], 5, 260
vi., 10S8
' I
Nitrobenzenesulphonamide
(S02.NH2).NO2=1.4
C6H604SNS
....
131
Limpricht
B., 8, 431 ; A.,
28, 896, 1027
177, 75
11
» »
»
....
131
Mahrenholz
A., 202, 331
38, 805
n
j> »
»
....
131
Hofmann
B., 13, 20
38, 389
11
)> »
))
135
Limpricht
B., 18, 2174, 2175
11
=1.3
)>
....
160-161
Goslich
B., 8, 352; A.,
28, 765 5 29,
180, 93
930
n
11
»
....
161
Limpricht
B., 8, 431; A.,
28, 896, 1027
177, 71
11
11 11
)>
....
161
Glaus and Moser
B., 11, 762
34, 865
n
11 11
»»
....
162
Biedermann
B., 8, 1675
29, 695
»
11 11
))
164
Hofmann
B., 13, 20
38, 389
!>
11 »
M
166
Limpricht
B., 18, 2174, 2175
11
=1.2
II
....
186
11
B., 8, 431 ; 18,
28, 896, 1028
2175; A., 177, 78
I)
11 >i
»>
....
188
11
B., 10, 320
32, 193
»
i) ii
jj
....
188
Bahlmann
A., 186, 307
32, 611
11
11 11
»
....
188
Hofmann
B., 13, 20
38, 389
Dinitro-/3-ethylthiophenene
S.Et.(NOj)j=1.3.(?)a
))
....
Liquid
Bonz
B., 18, 552
48, 767
Thienylmethylacetoxirne ....
S.(CMe : NOH)=1.3
C6H7OSN
110
Peter
B., 17, 2645
48, 141
Benzenesulphonamide
C6H5(S02.NH2)
06H7O2SN
A., 87, 299
147-148
Ascher & Meyer
B., 4, 326
24, 554
11
)»
j»
A., 159, 11
149
Otto and Ostrop
A., 141, 373
vi., 1048
)> .i.-
}I
M
J. [1852], 434
149
Lindon and Otto
Z. C. [2], 4, 39
vi., 273
ii
J)
»
....
149
Heumann and
B., 15, 1118
Kochlin
„
n
»
A., 140, 294
153
Stenhouse
P. E., 14, 351
v., 489, 523
11
»»
»
....
156
Hybbeneth
A., 221, 204
46, 72
Nitrothioxylene
CSHMej.N02
)»
....
Liquid
Messinger
B., 18, 1638
48, 1052
Nitroamidobenzenesulph-
NH2.N02.(S02.NH2)=1.2.?
C6H704SN3
....
155-156
Goslich
B., 8, 354; A.,
28, 765 ; 29,
onamide
180, 104
930
Nitrobenzenedisulphon-
(S02.NH2)2.NO2=1.3.5
C9H706S2N3
....
242
Limpricht and
B., 9, 551 ; A.,
30, 302; 32,
amide
Heintzelmann
188, 165
771
A cetylthiocyanopropimine
SCN.CH2.CMe:NAc
C6H8OSN2
**.*
130
Tscherniac and
C. R, 96, 494
44,568
Norton
11
»
)>
B., 16, 348
134
11 •
A. C. J., 5, 227
46, 665
Amidobenzenesulphonam-
NH2.(S02.NH2)=1.3
C6H802SN2
A., 177, 72
135
Limpricht
B., 8, 432
28, 896, 1027
ide
11 ]»
i) 11
))
....
142
Hybbeneth
A., 221, 204
46,72
Citracothiocarbamic acid....
NH2.CS.NH.CO.C3H4.C02H
C6H803SN2
....
222-223 d.
Pike
C. N., 28, 173;
27,50
B., 6, 1106
COMPOUNDS CONTAINING FIVE ELEMENTS.
663
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Benzenedisulphonamide ...
(SO.,NH2)2=1.3
C6H804S2N3
....
210
Nolting
B., 8, 1113
20, 395
„
» ,,
„
B., 9, 584
M9
Korner and Mon
G. I., 6, 133
31,81
selise
„
» »
„
....
229
Limpricht
B., 9, 552
30, 302
„
=1.2
„
....
233
„
B., 9, 553
30, 303
„
=1.4
„
B., 9, 584
288
Korner and Mon
G. I, 6, 133
31,81
selise
Carbamidocarbamindithio-
C02H.CH2.S.C(NH).NH.
C6H806S2N2
....
149 d.
Claesson
B., 14, 731
40, 715
glycollic acid
CO.S.CH.J.CO2H
Nitroxylenesulphonic acid
Me2.NO2.S03H=1.3.4.6
C6H903SN
....
122
Harmseu
B., 13, 1559
Ethylthiocarbimide oxide
NEt.CS.CS.NEt.O
C6HI0OS2N2
....
42
Sell
B., 6, 323
26, 881
i i
Ethylic oxythiocyanate (?)
C6H1002SN2(?)
....
b. 100
MM
A., 82, 279
Ethylic allylthiocarbamate
NH(C3H5).CS.OEt
CeHuOSN
210-215
Liquid
Hofmann
Z. C. [2], 5, 268 ;
vi., 1050
B.,2,119;A.,52,30
Isobutylic thioxamate ...
NH2.CS.C02BuP
C6Hn02SN
....
58
....
J. p. [2], 10, 201
Ethylic thiocyanformate
....
CuHnOjjSN
...*
43-44
....
J. p. [2], 9, 466 ;
alcoholate
10, 119
Isoamylic thiocarbamate ...
NH2.CS.O(C6Hn)
C6H13OSN
184
....
Johnson
A., 84, 337
6, 142 ; 1., 206
>, »
NH2.CO.S(C5HU)
„
....
107
Schone
J. p. [2], 30, 416
48, 512
Anhydrotriethylsulphamic
NEt3.SO..O
C6H1503SN
»*.*
91-5
Beilstein and
B., 16, 1267
44,971
acid
i i
Wiegand
Diethyltaurine
NEt,,C2H4.SO3H
„
....
151
James
....
47, 372
?
(Et.SO2)3N 1 0
C6H1507S3N
81-5
Zuckschwerdt
B., 7, 293; A.,
27, 674; 28, 344
174, 308
Dimethyldiethylsulph-
NMe-j-SOyNEtj
C6H1602SN2
229 p.d.
Liquid
Behrend
B., 15, 1611
42, 1282
amide
Ethylguanidine sulphate....
(CN3H4Et)2+H2S04
C6H2004SN6
....
169 d.
Letnii
B., 8, 767
29, 911
Nitrophenylthiocarbimide
NO2.(N:CS)=1.3
C7H402SN2
....
58
Steudemann
B., 16, 549
44, 801
„
„ ,,
„
275-280
60-5
„
B., 16, 2333, 2334
46, 307
Methenylamidothiophenol-
C6H4.S.C(OH) : N=1.4
C7H5OSN
B., 13, 10
136
Hofmann
B., 12, 1129
36, 806
oxide
Hydroxyphenylthiocarb-
OH.(N:CS)=1.2
„
• *••
193
Bendix
B., 11, 2264
36, 314
imide
)! ))
„ „
,,
MM
196
Diinner
B., 9, 466
30, 204
Sulphobenzimide
C6H4.CO.NH.S02=1.2
C7H5O3SN
....
220 u.c. ; p.d.
Fahlberg and
B., 12, 470
36, 629
Kemsen
Thiocarbanilsulphonic an-
C6H4.NH.CS.O.SO3
C?H603S2N
....
180-183 d.
Magatti
B., 11, 2267
36, 312
hydride
Benzonitrilsulphonamide....
(S02.NH2).CN=1.3
C7H602SN2
A., 106, 34
151-152
Wallach & Huth
B., 9, 428
Methylthiodinitrobenzene
SMe.(NOa)2=1.2.4
C7H604SN2
....
126
Willgerodt
B., 18, 330
48, 520
Sulphobenzimide sulphon-
S02.NH.CO.C?H3.(SO2.NH2)
CjHsOsSjN,
....
285 d.
Fahlberg
A. C. J., 2, 185
40, 817
amide
' =1.2.4 or 5
Dinitrotoluene sulphonic
Me.S03H.(N02)2=1.42.6
C7H607SN2
A., 155, 21
165
Schwanert
B., 10, 29; A.,
32, 470
acid
186, 353
Nitrobenzylsulphhydrate
NO2.(CH2.SH)=1.4
C7H702SN
....
140
Strakosch
B., 5, 698
25, 1027 ; vii.,
182
Nitrophenylthiocarbamide
NO2.(NH.CS.NH2)=1.3
C7H702SN3
....
157-158-5
Steudemann
B., 16, 550
44, 1802
Sulphaminebenzoic acid ....
CO2H.(SO2.NH2)=1.3
C7H7O4SN
....
a. 200
Usler
A., 106, 36
v., 485
» » .-
» I)
,,
B., 15, 1757
230
Eemsen & Palmer
A. C. J., 4, 142
1! ,,
» »1
„
A., 108, 343
?
Engelhardt
J. p., 75, 363
.. „ .."
=1.2
„
....
240
Fahlberg and
B., 12, 470
36, 629
Remsen
I! ,)
=1.4
„
A., 178, 299
280
Eemsen
A. C. J., 4, 161
Nitrotoluenesulphonic acid
Me.N02.SO3H==1.4.6
C7H706SN
A., 161, 8
130
Beilstein
A., 155, 23
» »
» ))
1)
A., 186, 351
133-5; sf. 130
Jenssen
B., 7, 56; A.,
27, 479 : 28, 77
172, 230
Dinitrotolueuesulphon-
Me.(N02)2.(S02.NH2)
C7H706SN3
B., 10, 31
203
Schwanert
A., 186, 359
32, 471, 612
amide
=!.(?). .4
Sulphaminesulphobenzoic
C02H.S03H.(S02.NH2)
C7H707S2N
165
Fahlberg
A. C. J., 2, 193
40, 817
acid
=1.2.4
664
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Hydroxyphenylthiocarb-
OH.(NH.CS.NH2)=1.2
C7H8OSN2
....
161 d.
Bendix
B., 11, 2263
36, 314
amide
„ „
=1.4
„
....
214 d.
Kalchoff
B., 16, 375
44, 735
Sulphobenzamide
(CO.NH2).SO3H=1.3
C7H803SN2
A., 106, 32
170
Limpricht and
A, 102, 253
v., 486
Uslar
Nitrotoluenesulphonamide
Me.N02.(S02.NHs)=1.2.4
C7HSO4SN2
....
128
Paysan
A., 221, 210
46, 72
„
n ii
„
....
128
Limpricht
B., 18, 2173
„
„ „
„
J. [1867], 678
128
Otto and Grtiber
A., 145, 23
vi., 287
„
=1.2.5
„
....
133-5
Limpricht
B., 18, 2184
48, 1234
D
=1.4.6
ji
....
186
Jenssen
B.,7,56;A.,172,233
27, 479 ; 28, 77
Benzylsulphonamide
Ph.CH2.S02.NH2
C7H902SN
....
102
Otto and Luders
B., 13, 1287
38, 812
„
H
„
105
Limpricht
B., 6, 535
26,1040;vii.,186
Toluenesulphonamide
Me.(SO2.NH2)=1.3
„
90-91
Hubner & Muller
Z. C. [2], 7, 14
24, 121
»
„ „
„
90-91
Hubner and Post
A., 169, 51
27, 60
„
n n
„
....
90-91
Remsen & Palmer
A. C. J., 4, 142
42, 1095
»
i) i>
„
....
91-92
Wolkow
Z. C. [2], 6, 542
vii., 1170
„
11 11
„
....
b. 100
Limpricht and
B., 7, 719 ; A.,
27, 991 ; 28, 79
Pechmann
173, 202
„
!» 11
„
....
104
Limpricht and
B., 7, 1394; A.,
28, 368, 898
Pagel
176, 298
»
11 1>
„
J. [1877], 943
104-105
Beckurts
B., 10, 945
32, 776
„
„ „
„
....
106-107
Neville and Win-
...*
37, 628, 631
ther
„
11 11
„
....
107
Muller and Wie-
B., 12, 1349
singer
„
11 1)
„
....
107-108
Claesson&Wallin
B., 12, 1853
38, 256
„
11 11
„
....
108
Chrustschoff
B., 7, 1166
28, 162
.,
=1.4
„
....
136
Claesson & Wallin
B., 12, 1853
38, 256
„
11 11
„
B., 10, 944
137
Heumann and
B., 15, 1118
Kochlin
„
!> 11
n
J. [1877], 943
137
Walkow
Z. C. [2], 6, 231
vii., 1168
„
11 11
„
....
137
Muller and Wie-
B., 12, 1348
singer
„
11 11
„
....
137
Chrustschoff
B., 7, 1167
28, 162
ii
11 11
„
....
139-140
Otto and Griiber
A., 142, 92
vi., 1060
„
=1.2
„
cryst.fr.H20
148
Jenssen
A., 172, 236
28,77
11 ....
11 11
„
fr. alcohol
155
„
„
„
„
11 11
„
fr. ether
155
M
„
„
,,
11 11
„
....
148
Limpricht
B., 6, 1010
27, 74
„
11 11
„
....
148
Gerver
A., 169, 373
27, 168
„ ....
11 1)
11
....
152-153
Hiibner & Terry
Z. C. [2], 7, 232
25, 1006
„
11 11
„
....
152-153
Hubner and Post
A., 169, 29
27, 58
„
!> 11
„
J*[1879],756
153-154
Wolkow
Z. C. [2], 6, 57
vii., 1169
11
11 11
„
J. [1877], 934
153-154
Beekurts
B., 10, 945
32, 775
„
11 1)
„
MM
153-154
Claesson&Wallin
B., 12, 1853
38, 256
11
11 11
„
....
154
Heffter
A., 221, 208
46,73
11
.1 11
„
....
154-155
Limpricht
B., 7, 450
27, 901
„
.1 11
„
fr. HS0
154-155
Lorenz
A., 172, 177
28, 82
j,
11 11
.
fr. alcohol
161
B
„
„
Amidotoluenesulphinic acic
Me.NH,,.S02H=1.4.6
„
....
132
Heffter
A., 221, 345
46, 455
Amidotoluenethiosulphonic
acid
=1.2.4
Me.NH2.(S02.SH)=1.2.4
C7H902S2N
....
175
d.w.m. 115
Paysan
11
A., 221, 360
11
46, 453
Toluidinedisulphonic acid
Nitrosulphobenzoic acid ...
Amidotoluenesulphon-
amide
Me.NH2.(S03H)2=1.2.(?)2
CO2H.N02.SO3H=1.3.4
Me.NH2.(SO2.NH2)=1.4.6
C7H906S2N
C;HBO9SN
C7H1002SN2
+2H20
240
130-131
164
Limpricht
Hart
Heffter
B., 18, 2182
A. C. J., ], 340
A., 221, 208
40, 1144
46, 73
Diamidotoluenethiosulph-
onic acid
=1.2.4
Me.(NH2)2.(S02.SH)=l.(?).,4
C7H1002S2N2
....
175
d. 152
Paysan
Perl
A., 221, 210
C. C. [1884], 468
46,72
48, 391
Diamidotoluenesulphonic
acid
Me.(NH2)2.S03H=l.(?)L.4
C7H1003SN2
A., 187, 324
nf. 280
Schwanert
B., 10, 31
32, 471, 612
COMPOUNDS CONTAINING FIVE ELEMENTS.
Gfi5
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
a-Toluenedisulphonamide
Me.(SO5.NH2)2=1.2.4
C7H1004S2N2
185
Gnehm
B., 10, 1276
32, 893
a- ,,
» »
»
....
183-186
Gnehm & Forrer
B., 10, 543
32, 612
a- „
» ;>
)1
....
186-187
Fahlberg
B., 12, 1052 ;
36, 804; 40, 816
A. C. J., 2, 192
a- „
>1 M
JJ
....
186
Blomstrand and
B., 5, 1086
26, 505 ; vii.,
Hakanssons
1171
0-
= ?
)>
....
216
u
»
»
/3-
= »
»
....
216 ; sf. 210
Limpricht
B., 18, 2180
?-
= '
J»
....
a. 260
Kornatzkin
A., 221, 191
46, 70
J-
=1.3.5
»
....
a. 240
Limpricht
B., 18, 2177
48, 1233
Toluenetrisulphonamide ...
Me.(SO2.NH.2)3=1.2.4.6
C-HnOeSjN,
....
a. 300 d.
Claesson
B., 14, 309
40, 429
Carbamidocarbonylsulph-
NH2.CO.NH.CO.S.C5Hn
C7H1402SN2
....
176
Scheme
J. p. [2], 30, 416
48, 512
amyl
Nitrodithiocyanobenzene....
(S.CN)2.NO2=1.3.?
C3H302S2N3
....
150
Gabriel
B., 10, 184
32, 325
Benzoylthiocyanate
Ph.CO.S.CN
C8H5OSN
d. 200
Liquid
Miquel
A. C. [5], 11, 300
32, 869
» ....
»
))
200-205 (i.v.)
»
C. R., 81, 1209
29, 571
„
MM
(C8H5OSN)n
160
»
A. C. [5], 11, 300
32, 870
Thiocarbimidobenzoic acid
C02H.NCS= ?
C8H502SN
d.w.m. 310
Rathke & Schiiffer
A., 169, 103
27, 164
Phthalic sulphimide
SO2.NH.CO.C6H3.CO2H
C8H505SN
uot constant
Stokes
A. C. J., 6, 262
48, 539
d.
= 12.1
Isophthalic „
=4.3.1
»
....
283-5 u.c.
Remsen & Coall
B., 12, 1436 ;
38, 258 ; 40,
A. C. J., 3, 204
1038
j> »
)I »
»
....
289
Jacobsen
B., 13, 1554
Terephthalic sulphimide ....
=5.4.1
))
....
1
A. C. J., 4, 197
Nitrotolylthiocarbimide ....
Me.NO2.NCS=1.2.4
C3H602SN2
....
56-57
Steudemann
B., 16, 2336
48, 307
Terephthalsulphinide
....
C8H604SN2
....
a. 300 d.
A.C.J.,2,405.413
Anisidinethiocarbinride ....
OMe.NCS=1.4
C8H?OSN
270
Liquid
Salkowski
B., 7, 1012
Oxethenylainidothiophenol
S.C6H4.N : C.CH2.OH
>»
....
176
Hofmann
B., 13, 1234
38, 887
1 '
?
....
C8H703SN
....
121
"Wenghoffer
B., 10, 443
32,447
Sulphamineisophthalic acid
(C02H)2.(SOi.NH2)=1.3.?
C8H7O6SN
282-284 u.c.
lies and Remsen
B., 11, 464
34, 505
Benzoylthiocarbamide
NH2.CS.NHBz
C8H8OSN
169-170 u.c.
Pike
B., 6, 755, 1107
26, 1132
j>
»
J)
....
171
Miquel
A. C. [5], 11, 313
32, 870
Salicylthiocarbamide
OH.(CO.NH.CS.NH2)=1.2
C8H802SN2
182
j»
A. C. [5], 11, 315
»
Thiouramidobenzoic acid....
CO2H.(NH.CS.N Hj) = 1 .3
)J
187
Traube
B., 15, 2118
44, 193
Methylic nitrophenylthio-
NO2.(NH.CS.OMe)=1.3
C9H803SN2
119-120
Steudemann
B., 16, 551
44, 802
earbamate
Ethylthiodinitrobenzene ....
SEt.(NO2)j=1.2.4
C8H804SN.,
113
Willgerodt •
B., 18, 330
48, 520
Sulphoterephthalamide ....
(CO.NH2)2.(SO3H)=1.4.5
C8H306SN2
a. 300
Schoop
B., 14, 226
40, 278
Methylic phenylthiocarb-
Ph.NH.CO.SMe
C8H9OSN
83-84
Will
B., 15, 340
amate
Phenthiacetamide
Ph.S.CH2.CO.NH2
»
....
104
Claesson
B. S. [2], 23, 441
29, 567
Phenoxythiacetamide
Ph.O.CH2.CS.NH2
J)
....
111
J. p. [2], 20, 279
Anhydrophenyltaurine ....
Ph.N.CH,.CH2.SO2
C9H902SN
69
Leymann
B., 18, 871
48, 787
i " i
Nitrotolylthiocarbamide ....
Me.NO2.(NH.CS.NH2)
C8H902SN3
....
176
Steudemann
B., 16, 2337
46, 307
=1.2.4
Sulphotoluamide ....
Me.(CO.NH2).SO3H
CSH9O4SN
154-155
Limpricht
B., 7, 450
27, 901
=1.3.2 or 6
Sulphaminetoluic acid
Me.C02H.(S02.NH2)=1.3.2
»
....
202-205
Jacobsen
B., 11, 902
11 »
=1.2.5
))
....
217 c.
»
B., 14, 39
40, 599
» »
=1.4.?
»
....
242
Kelbe and Baur
B., 16, 2565
46, 300
i) i)
=1.2.4
»)
243
Jacobsen
B., 14, 40
40, 599
» » ••••
=1.3.6
J»
235
lies and Remsen
B., 10, 1044
» »
» »
»
248
»
B., 11, 231, 889
34, 4ia
)! !)
» »
»)
254 c.
Jacobsen
B., 11, 896
» 1)
» »
)>
247-5-248 ;
lies and Remsen
B., 11, 1327 ; A.
36, 52
254-5-255 c.
C. J., 3, 205
t> 5)
=1.4.?
»
Ri'lS, 1433
267 u. c.
»
B., 11, 230
34, 412
H »
!> »
))
267
Remsen and Hall
A. C. J., 2, 50
42, 186
Sulphophenylglycocoll
....
C8H905SN
183-185
Zehenter
M. C., 5, 332
48, 55
Methylic amidosulphobenz-
NH2.SO3H.CO2Me=?
»)
188 d.
Hentschel
B., 18, 979
48, 792
oate
€66
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitroxylenesulphonic acid
Me2.NO2.SO3H=1.3.6.4
C8H906SN
122
Havnssen
B., 13, 1559
40, 49
„ „
„ „
M
132
Biesen
B., 18, 2191
Anisylthiocarbamide
OMe.(NH.CS.NH2)=l 2
CSH10OSN2
....
152
Mulhauser
B., 13, 923 ; A.,
38, 642; 42, 302
207, 246
Sulphaminetoluamide
Me.(SO2.NH2).(CO.NH2)
C8H1003SN2
....
218
Meyer and Baur
B., 13, 1499
40, 46
„
=1.3.4
„'
228
Fischli
B., 12, 618
36, 639
Nitrophenylxanthogenam-
N02.(NH.SO.OEt)=1.4
C8H1004SN2
....
175-176
Losanitsch
B., 15, 471
ide
Nitroxylenesulphonamide
Me2.N02.(S02.NH2)=1.3.6.4
„
179
Limpricht
B., 18, 2191
Dimethylthienylmethyl-
C4HSMe2.(CMe:NOH)
C8Hj OSN
....
65
Messinger
B., 18, 2302
48, 1205
acetoxime
Ethylbenzenesulphonamide
Et.(S02.NH2)=?
C8H1I02SN
....
108
Chrustachoff
B., 7, 1166
28, 162
Xylenesulphonamide
Me2.(S02.NH:)=1.3.2
,
95-96
Jacobsen
B., 10, 1015
32, 600
»
„ „
„
A., 184, 188
95-96
V
B., 11, 22
34, 411
„
» »
„
....
95-96
lies and Bemsen
B., 11,464; 579,
34, 505, 584,
889, 1328
724 ; 36, 52
„
„ „
ii
96
Jacobsen and
B., 11, 1536
36, 62
Weinberg
„
=1.3.4
„
B., 11, 889
110
lies and Bemseu
B., 10, 1043, 1199
32, 776 ; 34, 56
„
=1.3.?
ji
....
123
Witting and Post
B., 10, 745
32, 611
„
= 1.3.?
»
....
132
„
„
„
„
„ =1.3.5 or 2
„
132
lies and Bemsen
B., 10, 1043
32, 776
„
» jj
„
132
Bemsen
B., 10, 1199
34, 56
„
=1.3.4
.,
137
Limpricht
B., 18, 2188
„
» »
„
A., 184, 188
137
Jacobseu
B., .10, 1015
32, 600
„
„ „
„
137
V
B., 11, 20
34,411
„
» „
„
137
Bemsen and lies
B., 11, 465, 889 ;
34, 505, 724
A. C. J., 4, 192
„
» »
„
137
Jacobsen and
B., 11, 1536; 12,
36, 62, 643
Weinberg
606
„
„ „
„
138-139
Jacobaen
B., 18, 1760
48, 1052
„
=1.2.4
„
143
lies and Bemsen
B., 10, 1044
32, 776
„
» !)
„
....
142-144
Jacobsen
B., 14, 2626
„
1> »
91
144
„
B., 10, 1012; 11, 23
32,601
„
)) ),
„
....
144
Kriiger
B., 18, 1759
»
=1.4.?
„
....
147-148
Jacobsen
B., 11, 22
34, 411
»
=1.2.3
„
....
165
Kriiger
B., 18, 1760
48, 1053
Phenyltaurine
Ph.NH.(CH2)2.S03H
C8HUO3SN
260
Andreasch
M. C., 4, 138
44, 665
„ .... ....
„
,,
S77-S80 d.
James
47, 370
Dimethanilinesulphonic
NMe2.S03H=?
„
B., 6, 345,
149-150 u.c.;
Smyth
B., 7, 1238
28, 164
acid
663
d.
» »
» >•
„
B., 14, 2177
230
....
J. p. [2], 16, 463;
20, 259
Methoxytoluenesulphon-
Me.OMe.(S02.NH2)=1.4.6
„
150
Heffter
A., 221, 345
46, 454
amide
Phenyldimethylsulphon-
NMe2.SO2.NHPh
C8H1202SN2
84-85
Behrend
A., 222, 116
46, 285
amide
Ethoxybenzenesulphon-
OEt.(SO2.NH2)=1.3
C8H1305S2N2
233
Zander
A., 198, 28
38, 124
amide
Ethylleucazone sulphate ...
(C4H7ON3)2+H2S04
C8H1606SN6
161-5
Meyer & Constam
A., 214, 328
.44, 40
Amylenethiourethane
C4H9.CH(NH.CS.OEt)2
C8H1702SN
108
Bischoff
B., 7. 1083
28, 146
Ethylic oxalate thiocarb-
;CS(NH2)2].(CO2Et).,
C8H1804S2N4
150 d.
Nencki
B., 7, 780
27, 981
amide
Tetrethylsulphouamide ....
S02(NEg3
C8H2002SN2
249-251 d.
Liquid
Behrend
B., 15, 1612
42, 1282
Acetophenonethiocyanate
Ph.CO.CH2.S.CN
C9H7OSN
....
72-73
Dyckerhoff
B., 10, 120
32,327
„
„
)J
•*..
75
5)
B., 9, 1216
„
„
( ,, )n
....
203-204 d.
„
B., 10, 120
32, 327
Phenylcarbimideglycolide
PhN I C.S.CH2.CO.O
C,,H7O2SN
B., 12, 1594
148
Liebermann and
B., 13, 277 ; A.,
38, 659
Voeltzkow
207, 137
„
))
»
....
148
Lange
B., 12, 597
36, 651
COMPOUNDS CONTAINING FIVE ELEMENTS.
667
Name.
Constitution.
Formula.
Boiling
Point,
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Phenylcarbimiueglycolide
PhN.CO.S.CH,.CO
0^0^
B., 15, 516
148
Meyer
B., 14, 1662
i " i
Acetoxyphenylthiocarb-
OAc.(N:CS)=1.4
»
....
36
Kalckhoff
B., 16, 1831
44, 1110
imide
Methenylamidothiophenol-
C6H4.S.C(OAc):N=?
»
....
60
Hofmann
B., 13, 11
38, 388
acetate
1 1
Acetthiocarbamidophenol
C6H4.O.C(SAc):N=1.2
)J
120
Kalckhoff
B., 16, 1827
44, 1110
i i
Quinoline sulphouic acid ...
N.SO3H=ai ; j33
C9H703SN
nf. 260
Happ
B., 17, 192
46, 758
Hydroxyquinoline sulph-
N.OH=ai ; (3, or a.2
C9H704SN
270
Riemerschmied
B., 16, 725
44, 1148
onic acid
Anhydromethylsulph-
SO.j.NMe.CO.CoHjj.CO.jH
C9H705SN
191
Stokes
A. C. J., 6, 262
48, 539
amineplithalie acid
i i
=11.2
Anhydrosulphamineuvitic
SO2.NH.CO.C6H2Me.CO,H
»»
A.C.J.,2,130
270-272 c.
Jacobsen
A., 206, 183
40, 430
acid
"J =U.3.5
Phenylthioliydanto'in
Ph.N.CO.CH2.S.C : NH
i i
C9H8OSN2
....
178
Meyer
B., 10, 1965 ; 14,
34, 295 ; 40,.
1661
1039
»
jj
»
A., 207, 129
178
Andreasch
B., 15, 325; M.
42,407
C., 2, 776
Acetylphenylthiocarbiziue
NPh.CS.NAc
j>
....
186-187
Fischer and
A., 212, 329
42, 1095
1 1
Besthorn
Fr. phenylthiocarbimide ...
»
d.w.m. a 200
Aschan
B., 16, 1545
44, 1107
Phthalthiocarbamie acid ....
CO2H.(CO.NH.CS.NH2) =1.2
C9H803SN.,
A., 214, 25
171-172
Piutti
G. L, 12, 169
42, 1297
Ethylene phenylthiocarb-
NPh.CH2.CH2.COS
C9H9OSN
79
Will
B., 15, 344
42, 723
amate
1 1
Methenylamidothiophenol-
C,H4.S.C(OEt) I N
»
25
Hofmann
B., 13, 11
38, 388
ethoxide
1 1
Methylic benzoylthiocarb-
NHBz.CS.OMe
C,H9O2SN
....
97
Miquel
A. C. [5], 11, 330
32,871
amate
Mesitylenic sulphonimide
CsHjMej.CO.NH.SO,
C9H9O3SN
....
255 ; 262 c.
Hall and Eemsen
A. C. J., 2, 131 ;
40, 821
•J =1.3.5.6
3,216
Sulphaminecinnamic acid
(SO3. NH2).(C2H2.C02H) =1 .4
CBH9O4SN
d.w.m. 250
Palmer
A. C. J., 4, 161
42, 1204
Sulphamineuvitic acid
Me.(CO2H)2.(SO2.NH2)2
C9H9O6SN
....
279
Hall and Eemsen
A. C. J., 2, 136
40, 821
=1.3.5.6
Sulphaminexylidic acid ....
„ =1.2.5.4
»
MM
295-300
Jackson & Meyer
B., 16, 190
44,590
Acetylphenylthiocarb-
NHPh.CS.NHAc
C9H10OSN2
.*••
169-170
Miquel
A. C. [5], 11, 318
32, 870
amide
» »
tJ
)>
....
173
Schiff
B., 9, 570
30, 285
Phenylthiohydantoic acid
NHPh.C( : NH).S.CH2.C02H
C9H1002SN2
B., 14, 732
148-152
Jager
J. p. [2], 16, 20
32, 873
Ethylic nitrophenylthio-
N02.(NH.CS.OEt)=1.3
C9H1003SN2
....
115
Losanitsch
B., 16, 49
44, 583
carbamate
>! ))
» »
»
....
115
Steudemann
B., 16, 550
44,802
» i)
NO2.(NH.CO.SEt)=1.4
)»
....
175-176
Losanitsch
B., 15, 471
42, 955
Sulphaminecinnamide
(SO2.NH2).(C2H2.CO.NH2)
»
218
Palmer
A. C. J., 4, 161
42, 1204
=1.4
laopropylthiodinitrobenz-
SPi*.(NO2)j=1.2.4
C9H1004SN3
93-94
Willgerodt
B., 18, 330
48, 520
ene
Ethylic phenylthiocarb-
NHPh.CS.OEt
C9HUOSN
....
65
Hofmann
B., 2, 120 ; 3, 772
amate
i) »
I)
11
65
Schiff
B., 9, 1316
» »
»
J>
68-69
Bamberger
B., 15, 2164
» )>
)»
)J
B., 13, 684
71-72
Liebermann
A., 207, 145
42, 298
» »
)>
»
B., 13, 1575
73
Will
B., 15, 340
Benzylthiacetamide
Ph.CH2.S.CH2.CO.NH2
U
97
Gabriel
B., 12, 1641
38,34
Methylic tolylthiocarb-
Me.(NH.CO.SMe)=1.2
)>
70
Will
B., 15, 1317
42, 109O
amate
» )>
=1.4
)J
107
j)
B., 15, 1311
n
Acetamidothiocreaol
Me.SH.NHAc=1.2.4
»
....
195
Hesse
B., 14, 489
40, 596
» "••
„ =1.4.6
J)
240
) j
B., 14, 490
40, 597
Propenylbenzenesulphon-
C3H6.(S03.NHS)=?
C,HUOSSN
....
152
Meyer and Baur
B., 12, 2240
38, 166
amide
Tolylsulphonacetamide ....
Me.(SO2.CH2.CO.NH2)=1.4
C,HU0,SN
....
163-164
Otto
B., 18, 161
48, 537
4 Q 2
668
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Ethylic sulphaminebenz-
(S02.NH2).C02Et=1.3
C9HnO4SN
1
A., 106, 41, 387
oate
!) »
=1.4
J>
110-111 ;a.f.
Remsen
A., 178, 300
29, 258
94
Sulphethylbenzamic acid ....
....
))
261-262
....
A. C. J., 4, 197
Sulphaminemesitylenic
Me2.C02H.(S0.2.NH2)
))
....
247
Hall & Remsen
B., 10, 1040 ;
32, 777
acid
=1.3.5.6
A. C. J., 2, 131
ii "
ii u
U
....
259 ; 263 n.
Jacobsen
A., 206, 167 ;
36, 643; 40,
B., 12, 604
429
j) »
„ =1.3.5.2
n
A. C. J., 2,
276 c. ; d.
11
A., 206, 174 ;
36, 643 ; 40,
131
B., 12, 605
430
Sulphaminexylic acid
=1.3.4.6
»
....
268 c.
Jacobsen and
B., 16, 190
44, 589
Meyer
Nitromesitylenesulphonic
Me3.NO2.SO3H=1.3.5.2.4
CjHuOsSN
+ 1JH20
131
Rose
Z. C. [2], 7, 74 ;
24, 376 ; vii.,
acid
A, 164, 65
789
Ethoxyphenylthiocarb-
EtO.(NH.OS.NH2)=1.2
C9H12OSN2
110
Berlinerblau
J. p., 30, 97
48, 148
amide
Sulphaminemesitylenamide
Me2.(CO.NH.,).(S02.NH2)
C9H12O3SN2
287-288
A. C. J., 3, 218
=1.3.5.?
Ethylic disulphaminebenz-
(SO2.NH2)2.CO2Et=?
C9H1206S2N2
198-200
Fahlberg
A. C. J., 2, 185
40, 817
oate
Isopropylbenzenesulphon-
Pr/s.(SO2.NH2)=?
C9H130SSN
J., 1879, 760
95-5-96
Spica
G. I., 9, 433
38, 167
amide
i) »
=»
»
....
107
ii
•)
ii
I! »
» »
»
107-108
Meyer and Baur
B., 12, 2240
)I "
U »
»
....
112
Claus and Tonn
B., 18, 1241
,< II
=?
)>
127 u.c.
»
1>
48, 904
Propylbenzenesulphon-
Pr».(S02.NH2)=?
)J
....
110
Meyer and Baur
B., 12, 2239
amide
Mesitylenesulphonamide....
Me3.(S02.NH2)=1.3.5.6
)J
....
140+
Jacobsen
B., 15, 1857
»
ii «
>J
A., 184, 185
141-142
ii
B., 9, 257
30, 77
11
ii ii
))
141-142
Holtmeyer
Z. C. [1867], 686
vi., 301
Pseudocumenesulphon-
=1.3.4.?
»
A., 184, 185
175-176
Jacobsen
B., 9, 257
30,77
amide
» »
J» »
»
175
ii
B., 14, 2629
Hemiinellithenesulphon-
=1.2.3.?
JJ
....
196
11
B., 15, 1858
44,53
amide
Ethoxytoluenesulphon-
Me.OEt.(S02.NH2)=1.4.6
C9Hi303SN
136
Heffter
A., 221, 345
46, 454
amide
)i 11
=1.2.4
)»
137
Hayduck and
A., 172, 216 ;
27, 905, 1096 ;
Limpricht
B., 7, 554
vii.. 934
Phenyltanrocyamine
Ph.(CN.NH2)HN.C2H4.S03H
C9H1303SN3
....
nf. 300
James
....
47, 374
Tolyldimethylsulphamide
Me.(NH.SO2.NMe2)=1.4
C9H140,SN2
90-5
Behrend
B., 15, 1612
42, 1282
Ammonium mesitylene-
Me3.SO3NH4=1.3.5.6
C9H15O3SN
250 d.
Jacobsen
A., 145, 85
vii., 788
sulphonate
Oxethene toluidine acid
[C6H4Me.NH.CH2.CH2.OH]
C9H1505SN
110-111 d.
Demole
B., 7, 637
27,903
sulphate
+ H2S04
Benzylidene rhodanic acid
Ph.CH:C(SH).CO.S.CN
C10H7OS2N
200 u.c.
Neucki and Bour-
B., 17 2278
48,40
quin
Nitrostyrolenethiocyanate
....
Cn.HjOAN,
J. [I860], 405
111-112
....
A., 216, 325
0-Diazonaphthalene sulph-
(C10H7.N2.C10H7)H2S04
C10H804SN2
84-85
Scheiding
B., 8, 1652
29, 713
ate
Nitrouaphthalenesulphon-
NOS.(SOS.NH2)= ?
))
....
180
....
B. S., 26, 446
amide
i) »
= 1
J?
216
Cleve
B. S., 29, 415;
34, 677 ; 38, 47
B., 12, 1714
i>
11 =ala-2 i
)»
....
225
....
B. S., 24, 510
Tolylthiocarbimidegly-
C6H4Me.N : C.S.CH,.CO.O
C10H902SN
120
Voltzkow
B., 13, 1580
40, 43
collide
1 J
=1.2
11 l>
=1.4
ii
....
162
11
B., 13, 1579
H
COMPOUNDS CONTAINING FIVE ELEMENTS.
669
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
a-Nai ihthalenesulphon-
C10H-(S02.NH2)
C10HASN
A., 114, 135
150
....
Z. C. [1869], 711
amide
ft- n 5!
JJ
))
...*
212 ; 213
Cleve
B. S., 25, 258
30,82
ft- » »
JJ
51
317 c.
....
Z. C. [1869], 711
Thiophenesulphanilide ....
C4SH,.(SO2.NHPh)
C10H902S2N
96
Weitz
B., 17, 799
46, 1130
Methylic methylanhydro-
S02.NMe.CO.C6H3.C02Me
i i
C10H905SN
180
Stokes
A. C. J., 6, 262
48, 539
sulphamineplithalate
=?.2.1
Nitroiiaphthalenedisulph-
C10H5.N02.(S02.NH2)2
C10H906S2N3
B., 16, 570
285 d.
Alen
B. S., 39, 63
44, 596
onamide
Tolylthiohydantoin
C6H4Me.N.CS.NH.CH2.CO
C10H10OSN2
180 d.
Aschan
B., 17, 426
=1.4
jj ••*
» j»
»
183
Meyer
B., 10, 1966
34, 296
jj «••
j» »»
»
184 u.c.
Aschan
B., 16, 1544
44, 1107
a-Naphthalenedisulphon-
C10H6(S02.NH2)2
C10H1004S2N2
....
242-243
Ebert and Merz
B., 9, 599
30, 409
amide
ft' » )>
))
!>
nf. 305
?,
))
»
Ethylene p-tolylthiocarb-
C6H4Me.N.CO.S.C2H4
C10HUOSN
....
88
Will and Biel-
B., 15, 1316
42, 1091
amate
schowski
Ethylio benzoylthiocarb-
NHBz.CS.OEt
C10HU02SN
J. p., 10, 238
73-74
Miquel
A. C. [5], 11, 334
32, 871
amate
Sulphophenylsuccinamic
....
C.oH^O.SN
J. [1856], 506
160
Gerhardt and
A. C. [3], 47, 129
v., 524
acid
Chiozza
Benzoylethylthiocarbamide
NHBz.CS.NHEt
C10H13OSN2
....
134
Miquel
A. C. [5], 11, 316
32, 870
Tolylacetylthiocarbamide....
Me.(NH.CS.NHAc)=1.4
»
• •t*
175-176
..«•
B. S., 28, 103
Tolylthiohydantoic acid ....
C6H4Me.NH.C(: NH).S.CH2.
C10H1202SN2
176-182 d.
Ja'ger
J. p. [2], 16, 22
32, 873
CO2H=1.4
Ethylthiocarbamido-
CO2H.(NH.CS.NHEt)=1.3
»
194-195 u.c.
Aschan
B., 17, 430
46, 907
benzoic acid
d.
Ethylic nitrotolylthiocarb-
Me.N02.(NH.CS.OEt)=1.2.4
C10H1ASN2
95-5
Steudemann
B., 16, 2337
46, 307
amate
Isobuty Ithiodini trobenzene
SBu/s.(NO2)2=1.2.4
C10H1204SN2
71-72
Willgerodt
B., 18, 331
48, 520
Phenylmethylthiourethane
NPh : C(OEt).SMe
C10H13OSN
260-265 p.d.
Liquid
Liebermann
B., 13, 686; A.,
40, 44 ; 42, 298
207, 148
Ethylic tolylthiocarbamate
Me.(NH.CO.SEt)=1.2
I>
Liquid
»
B., 13, 1576 ; A.,
40, 45 ; 42, 299
207, 161
» »
)> )!
I»
....
66
Will
B., 15, 1317
42, 1091
»! ))
=1.3
I*
....
67-68
Liebermann
A., 207, 162
42, 299
„
=1.4
»
....
79
Will
B., 15, 1313
42, 1091
>> »
n »
»
87
Liebermann and
B., 13, 1576 ; A.,
40, 45; 42,299
Natanson
207, 160
Sulphaminepropylbenzoic
Pr«.(SO2.NH2).CO2H=1.2.4
C10H1304SN
....
212-213 c.
Remsen & Keiser
A. C. J., 5, 161
46, 457
acid
Sulphamineisopropyl-
Prt(S02.NH2).C02H=1.2.4
JJ
244 c.
Eemsen and Day
A. C. J., 5, 149
46, 456
benzoic acid
Diethylbenzenesulphon-
Et2.(S02.NH2)=1.4.5
C10H1502SN
97'5
A. C. J., 4, 197
amide
Methylpropylbenzene-
Me.Pr«.(SO2.NH2)=1.2.?
jj
crystalline
Claus & Hansen
B., 13, 898
sulphonamide
» »
=1.4.5
n
*...
73
Kelbe
B., 13, 1158
38, 878
') n
" »
»
73-5-74
Spica
B., 14, 654
40, 602
» >»
„ =1.4.6
»
110
Berger
B., 10, 976
32, 601
» »
=»
jj
MM
112
Paterno
G. I., 11, 124
40, 594
» »
» i)
i)
114-115
,,
G. I., 9, 397
38, 107
» »
=1.4.6(?)
j)
151 c.
Remsen and Day
A. C. J., 5, 149
46, 456
Methylisopropylbenzene-
Me.Prf.(S02.NH2)=1.3.?
»)
73
Kelbe
B., 13, 1400 ; A.,
40, 878; 42,
sulphonamide
210, 34
299
» »
" I!
»j
B., 16, 792
75-75-5
Spica
G. I., 12, 543
44, 460
I! ))
„ =1.4.5
jj
80-90
Jacobsen
B., 12, 433
36, 625
» )»
= 1.4.6
jj
....
97-98
)5
B., 12, 432
36, 624
)» »
» »
j»
....
97-98
Paterno & Spica
G. 1 , 9, 397
38, 107
670
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Methylisoprcpylbenzene-
Me.Pr0.(SOj.NH2)=1.3.?
C10H1502SN
A., 210, 37
108
Kelbe
B., 13, 1400
42, 301
sulphonamide
Methylisopropylsulphon-
=1.3.?
„
....
162
Kelbe and Czar-
B., 17, 1747
46, 1355
amide
nomski
Isodurenesulphonamid'e ....
Me4.(SO2.NH2)=1.2.3.5.6
„
....
118
Jacobsen
B., 15, 1854
44, 52
Ethylic dimethaniline-
NMe2.SO3Et=?
C10H1603SN
85
....
J. p. [2], 20, 263
sulphouate
Phenylthienylacetoxime ....
C4SH3.C(NOH).Ph
CUH9OSN
91-92
Comey
B., 17, 791
46, 1168
Thiophenic anilide
C4SH3.CO.NHPh
„
....
140
Leuckart and
B., 18, 2341
42, 1224
Schmidt
Cuminylthiocarbimide ....
MM
CnHnOSN
begins 245 ;
Liquid
Eaab
B., 10, 53
32, 894
d. 270
Dimethyiquinolinesulph-
N.Me3=a1;a1(3,
CnHn03SN
....
165-166
Berend
B., 17, 2717
48, 275
onic acid
it »
J} ^zaj ; p.ipj or dg
„
....
265-266
„
B., 17, 1489
46, 1197
Tolyl-a-methylthiohydan-
C6H4Me.N.CS.NH.
C,iH12OSN2
....
197 u.c.
Aschan
B., 17, 427
toi'n
CHMe.CO=1.4
Allylthiocarbamidobenzoic
C3H5.NH.CS.NH.C6H4.
C11H1202SN2
189 u.c. ; d.
„
B., 17, 431
46, 907
acid
CO2H=1.3
Tolylacetylthiobiuret
....
CnHl:iOS2N3
166
Tursini
B., 17, 586
46, 1141
Phenylmercapturic acid ....
....
C11H1303SN
B., 15, 1731
142-143
....
Z. P. C., 5, 335
Dimethylquinolinesulphate
N.Me2=a1|31a2;
CnH1304SN
....
225-228 p.d.
Engler & Kiehm
B., 18, 2247
48, 1246
Trimethylanhydrosulph-
S02.NH.C(OMe)2.C6H3.
CUH1306SN
144
Stokes
A. C. J., 6, 262
48, 539
aminephthalate
( 1
•
CO2Me=?.2.1
Phenyldiethylthiourethane
PhN : C(OEt).SEt
CnH16OSN
275 ; 278-
29-5-30-5
Liebermann
B., 13, 686 ; A.,
40, 44 ; 42, 298
280 c.; d.
207, 149
Isobutylic phenylthiocarb-
NHPh.CS.OBu3
„
....
75
Mylius
B., 5, 977
26, 267
amate
Methylic tolylthiourethane
C6H4Me.N : C(OEt).SMe
)»
a. 250 d.
Liquid
Liebermann
B., 13, 1577 ; A.,
40, 45 ; 42, 299
=1.2
207, 163
» »
=1.3
n
....
Liquid
„
„
„
» »
=1.4
„
a. 250 d.
Liquid
„
„
„
Sulphonamide of CnH16 ....
....
CnH17O2SN
....
64
Kelbe
B., 14, 1241
40, 809
Isobutyltoluenesulphon-
Me.Bu3.(S02.NH2)=1.3.?
ji
....
74-75
Kelbe and Baur
B., 16, 2562
46,300
amide
Butyltoluenesulphonamide
Me.Bu*.(SO2.NH2)=1.4.?
„
....
113
„
B., 16, 2565
„
a-Laurenesulphonamide ...
CnH15.(S02.NH2)
„
....
127
Eeuter
B., 16, 627
0-
„
„
2
„
B., 16, 628
Dinitrophenyl sulphide ...
S[C6H3(N02)2]2=(1.2.4)2
C12H609SN4
....
193
Beilstein and
B., 10, 1993; 11,
34, 139 ; 36,
Kurbatow
2056; A., 197, 77
230, 714
Dinitrophenylsulphone ...
S02[C6H3(N02)2]2=(1.2.4)2
CI2H6010SN4
....
240-241
H
1)
„
Dinitrohydroxyphenyl-
S02[C6H2.OH.(N02)2]2=?
C12H,012SN4
253 u.c.
Annaheim
B., 11, 1668
36,244
sulphone
Trinitrophenylic benzene-
Ph.S02.O.C6H2(NO2)3
C,2H7O9SN3
....
115-116
Schiaparelli
G. I., 11, 65
40, 603
sulphonate
Nitrophenyldisulphide ...
S2(C6H4.N02)2=(1.4)2
C12H804S2N2
....
181
Willgerodt
B., 18, 333
48, 519
Nitrophenylsulphone
S02(C6H4.N02)2
C12H806SN2
164
Gericke
A., 100, 211
vi., 277
»
„
„
....
168
Schmid
B., 9, 80
Trinitrobenzenesulphan-
fr. C6H4(NO2).S02.NH.
C12H808SN4
210
Michler and
B., 12, 1167
36, 922
ilide
C6H3.N02
Blattner
Nitrosulphobenzide
Ph.SO2.C6H4.NO2
C12H904SN
90-92
Gericke
A., 100, 209
vi., 277
Nitrophenylic benzene-
Ph.S03.C6H4.NO2=1.4
C12H906SN
....
82
Schiaparelli
G. I., 11, 65
40, 603
sulphonate
Diazophenylic benzene-
Ph.S02.N2.Ph
CTT f~\ C!"M"
12'^ 10 2*^ 2
....
75-76 d.
Konigs
B., 10, 1532
34, 220
sulphinate
Oxallylallylphenylthio-
NPh.CS.N(C3HJ2.CO2
161
Maley
Z. C. [2], 5, 261
vi., 1089
carbamide
i - i
Azobenzenesulphonic acid
Ph.N2.C6H4.SO3H=1.2
C12H1003SN2
127
Eichter
R. K. T., 309
Azoxybenzenesulphonic
Ph.N2O.C6H4.S03H=1.3
C12H1004SN2
60-70
Limpricht
B., 18, 1420
48, 984
acid
COMPOUNDS CONTAINING FIVE ELEMENTS.
671
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Azoxybenzenesulphonic
Ph.N2O.C6H4.S03H=1.4
C12H1004SN2
b. 100
Limpricht
B., 18, 1420
48, 984
acic
Benzenesulphonitranilide
N02.(NH.O2S.Ph)=1.2
11
....
104
Lellmann
B., 16, 594
44, 801
11
=1.3
„
131-132
11
B., 16, 595
11
11 '•
=1.4
„
139
11
11
11
Nitrodiphenylsulphon-
C6H4(N02).C6H4.S03H
„
228
Gabriel and Dam
B., 13, 1410
38, 890
amide
=(1.4)
bergis
Azobenzenedithiodi-
N2(C6H4.S02.SH)2=(1.3)2
C12H1004S4N2
91
Baur
A., 229, 353
48, 1140
sulphonic acic
11 11
11 11
ji
+ 1PI2O(2)
91-93
Limpricht
B., 18, 1471
48, 985
11 11
=(1-4),
„
b. 100
Baur
A., 229, 353
48, 1140
Azobenzenethiodisulphoni
S03H. C6H4.N2.C6H4.S02.SH
C12H1006S3N2
b. 100
11
11
„
acic
=(1.3)2
11 11
11 11
„
+xH20
b. 100
Limpricht
B., 18, 1472
48, 985
Azoxybenzenedisulphonic
ON2(C6H4.S03H)2=(1.3)2
C12H1007S2N2
....
125
Brunnemann
A., 202, 340
38, 807
acid
Benzenesulphanilide
Ph.SOj.NHPh
C12Hn02SN
102
Wallach
A., 214, 221
44, 48
11
11
11
....
105
....
A., 91, 107
11
„
„
MM
110
....
A., 100, 217
Diphenylsulphonamide ...
Ph.C6H4.S02.NH2
„
227-230
Gabriel & Deutsc
B., 13, 386
38, 476
Azophenolbenzenesulphon
HO.C6H4.N2.C6H4.S02.NH2
C12H1103SN3
A., 215, 231
212
Limpricht
B., 15, 1296
42, 1075
amide »
=1.4; 1.?
Ethylic a-nitronaphthalene
N02.(SO3Et)=a,a2;
C12HU06SN
....
101
Cleve
B. S. [2], 24, 510
34, 153
sulphonate
B., 10, 1723
11 *~ 11
11 =?
„
....
103
11
B. S. [2], 29, 415
34, 677
11 &- „
11 11
„
....
108
„
B., 12, 1714
38, 47
11 P~ 11
=1
„
B., 10, 1723
114
11
B. S. [2], 26, 446
34, 154
Dibenzsulphhydroxamic
(Ph.S02)2N.OH
C1JHU04S2N
....
109 d.
Konigs
B., 11, 617
acid
Phenylhydrazine benzene-
PLSOj-NHINHPh
C12H1202SN2
B., 8, 1007
130-131
Escales
B., 18, 895
48, 798
sulphinate
11 11
11
„
146
Fischer
A., 190, 132
34, 309
11 11
„
„
145
Konigs
B., 10, 1532
Phenylsulphamidoanilide
Ph.SO,,NH.C6H4.NH2=1.2
„
B., 14, 2184
168
Lellmann
A., 221, 1; B.,16,
44, 801 ; 46, 50
596
11
11 11
„
168
Schmid
B., 9, 80
Amidophenolsulphoanilide
OH.NH2.(SO2.NHPh)=1.4.6
C12H1203SN2
A., 205, 62
98
Post and Hoist
B., 13, 619
38, 642
„
=1.2.4
„
„
205
>i
B., 13, 618
Diphenyldisulphonamide....
(.C6H4.S02NH2)2=(1.4)2
C12H1204S2N2
a. 300
jrabriel & Deutsch
B., 13, 390
38, 477
Azobenzenedisulphon-
N2(C6H4.S02NH»)2=(1.4)2
C12H1204S2N4
....
176
Mahrenholz and
A., 202, 337
38, 805
amide
Gilbert
11
„ =meta ?
Jl
....
254
n
11
n
, 11
=1.3; 1.4
n
250
....
A., 215, 216
11
11 11
„
....
258
Jimpricht
B., 14, 1356
42, 517
11
=(1.3),
„
....
a. 260
11
B., 11, 1046
34, 722
11
11 11
„
....
295
Mahrenholz
A., 202, 336
38, 805
11
=(1.4),
n
....
d.w.m. 250
-iaar
B., 14, 1930
42, 195
11
=?
„
«...
nf. 300
jimpricht
B., 14, 1357
42, 517
Azoxy benzen edisulphon-
ON2(C6H4.S02NH2)2=(1.3)2
C12H1AS2N4
273
Jrunnemann
A., 202, 343
38, 807
amide
a-Naphthylthiourethane ....
C10H7.N:C(SH).OEt
C12H13OSN
....
96-97
Cosiner
B., 14, 62
/3-Naphthalenesulphon-
C10H7.S02.NHEt
C12H1302SN
....
82-5
^arleson
B. S. [2], 27, 360
2,490
ethylamide
"•- 11 11
,;
„
viscous
11
a
n
Phenylanimoiiium phenol-
OH.(SO,.NH,Ph)=1.4
C12H1304SN
d. 180-190
70
Kopp
B., 4, 978
5, 623 ; vii.,
sulphonate
918
'
NH2.02S.C6H4.N2.NH.C6H4.
C.jH^O.SjNs
....
83d.
lybbeiieth
A., 221, 204
6, 72
S02.NH2
Hydroxyazobenzenetri-
NH2.02S.CCH4.N2.C6H3
C12HI307S3N5
A., 215, 235
. 260
jimpricht
B., 15, 1297
sulphonamide
(OH).(S02.NH2)0=1.4;
672
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
j9-Azobenzenetetrasulphon-
N2[C6H3(S02.NH2)2]2
C12H1408S4N,
....
222
Reiche
A., 203, 71
38, 806
amide
=(1.1.3),
?-
=?
1>
229-230
Perl
G C. [1884], 468
48, 391
4th. Amidophenol sulphate
(C6H4.OH.NH:!),!+H2S04
C12H1606SN2
....
220 d.
Fittica
J. p. [2], 24, 1
42, 51
Amylic phenylthiocarbam-
NHPh.CO.StCj.H,,)
C12H17OSN
....
67
Schone
J. p. [2], 30. 416
48, 512
ate
Diethylic tolylthiocarb-
Me.[N:C(OEt)SEt]=1.2
JJ
a. 250 d.
Liquid
Liebermann and
B., 13, 1577 ; A.,
40, 45 ; 42, 299
amate
Natansou
207, 163
)> »
=1.3
»
a. 250 d.
Liquid
*>
»
»
11 )!
=1.4
J>
a. 250 d.
Liquid
u
»
j»
Ethylic mesitylthioure-
Me3.[N : C(SH).OEt]=1.3.5.6
»
....
88
Eisenberg
B., 15, 1015
48, 956
thane
Dipropylbenzenesulphon-
Pr2.(SOj.NH2)=1.4.5
C12H19O2SN
....
103
Kemsen and
A. C. J., 5, 161
46, 457
amide
Keiser
Nitrobenzenylamidothio-
fr. S.C6H4.N : CPh
C13H802SN2
....
188
Hofmann
B., 13, 1223
38, 885
phenol
1 1
Dinitrophenylic thiobenz-
SBz.(N02)2=1.2.4
C13H906SN2
....
113
Willgerodt
B., 18, 329
48, 519
oate
o-Hydroxybenzenylamido-
S.C6H4.N:C.C6H4.OH
C13H9OSN
129
Hofmann
B., 13, 1237
38, 887
thiophenol
i i
?
....
C^HjO-jSN
....
84
Gabriel and
B., 13, 389
Deutsch
Nitromethenylamidothio-
fr. S.C6H4.N:C.NHPh
C13H902SN3
....
247
Hofmann
B., 13, 12
38, 388
phenolanilide
1 J
Dinitrophenylbenzylthio-
(S.CH2Ph).(NO2)2=1.2.4
C13H1004SN2
....
128
Willgerodt
B., 18, 331
48, 520
ether
Dinitrodiphenylthiocarb-
CS(NH.C6H4.N02)2=(1.3)2
C13H1004SN4
B., 15, 470
160-161
Bruckner
B., 6, 1103
27, 77
amide
u »
» i>
Jl
....
160
Steudemann
B., 16, 550
44, 801
j> »
J> i)
1)
....
160-161
11
B., 16, 2333
46, 306
Phenylic phenylthiocarb-
NHPh.CO.SPh
Cj3HuOSN
125
Snape
....
47, 778
amate
Methyldiphenylamine
C6H4.SOn.C6H4.NMe
C13HnO2SN
222
Bernthsen
B., 16, 2901
46, 596
sulphone
i i
Nitrodiphenylthiocarb-
N02.(NH.CS.NHPh)=1.3
C^H.ASN,
145
Bruckner
B., 7, 1235
28, 166
amide
» »
» 3)
»>
>...
155
Losanitsch
B., 14, 2365
42, 183
Benzenesulphonbenzamide
Ph.SO2.NHBz
C13HUO3SN
J. [1856], 503
135-140
Gerhardt and
A. C. [3], 46, 145
i., 540
Chiozza
<> »
n
)J
A., 214, 211
147
Wallacli and
B., 11, 754
Gossmann
Nitrohydroxydiphenylthio-
NO2.C6H4.NH.CS.NH.C6H4.
C13HU03SN3
....
152
Steudemann
B., 16, 2335
46, 307
carbamide
OH=1.3; 1.4
Benzenesulphondinitro-
Ph.S02.NH.C6H3Me(NO:,)2
C13Hn06SN3
178
Lellmann
B., 16, 596
44, 801
toluide
=1.4.5.?
Hydroxydiphenylthiocarb-
NHPh.CS.NH.C6H4.OH
C13H12OSN2
....
146
Kalchoff
B., 16, 1829
44, 1110
amide
=1.2
11 11
=1.4
U
162
»
B., 16, 376
44, 735
Acetyl-a-naphthylthiocarb-
....
»J
....
198
....
B. S. [2], 28, 103
amide
Benzenesulphonbenzam-
Ph.SO2.N : CPh.NH2
C13H1202SN2
A., 184, 348
135
Wallach and
B., 11, 755
idine
Gossmann
11 ji
»
»
A., 108,215
139
....
A., 214, 218
Oxalylallyltolylthiocarb-
N(C,H5).CS.N(C0H:4Me).
J)
157
Maley
Z. C. [2], 5, 258 ;
vi., 1089
amide
i
J. [1869], 637
CO.CO=1.4
1
Dihydroxydiphenylthio-
CS(NH.C6H4.OH)2=(1.4)2
5?
.*..
222 d.
Kalchoff
B., 16, 1831
44,1110
carbamide
Benzenesulphonnitro-
Ph.SO2.NH.C6H3Me.NO2
C13H1204SN2
..»•
99
Lellmann
B., 16, 595 ; A.,
44, 801 ; 46,
toluide
=4.1.3
221, 1
51
Ethylic /3-naphthylthio-
C10H7.N:C(SH).OEt C13H13OSN
....
96-97
Cosiner
B., 14, 62
40, 606
carbamate
COMPOUNDS CONTAINING FIVE ELEMENTS.
673
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Toluenesulphonanilide ...
Me.(SO2.NHPh)=1.3
C13H130,SN
72
Miiller and
B., 12, 1349
Wiesinger
„
= 1.4
»
....
103
>»
B., 12, 1348
»
=1.2
?J
....
136
n
i)
Benzeuesulphontoluide ....
Me.(NH.O2S.Ph)=1.4
))
....
120
Wallach & Huth
B., 9, 427
Benzenesulphonamido-
Ph.SO2.NH.C6H3.Me.NH2
C13H1402SN2
....
146-5
Lellmann
B., 16, 597 ; A.,
44, 801 ; 46, 51
toluide
=4.1.3
221, 1
Phenylbutylthiohydanto'in
CO.NPh.CS.NH.CH.C4H9
C13H16OSN2
....
179 u.c.
Aschan
B., 16, 1545 ; 17,
44, 1107
i i
426
Toluylenediacetyldithio-
Me.(NH.CS.NHAc)3=?.1.3
C.A.OAN,
....
232
Lussy
B., 8, 668
28, 1036
carbamide
/3-Nitroanthraquinone-
C14H602-(N02).S03H
C14H.O7SN
....
250 d.
Glaus
B., 15, 1516
42, 1105
sulphonic acid
°' » 11
ii
)>
255 d.
»
B., 15, 1515
I!
Nitroanthraquinonedi-
C14H502(N02)(S03H)2
CuBtO^
....
181-182
Claus& Schneider
B., 16, 908
sulphonic acid
Anthraquinonesulphon-
C14H702-SO,NH2
C14H904SN
....
261
McHoul
B., 13, 692
40,52
amide
a-Amidoanthraquinone-
CMH60S.(NH3).S03H
C14H906SN
....
d.w.m. 360
Claus
B., 15, 1519
sulphonic acid
0- » )i
))
i)
a. 360 d.
)»
B., 15, 1520
Carbonylthiocarbanilide ....
Ph.N : C.NPh.CO.S ?
C14H10OSN2
87
Will
B., 14, 1486
40, 905
L i
Benzoylphenylthiocarb-
NPh.CS.NBz
»
186
Fischer and
A., 212, 330
42, 1095
izine
i 1
Besthorn
Naphthalene dinitrothio-
C10H8+C4SH2(N03)S
C14H1004SN2
50
Rosenberg
B., 18, 1778
48, 1051
phene
Phenylic benzoylthiocarb-
NHBz.CS.OPh
C14HU02SN
....
93
Miquel
A. C. [5], 11, 337
32, 872
amate
Phenylnitrobenzoylthio-
NHPh.CS.NH.CO.C6H4.NO2
C14H1103SN3
230 d.
D
A. C. [5], 11, 322
32, 870
carbamide
Phenylbenzoylthiocarb-
NHPh.CS.NHBz
C14H12OSN2
....
148-149
j>
A. C. [5], 11, 321
ii
amide
Benzphenylthiocarbamide
C6H4Bz.(NH.CS.NH2)= ?
>»
166
Dobner
A., 210, 246
42, 508
Phenylthiocarbamido-
NHPh.CS.NH.C6H4.CO2H
C14H1202SN2
B., 3, 244
190-191
Rathke and
A., 169, 106
27, 164
benzoic acid
=1.2
Schaflfer
11 11
» i)
»
191-192
Miquel
A. C. [5], 11, 324
32, 870
11 i»
=1.3
JJ
260-262 d.
Aschan
B., 17, 429
Nitrophenylnitrotolylthio-
NO2.C6H4.NH.CS.NH.
CHH1204SN4
188
Steudemann
B., 16, 2335
46, 306
carbamide
C6H3Me.OH=1.3; 1.4.5
Nitrobenzyldisulphide
S2(CH2.06H4.N02)2=(1.4)2
C14H1204S2N2
....
89
Strakosoh
B., 5, 698
25, 1028
Nitrotoluenesulphonbenz-
Me.N02.(S02.NHBz)=1.4.6
CI4H1ASN2
....
130
Wolkow
Z. C. [2], 7, 422
25, 147; vii.,
amide
1169
Diamidosulphobenzidedi-
S02(C6H3.NH2.C02H)2
C14H1206SN2
....
a. 350
Michael and
B., 10, 582
carboxylic acid
=(?.4.1)
Norton
Dinitrodimethoxysulpho-
S02(C6H3.N02.OMe)2
C14H1208SN2
....
214-215
Annaheim
A., 172, 49
27, 797
benzide
Benzenylph eny Ithio-
NHPh.CS.NH.CPh : NOH
CHH13OSN3
i..»
163
Kriiger
B., 18, 1060
48, 896
uramidoxime
Amidodiphenylsulphacetic
NH2.C6H4.06H4.S.CH2.CX).1H
C14H1302SN
a. 200
Gabriel and
B., 13, 1411
38, 890
acid
=(1.4)3
Dambergis
Nitrophenyltolylthiocarb-
C6H4Me.NH.CS.NH.C6H4.
C14H1302SNS
173
Steudemann
B., 16, 2335
46, 307
ainide
NO2=1.4 ; 1.3
Nitrotolylphenylthiocarb-
C6H3Me.N02.(NH.CS.NH
)»
....
143
»
B., 16, 2336
))
amide
Ph)=1.2.4
Toluenesulphobenzamide....
Me.(SO2.NHBz)=1.2
C14H1303SN
110-112
Wolkow
Z. C. [2], 6; 579
vll.,' 1169
») ....
=1.4
»
147-150
»
Z. 0. [2], 6, 578
vii., 1168
Nitrotoluenesulphonbenz-
C6H3Me(NO2).SO2.N : CPh.
C14H1304SN3
122-123
?i
B., 5, 142
25, 414
enylamidine
NH2=1.2.4
Ethylic nitrodiphenyl-
C6H4(N02).C6H4.S03Et
C14H1306SN
168-169
Gabriel
B., 13, 1410
sulphonate
=(1.4)2
4 R
674
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Toluenesulphonbenzenyl-
C6H4Me.SO2.N : CPh.NHs
C14H14O2SN2
....
114
Wolkow
B., 5, 141 ; Z. C.
25, 413 ; vii.,
amidine
=1.4
[2], 6, 577
1168
Nitrotoluenesulphotoluide
C6H3Me.N02.(S02.NH.
CHH1404SN2
....
130-131
11
Z. C. [2]
vii., 1174
C6H4Me)=1.2.4; 1.4
Azotoluenedisulphonic acid
N2(C6H3Me.S03H)2=(4.1.2)2
C11H1406S2N2
....
d.w.m. 190
Neale
A., 203, 80
38, 807
» »
11 11
))
+1$ H20
100
11
11
1)
Dimethamidosulpho-
Ph.S02.C6H4.NMe2
C14H1502SN
....
89
Michler and
B., 12, 1792
38, 108
benzide
Meyer
11
»)
n
81-82
Michler
B., 10, 1742
Toluenesulphotoluide
Me.(S02.NH.C6H4Me)=(1.3)2
H
....
103
Miiller
B., 12, 1349
jy «•«.
=(1.4),
)»
117
Wolkow
Z. C. [2], 6, 324
vii., 1168
„
»1 I)
»
....
118
Miiller
B., 12, 1348
jy ""
=(1.9),
»
134
Miiller
B., 12, 1348
Phenyltaurineanilide
NHPh.(CH2)2.SO2.NHPh
C14H1602SN2
....
74
Leymann
B., 18, 870
48, 786
Azotoluenedisulphonatnide
N2(C6H3Me.SO2NH2)2
C14H1804S2N4
250
Kornatzki
A., 221, 179
46, 71
=(2.1.3 or 5)s
n
=(4.1.2),
>»
....
270
Neale
A., 203, 82
38, 807
>i
» J)
J)
....
270
Heffter
A., 221, 208
46, 73
»
=(2.1.4),
))
....
300
Neale
A., 203, 76
38, 807
Sulphate of amidobenzoic
NH2.CO2H=1.2
C14H1608SN2
188
Hiibner
A., 149, 129
vi., 319
acid
)I 1!
=4th
))
....
225
Fittica
B., 9, 792
30, 412
i) ii
=1.2
*1
....
230
Hubner
Z. C. [2]
vi., 317
ii ii
» J)
J)
+H20
225
))
J»
ii
» 11
=1.3
>J
....
235
Fittica
J. p. [2], 13, 184;
30,412; 36,151
B., 9, 792
)! II
=4th
J)
• »..
240
ji
J. p. [2], 13, 184
36, 152
Methylphenylhydrazine-
(C7H10N2)2H2S04
C14H2204SN4
....
180
Tafel
B., 18, 1742
48, 1061
sulphate
Tetrethylbenzenesulphon-
Et4.(S02NH2)=1.2.3.5.6
CHH^O^SN
.*(•
104-105
Galle
B., 16, 1746
44, 1092
amide
Ethylcarbimidealdehyde
....
C14H3102S2N5
....
118-119
Schiff
B., 9, 573 ; G. I.,
30, 285 ; 31, 314
ammonia
4,244
?
C15H805SN4
MM
235
Stojentin
J. p. [2], 32, 1
48, 1195
Diphenylthiohydanto'in ....
CO.NPh.CS.NPh.CH2
i i
C15H12OSN2
A., 207, 123
176
Lange
B., 12, 595
36, 651
Thiocarbamidobenzoic acid
CS(NH.C6H4.C02H)2
C15HI204SN2
B., 3, 812
a. 300
Merz and Weith
Z. C. [2], 7, 45
24, 231
1! II
)»
»»
....
begins 300 d.
Rathke & Schaffer
A., 169, 102
27, 163
Dinitroditolylthiocarb-
CS[NH.C6H2Me(NO2),]2
C15H1203SN6
....
207
Steudemanu
B., 16, 2338
46, 307
amide
=(4.1.2.?),
Ethylic thiodiphenylcarb-
C12H3SN.C02Et
C15H1302SN
«...
109-110
Frankel
B., 18, 1845
48, 1130
amate
Benzylbeuzoylthiocarb-
NH2.CS.NBz.CH2Ph
C16H14OSN2
130
Miquel
B. S. [2], 25, 104
30,73
amide
» 11
NHBz.CS.NH.CH2Ph
»
145
11
A. C. [5], 11, 324
32, 871
p-Tolyl „
NHBz.CS.NH.C6H4Me
))
165
11
J)
)>
Acetoxydiphenylthio-
NHPh.CS.NH.C6H4.OAc
C15H1402SN2
....
137
Kalehoff
B., 16, 1831
44, 1110
carbamide
=1.4
Diphenyltaurocarbamic
....
C15H1403SN2
....
186-187 d.
Andreasch
M. C., 4, 136
44, 665
anhydride
Nitroditolylthiocarbamide
C6H4Me.NH.CS.NH.C6H3
C15H1502SN3
»•••
169
Steudemann
B., 16, 2338
46, 308
Me.NO2=1.4; 4.1.2
|
Xylenesulphobenzamide ...
Me2.(S02.NHBz)=1.3.4
C1SH1;03SN
....
149-151
Mahon
A. C. J., 4, 192
42, 1208
Cinnamaldehydeanilide
'Ph.CH : CH.CH : NPh
C15H1604SN
....
157
Peine
B., 17, 2118
46, 1345
sulphate
+H2SO4
Dianisylthiocarbamide ...
CS(NH.C,H4.OMe),=(1.2),
CI5H1602SN2
...*
134-5
Miilhauser
B., 13, 923 ; A.,
38, 642 ; 42, 302
207, 246
11 •••
=(1.4).
))
185
Salkowski
B., 7, 1012
28, 65
Dimethylquinolphenyl-
NHPh.CS.NH.C6H3(OMe)2
)J
137
Baessler
B., 17, 2123
46, 1330
thiocarbamide
=14.1
Dimethamidophenyltolyl-
C6H4Me.S03.C6H4.NMe2=1.4
C15H17O2SN
95
Michler & Meyer
B,, 12, 1793
38, 108
sulphone
COMPOUNDS CONTAINING FIVE ELEMENTS.
675
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
? (ortho)
NHPh.CH(OH).C6H4.O.CH2.
C15HI703SN
....
186
Rossing
B., 17, 2994
48, 388
CO2H+H2SO4
Oxallyldiphenyldithio-
NH:(CS.NPh.co),:
CTT f~\ Q "\T
16-*-*-ll^-'''l^2 3
....
215
Stojentin .
J. p. [21 32, 1
48, 1196
biuret
a-Naphthalenesulphon-
C10H7.SO.2.NHPh
Ci6H13O2SN
....
112
Carleson
B. S. [2], 27, 360
32, 490
anilide
18-
M
„
....
132
„
M
„
Carbonylthiocarbotoluide
S.CO.NPh.C:N.C6H4Me
C16H14OSN2
....
116
Will
B., 14, 1487
40, 906
i >
Phenylacetylthiocarb-
Ph.NH.CS.NAc.C6H4.CO2H
C16H1403SN2
....
159-160
Aschan
B., 17, 429
amidobenzoic acid
=1.3
•
Diphenyldiacetylthiodi-
S(NAcPh)2
C16H1602SN2
125-126
Smit
B., 8, 1447
29, 603
amine
Acetamidophenyl sulphide
S(C6H4.NHAc)2
„
....
213-5; 215
Merz and Weith
B. 4,390
24, 567; vii.,
1154
„ disulphide
S2(C6H4.NHAc).,
C16H1602S2N3
....
215-217
Schmidt
B., 11, 1171
34, 974
„ trisulphide
S3(C6H4.NHAc)3
C16H1602S3N3
....
213-214-5
„
„
„
Diethoxydinitrodiphenyl-
S02(C6H3.N02.OEt)2
C16H1608SN3
....
192
Annaheim
A., 172, 53
27, 797
sulphone
Benzenesulphocumenamide
Ph.SO2.NH.C10H1iO
C16H1703SN
J. [1856], 505
161
Gerhardt and
A. C. [3], 46, 151
ii., 177
Chiozza
Azobenzene-a-thymo-
Ph.N2.C,HMePr.OH.S03H
CI6H1804SN2
....
215-75 d.
Stebbins
B., 14, 2793 ;
42, 834
sulphonic acid
A. C. J., 3, 112
Diethylic azobenzenedi-
N3(C6H4.S03Et)2=(1.3)2
C16H1806S3N2
....
100
Mahrenholz and
A., 202, 336
38, 805
sulphonate
Gilbert
Di(phenylsulphonethyl)-
NH(C2H4.SO2.Ph)2
CWHI90482N
....
77
Otto
J. p. [2], 30, 321
48, 537
amine
Tolylimidotolylmethylthio-
C6H4Me.N : C(SMe).NH.
C^HjioO.S.jN.j
....
155-156
Will and Biel-
B., 15, 1310
carbamate sulphate
C6H4Me.H2SO4=(1.4)2
schowski
Azoxylenedisulphonamide
N2(C6H2Me2.S02NH2)2
C16H2004S2N4
....
174
Limpricht
B., 18, 2191
Di(phenylsulphonethyl)-
NH(C2H4.SO2.Ph)2.HNO3
C16H2007S2N2
....
189 d.
Otto and Dam-
J. p. [2], 30, 321
48, 537
amine nitrate
kohler
Xylidine sulphate
(C6H3Me2.NH2)2.H2SO4
C16H24O4SN2
198-210
IK*
Samonoff
J. R. [1882], 327
44, 180
Allylcarbimidealdehyde
[C3H5.N(OEt).CS.NC2H4]2
C16H3102S2N5
....
107-108
Schiff
G. I., 4, 244;
31, 313
ammonia
+NH3
B., 9, 571
a-Naphthalenesulphobenz-
C10H7.S02.NHBz
C17H1303SN
A., 114, 138
194-195
....
Z. C. [1871], 423
amide
Cymenesulph obenzeny 1-
C6H3MePr.S02.N : CPh.NH2
C17H20O2SN2
....
188
Wolkow
B., 5, 142
25, 414
amidine
Dimethylquinolthiocarb-
CS[NH.C,H3(OMe)3]2
C17HM04SN2
t*M
109
Bassler
B., 17, 2123
46, 1330
amide
= (?.4.1)2
Tolylimidotolylethylene-
CJ7H1,SN2.H2S04=(1.4)2
cnamo4sast
...*
194
Will and Biel-
B., 15, 1314
thiocarbamate
schowski
Sinapineth iocy anate
C16H22Oi,N.S.CN
C17H22O5SN2
....
176
Remsen & Coale
A. C. J., 6, 50
46, 1387
Anthracene + dini troth i o-
C14H10+C4SH2(N02)2
C18H1304SN2
....
162
Rosenberg
B., 18, 1778
48, 1052
phene
a-Naphthylbenzoylthio-
C10H7.NH.CS.NHBz
C19H14OSN2
• ...
172-173
Miquel
A. C. [5], 11, 326
32, 871
carbamide
Benzenesulphodiphen-
Ph.SO2.NPh2
C^H.ASN
124
Wallach
A., 214, 220
44, 48
amide
?
(Ph.S02)3NO
C18H1607S3N
A., 141, 371
98 ; 98-5
Konigs
B., 11, 618, 1590
34, 574
?
M
„
98-5
Otto and Ostrop
A., 141, 371
vi., 276
a-Naphthyldimethamido-
CloH,.S02.C6H4.NMe2
C18H1702SN
....
91
Michler and
B., 12, 1789
38, 108
phenylsulphone
Salath6
P" »
„
1)
115-116 u.c.
Michael & Adair
B., 10, 586
J
or C18H1904S2N3
C18H1704S2N,
112-115
A., 207, 129
?
or C1SH17O4S2N3
CI8H1904S2NS
jj
....
,.
Phenylurethane sulphide....
S2[C(OEt) : NPh]2
C18H2002S2N2
....
102
Liebermann and
B., 13, 1575; A.,
40, 45 ; 42, 299
Natanson
207, 159
Ditolylsulphonethylamine
NH(C2H4.SO2.C6H4Me)2
C18H2304S2N
MM
Liquid
Otto
J. p. [2], 30, 321
48, 538
=(1.4)2
Dimesitylenesulphamide ...
....
„
....
124
....
A., 184, 187
4 R 2
676
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
xAuthority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Dipseudooumenesulph-
...I
C18H2304SSN
....
177
....
A., 184, 185
amide
Benzoylthiodiphenylamine
C12H8NSBz
C19H13OSN
brown 167
170-5
Fraenkl
B., 18, 1844
48, 1130
Phenylsulphophenylbenz-
NHPh.CPh : N.S02.Ph
C19Hle02SN2
138-139
Wallach and
B., 11, 754; A.,
34, 670; 44, 48
amidine
Gossmann
214, 214
Furfuramide allylcarb-
CI5H1203N2+C3H8.NCS
C19H1703SN3
d. 135
118
Schiff
B., 10, 1191
34,47
imide
Amylic thiodiphenylallo-
(CPh:NO)2.C5H12S
C19H2202SN2
70
Hofmann
B., 4, 249
24, 394; vii.,
phanate
408
Nitronaphthylsulphide ...
S(C10H6.N02)2
CjoH.oO.SN,
230-231 u.c.
Ekstrand
B., 17, 2604
48, 171
A nthraquinone-m-sulphon-
C14H7O2.SO2.NHPh
C20H1304SN
...
193
M'Houl
B., 13, 692
40, 52
anilide
a-Naphthalenesulpho-
C10H7.S02.NH.C10H;
C2UH1502SN
82
Carleson
B. S. [2], 27, 360
32, 491
naphthalide
ft- » »
»
5)
....
177-5
V
)»
))
Benzenesulphodibenzanride
Ph.SO2.NBz2
C20H1;,O4SN
....
105
Gerhardt
J. [1856], 505
i., 540
Tolylsulphophenylbenz-
C8H4Me.NH.CPh : N-SO^Ph
C20H1302SN2
J. [1879], 438
145-146
Wallach and
A., 214, 216 ; B.,
44, 48
amidine
Gossmann
11, 755
Thallin sulphate
(C9H10NOMe)2.H2S04
CMH2ASN2
B.r. 18, 72
100 s.d.
Vulpius
A. P. [3], 22, 840
48, 399
Thiocarbanilidothiox-
NHPh. CS.CO.NPh.CS.
C21H17OS2N3
231
Stojentin
J. p., 32, 1
48, 1195
anilide
NHPh
p-Diazotrisulphotoluene
....
CS1H2206S3N2
190
Otto and Griiber
A., 145, 19
vi., 289
hydride
Dicuminylthiocarbamide ....
CS(NH.CIOH13)2
C2IH2802SN2
MM
128
Kaab
B., 10, 53
32, 894
Dimethamidophenylic
C14H7O2.SO2.C6H4.NMe2
C22H17O4SN
....
171
M'Houl
B., 13, 693
40,52
m-anthraquinone-sulph-
onate
Diisoamyloxydinitrodi-
S02(C6H3.N02.OC6HU)2
C^H-sOgSN,,
....
150-151
4nnaheim
A., 172, 57
27, 797
phenylsulphone
Phenylcarbimide +alde-
....
C22H8102S2N6
....
148 d.
Schiff
B., 9, 567
30, 285
hyde ammonia
Dithiotetraphenylcarb-
CO(NC12H8S)2
C26H16OS2N2
....
223-225
Fraenkl
B., 18, 1848
48, 1130
amide
?-piorate
C14H8S2+2C6H2.OH.(N02)3
C26H14014S2N6
....
146
Limpricht
B., 6, 534
26, 1032
Diphenyld ibenzoylthio-
S(NPhBz)2
C26H2()O2SN2
....
150
Smit
B., 8, 1448
20, 603
diamine
Benzoylphenylthiocarb-
CS(NH.C6H4Bz)2=(1.4)2
C27H2002SN2
A., 210, 273
166
Dobner & Weiss
B., 14, 1840
42, 177
araide
Tetranitrothionessal
....
C^H^SN,
....
a. 250
....
A., 144, 197
Succinylbenzoylbenzene-
MM
C30H2403S2N2
146
....
J. [1856], 507
sulphamide
Tetramethoxydiphenyl-
[.C6H2(OMe)2.NH.CS.
QoHsoOAN,
184
Baessler
B., 17, 2128
46, 1331
phenylthiocarbamide
NHPh]2=(?.1.4.?)s
Trisulphodiphenylnitric
(Ph.C6H4.S02)3NO
C36H27O.S3N
178
Gabriel & Deutsch
B., 13, 389
38, 477
oxide
Pseudoleucine
C36H78012SN6
>.••
210
Hesse
J. p., 70, 34
iii., 582
Cinchoniue sulphate
(C19H22ON2)2H2S04
C38H4606SN4
+2H2O
a. 100
Pastrew
....
i., 977
11 »
)>
H
196 u.c.
Skraup
A., 197, 352
36, 948
Trimethylic dithiophos-
MeS.(OMe)2PS
C3H902S2P
Liquid — 12
Kovalevsky
A., 119, 303
vii., 1122
phate
Triethylic trithiophosphate
Et3POS3
C6H15OS3P
....
Liquid — 18
Carius
A., 119, 289
vii., 1120
„ dithiophosphate
Et3P02S,
C6H1502S2P
....
Liquid — 18
D
)>
»
„ thiophosphate ....
Et3PO3S
C6H1503SP
....
Liquid — 18
»
)j
,,
Tetraethylic pentathio-
(EtS)2(EtO)2P2S3
C3H20O2S5P2
J. [1861], 586
71-2
»
A., 119,300
vii., 1124
pyrophosphate
Tetraethylic dithiopyro-
(EtO)4P2S2O
11
b. 160 d.
Liquid
D
A., 119, 299
vii., 1123
phosphate
Diethylic thiophosphenyl-
Ph.PS(OEt)2
C10H1602SP
....
Liquid
Kohler and
B., 9, 1054
30, 526
ate
Michaelis
COMPOUNDS CONTAINING FIVE ELEMENTS.
677
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Phenoxydiphenylphos-
PhO.S.PPh2
C18H15OSP
....
124
Michaelis&Coste
B., 18, 2115
48, 1215
phine sulphide
Triphenylic trithiophos-
Ph3POS3
CI8H15OS3P
....
72
....
J. p. [2], 10, 232
phate
Triphenylic thiophosphate
Ph3PO3S
C18H1503SP
390-394 s.d.
48-49
Kreysler
B., 18, 1719
48, 1056
)j »
1»
»
a. 300 d.
49
....
J. p. [2], 10, 233
Tribenzylphosphine oxide
5[(Ph.CH2)3PO]+S
CiosHujsOsSPs
....
211-212
Letts and Collie
T. E., 30, 181
42, 725
+s
Methyltriethylstibium
(MeEt3Sb)2SO4
C;H18O4SSb
....
100
Friedlander
J. p., 70, 443
i., 348
sulphate
Methylselenide nitrate ....
Me2Se(OH).N03(?)
C2H703SeN
90-5
Jackson
B., 8, 110
28, 553
Nitrobenzylseleniocyanate
C6H4.NOj.(CH2.SeCN)
Q.H.O.SeN,
A., 179, 16
122-5
ii
B., 8, 322
28, 1025
Phenoxydiphenylphos-
PPh2.Se.OPh
C18H15OSeP
114-115
Michaelis&Coste
B., 18, 2115
48, 1215
phinselenide
Phosphate of a base
formula uncertain
C4H1304N2P
170
Schreiner
A., 194, 68
36, 72
Nitrophosphenylic acid ...
C6H4(N02).PO(OH)2
C6H605NP
d. a. 200
132
Michaelis and
B., 8, 1312; A.,
29, 599 ; 34, 57
Benzinger
188, 276
» j»
))
))
....
140
Benzinger
B., 8, 501
28, 1205
Nitrophenylic phosphate ...
PO(OH)2(O.C6H4.N02)
C6H606NP
....
112
Eapp
A., 224, 156
46, 1337
Diazophosphenylic acid
N03.N2.C6H4.PO(OH)2
C6H606N3P
in.
188
Michaelis and
B., 9, 516 j A.,
30, 204; 34, 58
nitrate
Benzinger
188, 288
?
CHMe2.CH : CH(CMe :
C7H1504NP
....
169-170 d.
Michaelia
B., 18, 906
48, 748
NOH).PO(OH)2
Dinitrodiphenylic phos-
PO(OH)(O.C6H4.NO2)2
C12H908N2P
....
133-5
Rapp
A., 224, 156
46, 1338
phate
Phosphorous dianilide
(Ph.NH)2P.OH
CI3H13ON2P
C.N.,50,220
87
Jackson and
B., 16,570; A.C.
48, 254
Menke
J., 4, 380; 6, 89
Phosphoric dianilide
(Ph.NH)2PO.OH
C12H1302N2P
....
196
Michaelis& Soden
A., 229, 334
48, 1134
Trinitrotriphenylphosphine
PO(C6H4.N02)3
C18H1207N3P
d. a. 243
243
Soden
B., 17, 922
46, 1180
oxide
Trinitrotriphenylic phos-
PO(O.C6H4.N02)3=(1.2)3
C18H12010N3P
126
....
Z. C. [1870], 230
phate
» »
— 9
i) » — *
))
....
155
Eapp
A., 224, 156
46, 1333
Phosphenyldiamide
PON2Ph3
C18H15ON2P
....
b. 100
Wichelhaus
Z. C. [2], 6, 54
vi., 932
Diphenyh'c phosphanilate
Ph.NH.PO(OPh)2
C18H1603NP
....
127-129
Wallach and
B., 8, 1236
29, 263
Heymer
Orthophosphoric trianilide
PO(NHPh)3
C18H18ON3P
208
Michaelis & Sodei
A., 229, 334
48, 1134
Triamidotriphenylphos-
PO(C,H4.NH2)3
)»
....
259
Soden
B., 17, 923
46, 1180
phine oxide
Aniline diphenylic phos-
PH.NH3O.PO(OPh)2
C1SH13O4NP
....
160
Wallach and
B., 8, 1236
89, 263
phate
Heymer
Quinine hypophosphite ....
C20H2402N2+H3POa
CooH^O.NjP
150 p. d.
Smith
Z. P., 1, 159
v., 20
Diphenylmethylethyl-
C6H2(N02)3.0(PPh2MeEt)
C21H20OrN3P
86
Michaelis and
A., 207, 193
42, 306
phosphonium picrate
Link
Triacetamidotriphenyl-
PO(C6H4.NHAc)3
C^O^P
187-5
Soden
B., 17, 923
46, 1180
phosphine oxide
Tridimethamidotriphenyl-
POCC^-NMe,),
C24H30ON3P
150-152
Michaelis and
A., 229, 334
I
48, 1135
phosphine oxide
Soden
Triphenylbenzylphos-
PPh3(CH2Ph).N03
C26H2203NP
203d.
D
phonium nitrate
J>
Triphenylbenzylphos-
PPh3(CH2Ph).O.C6H2(N02)3
C»Htfl^f
148
jj
n
phonium picrate
Tribenzarnidotriphenyl-
PO(C6H4.NHBz)3
C39H3004N3P
180
Soden
B., 17, 923
46, 1180
phosphine oxide
1 (C.N., 50, 220)
(NHPh)7P302H2(?)
C42H4402N7P3
208
Jackson & Menke
A. C. J., 6, 89
48, 254
Protagon
~* TT C\ AT ~P
_
v-/160Jrl303v-'351' 5^
....
begins 200
Gamgee
B., 12, 1229
36, 950
C78
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diphenylmethylethyl-
C6H2(N02)3.0(PPh.,MeEt)
C21H2007N3As
95
Michaelis and
A., 207, 193
42, 305
arsonium picrate
Link
Stibtriethylnitrate
Et3Sb(N03)2
C6H1506N2Sb
62-5
....
»MI
i., 343
Stibtriamylnitrate
(C5Hn)3Sb(N03)2
C15H8306N2Sb
....
20
Berle
J. p., 65, 385
i., 340
Triethylallylthiocarb-
CS:NPEt3(C3H5)
ClnH20SNP
As., 1,48
68
Hofmann
P. T. [1860], 439 ;
iv., 610
phosphamide
B., 3, 766
Triethylphenylthiocarb-
CS : NPEtjPh
C^SNP
....
58
»
P. T. [1860], 432
n
phosphamide
Orthothiophosphoric tri-
PS(NHPh)3
C18H,SSN3P
J., 21,734
78
Chevrier
Z. C. [1868], 539
anilide
Triphenylbenzylphospho-
PPh3(CH2Ph).SCN
C^H^SNP
....
189
Michaelis and
A., 229, 334
48, 1135
nium thiocyanate
Soden
Dibrom-j3-thiophened i -
C4SBr2(S02Cl)j
C4Cl2Br204S3
brown 180
215 d.
Langer
B., 18,556
48, 766
sulphonyl chloride
Pentabrombenzenesulph-
C6Br5.S02Cl
C6ClBr5O2S
90
Limpricht and
B., 9, 479; A.,
30, 202, 30o
onyl chloride
Beckurts
181, 209
)I !>
})
»)
97
Limpricht
A., 191, 175
34, 495
» )»
»)
1)
....
153-154
Heinzelmann
A., 197, 311
36, 802
Trichlordibromnitroethane
C2013Br2(N02)
C2Cl3Br2O2N
120
Hoch
J. p. [2], 6, 96
26, 364; vii.,
259
Tetrachlorethylidenimide-
cci3.cci:N.POCi2
C2C1,ONP
255-259
78-81
Wallach
B., 15, 1608 ; A.,
32, 183
chlorphosphoryl
184, 25
» )»
3J
!»
255-259
s. 70-80
»
B., 8, 306
28, 884
Dinitrodibromthiophene ...
C4SBr2(N02)2
C4Br2O4SN2
....
134
Kreis
B., 17, 2075
46, 1314
679
V.-COMPOUNDS CONTAINING SIX ELEMENTS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Fluobenzenesulphonyl-
C6H4F.SO2C1=1.4
C6H4FC102S
....
36
Lenz
B., 10, 1136 ; 12,
36, 650
chloride
581
Fluobenzenesulphonamide
C6H4F.(SO2.NH2)=1.4
C6H6F02SN
....
123
»»
j>
32, 770; 36, 650
Chlorbromiodacrylic acid....
CjClBrl.COjH
C3HClBrI02
fr. H2O
110
Mabery & Lloyd
B., 15, 1756;
48, 1049
fr. CS2
115-116
A. C. J., 4, 92
Trimethylsulphinechlor-
Me3SIBrCl
C3H9ClBrIS
87 p.d.
Dobbin & Masson
47,61
bromiodide
Dibrom-|3-thiophenesulph-
C4SHBr2.SO2Cl
C4HClBrO2S,
Liquid
Langer
B., 18, 553
48, 765
onylchloride
„ -/3-thiophenic chlor-
C4SHBr2.COCl (identical)
C5HClBr2OS
250-270
SB-5
Bonz
B., 18, 2312
48, 1206
ide
» ~a~ » »
»> >J
M
....
39-5
»
»
»
Tetrabrombenzenesulph-
Br4.S02Cl=1.2.3.5.6
C6HClBr4O2S
....
85-91
Keinke
A., 186, 271
38, 464
onylchloride
»> »
»» >»
»
....
91-5
Limpricht and
B., 9, 477 ; A.,
30, 201, 305
Beckurts
181, 219
); )>
)» jy
)>
....
93
Knuth
A., 186, 300
32, 468
i» »
»* »
))
96-5
Limpricht
A., 191, 201, 227
34, 494
>J »
„ =1.2.3.4.5
1)
....
120
Lenz
A., 181, 46
30, 200
» »
j) j>
)>
....
120
Spiegelberg
A., 197, 295
36, 801
Tribroinbenzenesulphonyl-
Br3.SO2Cl=l.(?)3.6
C6H2ClBr3O2S
....
56
Limpricht
B., 8, 1070
89,82
chloride
n ))
!> ))
»
....
56
Bahlmann
A., 181, 208
30, 306
»» »
„ =1.3.5.6
»
62-63
Limpricht and
B., 9, 550; A.,
30, 302 ; 32,
Eeinke
186, 277
461
I! 1>
H >J
»
....
64-5
Limpricht
B., 9, 476
30, 201
11 1)
)> )»
»
....
64-5
Knuth
A., 186, 295
32,467
» »
J) I»
»)
64-65
Limpricht
A., 191, 196, 212
34, 493
)> JI
» =l.(?)2-6
»
....
72
Bahlmann
A., 181, 208
30, 306
J» »
» =?
J)
....
78
fieinke
A., 186, 271
32, 465
?» )>
„ =1.2.4.6
1]
....
85-5
Knuth
A., 186, 209
32, 469
» 1»
» »
)»
86
Lenz
A., 181, 40
30, 200
!» »
„ =1.2.4.5
»J
A., 186, 304
84-5
Keinke
A., 186, 289
38, 465
» ))
» J>
»
....
85-5
Spiegelberg
A., 197, 284
36, 799
)' >»
)) J)
)»
86-5
Limpricht
A., 191, 191
34, 493
J) »
„ =1.2.?.4
H
identical ?
120-121
Limpricht and
B., 9, 1862; A.,
31, 596 ; 32,
Goslich
186, 155
461
J> »
„ =1.2.3.5
»
»
137 ; cf. 123
Lenz
A., 181, 31
30, 199
» )>
» =»
>»
yellow
125
Limpricht
B., 8, 1068
29, 82
>J »
5J »
»
colourless
195
»
)>
)J
Dibrombenzenedisulph-
Br2.(SO2Cl)2=1.4.5.?
C6H2Cl,,Br2O4S2
....
161
Borus
A., 187, 367
32, 770
onylchloride
Dibrombenzeuesulphouyl-
Brj.SOsCa=1.2.4
CeHjClBrjOjS
A., 191, 180
31
Limpricht and
B., 9, 1861 ; A.,
31, 595 ; 32,
chloride
Goslich
186, 146
460
» )»
V »)
)3
....
34
Sachse
A., 188, 143
32, 752
?) »
» »
)»
....
34
Spiegelberg
A., 197, 257
36, 797
j> j>
„ =1.3.5
JJ
....
57-5
Lenz
A., 181, 28
30, 199
!> »
>» »
)1
A., 181, 202
57 '5
Limpricht
B., 8, 1066
29, 81
»1 »
» »
»
57-5
Sachse
A., 188, 143
32, 752
11 »
„ =1.4.5
N
....
70-5
Limpricht
B., 8, 1072
29,82
M »
» »
jj
....
70-5; 71
»
B., 9, 1859, 1868
31, 597
J> 1)
i) )»
»
....
71
»
B., 10, 318
32, 192
V )»
>» »
jj
71
Bahlmann
A., 181, 207
30, 306
680
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dibrombenzenesulphonyl-
Br2.S02Cl=1.45
C6H3ClBr202S
....
71
Limpricht
A., 186, 131
32, 4GO
chloride
»
)> J»
))
....
71
Bahlmann
A., 186, 313
32, 609, 610
»
» i»
3J
71
Sachse
A., 188, 143
32, 752
»
)> »
)J
....
71-72
Borus
A., 187, 350
32, 768
)>
„ =1.3.4
1)
....
79
Limpricht
A., 191, 234
34, 493
»
» =?
JJ
....
84
jt
B., 8, 1070
29, 82
!>
= 1.?.6
>
97-98
j,
B., 9, 1862
31, 596
»
'> »
)J
97-98
Bahlmann
A., 181, 207
30, 306
j»
=1.2.3
»
127
Sachae
A., 188, 155
32, 752
Brombenzenedisulphonyl-
Br.(S02Cl)2=1.2.6
C6H3Cl2BrO4S2
....
99
Heinzelmann
A., 188, 179
32, 773
chloride
>»
=1.2.4
J»
103
i)
A., 190, 222
34, 410
»
)» it
»
....
103-105
Meyer
B., 7, 1311
28, 259
»
» »
J)
....
103-105
Zander
A., 198, 11
38, 123
»
„ =1.3.2 or 4
M
....
104
»
A., 198, 29
38, 124
Chlorbenzenesulphonyl-
Cl.S02Br=1.4
C6H4aBrO2S
J. [1867], 630
52-53
Otto
A., 145, 324
vi., 274
bromide
Brombenzenesulphonyl-
Br.S02Cl=1.3
19
B., 7, 1352
Liquid
Limpricht
B., 7, 1352
28, 268
chloride
»
») J)
»
....
Liquid
»
A., 186, 134
32, 459
n
)> »
>»
....
Liquid
Berndsen
A., 177, 94
28, 1029
»
» =1-2
»
A., 177, 101
51
Limpricht
B., 10, 318
32, 193
»
!) ))
)»
51
Bahlmann
A., 181, 203; 186
30, 306; 32, 611
307
»
„ =1.4
JJ
....
69
Limpricht
B., 7, 1352
28, 268
»
» »
»
75
Nolting
B., 7, 1310
28, 264
»
» )>
»)
75
Goslich
B., 8, 352; A.,
28, 764;29,92»
180, 98
»
>J J)
»
....
75-76
Nolting
B., 8, 595, 596
i>
» )»
))
75-76
Siibner & Alsberg
Z. C. [2], 6, 389
vii., 153
)i
„ =?
5)
185-187
Limpricht
B., 14, 1361
42, 518
Disulphonylchloride brom-
CO2H,Br. (SOSC1) 2= 1.4. (?),
C7H3Cl2BrO6S2
151
Kornatzki
A., 221, 191
46, 70
benzoic acid
Chloride of Sulpho-p-brom-
C02H.Br.S02Cl or COCl.Br.
C7H4ClBrO4S
....
108
Bottinger
B., 9, 1252
31, 82
benzoic acid
S03H=1.4?
»
» »
»
155 d.
j>
B., 9, 803
30, 413
»
» i)
)>
....
176
j>
B., 9, 1252
31, 82
»
» »
J>
197 d.
»
A., 191, 18
34, 730
Tribromtoluenesulphonyl-
Me.Brs.SO2Cl=l.(?)3.4
H
Liquid
Limpricht
B., 7, 1355; A.,
28, 268
chloride
174, 355
Bromtoluenedisulphonyl-
Me.Br.(S02Cl)2=1.2.3.5
C7H5Cl2BrO4S.,
....
90
»
B., 18, 2177
48, 1233
chloride
»
=1.4(1),
J)
99
Kornatzki
A., 221, 191
46, 70
»
„ =1.4(2.6 or 3.5)
JJ
133 ; sf. 129
Limpricht
B., 18, 2179
48, 1233
Brombenzylsulphonyl-
Br.(CH2.SO2a)=1.4
CjHjClBrOsS
107
Mohr
A., 221, 215
46, 69
chloride
)»
>i »
))
115
Jackson and
A. C. J., 5, 264
46, 665
Hartshorn
Bromtoluenesulphonyl-
Me.Br.S02a=?
II
A., 169, 385
Liquid
Hayduck
A., 177, 60
28, 1030
chloride
•
»
=1.4.6
»
30-35
Jenssen
A., 172, 238
28, 78
»
» j>
J»
35
Hiibner and Post
A., 169, 21
27, 57
!>
» »
5>
35
Hasselbarth
B., 6, 411
26, 886
»
=1.3.5
»
....
52
Seville & Winther
B., 13, 1944
n
„ =1.2.3 or 5
»l
52-53
Hiibner and Post
A., 169, 40
27, 59
»
» »
»
....
53
Pagel
A., 176, 296
28, 898
!>
» »
1»
....
53
Limpricht
B., 7, 720
27, 991
1)
» »
»
53
j»
B., 7, 1393
28, 36S
1)
i) »
»
....
53
Pechmann
A., 183, 195
28, 80
n
=?
M
....
53
A., 173, 213
(fr. 1'4 toluidine)
1
COMPOUNDS CONTAINING SIX ELEMENTS.
681
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Bromtoluenesulphonyl-
Me.Br.SO2Cl=1.2.4
C7H6ClBr02S
....
54
Hayduck and
A., 172, 207; B.,
27, 905, 1095
chloride
Limpricht
7, 554
>j
=1.2.3
))
....
55-6-56-6
Neville & Winthei
B., 13, 1943
37, 628
j)
=1.4.5
))
A., 173, 208
61
Limpricht
B., 7, 719
27, 991
)>
)) »
)1
A., 169, 9
61-62
Neville &Winther
B., 13, 1947
37, 631
p-Bromphenylmercaptan
C2HClsO+C6H4Br.SH
C8H6Cl3BrOS
....
72
Baumann
B., 18, 887
48, 749
-(-chloral
Dibromxylenesulphonyl-
Me2.Br2.SO2Cl=1.3.(2)2.2
C8H7ClBr2O2S
107
Jacobsen and
B., 11, 1535
36,62
cliloride
Weinberg
Bromxylenesulphonyl-
Me2.Br.S02Cl=l 3.6.4
C8H8ClBrO2S
61
Weinberg
B., 11, 1063
34, 725
chloride
»
»
5)
....
61
Limpricht
B., 18, 2188
j3-Chloride of ethylic
CO2Et.Br.SO2Cl or COC1.
C9H8ClBrO4S
....
90-90-5
Bottinger
B., 9, 1252
31,82
sulphobrombenzoate
Br.SO3Et=1.4
a- „
?)
»>
....
165
J!
1)
»>
Dibrom-(3-naphthalene-
C10HsBr2.S02Cl
C10H5ClBr202S
....
108-109
Jolin
B. S. [2], 28, 517
sulphonylchloride
Bromnaphthalenesulph-
Br.SO2Cl=aia2
C10H6ClBrO2S
A., 147, 185
86-87
M
B. 8. [2], 28, 516
32, 902
onylchloride
»
), = ?«2
»I
....
90
»
B. S. [2], 28, 517
»
Chlornaphthalenesulph-
Cl.SO2Br=?
)>
....
115-116
Gessner
B., 9, 1504
31, 317
onylbromide
Bromcymenesulphonyl-
Me.Pr.Br.S02Cl=?
C10H12ClBr02S
....
80-81
Paterno and
G. I., 11, 124
40, 594
chloride
Canzeroni
Chloi-dibromacetamide ....
C01Br2.CO.NH2
C2H2ClBr2ON
***•
125
Neumeister
B., 15, 604
42, 944
Dichlorbromacetamide ....
CCl2Br.CO.NH2
C2H2Cl2BrON
253-255 d.
139
»
B., 15, 603
9)
Chlorbromacetamide
CHClBr.CO.NH2
C2H3ClBrON
....
126
Cech and Steiner
B., 8, 1174
29, 373
Brompropylenecarbamide
CO:(NH):C3H5Br+HCl
C4H6ClBrON2
....
143
Andreasch
M. C., 5, 33
46, 732
+ HC1
Chlorbromalacetamide ...
CaBr2.CH(OH).NHAc
C4H6ClBr2OaN
....
158
Jacobsen and
B., 15, 601
42, 938
Neumeister
Bromchloralacetamide
CCl2Br.CH(OH).NHAc
C4H6Cl2BrO2N
158
»
)J
>!
Dibromquinonechlorimide
Nitrochlorbrombenzene ....
C6H2Br2.NCl.O
i i
C6H2ClBr2ON
C6H3ClBr02N
d. 121
J. [1875], 325
80
46-8
MShlau
Korner
B., 16, 2845
G. I., 4, 305
46, 594
29, 220
Cl.Br.NO2=1.3.6
:l
=1.3.4
>J
»
49-5
»
jj
j»
)1
„ =1.4.6
»
»
68-6
»
>»
ji
»
=1.3.5
)1
»
82-5
»
»>
29, 221
Nitrochlorbromaniline ....
NH2.Cl.Br.N02=1.4.2.6
C6H4ClBrO2N3
J. [1875], 352
106-4
»)
v
29, 219
Dulcitolnitrochlorbrom-
....
C6H8ClBr012N4
115
....
A. C. [4], 27, 124
hydrin
Dibrompyridinebetame
+HC1
C5H3Br2N.CH2.CO.O+HCl
C7H6ClBr202N
begins d. 184
193
Gerichten
B., 15, 1253
42, 1110
Bromdichloraniidoaceto-
CHCl2.CO.C6H3Br.NH2
C8H6Cl2BrON
....
110-120
Baeyer & Bloem
B., 17, 968
46, 1027
phenone
=1.3.6
Bromamidoanisic acid
OMe.Br.NH3Cl.CO2H=?
C8H9ClBrOsN
....
186
Balbiano
G. I., 14, 234
48, 530
-I-HC1
Nitrosylchloridehesperid-
....
C10H14aBr2ON
130-131
Goldschmidfcand
B., 18, 2223
48, 1210
inedibromide
Ziirrer
Dinitrodibromdiphenyltri-
CCl3.CH(CcH,,Br.N02)2
C14H.Cl3Br204N2
....
168-170
Zeidler
B., 7, 1181
28, 148
chlorethane
Chlornaphthaquiuone-
C10H4C102.NH.C6H4Br=1.4
C16H8ClBrO2N
....
262
Plagemann
B., 15, 486
42, 973
bromanilide
Chlornaphthaquinone-
C10H4ClO2.NH.C6H3MeBr
C17HuClBr02N
....
185
»
B., 15, 487
IV
bromtoluide
=4.1.?
....
»
=2.1.?
»
....
212
v
»
)»
PC15 on bromeodei'ne
....
C18H19ClBr02N
131
Gerichten
A., 210, 113
42, 312
Diaceton ephosph orus-
C6H1002.PClBr2
C6H10ClBr202P
142
Michael is
B., 18, 901
48, 747
chlorobromide
4 s
682
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Allylthiocarbamidechloro-
NH2.CS.NH.C3H5ClBr
C4H8ClBrSN3
129-130
Maly
Z. C. [1867], 43 ;
v., 782
bromide
J. p., 100, 321
lodobenzenesulphonyl-
C6H4I.SO3C1=1.2
C6H4C1I02S
51
Limpricht and
B., 10, 321 ; A.,
32, 193, 611
chloride
Bahlmann
186, 326
i
ii 11
=1.4
1»
....
86-87
Lenz
B., 10, 1136
32, 770
lodotoluenedisulphonyl-
Me.I.(S02Cl)2=?
C7H5C12I04S2
....
143
Limpricht
B., 18, 2179
48, 1233
chloride
Diiodoquinonechlorimide....
C6HJ2.O.NC1=(?)2.4.1
C6H2C1I2ON
....
123
Seifert
J. p. [2], 28, 437
46, 431
1 1
Nitrochloriodobenzene ....
NOj.Cl.I=1.2.4(?)
C6H3C1I02N
J. [1875], 328
?
Korner
G. I., 4, 305
29, 221
ii
„ =1.3.6
»
))
63-3
jj
i)
»
11
„ =1.4.6
)J
1?
63-4
ii
11
))
Caffeinechloriodide + HC1
,,„
C^^C^IOoN,
175
Ostermeyer
B., 18, 2299
48, 1250
Diiodohydroxyquinoline
C9NH4(OH)I2+HC1
C8H6C1I2ON
....
100
ii
C. C. [1884], 937
48, 673
+HC1
Chloriodocinchonic acid
C,NH,ai.CO.H+HCl
CIOH8C1J02N
....
190
11
ii
n
+ HC1
Dimethylaminesulphonyl-
NMe2.SO2Cl
CjHjClOjSN
183-187
Liquid
Behrens
B., 14, 1810
42, 164
chloride
Chlortaurine
C2H3C1(NH3).S03H
C2H6C103SN
191-201
Spriug
B., 15, 446
42, 938
Nitrothiophenesulphonyl-
C4SH2(NO2).SO2C1
C4H2C1O4S2N
....
Liquid
Stiidler
B., 18, 535
48, 764
chloride
Diethylaminesulphonyl-
NEt2.SO2Cl
C4H10C102SN
208
Liquid
Behrend
B., 15, 1612
42, 1282
chloride
Dinitrobenzenesulphonyl-
(NO2)2.S02C1=1.2.3
C6H3C106SN2
,...
89
Sach.se
A., 187, 143
32, 752
chloride
» »
5»
i»
....
97
Limpricht
B., 9, 554
30, 303
Nitrobenzenedisulphonyl-
N03.(S02a)2=1.2.4
C6H3C12O6S2N
Liquid f.m.
Heinzelmann
A., 188, 166
32, 772
chloride
I! '!
=1.3.5
»
....
96
ii
A., 188, 164
32, 771
11 II
)» )»
)J
....
96
Limpricht
B., 9, 551
30, 302
Nitrochlorthiophenol
SH.C1.N02=1.3.6
C6H4C102SN
....
171
Beilstein and
B., 10, 1993; 11,
34, 139 ; 36,
Kurbatow
2057; A., 197, 79
231
,,
„ =1.4.6
)»
....
212-213
11
»
ii
Nitrobenzenesulphonyl-
NO2.S02C1=1.4
C6H4C1O.SN
Liquid
Limpricht
B., 8, 433 ; A.,
28/897, 1027
chloride
177, 74
!) »
=1.3
))
....
60-5
ii
ii
11
» »
» )»
Ji
61
n
B., 18,2174,2175
....
II 11
» ))
»
....
61
Glutz & Schrank
J. p. [2], 2, 223
....
ii ii
» J)
')
....
61
Goslich
B., 8, 354; A.,
28, 765 ; 29,
180, 93
930
ii 11
» )>
»J
....
61
Glaus and Moser
B., 11, 762
34, 865
ii n
=1.2
JJ
....
67
Limpricht
B., 8, 433; A.,
28, 897, 1028 ;
177, 77
32, 193
ii ii
!> II
))
67
Bahlmann
A., 186, 307
32, 611
Nitramidobenzenesulph-
N02.NH2.S02C1=1.2. 1
C6H6C104SN2
....
59-60
Goslich
B., 8, 354; A.,
28, 765 ; 29,
onylchloride
180, 103
930
Nitrochlorbenzenesulphon-
C1.N02.(S02NH2)=1.3.4
)J
158-159 u.c.
Laubenheimer
B., 15, 599
42, 953
amide
Chlorbenzenesulphonamide
C1.(SOS.NH.)=1.4
C6H6C1O2SN
....
142
Beckurts & Otto
B., 11, 2064
36, 229
si
>i ii
51
....
143-144
Goslich
A., 180, 107
29, 930
51
ii ii
5J
A., 143, 181
144
Otto and Brunner
A., 143, 100; 145,
vi., 273
326
II
=1.3
J)
148
Limpricht
B., 8, 1071
29, 82
11
» II
»
US
Goslich
A., 180, 110
29, 930
II
*' ' II
))
148
Hybbeneth
A., 221, 204
46, 72
11
=1.2
)5
182-5
Limpricht
B., 8, 1071
29, 82
?l
» ii.
Jl
A., 180, 110
188
Bahlmann
A., 186, 325
32, 610
COMPOUNDS CONTAINING SIX ELEMENTS.
683
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet
& J. Ch. Soc.
Ammonium chlorpheuol-
OH.Cl.SO3NH4='i
C6H8C1O4SN
...*
230
Petersen and
A., 157, 121
24,243
sulphonate
Predari
Nitromethenylamidothio-
c6H3(No2).N:oci.s
C7H3C1O2SN2
192
Hofmann
B., 13, 10
38, 388
phenolchloride
Dinitrotoluenesulphonyl-
Me.(NO3)3.SO3Cl=l.(?)2.4
C7H5C106SN2
....
125 ; sf. 123
Schwanert
B., 10, 31 ; A.,
32, 471, 612
chloride
186, 359
Nitrotolueuesulphonyl-
Me.NO2.SO2Cl=1.2.6
CyH.ClO.SN
36
Hesse
B., 14, 489
4Q, 596
chloride
>j
=1.4.6
)>
....
44
u
B., 14, 488
JJ
»
I> J»
>»
43-44-5
Jeussen
B., 7, 56; A.,
27, 479 ; 28, 77
172, 232
ji
=1.2.4
n
....
?
A., 145, 23
;)
=1.2.5
»»
50
Limpricht
B., 18, 2184
48, 1234
Chlortoluene sulphonamide
Me.Cl.(SOs.NH2)=1.2.4
C7H8C102SN
....
135
Paysan
A., 221, 210
46,72
j> »
=1.4.6
»)
....
138
Heffter
5»
46, 73
Ammonium sulphamine-
CO2NH4.C1.(S02.NH2)=1.4J
C7H9C104SN2
....
230-245
Collen and Bot-
B., 9, 1251
31,82
chlorbenzoate
tinger
Dinitroxylenesulphonyl-
Me2.(NO2)2.SO2Cl=1.3.6.2.4
C8H7a06SN2
123
Limpricht
B., 18, 2192
48, 1235
chloride
Nitroxylenesulphonyl-
Me2.N02.SOJCl=1.3.6.4
C8H8C1O4SN
....
98
>!
B., 18, 2174, 2191
chloride
Chlorxylenesulphonamide
Me2.Cl.(SO2.NH2)=1.3.4.6
C8H10C102SN
....
195
Jacobsen
B., 18, 1761
48, 1053
>j
„ =1.2.3.6
J)
....
199
Kriiger
B., 18, 1757
ij
=1.2.4.5
)»
....
207
)»
»
Diuitroxylenesulphon-
Me2.N02.(SO2.NH2)=1.3.6.4
C8H10C104SN3
....
193
Limpricht
B., 18, 2192
48, 1235
amide
Ethylic chlorphenylthio-
Cl.(NH.CSOEt)=1.4
C9H10C10SN
....
102-5
....
A., 176, 52
carbamate
Clilorphenylcystin
....
C9H10C102SN
....
182-184
Jaffe
B., 12, 1097
36, 79G
Dinitronaphthalenedi-
C10H4(N02)2(S02C1)2
C.eH.Ca.OAN,
....
218-5-219-5
Alen
B. S. [2], 39, 63 ;
44, 596
sulphonylchloride
B., 16, 570
Nitronaphthalenedisulph-
C10H6(N02)(S02C1)2
C10H5C1206S2N
...*
140-141
5)
»
»
onylchloride
» »
)J
»
185-187
»
»
n
Nitronaphthalenesulph-
NO2.SO2Cl=aia2
C10H6C104SN
....
113
Cleve
B.S. [2], 24, 510;
34, 153
onylchloride
B., 10, 1723
»
>. =1
»J
B., 10, 1723
125-5
11
B. S. [2], 26, 446
34, 154
D
„ =1
))
....
169
n
B.S.[2],29,414;
34, 676 ; 38, 47
B., 12, 1714
Dichlornaphthaleue-|3-
C10H,CI3.(SO,NH!1)
C10H7C12O2SN
....
245 d.
Widmann
B., 12, 966
36, 722
sulphonamide
Dichl ornaphthalene-a-
i»
»»
....
250 d.
)>
B., 12, 2233
38, 168
sulphonamide
Chlorphenylmercapturic
....
C11H12C1O3SN
....
153-154
Jaffe
B., 12, 1096
36, 796
acid
Dinitrodichlorphenyl
S(C,HaCl.NO,),=1.4.6
C12H:6C1204SN2
149-150
Beilstein and
B., 10, 1994; 11,
34, 139 ; 36,
sulphide
Kurbatow
2056; A., 197, 79
231
Dinitrodiphenyldisulph-
(.C6H3.N02.S02C1)2
C12H6as08S,N2
166
Gabriel and
B., 13, 1411
38, 890
onylchloride
Dambergis
Azobenzenedisulphonyl
N2[C6H,.(S02C1)2]2
C12H6C1408S4N2
58
Keiche
A., 203, 71
38, 806
chloride
Nitrodiphenyldisulphonyl-
C6H4(S02C1).C6H3(N02).
C12H7C1206S2N
....
130-131
Gabriel and
B., 13, 1411
38, 890
chloride
SO2C1
Dambergis
Dichlorazobeuzenesulph-
C6H4C1.N2.C6H3C1.S02C1
C12H7C1302SN2
..**
161
Calm
B., 15, 2559
44,341
onylchloride
=1.4; 1.4.2
Hydroxyazobeuzenetri-
C6H4(S02C1).N2.C6H2(OH)
C13H7a307S3N2
....
217-220
Limpricht
B., 15, 1297 ; A.,
42, 1075
sulphonylchloride
(S02C1)2=1.4 ; 1.4.0),
215, 235
Nitrodiphenylsulphonyl-
C6H4(N02).C6H4.S02C1
C12H,C1O4SN
....
178
Gabriel and
B., 13, 1409
38, 890
chloride
=(1.4)2
Dambergis
Azobenzenedisulphonyl-
N2(C6H4.S02C1)2=1.3 ; 1.4
C12H8C1204S2N2
....
120
Kodatz
A., 215, 215
44,478
chloride
4 s 2
684
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Azobenzenedisulphonyl-
N2(C6H4.SO2C1)2=1.3 ; 1.4
C12H8C1204S2N2
....
123-125
Limpricht
B., 14, 1358
42, 517
chloride
„
=(l-3)2
M
....
143
Janovsky
M. C., 3, 243
42, 834
„
„ „
„
145
Glaus and Moser
B., 11, 763
34, 865
„
ij jj
„
....
166
Mahrenholz
A., 202, 335
38, 804
M
» I?
„
....
166-167
Limpricht
B., 11, 1046
34, 722
„
„ „
„
....
166
„
B., 18, 1469
„
=(l-4)2
„
170
Janovsky
M. C., 3, 242
42, 834
„
„ „
„
....
215-218
Laar
B., 14, 1932
„
„ „
„
....
220-222
Limpricht
B., 14, 1375
42, 517
„
„ „
„
....
232
Laar
B., 14, 1930
42, 195
„
„ „
51
....
222
Bauer
A., 229, 353
48, 1141
„
„ „
„
....
222
Limpricht
B., 18, 1474
„
„ „
„
....
222
Rodatz
A., 215, 214
44, 478
Azoxybenzenedisulphonyl-
ON2(C6H4.SOsa)2=(1.3)2
C12HSC1206S2N2
....
138
Limpricht
B., 11, 1045
34, 722
chloride
»
)) J>
„
....
138
Brunnemann
A., 202, 343
38, 807
Azobenzenesulphonyl-
Ph.N2.C6H4.S02Cl=1.4
C12H9C102SN2
....
82
Janovsky
M. C., 3, 238
42,834
chloride
Azophenolbenzene-
HO.C6H4.N2.C6H4.SOi!Cl
C12H9C103SN2
122
Limpricht
B., 15, 1296
42, 1075
sulphonylchloride
=1.4; 1.?
„
» »
„
1
Rodatz
A., 215, 231
Phenamidobeuzene-
NHPh.S02Cl=1.4
C12H10C1O2SN
....
104
Wallach & Huth
B., 9, 426
sulphonylchloride
Chlorbenzenesulphon-
Cl.(S02.NHPh)=1.4
„
J. [1879], 417
120-121
„
B., 9, 425
anilide
Hydrazobenzenesulphonyl-
(.NH.C6H4.S02C1)2=(1.3)2
C^HnClO^Ns
....
a. 240
Limpricht
B., 11, 1048
34, 723
chloride
Amidodiphenylsulphone
Ph.S02.C6H4.NH3Cl
C12H12C1O2SN
....
90
Gencke
A., 100, 207
vi., 277
+HC1
Thiodiphenylcarbamic
C12H8SN.COC1
C13HSC1OSN
• *••
167-5
Fraenkel
B., 18, 1846
48, 1130
chloride
Benzenesulphamidobenz-
Ph.S02.N : CClPh
G1SH10C102SN
A., 108, 214
73-75
Wolkoff
B., 5, 140
25, 413
enylchloride
„
„
„
79-80
Wallach and
B., 11, 754 ; A.,
44, 48
Gossmann
214, 212
Nitroanthraquinone-
C14H6O2.NO2.S02C1
C14H6C106SN
....
194
Glaus
B., 15, 1516
42, 1105
sulphony Ichloride
Azotoluenetetrasulphonyl-
N2[C6H2Me(SO2Cl)2]2
C14H10C1408S4N2
....
91
Perl
C. C. [1884], 468
48, 391
chloride
Nitrotoluenesulphobenz-
Me.N02.(SO2.NClBz)=1.4.6
C14HUC104SN2
122-123
Wolkoff
Z. C. [2], 6, 422
vii., 1169
amide chloride
„
» ))
a
*•*•
125
„
B., 5, 141
25, 413
Toluenesulphobenzamide
Me.(SO2.NClBz)=1.4
C14H12C102SN
100
„
Z. C. [2], 6, 577 ;
25, 413; vii.,
chloride
B., 5, 140
1168
Azobenzyldisulphonyl-
N2(CH2.C6H4.S02C1)2=(1.4)S
C14H13C1204S2N2
....
149
Mohr
A., 221, 215
46, 70
chloride
Azotoluenedisulphonyl-
N2(C6H3Me.S02Cl)2= (4.1.2)2
„
....
194
Neale
A., 203, 81
38, 807
chloride
„
„ =(2.1.3 or 5)2
}J
218
Kornatzki
A., 221, 179
46, 71
„
=(2.1.4)2
„
220
Neale
A., 203, 76
38, 806
Phenyltaurineanilide
NHPh.(CH2)2.S02.NHPh
C14H17C1O2SN2
169 u.c.
Leymann
B., 18, 870
48, 786
+HC1
+HC1
Chloranisidinethiocarb-
CS(NH.C6H3C1.0Me)2
C16H14C1202SN3
....
152-5
Herold
B., 15, 1687
42, 1287
amide
=(1.?.2)2
Azoxylenedisulphonyl-
N2.(C6H2Me2.S02Cl)2
C16HI6C1204S2N2
.»<
86
Limpricht
B., 18, 2191
chloride
Di(phenylsulphonethyl-
NH2Cl(C2H4.SO2.Ph)2
C16H20C104S2N
.*..
192
Otto and Dam-
J. p. [2], 30, 321
48, 537
amine)+HCl
kcihler
a-Naphthalenesulphobenz-
C10H7(S02.NClBz)
C17H12C102SN
92-94
Wolkoff
B., 5, 142
25, 414
amide chloride
COMPOUNDS CONTAINING SIX ELEMENTS.
685
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Oxytriseleniocarbamide
C3H]<Cl3OSe3N6
d. 100
crystalline
Verneuil
C. R, 99, 1154
48, 377
+2HC1
?
POCl!!.NH.CCl2.CO2Et
C.H.jClANP
....
128-130
Wallach
B., 8, 303; A.,
28, 884; 32, 183
184, 17
?
POCl2.NEt.CCl2.CHCl2
C4H6C16ONP
140-150
Liquid
Wallach and
B., 13, 517 ; A.,
38, 547
Kamenski
214, 224
?
EtO.CHo.CN+PCL,
C4H;C13ONP
100-105
Liquid
Henry
B., 6, 261
26, 879
SbCl3 and quinine
SbClj-CjoH^O^^HCl
C20H26Cl602NoSb
....
80
Godeffroy
A. P. [3], 9, 434
32, 366
Nitrobromiodobenzene ....
Br.I.NO2=1.3.2(?)
C6H3BrIO2N
....
1
Korner
J. [1875], 330
„ ««-
„ =1.3.4
)J
J. [1875], 329
83-5
H
G. I., 4, 305
29, 222
„ ....
„ =1-4.5
)J
»
90-4
)J
»
29, 221
» ••••
„ =1.2.5
)J
»
103
»
j>
jj
»> ....
„ =1.3.6
»
j>
126-8
»
»»
29, 222
Nitrobromiodophenol
OH.Br.I.NO2=1.4.2.6
C6H3BrI03N
J. [1877], 549
104-2
»
J. [1867], 617
vi., 915
,i ....
=1.2.6.4
))
....
crystalline
)J
H
»
Nitrodibromdiiodotoluene
Me.Br2.L,.NO2=1.3.5.2.4.6
CjHjBr.il^jN
....
129
Wroblewsky
B., 9, 1055 ; A.,
30, 511
192, 212
Nitrodibromiodotoluene ....
Me.Br2.I.N02=1.3.5.4.6
C7H4Br2IO2N
....
69
j)
»)
30,511; 34,978
Nitrobromiodotoluene
Me.Br.I.NO2=1.2.3.?
C7HsBrI02N
86
)?
Z. C., 2, 7, 240
24, 713
„
„ =1.3.2.7
)J
....
solid
»
A., 168, 165
27,52
»»
=1.3.4.5(1)
»
....
118
»)
A., 168, 160
27, 51
Dibromiodoacettoluide ....
Me.Br2.I.NHAc=l.(?)2.2
C9H8Br2ION
....
121
»
A., 192, 211
Bromtarconium methiodide
CnHgBrOs.N.Mel
CjjHuBrlOjN
....
203-204 d.
Gerichten
A., 212, 171
42, 870
Bromtarcouium ethiodide
CnH8BrO3N.EtI
C13H13BrI03N
....
205-206 d.
»
A., 212, 173
»
Dibromthiohydantoin
NH.CS.NF.CBr2.CO
C3H2Br2OSN2
B., 13, 789
d.w.m.
Mulder
B., 8, 1263
1 J
130-140
Dibrom-j3-thiophene-
C4SHBr2(SO2.NH2)
C4H3Br202SsN
....
146-5-147
Langer
B., 18, 553
48, 765
sulphonamide
Dibrom-/3-thiophenedi-
C4SBr2(SO2.NH2)2
C4H4Br2O2S3N2
....
a., 270 p.d.
»
B., 18, 557
48, 766
sulphonamide
Dibrom-/3-thiophenamide
C4SHBr2(CO.NH2)
C5H3Br2OSN
identical ?
165-5
Bonz
B., 18, 2313
48, 1206
» -°- »
»
n
»>
167
»»
»
»
Nitrotribrombenzene-
Br3.N02.SO3H=1.3.5.2.4
C6H2Br3O5SN
....
100+
Eeinke
A., 186, 278
32, 463
sulphonic acid
i) )j
» »
»
124-125
Knuth
A., 186, 296
it it
» »
»;
....
202
Limpricht
A., 191, 196, 215
34, 496
)» »
„ =1.2.4.3.5
))
140-141
Spiegelberg
A., 197, 284
» »
» »
)t
-f3H20
125
»
M
)> i>
„ =1.2.3.4.5
)j
....
?
....
A., 181, 40
Diuitrotribromben zene-
Br3.(N02)2.(SO2NH2)
C6H2Br306SN3
255-260 d.
Limpricht
A., 191, 243
34, 497
sulphonamide
= 1.3.5.2.6.4
Nitrotetrabrombenzene-
Br4.N02.(S02NH2)
C6H2Br404SN3
a. 300
Limpricht and
B., 9, 478 ; A.,
30, 202, 305
sulphonamide
=1.2.4.5.3.6
Beckurts
181, 209
» i)
„ =1.2.3.5.4.6
»
crystalline
Limpricht
A., 191, 203
34, 495
)» »
„ =1.2.3.4.5.6
))
....
crystalline
Spiegelberg
A., 197, 302
36, 802
Pentabrombenzene-
C6Br5.(S02NH2)
C6H2Br602SN
A., 181, 228
d.w.m. 250
Limpricht and
B., 9, 479; A.,
30, 202, 305 ;
sulphonamide
Beckurts
191, 205
34, 49'
;> »
»
)>
....
nf. 290
Spiegelberg
A., 197, 312
36, 803
Nitrodibrombenzenesulph-
Br2.NO2.S03H=1.3.4.6
C6H3Br206SN
200
Limpricht
A., 191, 235
onic acid
N itrotribrombenzene
Br3.NO2.(SO2NH2)=1.3.5.2.4
C6H3Br304SN2
175 ; sf. 175
>»
B., 9, 477 ; A.,
30, 201; 34,
sulphonamide
191, 198, 218
494
» »
>i »
»
....
sf. 175
Knuth
A., 186, 297
32, 467
j> »
„ =1.3.5.2.4
»>
....
d.w.m. 210
Eeinke
A., 186, 280
32, 463
» 5)
„ =1.2.3.4.5
I?
202
Limpricht
B., 8, 1068
29,82
)> I!
» )i
J>
....
202
Lenz
A., 181, 43
30, 200
686
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
•Watts' Diet.
& J. Ch. Soc.
Nitrotribrombenzene
Br3.NOj.(SO2NH2)=l .2.4.3.5
C6H3Br304SN2
...•
260
Spiegelberg
A., 197, 288
36, 800
sulphonamide
Tetrabrombenzenesulphon-
Br4.(S02NH2)=1.2.3.4.5
C6H3Br4O2SN
181
Lenz
A., 181, 46
30, 200
amide
11 51
?J ))
„
....
2
Spiegelberg
A., 197, 295
36, 801
I? i)
=1.2.4.5.6
)>
....
a. 250
Limpricht and
B, 9, 477 ; A.,
30, 201, 305
Beckurts
181, 219
51 i5
=1.2.3.5.6
>;
A., 191, 2O1,
d.w.m. 250 ;
Reinke
A., 186, 271
32, 464
227
melts ou Pt
11 11
11 11
»j
....
a. 300
Knuth
A., 186, 300
32, 468
Amidotetrabrombenzene-
Br4.NH2.S03H=1.2.3.4.5.6
C6H3Br403SN
d. 130
Spiegelberg
A., 197, 302
36, 802
sulphonic acid
11 11
„ =1.2.3.5.6.4
))
A., 191, 204
?
Limpricht
A., 181, 223
Nitrobrombenzenesulph-
Br.NO2.SO3H=1.4.6
C6H4Br06SN
+2H20
130-135 d.
Limpricht and
B., 10, 319 ; A.,
32, 192, 609
onic acid
Eeinke
186, 316
Nitrodibrombenzenesulph-
Br2.NO2.(S02NH2)=1.4.(?)2
C6H4Br2O4SN2
....
178
Borns
A., 187,362
32, 769
onamide
55 »
=1.2.4
)»
....
210-211
Limpricht and
B., 9, 1862 ; A.,
81, 595 ; 32,
Goslich
186, 154
461
55 »
„ =1.3.4.6
))
nf. 240
Limpricht
A., 191, 237
34, 496
55 »
=1.3.4.5
»
d.w.m. 300
51
B., 8, 1067
29, 81
11 55
5» ))
5J
....
d.w.m. 300
Lenz
A., 181, 36
30, 199
Tribrombenzenesulphon-
Br3.(SO2NH2)=1.2.?.4
C6H4Br302SN
152
Limpricht and
B., 9, 1862; A.,
31, 596 ; 32,
amide
Goslich
186, 155
461
51 11
=1.(?)2.2
n
....
187
Bahlmann
A., 181, 208
80, 306
55 5i
=1.(02.2
»
....
202
15
55
51
55 55
„ =1.2.3.5
)>
210
Limpricht
B., 8, 1068
29, 82
55 rt
11 i>
?j
210
Lenz
A., 186, 31
30, 199
11 11
=1.4(1),
)»
identical ?
d.w.m. 200
Borns
A., 187, 365
32, 769
5 55
= 1.2.4.6
j»
v
?
Lenz
A.., 181, 40
55 55
„ =1.3.4.6
»
223
Spiegelberg
A., 197, 284
36, 799
55 ))
)> I?
i)
225
Eeinke
A., 186, 289
32, 465
55 55
» u
)T
S2S
Limpricht
A., 191, 191
84, 493
55 55
» jj
)>
....
d. 220-230
Knuth
A., 186, 304
32, 469
55 11
„ =1.3.5.6
»
d.w.m.
Reinke
A., 186, 277
32, 462
210-220
55 )5
i) i»
J»
....
d.w.m. 220
Limpricht
B., 9, 550
30, 302
55 55
)' ')
)}
v. 228 d.
d.220
Knuth
A., 186, 295
38, 467
55 55
» ))
J»
d.w.m. 220
Limpricht
A., 191, 196, 213
34, 494
55 55
= ?
»
nf. 260
11
B., 8, 1070
29,82
51 55
„ =1.2.5.6
»
v. 228
d. 220
11
B., 9, 476
30, 201
Amidotribrorubenzene-
NH2.Br3.SO3H=1.2. 4.6.3
C6H4Br303SN
d.w.m. 200
Reinke
A., 186, 298
32, 463
sulphonic acid
Nitrobrombenzenesulph-
Br.NO2.(S02NH2)=1.3.6
C6H5Br04SN2
*...
166
Limpricht
B., 18, 2186
48, 1234
onamide
5! >J
=1.4.5
»
A., 186, 126
169-170
11
B., 9, 1867
31, 596
» 55
=1.2.4
J>
....
176-177
Andrews
B., 13, 2129
40, 174
55 ))
11 11
^)
....
177
Goslich
A., 180, 100 ; B.,
28, 764 ; 29,
8, 353
929
55 51
„ =1.4.6
»J
....
205
Limpricht and
B., 10, 320 ; A.,
32, 192, 609
Bahlmann
186, 318
11 11
=1.?.6
J>
215
55
11
32, 192, 610
Dibroinbenzenesulphon-
Br2.(S02NH2)=1.2.4
CeHjBrjOjSN
167; 170
Limpricht and
B., 9, 1859, 1861 ;
31, 595 ; 32,
amide
Goslich
A., 186, 147
460
15 11
11 11
»
....
175
Sachse
A., 188, 143
32, 752
15 15
» 11
))
....
175
Limpricht
A., 191, 180
34, 492
55 51
11 »
)»
....
175
Spiegelberg
A., 197, 257
36, 798
'5 11
=1.3.4
»
....
188-190
Limpricht
B., 8, 1070
29, 82
55 11
>i 11
)3
....
190
15
A., 191, 234
34, 493
11 11
„ =1.4.5
)»
192
Limpricht and
B., 8, 1072 ; A.,
29, 82 ; 30, 306
Bahlmann
181, 207
COMPOUNDS CONTAINING SIX ELEMENTS.
687
Name,
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Dibrombenzeneaulph on-
Br2.(SO2NH2)=1.4.5
C6H5Br202SN
....
193
Limpricht and
B., 9, 1862,1868;
31, 596 ; 32,
amide
Bahlmann
A., 186, 132,314
460, 610
» »
„ „
M
193
Sachse
A., 188, 143
32, 752
>! 11
)' )i
„
193
Borna
A., 187, 350
32, 768
Tl 1)
= 1.3.5
,,
201-5
Limpricht
B., 8, 1066
29,81
11 !>
l> :i
51
203
Lenz
A., 181, 28
30, ]99
11 11
11 'i
„
203
Limpricht
A., 181, 202
30, 307
11 11
)l 11
11
203
Sachse
A., 188, 143
32, 752
11 11
=1.2.3
11
....
215
„
A., 188, 155
„
11 11
=1
„
252
Limpricht and
B., 9, 1862 ; A.,
30, 306; 31,
Bahlmann
181, 207
596
Amidodibrombenzene-
NH2.Br2.S03H=l. 2.4.5
C6H6Br203SN
d.w.m. 260
Keiuke
A., 186, 286
32, 465
sulphonic acid
11 11
11 11
M
....
d.w.m.
Knuth
A., 186, 301
32,468
Brombenzenesulphonamide
Br.(S02NH2)=1.3
C6H6BrO2SN
....
149 ; 156
Limpricht
B., 7, 1352
28, 268
„
11 11
,i
153-154
Berndsen
A., 177, 95
28, 1029
11
11 JJ
•
154
Limpricht
A., 186, 134
32, 459
„
= 1.4
11
....
160-161
Goslich
B., 8, 352; A.,
28, 764; 29,
180, 98
929
„
11 11
11
166
Nolting
B., 7, 1310; 8,
28, 264
597
„
= 1.2
„
180
Limpricht
B., 7, 1352
28, 268
»i
1) )1
„
....
186
Berndsen
A, 177, 102
28, 1030
„
n i>
„
....
186
Bahlmann
A., 181, 203, 307
30, 306, 611
„
=?
„
...
225-230
Limpricht
B., 14, 1361
42, 518
„
=»
„
....
252
Bahlmann
A., 181, 207
Amidobrombenzenesulph-
NH2.Br.S03H=1.2.5
C6H6Br03SN
nf. 170
Andrews
B., 13, 2126
40, 174
onic acid
Dibrombenzenedisulphon-
Br2.(S02NH2)2=1.4.5.?
C6H6Br204SaN.,
....
solid
Boms
A., 187, 367
32, 770
amide
Brombenzenedisulphon-
Br.(SO2NH2)2=1.3.2
C6H7Br04SsNs
....
210
Zander
A., 198, 29
38, 125
amide
,i
=1.3.4
1J
•
S38
„
A., 198, 11
38, 123
n 11
11 »
„
....
239
Heinzelmann
A., 192, 222
34, 410
11 11
„ =1.2.6
J1
....
245
,,
A., 188, 179
32, 773
Amidodibroiubenzenedi-
NH2.Br2.(S02.NH2).,
C6H7Br204S2N3
206
Borns
A., 187, 350
32, 770
sulphonamide
=?.1.4.(?)2
/3-S ulpham inebrombenzoic
Br.(SO2NH2).CO2H or
C7H6Br04SN
....
229-230
Bbttinger
B., 9, 1252 ; A.,
31, 82 ; 34, 730
acid
Br.SO3H.(CONH,)=U.4
191, 20
a- 11 i.
11 11
H
252-254
„
B., 9, 1252
31, 82
0- 11 11
11 11
11
....
262 d.
„
A., 191, 23
34, 730
Nitrobromtoluenesulphon-
Me.Br.N02.(S02NH2)
C7H7BrO4SN3
....
nf. 200
Hayduck
A., 174, 348
28, 461
amide
=1.2.?.4
Disulphaminebrombenzoic
C02H.Br.(S02.NH2)2
C-H7BrO6S2Na
a. 250
Kornatzki
A., 221, 191
46,70
acid
=1.4.(?)2
Bromtoluenesulphonamide
Me.Br.(S02NH2)=1.2.?
C7H8Br02SN
....
133-134
Hiibner and
Z. C. [2], 7, 618
26, 697 ; vii.,
Eetschy
1173
11
i, 11
„
....
133-134
Hiibner and Post
A., 169, 41
27, 59
11
•i 11
„
....
134-137
Limpricht
B., 7, 1392
28, 368
- . 11
» i,
1)
fr. CHC13
134-136
Pagel
A., 176, 296
28, 898
»
11 11
»
fr. HoO
135-136
„
„
11
'i
'i 11
„
fr. Et2O
136-137
„
„
11
11
i> >i
„
fr. EtOH
137
,,
B
»
=1.4.5 (?)
i,
....
134
Limpricht and
B., 7, 720; A.,
27, 991 ; 28,
Pechmann
173, 214
80
•i
=1.3.5
„
....
138-139
Neville and
B., 13, 1944
Winther
•I
= 1.2.3
„
146-3-147-2
B
B., 13, 1943
37, 628
11
=1.4.5 (?)
„
....
147
Limpricht
B., 7, 719
27, 991
11
=1.2.4
„
151
Limpricht and
B., 7, 554; A.,
27, 905, 1095
Hayduck
172, 207
688
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Bromtolueuesulphonamide
Me.Br.(SOaNH3)=1.4.5
C7H8BrO2SN
....
151-5
Hiibner& Eetschy
Z. C. [2], 7, 618
25, 697
»
!! !)
)»
....
151-152
Hiibner and Post
Z. C. [2], 6, 390 ;
27, 56 ; vii.,
A., 169, 9
1171
tt
11 )»
»)
1
Pechmann
A., 173, 209
»
» 11
II
....
151-5-152-3
Neville &Winther
B., 13, 1947
37, 631
D
=1.2.1
11
156-157
Limpricht and
B., 6, 1010; A.,
27, 74, 68
Gever
169, 385
j»
=1.3.6
II
....
162-165
Limpricht
B., 7, 451
87, 902
»
11 11
II
162-165
Weckwurth
A., 172, 199
27, 1094
H
=1.4.6
»I
166-167
Hiibner and Post
Z. C. [2], 6, 390 ;
27, 57;. vii.,
A., 169, 7, 22
1172
»
n 11
1)
166-5
Hiibner & Betschy
Z. C. [2], 7, 618
25, 697
!>
»i i)
II
fr. H2O
165-5
Jenssen
A., 172, 238
28, 78
J1
!! »
II
fr. EtOH
167-168
»
11
J!
»
= »
II
...»
260-267
Hiibner & Terry
Z. C. [2], 7, 232
25, 1006
»
» ))
It
....
d.-w.m. 230
Hayduck
A., 177, 60
28, 1031
#- Ammonium sulphamine-
Br.(S02NH2).CO2NH4 or
C7H9Br04SN3
....
125-126
Bottinger
B., 9, 1252
31,82
brombenzoate
Br.SO3NH4.(CONHj)=1.1.4
°- it i)
» 11
IJ
...*
203
»
11
11
Bromtoluenediaulphon-
Me.Br.(S02NH2)3=1.2.3.5
C7H9BrO4S2N3
....
236-238
Limpricht
B., 18, 2177
48, 1233
amide
» »
„ =1.4(2.6 or 3.5)
M
....
240
»
B., 18, 2179
!»
» »i
» =l-4(?)2
»>
....
a. 260
Kornatzki
A., 221, 191
46,70
Dibromxylenesulphon-
Me2.Br2.(SO2NH3)=1.3.4.6.2
C3H9Br2O2SN
....
220
Jacobsen and
B., 11, 1535
36,62
amide
Weinberg
Bromxylenesulphonamide
Me2.Br.(SO2NH3)=1.3.6.2
C8H10Br02SN
....
161
»
B., 11, 1536
!»
?>
„ =1.3.6.4
>I
....
194
»
B., 11, 1063
34, 725
»
>» )»
II
....
194
Limpricht
B., 18, 2188
«
=1.4.5.?
!»
206
Jacobsen
B., 17, 2379
48, 144
jj
„ =1.2.4.5
11
....
213
»
B., 17, 2374
48, 143
Bromphenylcysrtoin
....
C9H8BrOSN
...i
152-153
....
Z. P. C., 5, 332
Fr. bromphenylmereap-
....
C9H8BrO2SN
....
181
Baumann
B., 12, 809
36, 804
turic acid
4
Ethylic bronaphenylthio-
Br.(NH.CS.OEt)=1.4
C9H10BrOSN
105
Dennstedt
B., 13, 231
38, 634
carbamate
Bromphenyleyatin
Br.[S.CMe(NH3).C02H]
C9H10BrO2SN
....
180-182
Baumann
Z. P. C., 5, 317
42, 756
)» »»
H
1»
180-184
Jaffe
B., 12, 1096
36, 796
Ethylic j3-sulphaminebrom-
Br.(SO2NH2).CO2Et or
C9H10Br04SN
«...
128
Bottinger
A., 191, 22
34, 730
benzoate
Br.(S03Et).(CONH3)=1.1.4
Acetylpkenylthiocarb-
NHAc.CS.NH2BrPh
C9HuBrOSN2
....
270 d.
Miquel
A. C. [5], 11, 289
32, 870
amide-)-HBr
Dibrom-#-naphthalen«-
C10HiBr2.S02NH2
C10H7Br2O3SN
237-238
Jolin
B. S. [2], 28, 517
32, 902
sulphonamide
Bromnaphthaienesulphon-
Br.(S02NH,,)=a1a2
C10H8BrO3SN
190
)i
B. S. [2], 28, 516
))
amide
» »
>» »
1»
....
195
A., 147, 186
» »
=?
)1
....
205
Jolin
B. S. [2], 28, 516
Bromcynjenesulphonamide
Me.Pr«.Br.(SO2NH2)=?
C10H14Br02SN
....
191
Paterno
G. I., 11, 124
40, 594
>»
=1.4.2.?
1»
....
197 c.
Remsen and Day
A. C. J., 5, 149
46, 456
p-Bromphenylmercapturic
B., 15, 1732
CnH12BrO3SN
....
152
Baumann and
B., 12, 806 ;
36, 803
acid
Preusse
Z. P. C., 5, 311 •
»» n
....
*»
152
Jaffe
B., 12, 1094
36, 796
Di(nitrobromhydroxy-
S02(G6H2Br.OH.N08)3
C12H6Br308SN2
284-285
Annaheim
B., 9, 660
30, 290
phenyl)sulphone
• Tetrabromazobenzenedi-
N3(C6H3Br2.S02NH.,)2
O^H^r.O.S^
nf.
A., 215, 220
sulphonamide
=(1.2.4.5)2
»> »
„ =(1.2.6.4)2
1)
nf.
....
A., 215, 224
Brombeuzeneaulphon-
Br.(SO:.NHPh)=1.4
C12H10BrO2SN
119
Nolting
B., 8, 597
anilide
Dibromazotolueuedisulph-
N3(C6H2Me.Br.SOiNH2)3=
Cl4TII4Brs04S3N4
260
Kornatzki
A., 221, 179
46, 71
onamide
(4.1.!.2)2
COMPOUNDS CONTAINING SIX ELEMENTS.
689
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Dibromanisidine sulphate
OMe.Br2.NH2=l.(?)2.2
C14H16Br406SN2
....
177 p.d.
Staedel & Damm
B., 11, 1750; A.,
36, 239 ; 44,
217,55
663
Tri(amidodibrornphenyl)-
OP(C6H2Br2.NH2)3
ClsH12Br6ON3P
205 d.
Michaelis and
A., 229, 334
48, 1136
phosphine oxide
i
Soden
Phosphoric hexabromanil-
OP(NH.C6H3Br2)3
J>
252
»
)1
48, 1134
ide
Nitroiodothiophene
C4SH2I.NO3
C4H2IO2SN
....
74
Kreis
B., 17, 2074
46, 1314
lodobenzensulphonamide....
I.(S02NH2)=1.2
C6H6I02SN
170
Limpricht and
B., 10, 321 ; A..,
32, 193, 611
Bahlmann
186, 326
»
=1.4
»
183
Lenz
B., 10, 1136
32, 770
Methylpropaminethio-
CH2(SCN).CMe : NMe.HI
0,H9IOSN2
159-5
Tscherniac and
A. C. J., 5, 227
46, 665
cyanate+HI
Norton
lodotoluenesulphou amide
Me.I.(SO2NH2)=1.4.?
C7H8IO2SN
178-179
Glassner
B., 8, 561
28, 897
lodotoluenedisulphon-
Me.I.(S02NH2)3=?
C7H9I04S2N2
....
130-132
Linipricht
B., 18, 2179
48, 1233
amide
Di(nitroiodohydroxy-
SOj(C6H2I.OH.NO2)2
C12H6I208SN2
294-295
Annaheim
B., 9, 661
30, 297
phenyl)sulphone
Cmchoninesulphatoper-
8U20H24ON2+6H2SO4 4-
Ciso^^IieOaaSfi
+12H20
140-145
Jorgensen
J. p. [2], 14, 356
31, 714
iodide
6HI+I10
N16
Trimethylicphosphanilido-
S03Me.[NH.PO(OMe)2]=
C9H14O6SNP
114
Laar
J. p. [2], 20, 251
sulphonic acid
1.4
Triethylic phosphanilido-
SO3Et.[NH.PO(OEt)2]=1.4
C12H2006SNP
102
H
»
sulphonic acid
Dinitrotribrombenzene-
SO2a.Br3.(NO2)2=1.2. 4.6.3.5
C8ClBr306SN2
203d.
Limpricht
A., 191, 175
34, 497
sulphonylchloride
Nitrotetrabrombenzene-
S02Cl.Br4.NO2=1.2.3.4.6.5
C6ClBr404SN
146-147
Limpricht and
B., 9, 478; A.,
30, 202, 305
sulphonylchloride
Beckurts
181, 201
i»
)>
51
147-5
Limpricht
A., 191, 203
34, 495
»»
„ =1.2.3.4.5.6
»>
172-173
Spiegelberg
A., 197, 301
36, 801, 802
4 T
690
VI.— COMPOUNDS CONTAINING SEVEN AND EIGHT ELEMENTS,
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Nitrotribrombenzene-
Br3.NOa.S02Cl=1.2.3.4.5
C9HClBr3O4SN
....
116
Limpricht & Lenz
B., 8, 1068 ; A.,
29, 82 ; 30, 200
sulphonylchloride
181, 43
55
„ =1.2.4.3.5
„
143
Spiegelberg
A., 197, 288
36, 800
..
=1.3.5.2.4
55
....
142
Limpricht
B., 9, 477
30, 201
55 5>
„
brown 126
142
Reinke
A., 186, 280
32, 467
>(
55 55
„
....
144-145
Limpricht
A., 191, 198, 218
34, 494
1) 55
55 55
„
....
d.w.m. 180
Reinke
A., 186, 297
32, 463
Nitrodibrombenzene-
~R« "Wf i GO Ol — 1 \ f\ ?
OXftai^l *-/£• fj\J., V^l — — i. p'i.O. i
C6H5ClBr2O4SN
....
s. 0.
Limpricht and
B., 8, 1072; A.,
29, 83 ; 32, 769
sulphonylchloride
Borns
187, 362
55 55
=1.2.4. ?
„
....
98-99
Limpricht and
B., 9, 1862 ; A.,
31, 595; 32, 461
Goslich
186, 154
n
=1.3.4.6
„
....
115-5
Limpricht
A., 191, 237
34, 496
55 5)
„ =1.3.45
55
....
121 ; sf. 118
Limpricht and
B., 8, 1067 ; A.,
29,81; 30,199,
Lenz
181,36; 191, 193
308
Nitrobrombenzenesulphonyl-
Br.NO2.S02Cl=1.2.4
C6H3ClBr04SN
55
Goslich
B., 8, 353
28, 764
chloride
55 »1
55 55
„
....
K6-57
„
A., 180, 100
29, 929
55 55
„
....
sf. 40-50
Andrews
B., 13, 2128
....
=1.3.6
„
75
Limpricht
B., 18, 2186
48, 1234
55 15
=1.4.5
„
83
Limpricht and
B., 9, 1867 ; A.,
31,596; 32,459
Thomas
186, 126
15 55
=1.4.6
„
92
Limpricht and
B., 10, 319 ; A.,
32, 192, 609
Bahlmann
186, 318
).
55 l.J.D
„
....
97
„
„
32, 192, 610
Amidodibroinbenzenedi-
NH2.Br2.(SO2Cl)2=?.1.4.(2)2
C6H3Cl2Br204S2N
148
Borns
A., 187, 350
32, 770
sulphonylchloride
Nitrobromtoluenesulphonyl-
Me.Br.N02.S02Cl=1.2.?.4
C7H5ClBrO4SN
nf. 220
Hayduck
A., 174, 343
28,461
chloride
Hexabromazobenzenedi-
N2(C6HBrs.S02Cl)2 C12
H2a2Br604S2N2
....
222-224
Rodatz
A., 215, 227
44, 479
sulphonylchloride
=(1.2.4.6.3)2
Tetrabromazobenzenedi-
N2(C6H2Br2.SO2Cl)2 Ct,
H4Cl2Br404SaN2
232-233
„
A., 215, 220
55
sulphonylchloride
=(1.2.4.5)2
)5 )5
=(1.2.6.4)2
„
258-262
„
A., 215, 224
,.
Tetrabromazotoluenedi-
N2(C6HMeBr2.S02Cl)2 C14
H8Cl2Br4O4S2N2
243d.
Kornatzki
A., 221, 179
46,72
sulphonylchloride
=[2.1.(?)2.4]2
Dibromazotoluenedi-
N2(C6H2Me.Br.S02Cl)2 C14
Hloa2Br204S2N2
226
n
5>
46,71
sulphonylchloride
=(4.1.?.2)2
Phosphanilidosulphonyl-
C6H4.S02C1.(NH.POC12)
C6H6C1303SNP
102 or 158
Laar
J. p. [2], 20, 250
38, 321
chloride
Benzenesulphondichlor-
Ph.SO.XNH.PCy
CeH6Cl202SNP
130-131
Wichelhaus
Z. C. [2], 6, 54 ;
vi., 932
phosphamide
B., 2, 503
Ethylic chloride of dibrom-
C,
H15ClBr206SNP
•Ml
170
Laar
J. p. [2], 20, 258
....
phosphanilidosulphonic acid
691
VII.— COMPOUNDS CONTAINING SPECIAL ELEMENTS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Ag. Silver amylglycollate
C5Hu.O.CHs.CO2Ag
C7H1303Ag
....
110
Siemens
J. [1861], 449
11., 918
„ hydroxy-?-ate
MM
C8H1503Ag
....
120
Fossek
M. C., 4, 663
46, 38
„ triethoxybenzoate ...
(OEt)3.C02Ag=1.2.3.4
C13H1706Ag
....
d. 130
Will & Albrecht
B., 17, 2102
46, 1335
;> » •••
„ =1.2.3.5
»
200 d.
»
B., 17, 2100
»>
„ benzylsalicylate
(O.CH2Ph).CO2Ag=1.2
CuH.AAg
100
Perkin
6, 122
vl., 1007
„ melissate
C29H69.C02Ag
C30H5902Ag
94-95
Pieverling
A,, 183, 344
31, 587
Tetramethylammonium
NMe4.CN+AgCN
C6H12N3Ag
• ••>
211-212 u.c
Thompson
B., 16, 2341
46, 287
cyanide + AgCN
Silver amarine
....
C21H17N2Ag
....
218 u.c.
Claus&Kohlstoc
B., 18, 1850
48, 1132
Silver a-dichlorpropionate
CH3.CCl2.CO2Ag
C3H3Cl202Ag
d. 60
Beckurts & Otto
B., 18, 233
48, 507
Silver picramate
C6H2.NH2.(N02)2.OAg
C6H406N3Ag
....
165
Girard
C. B., 36, 421
iv., 407
Nitrotoluidine + AgNO3
C6H3Me.NH2.NO2 4- AgN03
C7H805N3Ag
....
131-132
Mixter
A. C. J., 1, 239
40, lisa
Tol\iidine+AgNO3
Me.NH2=1.4
C7H903N2Ag
101 d.
»
»
»
?
....
C13H1604N2Ag2
74-76
Golubeff
B., 7, 1651
28, 1203
Lepidine + AgNO3
(C10H9N)2+AgN03
C20H1803N3Ag
b. 100
Hoogewerff
B., 13, 1640
40, 110
m-Nitraniline+AgNOj ....
4(C6H4.N02.NH2)+AgN03
C24H24011N9Ag
124-125
Mixter
A. C. J., 1, 239
40, 1130
Diamarine+AgN03 „.
2(C21H13N2)+AgN03
C42H3603N5Ag
+H20
175 u.c.
Glaus &Kohlstock
B., 18, 1850
48, 1132
Tetranitroethylenedi-
C2Br2(N02)4+Ag20
C2Br209N4Ag2
d. 100
crystalline
Villiers
B. S. [2], 43, 322
48, 1044
bromi de + Ag2O
Thiocarbainide + AgCl
2CS(NH2)2+AgCl
C2H8ClS2N4Ag
....
175
Baumann
B., 8, 28
28, 632
J^i, Aluminium trimethide ....
AlMe3
C3H9A1
130
0+
Buckton&Odling
P. R, 14, 19;
iii., 983
As., 4, 112'
„ triethide (A.,
AlEtj
C6H15A1
194
Liquid —18
D
j?
»
114,242; 109,207)
„ tripropide ....
AlPra3
C9H21A1
240-245
Liquid
Cahours
C. E., 76, 133
26, 366; vii.}
1014
j» »
J»
))
248-252
Liquid
»
B. S. [2], 20, 190
(J. [1873], 518)
Benzene +A12C16
A13C16+6C6H8
^36-^36^6^2
3
Gustavson
B. S. [2], 31, 71
36, 308, 461
(B., 11, 2152)
Toluene+Al2Cl6
Al2Cl6+6C6H5Me
C42H48C16A12
....
Liquid — 17
»
B., 11, 2152
36, 308
Butylene+AlBr3
AlBr3+C4H,
C4H8Br3Al
Liquid —15
Gustavson
C. C. [1881], 1353
42, 27, 374
(B., 14, 2620)
Aluminium ethylate
(EtO)3Al.Al(OEt)3
C12H3006A12
360
115
Gladstone & Tribe
• •!•
29, 161
» )»
»
»
....
180
a
....
39, 11
„ triethylic
Al(CHAc.CO2Et)3
C18H27O9A1
...»
76
Conrad
A., 188, 269
4, 26
acetoacetate
„ propylate
(Pr»O)3Al.Al(OPr«)3
C18H4208A12
60
Gladstone&Tribe
....
9, 12
„ isobutylate ....
(Bu00)3Al.Al(OBu;3)3
C24H6406A12
....
140
»»
....
9,11
„ amylate
(C5HU.0)3A1.A1(O.C5HH)3
C30H6606A12
70
»
....
9, 12
A.U.. /3-Collidine aurochloride ....
C5NH2Me3+HAuCl4
C8H,.,Cl4Au
112
Hantzsch
A., 215, 1
44,84
Ethylmethylsulphine
SEtMe+EtAuCl4
C6HI3Cl4SAu
178,
Kriiger
J. p. [2], 14, 193
31, 187
ethaurochloride
4 T 2
692
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Diethylsulphine methauro-
SEt2+MeAuCl4
C6H13014SAu
192 d.
Kriiger
J. p. [2], 14, 193
31, 186
chloride
Trimethylamine auro-
NMe3+HAuCl4
C3H10Cl4NAu
220
Zay
G. I., 13, 420
46, 286
chloride
Butylamiue auroehloride ...
NH2Bu+HAuCl4
C4H12Cl4NAu
100
Wurtz
A., 93, 124
v., 737
Pyridine niethaurochloride
C5NH6+MeAuCl,
C6H8Cl4NAu
252-253
Ostermeyer
B., 18, 592
48, 813
Pipecoline auroehloride ...
C6H13N+HAuCl4
C6H14014NAu
130-131
Hesekiel
B., 18, 913
48, 812
Vinyldiethylamine auro-
NEt2C2H3+HAuCl4
5J
138-140
Ladenburg
B., 15, 1148
42, 1194
ehloride
Lutidine auroehloride
N.Me2=1.2.6
C7H10Cl4NAu
119
Epstein
B., 18, 883
48, 815
y-Ethylpyridine auro-
N.Et=1.4
»
....
120
Ladenburg
B., 16, 2061
44, 1152
ehloride
y-Isopropylpyridine auro-
N.Prf=1.4
C8H12Cl4NAu
79
)i
B., 17, 1122
46, 1048
ehloride
Pseudotropine auroehloride
C8H16N+HAuCl4
C8H16Cl4NAu
198
Ladenburg & Eoth
B., 17, 151
46, 761
Copellidine „
C8H17N+HAuCl4
C8H18Cl4NAu
....
105
Durkopf
B., 18, 923
48, 817
/3-Methylquinoline „
C10H9N+HAuCl4
C10H10Cl4NAu
145
Dobner & Miller
B., 18, 1642
Quinoline methauro-
C9H7N+MeAuCl4
)5
....
205
Ostermeyer
B., 18, 594
48, 814
chloride
p-Isopropylpyridine
C5NH4PrP + Mel + H AuCl4
C9H15Cl4INAu
128
Ladenburg and
B., 17, 1122
46, 1048
methiodide auroehloride
Schrader
? auroehloride
C5Hu02N+HAuCl4
C5H12Cl4O2NAu
+H20?
b. 100
Salkowski
B., 16, 1193
44, 925
Hydroxypicoline „
C6H8(OH)N-t-HAuCl4
C6H10Cl4ONAu
154
Etard
C. R, 92, 460
40, 1046
Methyldiacetonamine
C7H15ON+HAuCl4
C7H16Cl4ONAu
....
a. 90
Gotschmann
A., 197, 27
36, 1036
auroehloride
Piperethylalkamine
))
j)
....
129
Ladenburg
C. R, 93, 338
40, 1158
auroehloride
? auroehloride
C8H15ON+HAuCl4
C8HI6Cl4ONAu
198
u
A., 206, 274
40, 447
Tropine „
))
)>
210-212
Schmidt
B., 13, 373
38, 482
Valerobeta'ine „
CsHnOj-NMeadAuCL,
C9H20Cl402NAu
163
Corner & Menozzi
G. I., 13, 351
46, 425
Apoatropine „
017H21O2N+HAuCl4
C17H22Cl4O2NAu
106-108
Pesci
G. I. [1882], 59
42, 635
Pseudoatropine „
C^HjAN+HAuCl,
CJ7H24Cl4O3NAu
112-114
Ladenburg
A., 217, 87
44, 671
Atropine „
15
)»
....
135
Ladenburg and
B., 13, 380
38, 482
Meyer
» »
))
55
....
135
Ladenburg
B., 13, 110
38, 411
» »
5)
))
....
135
Planta
A., 74, 252
(J. [1850])
„ auroehloride
I)
)»
...,
135-137
Ladenburg
C. R, 90, 874
38, 561
>» »
»
»5
....
137-139
Pesci
G. I. [1882], 59
42, 634
Hyoscyamine „
55
>»
....
159
Ladenburg
B., 13, 110
38, 411
» »
55
))
159
Ladenburg and
B., 13, 380
38, 482
Meyer
Hyoscine „
55
J»
196-198
Ladenburg
A., 206, 274
40, 57, 446
[B., 13, 1549]
Methylphthalimide auro-
(C9H9ON)2+HAuCl4
C18H19Cl4O2N2Au
195-196 d.
Grcebe and Pictet
B., 17, 1174
46, 1019
ehloride
Cinchonine auroehloride ...
C19H22ON2+HAuCl4
C19H23Cl4ON2Au
100 +
Hesse
A., 122, 226
vi., 464
Boronglycide
B.CH2.CH.CH2
t 1
C3H5B
110-120
Liquid
Councler
J. p. [2], 18, 371
36, 622
Trimethylboride
BMe3
C3H9B
b. — 16
Frankland
P. T. [1862], 176
iii., 986
[A., 124, 144]
Triethylboride [A., 124, 135;
BEt3
cyfti5B
95
»
P. T. [1862], 167
ii., 526
j,
)5
»
95-97
Frankland and
J., 13, 386
Duppa
B.
COMPOUNDS CONTAINING SPECIAL ELEMENTS.
693
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Fluoborethylene (B., 12,
CH2:CH.BF2
C2H3F2B
124-125
Liquid
Laudolph
B. S. [2], 31, 503;
34, 483
1586)
C. R, 86, 671
Ethyleneborofluoride
C2H4+BF3
C2H4F3B
125-127
....
»
C. B., 85, 40
32, 864
Pheuylborochloride
Ph.BCJ2
C6H6C12B
175
0
Michaelis and
B., 13, 59; 15, 180
38, 395
Becker
Tolylborochloride
CaH4Me.BCl2=1.4
C7H7C12B
....
27
j>
B., 15, 185
42, 732
Acetoneboric acid ....
C^O+BAHj
CaH803B2
50
L.f.m.
Laudolph
C. B., 89, 173 :
36, 915
B., 12, 1582
Trimethylic borate
B(OMe)3
C3H903B
65
Solidifies
Schiff
As., 5, 186
n »
JJ
»
72
Liquid
Ebelmann and
A. C. [3], 17,59;
i.,650;vi., 363
Bouquet
A., 60, 252
Ethylic ethylborate
BEt(OH).OEt
C4H.uO2B
J. [1876], 469
s.b. 8
Frankland
P. B., 25, 165
30, 620
Methylic diethylic borate
B(OMe)(OEt)2
C6H1303B
100-105
Schiff
As., 5, 197
Phenylboric oxide
Ph.B:O
C6H6OB
a. 360
190
Michaelis and
B., 15, 184
42,732
•
Becker
Phenylboric acid
Ph.B(OH)2
C6H7O2B
MM
204
j)
B., 15, 181
42, 731
Ethylic diethylborate
BEt2.OEt
C6H15OB
102-103
Liquid
Fraukland
P. B., 25, 165 ;
30, 619
J. [1876], 469
Diethylic ethylborate
BEt(OEt)s
C6H1502B
125
A., 124, 139
»
P. T. [1862], 167
ii., 527
)) I) •••:
»
))
95-125 p.d.
Liquid
»»
P. B., 25, 165
30, 618
Triethylic borate
B(OEt)3
C6Hlb03B
119
A., 60, 252
Ebelmann and
J. P., 38, 215 ;
i., 650
Bouquet
J. [1856], 574
„ „
JJ
J»
119
....
Councler
B., 11, 1107
34, 775
,, „
))
»1
120 (760)
Schiff
As., 5, 161
vi., 361
„ ,, .... ....
JJ
J)
121
....
Bowmann
P. M. [3], 29, 548
Triethylene borate
B(O.C2H4.OH)3
C6H15O6B2
B., 11, 1106
161-7
Councler
J. p. [2], 18, 392
34, 775
Tolylboric acid
C6H4Me.B(OH)2=1.4
C7H9O2B
....
240
Michaelis and
B., 15, 185
42, 732
Becker
Triallylic borate (B., 9,
B(O.C3H6)3
C9H1503B
168-175
Liquid
Councler
J. p. [2], 18, 376
30, 395
486)
Diethylic isoamylic borate
B(OEt)2.OC6H11
C9H21O3B
173-175
Liquid
Schiff
As., 5, 193
vi., 364
Tripropylic borate
B(OPr«)3
»
172-175
Liquid
Cahours
C. B., 76, 1383 ;
26, 872 ; vii.,
J. [1874], 498
1013
„ „ ....
J»
»
175
....
V
C. C., 4, 482
)) 5» "••
»)
)>
174-5
....
Conncler
B., 11, 1107
34, 775
Triisopropylic borate
B(OPr0)3
jj
140 c.
Liquid
»
J. p. [2], 18, 389 ;
»>
B., 11, 1107
Diethylic phenylborate ....
Ph.B(OEt)2
C10H16O2B
176
Liquid
Michaelis and
B., 15, 184
42, 732
Becker
Diamylic tetraborate
B405(OC6Hn)2
^ioH22O7B4
a. 300
Ebelmann
A. C. [3], 16, 139
i., 649
Triisobutylic borate
B(OBu/3)3
C12H27O3B
212
Liquid
Councler
J. p. [2], 18, 382 ;
34, 21
B., 10, 1656
Ethylic diisoamylic borate
B(O.C6Hn)2.OEt
0
210-215
Liquid
Schiff
As., 5, 193
vi., 363
Pentaethylic ethyldiborate
B3Et(OEt)s
C12H3005B
112
Liquid
Frankland
P. B., 25, 165 ;
30, 618
J. [1876], 468
Triisoamylic borate
B(O.C6Hn)3
C15H33O3B
254 (760)
• •••
Schiff
As., 5, 189
vi., 363
» »
)»
»)
270-275
Liquid
Ebelmann and
A. C. [3], 17, 61
i., 649
Bouquet
j» >»
)J
»
272-275
....
Councler
B., 11, 1107
Cetylic metaborate
(C16H13.0).B:0
Ci6H13O2B
• •«•
58
Schiff
As., 5, 198
vi., 364
Tetraphenylic diborate ....
B20(OPh)4
C24H20O5B2
a. 300
....
....
v., 365
Trinaethylboride ammonia
BMe3.NH3
C3H12NB
110
56
Frankland
P. T. [1862], 176
iii., 986
Fluoboracetone
• •>•
C3H6F2OB
130-140
Landolph
C. E., 86, 1463
34, 774
(B., 16,962)
C3H60.3HF.B404
C3H9F3O5B4
120
Liquid —15
»
C. B., 96, 580
44, 655
0- !.
J)
»j
120-122
Liquid
»>
C. R, 89, 173; B.
36, 915
12, 1580
694
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
j3-Fluoboracetone
C3H60.3HF.B4O4
C3H9F306B4
90-92
36
Landolph
C.E., 89, 173 ;B.
36, 915
12, 1580
Fluoborcamphor
J. [1878], 640
C10H16F3OB
70
)>
G. E., 86, 539
34, 586
Ba. Barium acetate
(CH3.C02)2Ba
C4H6O4Ba
....
abt. 450
Tilden and Shen-
P. T., 1884
stone
„ oananthylate
(Q,Hlll.OajlBa
C14H2604Ba
238-239 d.
Mehlis
A., 185, 358
34, 135
„ isoxylate
Me2.CO2H=1.4.5
C18Hls04Ba
+4H20
100
Jacobsen
B., 14, 2111
42, 187
„ benzylphenoxy-
(CH2Ph.C6H4.O.CHMe.C02).
CsjHjoOgBa
+ H20
100 nearly
Mazzara
G. I. [1882], 261
48, 1072
propionate
Ba
„ o-naphthoylbenz-
(C10H7.CO.C6H4.C02)2Ba
CseHjABa
....
160
Ador and Crafts
C. R, 88, 1355
36, 940
oate
„ ricinostearolate ...
....
C36H6206Ba
....
135
Ulrich
B. S. [2], 9, 225
vi., 997
„ lithofellate
....
C40H7008Ba
185
Roster
G. I., 9, 364
38, 131
„ lithobilate
(C30H5706)2Ba
C60H114012Ba
109
»
G. I., 9, 462
38, 270
Barium isethionate
C4H1008S2Ba
320
....
MM
iii., 413
„ phenylsulphon-
(Ph.S02.CH2.C02)2Ba
C16H1408S2Ba
d. 110
Otto
B., 18, 158
48, 537
acetate
Barium aceturate
(NHAc-CHj-CO^Ba
C8H1206N2Ba
+5H20
200
Curtius
B., 17, 1670
46, 1307
„ „ .... ...
»
»
)»
d. 250-260
)»
)J
J)
„ hydrogen dinitro-
[C6H2(N02)2.OH.O]2Ba
C12H6012N4Ba
....
212-5
Typke
B., 16, 554
44,917
resorcinol
Be. Beryllium diethide
BeEt2
C4H10Be
185-188
Liquid
Cahoura
C. R, 76, 1383 ;
26, 871; vii.,
J. [1873], 520
1014
„ dipropide
BePr2
C6H14Be
244-246
Liquid — 17
»
»
»
Ca. Calcium succinate
(CH2)2:(C02)2Ca
C4H4O4Ca
....
180
Goldschmidt
M. C., 3, 136
42,602
„ levulate ....
(C4H7O.C02)2Ca
C10HI406Ca
+2H2O
abt. 100
Grote & Tollens
B., 7, 1375
28, 250
„ valerate
(C4H9.C02)2Ca
Ci0H20O6Ca
150 d.
....
....
v., 977
„ phenoxyacetate ....
(PhO.CH2.CO2)2Ca
C16H1406Ca
+3JH3O
120
Fritzsche
J. p. [2], 20, 267
38, 319
Cd. Cadmium diethide
CdEt,
C4H10Cd
200 ?
Liquid
....
J. [1856], 553
Ethyltetrahydroquinoline
(C9H10EtN.HCl)2CdCl2
C^CL.NjCd
105
Glaus and Stege-
B., 17, 1330
46, 1051
cadmiochloride
litz
Ethylglyoxaline cadmio-
(C3H3N : NEtMeI)2CdI3
C12H22I4N4Cd
151-152
Wallach
B., 16, 535
44,911
methiodide
Pipeline cadmioiodide
(C6H13N.HI)2CdI2
C12H28I4N2Cd
+H20
144-145
Hesekiel
B., 18, 912
48, 812
Hydro-a-isopropylpyridine
(C6H6PrfN.HI)2CdI2
C16H28I4N2Cd
132-133
Ladenburg
B., 18, 1589
48, 992
cadmioiodide
Cf. p-Phenylpyridine dichro-
C6H4PhN+H2Cr207
C11Hll07NC3r,
155 p.d.
Hantzsch
B., 17, 1519
46, 1194
mate
Lutidine dichromate
(C7H9N)2+H2Cr207
CI4H2007N2Cr2
92
Epstein
B., 18, 883
48, 815
Butylacridine chromate ....
C17H17N+H2CrO4
C17HI904NO
....
a. 100 d.
Bernthsen and
B., 17, 1509
46, 1183
Traube
Phenylmethylhydroxy-
(CHH.oONJ.+HAA
CjjHjsO^Crj
+ 5H20
177
Pinner
B., 18, 761
48, 752
pyrimidine dichromate
Benzylamarine dichromate
(C28H24N2)2+HsCr04
C66H6004N4Cr
....
90
Glaus and Kohl-
B., 18, 1852
48, 1133
stock
Chloriodoquinoline chro-
C9H7ClIN+H2Cr04
C9H9ClIO4NCr
160
Ostermeyer
C. C. [1884], 937
48, 673
mate
COMPOUNDS CONTAINING SPECIAL ELEMENTS.
695
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Copper hydrosorbate
(CHjMe.CHj.CH : CH.
C12H1804Cu
p. d. 100
180-185
Barringer and
A., 161, 307
vii., 1092
C02)2Cu
Fittig
„ ethylic acetoacetate
Cu(CHAc.CO2Et)2
C12H1306Cu
....
182
Conrad
A., 188. 269
34, 26
„ amylglycollate
(C5Hu.O.CH2.CO2)2Cu
C14H2606Cu
....
110
Siemens
J. [1861], 449
ii., 918
„ phenylglyoxalate....
(Ph.CO.C02)2Cu
C16H1006Cu
p. d. 140-150
160-170 d.
Claisen
B. 12, 628
36, 648
„ ethylio acetylaceto-
(C^AXCu
C16H2203Cu
....
148
James
47,7
acetate
„ pelargonate
(C8H17.C02)2Cu
Ci8H3404Cu
258
Giesecke
Z. C. [2], 6, 429
vii., 898
„ ethylic benzyl-
(C13H1304)2Cu
C26H2608Cu
180-190 d.
James
....
47, 11
acetoacetate
„ diheptylacetate ....
[(C7H15)2CH.C02],Cu
C32H6204Cu
227
Jourdan
A., 200
38, 314
,, oleate
(C17H33.C02)2Cu
C36H6604Cu
100
Chevreul
Eecherches, 205
iv., 194
Copper o-brombenzoate ....
(CjH.Br.CO^Cu
Cl4H10Br205Cu
+H20
257 d.
Ehalis
A., 198, 99
38, 119
Phenylthiocarbaniside +
3CSN3H3Ph.CuCl
C21H24ClS3N6Cu
144-145 d.
Kathke
B., 17, 297
46, 1018
CuCl
Iron urushate
(C14H1702)3Fe.3(C14H1802)
C84H105012Fe
....
105-110
Yoshida
43, 477
ji j»
(C14H1702)3Fe.9(C14H1802)
C163H213024Fe
+2H2O
105-110
»
....
»
Ethylie ferronitroso-
Et2Fe2(NO)4S2
C.H.AS^Fe,
....
78
Pavel
B., 15, 2609
44, 298
sulphide
Mercuric dimethide (A.,
HgMe2
C2H6Hg
93-96
Liquid
Buckton
P. E., 9, 91 ; A.,
iii., 927
85, 361 ; 92. 79 ; 130,
108, 103
108 ; Z. C. [1870], 25)
Mercuric diethide (A., 109,
HgEt2
C4H10Hg
158-160
Liquid
»
A., 108, 103
iii., 925
218 ; 112, 220)
„ diethide (A., 130,
))
)»
159
Z. C. [1866],
Frankland and
17, 415
H
109, 125)
376
Duppa
„ dipropide
HgPr°2
C6H14Hg
189-191
Liquid
Cahours
C. E., 76, 133;
26, 366 ; vii.,
J. [1873], 517
1014
„ diisobutide
HgBu*»2
C8H18Hg
205-207
Liquid
»
C. E., 77, 1403 ;
87, 349
J. [1873], 521
„ diisoamide
Hg(C5Hu)2
CIOH22Hg
....
....
A., 130, 111
„ diphenide (A.,
HgPh2
C12H10Hg
a. 300 d.
120
Dreher and Otto
Z. C. [2], 4, 685 ;
vi., 819
154, 93; 194, 148)
B., 1, 234
„ dibenzide
Hg(CH2Ph)3
C14H14Hg
....
a. 200
Campisi
C. E., 61, 86
vi., 821
„ ditolide
Hg(C6H4Me)2=(1.2)2
n
....
107
Michaelis & Panek
A, 212, 203
42, 959
„ (B., 7, 389)
» »
u
107
Ladenburg
A., 173, 165
»» jj .... ....
)) 11
»»
107
Coste & Michaelis
B., 11, 1889
„ (A., 154,
=(1.4),
»
....
235
Dreher and Otto
Z. C. [2], 4, 685
vi., 826
171)
,, ,, .... ...
1» ))
»
....
223-225
>»
B., 1, 235
,, j, ....
» »
»
235
Coste & Michaelis
B., 11, 1889
36, 163
„ (A., 173,
» It
j)
....
S88
Ladenburg
B., 7, 389
87, 803
163)
„ dixylide
Hg(C6H3Me2)2=(3.4.1)2
C16H18Hg
123
Jacobsen
B., 14, 2112
42,187
,, „ ....
=(4.2.1)3
)I
150
»
B., 17, 2374
48, 144
„ dioctide
Hg(C3H17)2
C'16H34Hg
d. 200
Liquid
Eichler
B., 12, 1880
38, 229
„ diisopropyl-
Hg(C6H4Pr0)2=(1.4)2
C.sH^Hg
....
109
Meyer & Muller
B., 15, 1906
44, 64
phenide
„ dinaphthide
Hg(C10H7)2
C^H^Hg
A.,. 154, 188
243
Otto and Mories
A., 147, 166
vi., 819
„ dicymide
Hg(C6H3MePr«)2
C.oH^Hg
>...
134
Paterno and
B., 10, 1749
34, 139
Colombo
Mercuric methylchloride ....
HgClMe
CH3ClHg
170
Seidel
J. p. [2], 29, 134
46, 1135
„ ethylchloride ...
HgClEt
C2HsClHg
A., Ill, 60
100
Diinhaupt
C. C. [1854], 263
iii., 925
696
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Mercuric ethylchloride ...
HgClEt
C2H6ClHg
190
Seidel
J. p. [2], 29, 134
46, 1135
„ isoamylchloride
HgCLC^,
C5HnClHg
A., 130, 114
86
Frankland and
17, 415
iii., 924
Duppa
,, phenylchloride....
HgClPh
CcH5ClHg
245
Heumann
B., 16, 1626
44, 1051
a a
>»
1>
250
Michaelis and
B., 15, 182
42, 732
(A., 154, 113)
Becker
„ phenylchloride....
J)
)»
....
251-252
Otto
J. p. [2], 29, 136
46, 1135
„ tolylchloride ...
HgCl.C6H4Me=1.4
C7H7ClHg
B., 15, 185
187-188
....
J. p. [2], 1, 185
Mercuric ethylbromide ....
HgBrEt
C2H5BrHg
A., 92, 375
„ phenylbromide....
HgBrPh
C6H5BrHg
275
J. p. [2], 1, 186
a a
»
>j
....
291
Otto
A., 154, 111
vi., 820
„ naphth} Tbromide
HgBr.C10H7
C10H7BrHg
195-196
n
A., 154, 190
Mercuric methyleneiodide
CH2I.HgI
CH2I2Hg
.».
108-109
Sakurai
B., 13, 2088
39, 485
Mercurous „
CH2I.Hg.HgI
CH2I2Hg2
....
230 p.d.
»
)>
39, 486
Mercuric methyliodide ....
HglMe
OH3IHg
143
»
)J
it
i> »
»
)>
143
Frankland
A., 85, 363
iii., 926
„ allyliodide
Hg.I.C3H6
C3H5IHg
B., 4, 670
135
Zinin
A., 96, 393 ; 140,
i., 142; iii.,
180 ; As., 3, 262
923
„ isoamyliodide ....
Hgl.C.H,,
C6HuIHg
A., 130, 113
122
Frankland and
17, 415
iii., 924
Duppa
„ phenyliodide ....
HglPh
C6H5IHg
A., 154, 109
265-266
Dreher and Otto
Z. C. [2], 4, 685
vi., 820
„ tolyliodide
HgI.C6H4Me=1.4
C7H7IHg
A., 154, 173
220
j>
J»
vi., 821
„ dinaphthyliodide
C10H?.I.Hg.I.C10H7
C2nH14I2Hg
185
Otto and Mories
A., 147, 164 ;
vi., 819
L 1
154, 189
Methylmercuric acetate ....
CH3.CO2.Hg.Me
C3H602Hg
142-143
Otto
Z. C. [2], 6, 25
vi., 818
Ethylmercuric acetate
CH3.CO2.Hg.Et
C4H302Hg
178
»
11
11
Mercuric phenylic acid ....
....
C6H602Hg
251-252
a
A., 154, 126
Phenylmercuric formate ....
H.CO2.Hg.Ph
C?H602Hg
171
11
A., 154, 118
Mercurous amylglycollate
C5H11.O.CH2.C02Hg
C7H1303Hg
170 p.d.
Siemens
J. [1861], 449
ii., 918
Phenylmercuric acetate ...
CH3.CO3.Hg.Ph
C8H802Hg
140
Dreher and Otto
Z. C. [2], 4, 685 ;
vi., 820
6,9; A., 154, 117
» 11
11
»1
....
148-149
....
J.p.[2], 1,179,186
Octylmercuric hydrate ....
C8H17.Hg.OH
C3H18OHg
75
Eichler
B., 12, 1882
38, 229
Pbenylmercuric propionate
CH3.CH2.CO2.Hg.Ph
C9H1002Hg
165-166
Otto
A., 154, 118
Tolylmercurie acetate
CH3.C02.Hg.C6H4Me=1.4
))
....
153
Dreher and Otto
A., 173, 174 ; Z. C.
vi., 821
[2], 4, 685 ; 6, 9
Naphthylmercuric acetate
CH3.C02.Hg.C10H7
C\.,H1002Hg
A., 154, 191
154
Otto and Mories
A., 147, 175
vi., 819
„ butyrate
C3H7.C02.Hg.C10H7
C14HH02Hg
....
200
Otto
A., 154, 193
Mercuric dimethyleugenol
Hg[C9H7(OMe)2]2
C^O.Hg
140
Wassermann
C. R, 88, 1206
36, 790
Mercuric thioethylate
Hg(SEt)2
C4H10S2Hg
76
Otto
B., 13, 1290
38, 796
11 a ••••
»
))
....
77
))
B., 15, 125
»1 !!
)J
J)
....
82
Will
B., 15, 339
11 1) •«•«
J)
))
85 ,
Debus
A., 72, 18
ii., 548
11 11 ••>•
)>
)*
....
86
Handw.
„ thiopropylate ....
Hg(SPr-)2
C6H14S2Hg
68
Romer
B., 6, 785
26, 1118;vii.,
1014
„ thiobutylate
Hg(S.CHMeEt)2
C8HI8S2Hg
....
189
Reymann
B., 7, 1288
28, 141
„ thioisoamylate ....
Hg(S.C5Hu)2
C10H22S2Hg
Liquid
....
....
i., 206
„ thiotolide
Hg(S.C6H4Me)2=(1.3),,
C14H14S2Hg
....
100
Hiibner and
Z. C. [2], 5, 500
vi., 291
Wallach
a n ••••
i> »
)i
123-126
»
»
91
11 !>
=(1.4)2
)»
crystalline
Marcker
A., 136, 79
11
„ thymothiocymene
Hg(S.C6H3MePr«)2=(3.1.4)2
C20H26S2Hg
abt. 78
Fittica
A., 172, 303
28,60
„ caniphorthio-
=(2.1.4).,
D
109
)!
a
»J
cymene
1 • 1
i
COMPOUNDS CONTAINING SPECIAL ELEMENTS.
697
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Phenylmercuric cyanide ....
Ph.Hg.CN
CrH5NHg
....
203-204
J. p. [2], 1, 181
Tetramethylammonium
(NMe4)Cy+HgCy2
C;H12N4Hg
....
275 u.c.
Glaus and Merck
B., 16, 2743
46, 338
cyanide + HgCy2
Mercuric metbylenechlor-
Cl.CH2.HgI
CH2ClIHg
129
Sakurai
41, 361
iodide
Chloraldehyde + Hg2Cl2 ....
CH.jCl.COH+Hg.A,
C^ClsOHg,
....
96
Satyzeff and
Z. C. [2], 3, 675
vi., 76
Glinsky
Ethylsulphide+HgCl2 ....
Et2S+HgCL
C4H10Cl2SHg
90
Loir
C. R, 26, 195
ii., 545
?
SEtMe+EtCl+2HgCl2
C5HI3Cl5SHg2
....
112
Kriiger
J. p. [2], 14, 193
31, 187
?
SEt2+MeCl+6HgCl2
C5H13Cl13SHg6
....
198
D
»
31, 186
?
SEt2+EtCl+4HgCl2
C6H15Cl9SHg4
....
100+
Dehn
As., 4, 83
v., 882
Mercuric thioethylate
Hg(SEt)2+CHI3
C9HslI3S2Hg2
....
85-5
Jackson and
B., 8, 1033
29, 364
iodoform
Oppenheim
Trichlorpyridine mercuro-
(CsH2Cl3N).HHgCI3
C6H3Cl6NHg
....
209
Ko'nigs & Geigy
B., 17, 1834
46, 1369
chloride
Dichlorpyridine „
(C5H3Cl2N).HHgCl3
C5H4Cl6NHg
....
183
»
B., 17, 1833
n
Lutidine mercurochloride
(C5NH3Me2).HHgCl3=?
C7H10Cl3NHg
....
155
Epstein
B., 18, 883
48, 815
» )>
=1.2.6
))
....
186
Ladenburg & Eoth
B., 18, 51
48, 558
») »
» >»
>J
....
188-189
Epstein
B., 18, 1749
>» »
(C:,NH3Me2).HHg2Cl5=1.2.4
C7H10Cl5NHg3
....
129
Hantzsch
A., 215, 56
» ji
» »)
»)
....
129-130
Michael
B., 18, 2026
j> »
)) n
»
+JH20
ISO
Ladenburg &Roth
B., 18, 914
48, 815
Trimethylphenylam-
(Me3PhNCl).Hga2
C9HI4Cl3NHg
....
187
Hiibner & others
A., 224, 331
46, 1318
monium mercurochloride
Viridiae „
(C12H19N).HHgCl3
C12H20Cl3NHg
MM
35
Thenius
J. [1861], 503
v., 1003
Valeritrine „
(C15H27N).HHgCl3
C^H^C^NHg
....
86-88
Lubavin
B., 6, 566
26, 1023
Dimethaniline „
(Ph.NMe2),,H2HgCl4
C16H24014N2Hg
....
149 u.c.
Klein
B., 11, 1743
36, 232
Ethylenediphenyldi-
(PhMe2NCl)2C2H4+2HgCl2
C18H26Cl6N2Hg2
....
175
Hiibner, Tolle,
A., 224, 331
46, 1318
methylammonium mer-
and Athen-
curochloride
stadt
Ethyltetrahydroquiuoline
(C9H10EtN)3.H2HgCl4
C22H32Cl4N2Hg
....
65
Claws & Stegelitz
B., 17, 1330
46, 1051
mercurochloride
Aniline mercurobromide ....
(Ph.NH2)2.HgBr2
C12H14Br2N2Hg
110-112
Klein
B., 13, 835
38, 633
o-Toluidine mercurobrom-
(CcH4Me.NH2),.HgBr3
C14H18Br2N2Hg
103-104 d.
j»
»
)J
ide
P- » „
I!
J)
....
120-121
11
»
)»
Aniline mercuroiodide ....
(Ph.NH.A.HgL,
C12H14IJN2Hg
J.[1871],705
60
Klein
B., 13, 835
38, 633
o-Toluidine „
(CcH4Me.NH2)2.HgBr2
C14H18I2N2Hg
....
d.w.m. 40-50
»
ji
»
p- „ „
»
»
81
)>
n
J)
?
....
C16H39I9N2Hg
150
....
11., 563
Triethvlmethylstibium-
2(SbMeEt.,I).3HgI2
C14H36IsSb2Hg3
b. 100
Friedlimder
J. p., 70; 433
i., 347
iodide mercuroiodide
Mercurophenylxanthamide
Hg(NPh.CS.OEt)2
ClsH2002S«Hg
....
78
Stephanowitz
B., 7, 692
27, 992
Methylmercuric nitrate ....
Me.Hg.NO3
CH303NHg
100
Strecker
A., 92, 79
iii., 927
Phenylruercuric nitrate ....
Ph.Hg.NO3
C6H503NHg
....
165-168 d.
J. p. [2], 1, 180
Mercuric dibenzamide
(C6H5.CO.NH)2Hg
C14H1202N2Hg
....
222-224
Oppenheim
B., 6, 1392
27, 272
„ acetanilide
(Ph.NAc)2Hg
C16H1602N2Hg
....
215
»
B., 7, 624
27, 891
„ isononylamide ....
(C8H17.CO~NH)3Hg
CJSH3602N2Hg
....
117-118
Kuhlhem
A., 173, 319
28, 334; vi''., 898
4 u
698
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Phenylmercuric thio-
Ph.Hg.S.CN
C7H6SNHg
....
220-227
J. p. [2], 1, 182
cyanate
1
(C3H5ClNO)2.HgO
C6H10Cl403N2Hg
100-110
Otto
R, 3, 257
iv., 729
Anthranil mercurochloride
C7H5ON+HgCl2
C7H5Cl2ONHg
....
174
Friedlander
B., 15, 2107
44, 188
Narccine ethomercuro-
(0,3H2909N).EtHgCl3
C25H34Cl309NHg
....
127 u. c.
Claus & Eitzfeld
B., 18, 1571
48, 996
chloride
Dimethyltolylphosphine
C6H4Me.POMe2 + HgCl,
C8H13Cl2OPHg
+HS0
156
Czimatis
B., 15, 2015
44,57
oxide mercurochloride
?
SEfcMe.EtCN.HgI2
C6H13I2SNHg
....
98
Kriiger
J. p. [2], 14, 193
31, 187
?
SEt2.MeCN.HgI2
;>
115
»
»
»»
Potassium formate
H.CO2K
CH02K
150
Souchay & Groll
G. J. C. [1859]
„ diformate
H.C02K+H.C02H
C2H304K
....
120 d.
Loriu
C. B., 82, 750
30,59
„ valerate
C4H9.CO2K
C5H9O2K
....
140
Gibbs
A.J.S.[2],15,118
v., 977
„ triacetate
....
CcH.AK
d. 170
112
Lescoeur
C. R, 78, 1046
„ hydroxyacetate
C6H4.OH.CO2K
C,HAK
....
200
Welden
J. p. [2], 15, 151
32, 338
„ amylglycollate
CsHn.O.CH., CO2K
C7H1303K
....
200-210
Siemens
J. [1861], 449
ii., 918
„ lignocerate
C23H47.C02K
C24H4-O2K
....
sf. 190
Hell & Hermanns
B., 13, 1719
40, 250
„ tripimarate
C19H29.CO2K-t-2C19H29.CO2H
CciiHsgOcK
121
Duvernoy
A,, 148, 143
vi., 945
Potassium thiocyanate ....
K.S.CN
CSNK
....
161-2
Pohl
J., 4, 59
Potassium brombenzoate....
C6H4Br.C02K=1.2
C?H8Br04K
+2H2O
245
Rhalis
A., 198, 99
38, 119
Potassium isethionate
HO.C2H4.SO3K
C2H5O4SK
300-350
MM
...»
iii., 413
„ phenolsulph-
C6H4(OH).S03K=1.3
C6HASK
....
200-210
Earth and Sen-
B., 9, 971
30, 410
onate
hofer
» »
)) »
1)
....
235-240
Solomrnanoff
Z. C. [2], 5, 294
vi., 924
)) »
=1.2
)>
....
240
Earth and Sen-
B., 9, 973
30, 411
hofer
» »
» ))
)»
....
240
Solommanoff
Z. C. [2], 5, 294
vi., 924
!! 11
=1.4
)>
....
nf. 240
»
j)
»
» 11
51 )>
))
....
nf. 260
Earth & Senhofer
B., 9, 973
30, 411
„ phenylsulphon-
Pli.S02.CH2.C02K
C8H7O4SK
+ xH2O
100 d.
Otto
B., 18, 159
48, 537
acetate
Ethylic potassiumcyan-
NK(CN).CO2Et
C4H5O2N2K
....
199
Biissler
J. p. [2], 16, 125
34, 215
amidocarbonate
Potassium sodium tartarate
C03Na.(CH.OH).,.CO2K
C4H4O0NaK
+4H20
70-80
Fresenius
A., 53, 234
v., 680
» » »
))
))
5)
50; sf. 37-5
Brandes
Br. Arch., 9, 108
Potassium ehlorphenol-
C6H3C1.0H.S03K
C6H4C104SK:
245
Predari
Z. C. [2], 6, 246
vi., 924
sulphonate
•-
Tetranitroethylenedichlor-
C2(N02)4C12.2KHO
C2HiCl209N4K2
....
detonates 147
Villiers
B. S. [2], 43, 322
48, 1044
ide+2KHO
Lithium acetate ....
CH3.C02Li+4H,O
C2H3O2Li
....
19
Berzelius
Lehrbuch
Magnesium diethide
MgEt2
C4H10Mg
....
A., 114, 240
....
A., 109, 206
K
COMPOUNDS CONTAINING SPECIAL ELEMENTS.
699
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Magnesium ethylic aceto-
Mg(CHAc.C02Et)2
C12H1806Mg
....
240 d.
Conrad
A., 188, 269
34,26
acetate
Magnesium benolate
Mg(C22H3902)2
C44H7804Mg
+3H2O
130
Hausknecht
A., 143, 40
vi., 257
Chlorophyllan
....
C.HbOcNdP.Mg,
....
110
Hoppe-Seyler
B. C. [1880], 375
38, 894
Sodium formate
H.COJSTa
CHO2Na
• •••
200
Souchay & Groll
G. J. C. [1859]
„ acetate
CH3.CO.jNa
C2H,02Na
....
319
Schoffgotsch
G. J. C. [1857]
„ .... ....
+ 2£H20
»
....
126
Zettnow
P. A., 142, 306
vii., 7
„ „
+ 3H20
J)
....
58-5
Tilden
....
45, 268
„ ,,
5» )J
)»
123
58
Jeannel
G. J. C. [1866]
„ „
)I )1
)»
120
59
Zettnow
P. A., 142, 306
24, 230
„ hydroxyacetate ....
....
C3H503Na
142-143
Heintz
A., 158, 291
vii., 717
» >i
HO.CH2.C02Na
11
....
nf. 160
Wislescenus
B., 6, 1395
27, 249
Disodium glyceride
C3H5.OH.(ONa)2
C3H603Na2
220
Loebisch & Looss
M. C., 2, 842
42,377
Sodium glyceride
C3H5(OH)2.ONa
C3H-O3Na
....
245 d.
Letts
25, 452
„ valerate
C4H9.CO2Na
C5H9O2Na
....
140
Zettnow
....
v., 977
,, triacetate ....
CH3.CO2Na+2CH3.CO2H
C6Hu06Na
d. 150
127
Lescceur
C. E., 78, 1046
27, 870
„ phenylic carbonate
PhO.CO2Na
C7H503Na
301-302
cryst.
Hentzschel
J. p. [2], 27, 39
44, 588
„ amylglycollate
C5Hn.O.CH2.C02Na
C7H1303Na
....
190-200
Siemens
J. [1861], 449
ii., 918
„ benzhydrilbenzoate
Ph.CH(OH).C6H4.CO2Na
C14Hu03Na
+ 4H20
90
Senff
A, 220, 225
46, 428
=1.3
„ lapachate
C6H9.C9H4.COsNa
C15H1303Na
+5H2O
50
Paterno
G. I., 12, 337
44, 210
„ brassidate
C21H41.C02Na
C^H^Na
....
a. 200
Hausknecht
A, 143, 40
vi., 367
„ cholesterate
....
C26H43ONa
....
150
....
vi., 448
„ glucate
3Na2O.4C12H16O9
C48H64039Na6
-t-9H2O
100
Reichardt
V. p. P., 19, 516
vii., 557
Sodium chloracetate
CH2Cl.CO2Na
C2H2C102Na
....
a. 100
Heintz
J. [1861], 144
vi., 19
„ chloride + dextrose
2C6H1206.NaCl
C12H24C1012Na
+H20
120
Hunt
AJ.S.[2],19,416
?
2C!£H2,iOn.3NaI
C24H44T3022Na3
+3H..O
90
Gill
....
24, 272
Sodium ethylic sulphate ....
EtO.SO2.ONa
CJHASNa
+H20
86
....
v., 624
„ isobutylmethyl-
CH2A.c.CMe2.S03Na
C6Hu04SNa
+ H20
95
Pinner
B., 15, 593
42, 943
ketonesulphonate
„ phenylsulphon-
Ph.S02.CH2.C02Na
C3H7O4SNa
....
d. 120
Otto
B., 18, 159
48, 537
acetate
Ethylic potassiumcyan-
NNa(CN).C02Et
C4H6O2N2Na
....
241
Biissler
J. p. [2], 16, 125
34, 214
amidocarbonate
Sodium dithymylphosphate
(C10H13)sNaP04
CMH2604PNa
....
74
Kreysler
B., 18, 1706
48, 1055
Sodium bronidichloracetate
CCl.,Br.CO2Na
CjajBrOiNa
+ 5H2O
100
Neumeister
B., 15, 603
42, 944
Carbamide+NaCl
CO(NH2)2.NaCl
CH4C10N2Na
....
60-70
Kichter
E. K. T., 11
Sulphibronibenzaldehyde
CBH3Br(SO2H).COH
C7H6BrO6S2Na
78
Bottinger
A., 191, 13
34, 731
+ NaHSO3
+NaHSO3
Lead tetramethide
PbMe4
C4H12Pb
110
Liquid
Butlerow
J. [1863], 476 ,
iii., 563
» ii
Jl
n
160
....
Cahours
A., 122, 68
. >»
„ tetraethide
PbEt4
cyHMPb
152
....
Bichter
E. K. T., 179
35, 245
(A., 112,226; 122,66)
„ tetraethide
J1
»
198-202 p.d.
Liquid
Buckton
P. M. [4], 17, 232
(J., 18, 21 2; A.., 109, 224)
Lead triethide (A., 88,318)
Et3Pb.PbEt3
C12H:loPb2
d.
Liquid
Klippel
J., 13, 381
4 u 2
700
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Lead acetate
(CH3.CO2),Pb
C4H604Pb
+3H2O
57
Hassenfratz
A. C., 28, 302
„ methylpropylacetate
(CHMePr*.CO,;),Pb
C^H^Pb
43
Liebermann
B., 17, 920
46, 1120
„ oenanthylate....
[ClLXCH^.CO.J.jPb
C14H2604Pb
....
78
Mehlis
A., 185, 358
34, 135
,, ,,
)J
1)
....
79-80
Franchimont
A., 105, 23
26, 1080
» »
J>
)J
....
00
Grimshaw
26, 1080
vii., 870
i) 11 •••• ••••
))
»
.y.
94-96
IT
)?
J)
„ anisate
(MeO.C6H4.C02).,Pb
C16H1406Pb
+H2O
80-90 p.d.
Engelhardt
J. p., 24, 417
vi., 172
„ diallyloxalate
[(C3H5);.C(OH).C02]2Pb
C16H2206Pb
-t-2H2O
100
Saytzeff
A., 185, 183
32, 883
„ laurate
(CuH.,3.C02)2Pb
C24H4c04Pb
b. 100
Muller
J. p., 58, 469
Hi., 475
11 11 »••
J?
»>
110-120
Heintz
A., 97, 271
ji
Pb-salt fr. canuba wax ....
C^XCO^Pb
C25H4604Pb
....
d. 125
Stiircke
A., 223, 283
46, 1281
Lead urushate
(C13H17.CO.,)2Pb
C28H3404Pb
....
110-115
Yoshida
43, 477
„ dibenzylcarboxylate
(CH2Ph.CHPh.C02)2Pb
C30H.,604Pb
....
146
Wurtz
C. R, 70, 350
vii., 427
„ ?-ate
(C14H29.002)2Pb
C30H3804Pb
....
113-5-114
Thorner
B., 12, 1637
38, 44
„ benzylphenoxypro-
(Ph.CH2.C6H4.O.CHMe.
C32H3006Pb
+H2O
100 nearly
Mazzara
G. I. [1882], 261
42, 1072
pionate
C02)2Pb
„ ricinoleate
(C17H33O.C02)2Pb
C36H6606Pb
....
100
Saalmiiller
A., 64, 108
v., Ill
„ stearate
(C17H35.C02)2Pb
C36H7004Pb
....
125
Chevreul
A. C. [2], 2, 354
v., 417
„ ?-ate
(CL,H,- COo'loPb
C H O Pb
110-111
Stiircke
A., 223, 283
46, 1281
„ lignocerate
V 23 47 2/2 v
1»
^4S-L-L94vy4I- u
I>
....
117
Hell
B., 13, 1719
40, 250
„ melissate
(C29H5!l.C02)2Pb
CJ311804Pb
....
118-119
Stiircke
A., 223, 283
46, 1281
Lead thioethylate
Pb(SEt)2
C4H10S2Pb
150
Otto
B., 13, 1290
38, 796
„ thiophenylate
Pb(SPh)2
C12H10S2Pb
....
a. 230
....
....
iv., 418
„ thiotolylate
Pb(S.C6H4Me)2=(1.3)2
C14H14S2Pb
....
70
Hiibner&Wallach
Z. C. [2], 5, 500
vi., 291
n 11
» 5J
»
....
76-78
u
11
11
Lead brombenzoate
(C6H4Br.C02)2Pb=(1.2)2
C16HuBr205Pb
....
176-180
Ehalis
A., 198, 99
38, 119
+Et.OH
Lead acetonesulphonate ....
(CH3.CO.CH,!.S03)2Pb
C6H1008S2Pb
+H30
140 ; d. 170
Bender
B., 4, 518
24,703; vii., 16
„ diethylic dipliosphate
[(EtO)2PO.O]2Pb
CgH^OsPsPb
....
180
Vogeli
A., 69, 180
iv., 592
„ glucosodiphosphate ...
o : [P0(o.cji11oi,).o]2pb
C12H22017P2Pb
....
187
Amatto
G. I., 1, 56
24, 925; vii., 562
Lead chlorhippurate
(CsH7ClON.COs),,Pb
C18H14a206N2Pb
110-120
Otto
A., 122, 129
iii., 160
Lead diamylic dithiophos-
[PS(O.C6Hu)2.S]2Pb
C20H4404S4P2Pb
b. 70
Korvalevsky
A., 119, 303
vii., 1123
phate
Triethylamine platino-
PtCy2(NHEt3.CN)2
C16H32N6Pt
....
80
Scholtz
W. A., 82, 1233
40, 708
cyanide
Platinocarbonylchloride ....
co:ptci3
CCl2OPt
195
Schiitzenberger
A. C. [4], 21, 350;
24, 1012 ; vii.,
J. [1870], 381
986
Platinodicarbonylchloride
:(GO)2:ptci2
C2Cl202Pt
....
142
!»
J)
11
Diplatinotricarbonyltetra-
CO.CO.PtCl2.CO.PtCl2
O3Cl4O3Pt2
....
130
i?
11
11
I _[
chloride
i»
)j
II
....
130-150
i>
A. C. [2], 15, 100
vi., 952
Ethylsulphide platinichlor-
Et2s.ptca2
>C4H10Cl3SPt
108
Loir
C. R, 26, 195
ii., 545
ide
Diethylmethylsulphine
(SEtMe.Et)2PtCl6
C10H26Cl6S2Pt
....
186 d.
Kriiger
J. p. [2], 14, 193
31, 187
platinochloride
» »
(SEt2.Me)2PtCl6
ii
....
214 d.
11
U
31, 186
Allylamine platinichloride
(Calls.NH^HPtCl,
C3H8Cl3NPt
cryst.
Liebermann
B., 16. 530
44, 909
Ethylallylamine platini-
(C3H5.NHEt).HPt(~!l3
C,,H12Cl3NPt
220
ii
11
JJ
chloride
COMPOUNDS CONTAINING SPECIAL ELEMENTS.
701
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Propionamidine platino-
(C3H8N2)2.H2PtCl6
C6H18Cl6N4Pt
....
199-200 d.
Pinner
B., 17, 178
46, 723
chloride
Diethylallylamine platini-
(C3H6.NEt2).HPtCl3
C7H16Cl3NPt
....
189
Liebermanu
B., 1G, 530
44, 909
chloride
Dipropylallylamine platini-
(C3H5.NPr«2).HPtCl3
C9H20Cl3NPt
152-153
M
B., 16, 529
»
chloride
Ethylallylamine platiuo-
(C3Hs.NHEt)2.H2PtCl6
C10H24Cl6N2Pt
....
154-156
»
B., 16, 526
»
chloride
Diethylformamidine
(NEt2.CH : NH)2.H2PtCl6
C10H26Cl6N4Pt
....
208-209
Pinner
B., 17, 180
46, 724
platinochloride
Pyridine methoplatino-
(C5NH5)2.Me2PtGl6
C12H16Cl6N2Pt
186-188
Ostermeyer
B., 18, 592
48, 813
chloride
Ethylglyoxaline metho-
(C3H3N : NEt).Me2PtCl6
C12H!2Cl6N4Pt
MM
194-195
Wallach
B., 16, 535
44, 911
platinochloride
Pipecoline platinochloride
(C6H13N).,.H2PtCl6
C12H23Cl6N2Pt
....
192
Hesekiel
B., 18, 912
48, 812
Capronamidine platino-
(C6HuN2)2.H2PtCl6
C12H30Cl6N4Pt
....
199 d.
Pinner
B., 17, 178
46, 723
chloride
Lutidiue platinochloride ....
(C7H9N)2PtCl4
C14H18Cl4N2Pt
204-205
Coninck
C. R, 96, 437
44, 740
» i>
(C7H9N)2.H2PtCl6
C14H20Cl6N2Pt
....
179-180
»)
i»
)J
;> »
N.Me2=1.2.4
J)
216
Epstein
B., 18, 883
48, 815
I) )l
» »
1J
....
216-217
Hantzsch
B., 17, 2909
48, 397
I) )>
j> »)
J>
....
217
»
A., 215, 56
>i I)
» j>
»
....
217
Michael
B., 18, 2025
n »
H »
J)
....
219-220
LadenLurg
B., 18, 1593
48, 816
,, >i
I! )J
)1
error
230
»
B., 18, 915
»
Diethylallylamine platino-
(C3H5.NEt2).H2PtCl6
C14H82Cl6N2Pt
....
128-130
Liebermann
B., 16, 526
44,909
chloride
Piperidine base platino-
(C7H16N)2.H2PtCl6
»
....
212
Ladenburg
B., 18, 50
48, 558
chloride
Isopropylpyridine platino-
N.Pr0=1.2
C16H24016N2Pt
••>«
169-170
D
B., 18, 1589
48, 992
chloride
)1 J5
„ =1-4
)>
....
203-204
)>
37
j)
;> »
» ;>
»
....
206
»
B., 17, 1122
46, 1048
Hydroisopropylpyridine
(C3H13N)2.H2PtCl6
C16H2SCl6N2Pt
....
193-193-5
i>
B., 18, 1589
48, 992
platinochloride
N.Pr0=1.2
Copellidine platinochloride
(C8H17N).H2PtCl6
C16H36Cl6N2Pt
....
145-147
Diirkopf
B., 18, 924
48, 817
» »
JJ
J»
+xH2O
105
j>
»
j)
Tetrahydroquiuoline
(C^N^Pta,;
C18H24Cl6N2Pt
200
Hoffmann
B., 16, 729
44, 1143
platinochloride
Methyltropidine „
(CaH^N^.H.PtGl,.
ClsH32Cl6N2Pt
....
120
Roth
B., 17, 158
46, 761
Methylquinoline „
(G9H,NMe)2.H2PtCl6
C20H,0016N2Pt
....
226-230
Fischer & Kuzel
B., 16, 165
44, 588
Quinoline methoplatino-
(C9H7N)2.Me2PtCli;
I)
....
230 d.
Ostermeyer
B., 18, 594
48, 814
chloride .
Methyltetrahydroquinoline
(C9H10MeN)2.HsPtCl6
C20H28Cl6N2Pt
177 d.
Hoffmann
B., 16, 732
44, 1144
platinochloride
Dimethylcopellidiue
(C8H15Mc2N).,H2PtCl6
C5()H44Cl,N.,Pt
....
93
Diirkopf
B., 18, 928
48, 817
platinochloride
Methylcopellidine metho-
(C8H16MeN)2.Me2PtCl6
)J
....
d. 254
>»
B., 18, 924
platinochloride
CJuinoliue ethoplatinochlor-
(C9H7N)2.Et2Pt016
CaH^CljN^t
....
226
Glaus and Tosse
B., 16, 1278
44, 1009
ide
?
(C!^,^),^^^!,
))
....
227
Beyer
J. p. [2], 31, 47
48, 672
Ethyltetrahydroqninoline
(C9H,0EtN)2.H2PtCl6
C22Ha,,Cl6N.!Pt
....
160 d.
Glaus & Stegelitz
B., 17, 1330
46, 1051
platinochloride
Methylamylpiperidine
[C6H0Me(CliH11)N]:,H2PtCl6
C22H48016N2Pt
....
140 ; sf. 100
Schotten
B., 15, 422
42, 982
platinochloride
Ethyltetrahydroquinoline
(C9H10EtN)2.Me.,PtCl6
C34H36Cl6N2Pt
...*
215
Glaus & Stegelitz
B., 17, 1331
46, 1051
niethoplatinochloride
Ethylamylaniline platino-
(Ph.NEt.C6H11)2.H2PtCl6
C!6H44Cl6N2Pt
....
100
Hofmann
A., 74, 156
iv., 452
chloride
702
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Quinoline amylplatino-
(C9H7N)J.(C6H11)JPtCl6
Ca.Hj.Cl.NjPt
220
Glaus and Tosse
B., 16, 1279
44, 1009
chloride
Methyldiphenylpyrazene
(C3N2HMePh)2.H2PtCl6
C32H30Cl6N4Pt
+ H20
160-200 d.
Knorr & Blank
B., 18, 314
48, 556
platinochloride
Diamidoamarine „
[C31H16N2(NH2)2]2.H2PtCl6
C42H42Cl6N8Pt
d.a. 250
Clans and Witt
B., 18, 1676
Benzylamarine „
[C21H17(CH2Ph)N2]2.H2PtCl6
C66H50Cl6N4Pt
d. 240
236 ; sf. 166
Glaus and Elba
B., 16, 1273
44, 983
„ ethoplatino
[C21H17(CH2Ph)N2].,.Et2PtCl6
C60H53Cl6N4Pt
d. 200
152
Glaus and Kohl-
B., 18, 1854
48, 1133
chloride
stock
Triethylphosphine platini-
(Et3P)2PtCl2
C12H30Cl2P2Pt
....
150
Cahours and Gal
Z. C., 13, 437
chloride
Trimethyltolylphosph-
(C6H4MelPMea)2PtClG
C20H32Cl6P2Pt
....
230
Czimatis
B., 15, 2015
44,57
onium platinochloride
=(l-4)i
Triethylphenylphosph-
(PPhEt3)2PtCI6
C24H40Cl6P2Pt
....
b. 100
Ananoff
B., 8, 497
28, 1204
onium platinochloride
Methyldiethylxylyl-
(C,HJMes.PEt!Me)sRCl6
C?6H44Cl6P2Pt
....
202
C/imatis
B., 15, 2016
44,58
phosphonium platino-
chloride
Diphenyldimethylphosph-
(PPh2Me2)2PtCy
C23H32ClcP2Pt
218
Michaelis & Link
A., 207, 210
42, 306
onium platinochloride
Diphenylmethylethyl-
(PPh2MeEt)2PtCl6
C3oH36Cl6P2Pt
....
220
»
)1
))
phosphonium platino-
chloride
Diphenyldiethylphosph-
(PPh2Et2)2PtCl6
C32H40Cl6P2Pt
....
218
»
))
J)
onium platinochloride
Dimethyltolylphosphine
(C6H4Me.PMe2)2.
»
....
226
Czimatis
B., 15, 2016
44, 57
benzylplatinochloride
(CH2Ph)2PtCl6=(1.4)2
Phenyltrimethylarsonium
(AsPhMe,)3PtCl6
C18H28016As2Pt
219
Michaelis & Link
A., 207, 193
42, 306
platinochloride
Diphenyldimethylarsoniuni
(AsPh2Me2)2PtCl6
C23H32Cl6As2Pt
....
219
!)
A., 207, 204
42, 305
platinochloride
Diphenylethylmethyl-
(AsPh2EtMe)2PtCl6
C30H36Cl6As2Pt
....
214 s.d.
j»
A., 207, 193
»
arsonium platinochloride
Quinine platinicyanide ...
(C20H24NA)2.H2PtCy4
C44H5004N8Pt
....
150-160 d.
Burg
J. [1865], 440
vi., 984
Ammonium platinithio-
(NH3)2Pt(CNS)2
C2H6S2N4Pt
....
100-110
Buck ton
7,22
v,, 513
cyanate
Lutidinedicarboxylic acid
C5NHMe2(C02H).H2PtCl6
C9HnCl6O4NPt
+6H2O
nf. 290
Michael
A., 225, 121
48,62
platinochloride
Collidinecarboxylic acid
C5NHMe3(C02H).H2PtCl6
C9H13Cl6O2NPt
+H20
198
)j
»
j>
platinochloride
Dimethylpseudoquinoxyl
C1IH11ON.H2PtCl6
CnH13a6ONPt
'•••
215
Knorr & Antrick
B., 17, 2877
48, 274
platinochloride
Ethylic collidinecarboxyl-
C5NHMe3(C02Et).H1!PtCl(i
CnH17ca6OaNPt
193
Michael
A., 225, 121
48, 62
ate platinochloride
m-Ethoxypyridine platino-
C5NH4(OEt).H2PtCl0
C14H20Cl602N2Pt
..*•
192
Fischer & Eenouf
B., 17, 1897
46, 1370
chloride
Diethylic collidine dicarb-
CjNMe^COjEtOj.HsPtCl,,
C14H21Cl6O4NPt
..,,
184
Hantzsch
A., 215, 1
44, 83
oxylate platinochloride
Nitrodiphenylmethyl-
C1,Hl3OsN3.H,PtCl,=1.2
C16H15Cl602N3Pt
....
198
Knorr & Jodicke
B., 18, 2261
48, 1248
pyrazene platinochloride
Lutidine carboxylic acid
N.Me2.CO2H=1.2.4.3
C16H2001604N2Pt
+2H..O
216
Michael
B., 18, 2024
48, 1245
platinochloride
Tropine platinochloride ....
(C8H16ON)2.H2PtCl6
C16H32Cl602N2Pt
....
198-200 d.
Schmidt
B., 13, 373
38, 482
m-Hydroxyquinoline pla-
(C9NH6.OH)2.H2PtCl6
C18H16Cl602N2Pt
....
244-245
Skraup
M. C., 3, 531
44, 95
tinochloride
Ethylic lutidinecarboxyl-
N.Me2.C02Et=1.2.4.3
C20F28CJ604N2Pt
....
191
Michael
B., 18, 2023
48, 1244
ate platinochloride
COMPOUNDS CONTAINING SPECIAL ELEMENTS.
703
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
Ethylic collidinecarboxyl-
(C5NHMe3.C02Et),.H2PtCl6
C22H32Cl6O4N2Pt
....
194
Hantzsch
A., 215, 1
44,84
ate platinochloride
?-platinochloride ....
(CltH,,01N)rH1PtCl.
C24H32Cl604N2Pt
....
195-196
Canzoneri
G. I., 14, 448
48, 751
Dimethylie collidinecarb-
[C5NMe3(OO2Me)2].:.H,,Pta6
C24H32Clc08N2Pt
200 d.
Hantzsch
B., 16, 1948
44, 1082
oxylate platinochloride
Ethylenediethyltoluylene-
(C9H10Et2ON2)2.H,,PtCl6
C26H42Cl602N4Pt
....
218
....
A., 210, 376
amidine platinochloride
Phenyllutidine carboxylic
(C5NHPhMe2.C02H)2
CJ^fHt04TSft
+H20
110-115
Hantzsch
B., 17, 2913
acid platiuochloride
H2PtCl6
Benzylamidobenzoic acid
NH(CH2Ph).C02H=1.2
J)
158 u.c.
Glaus & Glyckherr
B., 16, 1285
44, 1010
platinochloride
Ethylic phenyllutidine
(C16H1702N)2.H2PtCl6
C32H3,01604N2Pt
....
196
Hantzsch
B., 17, 2912
48, 397
carboxylate platino-
chloride
Fr. methyldiphenylpyr-
(C17H17ON2)2.H,.PtCl(i
C^ClAN.Pt
....
241
Knorr & Blank
B., 18, 315
48, 556
azene
Atropine platinochloride
(C^AN^.H.PtCl,
C^CIA^Pt
HM
208
Schmidt
B., 13, 370
38, 481
?-platinochloride
(C20H20ON2)2.H2PtCl6
C40H42Cl602N4Pt
....
190
Ostermeyer
B., 18, 595
48, 814
Dinitroamarine platino-
[C21H16N2(N02)2]2.H2Ptao
C42H34Cl603N3Pt
d.w.m. 220
Claus and Witt
B., 18, 1673
chloride
Papaverine ethoplatino-
(C31Hai04N)2.Et2PtCl6
C46H62Cl603NiPt
223 d ; u.c.
Claus & Huetlin
B., 18, 1578
48, 996
chloride
Hydrodimethylamarine
(C21H13Me2N20)2.Me2PtCl6
C^H^ClAN.Pt
244
Claus
B., 15, 2329
44, 203
methoplatinochloride
Hydrotrimethylamarine
(C21H17Me3N20)2.H2PtCl6
)»
1
195
»
i»
JJ
platinochloride
Narceme methoplatino-
(C23H2909N)2.Me2PtCl6
C4SHMCl6013NaPt
...»
189
Claus & Eitzfeld
B., 18, 1572
48, 997
chloride
„ ethoplatino-
(C23H!909N)2.Et2PtCl6
C50H68Cl6018N2Pt
....
170 u.c.
>!
B., 18, 1570
48, 996
chloride
Hydromethylbenzyl-
[CilH18Me(CH2Ph)N20]2.
CwH-d,01N4Pt
....
168
Claus
B., 15, 2327
44, 203
amarine platinochloride
H2PtClc
Benzylnarceiine platino-
(C23H28(CH2Ph)09N)2.
C,tHnpI1p18NtPt
+2H20
128 u.c.
Claus & Eitzfeld
B., 18, 1575
48, 997
chloride
H2PtCl6
.
Narceine benzylplatino-
(C23H29Oi)N)2.(CHPh)2Pta6
)J
....
165
»
B., 18, 1573
D
chloride
Triethylic phosphochlor-
(Eto)3p : ptcia
C6H16Cl203PPt
....
83
Schutzenberger
B. S.[2], 18, 101,
25, 1088 ; vii.,
platinate
and Fontaine
148
988
Ethylthiocarbanilide
(CJ6H16SN2)2.H2PtCl6
C30H34016S2N4Pt
+2H20
b. 100
Eathke
B., 14, 1777
42, 167
platinochloride
Phenylimidoethylphenyl-
[NPh:C(NEtPh).SEt]2.
C34H42Cl6S2N4Pt
....
110
Bernthsen and
B., 15, 567
42, 966
carbaminthiethyl pla-
H2PtCl6
Friese
,
tinochloride
?
C12H45C140CN5P2P
t, ....
150
Schutzenberger
B. S. [2], 18, 101,
vii., 989
148
Si. Silicontetramethide
SiMe4
C4H12Si
30
Liquid
Ladenburg
A.. 164, 300
26, 50
„ (A., 136, 203)
JJ
)j
30-31
....
Friedel & Crafts
B. S. [1863], 468
v., 266
Silicontriethylliydride
SiHEtj
C6H16Si
107
Liquid
Ladenburg
A., 164, 327 ; B.,
25, 806 : 26,
5,565
50; vii., 1082
Silicontetraethide
SiEt4
C3H20Si
152-5
Liquid
Friedel & Crafts
B. S. [1863], 468
v., 266
» (A., 127, 31)
j)
»
150-154
Friedel and
A. C. [5], 19, 390
38, 609
Ladenburg
„ (A., 138, 19)
»
)J
152-5
Ladenburg
B., 4, 731
24, 1039
5,
is
))
150
5)
B., 5, 565
25, 806
I)
i,
1 j
151-153
)»
A., 164, 330
26, 52 ; vii.,
1084
704
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Silicontripropylhydride ....
SiHPr«3
C9H2,,Si
170-171
Liquid
Pape
B., 14, 1873
42, 154
Silicouphenyltriethide
SiPhEt,
C12H20Si
230
Liquid
Ladenburg
B., 7, 388 ; A.,
27, 803
173, 159
Silicontetrapropide
SiPr«4
Ci2H23Si
213
Liquid
Pape
B., 14, 1874
42, 154
Siliconhexethide
Et3Si.SiEt3
Ci2H30Si2
250-253
Liquid
Friedel and
A. [5], 19, 401 ;
38, 609; vi.,
Ladenburg
C. K., 68, 920
1022
Silicontetraphenyl
SiPh4
C24H20Si
a. 360
228
Polis
B., 18, 1542
48, 973
Silicontetrabenzyl....
Si(CH2Ph)4
C28H28Si
....
127-5
»
B., 18, 1544
n
Silicontetratolyl
Si(C6H4Me)4=(1.4)4
»)
....
228
)'
B., 18, 1543
)>
Siliconethyltrichloride ....
SiEtCL,
C2H5Cl3Si
100
Liquid
Ladenburg
A., 164, 306
26, 49 ; vii.,
1082
Silioondiethyldichloride ....
SiEt,Cl2
C4H10Cl,Si
129
Liquid
)»
B., 4, 728
24, 1038
J) •"*
»
J)
128-130
Liquid
H
A., 164, 310
26, 50; vii.r
1082
Siliconphenyltrichloride ....
SiPhCl3
C6H5C]3Si
197
Liquid
)>
A., 173, 153; B.,
26, 1026
6,380
Silicontriethylchloride ...
SiEt3Cl
C6H15ClSi
143-5
Liquid
))
A., 164,315; B.,
25, 156 ; 26, 50
4, 902
Silicontolylchloride
Si(C6H4Me)Cl3=1.4
C7H7Cl3Si
218-220
Liquid
»»
A., 173, 165; B.,
27, 803
7, 390
Silicononylchloride
SiH2(CsH17)Cl
C8H19ClSi
180-190
....
Friedel
B. S. [2], 7, 322
vi., 1020
„ ....
)J
»J
185
....
....
A., 138, 20
Silicontriethylchlorphenyl
SiEt3.C6H4Cl
C12H19ClSi
260-265
....
Ladenburg
A., 173, 161
Silicontriethylbromide ....
SiEt3Br
C6H,5BrSi
161
....
Ladenburg
A., 164, 330
26, 52
»»
jj
M
159-163
....
»*
B., 5, 566
25, 807
Silicontripropylbromide ....
SiPr«3Br
CaH^BrSi
213
Liquid
Pape
B., 14, 1875
42, 154
Silicondiethyloxide
Et2SiO
C4H10OSi
a. 350
Liquid — 15
Ladenburg
A., 164, 31
26, 50 ; vii.,
1083
Diethylic silicate
(EtO)2SiO
C4H1003Si
350
Liquid
Ebelmann
A. C. [3], 16, 144
26, 746 ; v., 26S
» » •••• "••
»
)I
360
....
....
A., 57, 338
» »
>»
J>
358-360
...•
Hertkorn
B., 18, 1683
Tetramethylic orthosilicate
(MeO)4Si
C4H,.,04Si
120-122
Liquid
Friedel & Crafts
A. C. [4], 9, 36
v., 265-
Trimethylic orthosilicopro-
Et.Si(OMe)3
C5H1403Si
125-126
Liquid
Ladenburg
A., 173, 145 ; B.,
26, 488; vii..
pionate
5, 1081
1087
Trimethylic ethylic ortho-
(MeO)3(EtO)Si
C8H1404Si
133-135
....
Friedel & Crafts
A. C. [4], 9, 43
v., 265
silicate
Silicobenzoic acid
Ph.SiO.OH
C8H602Si
• •>•
92
Ladenburg
A., 173, 155
Triethylsilicol
SiEt3.OH
C6H16OSi
153-5
Liquid
j)
B., 4, 902
25, 156
?» .... ....
)»
J)
154
....
j»
A., 164, 316
26, 50 ; vii.,
1083
Silicontriethylate
SiHtOEt),
C6H16O8Si
134
....
Friedel and
A., 143, 124;
vi., 1020
Ladenburg
B. S. [2], 7, 322
Diethylic dimethylic
(MeO)2(EtO)2Si
C6H1804Si
143-144
....
Friedel & Crafts
A. C. [4], 9, 44
v., 265
orthosilicate
Hexamethylic disilicate ...
0[Si(OMe)3]2
C6H1807Si2
201-202-5
....
>J
A. C. [4], 9, 36
»
Silicotoluic acid
C6H4Me.(SiO.OH)=1.4
C7H8O2Si
....
150
Ladenburg
A., 173, 166
Triethylic orthosilico-
Me.Si(OEt)3
C7H1803Si
145-151
Liq uid
»
B., 6, 1030 ; A.,
.27, 40
acetate
173, 149
Triethylic methylic ortho-
(EtO)3(MeO)Si
C7H18O4Si
155- 157
....
Friedel & Crafts
A. C. [4], 9, 45
v., 265
silicate
Silicoacetic anhydride
Si(OAc)4
C8H12O8Si
148 (5-6)
110
Friedel and
A. C. [4], 27, 428;
26, 53; vii.,
Ladenburg
A., 145, 174
1084
Triethylsilicol acetate
SiEt3.OAc
C8Hls02Si
168
Liquid
Ladenburg
A., 164, 317 ; B.,
25, 609 ; 26, 51
5, 319
Triethylic acetylsilicate ....
(EtO)3Si.OAc
C8H1805Si
192-197
....
....
J. [1866], 491
v., 264
Triethylsilicol ethylate ....
Et3Si.OEt
C3H20OSi .
153
Liquid
Ladenburg
B., 4, 730; A.,
24, 1039 ; 26,
164, 313
50 ; vii., 1082
COMPOUNDS CONTAINING SPECIAL ELEMENTS.
705
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Silicononyl alcohol
C8H..SiH2.OH
C^OSi
190
Friedel and
B. S. [2], 7, 322;
vi., 1020
Ladenburg
A., 138, 23
Silicondiethyldiethylate ....
SiEt2(OEt)2
C8H2002Si
155-156
„
C. E., 66, 316;
24, 918 ; vi.,
A., 159, 259
1021
jj
„
J)
155-5 ; 155-8
Ladenburg
B., 4, 728 ; A.,
24, 1038; 26,
164, 300
49 ; vii., 1082
Triethylic orthosilicopro-
Et.Si(OEt)3
C8H2003Si
159
....
„
A., 164, 300
26, 49 ; vii.,
pionate
1082, 1087
jj
„
JJ
158-5
Friedel
A., 159, 259
24, 918
jj
,,
JJ
159-162
....
„
C. E., 66, 816
vi., 1020
Tetraethylic orthosilicate
Si(OEt)4
C8H2004Si
162-163
Ebelmann
A., 52, 334
(B., 8, 713)
„
„
165-5
Friedel & Crafts
S. J. [2], 43, 158
(B., 5, 327)
„
„
166-5
....
„
A. C. [4], 9, 45
24, 1039
j,
jj
u
166-5
Ebelmann
A. C. [3], 16, 144
v., 263
„ (J. [1875], 462)
„
„
166-5
....
Ladenburg
A., 164, 300
26,50
„ (B. S., 32, 118)
j/
JJ
165-169
....
Friedel
A. C. [4], 23, 430
25, 155
Tripropylsilicol
Pr«3Si.OH
C9H22OSi
205-208
....
Pape
B., 14, 1875
42, 154
Silicononylic acetate
C8H17.SiH2.OAc
C10H22O2Si
208-214
Friedel and
B. S. [2], 7, 322;
vi., 1020
Ladenburg
A., 138, 22
Tripropylsilicol acetate ....
Pr°3Si.OAc
CnH^OjSi
212-216
....
Pape
B., 14, 1875
42, 154
Isoamylic triethylic ortho-
(EtO)3(C6Hn.O)Si
CnH2604Si
216-225
Friedel & Crafts
A. C. [4], 9, 17
v., 264
silicate
Triethylic orthophenyl-
Ph.Si(OEt)3
Ca~SwOaSi
235
....
Ladenburg
A., 173,155
silicate
jj
„
„
237
Liquid
„
B., 6, 380
26, 1026
Tetrapropylic orthosilicate
(Pr«0)4Si
C12H2804Si
225-227
J. [1874], 49
Cahours
C. E., 76, 1383
26, 871
Diisoamylic dimethylic
(MeO)2(C6Hn.O)2Si
„
225-235
....
Friedel & Crafts
A. C. [4], 9, 46
v., 265
orthosilicate
Silicoheptyl oxide
O(SiEt,)2
C13H30OSi2
224-229
Ladenburg
B., 4, 730
24, 1039
„
„
„
230-235
....
„
A., 147, 364
vii., 1084
jj
„
jj
231
„
A., 164, 326
26, 52
Hexethylic disilicate
0[Si(OEt)3]s
C12H300;Si2
125-130
....
....
A., 57, 341
v., 264
„ (J-, 19, 489)
„
„
233-238
Friedel & Crafts
A. C. [5], 7, 472
„
jj
„
235-237
Friedel and
B. S. [2], 9, 358 ;
vi., 1021
Ladenburg
A., 147, 362
Diisoamylic diethylic
(EtO)2(C6Hn.O)2Si
C14H3304Si
245-250
Friedel & Crafts
A. C. [4], 9, 19
v., 264
orthosilicate
Tetraisobutylic ortho-
(BuPO)4Si
C16H3604Si
256-260
J. [1874], 349
Cahours
C. E., 77, 1403
27, 349
silicate
Diethylic silicate
[(EtO)2SiO]4
Ci»H40012Si4
270-290
Liquid
Troost
A. C. [5], 7, 472
30, 599
Triisoamylic ethylic ortho-
(EtO)(C5Hn.O)3Si
C.-H^Si
280-285
....
Friedel & Crafts
A. C. [4], 9, 19
v., 264
silicate
Tetraisoamylic
(C5Hn.O)4Si
C20H4404Si
324; 322-325
....
Ebelmann
A.C. [3], 16, 144;
v., 263
orthosilicate
A., 57, 344
Tetraphenylic „
(PhO)4Si
CMH2004Si
417-420
47-48
Hertkorn
B., 18, 1680
48, 1056
Tetratolylic „
(C6H4Me.O)4Si=(1.2)4
CjsHjgO^Si
435-438
L. f. m.
„
B., 18, 1687
48, 1056
jj jj
„ =(1.3)4
„
443-446(720)
Liquid
„
B., 18, 1688
jj
jj »
=(l-4)4
„
442-445
69-70
„
B., 18, 1689
jj
Tetraxylic „
(C6H3Me2.0)4Si=(1.3.?)4
C32H3604Si
453-457
L.f.m.
„
B., 18, 1690
u
jj »
=(1-2.?),
„
460 (760) ;
s.f.m. ; n.f.
n
B., 18, 1691
»
350-360(120)
ord. temp.
Tetra-a-naphthylic ortho-
(C10H7.0)4Si
C40H2904Si
425-430 (130)
crystalline
„
B., 18, 1696
48, 1057
silicate
Tetra-(3-naphthylic ortho-
„
J)
430 (133)
crystalline
n
B., 18, 1697
"
silicate
Tetraisobutylphenylic
(C6H4Bu0.O)4Si
C40H6204Si
380 (120)
s.f.m.
„
B., 18, 1692
48, 1056
orthosilicate
Tetrathymylic orthosilicate
(C6HMePr«.O)4Si=(1.4.5)4
„
450 (760)
47-48
„
B., 18, 1694
48, 1057
;j jj
u ,j
„
340-345(69-5)
....
„
„
»
Tetracarvacrylic „
=(1.46)4
"
380-390'(118)
L.f.m.
"
"
4i
706
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Tetramenthylic ortho-
(C10H19.0)4Si
C40H7604Si
350 (155)
82
Hertkorn
B., 18, 1695
48, 1057
silicate
Tetraisoamylphenylic
(C5Hu.C6H4.0)4Si
C44H6004Si
390-397 (118)
s.f.m.
>i
B., 18, 1693
J)
orthosilicate
Silicon tetrathiocyanate ....
Si(S.CN)4
C4S4N4Si
300
142
Miquel
A. C. [5], 11,343;
31, 706 ; 32, 872
C. C. [1876], 516
Methoxysilicon trichloride
MeO.SiCl3
CH3Cl3OSi
82-86
Friedel and Crafts
A. C. [4], 9, 41
v., 265
Ethoxyailicontrichloride ....
EtO.SiCL,
C2H5013OSi
104
....
»
A. C. [4], 9, 15
v., 264
„
»
)J
104
....
Ladenburg
A., 164, 300
26, 52
Dimethoxysilicondi-
(MeO)2SiCl2
C2H6Cl2O2Si
98-103
....
Friedel and Crafts
A. C. [4], 9, 40
v., 265
chloride
Trimethoxysiliconchloride
(MeO)3SiCl
C3H9ClO3Si
114-5-1 15-5
....
»
JI
ii
Diethoxysilicondichloride
(EtO)2SiCl2
C4H10Cl202Si
136-138
»
A. C. [4], 9, 14
v., 264
n
n
?i
137
....
Ladenburg
A., 164, 300
26, 52
Dipropoxysilicondichloride
(Pr«0)2SiCL,
C^Cl^i
185-188
J. [1874], 498
Cahours
C. R., 76, 1383
26, 871
Ethoxysilicondiethyl-
EtO.SiEt2Cl
C8H16C10Si
146-148; 148
Liquid
Ladenburg
B., 4, 728; A.,
24, 1038 ; 26,
chloride
164, 309
50; vii., 1082
Diethoxysiliconethyl-
(EtO)2SiEtCl
C6H15C102Si
148-153
....
H
A., 164, 307
26,52; vii., 1082
chloride
Triethoxysiliconchloride ....
(EtO)3SiCl
C6H16C103Si
156
....
»
A., 164, 300
26, 52
»
!>
J)
156
....
Friedel
B. S. [2], 7, 322
vi., 1020
», ••••
11
)>
155-157
Friedel and Crafts
A. C. [4], 9, 11
v., 264
Tripropoxysiliconchloride
(Pr°O)3SiCl
C9H21C103Si
208-210
J. [1874], 497
Cahours
C. R., 76, 1383
26, 871
1
(EtO)b(NH2)Si2O
0,nHn,O«NSio
280 (i.v.)
Troost
A. C. [5], 7, 453
30, 599
^10 ^ST^fi-1^ 012
Tin diethide
SnEt2
C4H10Sn
150 d.
Liquid — 12
Frankland
P. T. [1852]
v., 827
n ii
n
»
176-180
....
Buckton
J., 11, 392
„ tetramethide (B., 3, 358)
SnMe4
C4H12Sn
78
Liquid
Ladenburg
As., 8, 77
vii., 1160
(J., 12, 427)
J)
»
140-145
....
Cahours
A., 114, 369
v., 834
„ ethotrimethide
SnEtMe3
C5H14Sn
125-128
....
,i
A., 122, 59
n
„ diethodimethide
SnEt2Me2
C6H16Sn
144-146
Liquid — 13
Frankland
A., 144, 157 ;
ii
P. T. [1852]
„ triethomethide
SnEt3Me
C7HI8Sn
162-163
Cahours
A., 122, 60
ii
„ tetrethide( A., 112,223)
SnEt4
C8H20Sn
179-180
....
Ladenburg
B., 3, 355
(A., Ill, 46)
M
)»
180
....
Cahours
J., 12, 420
„ (A., 109, 226)
I)
)J
181
Liquid —13
Fraukland
P. T. [1852]
v., 831
„ phenyltriethide
SnPhEt3
C^Sn
254
Liquid
Ladenburg
A., 159, 251 ;
24, 225
B, 4, 17
„ tetrapropide
SnPr«4
C^H^Sn
222-225
J. [1873], 519
Cahours
B. S., 20, 190
„ triethide
Et3Sn.SnEt3
C12H30Sn2
240-245
....
D
A., 114, 244, 361
») i)
11
11
265-270 p.d.
....
Ladenburg
As., 8, 63
vii., 1159
„ (B.,3,355,647)
11
11
268-272
....
j»
Z. C., 13, 604
Tin dimethyldichloride ...
SnMe2012
C2H6012Sn
188-190
90
Cahours
A., 114, 227, 354
v., 832
„ diethyldichloride
SnEtjClj
C4H10012Sn
220
60
ii
ii
v., 827
» »
»
>1
....
84-5
Ladenburg
As., 8, 60 ; B., 4,
24, 223; vii.,
19
1160
„ diisopropyldichloride
SnPr02Cl2
C6H14012Sn
....
56-5-57-5
Cahoura
C. R., 88, 1112
36, 919
„ dipropyldichloride ...
SnPr«2Cl2
»
....
80
ii
C.R.,88,725,1112
36, 622, 918
„ triethylchloride
SnEt3Q
C6H15ClSn
205-208
....
Ladenburg
B., 4, 17
24, 225
» 11
,f
»
208-210
0
Cahours
J., 12, 425
v., 829
„ phenylethyldichloride
SnPhEtCl2
C8H10012Sn
B, 4, 18
45
Ladenburg
A., 159, 258
24, 225
„ diisobutyldichloride ...
SnBu02Cl2
C8H18012Sn
260-262
a. 5-6
Cahours
C. R., 89, 68
36, 919
„ diphenyldichloride ...
SnPhjCL,
C12H10012Sn
333-337 d.
42
Aronheim
A., 194, 159
36, 249
„ tripheuylchloride
SnPh3Cl
Ci8H15ClSu
....
105
ii
B., 12, 509
j» »
1)
11
....
106
ii
A., 194, 172
36, 250
COMPOUNDS CONTAINING SPECIAL ELEMENTS.
707
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Tin dimethyldibromide ....
SnMe2Br2
C2H6Br2Sn
208-210
Cahours
A., 114, 227, 354
v., 832
„ diethyldibromide
SnEt2Br2
C4H10Br2Sn
232-233
„
„
v., 827
„ triethyldibromide
SnEt3Br
C6H15BrSn
222-224
„
„
v., 829
„ diphenyldibromide ....
SnPh2Br2
C12H10Br2Sn
....
38
Aronheim
A., 194, 166
36, 250
Tin dimethyldiiodide
SnMe2I2
C2H6I2Sn
228
28
Cahours
A, 114, 369
v., 833
„ trimethyliodide
SnMe3I
C3H9ISn
170
....
Ladenburg
As., 8, 77
vii., 1160
„ (A., 122, 56)
j)
„
188-190
Cahours
A., 114, 377
v., 833
„ diethyldiiodide
SnEt2I2
C4H10I2Sn
246
42
Frankland
P. T. [1852]
v., 827
„ „
„
„
245-246
42
Cahours
J., 12, 421
„ (A., 85, 335)
„
„
245
44-5
Ladenburg
As., 8, 60
„ diisopropyldiiodide ....
SnPr/32Is
C6H14I2Sn
265-268
....
Cahours
C. E., 88, 1112
36, 919
„ dipropyldiiodide
SnPr«2Ia
„
270-273
Liquid —20
„
C.E.,88,725,1112
36, 622, 918
„ triethyliodide
SnEt3I
C6H15ISn
180-200
A., 84, 326
Lowig
J., 5, 588
„ „
„
„
231
....
Ladenburg
As., 8, 64
vii., 1159
„ „
„
„
235-238
Cahours
A., 114, 248, 361
v., 830
„ diisobutyldiiodide
SnBuS2Ij
C8H18I2Sn
290-295
Liquid
„
C. E., 89, 68
36, 919
„ triisopropyliodide
SnPrS3l
C9H21ISn
256-258
....
„
C. E., 88, 1112
„
„ tripropyliodide
SnPr«3I
„
260-262
Liquid
„
„
36, 918
» »
„
„
262-264
....
„
C. E., 88, 725
36, 622
„ „
71
„
269-270
....
„
C. E., 76, 133;
26, 366 ; vii.,
J. [1873], 519
1015
„ triisobutyliodide
SnBu03I
C12H!7ISn
284-286
Liquid
„
C. E., 89, 68
36, 919
„ tributyliodide
SnBu«3I
„
292-296
Liquid
„
C. E., 77, 1403
27, 349
,, tripentyliodide
Sn(C5Hn)3I
C^H^ISn
302-305
Liquid
»
C. E., 89, 68
36, 919
Tin trimethylethylate
SnMe3.OEt
C5H14OSn
66
Ladenburg
B., 3, 358
i
„ triethylhydroxide
SnEt3.OH
C5H16OSn
269-273
43
„
As., 8, 74
vii., 1160
„ „
„
„
271
66
„
B., 4, 19
„ „
....
( ,. )«
....
100
„
As., 8, 74
vii., 1160
„ triethylic formate
H.C02.SnEt3
C7H1602Sn
....
56-60
v., 830
„ „ acetate
CH3.C02.SnEt3
C8H1802Sn
230
....
....
ii
„ triethylethylate
SnEt3.OEt
C8H20OSn
190-192
Liquid
Ladenburg
As., 8, 66
•vii., 1160
„ triisopropylhydroxide
SnPr«3.OH
CaHj-jOSn
....
cry st.
Cahours
C. E., 88, 1112
36, 918
„ triisobutylhydroxide...
SnBuS3.OH
C12H28OSn
311-314
„
C. E., 89, 68
36, 919
„ triethylic benzoate ....
Ph.CO2.SnEt3
C13H2002Sn
80
Kulnicz
J. p., 80, 60
v., 830
„ tripentylhydroxide ....
Sn(C6Hu)3.OH
C^H^OSn
335-338 p.d.
Liquid
Cahours and
C. E., 89, 68
36, 919
„ diphenyldiethylate ....
SnPh2(OEt)a
C16H20O2Sn
124
Aronheim
A., 194, 172
„ triphenylhydroxide ....
SnPh3.OH
C18H16OSn
....
117-118
»
A., 194, 174
Tin tetrathioethylate
Sn(SEt)4
C8H2084Sn
200 (i.v.)
Liquid — 40
Claesson
B.S.[2],25,183;
31,585; 32,295
J. p. [2], 15,193
Tin diphenylchlorobromide
SnPh2ClBr
C,2H10ClBrSn
....
39
Aronheim
A., 194, 160
36, 250
Tin diphenylchloriodide ....
SnPh2ai
C12H10ClISn
69
Aronheim
A., 194, 162
36, 250
Tin tetrachlo ride + ethyl-
SnCl4+Et2O
C4H10Cl4OSn
80
Lewy
C. E., 21, 371
v., 809
oxide
„ „ +amyl-
SnCl4+2(C6Hu.OH)
Ci0H24Cl4OjSn
— 10 to —17
Bauer and Klein
J. p. [2], 4, 376
vi., 110
alcohol
„ diphenylhydroxy-
SnPh2Cl.OH
C12HuClOSn
....
187
Aronheim
A., 194, 154
36, 249
chloride
Fr. 4th amidobenzoic acid
C6H4.NH3Cl.C02H+SnCl2
C7H8Cl302NSn
143
Fittica
B., 8, 710, 742
28, 1195
Fr. m-amidobenzoic acid ....
M
H
250
"
H
"
4x2
708
ORGANIC COMPOUNDS.
Name.
Constitution,
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Ti. Titanium tetrachloride
TiCl4+AcCl
C2H3Cl5OTi
....
25-30
Bertrand
B. S. [2], 33, 403
38, 624
+acetylchloride
„ ethoxytrichloride
TiCl3.OEt
C2H5Cl3OTi
186-188
76-78
Bedson
29, 313
„ tetrachloride
Tia4+Et2O
C4H10Cl4OTi
118-120
42-45
„
....
„
+ ethyloxide
„ tetrachloride
TiCl4+BzCl
C7H5Cl6OTi
....
65
Bertraud
B. S. [2], 34, 631
40, 273
-f-benzoylchloride
TL Thallium diethylchloride....
TlEt2Cl
C4H10C1T1
B., 7, 301
d. 190
Hartwig
A., 176, 257
28, 1003
i, »
»
J)
d. 225
Hansen
B., 3, 10
Thallium diethyliodide ....
TIEtjI
C4H10IT1
B., 7, 301
d. 195
Hartwig
A., 176, 257
28, 1003
Thallium formate
H.C02T1
CHO2T1
b. 100
Kuhlmann
C. E., 58, 1037
v., 754
„ ethylate
Tl.OEt
C2H6OT1
— 3
Lamy
C. E., 55, 286
v., 757
Dithallium mallate
C02T1.CH2.CH(OH).C02T1
C4H406T12
b. 100'
Kuhlmann
C. E., 58, 1037
v., 754
Thallium diethylhydroxide
TlEt2.OH
C4HUOT1
B., 7, 301
d. 211
Hartwig
A., 176, 257
28, 1004
„ isoamylate
T1(O.C5HU)
C.H.jOTI
....
Liquid 20
Lamy
C. E., 55, 286
v., 757
„ diethylacetate ....
TlEt2.OAc
C6H1303T1
245 s.d.
212
Hartwig
A., 176, 257 ; B.,
27, 675 ; 28,
7, 300
1003
Thallium diethylsulphate
(TlEt2)2S04
C8H2004ST12
B., 3, 11 ; 7,
d. 205
Hartwig
A., 176, 257
28, 1003
300
Thallium diethylnitrate ....
(TlEt2)N03
C4HI003NT1
B., 3, 11 ; 7,
d. 236
Hartwig
A., 176, 257
28, 1003
300
Thallium diethylphosphate
(TlEt2)3P04
C12H3004PT13
B., 7, 300
d. 189
Hartwig
A., 176, 257
Thallium thiocarbamide
CS(NH2)2T1S04
CH40482N2T1
MM
140-145 p.d.
Pratorius and
J. p. [2], 21, 129
38, 372
sulphate
Seidler
V. Vanadium oxychloride
Et2O+VOCl3
C4H10C1AV
....
b. 20
Bedson
....
29, 311
+Et20
"W. Tungsten tetramethyl-
WMe4I2
C4H12I2W
J. [1856], 373
110
Cahours
A., 122, 70; J.
v., 915
diiodide
[1861], 353
Zn. Zincdimethide(A.,85,347)
ZnMe2
C3H6Zn
46
A., 173, 147
Frankland and
A., 130, 119
17, 30 ; v., 1078
Duppa
(A., 111,62;
„
„
47
Liquid
Ladeuburg
B., 6, 1030
27,41
144, 2)
„ diethide (A., 95, 28 ;
ZnEt2
C4H10Zn
118
Liquid —22
Frankland and
J., 8, 577
v., 1076
123, 245 ; 126, 248 ; 152,
Duppa
220,321; 174, 302; B. S.,
2,51)
Zinc dipropide
ZnPr«2
C6HI4Zn
142-143
Gladstone & Tribe
B. S., 19, 552 ;
21, 130
(B., 6, 1137)
„
„
146
Liquid
„
J. [1873], 518
26, 968 ; 39, 6
„ „ ....
„
„
148
....
Schtscherbakow
B., 14, 1711
„ „
„
„
150
Pape
B., 14, 1873
„ „
H
,,
158-160
....
Cahours
B. S. [2], 20, 190
„ diisobutide
ZnBu02
C8H18Zn
166
....
Thurnlackh
A., 223, 106
46, 1117
„ (B.S,21,357
„
„
185-188
Liquid
Cahours
C. E., 77, 1403
27, 349
„ diisoamyl(A.,130,122
Zn(C5Hu)2
C10H22Zn
220
....
Frankland
J., 16, 473
v., 1075
„ (A.,85,360)
»
» .
220
Gladstone & Tribe
....
26, 680
COMPOUNDS CONTAINING SPECIAL ELEMENTS.
709
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts'Dict.
& J. Ch. Soc.
Zinc ethylbromide
ZnEtBr
C2H5BrZn
....
62
Gladstone & Tribe
27, 411
vii., 478
Zinc acetate
Zn(OAc)2
C4H6O4Zn
....
190-195
Larocque
B., 12, 13
„ „ (A., 34, 220)....
»
))
....
241-ZJ&
Franchimont
!>
36, 452
» »
»
))
+2H20
235-237
»
IJ
)I
„ methoxysuccinate ....
„ /3-hydroxypropionate
CO2.CH(OMe).CH2.CO2.Zn
i i
C5H606Zn
C6H1006Zn
+ 4H20
d. 220
b. 60
Purdie
Wislicenus
J. p. [2], 7, 44
47, 864, 872
24, 236
[CH2(OH).CH2.CO2]2Zn
„ valerate
(C4H9.CO2)2Zn
C10H1304Zn
....
140
v., 977
„ methylpropylacetate
(CHMePr«.C02)2Zn
C12H22O4Zn
72
Liebermann
B., 17, 920
46, 1120
»» i)
J>
)1
72
Kelbe & Warth
B., 15, 310
„ cenanthylate
(C6H13.C02)2Zn
Cl4H2604Zn
....
130
Grimshaw
26, 1079
vii., 870
D » .... ....
»
>»
....
131-132
Franchimont
A., 165, 237
D
„ octylate
(C7H15.C02)2Zn
C16H3004Zn
135-136
Remsen
A., 171, 380
27, 1155
„ caprylate
))
»
....
136
rj
1)
»
„ /3-benzoylbenzoate ....
(C6H4Bz.C02)2Zn
C^H^OsZn
+2H2O
140
Plascuda
B., 7, 987
28,75
„ oleate
(C17H33.C02)2Zn
C36H6604Zn
....
b. 100
Chevreul
Recherches, 205
iv., 194
Oxalmethyline+Zn012 ....
(C4H6N,,HCl)2.ZnCl2
CaH^Cl.N.Zn
....
128
Wallach and
B., 14, 423
40, 572
Schulze
Ethylglyoxaline methyl-
(C,HjN : NEt-MeCl^ZnClj
CuHjjCl.N.Zn
....
157-159
WaUach
B., 16, 535
44,911
zincochloride
Oxalpropyline+ZnClj
(C8H14N2.HCl)2.ZnCl2
C16H30Cl4N4Zii
....
92
Wallaeh and
B., 14, 424
40, 573
Schulze
Oxaliaoamylisoamyline
[C7H11(C5H11)N2.HCl]2ZnCl2
C24H4,Cl4N4Zn
....
86-87
Radziszewaky
B., 17, 1296
46, 986
+ ZnClj
and Szul
Malachite green zincochlor-
3(C23H24N2.HCl).2ZnCl2
C69H76Cl7N6Zn2
....
130 d.
Doebner
B., 13, 2224
40, 165
ida
Triethylphosphine oxide
2(Et3PO).ZnI2
C12H30I2O2P,,Zn
....
99
....
iv., 613
+ Znls
PART III.
1. Vapour tension and boiling point tables of simple
substances.
2. Ditto of mixed substances, such as mixed liquids and
saline solutions.
3. Freezing and melting points of mixtures, including
cryohydrates.
4. Miscellaneous melting and boiling point data, such as
melting and boiling points of fats, oils, &c.
5. Volumes and corresponding years of issue of the more
important chemical and physical periodicals.
6. Alphabetical index of root carbon compounds.
N.B. — When there are several series of observations of the vapour tensions or boiling
points of the same substance the series which is considered the most reliable is frequently
indicated by an asterisk.
712
I.— VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE
SUBSTANCES.
Mercury — Regnault, M.A.S. 21, 502 ; 26, 520; P.A. Ill, 411 ; Watts' Diet., iii., 94. Ramsay and Young, 47, 656;
49, 37. Carnelley. Results obtained in 1880, but not yet published.
Bromine.
Ramsay and Young.
49, 458.
Ramsay and
Young.
Regnault.
Carnelley.
Hageu.
Hertz.
Ramsay and
Young.
Regnault.
Carnelley.
° s.
— 16-65
—14-
mm.
20
25
*
mm.
mm.
mm.
inm.
mm.
mm.
mm.
mm.
— 12-
30
O
— 10-05
35
0
0-0200
[0-00021]
0-015
0-00019
360
785-107
797-74
800-
— 8-4
40
10
0-0268
0-018
0-00050
365
855-223
— 7-0
45
20
0-0372
JP
0-021
0-0013
370
930-335
954-65
960'
— 7'1 m.p.
30
*
0-0530
0-026
0-0029
375
1010-47
— 5-05 1.
50
40
0-008
0-0767
i'8
0-033
0-0063
380
1096-22
1139-65
1120-
+ 8-20
100
50
0-015
0-1120
*°-S §
0-042
0-013
385
1186-67
16-95
150
60
0-029
0-1643
.5 -2'B
0-055
0-026
390
1283-71
1346-71
1390-
23-45
200
70
0-052
0-2410
flj ® O
0-074
0-050
395
1386-60
33-05
300
80
0-092
0-3528
£ o.
0-102
0-093
400
1495-60
1587-96
1629-
40-45
400
90
0-160
0-5142
> * -w
0-144
0-165
405
1611-19
46-80
500
100
0-270
0-7455
2 EE £
0-210
0-285
410
1733-79
1863-73
1830-
51-95
600
107
1-000
H
415
1863-36
56-30
700
110
0-445
1-0734
....
0-478
420
2000-21
2177-53
2120-
58-75
760
120
0-719
1-5341
[0-51]
....
0-779
425
2145-57
130
1-137
2-1752
1-24
430
2298-80
2533-01
2420"
135
1-409
CJ
435
2459-41
Hydrogen.
140
145
1-754
2-172
3-0592
-S '"
0)
....
1-93
440
445
2628-79
2807-53
2933-99
2800-
c.t.— 174-2 (98-9 ats.)
calcl Sarrau, W. 20,
150
2-680
4-2664
a
2-93
450
2996-06
3384-35
3179-
254 ; b.p.— 215 (760)
155
3-287
>->
455
3192-69
calc"1 Mills, C.N. 50,
160
165
170
4-013
4-879
5-904
5-9002
8-0912
a
4-38
6-41
460
465
470
3399-50
3616-22
3843-68
3888-14
4449-45
3530-
3950-
179; compressed — 140
(650 ats.), and pressure
released gives momen-
175
180
7-116
8-535
11-00
B
9-23
475
480
4080-10
4327-14
5072-43
4500-
tary liquefaction and
solidification. Pictet,
185
10-204
*
485
4585-95
C.R. 86, 106; viii., 857;
190
195
200
12-137
14-403
17-015
14-84
19-90
- ^
£ o
o C
16-0
13-07
18-25
490
495
500
4856-74
5139-89
5434-99
5761-32
6520-25
4950-
5446-
liquefies in boiling O
(100— 200 ats.). Wrob-
lewski and Olzewski ;
205
210
20-028
23-482
26-35
1-8
25-12
505
510
5741-86
6059-16
7353-44
5930-
approaches liquefac-
tion— 200. Wroblew-
215
27-447
O -2
515
6391-49
ski, M.C. 6, 204 ; 48,
220
31-957
34-70
I"
....
34-90
520
6736-60
8264-96
6553'
715 ; grey cloud— 208
225
37-083
....
W., 16, 618;
W., 17, 199
to —211, ibid.; C.R.
£
N., 26, 167
100, 982 ; 48, 861 ; does
230
235
240
245
42-919
49-466
56-919
65-241
45-35
58-82
ft
1
|
The following have been obtained by
Ramsay and Young.
not obey Charles' Law,
b. — 193, ibid. ; still
gaseous— 220 (180 ats.).
250
74-592
75-75
«
P.
T.
T.
Olz6wskij C.R. 101,
238 ; 48, 1101.
255
85-010
2
~
260
96-661
96-73
265
109-556
mm.
»
°
Iodine. — Ramsay and
270
123-905
123-01
122-3
10
177-0
184-3
Young. 49, 460.
275
139-802
50
233-9
235-5
280
157-378
155-17
157-8
100
261-3
261-2
0
mm.
285
176-733
150
278-5
277-97
85 s.
20
290
, 197-982
194-46
201-0
200
291-3
290-44
92-2
30
295
221-251
300
310-0
309-21
10215
50
300
246-704
242-15
254-0
400
324-0
323-44
109-05
70
305
274-443
500
335-2
335-03
114-15
90
310
304-794
299-69
600
344-7
344-87
114-2 m.p
315
337-753
333-0
700
352-9
353-48
117-01.
100
320
373-528
368:73
350-0
800
360-1
361-0
128-9
150
325
412249
900
366-8
368-0
137-05
200
330
454-277
450-91
425-0
1000
372-4
374-2
150-7
300
335
499-656
1500
396-2
400-1
160-9
400
340
548-715
548-35
525-0
2000
420-0
169-05
500
345
601-583
3000
450-1
176-0
600
350
658-515
663-18
650-0
5000
....
492-6
182-0
700
355
719-772
P.M. [5], 20, 524
P. M. [5], 21, 5
185-3
700
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
713
Nitrogen,
c.— 29 (300 ats.) and
suddenly released.
Cailletet, C.E. 85 ;
A.C. [5], 15, 132.
Nitrogen (coi
—148-91
— 149-15
—149-925
— 150-05
—150-4
itinued) : —
ats.
27-465
26-867
26-414
25-93
25-093
Oxygen (continued) : —
Cailletet, C.E. 85; A. C.
[5], 15, 132. c.t.— 113
(ibid.). C.E. 86, 97;
N. 32, 584.
Oxygen (con
—195-13
— 194-4
—194-2
— 193-58
— 193-1
—192-71
-192-53
—192-31
— 192-3
—192-13
— 191-98
— 191-88
—191-6
— 191-35
— 190-8
— 190-5
-190-05
—190-0
—181-5
c.t.— 118-0
tinued) : —
mm.
59
60
62
64
68
71
74
76
77
78
80
82
84
86
90
100
140
160
740
ats.
50
Oxygen (con
— 138-15
— 138-7
tinued) : —
mm.
25-65
25-04
Air (contij
Waals, W.I
0
c.t— 158
Wroblewski,
174;M.C.6
102, 1011 ;
O
—191-2
-187 to
—191-4
—146-6
Olzewski, C.:
101, 239;
48, 1101 :—
—220
—205
—191-4
-176
—169
— 160-5
—158-5
—152-0
— 146
—142
c.t. — 140
lued) : —
. 1, 10:—
ats.
14-5
C.N. 51,
,204; C.E.
48, 715 :—
ats.
1
mm.
740
ats.
45
B. 99, 184 ;
46, 1257 ;
mm.
10
(i. V.)
mm.
760
ats.
4-0
6-8
12-5
14-0
20-
27-5
33-
39-
—140-46
— 140-69
—141-17
—141-58
— 142-48
— 142-97
— 143-27
—143-85
—144-17
—144-4
—144-63
— 144-97
—145-2
—145-3
—145-52
— 145-72
—145-89
23-28
22-09
21-21
20-63
19-97
19-39
19-10
18-61
18-22
17-98
17-74
17-38
17-20
17-02
16-83
16-62
16-37
b.p.-123'S (42-1 ats.),
calcd. Sarrau, C.R.
[1882].
c.t. — 1 1 3 (50 ats.) quoted
by Dewar, P.M. [5],
18, 214=Wroblewsky,
C.E. 97, 309.
—150-9
— 151-01
— 151-2
— 151-55
24-896
24-465
23-578
23-217
Olzewski, CJ
100, 350;
B. r. 18, 136
48, 475 ; 41
—225
s.— 214
—213
—194-4
— 160-5
— 148-2
S. 99, 133;
101, 238;
; 46, 1257;
5, 1101 :—
mm.
4
60
(i.v.)
760
ats.
17
31
35
m.b.— 211-5
—211-5
—181-4
— 175-4
—166-1
—159-9
— 155-6
—151-6
—148-6
.. l/lfi'C*
*
mm,
4-
9-
760-
ats.
2-16
4-25
6-23
8-23
10-24
12-3
13-7
32-6
34-4
36-3
38-1
40-4
43-0
45-5
46-7
47-6
49-7
50-8
I. 100, 351 ;
,137.
— 151-79
— 151-925
23-087
22-877
— 153-24
—153-46
—153-67
— 153-95
—154-15
— 154-35
21-462
21-103
20-672
19-521
19-027
18-693
— 154-85
—155-04
18-573
18-193
Eamsay an
P.M. [5],
Calculated
zewski and
ski's numbe
—209-5
—201-4
—197-2
—194-4
—189-5
137-5
i Young,
21, 42-44.
from Ol-
Wroblew-
rs : —
mm.
9
50
100
150
300
400
500
600
700
800
1000
1500
2000
3000
5000
10000
15000
20000
30000
40000
— 130-3
—129-0
1 OQ.A
—123-7
—124-3
—124-85
—125-2
— 125-4
— 125-55
— 125-9
— 126-3
mm.
43-5
42-4
41-47
41-15
40-75
40-34
39-91
39-41
39-09
38-68
38-25
37-94
37-53
37-03
Wroblewski,
979 ; 102, 1
6, 204; B.
48, 715, 861
—206
—204
s.— 203
—202-5
-202-
—201-7
—201-25
—201-
—193-
-193-2
—153-7
— 146-6 ,
c.t.— 146-35
C.E. 100,
Oil ; M.C.
r. 18, 312 ;
:—
mm.
42
60
65
70
79-8
80
100
120
740
ats.
1
20-7
32-2
32-08
The followin
tions were
with rising
—160-22
— 159-61
— 158-85
g observa-
obtained
Dressure : —
ats.
14-09
14-48
14-93
15-26
15-46
— 126-8
—125-6
—124-0
— 122-6
— 121-6
— 120-7
— 119-5
c.t.— 118-8
Olzewski, C.I
B. r. 18
— 158-125
— 157-675
lZD O
—127-1
— 127-5
—127-85
— 128-0
—128-6
Mixture of
and 1 vol. '.
ski, C.E. 1C
1101 :—
—220
Still liquid
1 vol. Air
f. Olzew-
1,239; 48,
mm.
IS
4
— 157-54
—158-57
—159-51
i fin-nfi
15-395
15-00
14-605
14-07
—185-5
— 184-0
—182-6
181-4
Wroblewski,
981 ; 102,
6,204; B.r.
382 ; 48, 71
—200-4 is
still li-
quid
— 199-95
—199-4
199-25
C.E. 100,
L010 ; M.C.
18, 312; 19,
15, 861 :—
mm.
20
22
26
28
30
32
36
38
40
42
44
47
50
52
54
56
58
— 129-0
— 129-2
—129-3
— 129-5
—129-8
36-61
36-22
35-91
35-55
35-28
34-86
34-65
34-32
34-07
33-75
33-49
33-19
32-94
32-65
32-4
179"3
— 147-5
30-845
30-945
31-04
31-145
—175-1
172'0
—147-35
—147-2
—167-1
—160-0
-148-6
Mixture of 2
1 vol. O.
Eemains liqu
and under
sure.
vols. H and
Ibid •
—146-45
—146-55
— 146-5
ats.
32-40
32-28
32-14
31-98
For Air and mixtures of
O and N, see next
column but two.
— 130-05
— 130-8
— 131-1
- niM^
— 140-8
-134-5
— 125-1
id at — 213°
high pres-
—198-7
—117-4
Phospfc
Joubert, C.E.
7,10
5
10
20
30
40
100
orus.
[1874]; B.,
38.
mm.
•03
•05
•11
•25
•48
3-44
—146-7
Oxygen.
—140 (320 ats.) and
pressure suddenly re-
leased produces mo-
mentary liquefaction.
Pictet, C.E. 85, 1214,
1276; 86, 37, 106; C.N.
37, 1, 83 ; viii., 857.
— 131-7
— 146-81
-147-0
—147-45
— 147-65
—147-72
31-25
30-905
30-59
30-305
30-025
— 198-3
—198-
—197-7
—197-5
— 196-6
— 196-3
— 196-2
— 196-0
—195-5
—195-44
— 131-8
— 132-0
—132-3
-132-6
Ail
(Mixture of '.
Cailletet, C.
J. [1877], 6!
O
c.— 27
—140
I
ST and O.)
R. 85, 101 6;
i:—
ats.
300
suddenly
released.
ats.
200
1 ^T-9
31-675
30-51
29-46
28-395
27-35
26-45
—146-85
—147-3
-147-67
— 148-02
31-47
30-556
29-945
29-322
28-657
—134-1
— 135-1
— 135-85
— 136-8
—137-65
—29 (300 ats.) and pres-
sure suddenly released
produces liquefaction.
— 148-205
—195-3
4 v
714
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Phosphorus (cont.) : —
Boron trichloride,
Hydrochloric acid
Phosphorus trichloride
Antimony triiodide
Water (continued) : —
Troost and Hautefeuille,
BC13.
(continued) : —
(continued): —
(continued) : —
iiim.
C.E. 76, 76.
Regnault, M.A.S. 26,
s.— 115, Olzewski, GN.
55
mm.
408-46
.
mm.
92
566-757
Red Phosphc
255:
360
>rus, m.p.
ats.
0-6
339:
—20
— 15
—10
mm.
159-46
200-69
250-54
51, 174.
c. 15 (25 ats.), Seelig
[1886].
c.t. 52-3 (86ats.), Dewar,
P.M. [5], 18, 214;
60
65
70
75
485-63
573-86
674-23
787-61
330
340
350
360
165
204
252
310
93
94
95
96
588-406
610-740
633-778
657-535
440
1-75
— 5
310-30
C.N. 51, 29.
370
377
97
682-029
0
381-32
c.t. 51 — 51°-5, Vincent
Silicon
380
458
98
707-280
Sulphur.
+ 5
10
465-03
562-94
audChappuis.C.R. 100,
1217 ; 48, 861.
tetrachloride, SiCl4.
Regnault, M.A.S. 26,
390
400
552
662
99
100
733-305
760-00
Ramsay and Young,
P.M. [5], 20, 524; 21,
41 :—
15
20
676-57
807-50
b. p. —35° (760); c.t. 5V5
(96 ats.). Ibid., C.R.
339
0
—20
mm.
26-49
410
420
430
790
937
1107
101
102
103
787-59
816-01
845-28
25
957-29
101, 428.
ni ill
30
1127'50
— 15
35-28
440
1301
104
875-41
O
395-
410-7
300
400
35
40
1319-66
1535-25
Mercuric chloride,
— 10
— 5
46-46
60-52
450
470
1522
2054
105
106
906-41
938-31
423'1
500
45
1775-69
HgCl2.
0
78-02
107
971-14
434-0
600
50
2042-25
Carnelley. Results ob-
+ 5
99-59
Water.
108
1004-91
443-1
700
55
2336-17
tained 1880, but not
10
125-90
Melts
Pressure.
109
1039-65
451-6
800
60
2658-52
yet published : —
15
157-74
ats.
110
1075-37
459-0
900
65
3010-24
o
mm.
20
195-86
— 0-059
8-1
111
1112-09
466-0
1000
70
3392-12
47
[1-0]
25
241-15
— 0-129
16-8
112
1149-83
515-2
2000
75
3804-79
240
200
30
294-49
— 18-0
13000- *
113
1188-61
547-8
3000
80
4248-28
250
249
35
356-83
114
1228-47
85
4720-11
260
308
40
429-08
•00747° per atmosphere.*
115
1269-41
270
379
45
512-32
Thomson, Hi., 76 ; *Mous-
116
1311-47
Regnault, M.A.S. 26,
271
387
50
607-46
son, A.C. [3], 56, 252.
117
1354-66
530:—
Hydrochloric acid,
s. 275
420
55
715-44
118
1399-02
O
390
mm.
272-31
HC1.
Faraday, P.T. 113, 189;
280
m.p. 288
465
554
60
65
837-23
973-74
Regnault, M.A.S. 21,
624 ; expressed in mm.
119
120
1444-55
1491-28
400
328-98
135, 15
K .
290
566
reduced to 0°, and
121
1539-25
o : —
410
395-20
•
ats.
300
688
Hydriodic acid, HI.
60 metres above sea
122
1588-47
420
472-11
—73-3
1-8
305
757
Faraday, P.T. 135, 155: —
level : —
123
1638-96
430
560-98
—67-8
2-38
310
832
0
ats.
124
1690-76
440
663-11
—62-2
3-12
320
1002
—17-8
2-9
a
mm.
125
1743-88
450
779-89
—45-5
6-30
330
1201
0
3-97
—32
0-320
126
1798-35
460
912-74
—34-4
9-22
339
1410
+ 15-6
5-86
—30
0-386
127
1854-20
^
28'9
10-92
340
1434
25
0'605
198
1Q1 1 -A^l
4iO
480
10o3'17
1232-70
—23-3
12-82
350
1707
Antimony triiodide
—20
0-927
14O
129
l&LL ti
1970-15
490
1422-88
—17-8
15-04
360
2024
Shi,.
— 15
1-400
130
2030-28
500
1635-32
— 3'9
23-08
370
2389
Carnelley. Results ob-
—10
2-093
131
2091-94
510
1871-57
+ 4'4
30-67
380
2811
tained in 1880, but not
— 5
3-113
132
2155-03
520
2133-30
lO'O
40-0
390
3295
yet published : —
0
4-600
133
2219-69
KOA
94.91 'Q7
400
3850
+ 5
6-534
134
2285-92
<jtj\J
540
_ i _ i . ' i
2739-21
Ansdell, C.N. 41, 75;
410
4481
153-4
lUlYl,
[1-0]
r-i ,Q-|
10
i p
9-165
135
2353-73
550
3086-51
P.R. 34, 113:—
170
[1-8]
15
12 '699
136
2423-16
560
3465-33
ats.
Phosphorus tri-
m.p. 171
[1-9]
20
17-391
137
2494-23
570
3877-08
O
4-0
29-8
chloride.
180
[2-6]
25
23-550
138
2567-00
9'25
33-9
Regnault, M.A.S. 26.
190
[3-6]
30
31-548
139
2641-44
Boron trifluoride,
13-8
18-1
37-75
41-8
339
mm.
200
210
[5-0]
[6-9]
35
40
41-827
54-906
140
141
2717-63
2795-57
BF3.
22-0
45-75
0
37-98
220
[9-4]
45
71-391
142
2875-30
Faraday, P.T. [1845]
26-75
51-0
+ 5
49-09
230
[12-7]
50
91-982
143
2956-86
155:—
QQ./I
10
62-88
240
17-0
55
117-478
144
3040-26
O<5 4
58 '85
jits.
15
79-85
250
22-5
60
148-791
145
3125-55
39 '4
66 '95
—73-3
4-61
44-8
75-2
' 20
100-55
260
29-7
65
186-945
146
321274
—63-3
7-50
48-0
80-8
25
125-59
270
38-8
70
233-093
147
3301-87
—57-8
9-23
49-4
84-75
30
155-65
280
50-0
75
288-517
148
3392-98
—54-4
10-00
50-56
85-33
35
191-45
290
64-6
80
354-643
149
3486-09
—52-2
11-54
c.t. 51-25
40
233-78
300
82-4
85
433-041
1 150
3581-23
45
283-46
310
104
90
525-450
151 3678-43
50
341-39
320
131
91
545-778
152 ! 3777-74
VAPOUR TENSION" AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
715
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
0
mm.
0
mm.
0
ats.
.
mm.
c.t. 370 (195 ats.), calcd.
mm.
153
3879-18
214
15497-17
133-91
3
83-0
400
Strauss, W.B. [1883],
— 14-2
1-5366
154
398277
215
15801-33
144-00
4
88-7
500
676.
•1
1-5492
155
4088-56
216
16109-94
152-22
5
93-5
600
— 14-0
1-5618
156
4196-59
217
16423-15
159-22
6
97-7
700
— 13-9
1-5745
157
4306-88
218
16740-90
165-34
7
100-0
760
Brock (Trav. et Mem. du
•8
1-5874
158
4419-45
219
17063-29
170-81
8
101-45
800
Bur. intern, des Poids
•7
1-6004
159
4534-36
220
17390-36
175-77
9
104-8
900
etMes.,I.A. 33 [1881]).
•6
1-6135
160
4651-62
221
17722-13
180-31
10
107-85
1000
Vap. tension of Water
•5
1-6267
161
4771-28
222
18058-64
184-50
11
120-2
1500
expressed in Mercury
•4
1-6399
162
4893-36
223
18399-94
188-41
12
129-5
2000
at 0° in 45° Lat. and at
•3
1-6532
163
5017-91
224
18746-07
192-08
13
143-5
3000
sea level, calcd. from
•2
1-6667
164
5144-97
225
19097-04
195-53
14
154-2
4000
Eegnault's results : —
•1
1-6803
165
5274-54
226
19452-92
162-85
5000
*
1 11 1 1 1
—13-0
1 "6939
166
167
5406-69
5541-43
227
228
19813-76
20179-61
Arago and Dulong, AC.
roi AQ 74 •
170-1
177-0
6000
7000
o
-19-0
—18-9
1-0288
1-0376
—12-9
•8
1-7076
1-7214
168
5678-82
229
20550-48
L^Ji *»» i * • —
182-9
8000
•8
1-0465
•7
1-7353
169
5818-90
230
20926-40
0
ats.
192-65
10000
•7
1-0555
•6
1-7493
170
"SQfil 'fifi
100
1
212-3
15000
•R
1 'OfiAfi
•5
T7634
171
t*t7Ui. VU
6107-19
Fairbairn and Tate, P.T.
112-2
1-5
227-5
20000
\j
•5
i VAJ^v)
1-0737
•4
1-7776
172
6255-48 t
150, 220 ; iii., 93 :—
121-4
2
•4
1-0828
•3
1-7920
173
6406-60 '
0
mm.
135-1
3
Magnus, P.A. 61, 225: —
•3
1-0920
•2
1-8065
174
6560-55
58-20
135-9
145-4
4
mm.
•2
1-1013
•1
1-8210
175
6717-43
68-51
219-9
153-1
5
19-9
17-28
•1
1-1107
— 12-0
1-8357
176
6877-22
70-76
240-0
160-2
6
24-2
22-48
—18-0
1-1202
-11-9
1-8504
177
7039-97
77-18
316-7
166-5
7
29-9
31-40
— 17-9
1-1298
•8
1-8653
178
7205-72
77-49
320-2
172-1
8
35-0
41-89
•8
1-1394
•7
1-8802
179
7374-52
79-40
345-9
181-6
10
40-9
57-66
•7
1-1491
•6
1-8953
180
7546-39
83-49
406-6
190-0
12
44-8
70-70
•6
1-1588
•5
1-9105
181
7721-37
86-83
466-3
197-2
14
48-4
84-39
•5
1-1686
•4
1-9258
182
7899-52
92-66
581-2
203-6
16
49-8
91-05
•4
1-1785
•3
1-9412
183
8080-84
117-16
1361-7
209-4
18
52-5
104-76
•3
1-1885
•2
1-9567
184
8265-40
118-23
1410-1
214-7
20
54-1
112-40
•2
1-1985
•1
1-9723
185
8453-23
118-45
1419-6
226-3
25
57-9
134-88
•1
1-2086
— 11-0
1-9880
186
8644-35
124-16
1697-7
236-2
30
61-2
157-04
-17-0
1-2187
-10-9
2-0038
187
8838-82
128-41
1935-4
244-8
35
68-7
219-88
— 16-9
1-2290
•8
2-0198
188
9036-68
130-67
2070-8
252-5
40
72-2
255-81
•8
1-2393
•7
2-0359
189
9237-95
131-77
2138-9
265-9
45
82-3
388-59
•7
1-2497
•6
2-0520
190
9442-70
134-05
2287-9
•6
1-2602
•5
2-0683
191
192
9650-93
9862-71
134-86
137-45
2342-6
2529-8
Ramsay and Young,
WUllner, P.A. 103,541:—
•5
•4
1-2707
1-2814
•4
•3
2-0847
2-1012
193
10078-04
139-21
2655-2
P.T. [1884], 477 :—
0
mm.
•3
1-2922
•2
2-1178
194 -,
10297-01
141-80
2864-6
*
mm.
19-9
16-69
•2
1-3030
•1
2-1346
195
10519-63
142-36
2901-9
—15-9
1-0
24-2
22-25
•1
1-3139
— 10-0
2-1514
196
10745-95
144-74
3105-1
—15-2
1-25
29-9
30-66
— 16-0
1-3248
- 9-9
2-1683
197
10975-00
—13-3
1-45
35-0
41-49
—15-9
1-3358
•8
2-1854
198
199
200
11209-82
11447-46
11688-96
Herwig, P.A. 137, 19,
592 ; 141, 84 ; vi.,
(J82 ;
— 11-1
- 9-7
— 6-7
1-65
1-95
2-55
40-9
44-8
48-4
57-61
70-49
84-62
•8
•7
•6
1-3470
1-3582
1-3695
•7
•6
•5
2-2026
2-2199
2-2374
201
11934-37
lllll)
— 5-6
2-85
49-8
90-14
•5
1-3809
•4
2-2550
202
12183-69
40
54-95
- 3-7
3-2
52-5
103-56
•4
1-3924
•3
2-2727
203
12437-00
55
117-81
— 2-6
3-7
54-1
110-61
•3
1-4039
•2
2-2905
204
12694-30
69-8
230-23
57-9
134-24
•2
1-4155
•1
2-3085
205
12955-66
85
430-55
Ibid., P.M. [5], 20, 517,
61-2
156-61
•1
1-4272
— 9-0
2-3266
206
13221-12
95
629-59
524; 21, 35:—
68-7
219-89
—15-0
1-4390
— 8-9
2-3448
207
13490-75
mm.
72-2
257-00
—14-9
1-4509
•8
2-3632
208
209
13764-53
14042-52
Zeuner, Grundziige der
mechanisehen Warme-
11-3
38-3
10
50
82-3
391-90
•8
•7
1-4629
1-4750
•7
•6
2-3816
2-4002
210
14324-80
theorie, 1877 :—
51-7
100
-18 to -2 (1), Luvini,
•6
1-4872
•5
2-4189
211
14611-32
cits.
60-1
150
C.B. 98, 1536; 46, 957.
•5
1-4994
•4
2-4378
212
14902-22
100
i
66-6
200
.£.370 (195-5 ats.),Dewa.r,
•4
1-5117
•3
2-4567
213
15197-48
120-60
2
75-9
300
P.M. [5], 18, 214.
•3
1-5241
•2
2-4758
4 Y 2
716
VAPOUE TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
mm.
o
mm.
mm.
mm.
.
mm.
.
mm.
—8-1
2-4950
—2-0
3-9499
4-1
6-1118
10-2
9-2623
16-3
13-7705
22-4
20-1130
—8-0
2-5143
-1-9
3-9790
•2
6-1546
•3
9-3241
•4
13-8582
•5
20-2355
—7-9
2-5338
•8
4-0082
•3
6-1977
•4
9-3863
•5
13-9464
•6
20-3586
•8
2-5534
•7
4-0376
•4
6-2410
•5
9-4488
•6
14-0351
•7
20-4824
•7
2-5731
•6
4-0672
•5
6-2846
•6
9-5117
•7
14-1243
•8
20-6068
•6
2-5930
•5
4-0970
•6
6-3285
•7
9-5750
•8
14-2141
•9
20-7319
•5
2-6130
•4
4-1271
•7
6-3727
•8
9-6387
•9
14-3043
23-0
20-8576
•4
2-6332
•3
4-1574
•8
6-4171
•9
9-7027
17-0
14-3950
•1
20-9840
•3
2-6535
•2
4-1878
•9
6-4618
11-0
9-7671
•1
14-4862
•2
21-1110
•2
2-6740
•1
4-2185
5-0
6-5067
•1
9-8318
•2
14-5779
•3
21-2388
•1
2-6946
-1-0
4-2493
•1
6-5519
•2
9-8969
•3
14-6702
•4
21-3672
—7-0
2-7153
-0-9
4-2803
•2
6-5974
•3
9-9624
•4
14-7630
•5
21-4964
—6-9
2-7362
•8
4-3116
•3
6-6432
•4
10-0283
•5
14-8563
•6
21-6262
•8
2-7572
•7
4-3430
•4
6-6893
•5
10-0946
•6
14-9501
•7
21-7567
•7
2-7784
•6
4-3747
•5
6-7357
•6
10-1614
•7
15-0444
•8
21-8879
•6
2-7997
•5
4-4065
•6
6-7824
•7
10-2285
•8
15-1392
•9
22-0198
•5
2-8211
•4
4-4385
•7
6-8293
•8
10-2960
•9
15-2345
24-0
22-1524
•4
2-8427
•3
4-4708
•8
6-8765
•9
10-3639
18-0
15-3304
•1
22-2857
•3
2-8644
•2
4-5032
•9
6-9240
12-0
10-4322
•1
15-4268
•2
22-4196
•2
2-8863
•1
4-5359
6-0
6-9718
•1
10-5009
•2
15-5237
•3
22-5543
•1
2-9083
o-o
4-5687
•1
7-0198
•2
10-5700
•3
15-6212
•4
22-6898
—6-0
2-9304
+0-1
4-6017
•2
7-0682
•3
10-6394
•4
15-7192
•5
22-8259
—5-9
2-9527
•2.
4-6350
•3
7-1168
•4
10-7093
•5
15-8178
•6
22-9628
•8
2-9751
•3
4-6685
•4
7-1658
•5
10-7796
•6
15-9169
•7
23-1003
•7
2-9977
•4
4-7022
•5
7-2150
•6
10-8503
•7
16-0166
•8
23-2386
•6
3-0205
•5
4-7361
•6
7-2646
•7
10-9214
•8
16-1168
•9
23-3777
•5
3-0434
•6
4-7703
•7
7-3145
•8
10-9928
•9
16-2176
25-0
23-5174
•4
3-0665
•7
4-8047
•8
7-3647
•9
11-0647
19-0
16-3189
•1
23-6579
•3
3-0898
•8
4-8393
•9
7-4152
13-0
11-1370
•1
16-4208
•2
23-7991
•2
3-1132
•9
4-8741
7-0
7-4660
•1
11-2097
•2
16-5233
•3
23-9411
•1
3-1368
1-0
4-9091
•1
7-5171
•2
11-2829
•3
16-6263
•4
24-0838
—5-0
3-1605
•1
4-9443
•2
7-5685
•3
11-3564
•4
16-7299
•5
24-2272
—4-9
3-1844
•2
4-9798
•3
7-6202
•4
11-4304
•5
16-8341
•6
24-3714
•8
3-2084
•3
5-0155
•4
7-6722
•5
11-5048
•6
16-9388
•7
24-5164
•7
3-2326
•4
5-0515
•5
7-7246
•6
11-5797
•7
17-0441
•8
24-6620
•6
3-2570
•5
5-0877
•6
7-7772
•7
11-6550
•8
17-1499
•9
24-8084
•5
3-2815
•6
5-1240
•7
7-8302
•8
11-7307
•9
17-2563
26-0
24-9556
•4
3-3062
•7
5-1606
•8
7-8834
•9
11-8069
20-0
17-3632
•1
25-1035
•3
3-3310
•8
5-1975
•9
7-9370
14-0
11-8835
•1
17-4707
•2
25-2523
•2
3-3560
•9
5-2346
8-0
7-9909
•1
11-9605
•2
17-5789
•3
25-4018
•1
3-3812
2-0
5-2719
•1
8-0452
•2
12-0380
•3
17-6877
•4
25-5521
—4-0
3-4065
•1
5-3094
•2
8-0998
•3
12-1159
•4
17-7971
•5
25-7032
—3-9
3-4320
•2
5-3472
•3
8-1547
•4
12-1943
•5
17-9071
•6
25-8551
•8
3-4576
•3
5-3852
•4
8-2099
•5
12-2731
•6
18-0176
•7
26-0077
'7
3-4834
•4
5-4235
•5
8-2655
•6
12-3523
"7
18-1288
•8
26-1612
•6
3-5095
•5
5-4620
•6
8-3214
•7
12-4320
•8
18-2406
•9
26-3155
•5
3-5357
•6
5-5008
•7
8-3777
•8
12-5122
•9
18-3529
27-0
26-4705
•4
3-5620
•7
5-5398
•8
8-4342
•9
12-5928
21-0
18-4659
•1
26-6263
•3
3-5886
•8
5-5790
•9
8-4911
15-0
12-6739
•1
18-5795
•2
26-7830
•2
3-6153
•9
5-6185
9-0
8-5484
•1
12-7554
•2
18-6937
•3
26-9405
•1
3-6422
3-0
5-6582
•1
8-6061
•2
12-8374
•3
18-8085
•4
27-0987
—3-0
3-6693
•1
5-6981
•2
8-6641
•3
12-9198
•4
18-9240
•5
27-2578
—2-9
3-6966
•2
5-7383
•3
8-7224
•4
13-0027
•5
19-0400
•6
27-4177
•8
3-7240
•3
5-7788
•4
8-7810
•5
13-0861
•6
19-1567
•7
27-5784
"7
3-7516
•4
5-8195
•5
8-8400
•6
13-1700
"7
19-2740
•8
27-7399
•6
3-7794
•5
5-8605
•6
8-8993
•7
13-2543
•8
19-3920
•9
27-9023
•5
3-8074
•6
5-9017
•7
8-9589
•8
13-3392
•9
19-5105
28-0
28-0654
•4
3-8355
•7
5-9432
•8
9-0189
•9
13-4245
22-0
19-6297
•I
28-2294
•3
3-8638
•8
5-9850
•9
9-0792
16-0
13-5103
•1
19-7496
•2
28-3942
•2
3-8923
•9
6-0270
10-0
9-1398
•1
13-5965
•2
19-8701
•3
28-5599
•1
3-9210
4-0
6-0693
*1
9-2009
•2
13-6832
•3
19-9912
•4
28-7265
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
717
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
.
mm.
.
mm.
.
mm.
o
mm.
0
mm.
0
mm.
28-5
28-8939
34-6
40-8664
40-7
56-9540
46-8
78-2696
52-9
106-1351
59-0
142-0973
•6
29-0622
"7
41-0942
•8
57-2580
•9
78-6697
53-0
106-6546
•1
142-7640
•7
29-2313
•8
41-3231
•9
57-5633
47-0
79-0714
•1
107-1764
•2
143-4334
•8
29-4013
•9
41-5531
41-0
57-8700
•1
79-4749
•2
107-7005
•3
144-1054
•9
29-5722
35-0
417842
•1
58-1781
•2
79-8802
•3
108-2268
•4
144-7801
29-0
29-7439
•1
42-0164
•2
58-4877
•3
80-2874
•4
108-7553
•5
145-4575
•1
29-9165
•2
42-2498
•3
58-7988
•4
80-6963
•5
109-2860
•6
146-1376
•2
30-0900
•3
42-4843
•4
59-1113
•5
81-1071
•6
109-8190
•7
146-8204
•3
30-2644
•4
42-7199
•5
59-4252
•6
81-5197
•7
110-3542
•8
147-5059
•4
30-4396
•5
42-9567
•6
59-7406
•7
81-9341
•8
110-8916
•9
148-1940
•5
30-6157
•6
43-1946
•7
60-0575
•8
82-3503
•9
111-4312
60-0
148-8848
•6
30-7928
•7
43-4337
•8
60-3758
•9
82-7684
54-0
111-9730
•1
149-5784
•7
30-9707
•8
43-6739
•9
60-6955
48-0
83-1883
•1
112-5171
•2
150-2747
•8
31-1494
•9
43-9152
42-0
61-0167
•1
83-6100
•2
113-0634
•3
150-9738
•9
31-3291
36-0
44-1577
•1
61-3394
•2
84-0336
•3
113-6120
•4
151-6757
30-0
31-5096
•1
44-4013
•2
61-6636
•3
84-4590
•4
114-1629
•5
152-3804
•1
31-6910
•2
44-6462
•3
61-9893
•4
84-8862
•5
114-7161
•6
153-0879
•2
31-8734
•3
44-8922
•4
62-3164
•5
85-3153
•6
115-2716
•7
153-7982
•3
32-0567
•4
45-1394
•5
62-6450
•6
85-7462
•7
115-8293
•8
154-5112
•4
32-2410
•5
45-3878
•6
62-9751
•7
86-1789
•8
116-3893
•9
155-2270
•5
32-4262
•6
45-6374
•7
63-3067
•8
86-6135
•9
116-9516
61-0
155-9456
•6
32-6124
•7
45-8882
•8
63-6398
•9
87-0499
55-0
117-5162
•1
156-6671
•7
32-7995
•8
46-1402
•9
63-9744
49-0
87-4882
•1
118-0831
•2
157-3914
•8
32-9875
•9
46-3934
43-0
64-3104
•1
87-9284
•2
118-6524
•3
158-1186
•9
33-1765
37-0
46-6477
•1
64-6479
•2
88-3705
•3
119-2241
•4
158-8486
31-0
33-3664
•1
46-9032
•2
64-9870
•3
88-8146
•4
119-7982
•5
159-5815
•1
33-5573
•2
47-1600
•3
65-3277
•4
89-2606
•5
120-3746
•6
160-3173
•2
33-7491
•3
47-4180
•4
65-6700
•5
89-7086
•6
120-9534
•7
161-0559
•3
33-9419
•4
47-6773
"5
66-0138
•6
90-1586
•7
121-5346
•8
161-7974
•4
34-1356
•5
47-9378
•6
66-3593
•7
90-6105
•8
122-1182
•9
162-5417
•5
34-3303
•6
48-1996
"7
66-7063
•8
91-0644
•9
122-7042
62-0
163-2889
•6
34-5259
•7
48-4626
•8
67-0549
•9
91-5202
56-0
123-2925
•1
164-0390
•7
34-7225
•8
48-7268
•9
67-4050
50-0
91-9780
•1
123-8832
•2
164-7921
•8
34-9201
•9
48-9923
44-0
67-7568
•1
92-4378
•2
124-4764
•3
165-5482
•9
35-1186
38-0
49-2590
•1
68-1101
•2
92-8995
•3
125-0720
•4
166-3073
32-0
35-3181
•1
49-5270
•2
68-4650
•3
93-3632
•4
125-6700
•5
167-0693
•1
35-5186
•2
49-7963
•3
68-8215
•4
93-8289
•5
126-2705
•6
167-8342
•2
35-7201
•3
50-0668
•4
69-1796
•5
94-2966
•6
126-8734
•7
168-6021
•3
35-9226
•4
50-3386
•5
69-5393
•6
94-7662
•7
127-4788
•8
169-3730
•4
36-1261
•5
50-6117
•6
69-9006
•7
95-2378
•8
128-0866
•9
170-1468
•5
36-3307
•6
50-8861
•7
70-2636
•8
95-7114
•9
128-6968
63-0
170-9236
•6
36-5363
•7
51-1618
•8
70-6281
•9
96-1869
57-0
129-3095
•1
171-7034
•7
36-7429
•8
51-4388
•9
70-9942
51-0
96-6644
•1
129-9247
•2
172-4863
•8
36-9505
•9
51-7170
45-0
71-3619
•1
97-1439
•2
130-5424
•3
173-2722
•9
37-1592
39-0
51-9965
•1
71-7313
•2
97-6255
•3
131-1627
•4
174-0611
33-0
37-3689
•1
52-2773
•2
72-1024
•3
98-1093
•4
131-7855
•5
174-8531
•1
37-5796
•2
52-5595
•3
72-4751
•4
98-5951
•5
132-4108
•6
175-6481
•2
37-7914
•3
52-8430
•4
72-8495
•5
99-0830
•6
133-0386
•7
176-4461
•3
38-0042
•4
53-1279
•5
73-2256
•6
99-5730
•7
133-6689
•8
177-2472
•4
38-2180
•5
53-4141
•6
73-6034
•7
100-0651
•8
134-3017
•9
178-0513
•5
38-4329
•6
53-7016
•7
73-9829
•8
100-5594
•9
134-9371
64-0
178-8585
•6
38-6488
"7
53-9905
•8
74-3641
•9
101-0557
58-0
135-5750
•1
179-6688
•7
38-8657
•8
54-2807
•9
74-7469
52-0
101-5541
•1
136-2154
•2
180-4822
•8
39-0837
•9
54-5722
46-0
75-1314
•1
102-0547
•2
136-8585
•3
181-2988
•9
39-3027
40-0
54-8651
•1
75-5176
•2
102-5573
•3
137-5042
•4
182-1185
34-0
39-5228
•1
55-1594
•2
75-9056
•3
103-0621
•4
138-1525
•5
182-9414
•1
39-7440
•2
55-4550
•3
76-2953
•4
103-5690
•5
138-8034
•6
183-7674
•2
39-9663
•3
55-7521
•4
76-6867
•5
104-0780
•6
139-4569
•7
184-5965
•3
40-1897
•4
56-0505
•5
77-0799
•6
104-5891
•7
140-1131
•8
185-4288
•4
40-4142
•5
56-3503
•6
77-4748
•7
105-1023
•8
140-7719
•9
186-2642
•5
40-6398
•6
56-6515
•7
77-8713
•8
105-6176
•9
141-4333
65-0
187-1028
718
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
0
mm.
.
mm.
mm.
mm.
mm.
0
mm.
65-1
187-9446
71-2
245-7230
77-3
317-7607
83-4
406-7006
89-5
515-5583
95-6
647-8118
•2
188-7896
•3
246-7821
•4
319-0747
•5
408-3157
•6
517-5275
•7
650-1966
•3
189-6378
•4
247-8451
•5
320-3933
•6
409-9362
•7
519-5031
•8
652-5889
•4
190-4893
•5
248-9120
•6
321-7165
•7
411-5621
•8
521-4849
•9
654-9885
•5
191-3440
•6
249-9828
•7
323-0442
•8
413-1934
•9
523-4731
96-0
657-3956
•6
192-2020
•7
251-0575
•8
324-3765
•9
414-8301
90-0
525-4676
•1
659-8101
•7
193-0632
•8
252-1361
•9
325-7134
84-0
416-4721
•1
527-4685
•2
662-2321
•8
193-9277
•9
253-2185
78-0
327-0549
•1
418-1196
•2
529-4757
•3
664-6616
•9
194-7954
72-0
254-3048
•1
328-4010
•2
419-7725
•3
531-4893
•4
667-0985
66-0
195-6663
•1
255-3950
•2
329-7518
•3
421-4309
•4
533-5093
•5
669-5430
•1
196-5405
•2
256-4892
•3
331-1073
•4
423-0948
•5
535-5358
•6
671-9951
•2
197-4180
•3
257-5874
•4
332-4674
•5
424-7642
•6
537-5687
•7
674-4547
•3
198-2989
•4
258-6895
•5
333-8321
•6
426-4390
•7
539-6080
•8
676-9219
•4
199-1831
•5
259-7955
•6
335-2016
•7
428-1194
•8
541-6538
•9
679-3967
•5
200-0707
•6
260-9055
•7
336-5757
•8
429-8053
•9 ,
543-7062
97-0
681-8791
•6
200-9616
•7
262-0194
•8
337-9546
•9
431-4968
91-0
545-7650
•1
684-3692
•7
201-8558
•8
263-1373
•9
339-3382
85-0
433-1938
•1
547-8303
•2
686-8669
•8
202-7534
•9
264-2591
79-0
340-7265
•1
434-8964
•2
549-9022
•3
689-3723
•9
203-6543
73-0
265-3849
•1
342-1196
•2
436-6046
•3
551-9807
•4
691-8854
67-0
204-5586
•1
266-5148
•2
343-5174
•3
438-3184
•4
554-0657
•5
694-4062
•1
205-4662
•2
267-6488
•3
344-9200
•4
440-0378
•5
556-1573
•6
696-9348
•2
206-3773
•3
268-7869
•4
346-3274
•5
441-7628
•6
558-2555
•7
699-4712
•3
207-2918
•4
269-9290
•5
347-7396
•6
443-4935
•7
560-3604
•8
702-0153
•4
208-2097
•5
271-0752
•6
349-1566
•7
445-2298
•8
562-4719
•9
704-5673
•5
209-1311
•6
272-2254
•7
350-5784
•8
446-9719
•9
564-5900
98-0
707-1271
•6
210-0559
•7
273-3798
•8
352-0051
•9
448-7196
92-0
566-7149
•1
709-6947
•7
210-9841
•8
274-5382
•9
353-4366
86-0
450-4730
•1
568-8465
•2
712-2702
•8
211-9158
•9
275-7008
80-0
354-8730
•1
452-2321
•2
570-9847
•3
714-8536
•9
212-8509
74-0
276-8675
•1
356-3143
•2
453-9969
•3
573-1297
•4
717-4449
68-0
213-7895
•1
278-0383
•2
357-7604
•3
455-7675
•4
575-2815
•5
720-0442
•1
214-7316
•2
279-2133
•3
359-2115
•4
457-5438
•5
577-4400
•6
722-6514
•2
215-6772
•3
280-3925
•4
360-6675
•5
459-3260
•6
579-6053
•7
725-2665
•3
216-6264
•4
281-5758
•5
362-1284
•6
461-1139
•7
581-7775
•8
727-8897
•4
217-5791
•5
282-7633
•6
363-5943
•7
462-9077
•8
583-9564
•9
730-5209
•5
218-5353
•6
283-9550
•7
365-0651
•8
464-7073
•9
586-1422
99-0
733-1602
•6
219-4950
•7
285-1509
•8 .
366-5409
•9
466-5127
93-0
588-3349
•1
735-8075
•7
220-4583
•8
286-3510
•9
368-0217
87-0
468-3240
•1
590-5344
•2
738-4629
•8
221-4250
•9
287-5554
81-0
369-5075
•1
470-1412
•2
592-7408
•3
741-1265
•9
222-3953
75-0
288-7640
•1
370-9983
•2
471-9644
•3
594-9542
•4
743-7981
69-0
223-3691
•1
289-9769
•2
372-4941
•3
473-7934
•4
597-1744
•5
746-4779
•1
224-3464
•2
291-1940
•3
373-9950
•4
475-6284
•5
599-4016
•6
749-1659
•2
225-3274
•3
292-4154
•4
375-5009
•5
477-4693
•6
601-6358
•7
751-8621
•3
226-3121
•4
293-6411
•5
377-0119
•6
479-3162
•7
603-8770
•8
754-5665
•4
227-3005
•5
294-8711
•6
378-5279
•7
481-1619
•8
606-1251
•9
757-2791
•5
228-2925
•6
296-1054
•7
380-0491
•8
483-0278
•9
608-3804
100-0
760-0000
•6
229-2882
•7
297-3440
•8
381-5753
•9
484-8927
94-0
610-6426
•1
762-7272
•7
230-2876
•8
298-5870
•9
383-1067
88-0
486-7635
•1
612-9119
•2
765-4666
•8
231-2907
•9
299-8343
82-0
384-6432
•1
488-6403
•2
615-1883
•3
768-2124
•9
232-2975
76-0
303-0860
•1
386-1848
•2
490-5232
•3
617-4718
•4
770-9666
70-0
233-3079
•1
302-3421
•2
387-7316
•3
492-4121
•4
619-7624
•5
773-7291
•1
234-3220
•2
303-6025
•3
389-2836
•4
494-3071
•5
622-0602
•6
776-5000
•2
235-3399
•3
304-8674
•4
390-8407
•5
496-2083
•6
624-3651
•7
779-2793
•3
236-3615
•4
306-1367
•5
392-4031
•6
498-1155
•7
626-6772
•8
782-0670
•4
237-3867
•5
307-4104
•6
393-9706
•7
500-0288
•8
628-9965
•9
784-8632
•5
238-4157
•6
308-6885
•7
395-5434
•8
501-9483
•9
631-3230
101-0
787-6678
•6
239-4484
•7
309-9711
•8
397-1214
•9
503-8740
95-0
633-6567
Boiling Points of Water
•7
240-4848
•8
311-2582
•9
398-7047
89-0
505-8059
•1
635-9976
at different pressures.
•8
241-5249
•9
312-5497
83-0
400-2933
•1
507-7439
•2
638-3459
Ibid. 46 [1881].
•9
242-5687
77-0
313-8457
•1
401-8872
•2
509-6881
•3
640-7014
0
mm.
71-0
243-6163
•1
315-1462
•2
403-4863
•3
511-6386
•4
643-0642
96-9243
680-0
•1
244-6677
•2
316-4512
•3
405-0908
•4
513-5953
•5
645-4343
•9284
•1
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
719
Water (continued) : —
Water; (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
0
mm.
»
mm.
o
mm.
° mm.
0
mm.
0
mm.
96-9324
680-2
97-1813
686-4
97-4284
692-6
97-6736
698-8
97-9169
705-0
98-1585
711-2
•9364
•3
•1853
•5
•4323
•7
•6775
•9
•9208
•1
•1624
•3
•9404
•4
•1893
•6
•4363
•8
•6814
699-0
•9247
•2
•1662
•4
•9445
•5
•1933
•7
•4403
•9
•6854
•1
•9286
•3
•1701
•5
•9485
•6
•1973
•8
•4442
693-0
•6893
•2
•9326
•4
•1740
•6
•9525
•7
•2013
•9
•4482
•1
•6933
•3
•9365
•5
•1779
•7
•9566
•8
•2053
687-0
•4522
•2
•6972
•4
•9404
•6
•1818
•8
•9606
•9
•2093
•1
•4561
•3
•7011
•5
•9443
•7
•1856
•9
•9646
681-0
•2133
•2
•4601
•4 •
•7051
•6
•9482
•8
•1895
712-0
•9686
•1
•2173
•3
•4641
•5
•7090
•7
•9521
•9
•1934
•1
•9727
•2
•2213
•4
•4680
•6
•7129
•8
•9560
706-0
•1973
•2
•9767
•3
•2253
•5
•4720
•7
•7169
•9
•9599
•1
•2012
•3
•9807
•4
•2293
•6
•4760
•8
•7208
700-0
•9638
•2
•2050
•4
•9847
•5
•2333
"7
•4799
•9
•7247
•1
•9677
•3
•2089
•5
•9888
•6
•2373
•8
•4839
694-0
•7287
•2
•9716
•4
•2128
•6
•9928
•7
•2413
•9
•4879
•1
•7326
•3
•9755
"5
•2167
•7
•9968
•8
•2453
688-0
•4918
•2
•7365
•4
•9794
•6
•2205
•8
97-0008
•9
•2493
•1
•4958
•3
•7405
•5
•9833
•7
•2244
•9
•0049
682-0
•2532
•2
•4997
•4
•7444
•6
•9872
•8
•2283
713-0
•0089
•1
•2572
•3
•5037
•5
•7483
•7
•9911
•9
•2322
•1
•0129
•2
•2612
•4
•5077
•6
•7523
•8
•9950
707-0
•2360
•2
•0169
•3
•2652
•5
•5116
•7
•7562
•9
•9989
•1
•2399
•3
•0209
•4
•2692
•6
•5156
•8
•7601
701-0
98-0028
•2
•2438
•4
•0250
•5
•2732
•7
•5195
•9
•7641
•1
•0067
•3
•2476
•5
•0290
•6
•2772
•8
•5235
695-0
•7680
•2
•0106
•4
•2515
•6
•0330
•7
•2812
•9
•5275
•1
•7719
•3
•0145
•5
•2554
•7
•0370
•8
•2852
689-0
•5314
•2
•7758
•4
•0184
•6
•2592
•8
•0410
•9
•2891
•1
•5354
•3
•7798
•5
•0223
•7
•2631
•9
•0451
683-0
•2931
•2
•5393
•4
•7837
•6
•0262
•8
•2670
714-0
•0491
•1
•2971
•3
•5433
•5
•7876
•7
•0301
•9
•2709
•1
•0531
•2
•3011
•4
•5472
•6
•7915
•8
•0340
708-0
•2747
•2
•0571
•3
•3051
•5
•5512
•7
•7955
•9
•0379
•1
•2786
•3
•0611
•4
•3091
•6
•5551
•8
•7994
702-0
•0418
•2
•2825
•4
•0651
•5
•3130
•7
•5591
•9
•8033
•1
•0457
•3
•2863
•5
•0691
•6
•3170
•8
•5631
696-0
•8072
•2
•0496
•4
•2902
•6
•0732
•7
•3210
•9
•5670
•1
•8112
•3
•0535
•5
•2941
•7
•0772
•8
•3250
690-0
•5710
•2
•8151
•4
•0574
•6
•2979
•8
•0812
•9
•3290
•1
•5749
•3
•8190
•5
•0613
'7
•3018
•9
•0852
684-0
•3330
•2
•5789
•4
•8229
•6
•0652
•8
•3057
715-0
•0892
•1
•3369
•3
•5828
•5
•8269
•7
•0691
•9
•3095
•1
•0932
•2
•3409
•4
•5868
•6
•8308
•8
•0730
709-0
•3134
•2
•0972
•3
•3449
•5
•5907
•7'
•8347
•9
•0769
•1
•3172
•3
•1012,
•4
•3489
•6
•5947
•8
•8386
703-0
•0808
•2
•3211
•4
•1052
•5
•3529
•7
•5986
•9
•8425
•1
•0846
•3
•3250
•5
•1092
•6
•3568
•8
•6026
697-0
•8465
•2
•0885
•4
•3288
•6
•1133
•7
•3608
•9
•6065
•1
•8504
•3
•0924
•5
•3327
•7
•1173
•8
•3648
691-0
•6105
•2
•8543
•4
•0963
•6
•3366
•8
•1213
•9
•3688
•1
•6144
•3
•8582
•5
•1002
•7
•3404
•9
•1253
685-0
•3727
•2
•6184
•4
•8621
•6
•1041
•8
•3443
716-0
•1293
•1
•3767
•3
•6223
•5
•8660
•7
•1080
•9
•3481
•1
•1333
•2
•3807
•4
•6262
•6
•8700
•8
•1119
710-0
•3520
•2
•1373
•3
•3847
•5
•6302
•7
•8739
•9
•1158
•1
•3558
•3
•1413
•4
•3886
•6
•6341
•8
•8778
704-0
•1196
•2
•3597
•4
•1453
•5
•3926
•7
•6381
•9
•8817
•1
•1235
•3
•3636
•5
•1493
•6
•3966
•8
•6420
698-0
•8856
•2
•1274
•4
•3674
•6
•1533
•7
•4006
•9
•6460
•1
•8895
•3
•1313
•5
•3713
•7
•1573
•8
•4045
692-0
•6499
•2
•8934
•4
•1352
•6
•3751
•8
•1613
•9
•4085
•1
•6539
•3
•8974
•5
•1391
•7
•3790
•9
•1653
686-0
•4125
•2
•6578
•4
•9013
•6
•1429
•8
•3829
717-0
•1693
•1
•4165
•3
•6617
•5
•9052
"7
•1468
•9
•3867
•1
•1733
•2
•4204
•4
•6657
•6
•9091
•8
•1507
711-0
•3906
•2
•1773
•3
•4244
•5
•6696
•7
•9130
•9
•1546
•1
•3944
•3
720
VAPOUK TENSION AND BOILING POINT TABLES OP SIMPLE SUBSTANCES.
Water (continued) :—
Water (continued): —
Water (continued) : —
Water (continued) : —
Water (continued) : —
Water (continued) : —
„
mm.
0
mm.
0
mm.
mm.
0
mm.
0
mm.
98-3983
717-4
98-6363
723-6
98-8726
729-8
99-1073
736-0
99-3402
742-2
99-5715
748-4
•4021
•5
•6401
•7
•8764
•9
•1110
•1
•3440
•3
•5752
•5
•4060
•6
•6440
•8
•8802
730-0
•1148
•2
•3477
•4
•5790
•6
•4098
•7
•6478
•9
•8840
•1
•1186
•3
•3514
•5
•5827
•7
•4137
•8
•6516
724-0
•8878
•2
•1223
•4
•3552
•6
•5864
•8
•4175
•9
•6554
•1
•8916
•3
•1261
•5
•3589
•7
•5901
•9
•4214
718-0
•6593
•2
•8954
•4
•1299
•6
•3627
•8
•5938
749-0
•4252
•1
•6631
•3
•8992
•5
•1336
'7
•3664
•9
•5975
•1
•4291
•2
•6669
•4
•9030
•6
•1374
•8
•3702
743-0
•6013
•2
•4329
•3
•6707
•5
•9068
•7
•1412
•9
•3739
•1
•6050
•3
•4368
•4
•6745
•6
•9106
•8
•1449
737-0
•3776
•2
•6087
•4
•4406
•5
•6784
•7
•9144
•9
•1487
•1
•3814
•3
•6124
•5
•4445
•6
•6822
•8
•9182
731-0
•1525
•2
•3851
•4
•6161
•6
•4483
•7
•6860
•9
•9220
•1
•1562
•3
•3889
•5
•6198
•7
•4522
•8
•6898
725-0
•9258
•2
•1600
•4
•3926
•6
•6235
•8
•4560
•9
•6936
•1
•9295
•3
•1638
•5
•3963
•7
•6273
•9
•4599
719-0
•6975
•2
•9333
•4
•1675
•6
•4001
•8
•6310
750-0
•4637
•1
•7013
•3
•9371
•5
•1713
•7
•4038
•9
•6347
•1
•4676
•2
•7051
•4
•9409
•6
•1751
•8
•4075
744-0
•6384
•2
•4714
•3
•7089
•5
•9447
•7
•1788
•9
•4113
•1
•6421
•3
•4752
•4
•7127
•6
•9485
•8
•1826
738-0
•4150
•2
•6458
•4
•4791
•5
•7165
•7
•9523
•9
•1863
•1
•4187
•3
•6495
•5
•4829
•6
•7204
•8
•9561
732-0
•1901
•2
•4225
•4
•6532
•6
•4868
•7
•7242
•9
•9599
•1
•1939
•3
•4262
•5
•6569
•7
•4906
•8
•7280
726-0
•9637
•2
•1976
•4
•4299
•6
•6606
•8
•4945
•9
•7318
•1
•9674
•3
•2014
•5
•4337
•7
•6643
•9
•4983
720-0
•7356
•2
•9712
•4
•2051
•6
•4374
•8
•6681
751-0
•5021
•1
•7394
•3
•9750
•5
•2089
•7
•4412
•9
•6718
•1
•5060
•2
•7432
•4
•9788
•6
•2127
•8
•4449
745-0
•6755
•2
•5098
•3
•7471
•5
•9826
•7
•2164
•9
•4486
•1
•6792
•3
•5137
•4
•7509
•6
•9864
•8
•2202
739-0
•4523
•2
•6829
•4
•5175
•5
•7547
•7
•9902
•9
•2239
•1
•4561
•3
•6866
•5
•5213
•6
•7585
•8
•9939
733-0
•2277
•2
•4598
•4
•6903
•6
•5252
•7
•7623
•9
'9977
•1
•2315
•3
•4635
•5
•6940
•7
•5290
•8
•7661
727-0
99-0015
•2
•2352
•4
•4673
•6
•6977
•8
•5329
•9
•7699
•1
•0053
•3
•2390
•5
•4710
•7
•7014
•9
•5367
721-0
•7737
•2
•0091
•4
•2427
•6
'4747
•8
•7051
752-0
•5405
•1
•7775
•3
•0128
•5
•2465
•7
•4785
•9
•7088
•1
•5444
•2
•7813
•4
•0166
•6
•2502
•8
•4822
746-0
•7126
•2
5482
•3
•7852
•5
•0204
•7
•2540
•9
•4859
•1
•7162
•3
•5520
•4
•7890
•6
•0242
•8
•2577
740-0
•4896
•2
•7199
•4
•5559
•5
•7928
•7
•0280
•9
•2615
•1
•4934
•3
•7236
•5
•5597
•6
•7966
•8
•0318
734-0
•2652
•2
•4971
•4
•7273
•6
•5635
•7
•8004
•9
•0355
•1
•2690
•3
•5008
•5
•7310
•7
•5674
•8
•8042
728-0
•0393
•2
•2728
•4
•5045
•6
•7347
•8
•5712
•9
•8080
•1
•0431
•3
•2765
•5
•5083
•7
•7384
•9
•5750
722-0
•8118
•2
•0469
•4
•2803
•6
•5120
•8
•7421
753-0
•5789
•1
•8156
•3
•0506
•5
•2840
•7
•5157
•9
•7458
•1
•5827
•2
•8194
•4
•0544
•6
•2878
•8
•5194
747-0
•7495
•2
•5865
•3
•8232
•5
•0582
•7
•2915
•9
•5232
•1
•7532
•3
•5904
•4
•8270
•6
•0620
•8
•2953
741-0
•5269
•2
•7569
•4
•5942
•5
•8308
•7
•0658
•9
•2990
•1
•5306
•3
•7606
•5
•5980
•6
•8346
•8
•0695
735-0
•3028
•2
•5343
•4
•7643
•6
•6019
•7
•8384
•9
•0733
•1
•3065
•3
•5381
•5
•7680
•7
•6057
•8
•8422
729-0
•0771
•2
•3102
•4
•5418
•6
•7717
•8
•6095
•9
•8460
•1
•0808
•3
•3140
•5
•5455
•7
'7754
•9
•6133
723-0
•8498
•2
•0846
•4
•3177
•6
•5492
•8
•7791
754-0
•6172
•1
•8536
•3
•0884
•5
•3215
•7
•5529
•9
•7828
•1
•6210
•2
•8574
•4
•0922
•6
•3252
•8
•5567
748-0
•7865
•2
•6248
•3
•8612
•5
•0959
•7
•3290
•9
•5604
•1
•7902
•3
•6287
•4
•8650
•6
•0997
•8
•3327
742-0
•5641
•2
•7938
•4
•6325
•5
•8688
•7
•1035
•9
•3365
•1
•5678
•3
•7975
•5
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
721
Water (continued) :--
Water (continued) : —
Water (continued) :—
Water (continued) : —
Water (continued) : —
Water (continued) : —
0
mm.
0
mm.
0
mm.
0
mm.
0
mm.
o
mm.
99-8012
754-6
100-0293
760-8
100-2559
767-0
100-4809
773-2
100-7043
779-4
100-9263
785-6
•8049
•7
•0330
•9
•2595
•1
•4845
•3
•7079
•5
•9299
•7
•8086
•8
•0367
761-0
•2632
•2
•4881
•4
•7115
•6
•9334
•8
•8123
•9
•0403
•1
•2668
•3
•4917
•5
•7151
•7
•9370
•9
•8160
755-0
•0440
•2
•2704
•4
•4953
•6
•7187
•8
•9406
786-0
•8197
•1
•0477
•3
•2741
•5
•4989
•7
•7223
•9
•9441
•1
•8234
•2
•0513
•4
•2777
•6
•5026
•8
•7259
780-0
•9477
•2
•8271
•3
•0550
•5
•2814
•7
•5062
•9
•7295
•1
•9513
•3
•8308
•4
•0587
•6
•2850
•8
•5098
774-0
•7331
•2
•9548
•4
•8344
•5
•0623
•7
•2886
•9
•5134
•1
•7366
•3
•9584
•5
•8381
•6
•0660
•8
•2923
768-0
•5170
•2
•7402
•4
•9620
•6
•8418
•7
•0696
•9
•2959
•1
•5206
•3
•7438
•5
•9655
•7
•8455
•8
•0733
762-0
•2995
•2
•5242
•4
•7474
•6
•9691
•8
•8492
•9
•0770
•1
•3032
•3
•5278
•5
•7510
•7
•9727
•9
•8529
756-0
•0806
•2
•3068
•4
•5315
•6
•7546
•8
•9762
787-0
•8566
•1
•0843
•3
•3105
•5
•5351
•7
•7582
•9
•9798
•1
•8603
•2
•0880
•4
•3141
•6
•5387
•8
•7618
781-0
•9833
•2
•8639
•3
•01*16
•5
•3177
•7
•5423
•9
•7653
•1
•9869
•3
•8676
•4
•0953
•6
•3214
•8
•5459
775-0
•7689
•2
•9905
•4
•8713
•5
•0989
•7
•3250
•9
•5495
•1
•7725
•3
•9940
•5
•8750
•6
•1026
•8
•3286
769-0
•5531
•2
•7761
•4
•9976
•6
•8787
•7
•1062
•9
•3323
•1
•5567
•3
•7797
•5
101-0011
•7
•8824
•8
•1099
763-0
•3359
•2
•5603
•4
•7833
•6
•0047
•8
•8860
•9
•1136
•1
•3395
•3
•5639
•5
•7868
•7
•0083
•9
•8897
757-0
•1172
•2
•3432
•4
•5675
•6
•7904
•8
•0118
788-0
•8934
•1
•1209
•3
•3468
•5
•5712
•7
•7940
•9
•0154
•1
•8971
•2
•1245
•4
•3504
•6
•5748
•8
•7976
782-0
•0189
•2
•9008
•3
•1282
•5
•3540
•7
•5784
•9
•8012
•1
•0225
•3
•9044
•4
•1318
•6
•3577
•8
•5820
776-0
•8048
•2
•0261
•4
•9081
•5
•1355
•7
•3613
•9
•5856
•1
•8083
•3
•0296
•5
•9118
•6
•1392
•8
•3649
770-0
•5892
•2
•8119
•4
•0332
•6
•9155
•7
•1428
•9
•3686
•1
•5928
•3
•8155
•5
•0367
•7
•9192
•8
•1465
764-0
•3722
•2
•5964
•4
•8191
•6
•0403
•8
•9228
•9
•1501
•1
•3758
•3
•6000
•5
•8227
•7
•0438
•9
•9265
758-0
•1538
•2
•3794
•4
•6036
•6
•8262
•8
•0474
789-0
•9302
•1
•1574
•3
•3831
•5
•6072
•7
•8298
•9
•0509
•1
•9339
•2
•1611
•4
•3867
•6
•6108
•8
•8334
783-0
•0545
•2
•9376
•3
•1647
•5
•3903
•7
•6144
•9
•8370
•1
•0581
•3
•9412
•4
•1684
•6
•3940
•8
•6180
777-0
•8406
•2
•0616
•4
•9449
•5
•1720
•7
•3976
•9
•6216
•1
•8441
•3
•0652
•5
•9486
•6
•1757
•8
•4012
771-0
•6252
•2
•8477
•4
•0687
•6
•9523
•7
•1793
•9
•4048
•1
•6288
•3
•8513
•5
•0723
•7
•9559
•8
•1830
765-0
•4085
•2
•6324
•4
•8549
•6
•0758
•8
•9596
•9
•1866
•1
•4121
•3
•6360
•5
•8584
•7
•0794
•9
•9633
759-0
•1903
•2
•4157
•4
•6396
•6
•8620
•8
•0829
790-0
•9670
•1
•1939
•3
•4193
•5
•6432
•7
•8656
•9
•0865
•1
•9706
•2
•1976
•4
•4230
•6
•6468
•8
•8692
784-0
•0900
•2
•9743
•3
•2012
•5
•4266
•7
•6504
•9
•8727
•1
•0936
•3
•9780
•4
•2049
•6
•4302
•8
•6540
778-0
•8763
•2
•0971
•4
•9816
•5
•2085
•7
•4338
•9
•6576
•1
•8799
•3
•1007
•5
•9853
•6
•2122
•8
•4374
772-0
•6612
•2
•8835
•4
•1042
•6
•9890
•7
•2158
•9
•4411
•1
•6648
•3
•8870
•5
•1078
'7
•9927
•8
•2194
766-0
•4447
•2
•6684
•4
•8906
•6
•1113
•8
•9964
•9
•2231
•1
•4483
•3
•6720
•5
•8942
•7
•1149
•9
100-0000
760-0
•2267
•2
•4519
•4
•6756
•6
•8977
•8
•1184
791-0
•0037
•1
•2304
•3
•4555
•5
•6792
•7
•9013
•9
•1220
•1
•0073
•2
•2340
•4
•4592
•6
•6828
•8
•9049
785-0
•1255
•2
•0110
•3
•2377
•5
•4628
•7
•6864
•9
•9085
•1
•1291
•3
•0147
•4
•2413
•6
•4664
•8
•6900
779-0
•9120
•2
•1326
•4
•0183
•5
•2450
•7
•4700
•9
•6936
•1
•9156
•3
•1361
•5
•0220
•6
•2486
•8
•4736
773-0
•6971
•2
•9192
•4
•1397
•6
•0257
•7
•2522
•9
•4773
•1
•7007
•3 1
•9227
•5
•1432
•7
A _
722
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Water (continued) : —
Water (continued) : —
Nitrous oxide (cont.) : —
Sulphur dioxide(cont-): —
Hydrogen sulphide
Ammonia (continued) : —
0
101-1468
mm.
791-8
101-3658
mm.
798-0
O
25
ats.
61-38
Regnault, M.A.S. 26,
(contiuu
sd): —
ats.
0
— 5
ats.
3-45
•1503
•9
•3693
•1
30
68-03
535 ; iii., 94 : —
— 3-3
9-36
0
4-19
•1539
792-0
•3728
•2
35
75-36
0
ats.
+ 10-0
14-14
+ 5
5-04
•1574
•1
•3764
•3
40
83-37
—30
0-39
11-1
14-60
10
6-02
•ifiifi
'2
•M7QQ
•4
—25
0-49
15
7-14
HJ 1 VJ
•1645
•1680
•3
•4
o i yy
•3834
•3869
•5
•6
Cailletet, Arch, de Gen.,
66, 16 [1878]:—
—20
— 15
0-63
0-80
Regnault, M.A.S. 26,
535 • iii. aA '
20
25
8-41
9-84
•1716
•5
•3904
•7
0
ats.
— 10
1-00
30
11-45
•1751
•6
•3940
•8
—92
ro
— 5
1-25
7°8
mm.
441 '4
35
13-25
•1787
•7
•3975
•9
—90
1-10
0
1-53
40
15-26
•1822
•8
•4010
799-0
—84
1-40
+ 5
1-87
—30
3-69
45
17-48
•1857
•9
•4045
•1
—80
1-90
10
2-26
—25
4-93
50
19-95
•1893
793-0
•4080
•2
— 74
2-60
15
2'72
—20
5-83
55
22-66
•1928
•1
•4115
•3
-70
3-15
20
3-24
— 15
6-84
60
25-63
•1964
•2
•4151
•4
—64
4-20
25
3-84
— 10
8-01
65
28-90
•1999
•3
•4186
•5
-60
5-05
30
4-52
— 5
9-30
70
32-47
•2034
•4
•4221
•6
—54
6-32
35
5-28
0
10-80
75
36-35
•2070
•5
•4256
•7
—50
7-63
40
6-15
+ 5
12-48
80
40-59
•2105
•6
•4291
•8
—44
9-60
45
7-11
10
14-34
85
45-17
•2141
•7
•4326
•9
—40
11-02
I 50
8-19
15
16-38
90
50-14
•2176
•8
•4362
800-0
—34
13-19
55
9-38
20
18-62
95
55-52
•2211
•9
•4397
•1
60
10-69
25
21-07
100
61-32
•2247
794'Q
•4432
•2
Dewar, P.M. [5], 18,
65
12-11
30
23-73
•2282
•1
•4467
•3
212
mm
35
26-B2
Vincent & Chappuis, C.R.
•2317
•2
•4502
•4
—125
25
Sajotschewski, W.B. 3,
40
29-72
101, 428; 48, 1105:—
•2353
•3
•4537
•5
ats.
741:—
45
32-83
O
ats.
•2388
•4
•4572
•6
c.t. 35-4
75
0
ats.
50
36-60
c.t. 131
113
•2423
•5
•4607
•7
Andrews, C.N. 4, 158 :—
50
8-43
55
40-38
— 38-5
i-o
•2459
•6
•4642
•8
.
60
11-09
60
44-39
•2494
•7
•4678
•9
c.t. 36
ats.
1
70
14-31
65
48-63
Dewar, P.M. [5], 18,214;
•2529
•8
Seelig [1
2Q£!~1 .
80
18-09
70
53-10
C.N. 51,
oq.
5ODj I
•2565
•2600
•2635
•9
795-0
•1
Nitrous oxide, N20.
Faraday, P.T. 135, 155 ;
C.N. 51, 174:—
c. 15
ats.
31
90
100
120
22-47
27-82
41-56
c.t. 130
Seelig [If
ats.
115
IQfTl .
Dewar, P.M. [5], 18,214;
C.N. 51, 29:—
5ot)J .
•2671
•2706
•2741
•2
•3
•4
—87-2
ats.
ro
Nitric oxide, NO.
Olzewski, C.R. 100,942;
150
c.t 155-4
71-45
78-9
J
c.t. 108-2
ats.
92
c. 15
ats.
7
•2777
•2812
•2847
•2883
•5
•6
•7
•8
—73-3
—62-0
—59-4
—51-0
1-77
3-00
3-58
5-00
B.r. 18, 313 ;
0
—176-5
s. —167-0
*», oou: —
mm.
18
138
Ladenburg, B. 11, 818;
34, 633: —
» ats.
Seelig [11
c. 15
386] :—
ats.
10
Hydrogen arsenide,
AsH3.
Faraday, P.T. 135, 155 :—
— 45 '6
6'89
ats.
c.t. 157-161
I
•2918
•2953
•2988
•9
796-0
•1
—40-0
—31-7
8-71
12-04
—153-6
— 138-8
—129-0
1-0
5-4
10-6
Drion, A.C. [t
], 56, 37 :—
ats.
Ammonia, NH3.
Faraday, P.T. 135, 155 :—
—59-4
—53-3
ats.
0-94
1-26
•3024
•2
— 17-8
19-34
—119-0
20-0
c.t. 140
?
°
ats.
—46-7
1-73
•3059
•3094
•3
•4
— 3-9
— 1-7
28-90
33-40
—iio-o
— 105-0
31-6
41-0
Seelig [1
386]:—
ats.
—17-8
— 3-3
2'48
4-04
—30-6
-17-8
3-32
5-21
•3129
•5
0
32-00
—100-9
49-9
c. 15
3
+ 9-4
5'83
— 12-2
6-24
'6
97'5
57'8
28'3
lO'OO
0
8-95
•3200
•7
Regnault, M.A.S. 26,
c.t. — 93-5
71-2
Hydrogen sulphide,
49-4
10-30
+ 4-4
10:0
10-05
11-56
•3235
•3271
•3306
'8
•9
797-0
535
—25
ats.
20-65
Sulphur dioxide.
Faraday, P.T. 135. 155:—
Faraday, P.T. 135, 155:—
Regnault, MJ
iii., 94 ; vi
LS.26, 535;
102 •
15-6
13-19
•3341
•1
—20
23-14
ats.
0
ats.
o
mm.
Olzewski, C.N. 51, 174 :—
•3376
•2
— 15
25-90
—17-8
0-725
—73-3
1-02
—78-2
240
o
•3412
•3
— 10
28-96
— 7-2
1-12
—67-8
1-09
—40
528-6
Remains liquid — 102
•3447
•4
— 5
32-34
— 3-3
1-33
—58-9
1-50
ats.
Solidifies -118
•3482
•3517
•5
•6
0
+ 5
36-08
40-21
+ 4-4
23-1
1-78
3-28
—45-5
-31-1
2-35
3-95
—30
—25
1-14
1-45
Seelig [1
386] :—
ats.
•3552
•7
10
44-76
32-2
. 4-35
—28-9
4-24
—20
1-83
c. 15
8-5
•3588
•8
15
49-77
37'8
5'16
— 18-9
5-90
— 15
2-24
•8893
•9
20
55-30
—17-8
6-10
-10
2-82
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
723
Methane, CH4.
Acetylene (cont.) : —
Ethylene (cont.) :—
Benzene (cont.) : —
Benzene (cont.) : —
Naphthalene (cont.) : —
Wroblewski, C.R. 99,
136;B.r. 17, 412;C.N.
0
36-9
ats.
67-96
Seelig [1886] :—
75
mm.
643-18
0
20-1
mm.
75
o
210
mm.
639
51, 174; 46, 1275:—
c.t. 37-05
~
c. 15
ats.
42-5
80
751-86
79-1
725
218
760
0
mm.
85
874'63
80-1
760
220
808
—155
—130-9
760
ats.
67
Dewar, P.M. [5], 18,
214; C.N. 51, 29:—
° ats.
Ramsay and Young,
P.M. [5], 20, 524 ; 21,
90
95
100
1012-75
1167-46
1340-05
Sajotschewski, W.B.
3, 741 ; 45, 138 :—
230
240
250
1008
1244
1519
—113-4
16-4
c.t. 37
68
41 : —
105
1531-83
O
ats.
256
1704
— 113
16-0
o
mm.
10
110
1744-12
c.t. 280-6
49-5
260
[1836]
—150
— 98'2
— 98
— 86
*7K>f\
24'9
25
40
Ethylene, C3H4.
Faraday, P.T., 135,
155 ; C.N., 51. 174 :—
—133-5
—126-25
—121-6
50
100
150
115
120
125
1978-22
2235-44
2517-06
Dewar, P.I
214 ; C.N.
H. [5], 18,
51, 29 :—
ats.
270
280
290
[2198]
[2606]
[3065]
— 75 9
52 '5
ats.
—118-1
200
130
2824-35
c.t. 2917
60-4
300
[3574]
c.t. — 73-5
56'8
—76-1
4-6
- 113'0
•?no
135
3158-51
0
Remains liquid at — 160
—73-3
—67-8
4-82
5-44
—109-0
O\J\J
400
140
145
3520-73
3912-11
Toluene, C7H8.
Turpentine, C10H16.
Olzewski, C.R. 100, 941 ;
[—62-0
—59-4
6-5]
6 '89
Ethane, C2H6.
150
155
4333-71
4786-51
Kahlbaum, B., 17,
1261 :—
Regnault, M.A.S., 26,
339 ; iii., 94 :—
B.r.18,313; 48,860:—
—51-1
9-14
Cailletgt,C.R. 85,851:—
160
5271-43
o
mm.
*
0
mm.
—45-6
11-10
O
ats.
165
5683-03
— 2-2
0
0
mm.
—201-5
s. —185-8
5
80
—40-0
13-46
4
46
170
6340-72
+ 4-5
1 A«A
5
1 A
+ 10
2 '07
2-94
ats.
•• 31'7
17-75
Dewar, P.M. [5], 18,
10 0
1 K.A
10
I K
20
4-45
— 164-0
—153-8
—138-5
—126-8
1-0
2-24
6-2
11-0
—23-3
—17-8
e.— 1-0
22-94
26-90
42-0
214 ; C.N.
o
c.t. 35
51, 29 :—
ats.
45-2
Ramsay and Young,
P.R, 31, 194; P.T.
[1884], 464; 45, 138:—
1O \J
19-3
227
34-5
10
20
25
50
30
40
50
60
6-87
10-80
16'98
26'46
—110-6
-105-8
21-4
26-3
40-0
Olzewski, C.R. 99, 133 ;
101, 238; 46, 1257;
48, 1101 :—
Amylene, C6HW.
Guthrie, P.M. [5], 18,
El H ,
0
—5-21 s.
—4-80 s.
—3-77 s.
mm.
17-60
17-90
19-60
42-4
111-0
75
760
70
80
90
40-64
61-30
90-61
— 93-3
— 85-4
49-0
9
mm.
ol /
—2-80 s.
20-80
Octane, C8H18.
100
131-11
c.t. — 81-8
54-9
1.— 162
— 150-4
1
9-8
0
18-4
mm.
356-5
—1-72 s.
—1-28 s.
22-35
23-40
Lemoine, B.S. 41, 161 ;
46, 1106 :—
110
120
185-62
257-21
Dewar, N. 28, 551 :—
—148-0
12
Dewar, P.M. [5], 18,
—0-20 s.
25-50
O
mm.
130
348-98
0
ats.
—139-0
31
214 ; C.N. 51, 29 :—
+0-90 s.
26-70
31
27
140
464-02
c.t. b. —100
39
— 132-0
56
0
ats.
l-20s.
27-30
63
110
150
605-20
Ibid., P.M. [5], 18, 214 ;
—129-7
—126-0
72
107
c.t. 19V6
33-9
2-60 s.
2'98 1.
29-90
31 '90
82
121
212
779
155
160
686-37
775-09
C.N. 51, 29:—
— 122
146
3-00 s.
31-40
165
871-27
0
ats.
— 115-5
246
Benzene, C6H6.
170
975-42
c.t. —99-5
50
—111
346
Regnault, M.A.S. 26,
m.p. 3'30
3-60 1.
32-55
Naphthalene.
175
1090-11
Sarrau, C.R. 94, 720 :—
—108
441
339 ; P.A. Ill, 408;
4-01 1.
32-40
Carnelley. Not yet
180
120/-92
0
ats.
— 105
546
iii., 94 :—
4 '08 1.
33"35
published : —
185
1336-45
-75-7
46-8
— 103
750
O
mm.
4-46 1.
34-05
0
mm.
190
1473-24
—20
5-79
42
[1-0]
Acetylene, C2H3.
Cailletet, N. 32, 584 :—
—15
— 10
8-82
12-92
4'50 1.
6-32 1.
33'20
37-10
50
60
[1-54]
[2-7]
Ibid., P.M. [41, 8, 271 :—
CailletSt,C.R. 85, 851:—
„
mm.
— 5
18-33
8-20 1.
40-90
70
L J
[4-4]
o
mm
o
ats.
—103
760
0
25-31
9-60 1.
44-40
m.p. 79
[6-9]
0
2-1
1
48
80 -0
755-7
ftO
Waals, P.R. 37, 354 ;
+ 5
34-17
ats.
80
[7-2]
10
2-3
1 Q
Do
00
W.B. 4, 704 :—
10
45-25
.t. 291-5
90-5
90
[11-6]
20
4-3
1O
oo
15
58-93
100
[17-9]
30
7-0
25
94
0
c.t. 9-2
ats.
58
20
75-65
106
23-0
40
11-2
31
103
25
95-91
Schall, B., 17, 2202,
110
27-1
50
17-2
Sarrau C R 94 «4fi •
cc\
Of?«Q
Ansdell, P.R. 29, 209 :—
ats.
30
35
120-24
149-26
2568
o
mm.
120
130
40'3
58-6
DO
70
20 y
41-9
0
ats.
c.t. 1-5
43-5
40
183-62
— 3-3
0
140
83-7
80
61-2
—23
11-01
Dewar, P.M. [5], 18,
45
224-06
— 0-6
5
150
118
90
91-0
—10
17-06
212 ; C.N. 51, 29 :—
50
271-37
+ 1-3
10
160
163
100
134-9
0
21-53
55
326-41
3-3
15
170
219
110
187-3
13-5
32-77
0
c.t. 10-1
ats.
51
60
390-10
51
20
180
292
120
257-0
20-15
39-76
mm.
65
463-43
6-4
25
190
386
130
347-0
31-6
56-20
—140
25 ;
70
547-42
13-8
50
200
500
140
462-3
4 z 2
724
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Turpentine (cont.) : —
Carbon tetrachloride
Carbon tetrachloride
Hexachlorethane,
Carbon tetrabromide
Carbon monoxide
o
mm.
(continued) : —
(continued) : —
C2CI6.
(continued) : —
(continued) : —
150
604-5
0
mm.
Winkelmaim, W. 9,
Staedel and Hahn, B. 1 1
0
mm.
o
ats.
160
170
777-2
989-0
115
120
2129-15
2393-67
372, 385 :—
o Tnm_
1736, 1'
'38:—
150-0 (1)-,
150-5' (2)j
280
— 155-80
— 155-35
15-54
15-70
180
1225-0
125
2682-41
6-69
47-5
O
185-5
mm.
776-73
160-25 (1) j
OOA
— 155-10
15-87
190
1514-7
130
2996-88
20-86
95-0
186-4
787-70
161-0 (2)J
ooD
— 154-84
16-12
200
1865-6
135
3338-56
28-20
123-6
187-0
800-66
165-5 (2)
430
— 154-73
16-21
210
2251-2
140
3709-04
28-56
127-9
188-7
820-60
169-5 (2)
482
220
2690-3
145
4109-99
29-09
131-5
189-0
826-45
175-0 (2)
558
— 151-95
18-6
222
2778-5
150
4543-13
34-69
166-7
189-6
839-54
189-5
760
— 151-6
18-91
- KE
fimn-91
r>ft.QA
1 on-O
— 151-29
19-39
Oil of lemon. ClnH1B.
160
OUlw 21
5513-14
44-86
i tj\j \j
250-7
189-8
191
847-42
872-21
— 151-15
19-74
J 1U ID
Eegnault, P. A. Ill,
165
6053-83
52-89
336-8
191-5
881-40
Carbon monoxide,
— 150-85
19-98
410:—
170
6634-37
55-26
380-0
192-4
893-22
CO.
— 150-38
20-48
o
mm.
175
7256-87
59-58
427-9
193
913-21
Olzewski, O.K. 99, 706 ;
— 150-03
20-80
100
70-0
180
7923-55
68-38
574-1
193-7
919-31
48, 14: —
— 149-63
20-84
115-1
129-1
185
8636-78
77-16
757-5
194-4
939-25
Solidifies —211 (i.v.).
— 149-25
21-6
115-4
129-4
190
9399-02
atst
195-5
964-18
0
mm.
—149-1
21-92
124-8
178-3
76-52
1
195'6
973'15
— 190-0
760
—148-63
22-38
125-0
179-0
101-37
2
196'7
992-05
ats.
—148-25
22-97
137-0
263-4
Ibid., P.A. 111, 408 :—
117-90
3
197
1001-00
— 172-6
4-6
—147-73
23-58
147-4
357-0
o
mm.
130-50
4
197-4
1005-06
— 168-2
6-3
—147-50
24-1
155-5
449-2
0
30-5
141-18
5
197'8
1010-05
— 155-7
14-8
—146-53
25-12
165-1
576-5
5
40-1
150-19
6
198
1021-85
—154-4
16-1
—146-08
26-55
1 *7 A -O
^ _
10
52-1
158-12
7
— 152-0
18-1
174 2i
201-6
1439-7
15
67-1
*
— 150-0
20-4
—145-55
27-42
223-3
236'6
2328-0
3213'5
20
25
85-5
108
Piamsay and Young,
185-0
185-5
765-02
779-08
— 148-8
— 147-7
21-5
23-4
—145-17
—144-47
28-09
29-27
239-7
4374-4
30
135
P.M. [5], 20, 524 :—
185-9
790-04
— 145-3
25-7
—143-87
29-99
35
168
0
mm.
186-3
801-99
c t. 139-5
35-5
1 43'55
30'63
Carbon tetrachlor-
ide, COL..
40
45
50
207
252
305
8
22
31
50
100
150
187-2
188-0
188-8
820-86
835-86
853-66
—143-2
—142-62
—142-1
31-31
32-0
32'97
Ibid, C. R 100, 351 ;
Regnault, M.A.S. 26,
55
368
38
200
190-0
865-56
48, 476 :—
—141-53
33-67
339:
O
*
mm.
60
65
440
522
48-8
57
300
400
190-2
191-0
86976
882-76
begins
mm.
100
—141-26
—141-1
34-42
34-6to35'2
— 20
— 15
9-80
13-55
70
75
616
723
63-3
69
500
600
193-2
195-0
930-86
964-43
s. — 207
complete
b. 100
c.t. —140-2
39-0
i r\
^ O.A *7
73-8
700
-iqe.q
QQl-41
s. —211
— 10
— 5
lo 47
24-83
80
85
844
979
78
800
197-0
tjy L *±j
1009-28
—220-5
4
0
32-95
90
1129
82
900
198-5
1033-30
Carbon dioxide, C02.
+ 5
10
43-19
55-97
95
100
1296
1481
86
100-9
1000
1500
199-0
1044-16
Wroblewski, C.E. 100,
981 ; M.C. 6, 204 ; B.r.
Faraday, P.T. 135, 155;
I., 772 :—
15
71-73
105
1684
112-3
2000
Staedel, B. 15, 2563:—
18, 31 2; 48, 715; 861:
0
ats.
20
90-99
110
1907
130'1
3000
mm.
—79-4
1-14
25
114-30
115
2150
154-9
5000
186-601
£00
0
—201-6
mm.
40
—77-2
1-36
30
142-27
120
2415
192-201
900
—201-5
60
—70-5
2-28
35
175-55
125
2702
Dewar, P.M. [5], 18,
196-797
1000
s.— 199
90 to 100
—63-2
3-60
40
214-81
130
3013
214 ; C.N. 51, 29 :—
200-640
1080
— 198-83
100
—62-0
3-75
45
260-82
135
3349
O
ats.
193-75
112
—59-4
4-60
50
314-38
140
3711
c.t. 282
57-6
— 198-5
120
s.— 57-0
5-33
55
60
376-29
447-43
145
150
4101
4520
Avenarius, P.A. 151,
303 : —
Carbon tetrabrom-
ide, CBr4.
— 1984
— 197-5
140
160
—51-0
—48-8
6-75
7-70
65
528-74
155
4970
Bolas and Groves, 24,
-190-0
735
—455
8-88
70
621-15
160
5454
c.t. 292'5
ats.
1
780:—
ats.
-40-0
11-00
75
725-66
165
5974
(1) From CSj.
—159-7
12-8
-36-6
12-50
80
843-29
170
6535
Hannay and Hogarth,
(2) From brompicrin.
—159-15
13-14
—30-5
15-45
85
975-12
175
7139
P.E. 30, 178 ; C.N. 41,
o
mm.
— 158-2.3
13-47
—26-1
17-80
90
1122-26
180
7792
103:—
101-75
50
— 157-96
13-95
—23-0
19-38
95
1286-86
185
8501
120-5 (I),
-157-43
14-38
—20-0
21-50
100
1467-09
190
9273
0
c.t. 277-9
. 58-i
121 (2)}
100
— 156-78
14-65
— 17-8
22-84
105
1667-19
195
10117
143 (1)-,
— 156-58
14-83
— 15-0
24-70
110
1887-44
143-5 (2)J
228
1 Kf'-*}!
15-19
1 O«O
26-80
!
lOO ol
*• ^
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
725
Carbon dioxide
Carbon dioxide Carbon dioxide
Carbon disulphide
Carbon disulphide
Cyanogen, C2N3.
(continued) : —
(continued) : — (continued) : —
(continued) : —
(continued) : —
Faraday, P.T. 135, 155 ;
o
ats.
Sarrau, C.E.
94, 719 :— Pictet, C.N. 51, 174 :—
Winkelmann, W. 9, 374,
0
mm.
N. Bibl. Univ., 59,
— 9-4
29-10
0
ats. 0
393 ; 38, 692 :—
41
638-7
162 ; ii., 276 :—
— 5-0
33-15
c.t. 32
77 —140 i.v.
0
mm.
42
660-5
r
38-50
— 6-37
95
43
682-9
0
ats.
i
36-00
Dewar, P.M. [5], 18, 212,
214 ; C.N. 51, 174 :— Seelig [18861 •—
+ 8-90
26-38
190
380
44
45
705-9
729-5
m.p. — 34-4
—17-8
12'2
b. I'O
1-25
1"53
o
mm. o ats.
ate.
46
753-75
Mareska and Donny,
—115
25 c. 15 52
46-25
1
47
77R-fi
— 6-7
1-89
i., 772 :—
c.t. 31-9
ats.
77
69-25
2
48
i t O \)
804-1
— 2-8
2-20
o
ats.
34-45
3
0
2-37
—20-0
23-6
O£J*1 ^7
49
830'25
+ 3-6
2-72
—15-0
25-3
Carbon disulphide, CS3.
9b 17
i n^-ftR
•
K
50
857-1
6-9
3-00
lO'O
27-5
The three following series of observations are
1UO OO
114-21
i)
6
8-9
3-17
- 5-0
0
36-0
42
by Eegnault : —
M.A.S. 26,
P.M. [4], 8, P.A. Ill,
121-59
7
Ibid., P.M. [5], 20, 524 ;
10-0
11-1
3-28
3-36
128*25
21 35 ;
+ 6-3
46
339
271
407 ; iii., 94
i •> t .0/1
17-2
4-00
Io4 o4
10-0
52
*
139-97
10
— 18-95
mm.
50
21-1
4-50
15"5
57
O
mm.
mm.
mm.
23-3
4-79
—20
47-30
....
43-5
— 5-3
100
19'0
63
34 '2
6 '50
— 16
58-8
+ 3-5
150
23-5
68
—15
61-64
60-9
Eamsay and Young, 47,
10-2
200
35-0
6-64
27-0
74
—10
79-44
79-0
81-0
653:—
20-2
300
39-4
7-50
30-7
80
o
mm.
— 5
101-29
....
104-4
0
127-9
2775
400
0
127'91
127-3
132-0
1
133-85
33-9
500
Bunsen, P.A. 46, 101 : —
Eegnault, M.A.S. 26,
+ 5
160-01
2
140-05
39-15
600
0
ats.
535 ; J. [1863], 66 :—
10
198-46
199-3
203-0
3
146-45
43-75
700
—20-7
TOO
o
ats.
15
244-13
4
153'1
47-8
800
—20
1-05
—25
17-12
20
298-03
298-2
301-8
5
160'0
51-5
900
— 15
1-45
—20
19-93
25
361-13
g
167'15
55-0
1000
—10
1-85
— 15
23-14
30
434-62
434-6
7
174-6
68-9
1500
— 5
2-30
— 10
26-76
35
519-66
8
182-25
79-3
2000
0
2-7
— 5
30-84
40
617-53
617-5
617-0
q
190'2
95-7
3000
+ 5
3-2
0
35-40
45
729-53
o
10
198-45
118-7
5000
10
3-8
+ 5
40'47
50
857-07
852-7
11
207-0
15
4-4
10
46'05
55
1001-57
12
215-8
20
5-0
15 .
52-17
60
1164-51
1162-6
1163-7
13
224-95
Cagniard de la Tour,
20
58-84
65
1347-52
14
234-4
P.E. 30, 183 :—
Dewar, P.M. [5], 18,
25
66-07
70
1552-09
1549-0
15
244-15
0
ats.
214:—
30
73'84
75
1779-88
16
254-25
c.t. 275
77-8
0
ats.
35
82-17
80
2032-53
2030-5
2033-8
17
264-65
c.t. 124
61-7
40
45
91-03
100-41
85
90
(\K
2311-70
2619-08
2623-1
18
19
275-4
286-55
Hannay and Hogarth,
P.R 30, 183 ; C.N.
Seelig [16
0
86]:—
ate.
95
2966"34
20
298-05
41, 103 :—
c. 15
4
Cailletgt, Arch, de Gen.
100
3325-15
3321-3
3329-5
21
309'9
66, 16 [1878] :—
105
3727-19
22
322-1
c.t. 272-96
77-9
Chloroform, CHC13.
o
—80
—74
ats.
1-00
1-55
110
115
120
4164-06
4637-41
5148-79
4136-3
5121-6
5145-4
23
24
25
334-7
3477
361-1
Dewar, P.M. [5], 18,
214; C.N. 51- 29 :—
Herwig, P.A. 137 and
141 :—
—70
2-08
125
5699-69
26
374-95
7
sts
o
30-4
mm.
243-08
—64
3-10
130
6291-60
6260-6
27
389-2
c.t. 277-7
78-1
39-8
354-77
—60
3'90
135
6925-90
....
6895-0
28
403-9
49-8
514-07
—54
—50
5'46
6-80
136
140
7603-96
7029-2
7556-9
29
30
419-0
434-6
Guthrie, P.M. [5], 18,
Dewar, P.M. [5], 18,
—44
8-72
145
8326-92
31
450-65
512 : —
214; C.N. 51, 29:—
—40
10-25
150
9095-94
32
467-15
«
mm.
ftK-t ,f*
0
ats.
— 34
10-70
13'8
ZOl O
. OfJQ
33
484-15
16'0
264-8
"~*"
Herwig, P.A. 137 and 141 ; vi.,
fiftO «
34
501-65
19-02
284-5
Guthrie, P.M. [5], 18,
Andrews, C.N. 4, 158 ;
o
mm. o mm.
35
519-65
511 :—
P.T. 159, 575; P.M.
[4], 39, 150 ; P.A. Erg.
8-5
14-2
183-09 35-9 531-59
234-45 40'0 614'45
36
37
538-15
557-15
Coleman, C.N. 51, 174 :—
13-8
mm.
158-4
20*1
5,64; J. [18611. 40:—
294-12 50-0 856-50
38
576-75
Solidifies —116
16-0
169-2
o
32-0
ats.
461-54
39
696-85
19-02
190-7
c.t. 30-92
77
40
617-5
726
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Chloroform (continued) : —
Methylchlorlde,
Ethyl chloride (cont.) : —
2hlorbenzene(cont.) : —
Chlorbenzene (cont.) : —
Regnault gives the following results : (1) by
ebullition ; (2) by tension : —
M.A.S. 26. P.M. F41, 8, P.A. Ill,
CH3C1.
Regnault, M.A.S. 26,
535 : —
o
70
75
mm.
4405-03
4982-72
o
18-1
22-6
mm.
5
7-5
101
102
mm.
302-5
312-5
339.
' 271.
407; iii., 94.
80
5614-11
26-3
10
103
322-3
o
ats.
85
6301-61
29'7
12'5
104
333-35
30
0762
mm.
mm.
mm.
90
7047-51
32'6
15
105
344-15
+ 10
20
160-47
130-4 (2)
190-2 (2)
0
160-5
—20
— 10
0
1-16
1-72
2-49
95
100
7853-92
8722-76
35-6
37-2
17-5
20
106
107
1 AQ
355-25
366-65
070-0
25
30
200-18
247-51
276-1 (2)
+ 10
20
3-51
4-83
Sajotschewski, W.B. 3,
741:—
391
41-0
KO.O
22-5
25
KA
lUo
109
109-8
o to o
390-25
400-0
35
303-49
30
6-50
52 3
50
36
....
r 342-2 (2)
L 313-4(1)
35
7-49
O
110
ats.
14-81
59-0
129-0
75
760
110
111
402-55
415-1
A O*7 «flK
40
369-26
364-0 (1)
366-2
Vincent and Chappuis,
130
20-92
112
113
427 95
441-15
45
50
446-01
535-05
524-3 (1)
C.R. 100, 1218; 101,
428; 48, 861, 1105:—
140
150
25-27
30-22
Ramsay and Young, 47,
646, 654; P.M. [5],
114
115
454-65
468-5
55
637-71
160
35-85
20, 524 ; 21, 39 :—
116
482-65
60
755-44
738-0 (1)
751-0
o
—23-7
ais.
1
170
42-00
o
*
mm.
117
497-2
70
889-72
1042-11
976-2 (1)
+35
40
7-5
8-75
c.t. 182-6
52-60
25-0
30
11-4
14-95
117-2
118
500-0
512-05
75
1214-20
50
11-2
Vincent and Chappuis,
35
19-45
119
527-25
80
1407-64
1367-8 (1)
1404-6
60
14-3
C.R. 101, 428; 48,
40
25-1
120
542-8
85
1624-10
70
17-87
1105:—
45
32-1
121
5587
90
1865-22
1811-5 (1)
80
22-15
0
ats.
50
40-75
122
575-05
95
2132-85
90
27-65
— 12-5
1
55
51-35
123
591-7
100
2428-54
2354-6 (1)
2426-5
100
33-90
c.t. 182-5
54
60
64-2
123-5
600-0
105
27
54-03
110
41-0
65
79-6
124
608-75
110
3110-99
3020-4 (1)
120
49-8
Ramsay and Young,
70
97-9
125
626-15
115
120
3501-03
3925-74
3818-0 (1)
3916-2
130
135
61-0
65-0
P.M. [5], 20, 524 ; 21,
38:—
70-5
71
100-0
101-95
126
127
643-95
662-15
125
4386-60
140
70-6
O
mm.
72
106-1
128
680-75
130
4885-10
4721-0(1)
141
72-0
—24-3
150
73
110-41
129
699-65
135
5422-53
c.t. 141-5
73-0
—18-7
200
74
114-85
129-0
700-0
140
6000-16
....
5965-8
—10-1
300
75
119-45
130
718-95
145
6619-20
3 "6
400
76
124-2
131
738-65
- ...
150
155
7280-62
7985-35
....
7226-5
Ethyl chloride,
+ 1-9
6-3
500
600
77
78
129-1
134-15
132
135
758-8
822-0
160
8734-20
vjHjwl.
10-3
700
165
9527-82
Drion, A. C. [3], 56, 33:—
14-0
800
80
144-8
0
ats.
17-1
900
80-9
150
"Winkelmann, W. 9,
369:—
Ramsay and Young,
P.M. [5], 20, 517,
c.t. 170 s
Regnault, M.A.S. 26,
20-0
32-0
1000
1500
OAAA
81
82
150-3
156-05
Benzylchloride,
Ph.CH3Cl.
o
mm.
524:—
339; P.A. Ill, 408:—
55'5
4\J\J\J
3000
83
161-95
Kahlbaum, B. 17, 1261;
23-79
190
o mm.
84
168-0
40-67
380
25-0 200
o
—20
mm.
187-55
75-1
5000
85
174-25
18, 2107: —
ats.
34-7 300
239-60
86
181-7
,1 Q.O
mm.
—15
60-18
82-59
97-55
109-04
118-56
1
2
3
4
5
42-0 400
48-0 500
53-2 600
57-9 700
61-0 760
— 10
— 5
0
+ 5
10
302-09
376-72
465-18
569-32
691-11
Propyl chloride,
Pr-Cl.
Vincent and Chappuis,
C.R. 103, 379 ; B.r. 19,
700 .
87
88
88-8
89
90
187-3
194-1
200-0
201-15
208-35
4o o
58-7
63-5
66-1
68-8
n-0
•
5
7-5
10
12-5
1 ^
126-78
134-08
140-66
146-70
6
7
8
9
1 A
61-8 800
65-3 900
68-7 1000
82-1 1500
15
20
25
30
832-56
996-23
1184-17
1398-99
/ oo . —
o
57-5
c.t. 221
ats.
1
49
91
92
93
94
215-8
223-45
231-3
239-35
O
73-8
76-1
783
80-5
LO
17-5
20
225
25
152'34
10
^uuo
35
1643-24
95
247-7
108-3 3000
40
1919-58
Chlorbenzene,
96
256-2
121-0 4000
131-2 5000
45
50
2230-71
2579-40
C6H6C1.
Kahlbaum, B. 17, 1261
97
98
265-0
274-0
102-8
179-0
75
760
140'0 6000
55
2968-43
18, 2107, 3149 :—
99
283-25
148-0 7000
60
3400-54
mm
100
29275
155-0 8000
65
3878-52
6-8
0
100-7
300-0
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
727
p-Chlortoluene,
Ethylenebromide
Ethyl bromide,
Ethyl bromide (cont.) : —
Brombenzene (cont.) : —
Brombenzeue (cont.) :—
C6H4MeCl.
Kahlbaum, B. 17, 1261 ;
(continu<
0
sd):-
mm.
C2H6Br.
Reguault, M.A.S. 26,
o
125
mm.
7339
o
58-1
mm.
22-5
o
148
mm.
61575
25
13-51
130
8101
60-1
25
149
632-25
18, 2107 : —
339: —
30
17-20
135
8919
70-7
50
150
649-05
0
28-1
mm.
0
35
21-80
o
—20
mm.
59-16
140
9794
77-3
75
151
666-25
40-3
5
40
27-49
—15
78-09
156-0
760
152
683-8
45-1
48-9
52-1
54-9
7-5
10
12-5
15
45
50
55
60
34-47
42-99
53-31
65-75
101-54
130-58
165-57
207-21
EEerwig, P.A.
vi., 68;
25
37 and 141;
!:—
mm.
474-8
152-9
153
154
155
700-0
701-65
719-95
738-55
—10
— 5
0
+ 5
Ramsay and Young, 47,
•647,655; P.M. [5], 20,
524 ; 21, 39 :—
57-7
17-5
65
80-64
10
257-40
35
689-5
*
156
757-55
59-6
20
70
98-36
15
316-92
43
904-0
0
mm.
157
776-95
617
22-5
75
119-34
20
387-03
45
12-4
158
7967
637
77-7
84-9
25
50
75
80
85
90
144-02
172-92
206-58
25
30
35
469-07
564-51
674-92
Ramsay and Young,
P.M. [5], 20, 524 ; 21,
OD
50
55
60
16-0
20-5
26-1
158-2
159
160
800-0
816-9
837-45
161-5
760
95
inn
245-51
OQrvjQ
40
801-92
3o :-
65
tjf\
33-0
i\j\j
£t\t\J tO
45
947-28
i)o.r»
mm.
e/\
70
41 "4
Bromoform,
105
110
342-11
401-08
50
55
1112-79
1300-35
— ZG 0
—10-2
oO
100
74-0
75
50-0
51-6
P-Bromtoluene,
CHBr3.
115
468-13
60
1511'92
— 2'0
150
80
63-9
C6H4MeBr.
Kahlbaum,B. 17,1259;
120
544-06
65
1749-47
+ 4'0
200
85
V8-6
Kahlbaum, B. 17, 1261 ;
18, 2107 :—
125
629-66
70
2015-06
13'8
300
90
96-0
18, 2107 :—
|
25-7
mm.
0
130
135
725-77
833-26
75
80
2310-73
2638-57
20'9
26-8
400
500
91-3
95
100-0
116-4
44-4
mm.
0
34-2
37-8
40'9
5
7-5
10
140
145
150
953-00
1085-89
1232-83
85
90
95
3000-63
3398-95
3835-53
31P7
36-0
40-0
600
700
800
100
101-9
105
140-1
150-0
167-4
55-4
59-6
63-4
5
7-5
10-0
43'5
45-8
48-1
50-2
52-3
54-3
12-5
15-0
17-5
20
22-5
25
155
160
165
170
175
180
1394-73
1572-49
1766-99
1979-14
2209-77
2459-73
100
105
110
115
120
125
4312-32
4831-22
5394-01
6002-41
6658-00
7362-25
43'3
46-6
59-8
69-7
85-0
106-3
900
1000
1500
2000
3000
5000
110
110-2
115
120
121
122
1987
200-0
234-4
274-9
283-65
292-6
66-7
69-8
72-6
75-2
77-4
79-6
12-5
15
17-5
20
22-5
25
66-0
50
185
2729-84
130
8116-49
122-8
300-0
95-7
50
73-4
150-0
75
760
190
3020-83
135
140
8921-92
9779-56
Isoamyl bromide,
CjH^Br.
123
124
•toe
30175
311-15
OOfVQ
104-4
183-0
75
760
1ZO
OZU O
Tribromethane,
Kahlbaum, B. 17, 1260:—
Ibid., P.A. 111, 408,
5-0
mm.
0
126
127
330-7
340-8
CHBr2.CH2Br.
0
inm.
409:—
12-4
5
128
351-15
Carnelley, not yet pub-
Anschutz, A. 221, 133 ;
9-7
0
O
mm.
17'6
10
129
361-8
lished : — (para-)
B. 16, 2918 :—
19'0
5
+ 20
380
22'4
15
130
372-65
mm.
26-0
10
25
463
27-0
20
131
383-75
0
mm.
73
11-5
31-4
15
30
560
30-6
25
132
395-1
80
28-9
83
18
36-1
20
35
671
43-5
50
132-4
400-0
90
42-0
187
751
39-3
25
40
799
50-8
75
133
406-7
100
60-6
58-2
75
45
946
118-6
760
134
418-6
110
85-9
129-0
760
50
1112
135
430-75
120
120-1
Ethylenebromide,
55
1299
136
443-2
130
165-8
CjjHjBro.
60
1511
Brombenzene,
137
455-9
140
226
Regnault, M.A.S. 26,
65
1747
C8H6Br.
138
468-9
150
304
339:—
Ramsay and Young,
70
2011
Kahlbaum, B. 17, 1261 ;
139
482-2
160
406
o
*
mm.
P.T. [1884] 470:—
75
2305
18,2107,3149:—
140
495-3
170
535
—20
1-73
0
mm.
80
2630
HI HI
140-3
500-0
180
698
— 15
2-03
—1-9 s.
1-35
85
2989
15-8
0
141
509-7
190
901
— 10
2-48
—1-91.
1-25
90
3384
29-8
5
142
523-9
200
1152
— 5
3-09
-17 1.
1-35
95
3817
36-3
7-5
143
538-4
210
1459
0
3-92
ats.
100
4290
41-5
10
144
553-2
220
1831
+ 5
5-01
130—132
1
105
4806
45-7
12-5
145
568-35
230
2278
10
6-42
Sample not quite pure.
110
5267
49-6
15
146
583-85
15
8'25
115
5974
52'8
17-5
J 599-65
20
10-57
120
6631
55-7
20
1- 600-0
728
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Bromnaphthalene,
Bromnaphthalene
Ethyl iodide (cont.) : —
Formic acid, CH20
Formic acid (cont.) : —
Methyl alcohol (cont.) : —
C10H7Br.
(continued) :—
Eamsay and Young
Landolt, As. 6, 129 :—
o
mm.
o mm.
1U /
Ramsay and Young, 47,
653, 656 ; P.M. [5],
249
mm.
377-3
P.M. [5], 2
0, 524 :—
mm.
10
mm.
18-4
30-7
37-7
50
75
75 1032-14
80 ' 1238-47
20, 524 ; 21. 40 :—
250
386-35
18-0
100
15
24-1
105-3
760
85 1470-92
251
395-6
27-0
150
20
31-4
90 1741-67
•
i in
mm.
3'6
251-5
400-0
34-0
200
25
40-4
95
2051-71
j. i.\j
115
4-4
252
405-05
44-7
300
30
51-6
Eichardson,
40, 765 :—
100
2405-15
120
5-45
253
414-65
52-7
400
35
65-4
0
5-7
mm.
13-46
105
2806-27
125
6-8
254
424-45
59-2
500
40
82-3
6-1
14-60
110
3259-60
130
8-5
255
434-45
45
102-7
7-2
13-46
115
3769-80
135
10-6
256
444-65
50
127-2
10'2
17-44
120
434177
140
13-15
257
455-0
Propyl iodide, Pral
55
156-5
13-2
20-93
125
4980-55
145
16-2
258
465-6
Brown, P. E. 26, 244,
60
191-2
18-5
28-66
130
5691-30
150
19-8
259
476-35
247 ; 32, 837 :—
65
232-1
21-7
32-94
135
6479-32
155
24-0
260
487-35
o
mm.
70
280-0
227
34-59
140
7337-10
160
28-85
261
498-55
53-06
138-6
75
335-6
29-7
48-08
145
8308-87
165
34-4
261-1
500-0
53-17
139-8*
80
399-8
31-0
50-00
150
9361-35
170
40-75
262
509-9
53-26
139-6
85
473-7
35-7
65-02
175
48-05
263
521-5
56-17
157-9*
90
558-0
39-1
73-26
Eamsay and Young,
180
56-45
264
533-35
61-80
195-9
95
653-8
44-3
84-82
P.M. [5], 20, 524 ; 21,
185
66-1
265
545-35
62-37
200-0
100
762-0
44-45
82-97
37:—
190
77-15
266
557-6
62-70
203-0*
46-2
99-165
0
mm.
195
89-75
267
570-05
70-45
269-6
46-9
100
— 14-0
10
200
104-05
268
582-7
73-51
300-0
Kahlbaum, B. 16, 2480
56-1
150
+ 10-0
50
205
120-2
269
595-6
79-11
365-3
17, 1259, 1267; 18
63-1
200
22-0
100
210
138-4
269-3
600-0
81-95
400-0
3147 :—
69-0
250
30-0
150
212-9
150-0
270
608-75
84-15
431-3*
0
mm.
74-1
300
35-9
200
215
158-85
271
622-1
88-84
500-0
11-3
0
78-8
350
44-6
300
216
163-25
272
635-7
90-05
520-0
13'8
5
82-8
400
51-0
400
217
167-7
273
649-5
94-70
600-0
15'8
10
86-5
450
56-3
500
218
172-3
274
663-55
96-81
640-4
17'9
15
89-5
500
60-9
600
219
176-95
275
677-85
99-83
700-0
19-9
20
92-0
550
64-8
700
220
181-75
276
692-4
100-21
707-1
20-3; 26
22-0
94-5
600
68-1
800
221
186-65
276-5
760-0
100-45
712-7*
21'8
24'84
967
650
71-1
900
222
191-65
277
707-15
101-37
732-1
22-0
25-0
98 "9
700
701 (?)
1000
223
196-75
. 278
722-15
102-63
760-0
22-6
27-66
101-0
750
85-9
1500
223-6
224
200-0
202-0
279
280
737-45
752-98
• Pt. foil in liquid.
23'7
24-6
30-0
32-58
1017
762-52
94-1
107-1
2000
3000
225
207-35
281
768-70
25-6
35-0
125-1
5000
226
227
OOQ
212-8
218-4
OO/l •! K.
282-9
285
800
834-35
Isopropyl iodide,
Pi-PL Ibid. :—
27-3
27-9
29-1
40-0
41-40
45-0
Methyl alcohol,
CH40.
Eichardson, 49, 762,
iZO
229
-_ 1 15
230-0
O
48-90
mm.
187-9
30-5
307
49-66
50"0
Eegnault, M.A.S. 26,
339 ; P.A. Ill, 408 :—
775:
0
mm.
230
231
235-95
242-05
Ethyl iodide, C3H6I.
50-50
54-43
200-0
232-6
32-2
55-0
—20
mm.
6-27
— 10-1
— 8'3
15-05
17'3
232
248-3
Eegnault, M.A.S. 26,
55-93
245-9
337
60-0
—15
9-29
— 7-3
18-76
233
254-65
339; P.A. Ill, 409:—
61-33
300-0
35'1
65-0
—10
13-47
— 6-3
19-26
36*2
70'0
234
235
236
261-2
267-85
274-65
O
0
+ 5
mm.
41-95
54-14
62-40
69-63
69-70
311-2
399-7
400-0
37-6
37-7
74-54
75
— 5
0
+ 5
19-17
26-82
36-89
— 5-3
— 4-8
— 3-3
21-24 (?)
20-54 (?)
24-33
237
281-6
10
69-20
72-3
437-4
383
80
10
50-13
— 2-3
25-23
238
288-7
15
87-64
74-71
472-8
39-2
85
15
67-11
— 17
26'92
239
295-95
20
110-02
76-44
500-0
40-2
90
20
88-67
+ 0-2
28'67
239-5
300-0
25
136-95
78-13
530-6
41-1
95
25
115-99
0-7
32-06
240
303-35
30
169-07
80-52
570-6
42-0
100
30
149-99
2-2
35-15
241
242
243
310-9
318-65
326-5
35
40
45
Kfi
207-09
251-73
303-77
•)f* 4 ,f\
82-11
83-79
87-13
600-0
631-9
700-0
100-6
760-0
35
40
45
192-01
243-51
306-13
4-2
4-7
6-25
38-30 (?)
36-89 (?)
43-88
Schall, B. 17, 2568 :—
244
334-55
*JU
ou-4 U
87-64
709-9
50
381-68
7-7
48-87
245
342-75
55
433-21
8966
754-8
15-8
uuu .
10
55
472-20
8-5
48-97
246
351-1
60
512-25
89-86
• 760-0
17-9
15
60
579-93
9-0
50-00
247
359-65
19-9
20
65
707-33
11-2
55-82
248
368-4
22-0
25
70
857-10
12-2
58-48
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
729
Methyl alcohol (cont.): —
Acetic acid (cont.) : —
Acetic acid (cont.) : —
Acetic acid (cont.) : —
Acetic acid (cont.) : —
Acetic acid (cont.) : —
0
mm.
0
mm.
Solid acid : —
0
mm.
0
mm.
o
mm.
21-8
100
—5-11
3-35
o
mm.
60
107-3
4-70
4-75
68-5
127-5
29-0
150
—2-40
3-90
0
3-23
70
155-2
6-01
5-OOt
69-1
131-9
35-9
200
—0-69
4-27
3-57
4-06
80
232-9
7-06
5-25
70-0
137'lt
40-5
250
+ 1-36
5-23
6-92
5-08
90
346-7
7-13
5-40
71-6
146-3
44-4
300
1-53
4-83
9-96
6-28
100
473-0
8-56
5-95
72-4
150'Ot
479
51-0
350
400
3-09
3-81
5-27
5-99
11-49
12-43
6-97
7-48
cf. Kahlbaum,B. 18,3148.
9-14
9-70
6'OOt
6-20
73-2
76-4
156-2
177-3
54-0
450
5-52
5-97
13-14
7-86
10-00
6'34t
78-8
194-4
56-5
500
7-21
6-64
Ramsay and Young, 47,
10-60
6-50
79-8
199-5
58-5
60-5
550
600
8-19
9-09
7-01
7-81
Landolt, As. 6, 129 :—
44; 49,805; P.T.[1884],
464 ; [1886], 112 ; B.r.
10-70
11-64
6-75
7'OOt
79-9
80-0
200'Ot
202-lt
62-4
650
10-91
8-12
O
0
mm.
7'6
18, 136; B. 19, 71;
12-30
7-30
81-65
215-2
64-1
700
10-95
8-48
5
9'6
P.M. [5], 21, 45; cf.
13-91
8-OOt
83-4
228-0
65-9
750
13-13
9-29
10
• ' V
12-1
Kahlbaum, 19, 2863.
13-70
8-10
83-9
236-3
14-74
10-23
i K
i R*I
0 ... . .
14-20
8-30
84-6
242-1
15-92
10-87
10
ID 1
feoliu acid : —
14-39
8-45
87-5
267-8
Methylic formate,
18-23
12-34
20
25
18'9
23'5
„
*
mm.
14-72
8-50
90-0
292-8t
C2H402.
30
29-1
—5-68
1-3
14-90
8-55
90-75
300'Ot
Schumann, W. 12, 46;
Solid acid : —
35
35-9
—0-60
1-95
15-88
9'OOt
91-4
307-9
B., 14, 1273 :—
40
44-1
—o-ii
2'OOt
15-50
9-10
94-5
344-3
0
mm.
—7-55
3-25
+ 1-85
2-35
15-60
9-15
97-4
376-4
—23-9
54
—5-83
3-56
45
54'0
2-86
2-80
15-70
9-35
98-6
396-3
—23-3
58
—4-24
3-93
50
66 '0
4-10
3'OOt
16-75
10-45
98-9
400-Ot
—15-6
91
—2-56
4-26
55
80"3
5-32
3-30
17-00
9-75
100-0
416'5t
— 6-5
143
—0-82
4-71
60
OK.
97'4
6-30
3-70
17-60
io-oot
100-6
425-2
— 2-3
169
0
4-89
DO
117'8
6-41
3-75
18-60
11-10
103-3
460-3
o-o
192
70
142'0
6-68
3-85
19-20
11-05
105-15
500'Ot
+ 0-4
197
0
378
75
170-6
7-14
4-OOt
20-00
n-sot
105-45
501-8
0-7
200
1-23
4-02
80
204'3
7-20
4-05
20-10
12-00
107-45
540-0
5-1
244
3-51
4-59
85
244
8-40
4-25
20-90
12-45
110-0
582-6t
8-9
289
5-52
5-18
90
290'6
8-50
4-35
21-40
12-65
110-4
587-1
13-1
352
95
345'2
8-72
4-60
21-68
12-85
111-0
600'Ot
18-4
437
Liquid acid : —
100
4085
9-16
4-70
22-05
13-05
112-4
623'*
20-2
474
—5-38
3-21
105
110
482 '5
567-8
9-60
5-OOt
22-4
12-90
113-4
642-6
21 "4
23-6
501
548
+ 3-03
5-35
4-96
5-59
115
120
667-0
781-1
10-40
11-39
5-30
5-75
23-0
23-4
13-65
13-80
1141
116-45
657-5
700'Ot
257
31-0
32-3
34-7
38-2
592
730
760
837
950
7-01
7-40
8-61
10-33
6-06
6-22
6-57
7-28
125
130
135
140
912-3
1062-8
1234-9
1431-3
11-67
11-70
12-15
12-60
13-30
6-OOt
6-15
6-05
6-65
6'75
25-6
27-2
27-3
30-0
31 "3
15-95
16-80
17-45
19-9
21'8
117-15
120-0
130-0
140-0
717-9
794-Ot
1040-Ot
1381 -Ot
40-9
1043
11-09
12-24
7-52
8-03
cf. Horstmann, B. 3, 80 ;
13-37
7'OOt
32-7
22-9
Richardson, 49, 765,
43'2
1133
12-25
8-05
11, 1292 :—
13-96
7-30
36-1
28-3
776:—
45'6
1236
15-18
9-39
14-30
7-20
36-9
28-9
0
mm.
47'1
47-9
49-8
1300
1327
1414
18-79
21-57
11-37
13-26
Bineau, quoted by
Ramsay, 47, 45 : —
14-58
14-80
15-15
7-95
8-OOt
8-40
40-0
40-1
43'8
34 -Ot
34-3
41-7
2-72
5-59
6-11
4-0
4-9
5-0
1-32
3-96
o
15
mm.
77
15-40
8-75
48-0
50-Ot
6-87
5-1
Acetic acid, CaH4O3.
3-54
5-77
4-50
5-14
22
QO
14-5
15-60
15-80
8-55
8-85
48-2
48-5
51-3
51-7
7-06
7-62
5-25
5-50
Regnault, M.A.S. 26,51 ;
7-04
5-61
BB
30
16-09
8-95
49-2
53-7
8-27
5-90
P.M. [4], 9, 23.
7-09
5-53
Naumami, A. 155, 325 :—
16-08
9-OOt
49-65
55-6
9-70
6-20
Liquid acid : —
7-17
5-57
0
mm.
i w^
16-20
9-10
50-0
56'2t
10-60
6-50
8-07
5-79
1OO
16-32
9-15
50-5
58-1
10-7
6-75
°
mm.
f\*f71
4-36
5-63
9 71
6'42
16"41
9-45
53-5
66'7
14-72
8P5
6-55
6'37
12-12
7-33
Wiillner,P.A. 103,529:—
57-4
78-7
15-5
9-1
7-62
6-83
14-33
8-42
0
mm.
Liquid acid : —
*
59-6
87-6
17-0
9-75
10-09
7-80
14-87
8-59
14
157
0
3'5t
60-0
88-3t
20-1
12-0
14-43
10-02
17-23
9-85
20
19-0
2-72
4-0
61-8
96-3
25-6
15-95
17-09
11-61
19-84
11-46
30
30-5
4-20
4-25
62-9
100-Ot
31-3
21-8
19-91
13-56
22-37
13-15
40
45-5
9S-3S
i R-afi
KO
79
+ OVitainfifl bv internolation.
5 A
730
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Acetic acid (cont.) : —
Ethyl alcohol (cont.) : —
Ethyl alcohol (cont.) :—
Ethyl alcohol (cont.) : —
Ethyl alcohol (cont.) : —
Ethyl alcohol (cont.): —
o
mm.
o
mm.
0
mm.
o
mm.
0
mm.
o
mm.
36-1
28-3
40
133-69
140
5637-7
5-0
17-70
11-2
25-91
17-4
37-68
1
40-1
34-3
45
172-18
150
7257-8
•1
17-80
•3
26-07
•5
37-91
481
50-0
50
219-90
152
7617-3
•2
17-93
•4
26-23
•6
38-14
.Q _
M-7
KK
97Q. KQ
~
18 '04
•5
26'39
"7
38 "36
57-4
1
78-7
HO
60
— * • >. /
350-21
Vap. tension of absolute
•4
18-16
•6
26-55
•8
38-59
59-6
87-6
65
436-90
alcohol calculated from
•5
18-27
•7
26-71
•9
38-82
62-5
100-0
70
541-15
Eegnault's measure-
•6
18-38
•8
26-87
18-0
39-05
68-5
127-5
75
665-54
ments (M. A.S. 26, 349,
•7
18-50
•9
27-03
•1
39-29
69-1
131-9
80
812-91
see above) by Bunsen,
•8
18-61
12-0
27-19
•2
39-53
72-3
150-0
85
986-40
Gasomet. Meth. Tab.
•9
18-73
•1
27-36
•3
39-77
73-2
156-2
90
1189-30
3.:—
6-0
18-84
•2
27-53
•4
40-01
79-5
200-0
95
1425-13
0
mm.
•1
18-96
•3
27-70
•5
40-25
81-65
215-2
100
1697-55
o-o
12-73
•2
19-08
•4
27-87
•6
40-49
85-5
250-0
105
2010-38
•1
12-82
•3
19-20
•5
28-04
•7
40-73
90-7
300-0
110
2367-64
•2
12-91
•4
19-32
•6
28-21
•8
40-97
91-4
307-9
115
2773-40
•3
13-01
•5
19-44
•7
28-38
•9
41-21
95-1
350-0
120
3231-73
•4
13-10
•6
19-56
•8
28-55
19-0
41-45
98-9
400-0
125
3746-88
•5
13-19
•7
19-68
•9
28-72
•1
41-71
100-6
425-0
130
4323-00
•6
13-28
•8
19-80
13-0
28-89
•2
41-96
102-2
450-0
135
4964-22
•7
13-37
•9
19-92
•1
29-07
•3
42-22
105-4
500-0
140
5674-59
•8
13-46
7-0
20-04
•2
29-25
•4
42-47
105-45
501-8
145
6458-10
•9
13-56
•1
20-17
•3
29-43
•5
42-73
108-3
550-0
150
7318-40
1-0
13-65
•2
20-30
•4
29-61
•6
42-98
110-4
587-1
155
8259-19
•1
13-74
•3
20-43
•5
29-79
•7
43-24
111-2
600-0
•2
13-84
•4
20-55
•6
29-97
•8
43-49
113-8
650-0
Jbid.,C.R. 50, 1067 ; P.A.
•3
13-93
•5
20-68
•7
30-15
•9
43-75
Ill, 407 ; iii. 94 :
114-1
657-5
o mm.
•4
14-03
•6
20-81
•8
30-33
20-0
44-00
116-5
700-0
0
12-83
•5
14-12
•7
20-93
•9
30-51
•1
44-27
117-15
717-9
10
24-30
•6
14-22
•8
21-06
14-0
30-69
•2
44-54
119-0
750-0
20
44-48
•7
14-31
•9
21-19
•1
30-88
•3
44-81
30
78-49
•8
14-41
8-0
21-31
•2
31-07
•4
45-08
Dimethyl oxide,
40
50
133-64
219-88
•9
2-0
14-50
14-60
•1
•2
21-45
21-58
•3
•4
31-26
31-45
•5
•6
45-35
45-61
C2H60.
60
350-26
•1
14-70
•3
21-72
•5
31-64
•7
45-88
Eegnault, M.A.S. 26,
70
541-21
•2
14-79
•4
21-85
•6
31-84
•8
46-15
535:—
80
812-76
•3
14-89
•5
21-99
•7
32-03
•9
46-42
o
ats.
90
1188-43
•4
14-99
•6
22-12
•8
32-22
21-0
46-69
— 30
'759
100
1694-92
•5
15-09
•7
22-25
•9
32-41
•1
46-98
— 20
1*16
110
2361-63
• 6
15-19
•8
22-39
15-0
32-60
•2
47-26
— 10
1*72
o
2'47
120
3219-68
•7
15-29
•9
22-52
•1
32-80
•3
47-55
130
4301-04
•8
15-39
9-0
22-66
•2
33-01
•4
47-83
4-10
3"40
i ***
20
4-72
140
5637-00
•9
15-49
•1
22-80
•3
33-21
•5
48-12
150
7258-73
3-0
15-59
•2
22-94
•4
33-41
•6
48-40
30
6*29
Ibid., P.M. [4], 8, 271 :—
o mm.
•1
•2
15-69
15-79
•3
•4
23-08
23-23
•5
•6
33-61
33-82
•7
•8
48-69
48-97
Ethyl alcohol,
—21
3-12
•3
15-90
•5
23-37
•7
34-02
•9
49-26
C2H60.
—20
3-34
•4
16-00
•6
23-51
•8
34-22
22-0
49-54
Eegnault, M.A.S. 26,
—10
6-50
•5
16-10
•7
23-65
•9
34-42
•1
49-84
339:—
0
12-73
•6
16-21
•8
23-79
16-0
34-62
•2
50-14
o mm.
+ 10
24-08
•7
16-31
•9
23-94
•1
34-84
•3
50-44
—20
3-34
20
44-0
•8
16-41
10-0
24-08
•2
35-05
•4
50-74
—15
5-10
30
78-4
•9
16-52
•1
24-23
•3
35-27
•5
51-04
—10
6-47
40
134-1
4-0
16-62
•2
24-38
•4
35-48
•6
51-34
— 5
9-09
50
220-3
•1
16-73
•3
24-53
•5
35-70
•7
51-64
0
12-70
60
350-0
•2
16-84
•4
24-68
•6
35-91
•8
51-94
+ 5
17-62
70
539-2
•3
16-95
•5
24-83
•7
36-13
•9
52-24
10
24-23
80
812-8
•4
17-05
•6
24-99
•8
36-34
23-0
52-54
15
32-98
90
1190-4
•5
17-16
•7
25-14
•9
36-56
•1
52-8ft
20
44-46
100
1685-0
•6
17-27
•8
25-29
17-0
36-77
•2
53-17
25
59-37
110
2351-8
•7
17-38
•9
25-44
•1
37-00
•3
53-49
30
78-52
120
3207-8
•8
17-48
11-0
25-59
•2
37-23
•4
53-81
35
102-91
130
4331-2
•9
17-59
•1
25-75
•3
37-45
•5
54-12:
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
731
Ethyl alcohol (cont.):—
Ethyl alcohol (cout.) : —
Ethyl alcohol (cont.) : —
Ethyl alcohol (cont.) :—
Ethyl alcohol (cont.) : —
Acetone, CO(CH3)2.
o
mm.
0
mm.
0
mm.
o
mm.
o
mm.
Regnault, M.A.S. 26,
23-6
54-44
29-8
77-55
5-43
17-75
52
242-05
27-3
71-11
339 ; P. A. Ill, 408 :—
•7
54-75
•9
77-98
6-55
18-85
53
253-8
29-6
80-61
o
mm.
•8
55-07
30-0
78-41
7-65
20-15
54
265-9
30-7
82-86
20
197-63
•9
55-38
9-15
22-15
55
278-6
34-0
100
25
226-27
24-0
•1
55-70
56-04
Herwig, P. A. 137 and 141 ;
vi., 682. Contained a
10-72
12-39
24-90
27-60
56
56-8
291-85
300
32-8
34-8
95-1
104-81
30
35
281-00
345-15
•2
56-37
trace of water : —
14-09
30-60
57
305-65
35-3
107-22
40
420-15
•3
56-70
o
mm.
15-87
34-00
58
319-95
36-6
114-59
45
507-52
•4
57-03
23
50-23
16-69
35-90
59
334-85
37-3
119-97
50
602-86
•5
57-37
30-5
77-58
17-65
37-90
60
350-3
40-1
138-41
55
725-95
•6
57-70
36-4
108-0
18-55
40-00
61
366-4
41-8
150
60
860-48
•7
58-03
41-9
144-7
19-96
43-95
62
383-1
42-2
155-59
65
1014-32
•8
58-36
47-8
196-5
20-86
46-55
63
400
43-1
162-96
70
1189-38
•9
58-70
57-8
315-8
22-55
51-45
64
418-35
43-8
165-41
75
1387-62
25-0
59-03
62-9
396-83
23-43
53-95
65
437
46-5
189-56
80
1611-05
•1
59-38
69-9
537-63
24-46
57-60
66
456-35
47-2
199-18
85
1861-81
•2
5973
25-37
60-50
67
476-45
47-4
200
90
2141-66
•3
60-08
26-46
64-70
68
497-25
49-6
222-87
95
2452-81
•4
60-43
Kahlbaum,B. 16, 2480;
27-25
67-60
68-1
500
50-05
226-99
100
2797-27
•5
60-78
17, 1259; 18, 2856:—
28-03
69-90
69
518-85
52-1
250
105
3177-00
•6
61-13
0
—4-5
mm.
0
29-36
75-75
70
541-2
52-8
257-52
110
3593-96
•7
61-48
+ 1-5
5
32-60
90-6
71
564-35
53-7
269-83
115
4050-02
•8
61-83
6'5
10
72
588-35
55-5
258-49
120
4546-86
•9
62-18
9'5
15
0
12-24
72-45
600
56-0
300
125
5086-25
26-0
62-53
12-4
20
10
23-77
73
613-2
57-3
320-87
130
5669-72
•1
62-90
12-8
20-5
20
44-00
74
638-95
59-8
349-02
135
6298-68
•2
63-27
14-4
25
30
f\f\
78-06
1 I Q A ,Q
75
665-55
59-5
350
140
6974-43
•3
•4
63-64
64-01
17-4
21'0
30-86
41-32
yu
110
1 1 !M •>
2356
76
76-1
693-1
700
61-0
62-5
370'12
400
Winkelmann, W. 9, 366;
•5
64-37
23-5
50
130
4320
77
721-55
65-5
450
38, 692 : —
•6
64-74
24-4
54-86
140
5666
78
751-0
65-8
451-48
0
21-17
ats.
i
•7
65-11
24-8
56-86
150
7326
79
781-45
68-3
500
37-32
4
i
•8
65-48
26-2
61-96
160
9366
79-65
800
68-8
513-76
56-32
1
1
•9
65-85
29-0
75
170
11856
80
812-9
70-5
550
78-03
2
27-0
66-22
78-2
760
180
14763
82-6
900
71-1
569-64
92-30
3
•1
66-60
190
18178
85-4
1000
72-5
600
103-26
4
•2
66-99
*
200
22164
96-8
1500
73-8
642-98
112'30
5
•3
67-38
Ramsay and Young, P.T.
210
26821
105
2000
74-1
650
120-08
6
•4
6777
[1886], 127, 154:—
220
32097
117-6
3000
76-1
700
126-95
7
•5
68-15
O
mm.
230
38176
135-3
5000
78-0
750
133-15
3
•6
68-54
-5
8-60
240
45504
162-7
10000
78-2
760
138-81
9
•7
•8
68-93
69-31
—4-67
—4-27
8-75
9-20
c.t. 243-6
ats.
62-8
180-5
194-1
15000
20000
Sajotschewski, W.B.
3, 741 :—
144-05
10
•9
28-0
69-70
70-02
—3-36
—2-50
9-80
10-25
Ibid., 47, 654; P.M. [5],
20, 524 ; 21, 36 :—
Richardson, 49, 762,775;
B.r. 19, 808 :—
o
c.t. 234-3
ats.
62-1
Ethylic formate,
•1
70-49
—1-63
10-75
CoH,02
•2
70-89
—1-60
10-90
3-75
U1JI1.
10
O
—3-3
Mini.
10-23
Hannay and Hogarth,
o o a
Schumann, W. 12, 47 ;
•3
71-29
—1-10
11-05
22
50
+4-2
16-89
P.R. 30, 18
3, 484:—
B. 14, 1273 :—
•4
71-69
—0-92
11-35
34-5
100
4-8
17-94
O
ats.
o
mm.
c.t. 234'6
65
•5
72-09
—0-79
11-60
40
133-7
7-3
22-39
—9-5
40
•6
72-49
—0-39
11-85
41
140-75
8-8
23-31
Strauss, W.B. 6, 282 :—
+1-2
81
•7
72-89
—0-13
12-05
42
148-1
9-8
24-51
0
ats.
9-5
121
•8
73-29
-fO-09
12-45
42-3
150
10-7
25-80
c.t. 240-6
?
20-1
200
•9
73-69
0-54
1270
43
155-8
13-6
30-67
De la Tour, P.R. 30,
20-9
206
29-0
74-09
0-70
12-85
44
163-8
17-2
38-57
184:—
26-2
256
•1
74-53
0-99
13-00
45
172-2
19-8
45-22
0
ats.
29-6
291
•2
74-96
1-28
13-15
46
181-0
21-8
50-0
at. 258-7
119
33-2
342
•3
•4
75-39
75-82
1-63
2-31
13-75
14-20
47
48
190-1
200
22-6
23-1
51-96
54-86
Ramsay, P.R. 38, 330 ;
38-2
41-5
419
477
•5
76-25
2-78
14-85
49
209-6
23-5
56-25
48, 1178 : —
44-9
541
•6
76-68
3-47
15-45
50
220-0
25-3
62-48
o
c.t. 243-6
BMMfe
64-3
49-4
638
-7
77-12
A-R7
Ifi-QO
•a
OOA.Q
nc.Q
fift-Qfi
53-1
730
I • 4w -i «^f
1 u a\f ui
_->U 0 £i\J ' >
DO tj\J
5 A 2
732
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Ethylic formate
(continued) : —
O mm
Propionic acid
O
105
(cont.) : —
mm.
229-7
Propionic acid (cont.) : —
Eichardson, 49, 766,
776 ; B.r. 19, 808 :—
Propyl alcohol
0
35-6
(cont.) : —
mm.
39-6
Propyl alcohol (cont.) : —
Nadejdine,W.B.[1883],
678:—
Acetic anhydride,
C4H603.
Kahlbaum, B. 16, 2481 ;
54-4
760
110
274-4
O
mm.
39-7
50-0
O
ats.
B. 17, 1259, 2570 ; 18,
56-4
814
115
327-1
13-9
2-49
43-2
62-18
c.t. 258
?
2107 ; 46, 141 :—
61-2
961
120
389-0
14-7
2-98
47'3
75-0
—
O
mm.
65-9
1124
125
462-0
15-82
2-74
96-6
760
Glycerol, C3H803.
26-8
o-o
69-0
1243
130
547-5
16-7
3-59
Eichardson, 49, 764 ;
34'2
5
70-2
1300
135
650-2
20-2
2-99
Eichardson, 40, 763 ;
B.r. 19, 808 :—
37'2
7'5
73-0
1408
140
765-2
20-45
3-98
B.r. 19, 808 :—
0
mm.
39-9
10
145
902-3
24-7
4-98
O
mm.
118-45
•238
42-6
12'5
150
1062-0
28-7
4-73
2-0
4-59
118-75
•298
44-5
15
Methylic acetate,
155
1248-6
31-7
5-48
4-8
5-19
120-77
•348
44-6
15-02
C8H,Or
35-7
6-97
6-2
5-78
122-92
•398
47-0
17-5
Schumann, W. 12, 47 ;
B. 14, 1273 :—
Schall, B. 17, 2568 :—
39-7
46-7
8-37
13-20
10-8
11-45
7-84
8-56
123-85
127-91
•448
•499
49-2
50-8
20
22-5
0
mm.
O
46'5
111111.
10
49-6
15-84
11-7
8-83
130-8
1-891
52-4
25
-9-5
27
51'6
15
55-0
22-02
13-45
9-49
134-8
1-941
53-4
25-86
o-o
57
55-4
20
56-2
21-92
14-9
10-96
137-0
2-000
59-0
33-70
+8-8
95
59'0
25
60-12
19-44
20-7
15-46
138-39
2-191
62-6
41-24
18-9
159
71'6
50
65-2
35-87
23-7
18-82
139-04
2-338
66-4
50
217
183
77'2
75
72-0
50-0
28-2
24-96
141-04
2-49
68-2
53-04
23-5
200
141-8
760
77-7
66-27
30-6
29-04
143-64
3-046
75-3
75
24-2
204
.1^1-1
81-2
76-73
33-8
34-90
147-06
3-385
81-2
105-46
31 "2
zoO
83-2
86-45
33-7
35-23
151-99
4-083
136-4 \
760
34-7
323
Kahlbaum, B. 16, 2480 ;
86-7
100-0
35-1
39-81
161-25
6-527
137-9 >
37-4
364
17, 1259; 18, 2107,
87-7
104-14
36-7
40-74
162-45
8-115
40-2
407
3147; 19, 2864; 46,
92-7
131-34
38-2
45-50
171-05
12-694
Dimethylic oxalate,
43'6
465
141:—
96-4
150-0
39-2
47-40
172-80
12-745
C4H604.
45-7
48-7
r I .0
503
562
O
34-7
41-1
mm.
o-o
5-0
100-7
103-2
176-39
196-56
40-3
41-7
50-00 1
54-88
183-25
195-30
20-461
34-369
Eegnault, P.A. Ill,
410:—
Ol O
103-5
200-0
43-7
61-67
200-8
44-865
56-2
730
43-9
7'5
108-7
247-89
44-7
65-21
201-3
45-61
109-4
iii nil
117-3
57-5
760
46 '5
lO'O
108-9
250-0
46-7
73-50
211-5
65-61
109-5
117-5
60-1
847
49-0
12-5
113-3
300-0
48-7
83-53
220-3
100-813
125-98
222-7
63-3
946
51'2
15'0
113-7
303-44
48-1
84-32
229-5
137-95
126-06
222-9
67-7
1088
53-4
17-5
1177
350-0
52-4
100-0 1
241-8
201-225
136-5
320-1
71-4
1237
55-4
20'0
120-3
388-80
53-9
106-92
250'3
231-872
145-1
423-4
73-0
1300
56'5
21'31
121-5
400-0
55-7
119-25
260-4
385-326
1557
591-4
75-4
1404
57'1
57-6
22'0
22-46
125-3
"I OC.yf K
450-0
56-5
129-23
141-O
2nd Experiment.
164-3
1 GA .R
761-3
57-2
22-50
I/O 4O
453 5
59 7
1*±O \J
122-8
lD-± O
7oo o
Propionic acid,
59-0
25-0
128-4
500-0
60-7
150-0
127-91
0-746
190-65
1589-8
C3H602.
62-8
30'0
131-1
550-0
62-5
163-96
135-51
1-165
217-2
2958-7
Landolt, As. 6, 129 :—
63-5
31-34
132-7
572-25
66-5
200-0 1
136-52
2-340
228-9
3875-9
0
mm.
65-7
35-0
133-4
600-0
66-2
214-75
145-55
3-285
237-2
4849-7
10
5-4
68-0
40'0
135-6
650-0
68-7
220-74
152-34
4-659
242-9
4867-8
15
6-7
68-8
41-7
1377
700-0
71-4
250-0
163-36
7-417
253-5
6203-1
20
8-3
69'2
44'2
140-0
750-0
74-5
287-3
169-70
12-059
25
30
10-3
12-7
70-0
70-4
45-0
47-3
140-3
760-0
75-3
78-8
300-0 1
350-0 1
175-52
183-40
15-683
20-512
Propylic formate,
35
15-6
71-6
50'0
79-2
358-75
192-0
30-62
C4H802.
40
19-2
73-2
55-0
Propyl alcohol,
81-8
400-0 f
199-8
41-81
Schumann, W. 12, 47 ;
45
23-5
74-3
60-0
C3H80.
84-2
450-0 t
205-8
52-767
B. 14, 1273 :—
50
55
28-7
35-0
75-4
76-4
65-0
70-0
Kahlbaum, B. 16,2480;
17, 1259 :—
857
86-9
477-51
500-0 1
211-5
217-3
68-703
86-725
0
9-0
mm.
38
J.T
60
42-7
77'2
75'0
O
mm.
89-0
550-0 1
224-3
115-25
<41
65
51-9
78-2
80'0
6
0
90-2
566-22
227-0
130-535
20'0
61
70
75
62-9
76-2
78-9
79-7
85-0
90-0
11-8
16-3
5
10
90-8
92-6
600-0 1
650-0 1
229-8
237-1
144-87
183-503
24'7
29-2
OO./1
78
101
80
92-0
80-2
95-0
20-6
15
94-1
700-0 1
246-4
239-95
oo 't
1 A Q
85
110-8
80'8
lOO'O
22-3
16-78
97-2
745-95
248-5
258-627
37'8
14r>
90
133-5
139-4
760
24-6 .
. 20
96-0
750-0 1
245-3
266-85
41'6
4VO
175
200
95
160-3
27-8
25
257-3
347-092
*±<J \J
A VI
100
192-1
31-4
30-2
t By interpolation.
'iO 1
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
733
Propylic formate
Methylic propionate
laobutyric acid (cont.) : —
Butyric acid (cont.) : —
Butyric acid (cont.) : —
Diethyloxide (cont.) : —
(continu
o
ed):-
mm.
(eontinii
o
ed):—
HUM.
Eichardson, 49, 761 ;
o
35
mm.
12-2
o
70-9
mm.
17-5
Olzewski, C.N. 51, 174 :—
49-5
240
24-9
82
B.r. 19, 808 :—
40
14-5
73-0
20-0
Solidifies —129°.
^•Q
282
33'2
1 OK
Ati
T7-9
7r.o
91 -Aft
tlO £/
56-7
312
35-5
xav
141
23-8
111111.
0-996
•4O
50
J. i &
20-4
fO _
74-8
Zii *±O
22-0
Eegnault, M.A.S. 26,
64-9
437
38-5
161
32'6
2-195
55
24-2
75-0
22-5
339:—
72-9
580
41-2
182
34-55
2-798
60
28-6
76-9
25-0
*
76-2
652
43-7
200
37-55
3-584
65
33-7
80-5
30-0
o
—20
mm.
68-9
79-9
730
45-6
216
38-8
3-787
70
39-9
81-4
31-94
—15
89-31
81-0
760
50-0
260
44-05
5-873
75
47-1
83-2
35-0
—10
114-72
82-5
796
55-0
318
48-55
7-366
80
55-6
85-9
40-0
— 5
146-06
86-3
905
59-4
377
51-8
12-158
85
65-5
87-5
43-12
0
184-39
90-4
1027
63-7
439
64-8
18-436
90
77-3
87-8
45-0
+ 5
230-89
92-5
1097
67-1
496
67-2
20-9
95
91-0
89-8
48-9
10
286-83
95-3
1192
70-0
550
70-6
24-73
100
107-1
90-3
50-0
15
353-62
98-2
1298
74-3
633
76-4
34-78
105
125-9
91-7
55-0
20
432-78
98-3
1300
78-4
733
84-8
50-0 1
110
148-1
92-9
60
25
525-93
101-1
1412
79-9
760
89-8
66-37
115
173-0
94-0
65
30
634-80
82-0
824
92-3
Qfi-O.
72-71
QQ-AQ
120
204-1
95-9
70
35
761-20
89'9
1052
V\) o
oy uy
125
240-0
97-1
75
40
807-04
Ethylic acetate,
/-t TT r\
93-1
96-3
1159
1275
98-8
99-2
97-79
loot
130
135
281-2
329-3
97-9
98-7
80
85
45
50
1074-15
1264-83
Schumann, W. 12,47;
97-0
99-7
1300
1398
103-8
104-8
129-75
127-90
140
145
386-1
450-8
99-9
101-0
90
95
55
60
1481-06
1725-01
B. 14, 12
o
16 : —
ll 1 II I
107-3
147-09
150
529-1
102-1
100
65
1998-87
13-0
53
107-8
150-0 1
155
617-9
161-5
760
70
2304-90
9O-1
Isobutyric acid,
110-3
160-0
160
723-1
75
2645-41
4i\j i
22-0
30-6
33-3
81
123
139
C4H802.
Schumann, W. 12, 47 ;
B. 14, 1273 :—
111-8
114-5'
115-8
177-24
200-0 1
205-29
165
170
175
844-4
986-2
1151-4
Ramsay and Young, B.
19, 2110 :—
80
85
90
3022-79
3439-53
3898-26
36-2
158
o
mm.
119-3
236-03
180
1342-0
O
mm.
95
4401-81
38-9
177
113-8
200
120-8
250-0 1
20-3
0-35
100
4953-30
41"4
200
153-3
760
123-0
279-04
50
5-2
105
5556-23
42-1
202
168-9
1300
124-3
283-66
Schall, B. 17, 2569 :—
60
9-5
110
6214-63
45-2
233
125-9
300-0 1
o
[ill;]
70
16-3
115
6933-26
48-3
266
01 Q
Kahlbaum, B. 16, 2480 ;
126-8
130-4
308-57
350-0 1
63-4
68-7
10 '
15
80
90
27-5
44-5
120
7719-20
567
60-3
O LO
371
422
17, 1259; 18, 2107;
19, 2864 ; 46, 141 :—
130-55
131-20
358-76
358-84
73-0
76-9
20
25
100
110
73-1
110-2
Ibid., P.M. [4], 8, 271 :—
67-3
545
O
39-9
mm.
o
134-5
400 1
90-3
50
120
164-3
O
mm.
70-3
605
49-3
5
133-80
406-59
971
75
130
241-5
— 20
69-2
72-9
665
52-9
7'5
136-05
411-19
157-0
760
140
345-7
— 10
113-2
75'7
729
KK.Q
in
138-0
450 1
150
488-5
0
182-3
77-1
77-7
760
772
tjtj O
57-5
58 '5
L\J
11-36
12'5
141-0
139-8
500 t
522-03
Schumann, B. 18, 2085 :—
160
163-8
676-3
7601
10
20
286-5
434-8
143-8
550 t
30
637-0
80'2
849
60'8
15'0
o
mm.
87-2
1051
63-2
17'5
146-1
600 1
15-8
6-5
40
913-6
89-2
1117
69-2
1814
1487
650 1
84-0
36-0
Diethyloxide,
50
1268-0
91-8
1208
65-4
20'0
150-8
700 1
155-5-160 u.c.
730
C4H100.
60
1730-3
153-0
750 1
Drion AC [3156-133:
70
2309-5
94-3
95-5
1300
1347
67'5
69-8
72-8
22'5
25-0
28-84
153-3
t Interp
761-27
olated.
Kahlbaum, B. 16, 2480 ;
17, 1259, 1267, 1271 ;
o
c.t. 190-5
JT f
ats.
80
90
100
2947-2
3899-0
4920'4
97-0
1403
73-8
30-0
18, 2107, 3147; 19,
Ladenburg, B. 11, 828;
110
6249"0
76-9
35-0
2864 ; 46, 141 :
34, 633 :—
1 -1 />
78-8
39-36
Butyric acid,
o
mm.
o
lib
70762
Methylic propion-
79-0
40-0
C4H802.
49-0
0
c.t. 196.
ate, C4HgO2.
81-4
45-0
Landolt, As. 6, 129 : —
57-3
5
Strauss, W.B. 6, 282 :—
Ibid., P. A. Ill, 407; iii.,
Schumann, W. 12, 47 ;
83-0
50-0
0
mm.
60-6
7-5
o
ats.
94:—
B. 14, 1273 :—
85-0
61-4
10
5-2
63-6
10-0
c.t. 195-5
1
O
mm.
o
4-5
mm.
34
88-3
152-0
75-0
760-0
15
20
6-2
7-3
63-5
66-3
10-06
12-5
De la Tour and Wolf,
B., 11, 822: —
— 20
— 15
67-5
87-9
17-1
58
25
8-7
67-9
14-0
o
— 10
113-3
23-4
77
30
10-3
68-7
15-0
c.t. 200.
— 5
144-8
734
VAPOUR TENSION AND BOILING POINT TABLES OP SIMPLE SUBSTANCES.
Diethyloxide (cont.) : —
Isobutyl alcohol,
Isobutyl alcohol
Isobutylic formate
Propylic acetate
Methylic butyrate
o
mm.
Bu^.OH.
(continued) : — •
(continued) : —
(continued) : —
(continued) : —
0
183-3
Kahlbaum, B. 16, 2480 ;
0
mm.
0
mm.
0
mm.
o
mm.
+ 5
230-1
90-3
378-12
59-4
200
11-8
15
82-3
398
17, 1259 ; 46, 141 : —
10
286-4
91-55
399-35
59-6
203
16-2
20
84-2
423
o
mm.
15
353-6
7-6
0
91-8
400f
63-5
236
21-2
25
87-3
467
20
433-3
17-9
5
92-8
418-12
68-5
286
33-8
50
89-6
509
30
637-0
25-2
9-46
92-95
428-94
73-0
336
39-1
75
91-7
543
40
909-6
26-4
10
94-4
450f
77-2
392
100-8
760
94-2
590
50
1268-0
OO-K
i ^
95-4
468-98
80-9
448
98-3
673
60
70
1728-5
2309-5
«3o O
38-0
42-0
iO
20
25
95-8
97-0
478-12
500f
83-9
87-2
491
548
Ethylic propionate,
/"I T T /"I TT /~t /~\ TJ1 i.
100-8
101-6
732
743
80
3024-4
45'2
30'2
98-05
524-86
89-9
594
\J l~l.jTl. J Jlp-V-A JnlljLi.
102-3
760
90
3899-0
50'0
42 "48
96-80
527-36
93-1
654
Schumann, W. 12, 47 ;
104-4
807
100
4950-8
52-2
50
99-4
550f
96-3
733
B. 14, 1273 :—
108-5
913
110
6249-0
56-0
75
100-7
575-65
97-9
760
0
26-0
mm.
39
109-6
944
120
7702-2
106-4
760
101-55
593-86
102-1
863
31-5
52
113-1
1044
101-4
600f
105-8
958
35"4
66
116-1
1140
102-75
626-26
109
1067
119-7
1256
Herwig, P.A. 137 and
Richardson, 49, 763 ;
102-8
630-89
112-3
1178
38 '8
77
120-9
1300
~Rr IP 8ft8 •
41 '9
89
141 ; vi., 683 :—
1 >. 1 . 1.J7, OVO .
103-3
650t
115-1
1279
43-5
97
122-3
1350
o
18-2
25-0
35-0
mm.
405-16
530-16
769-73
25-3
32-8
35-4
37-9
42-0
46-7
46-8
11-21
18-44
21-42
26-16
33-12
44-07
42-92
104-8
104-8
105-3
105-8
107-0
107-7
Pawlewski, I
669-11
680-83
700t
708-36
750t
755-11
-. 16.2634:
115-8
118-5
1300
1396
47-7
51-2
54-7
58-3
60-7
61-8
65-9
117
138
158
183
200
207
243
123-4
1390
Methylic isobuty-
rate,
CHMea.C02Me.
Schumann, "W. 12, 47 ;
B. 14, 1273 :
Propylic acetate,
CH3.CO3Pr«.
Schumann, W. 12, 47 ;
Winkelmann, W. 9. 364 ;
38, 692 :—
o
ats.
49-0
50'Ot
46, 252 : —
B. 14, 1273 :—
70-0
283
— 13'86
1
mill.
o
50-8
55-66
o ats.
o
mm.
73-2
323
23
48
0'50
21 "0
31
4
52-8
62-68
c.t. 234-9
?
76-2
361
26
56
+ 16'70
28'8
47
2
54-9
71-61
83
o.p.
79-0
402
32-3
75
34-96
1
37"!
65
e r .Qhf
58-8
85-86
83-0
461
37-5
94
OO O/
57-8
88-76
398
74
86-7
522
41-6
113
69-61
80-21
3
61-3
98-68
Propylmethyl
43-7
47'6
87
104
90-6
597
44-6
130
61-8
100-Ot
ketone,
94-2
668
47-5
150
88'96
5
52'0
126
96-47
6
62-3
103-04
C3H7.CO.CH3.
59-9
175
97-2
734
51-1
172
103-08
7
66-0
116-29
Kahlbaum, B. 17, 1260:—
63-1
200
98-3
760
55-0
200
109-00
8
65-8
123-92
0
mm.
64-7
215
100-5
812
573
221
66-0
124-62
21
0
105-7
954
61-9
264
114-37
9
67 "8
240
119-39
10
68-8
134-11
7-6
5
71-4
277
109-6
1066
65-6
306
69-8
150t
11-9
10
75-4
322
113-1
1178
69-3
348
69-9
151-2
14-8
15
79-3
372
115-3
1250
72-3
387
Ramsay, P.M. [5], 20,
71-8
166-62
17-9
20
83-8
436
116-9
1300
76-1
445
524 ; 21, 37 ; P.R. 31,
73-8
182-38
20-9
25
87-3
493
117-9
1331
80-6
520
194 ; 42, 136 :
74-8
194-68
32-1
50
84-4
592
0
— 12-7
mm.
100
75-5
75-9
200t
204-09
38-4
88-9
75
760
90-8
95-7
552
649
Methylic butyrate,
87-6
91-0
658
734
— 4-5
150
77-2
213-77
99-7
100'8
733
760
CHs.(CH3)2.C02Me.
92-3
760
+ 1-8
200
78-7
226-82
Schumann, W. 12, 47 ;
99'7
946
11-0
18-0
23-7
28-5
32-7
36-3
39-9
300
400
500
600
700
800
900
78-7
80-55
80-5
81-0
81-3
83-6
84-8
229-45
244-61
250t
259-56
259-00
284-30
297-59
Isobutylic
H.CO
Schumann, ^
B. 14, 1
0
29-8
33-5
formate,
i DU^ •
IV. 12, 47 ;
273:—
mm.
51
64
104-6
108-3
112-3
114-3
117-3
119-2
119-8
m.Q
851
956
1069
1138
1230
1300
1317
1 *5Q1
B. 14, 1
o
43-0
47-3
52-1
55-4
63-0
273:—
mm.
81-6
105
127
141
192
102-5
105-9
108-7 •
110-6
111-1
112-7
1035
1137
1242
1800
1316
1370
43-0
1000
85-0
soot
37-8
76
9
loyi
63-9
200
55-5
1500
85-3
304-47
40-4
88
66-9
225
Isovaleric acid,
65-0
2000
87-3
332-32
44-3
104
Kahlbaum, B. 17, 1259:—
70-3
258
CHMe3.CH2.CO2H.
79-8
3000
87-8
347-47
50-6
138
o
mm.
73-0
281
Landolt, As. 6, 129:-
100-4
5000
88-8
350t
55-3
. 169
— 13-2
0
77-0
327
o
mm.
— 2-4
5
78'4
347
10
4-6
t Interpolated.
+ 5-6
10
81-0
376
15
5-4
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
735
Isovaleric acid (cont): —
Isovaleric acid (cont.) : —
Isovaleric acid (cont.) : —
Isoamyl alcohol,
Isoamyl alcohol (cont.): —
Phenol (continued) : —
o
mm.
o
mm.
0
mm.
CHMe,.CHo.CH2.OH.
0
mm.
° mm.
20
6-3
837
20-0
106-27
55-89
a » ~,
Schall, B. 17,2568:—
95-65
191-75
210
1534
25
7-4
85-8
22-0
112-09
63-81
96-8
200-0
213
1659
o
mm.
30
8-7
86-1
22-5
112-62
72-27
41-2
10
99-2
220-6
220
1953
35
10-2
88-4
25-0
114-65
81-48
47-4
15
101-5
250-0
230
2447
40
12-0
90-0
27-28
116-70
88-80
51-8
20
101-8
253-59
45
14-0
91-6
30-0
124-05
122-30
55'5
103-7
273-52
50
16-4
94-9
35-0
133-0
175-16
66-0
50
103-8
276-15
Mesityl oxide,
55
19-3
97-0
40-0
138-25
218-11
71-5
7fi
104-0
279-04
C6H100.
60
22-6
99-8
45-0
143-05
256-19
i J. «J
130-5
1 *j
760
105-9
300-0
Kahlbaum, B. 17, 1260 ;
65
26-4
99-2
45-92
148-67
312-09
106-8
304-74
18, 2107:—
70
30-9
100-7
50-0
150-3
368-39
107-0
314-72
0
mm.
75
36-2
102-2
55-0
153-1
369-53
Kahlbaum, B. 17,1259;
107-7
319-71
7-3
0
80
42-3
103-2
60-0
158-27
434-04
18, 2107 :—
108-8
334-42
18'5
22-8
5
75
85
49-4
104-3
65-0
162-4
492-77
o
mm.
109-3
345-96
23-3
0
26'5
10
90
57-8
105-2
70-0
165-62
551-88
33-4
5
109-5
350-0
29-9
12-5
95
67-4
105-8
71-94
171-25
673-25
110-9
370-44
37"7
7-5
32'8
15
100
78-8
106-1
75-0
176-0
745-59
41'4
10
111-5
387-0
35-5
17-5
105
92-0
106-9
80-0
111-8
388-67
44'6
12'5
37'9
20
110
107-3
107-5
85-0
55-4
3-39
47-4
15
112-8
400-0
40-2
22-5
115
125-6
107-9
90-0
73-51
10-71
114-3
417-7
49'7
17"5
42'5
25
120
145-9
108-5
95-0
88-85
23-99
51-8
20
115-9
450-0
55-0
50
125
170-6
109-1
100-0
96-1
34-88
53-7
22-5
115-8
452-2
61-5
75
130
198-1
1737
760
106-22
58-15
55-5
25
118-5
500-0
130
760
135
231-5
111-36
62-59
118-8
524-21
140
145
150
268-5
313-5
363-4
Richardson, 49, 761 ;
B.r. 19, 808 :—
115-42
123-85
130-0
80-73
122-59
15478
66'0
71-5
129-7
50
75
760
121-1
120-8
121-0
524-36
536-81
550-0
Ethylic aceto-
cetate,
155
421-9
o
51-3
mm.
2-59
133-01
174-01
123-6
591-75
CH2Ac.CO.jEt.
160
491-2
59-4
3-63
135-02
185-55
Richardson, 49, 761 ;
123-5
598-4
Kahlbaum, B. 17, 1260:—
165
571-4
60-8
4-68
138-04
218-26
B.r. 19, 808 :—
•Je
123-2
600-0
O
39 '9
mm.
Q
170
662-9
69-9
8-21
142-25
253-44
0
mm.
124-8
628-92
K.A .0
175
769-6
88-2
22-89
146-36
292-31
347
7-27
125-4
650-0
D4 o
i n
180
893-3
92-9
28-47
151-29
349-72
41-9
9-97
128-55
681-46
65 '9
10
1 PV
185
1043-7
102-4
46-98
155-01
399-95
46-5
14-0
127-7
700-0
10
OA
190
1203-0
107-8
56-22
155-11
398-61
47-8
15-67
129-6
750-0
QA .£>
•u
OR
111-8
74-35
157-20
434-53
53-8
21-87
O*± -
mO
Schall, B. 17
0
70-9
, 2569 :—
mm.
10
120-55
124-4
128-8
104-96
125-71
155-87
158-26
163-45
171-15
440-91
526-52
673-23
58-3
65-55
66-68
29-34
42-85
46-58
Pawlewski, B
o
c.t. 306-6
16, 2634:—
ate.
99-5
181-0
75
760
78-5
15
130-9
186-93
174-93
744-99
67-8
48-16
Olzewski, C.N. 51, 174:—
83-6
20
136-4
212-01
68-3
50-0
Remains liquid —102°.
Propionic anhy-
88-4
25
140
264-05
The following were inter-
70-3
56-56
dride,
100-7
50
145-8
299-31
polated from the three
72'8
63-93
(CH3.CH2.CO)20.
105-3
75
151-8
270-67
preceding series : —
73-0
65-46
Phenol, C6H60.
Kahlbaum, B. 16, 2480 ;
176-3
760
155-8 .
436-72
«
74-25
69-61
Carnelley, unpublished :
17, 1259; 18,2107; 46,
157-6
479-06
o
1 f\A 'f\
mm.
Kf\
76-8
79-06
0
mm.
141 : —
Kahlbaum, B. 16,
2480 ; 17, 1259, 1267,
1271 ; 18, 2107, 3147 ;
161-3
173-3
557-0
645-19
104 U
119-3
129-5
50
100
150
77-65
78-05
81-50
82-87
85-66
100-0
130
135
140
166
194
228
0
42-0
52-0
mm.
0
5
19, 2865 ; 46, 141 :—
51-79
2-74
136-5
200
81-55
100-04
145
259
55-6
7-5
o mm.
56-25
3-33
142-0
250
82-05
102-55
150
307
59-1
10
53-6
o-o
58-74
3-93
147-4
300
84-4
116-6
155
356
62-3
12-5
63-1
5-0
62-72
4-98
151-5
350
84-9
107-18
160
407
65-1
15
67-8
7-5
65-45
5-72
155-5
400
85-8
113-61
165
467
67'8
17-5
71-8
10-0
73-51
9-95
159-0
450
88-95
143-0
170
547
67-5
17-94
72-4
10-58
84-12
18-91
162-2
500
89-55
145-5
175
630
70-4
20
72-6
10-68
89-35
24-29
165-0
550
90-20
150-0
180
731
72-0
21-44
75-3
12-5
92-51
28-37
167-8
600
90-55
150-98
188
949
72-8
22-5
78-4
14-9
93-32
29-87
170-4
650
90-6
155-56
190
1009
75-1
25
78-5
15-0
93-82
31-09
173-0
700
91-9
164-93
195
1149
77-2
28-06
99-6
16-0
96-81
35-98
175-8
750
92-3
167-92
200
1249
80-0
33-42
81-2
17-5
101-38
42-45
93-7
175-87
205
1399
82-7
38-06
736
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Propionic anhydride
(continued) : —
Amylic formate (cont.): —
o mm.
Isobutylic acetate
(continued) : —
Ethylic butyrate,
CH3.(CH2)2.C02Et.
Ethylic isobutyrate
(continued) : —
Benzaldehyde
o
77-1
(cont.) : —
mm.
25
0
85*0
86*7
mm.
44-02
50
108-2
109-7
110*9
482
506
523
0
135*5
135*9
mm.
1300
1313
Schumann, W. 12, 47 ;
B. 14, 1273 :—
o mm.
0
116-9
120-3
mm.
923
1015
88-3
94-8
50
75
93*2
75
113-8
569
137-4
1364
42-0
39
123-1
1098
180
760
167-0
760
114*9
589
45-3
46
126-0
1180
117-0
627
46-4
50
128-8
1277
Benzole acid,
118-8
664
Kahlbaum, B. 17, 1259 ;
49-8
59
129'3
1300
C7H6O2.
Diethylic oxalate,
119*8
685
18, 2107 :—
53-3
69
131-6
1374
Carnelley, not yet pub-
(COsEt)2.
120-2
697
O
mm.
58-0
82
===-==-------==
lished : —
Schall, B. 17, 2570 :—
121-8
726
5'4
1 0*7
0
62-4
99
Methylie valerate,
0
mm.
0
83*9
91*6
96-5
mm.
10
15
20
122-8
123-3
123-5
124-9
748
760
764
794
16*1
18*8
21-2
7-5
10
12-5
67-6
73-7
75-4
78-2
125
161
173
193
C4H,.CO2Me.
Schumann, W. 12, 47 ;
B. 14, 1273 :—
O TT»TT1_
140
150
160
170
17
24
36
57
100-8
25
125*9
818
23-3
15
79-2
200
45-4
50
180
88
113-2
50
127-2
851
25-2
17-5
81*2
216
48-5
58
190
129
118-6
75
128*7
885
27-0
20
83-8
234
51-9
67
200
176
185-3
760
130-1
923
28-7
22-5
87-2
267
54-6
79
210
249
131-7
960
30-4
25
89-8
290
58-1
91
220
346
Kahlbaum, B. 17, 1260 ;
132-8
986
42-5
50
92-1
316
60-7
103
230
474
18, 2107 :—
134*1
1025
49-7
75
95-1
346
63-0
116
240
609
O
mm.
135*5
1067
112-0
760
101-3
430
67-8
137
250
773
59-1
0
136-9
1105
—
105-2
485
75-3
187
260
930
73-6
5
140"5
1209
108-8
540
77-2
200
270
1107
79-6
7-5
143-7
1300
Propylic propionate,
112-4
612
78-0
207
280
1347
83-9
0*7.0
10
CH3.CH3.C02Pra.
115-5
676
81-2
230
290
1580
O/ 0
12 O
Schumann, AV. 12, 4/ ;
118-2
729
83-6
251
300
1827
91-0
93-7
96-5
98-6
100-8
15
17-5
20
22-5
25
Isobutylic acetate,
CH3.CO2.CH2.CHMe2.
Schumann, W. 12, 47 ;
B. 14, 1273 : -
B. 14, IS
0
52*9
58-1
61-3
'73 :—
mm.
57
74
85
119-9
121-7
125-4
127-9
132-8
760
806
894
961
1098
86-0
89-3
92-7
94-9
lOO'O
275
309
352
382
453
CEnanthol,
C6H13.COH.
Kahlbaum, B. 17, 1260 ;
113-2
50
o
21-8
mm.
17
64*7
98
136-2
1202
102-6
496
18, 2107 :—
118-6
75
36-8
33
677
114
139-1
1300
108-9
594
0
31 "7
mm.
o
185-3
760
50-6
67
70-7
129
140-9
1361
111-2
650
5
KA*C)
fTQ
74*2
149
142*3
1406
1 1 P)-A
731
.__
• > \ A
1 O
78'5
174
A 1<J ^
42-7
7'5
Amylic formate.
56-7
87
82*0
200
___====_=^==
116-4
757
45-5
10
Schumann, W. 12, 47;
60-2
102
82-2
202
116-7
760
48-1
12-5
B. 14, 1273 :—
62-9
114
86 "0
231
Ethylic isobutyrate,
121*3
860
50-5
15
O
mm.
64-8
125
89'0
262
CHMe.j.CHj.COjEt.
128*7
1063
52-5
17-5
21-0
12
69-3
150
92*1
294
Schumann, W. 12, 47 ;
131-5
1146
54*4
20
31-3
22
75*9
196
95-5
327
B. 14, 1273 :—
133-9
1227
56*2
22-5
41-8
39
76-6
200
o mm.
135-7
1286
57*8
25
99*3
372
49-0
50
79-2
221
30-1
34
136-0
1300
69*7
50
102 "3
411
54-9
63
85-3
275
43-8
61
138-0
1366
76'9
75
105"7
460
66-0
102
92*1
349
1 1 A-l
KOQ
48'2
76
155*0
760
71-8
127
96-6
406
liU 1
1 1 I**'.
DjMf
58-9
121
74-0
140
98-3
433
llo u
63-6
148
Benzaldehyde,
77-6
160
101-2
477
118*2
676
67-2
172
C7H6O.
Isobutylic propion-
120*9
730
80-1
178
103-3
513
71-1
200
Kahlbaum, B. 17, 1260 ;
ate,
83-2
200
106-6
570
122-2
760
72-1
209
18, 2107; cf. Schall,
CH3.CH2.CO2Bui3.
85-9
221
110-2
630
123-5
792
76-3
243
B. 17, 2570 :—
Schumann, W. 12, 47 ;
126*4
858
87-9
238
115-1
737
80-3
284
o
mm.
B. 14, 1273 :—
89*8
256
116-3
760
129-3
935
83-5
322
46-6
0
o
mm.
93-0
286
117-1
780
133-4
1049
87-2
366
57-3
5
65*8
52
95-8
318
119-9
842
136-2
1131
90-8
412
61-2
7-5
68*2
60
96-2
321
122-1
905
140-1
1247
95-2
474
64-3
10
71-8
70
98-7
350
125
975
141-7
1300
99-1
542
66-9
12-5
76-8
96
100-0
368
127-2
1036
143-3
1357
1037
628
69-3
15
80-0
109
102-3
397
129-4
1108
144-9
1401
108-7
732
71-6
17-5
90-7
170
104-5
426
131-5
1167
110-1
760
73-7
20
94-4
198
105-8
445
134-6
1275
112-9
823
75-7
22-5
95-0
200
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
787
Isobutylic propionate
Propylic isobutyrate
Methylic salicylate,
Methylic salicylate
Amylic propionate
Isobutylic isobutyrate
(continued) : —
(continued) : —
C6H4.OH.COsMe=1.2.
(continued) : —
(continued) : —
(continued) : —
o
mm.
o
mm.
Kamsay & Young, 47,
o
mm.
o i mm.
o
mm.
98-7
229
61-0
54
650, 655; P.M. [5],
205-7
500-0
109-6 158
85-8
100
103-6
271
66-0
70
20, 524; 21, 40:—
206
504-35
113-9
184
90-6
122
108-2
317
70-2
83
0
mm.
207
517-25
116-9
200
94-0
140
113-9
383
77-6 114
70
2-4
208
530-4
119-2
219
97-8
161
118-0
441
81-9
134
75
3-4
209
543-8
124-8
262
100-4
178
128-0
589
86-8
164
80
4-6
210
557-5
128-8
301
103-8
200
131-5
656
90-3
188
85
6-05
211
571-45
133-0
344
105-8
214
135-3
732
92-0
200
90
7-8
212
585-7
137-5
399
109-4
243
136-8
760
96-5
233
95
9-95
213
600-0
142-4
456
117-3
315
139-0
810
106-0
326
100
12-6
214
615-05
146-3
512
120-3
347
142-9
900
110-0
369
105
15-85
215
630-15
150-5
582
124-8
398
149-0
1059
114-6
427
110
19-8
216
645-55
154-5
648
128-0
441
152-5
1159
118-8
485
115
24-55
217
661-25
158-9
732
136-4
572
155-7
1255
123-4
560
120
30-25
218
677-25
160-2
760
141-6
662
156-9
1300
127-5
633
125
37-1
219
693-6
163-2
819
144-7
730
158-2
1341
132-4
731
130
45-3
219-4
700-0
173-2
1062
146-6
760
160-0
1401
133-9
' 760
132-5
50
220
710-1
178-4
1208
150-7
843
i Qfi.Q
QO"5
1 OK.
KK.f\K
ooi
tya<7'f\K
m'9
1 1(\(\
154-3
928
Propylic butyrate,
lob o
144-6
1020
loo
140
oo Oo
66-55
nil
222
744-35
£t
181-6
1310
159-8
1067
PTT CPTT 1 PO P a
148-9
1142
145
80-0
223
761-9
165-0
1217
Schumann, W. 12, 47 ;
B. 14, 1273 : —
151-3
153-2
1243
1300
150
151-3
95-6
100
224
225
779-85
798-1
Isobutylic butyrate,
167-8
168-1
1300
1310
154-3
1335
155
113-6
225-1
800-0
CH3.(CH2)2.C02Bu0.
57-0
34'
•1
160
134-25
Schumann, W. 12, 47 ;
B. 14, 1273 :—
Kahlbaum, B. 17, 1260 :
71-0
OX
61
165
157-85
Pheneto'il,
o
74-3
mm.
46
o
24-4
mm.
0
76-1
79-9
75
89
Ethylie valerate,
170
172-5
184-7
200
Kahlbaum, B. 17, 1260 ;
83-6
65
34-4
42 '2
5
10
18 2107 •
92'6
90
85-4
115
Schumann, W. 12, 47 ;
175
215-1
o
nun.
98-2
116
47-7
15
91-5
144
B. 14, 1273 :—
176
221-65
48-3
0
105-4
150
52-4
20
97-9
180
o
mm.
177
228-3
55-2
5
113-0
200
56-4
25
101-2
200
55-1
31
178
235-15
58-4
7-5
117-3
233
70-5
50
101-9
205
60-2
45
179
242-15
61-2
10
123-8
284
77-0
75
106-9
243
64'2
60
180
249-35
63-6
12-5
130-5
356
147-5
760
112-4
299
68'1
73
181
256-7
65'9
15
435
115-2
330
72-0
89
182
264-2
67-9
17-5
141'3
492
117-8
363
76-2
107
183
271-9
70-0
20
145-9
556
Propylic valerate,
122-2
414
81-4
130
184
279-75
71-8
22-5
149-8
626
C4H9.C02Pr«.
125-7
464
87-2
162
185
287-8
73-6
25
155-5
730
Schumann, W. 12, 47 ;
129-1
514
92-3
200
186
296-0
87-7
50
156-9
760
B. 14, 1273 :—
129-6
524
93'2
206
186-5
300-0
96-2
75
160'7
842
o
mm.
130-4
133-1
535
577
98-6
104-1
250
300
187
188
304-45
313-05
172
760
164-7
931
77-2
83-0
43
62
1 Ofi.fJ
i • 1 • *
lOS'fi
355
169'7
1058
87'0
73
lob o
141-0
o4o
729
AVO O
112-6
399
189
190
321 '85
330-85
Amylic propionate,
173-5
175-4
1172
1222
89-5
81
142-7
145-7
760
827
116-9
120-5
455
508
191
192
340-05
349-45
CH3.CH2.C02(C5H11).
Schumann, W. 12, 47;
177-4
178-0
1292
1300
927
103-8
95
143
149-3
909
124-4
574
193
359-05
B. 14, 1273 : —
108 "5
1 1 9-fi
175
152-8
996
128-6
646
194
368-85
o
linn.
11.4 b
156-1
1086
132-7
729
195
378-9
21-8
4
Isobutylic isobuty-
114-5
215
159-6
1185
134-3
760
196
389-15
36-8
6
rate,
120-2
259
160-2
1208
139-4
875
197
399-6
50-4
12
CHMe2.CO2Bu0.
124-4
299
163-7
1300
143-2
146"3
975
1056
197-05
400-0
A i A.Q
69-5
7Q-9
29
4.7
Schumann, W. 12, 47 ;
129-1
133-4
346
397
Propylic isobutyrate
CHMe^CO,Pr«.
150-4
152-8
1166
1246
199
200
41U o
421-2
432-35
< •' -
85-2
89-3
*± t
60
72
B. 14, li
O
!73:—
*
mm.
137-4
141-4
449
504
M i
Schumann, W. 12, 47 ;
154-6
1300
201
443-75
93-3
85
65-3
43
144-6
555
B. 14, 1273 : —
155-1
1321
202
455-35
93-7
89
69-1
50
148'0
612
157-5
1407
203
467-25
96-5
96
74-7
60
150-7
658
49-5
32
204
479-35
99-1
106
77-3
70
154-5
728
56-1
43
205
491-7
103-8
128
81-2
82
155 "9
760
"38
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Propylic v
(continue
o
164-2
168-2
172-1
172-8
177-2
179-1
alerate
d):-
mm.
949
1052
1155
1165
1300
1349
Amylie bt
(continue
o
154-5
159-2
163-0
167-2
170-4
177-0
178-6
181-7
186-5
190-9
198-1
201-0
204-3
ityrate
d):-
mm.
390
447
499
562
617
732
760
820
924
1033
1216
1300
1394
Isobutylic
(continue
o
137-0
140-7
144-8
148-8
152-9
156-7
160-1
164-0
167-5
168-7
173-6
175-4
178-8
181-6
183-2
186-8
190-9
191-1
valerate
ri):-
mm.
303
342
386
435
491
543
599
668
734
760
858
905
982
1053
1093
1185
1292
1300
Camphor (c
o
154-0
154-3
157-9
160-1
168-0
m.p. 175-0
184-5
ont.) : —
mm.
188-8
197-6
218-5
240-7
297-8
354-0
431-0
Isobutylic
(continu
o
113-7
117-7
121-2
124-4
1271
129-7
146-0
153-6
237-0
Denzoate
3d):—
mm.
12-5
15
17-5
20
22-5
25
50
75
760
Dimethy]
NH(CI
Vincent and
ibid. :
o
8
163
amine,
I3)2-
Chappuis,
ats.
1
56
E thy la]
C3H5.1>
Ibid., C.E. 10
19, 732
o
18-5
177
nine,
fH2.
3, 379 ; B.r.
,
ats.
1
66
Octyl al<
C8Hlf
Kahlbaum
1259:
0
66-6
71-2
75-4
79-0
82-3
84-6
94-4
102-9
178-5
johol,
0.
, B. 17,
TT1TT1-
0
5
10
15
20
25
50
75
760
Ibid., page
o
136
149-8
168-0
174-6
1767
178-3
178-9
179-5
180-3
181-2
181-3
181-9
182
182-6
182-8
183-4
184-5
198-7
207-3
463:—
mm.
94-9
152-1
274-1
327-6
350-6
363-6
370-3
378-7
385-9
393-3
394
398-6
400-8
405-3
407-4
412-8
421-1
593-2
746-3
Isoamylic 1
C6H5.C02
CHM
Kahlbaum, E
18, 2107 ; c
B. 17, 2£
o
105-4
115-5
120-6
124-8
128-6
132-0
135-3
138-4
141-5
144-8
165-8
174-7
262-0
jenzoate,
(CH2)2.
e,.
. 17, 1260 ;
f. Schall,
70:—
mm.
0
5
7-5
10
12-5
15
17-5
20
22-5
25
50
75
760
Amylie iso'
CHMe2.CO
Schumann,
o
82-9
90-0
94-0
100-0
107-0
112-8
117-1
122-4
124-3
126-8
131-5
134-9
143-7
147-6
153-9
157-6
167-5
168-8
172-8
178-1
183-2
191-4
192-1
Dutyrate,
3(C6HU).
ibid. : —
mm.
43
54
66
81
106
128
154
187
200
213
252
280
370
416
492
551
730
760
838
953
1085
1300
1312
Trimethy
N(CE
Ibid., C.E. 1C
1105:
0
9-3
160-5
lamine,
[3)3-
1, 427 ; 48,
ats.
1
41
Cuminol,
Kahlbaum, I
18, 2107;
B. 17, 2570
o
74-5
92-1
98-5
103-5
108-3
112-3
115-3
117-9
120-3
122-5
137-8
145-9
232-0
C]0H120.
. 17, 1260 ;
cf. Schall,
Ethylic sa
C6H4.OH.C(
Kahlbaum, I
18, 210
0
80-0
94-0
99-4
104-8
109-3
113-0
116-2
119-0
121-7
124-1
139-1
145-7
231-5
lieylate,
)2Et =1.2.
. 17, 1260 ;
7:—
mm.
0
5
7-5
10
12-5
15
17-5
20
22-5
25
50
75
760
mm.
0
5
7-5
10
12-5
15
17-5
20
22-5
25
50
75
760
Propyla
OH3.CH2.C
Ibid., C.R. 1C
19, 7k
0
49
218
mine,
H2.NH2.
3, 379 ; B.r.
; .
ats.
1
50
Isoamy]
valer
CHMea.C
(CH2)2.C
Kahlbaum, ]
18, 2107;
B. 17, 2569
o
43-5
58-9
65-3
71-0
75-9
80-2
83-7
86-6
88-9
91-0
102-8
110-9
194-0
ic iso-
ate,
H3.C03.
:HMe2.
5. 17, 1260 ;
cf. Schall,
mm.
0
5
7-5
10
12-5
15
17-5
20
22-5
25
50
75
760
Diethyli
NH(C2
Ibid.
0
57
216
imine.
H-sV
ats.
1
40
Diethyl
C16H1
Kahlbaum, B
0
3-5
8-5
12-6
16-5
20-2
23-0
32-8
40-5
102-2
acetal,
A-
.17,1260:—
Camphor,
Bamsay an
P.T. [1884],
O
20
35
41-2
48-9
62-4
78-4
92-4
100
101
109-4
116-7
127-4
132
134-2
136-3
140-3
141-7
147-0
CioH16O.
i Young,
45, 463 :—
mm.
1-0
1-8
1-7
7-2
6-4
9-5
15-4
22-6
27-2
35-0
46-0
66-3
78-1
88-6
92-8
• 105-0
109-4
155-1
nun.
0
5
10
15
20
25
50
75
760
Pyridine,
Kahlbaum, '.
18, 21(
o
— 5-2
+ 7-3
11-7
15-4
18-6
21-5
24-0
26-3
27-5
30-3
42-2
48-0
114-5
C6H6N.
B. 17, 1261 ;
)7:—
mm.
0
5
7-5
10
12-5
15
17-5
20
22-5
25
50
75
760
Amylie b
CH3.(CH
(C6H
Schumann, "*
B. 14, 1
o
92-6
97'5
102-0
107-2
111-9
117-0
123-2
132-6
133-2
138-7
143-4
147-8
151-4
utyrate,
0)o. CO2
ll)~-
iV. 12, 47;
273:—
mm.
47
57
65
78
95
117
142
200
202
241
277
317
357
Isobutylic
C4H9.C(
Schumann
o
80-5
89-4
94-6
96-9
100-1
104-6
109-4
114-7
117-9
120-6
123-9
124-2
128-9
133-4
valerate,
D2BuP.
ibid. : —
mm.
41
55
67
74
84
99
119
144
159
176
199
200
231
269
Methyl
CH3.1
Vincent anc
O.K. 101,
1105 :—
0
— 2
+155
amine,
*H2.
Chappuis,
427 ; 48,
ats.
1
72
Isobutylic
C6H6.C
Kahlbaum, ]
18, 21(
o
83-6
97-9
104-7
109-5
benzoate
02Bu".
?. 17, 1260 ;
)7 :—
mm.
0
5
7-5
10
VAPOUR TENSION AND BOILING POINT TABLES OF SIMPLE SUBSTANCES.
Piperidine, C5HUN.
Aniline (cont.) : —
Picoline, C6H,N.
Xylidine (cont.) : —
Ethylene chlorobromide
Nitrobenzene (cont.) :— -
Kahlbaum, B. 17, 1261:—
o
mm.
Kahlbaum, B. 17, 1261 ;
0
mm.
(continued) : —
o
mm.
0
mm.
135
172-5
18, 2107 :—
125-8
50
From CjHiBr,.
98-1
20
-6-1
0
139-4
200-0
0
mm.
130-8
75
0
mm.
100-3
22-5
+3-5
5
140
204-6
1-9
0
211-5
760
87-02
400
205-0
760
9-2
10
145
241-5
15-2
5
93-74
500
13-6
15
150
283-7
20-2
7-5
99-36
600
17-2
20
151
292-8
24-4
10
Quinoline, C9H,N.
105-30
700
20-0
25
15175
300
28-2
12-5
Ibid. :—
108-54
760
Allylthiocarbamide,
30-4
50
152
302-15
31-5
15
o
Qfi
mm.
110-07
800
C3H5.NCS.
38-3
75
153
311-75
34-6
17-5
OD
113-94
900
Kahlbaum, ibid. :—
106-0 760
154
321-6
37-4
20
117-96
1000
o
mm
155
331-7
39-4
22-5
106-4
10
37-2
156
342-05
42-0
25
112'6
15
41-5
10
Aniline, C6H7N.
157
352-65
57-3
50
118-0
20
Diehlorhydrin,
45-1
12-5
' o /
Kahlbaum, B. 17, 1261 ;
158
363-5
66-6
75
121-9
25
C3H6C120.
48-4
15
18, 2107, 3149 :—
159
374-6
126-2
760
136 "5
1 AA-A
50
Kahlbaum, B. 18,2107:—
51-3
17-5
O
mm.
160
386-0
1<4<4 o
75
o
mm.
53-8
20
55-4
0
161
397-65
238-0
760
67-0
7-5
55-8
22-5
GK.K
1 fil -O
Triethylamine,
70"2
10
1 /Ift-O
DO O
69-3
7-5
10
IDl -
162
163
409-6
421'8
N(C2H5)3.
Vincent and Chappuis,
Ethylidene ehloro-
72-8
75-1
12-5
15
I4o ~,
75-6
12'5
164
434-3
C.E. 103, 379 ; B.r. 19,
bromide,
77-4
17-5
78-3
15
165
447-1
733 :—
CH3.CHClBr.
79-5
20
Phenylthiocarb-
80-7
17-5
166
460-2
o
on
ats.
Staedel, B, 15, 2563 :—
81-5
22-5
amide, C6H5.NCS.
83-0
20
167
473-6
89
259
1
30
o
63-63
mm.
400
182-0
760
Kahlbaum, ibid. : —
85-1
22-5
168
487-25
69-93
500
0
mm.
87'2
25
168-9
500
75-34
600
86'3
7'5
100-9
50
169-
501-25
Dipropylamine,
80'03
700
Bromal, C2HBr30.
91-1
10
108-2
75
170
515-6
NH(C3H7)2.
82'69
760
Kahlbaum, ibid. : —
95-4
12-5
182-0
760
171
530-2
Vincent and Ohappuis,
84-35
800
o
mm.
99-2
15
172
545-2
*A W
58-6
7-5
102-8
17-5
88'19
900
173
560-45
62-4
10
106-2
20
Ramsay and Young, 47,
174
576-1
o
97
ats.
1
91-68
1000
65-7
12-5
109-0
22-5
649, 655 ; P.M. [5], 20,
175
592-05
277
31
94-26
1080
68-7
15
218-5
760
524 ; 21, 39 :—
175-5
600
71-2
17-5
0
80
mm.
18-8
176
177
608-35
625'05
Xylidine, C8HnN.
Ethylene chloro-
73-5
75-2
20
22'5
85
90
95
100
24-0
30-1
37-3
45-9
178
179
180
642-05
659-45
677-15
Kahlbaum, B
18, 210'
0
67-1
. 17, 1261 ;
7 :—
mm.
0
brom
CHZC1.C
Staedel, B. 1!
PVr»m C*
ide,
H2Br.
174
760
)n distillation of benz-
ene, toluene, xylene,
turpentine, carbon
>, 2563 : —
102
50-0
181
695-3
81-5
5
Jj I Mill V>«.
o
mm.
Nitrobenzene,
tetrachloride, nitro-
105
56-2
181-25
700
88-0
7-5
85-53
400
benzene, ethylbromide,
110
115
68-5
83-1
182
183
713-75
732-65
93-1
97-6
10
12-5
92-50
98-22
500
600
Kahlbaum, ibid. : —
ethylic benzoate, and
naphthalene in a
119-9
100-0
184
751-9
101-6
15
103-12
700
83-5
llllil,
7-5
current of steam, see
120
100-4
185
771-5
104-8
17-5
106-07
760
87-0
10
Naumann, B. 10, 1421,
125
120-8
186-4
800
107-6
20
107-78
800
90-0
12-5
1819, 2014, 2099 ; 11,
130
144-7
190
875-7
109-6
22-5
111-93
900
92-9
15
33, 204, 429, 689.
131
150-0
111-3
25
11574
1000
95-5
17-5
5 B 2
740
II.— VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES,
e.g., MIXED LIQUIDS AND SALINE SOLUTIONS.
0 C.= temperature or boiling point, mm. = tension in millimetres of Mercury. Ats. = ditto in atmospheres. W = parts of anhydrous salt
in 100 parts of water. Sat. = saturated.
A.— VAPOUK TENSIONS OF AQUEOUS SOLUTIONS.
Potassium fluoride, KF.
Potassium fluoride (continued) : —
Barium chloride (continued) : —
Calcium chloride (continued) : —
Tammann, W. 24, 535.
mm.
268-5
mm.
164-8
mm.
127-4
mm.
221-2
mm.
216-5
mm.
203-2
o
104
ats.
1
W.
25-8
Tension of
Tension of Solution.
302-2
187-0
145-4
240-5
234-2
221-4
105
j,
29-4
pure H2O.
8-5 W.
19-41 W.
330-2
204-2
158-8
272-6
266-8
251-2
106
32-6
379-1
237-9
185-4
305-0
297-9
281-5
107
M
35-6
mm.
mm
mm
22-6
20-6
19-1
386-3
239-8
188-7
353-4
345-4
326-1
108
,,
38-5
34-5
32-3
30-1
436-4
273-5
215-1
398-3
388-3
367-4
109
»
41-3
41-7
39-3
36-2
501-1
314-8
249-5
431-7
421-2
398-4
110
»
44-0
53-7
50-9
46-9
565-4
359-9
....
487-6
477-7
450-9
111
„
46-8
65-3
62-1
56-8
628-4
398-8
....
527-4
516-0
487-5
112
„
49-7
7 fi
_
577-0
564-5
532-5
113
52-6
90-1
104-4
85-9
99-7
79-1
92-5
Aluminium chloride, A12C16.
642-3
705-0
627-7
687-0
594-4
652-4
114
115
jj
55-6
58-6
114-9
109-8
101-5
Gerlach, Sp. gw. Salzlosungen,
775-0
755-3
715-3
116
„
61-6
133-1
126-5
117-8
103:—
117
„
64-6
151-2
144-6
133-6
103-4
ats.
1
W.
23-7
39-93 W.
50-97 W.
118
»
67-6
168-8
178-8
161. -2
170-1
149-3
157-9
112-8
•
62-1
95-0
mm.
87-4
mm.
86-1
120
j>
73-6
198-8
189-1
174-6
121-5
112-1
110-4
"
220-4
210-5
195-0
Barium chloride, BaCl2.
143-2
132-5
130-8
"
243-8
232-2
215-4
Legrand, A.C. [2], 59, 432; iii.,89:—
158-3
146-0
144-0
"
86-0
268-5
256-2
237-5
o
ats.
W.
183-7
168-8
166-2
125
"
RQ-1
302-2
287-7
267-8
100-5
1
11-0
221-2
203-7
200-3
1 9ft
"
Oi/ L
QO.O
330-2
314-1
292-0
101-0
N
19-6
240-5
222-6
216-1
liO
1 9Q
"
.'_ ^
379-1
362-2
336-6
101-5
B
26-2
272-6
250-9
245-6
Izo
"
1 C\A'fi
386-3
368-3
342-0
102-0
32-5
305-0
280-6
275-1
"
1U4 O
IIO'Q
436-4
501-1
416-7
478-4
386-9
443-4
102-5
103-0
»
38-6
44-5
353-4
398-3
325-2
366-9
319-0
359-1
134
1 *%f\
>j
!)
i iw y
117-2
565-4
539-1
506-0
103-5
„
50-3
431-7
397-7
389-7
1OU
"
19Q-Q
628-4
....
559-4
104-0
56-0
487-6
449-3
441-1
"
LjLty ij
763-5
725-1
674-4
104-4
»
60-1 sat.
527-4
486-1
476-2
ROA-O
142
"
142-8
54-73 W.
73-42 W.
Griffiths, Q.J.S. [1825], 18, 90 :—
642-3
592-3
520 .5
580-1
144
146
»
149-4
156-2
•^^—
111711
o
104-4
ats.
1
w.
81-81 sat.
705-0
649-5
635-7
148
5)
163-2
22-0
7-7
775-0
713-8
699-5
150
170-5
34-5
19"0
13'3
Gerlach, Sp. gw. Salzlosungen,
152
178-1
41-7
23-2
16-5
102:—
154
"
186-0
53-7
31-1
22-6
0
ats.
W.
Calcium chloride, CaC)2.
156
.
194-3
65-3
38-4
27-9
100-6
1
11-1
Gerlach, Sp. gw. Salzlosungen,
158
203-0
78-6
46-7
34-6
101-9
5)
25-0
101:—
160
212-1
90-1
53-1
40-1
Tammann, W. 24, 549 :—
o
101-4
ats.
1
W.
11-1
162
„
221-6
104-4
114-9
617
RQ-0
46-3
^9-0
Tension of
Tension of Solution.
104-2
25-0
164
166
"
231-5
24 1-9
133-1
\JiJ \J
80-2
tiZt \f
60-5
pure H2O.
13-27 W.
39-10 W.
109-7
M
42-9
168
"
252-8
_^^_
j
118'0
ftfi-fi
TJ
151-2
91-1
69-5
,, ~~ ~
170
264-2
mm.
mm.
mm.
168-8
102-5
78-5
95-0
93-0
87-0
Legrand, A.C. [2], 59, 437:—
172
„
276-1
178-8
108-2
82-7
121-5
119-6
112-3
o
ats.
W.
174
„
288-5
198-8
120-5
93-1
143-2
140-6
132-3
101
1
10-0
176
I)
301-4
220-4
134-4
103-8
158-3
155-4
145-9
102
H
16-5
178
„
314-8
243-8
149-2
115-9
1837
179-5
169-0
103
„
21-6
179-5
R
325-0 sat-
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES.
741
Calcium chloride (continued) : —
Calcium chloride (continued) : —
Calcium chloride (continued) : —
Coesium chloride, CsCl.
Lescoaur, B. 14, 1392 ; C.E
92,1158:—
Regnault, P.M.[4], 8, 276 ; C.R. 39, 309 :
Hammerl, W.A. 72, 8 ; viii., 947.
Tammann, W. 24, 537 ; B.r. 18, 313.
100
100
mm.
26(?)
W.
1340-6
708-8
0
52-0 t
61-58
mm.
82-52
136-61
H2 *
o
102-7
110-9
ats.
1
W.
16-69
40-05
Tension of pure
H20.
Tension of
Solution, 28-92 W.
100
59
598-7
71-80
219-44
"^ «4-C O
120-5
70-94
mm.
mm.
100
60
309-9
87-54
434-19
M 0 £
<4-i rj O
131-8
107-9
32-2
30-3
100
132
295-0
129-86
1807-15
° II
p t -g Q
140-3
140-4
71-6
66-8
100
132
197-6
136-30
2182-35
B 2 2
0) &
151-2
182-5
84-6
78-1
100
134
156-1
142-79
2702-13
162-4
242-4
99-8 '
93-1
100
132
152-6
147-91
3123-69
-H- PH
112-4
m«rt
105-0
1 I Q. «
100
100
133
204
140-8
117-5
78-45
198-41
i
Tammann, W. 24, 550 ; B.r.
0
160-4
llo 4
150-4
100
433
62-0
79-1
282-92
o> *5 <u
tuO ^
18, 313 :—
188-6
176-9
100
580
44-9
85-1
362-49
J3 £3 O
B * <l
Tension of
Tension of Solution.
212-1
199-2
100
740
7-6
91-1
479'17
"o
pure H2O.
8-74 W. 16-70 W.
2447
230-0
102'2
754-71
0:
285'3
269-4
Wullner, P.A. 110, 575 :—
mm.
mm.
mm.
336-7
317-4
Tension of
Tension of Solutions.
45-5
43-0
40-9
382-5
360-2
o/V
54'2
51 "0
48 "6
v^.
pure H2O.
1 W.
7-5 W.
15 W.
SOW.
88-1
84-3
80-8
415-0
390-8
^_^_
__^_
^_^_
^^^_
488-4
460-0
104'7
100-2
95"9
mm.
mm.
mm.
mm.
527-3
496-8
16-2
13-71
13-678
13-212
12-738
10-915
127-4
122-3
116-9
599'2
564'9
18-4
15-747
15-709
15-050
14-651
12-454
136-6
131-3
126-0
652'1
613'2
19-84
17-212
17-170
16-515
15-867
13-579
156-5
150-3
144-6
760"!
715-0
20-4
91-ftl
17-826
1 Q*d.7Q
17-783
1 Q.OQO
16-384
14-193
1 V9QR
184-4
991 'Q
177-3
214'0
170-2
205 "6
fii • <
23-28
26-05
L tj ** / tJ
21-272
25-058
21-211
24-992
lo ooo
19-977
23-866
19-132
22-830
1 '* -i.'O
16-594
19-834
ftfiL •)
243-2
273-2
234-8
264-1
224-9
253-4
Hydrochloric acid, HC1.
28-35
28-684
28-609
27-296
26-105
22-632
306-0
296-1
284-6
Kirwan, quoted by Dalton.
32-22
35-8
35-709
34-215
32-725
28-358
347-8
336-0
322-9
New System, 2, 295 :—
34-9
41-595
41-495
39-960
38-125
33-360
375-7
363-5
349-4
o
ats.
W.
15'56
1
91 "57
37-5
48-261
48138
46-079
43-893
38-430
408-8
395-2
380-1
48-89 ?
34-41
38-93
51-866
51-734
49-385
47-400
41-140
453-2
438-6
421-7
"
62'78 ?
30 '55
40-66
56-708
56-564
54-030
51-752
45-150
496-4
479-9
461-6
76-67
27-55
43-05
64-496
64-330
61-519
58-359
51-496
550-8
532-6
512-1
87'78
25'00
45-55
73-274
73-098
70-298
67-338
58-752
604-7
584-4
561-0
100-0
23-00
48-69
86-21
86-008
83-092
79-279
69-360
704-7
679-5
654-5
102-78
21-21
51-7
100-078
99-837
96116
91-959
80-035
765-1
739-1
711-4
105-56
n
53
106-636
106-384
102-476
98-324
85-529
108-89
18-34
55-69
121-514
121-232
117-155
112-267
97-532
20-12 W. 42-83 W.
111-11
13-76
58-3
137-458
137-141
132-509
126-986
110-694
—
108-89
„
11-00
58-7
140-062
139-724
134-974
128-513
111-680
mm.
mm.
9-1 7
40"5
35 "6
107"22
1 /
60
148-791
148-451
143-514
137-541
120-093
R'QA
54"2
48'1
42-4
105"56
,,
o y4
60-6
153-019
152-667
147-643
140-974
123-662
RR-l
79"!
68 "9
103-89
B
5-50
62:28
63-13
165-456
171-583
165-057
171-184
159-191
165-417
151-813
157-981
132-200
138-330
OO i
104-7
197-4
94-3
115'3
82-2
100-5
102-22
101-11
)!
2-72
1-38
64-10
179-537
179-123
173-124
165-741
144-640
i — i *±
65-64
191-075
190-612
183-482
175-100
151-939
136-6
124-0
108-0
Roscoe and Dittrnar, 12, 146 :—
68-45
217-902
217-395
210-113
200-954
175-180
156-5
142-3
124-7
o
mm.
W.
70-60
239-273
238-726
230-852
220-571
192-571
184-4
167-1
146-8
62
100
29-53
72-20
256-287
255-702
247-655
236-415
206-976
221-9
202-1
177-1
77
210
28-37
74-38
281-908
281-280
272-657
260-738
228-752
243-2
221-2
194-4
85
300
27-71
76-83
311-429
310-719
300-483
287-417
251-954
273-2
248-8
218-3
91
380
27-06
78-80
337-747
336-985
326-062
312-235
273-511
306-0
279-0
244-7
97
490
26-42
80-60
363-427
362-621
351-489
336-419
295-245
347-8
317-1
279-0
103 620 25-94
375-7
342-8
301-3
82'63
393'831
392'950
380-622
364'369
319'333
372'3
328-8
'
84-80
86-50
87-65
429-516
459-212
480-175
428-547
458-191
479-102
415-097
443-861
464-175
396-421
424-990
443-954
348-160
372-988
389-703
453-2
496-4
414-0
453-2
364-9
399-8
Mercuric chloride, HgCl2.
Griffiths, Q.J.S. [1825], 18, 90:—
89-93
524-150
522-989
506-098
484-150
427-868
550-8
KO4-7
503-2
551'7
444-0
486-8
o ats.
101-1 i
sat.
92-2
571-031
569-799
552-288
528-193
468-730
\JV± i
94-65
625-630
624-270
605-282
578-777
511-913
704-7
644-1
569-2
Hannay, 26, 573 :—
96-85
678-310
676-830
645-962
627-454
554-587
765-1
700-3 620-0
0
ats.
99-30
741-280
739-698
718-280
687-332
607-766
100-8
1 sat.
742
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES :
Mercuric chloride (continued) : —
Potassium chloride (continued) : —
Potassium chloride (continued) : —
Lithium chloride (continued) : —
Eaoult, C.E. 87, 169; 36, 4 :—
Berzelius,
Lehrbuch, 3, 93 :—
Legrand, A.C. [2], 59, 432 : —
Tension of
Tension of Solutions.
o
100
mm.
759-56
1 W.
o
108-3
ats.
1 Sat.
O
100-5
ats.
1
W.
4-7
pure H2O.
8-01 W.
14-49 W.
Gerlach, Sp. gw.
Salzlosungen, 94 : —
101-
101-5
»
9-0
13-2
mm.
471-2
mm.
441-0
mm.
412-9
101-1
ats. W.
1 11-1
102-
H
17-1
517-4
482-9
452-9
Potassium chloride, KC1.
103-4
25-0
102-5
H
20-9
558-3
521-4
489-1
103-
24'5
604-3
564-5
529-2
Kremers, P.A. 99, 43 :—
Eaoult, C.E. 87, 169; 36, 4:—
103-5
28-0
660-4
617-4
578-9
1 ats.
o
mm.
104-
31-4
697-6
649-0
610-3
110 1 1
Sat.
100
756-58 1 W.
104-5
"
34-6
17-8
752-1
700-8
658-7
Wullner, P.A. 103, 545 :—
105-5
„
O 1 O
41-0
22-64 W. 32-36 W.
Tension of
Tension of Solutions.
106-
D
44-2
° c.
106'5
47'4
mm.
mm.
pure H2O.
1 W.
10W.
20 W.
107-
50-5
59-5
46-6
40-9
1 A*7.K
.
67-8
53-0
46-6
mm.
mm.
mm
mm.
107 5
,,
Oo'7
23-1
21-01
20-94
20-31
19-62
108-
J,
56-9
77-4
60-5
53-1
27-1
26-66
26-57
25-76
24-77
108-3
59-4
92-1
72-0
63-5
100-8
79-0
69'7
29-1
29-95
29-85
28-91
28-01
See also Pouchon, C.E. 89, 753 ;
112-9
88-5
777
31-5
34-36
34-234
33-17
31-78
38, 211.
126-6
99-4
877
37-3
48-25
48-068
46-46
44-58
161 '3
127'4
112"6
39-4
53-14
52-939
51-16
49-07
41-5
59-48
59-249
57-20
54-82
Lithium chloride, LiCl.
187-2
131-1
44-0
67-79
67-502
64-91
62-04
Kremers, P.A. 99, 43 :—
207-6
228-1
164-2
181-9
145-6
159-5
47-3
80-33
79-982
76-82
73-40
o ats.
49-1
87-93
87-583
84-46
80-99
171
1
sat.
254-5
202-1
178-1
286-4
226-5
200-3
51-7
100-00
99-547
95-54
90-89
Gerlach, Sp. gw. Salzlosungen,
324'4
257-4
228-0
65-1
118-04
117-571
113-32
108-70
96:—
351-5
2787
246-8
56-5
126-24
125-711
121-05
115-56
O
ats.
W.
379-9
302-4
268'3
58'5
138-76
138-186
133-22
127-08
1007
1
5-26
397-9
316'4
280"7
62-5
166-98
166-256
159-67
152-55
102-3
);
11-1
433'1
344-7
306 "3
64-5
182-12
181-387-
174-92
167-32
105-1
,1
17.7
471 "2
375 '6
333'3
65-6
201-07
200-257
193-07
184-67
109-2
25-0
517'4
412'2
366'5
68-9
70-5
222-29
238-24
221-389
237-254
213-11
228-38
204-42
218-52
114-0
119-9
"
33-3
42-9
558-3
444-6
395-5
604"3
428'2
72-5
260-60
259-458
249-05
237-90
127-1
»
53-9
660'4
526-8
469-2
75-4
293-30
292-082
281-08
269-05
135-6
»
66-6
697-6
556-7
495-3
78-7
81-5
336-33
376-85
334-940
375-336
322-63
361-78
308-35
346-50
Tammanu, W. 24, 546 ; B.r. 13,
752-1
600-1
535-9
83-4
86-0
406-57
450-34
404-879
448-461
389-53
43179
372-67
412-53
Tension of
sm : —
Tension of Solutions.
Magnesium chloride, MgCl3.
88-7
92-6
500-00
579-67
497-916
577-282
479-50
556-21
457-97
531-48
pure H2O.
8-01 W.
14-49 W.
Gerlach, Sp. gw. Salzlosungen,
98:—
94-9
631-44
628-756
604-89
577-47
mm.
mm.
mm.
o
ats.
W.
100-3
768-20
765-111
737-42
706-30
59-5
....
51-5
101-6
1
11-1
67-8
63-1
58-8
106-2
B
25-0
77-4
72-4
67-9
115-6
42-9
Tammann, W. 24, 530 ; B.r. 18, 313 :—
92-1
85-8
80-3
Tension of pur.
Tension of Solutions.
100-8
94-0
87-5
Tammann, W. 24, 551 ; B.r. 18,
H2O. 13-82 W.
26-75 W.
27-34 W.
112-9
104-9
98-6
313:—
126-6
110-4
Tension of Solutions.
mm.
mm.
mm.
mm.
161-3
150-7
141-0
Tension of
74-0
69-7
65-4
65-3
187-2
175-1
163-6
pure H2O.
12-22 W.
24-24 W.
198-0 185-7
175-0
174-0
207-6
194-1
181-6
mm.
mm.
mm.
249-5 234-6
220-0
218-6
228-1
213-6
100-2
28-0
24-0
378-3 354-9
332-8
331-5
254-5
238-7
222-9
46-5
43-0
40-1
483-8 454-8
425-3
423-8
286-4
266-8
250-4
55-0
51-5
47-5
553-5 519-3
487-5
485-2
324-4
303-3
283-8
65-0
60-5
55-6
7087 666-3
624-9
622-2
351-5
327-8
307-5
75-0
70-2
64-1
758-0 712-7
668-2
665-0
379-9
355-7
332-7
85-7
80-4
73-5
397-9
372-4
348-3
97-8
91-5
84-2
433-1
405-4
379-8
111-8
105-1
96'6
MIXED LIQUIDS AND SALINE SOLUTIONS.
743
Magnesium chloride (continued) : —
Sodium chloride (continued) : —
Sodium chloride (continued) : —
Sodium chloride (continued) : —
Tension of
Tension of Solutions.
o
1 AO.O
ats.
i
W.
17"1?
Jones. 33, 182 :—
Baoult, C.R 87. 167 : 36. 4 :—
pure H2O.
12-22 W.
24-24 W.
iwo «>
105-3
i
ji
Lit
25-0
o
ate.
O
mm.
W.
mm.
mm.
mm.
107-6
»
33-3
108-25
1
sat.
100
755-41
1
125-9
139-4
118-7
131-1
109-0
120-3
Bischoff, Storer's Diet. Sol. 182 :—
154-1
144-9
132-0
o
101-50
ats.
1
W.
5-26
Legrand, A.C. [2], 59, 431 :-
Guthrie, P.M. [4], 49, 6 and 17 :—
175-6
164-5
151-3
103-03
n
11-1
ats.
W.
O
ats.
W.
213-8
201-3
184-1
104-63
»
17'7
O
100-5
1
4-4
100-4
1
0
241-8
228-0
208-9
106-26
)»
25-0
101
7-7
101-0
»
5-55
270-4
254-5
233-7
107-93
)i
33-3
101-5
JJ
10-8
101-2
3)
7-03
299-8
282-4
258-9
107-9 to \
41 "6
102
))
13-4
101-7
»
8-55
329-0
309-7
284-6
108-99 f
j>
102-5
15-9
102-0
»»
10-12
383-4
360-1
331-8
See also Pauchon, O.K. 89, 753 ;
103
18-3
102-4
))
11-74
419-7
395-2
363-6
38, 211.
103-5
20-7
102-6
))
13-41
463-5
497-4
436-4
468-4
402-0
431-2
Karsten, Archiv. 20, 45 ; v., 337 : —
O «,*„ TXT
104
104-5
»
23-1
25-5
103-0
103-4
))
»)
15-11
16-89
539-5
509-0
469-6
100-21
lUMh
1
1-01
105
27-7
104-0
JJ
18-71
592-4
557-5
514-7
101-10
5-26
105-5
29-8
104-2
)>
20-59
669-3
631-6
582-5
102-38
11-1
106
n
31-8
104-7
)J
22-53
762-1
717-0
663-5
103-83
)»
17-7
106-5
»
33-9
108-8
»
35-6 sat.
103-99
»
177
107
»
35'8
Sea- water from Dover, and contain-
33-14 W.
61-23 W.
105-46
))
25-0
107-5
J>
377
ing 6'58 per cent, solid matter,
mm.
mm.
107-27
I)
33-3
108
J)
39-7
boiled at 100"-6 (760).
28-0
22-3
17-1
108-83
)5
40-8
108-4
?)
41-2
46-5
36-8
29-5
55-0
43-8
35-0
WUUner, P.A. 103, 542 :—
65-0
51-7
41-5
Tension of Solutions.
75-0
59-2
47-4
Tension of
85-7
67-9
53-8
°C.
pure water
1 W.
5 W.
10W.
15 W.
20 W.
25 W.
30 W.
97-8
77-8
62-3
'
^— —
-
mm.
111-8
89-6
72-2
19-9
17-28
17-13
16-30
15-81
15-01
••««
13-22
125-9
100-8
81-0
24-2
22-45
22-26
21-27
20-37
19-48
....
17-29
139-4
111-5
90-1
29-9
31-36
31-15
30-25
29-31
27-88
....
24-97
154-1
123-0
98-5
30-8
33-02
32-75
30-14
28-85
27-75
26-06
....
175-6
140-7
113-8
35-0
41-82
41-52
40-03
38-71
37-12
33-69
213-8
171-5
138-7
35-4
42-74
42-43
39-40
37-97
36-73
34-99
....
241-8
194-4
157-0
39-5
53-43
53-06
....
49-66
47-97
46-28
44-10
270-4
218-0
176-8
40-9
57-61
57-23
55-54
54-05
51-86
....
46-00
299-8
241-6
196-0
40-9
57-61
57-23
55-59
54-09
52-39
50-13
...*
45-76
329-0
265-1
215-5
42-6
62-97
62-55
58-81
57-02
54-64
51-96
«••«
383-4
309-3
252-5
44-8
70-27
69-82
68-08
66-15
63-47
..*
»•*
59-18
4197
339-3
277-2
45-7
73-98
73-50
69-11
67-13
64-56
61-58
....
463-5
374-8
307-3
48-4
84-36
83-80
81-49
79-20
76-43
72-74
....
66-52
497-4
402-9
329-7
49-1
87-93
87-36
....
82-29
79-81
76-44
73-07
....
539-5
438-7
359-9
49-8
91-09
90-50
88-25
85-28
82-11
79-73
....
72-89
592-4
480-7
395-1
52-5
104-49
103-87
101-41
98-34
95-82
92-05
....
83-57
669-3
545-0
449-1
53-8
110-87
110-18
....
103-84
101-27
96-62
93-15
....
762-1
621-2
514-7
54-1
112-59
111-88
109-12
105-95
101-98
99-03
....
90-41
56 '6
126-84
126'04
118-33
115-15
110-69
106-65
Sodium chloride, NaCl:
Legrand, Gm. 1, 269 ; iii., 89 :—
57-9
59-0
60-6
134-88
142-01
152-99
134-05
141-18
152-07
130-83
137-89
126-77
134-03
142-61
123-80
129-48
139-22
118-26
125-33
130-34
108-04
0
108-4
ats.
1
W.
41-2
60-9
155-09
154-15
....
145-00
142-81
136-30
131-55
....
61-2
157-29
156-34
152-54
143-83
137-60
....
Griffiths, Q.J.S. [1825], 18, 90 :—
62-2
165-07
164-04
....
154-80
144-56
139-17
....
0
ats.
W.
63-8
177-11
176-08
....
167-18
162-33
156-35
149-73
106
1
30 sat.
64-7
184-45
183-40
....
173-28
169-54
....
158-60
....
Gerlach, Sp. gw. Salzlosungen, 93 : —
64-8
185-27
184-18
175-39
170-25
163*82
157-30
....
0
ats.
W.
67-8
211-73
210-52
198-79
193-95
....
181-66
....
100-9
1
5-26
67-9
212-67
211-44
....
200-82
194-60
186-23
182-41
....
101-9
»
111
68-6
219-36
218-00
212-53
206-52
201-56
191-87
....
744
VAPOUR TENSIONS AND BOILING POINTS OP MIXED SUBSTANCES:
Sodium chloride (continued) :—
Rubidium chloride (continued) : —
Tension of
Tension of Solutions.
Tension of
Tension of Solutions.
O ft
jure water.
1 W.
5W.
10W.
15 W.
20 W.
25 W.
SOW.
pure H2O.
15-08 W.
34-93 W.
mm.
mm.
mm.
mm.
68-7
220-24
218-99
....
208-20
201-93
194-65
....
66-4
63-2
59-6
72-2
256-27
254-76
....
241-76
234-85
226-07
216-49
80-0
77-0
72-5
75-3
292-20
290-50
....
275-73
....
258-00
247-06
....
91-2
87-7
82-2
75-5
294-66
292-88
....
277-69
....
258-65
248-00
105-9
101-4
95-0
78-6
335-01
333-14
....
296-07
285-72
...»
116-8
112-1
104-9
82-2
388-33
386-09
....
366-75
....
342-13
328-92
....
133-2
127-9
120-3
85-7
445-09
442-48
....
419-79
....
392-51
379-19
148-8
143-1
134-4
88-5
496-15
493.30
467-51
....
436-21
....
169-3
161-9
152-4
91-2
549-92
546-64
534-08
517-55
....
483-22
....
187-4
180-6
169-8
92-0
566-76
563-32
....
532-93
....
497'21
216-1
207-6
195-4
92-0
566-76
563-19
....
532-52
514-92
492-00
....
242-6
233-0
219-8
100-5
775-40
770-95
730-50
712-48
682-99
284-2
273-1
257-3
100-7
779-26
774-46
....
729-95
....
684-27
....
315-2
302-6
285-8
337-4
324-1
305-1
Tammann,
Tension of
pure H2O.
W. 24, 537 ; B.r. 18,
313 :—
Tension of Solutions.
Tension of
pure H2O.
mm.
KAQ-O
Tension of Solutions.
Ammonium
Tammann,
Tension of
chloride (continued) : —
W. 24, 544 ; B.r. 13,
313:—
Tension of Solutions.
360-2
385-2
414-0
448-3
473-1
346-8
370-9
398-5
431-1
455-7
326-2
349-0
374-8
405-6
4287
35-66 W.
mm.
14-78 W.
21-94 W.
O\JO O
541*5
413"5
pure H20.
6-06 W.
24-38 W.
502-5
484-5
456-1
mm.
mm.
mm.
88-6
80-7
76-0
598-1
457-9
mm.
mm.
mm.
584-9
563-8
530-6
103-2
93-3
88-7
670-4
512-6
43-2
37-4
654-2
630-4
594-1
121-4
110-9
104-9
770-9
590-1
57-1
....
49-3
695-1
668-3
630-0
142-5
129-8
122-3
72-7
....
62-2
768-5
737-8
695-2
ieri
177-4
146 "8
162-0
139-.3
151-1
Ammonium chloride, NBUC1.
99-7
238-8
....
85-6
205-3
43-23 W.
76-51 W.
194-8
218-9
177-5
199-0
167-8
188-5
Berzelius,
o
Lehrbuch, J
ats.
, 280 :—
W.
305-0
366-3
295-7
354-2
262-9
315-6
40-2
mm.
35-7
mm.
31-3
245-9
224-7 '
211-3
114-2
1
88-9 sat.
542-5
525-3
467-7
47-0
40-7
36-4
285-9
292-5
260-2
266-8
246-1
252-4
Griffiths, Q. J.S. [1825], 18, 90 :—
581-8
673-0
564-3
653-5
502-1
581-6
57-0
66-4
49-7
57-6
44-1
51-2
323-2
294-6
278-9
o
ats.
W.
768-1
744-4
664-9
80'0
69'5
62'1
417-1
381-1
360-3
113-5
1
100 sat.
91'2
79'3
70"3
431-4
472-3
393-5
430-6
371-7
407-1
Gerlach, Sp. gw. Salzlosungen, 97 : —
28-52 W.
48-04 W.
105-9
116-8
91-6
101-3
81-2
89-5
503-3
541-5
598-1
459-0
494-6
5467
433-8
467-7
516'9
0
101-7
104-4
ats.
1
it
W.
11-1
25-0
43-2
57-1
mm.
36-4
48-2
mm.
43-0
133-2
148-8
116-0
129-6
102-9
115-0
670-4
770-9
611-9
703-7
5787
666-6
Legrand, A.C
o
101
!. [2], 59, 43f
ats.
X
' ; iii., 89 :—
W.
7'8
72-7
99-7
238-8
60-5
83-0
198-8
54-7
74-6
177-8
169-3
187-4
216-1
147-4
162-8
189-0
130-9
145-2
168-6
305-0
254-8
227-6
242'6
212-1
188-0
35-66 W.
102
»
13-9
366-3
305-1
272-2
284-2
247-9
220-4
mm
103
»
19-7
542-5
452-7
402-6
315-2
275-4
243-6
88-6
66-7
104
»
25-2
581-8
485-6
337-4
294-9
261-6
103-2
78-2
105
»
30'5
673-0
562-8
360-2
315-1
....
121-4
92-0
106
»
35-7
768-1
642-3
385-2
336-9
299-3
142-5
108-4
107
»
41'3
414-0
362-2
321-7
161-1
121-6
108
H
47-3
448-3
391-6
347-5
177-4
194-8
218-9
134-8
148-2
166-2
109
110
111
1)
53-5
59-9
66-4
Rubidium chloride, RbCl.
Tammann, W. 24, 536 ; B.r. 18,
Q1 Q .
473-1
502-5
584-9
414-4
440-3
512-2
367-5
391-2
455-2
245-9
285 '9
186-8
112
113
»
73-3
80-5
Tension of
Tension of Solutions.
654-2
695-1
574-0
609-6
508-5
540-9
292-5
222-2
114
,,
88-1
pure H2O.
15-08 W.
34-93 W.
768-5
673-2
598-7
114-2
88'9 sat.
•MMM
- ----- -
__ —
323*2
246*5
4.1 7*1
on Q.K
"Ronnlt P T> Q*7 1 an . Oft A .
mm.
AO9
mm.
QQ.Q
mm.
*±L 1 i
431-4
oiy t>
329-0
-tvHOUll, V^.
mm.
W.
*±\J —
47-0
oo o
45-3
42-6
472-3
359-8
100
755-71
1
57-0
54-4
51-3
MIXED LIQUIDS AND SALINE SOLUTIONS.
745
Strontium chloride, SrCl2.
Strontium chloride (continued) : —
Barium bromide (continued) : —
Hydrobromic acid, HBr.
Kremers, P.A. 92, 499 :—
Tension of
Tension of Solutions.
Tension of
Tension of Solutions.
Storer, Diet. Solubilities, 75 :—
0
ats.
pure H2O.
41-13 W.
pure H2O.
67-03 W.
99-83 W.
o
ats.
114
1
sat.
b. 100
1
sat.
mm.
mm.
mm.
mm.
mm.
a. 100
more dil.
Legrand, A.C. [2], 59, 436 ; iii., 89:—
160-4
139-0
258-5
216-5
192-7
0
ats.
W.
188-6
164-4
296-9
247-8
221-1
101
1
167
212-1
185-8
332-8
279-7
249-0
Potassium bromide, KBr.
102
„
25-2
244-7
2135
370-0
310-1
276-0
Kremers, P.A. 97, 15, 20 :—
103
„
32-1
285-3
250-2
418-8
351-3
313-6
0
ats.
104
„
37-9
336-7
293-6
474-0
397-8
355-8
112
1
sat.
105
»
43-4
382-5
334-8
517-2
435-2
389-3
Kaoult, C.E. 87. 169 : 36, 4 :—
106
.,
48 '8
415-0
363-1
561-1
471-3
422-2
107
H
54-0
488-4
428-6
608-0
511-5
458-4
o
100
mm.
757-64
1 W.
108
11
59-0
527-3
462-8
616-6
518-8
464-9
109
„
63-9
599-2
526-2
658-9
553-0
496-9
Tammann, W. 24, 530 ; B.r. 18,
110
„
68-9
652-1
571-9
699-4
587-9
528-2
313 :—
111
1 1 o
. »
74-1
760-1
669-0
764-0
641-3
578-5
Tension of
Tension of Solutions.
ua
113
»
85-3
pure H2O.
24-63 W.
35-40 W.
Ql -9
Barium bromide, BaBr,.
Calcium bromide. CaBr2.
))
yi _
' &
mm.
mm.
mm.
115
97-5
Kremers, P.A. 99, 43 :—
Tammann, W. 24, 553 ; B.r. 18,
196-8
184-9
178-6
116
104-0
0
ats.
313:—
242-8
227-7
220-1
117
„
110-5
113
1
sat.
Tension of
Tension of Solutions.
298-0
278-5
269-3
1 17*85
»
117'5sat.
Tammann, W. 24, 552 ; B.r. 18,
pure H2O.
26-32 W.
46-70 W.
380-8
502-3
356-0
469-5
343-6
453-2
Tammann, W. 24, 549 ; B.r. 13,
313:—
mm.
mm.
mm.
559-0
522-8
503-7
313:—
Tension of
Tension of Solutions.
63-0
59-0
54-1
639-2
598-8
576-5
Tension of
Tension of Solutions.
pure H2O.
22-47 W.
46-04 W.
80-8
Qft-fi
75-1
91 "8
69'3
85 "0
769-4
718-1
695-0
pure H2O.
10-6 W.
26-6 W.
mm.
mm.
mm.
i7O U
120-9
112-8
104-3
57-6
54-6
51-2
159-4
148-3
139-1
44-45 W.
68-57 W.
mm.
mni.
11 LI) L.
27-2
MM
24-2
73-4
69-4
65-2
182-8
170-7
159-7
111 m.
mm.
40-9
....
37-4
87-8
82-9
78-2
213-2
199-0
186-0
196-8
173-0
161-6
58-1
51-9
101-4
96-2
89-9
241-1
224-1
209-6
242-8
213-0
199-4
71-6
65-8
121-3
115-9
107-9
273-3
254-9
239-0
298-0
261-1
243-4
84-6
77-4
141-3
135-1
125-9
324-3
302-4
284-1
380-8
332-7
310-0
99-8
96-5
91-3
162-2
154-7
144-5
365-1
340-4
319-6
502-3
438-0
406-9
112-4
109-0
102-9
195-2
186-7
174-6
411-9
384-7
361-4
559-0
488-0
452-8
127-0
123-4
116-4
227-3
216-8
202-5
495-7
462-0
434-9
639-2
558-5
517-5
160-4
155-4
146-6
258-5
246-9
231-3
554-4
518-7
486-8
769-4
671-4
.**>
188-6
183-7
173-2
296-9
283-5
264-5
632-2
590-4
554-2
212-1
244-7
206-5
238-6 .,
194-5
224-8
332-8
370-0
3187
352-9
298-3
329-6
680-3
775-6
634-6
723-2
596-9
680-0
Lithium bromide, LiBr.
41S-R
d.OO'4
O*7K -O
Tammann. ibid. : —
285-3
336-7
277-9
327-5
262-5
308-6
110 o
474-0
*±\J\J 4t
452-1
424-6
106-5 W.
150-0 W.
Tension of
Tension of Solutions.
382-5
372-2
352-2
517-2
494-3
464-2
mm.
mm.
pure H2O.
19-39 W.
34-90 W.
415-0
403-6
381-7
561-1
535-8
503-2
63-0
43-8
37-4
488-4
475-2
449-5
608-0
581-1
544-6
80-8
55-7
47-8
mm.
23'4
mm.
mm.
18-8
527-3
513-1
4857
616-6
590-1
552-3
98-6
68-1
58-3
39"4
34'5
30'7
599-2
583-7
552-5
658-9
630-2
590-4
120-9
83-7
72-0
54'5
48'6
43-5
652-1
632-9
600-7
699-4
668-2
626-6
159-4
•111-3
95-8
7Q-1
71'6
64-7
760-1
739-1
702-7
764-0
728-4
685-3
182-8
127-4
110-5
1 f JL
96-1
87-0
78-5
67-03 W.
99-83 W.
213-2
149-5
129-0
108-4
98-2
88-9
41-13 W.
241-1
168-6
145-9
119-1
108-3
98-3
27-2
mm.
22-8
57-6
73-4
mm.
47-3
60-8
mm.
41-9
55-0
273'3
324-3
365'1
191-3
228-0
257-0
165-9
198-3
224-2
148-5
172-7
135-1
158-0
123-4
144-8
40-9
68-1
71-6
84-6
99-8
112-4
35-3
49-5
62-3
73-1
86-5
97-8
87-8
101-4
121-3
141-3
162-2
195-2
72-8
84-4
100-6
117-3
135-2
162-5
64-8
74-6
89-3
104-2
120-0
144-4
411-9
495-7
554-4
632-2
680-3
775-6
290-9
352-8
393-2
448-7
484-7
555-5
253-8
310-3
344-4
393-4
427-7
504-0
190-6
204-9
220-5
248-9
270-5
285-3
01 7.1
174-7
187-6
202-4
228-8
249-2
262-2
291 '8
159'1
170-8
183-5
208-7
226-9
238-9
266'1
127'0
nn-fi
227-3 189'3
168 -7
Ol 1 1
5c
746
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES:
Lithium bromide (continued) : —
Magnesium bromide (continued) : —
Sodium bromide (continued) : —
Ammonium bromide (continued) : —
Tension of
Tension of Solutions
Tension of
Tension of Solutions
Tension of
Tension of Solutions
Tension of
Tension of Solutions.
pure H2O.
19-39 W.
34-90 W
pure H2O.
18-23 W.
32-41 W.
pure H2O.
18-24 W.
31-93 W.
pure H2O.
55-60 W.
60-82 W.
mm.
mm.
mm.
mm.
mm.
mm.
mm.
mm.
mm.
mm.
338-9
mm.
311-4
mill.
283-7
174-6
166-4
157-5
104-8
98-5
92-6
62-9
51-3
50-1
369-4
340-1
309-9
193-9
185-5
175-8
125-7
118-4
111-5
91-3
74-6
72-8
385-7
354-8
323-7
223-6
214-0
203-3
136-6
128-6
120-7
121-9
99-4
96-7
408-5
375-3
342-7
260-0
247-5
235-2
150-0
141-4
1327
166-9
136-6
133-5
461-9
424-3
387-6
286-4
271-8
258-5
167-0
157-2
147-7
222-2
183-4
178-1
506-3
464-1
424-3
313-1
298-0
282-7
188-3
177-2
166-2
362-4
296-4
290-3
538-8
494-2
451-7
340-9
324-6
308-7
211-2
198-0
186-0
463-9
378-6
370-8
578-5
530-9
485-7
375-8
357-1
339-4
222-0
208-5
195-6
550-0
449-7
440-5
628-2
576-5
527-3
435-1
412-9
393-0
243-7
228-2
214-5
777-8
635-1
622-0
672-1
616-5
564-5
475-1
452-4
429-9
281-7
264-2
247-8
765-7
703-1
642-8
539-3
512-4
487-5
348-5
326-8
306-2
593-8
564-6
537-2
383-6
359-7
337-5
671-5
640-1
609-6
431-3
404-1
379-7
Strontium bromide, SrBr2.
51-82 W.
79-89 W.
718-7
682-6
649-8
481-8
451-9
428-1
Tammann, ibid. : —
mm.
mm.
758-7
720-8
686-8
541-3
506-6
475-7
Tension of
Tension of Solutions.
23-4
16-0
12-9
606-8
568-8
533-4
pure H2O.
20-24 W.
43-15 W.
39-4
27-7
21-9
50-77 W.
88-10 W.
682-8
640-5
601-5
54-5
39-3
31-2
768-9
719-9
675-6
mm.
mm.
mm.
79-1
57-9
46-3
mm.
mm.
75-7
72-6
68-5
961
70-3
56-2
22-8
18-2
15-2
41-01 W.
57-55 W.
91-6
86-7
82-6
108-4
79-5
64-2
28-8
23-1
19-5
mm
Ill Til
113-0
107-8
102-2
119-1
88-4
71-1
36-6
29-5
24-4
67-2
56-9
51-7
130-6
126-2
118-9
148-5
110-3
89-6
45-4
36-6
30-6
72-2
60-9
55-3
153-7
147-4
138-9
172-7
129-6
104-9
54-5
44-5
36-9
81-0
68-6
62-6
174-7
169-1
159-1
190-6
142-3
114-8
69-1
56-3
47-0
87-7
73-5
67-0
198-2
190-6
180-4
204-9
152-7
123-8
88-2
72-5
60-4
104-8
88-7
80-4
232-1
223-2
210-7
220-5
164-3
133-5
106-7
87'4
72-9
125-7
106-5
96-3
266-4
255-9
241-3
248-9
186-4
150-8
135-0
110-8
93-0
136-6
115-2
104-1
291-9
281-1
265-6
270-5
202-9
165-0
146-1
120-8
101-3
150-0
126-5
114-5
329-5
317-3
299-2
285-3
213-9
172-7
174-6
144-0
120-8
167-0
140-6
127-4
363-6
348-8
330-1
317-1
238-0
192-9
193-9
160-8
135-3
188-3
158-3
143-5
431-5
413-8
391-1
338-9
254-6
206-4
223-6
185-2
156-0
211-2
178-7
160-7
484-9
466-6
441-3
369-4
277-3
225-2
260-0
219-4
182-4
222-0
186-0
1687
550-0
527-7
499-4
385-7
289-4
235-4
286-4
241-3
200-8
243-7
204-4
185-1
616-2
592-2
560-4
408-5
307-0
250-3
313-1
263-3
219-6
281-7
236-3
213-2
706-0
679-0
643-3
461-9
347-2
282-5
340-9
286-9
239-6
348-5
292-5
266-1
774-2
744-3
702-4
506-3
380-3
310-1
375-8
314-5
263-9
383-6
322-0
290-9
538-8
405-0
330-5
435-1
364-3
306-9
431-3
361-7
331-5
71-95 W.
134-5 W.
578-5
434-6
475-1
397-6
335-4
481-8
403-5
366-4
•
628-2
472-6
....
539-3
451-4
381-4
541-3
453-4
410-1
75-7
mm.
62'7
mm.
50-8
672-1
506-0
MM
593-8
497-2
421-2
606-8
508-9
462-1
91'6
75 '6
61 '3
765-7
577-5
671-5
562-3
478-2
682-8
572-6
519-5
113-0
94-5
77"!
718-7
602-1
511-2
768-9
644-7
586-1
130-6
109-4
89-5
TVTfi rfnpcintYi HVOTYII HP "M"r*R»»
758-7
635-8
541-1
1 ^Q-*7
1 OQ'/i
1 f\t^' \
•LVAnltJIitjol 14.111 ML Uilll LIL/ j .» 1 „ 1 » 1 ...
Tammann, ibid.: —
Sodium bromide. Na.Kr.
Ammonium bromide, NHJBr.
lOo /
174-7
Izo 4
143-8
.LOO 4
120-3
Tension of
pure H2O.
Tension of Solutions.
Jremers, P. A
o
J
. 97, 14, 20 ;
of g
v., 331 :—
Tami
Tension of
nann, ibid.: —
Tension of Solutions.
198-2
232-1
165-8
194-2
136-4
160-0
18-23 W.
32-41 W.
266'4
222'7 •
184"0
1 "
121
1
sat.
pure H2O.
14-52 W.
28-87 W.
mm.
mm.
mm.
291-9
244-1
202-7
22-8
21-2
20-2
Tammann, W. 24, 538 ; B.r. 18,
mm.
mm.
mm.
329-5
275-8
228-4
28-8
27-3
25-5
313:—
62-9
60-3
56-9
363-6
304-4
253-0
36-6
34-5
32-5
Tension of
Tension of Solutions.
91-3
87-1
82-2
431-5
361-8
301-5
45-4
42-7
40-4
r^n*.rt TT f"l
121-9
116-1
110-2
484-9
408-2
340-3
54-5
51-3
48-7
pure H2U.
18-24 W.
31-93 W.
166-9
159-3
151-2
550-0
461-3
385-4
69-1
65-2
62-0
mm.
mm.
mm.
222-2
212-7
201-3
616-2
518-5
433-0
88-2
83-7
79-3
67-2
63-0
59-1
362-4
345-7
328-0
706-0
594-4
4977
106-7
100-8
95-5
72-2
67-8
63-5
463-9
442-6
420-0
774-2
653-2
548-5
135-0
127-5
121-4
81-0
76-3
'71-4
550-0
525-7
498-4
146-1
139-3
131-8
87-7
82-2
77-0
777-8
741-0
702-9
MIXED LIQUIDS AND SALINE SOLUTIONS.
747
Potassium iodide, KI.
Lithium iodide (continued) : —
Sodium iodide (continued) : —
Sodium silicofluoride,
Baup, iv., 705 :—
Tension of
Tension of Solutions.
Tension of
Tension of Solutions.
Na2SiFe.
0
120
ats.
1
sat.
pure H2O.
11-16 W.
32-7 W.
pure H2O.
13-22 W.
43-97 W.
Stolba, J.
O
p., 90, 193
ats.
v., 271.
Gay Lussac in Thomson's system,
mm.
150-6
mm.
146-2
mm.
135-9
mm.
430-9
mm.
4197
mm.
379-5
101
1
sat.
o
120
1O.51 : — •
ats.
1
sat.
183-1
209-9
253-6
177-3
203-9
245-9
165-6
189-9
229-8
470-9
529-2
582-3
458-0
5157
566-2
415-0
467-2
513-1
Potassium hydroxide, KOH.
Griffiths, Q.J.S. [1825], 18, 90 :—
Kremers
P. A. 97, If
>, 20 :—
290-5
282-4
263-7
643-6
626-6
567-7
0
begins 158
ats.
1
sat.
o
"1 1 Q
ats.
326-4
317-0
295-8
693-5
673-1
609-9
119
.
sat.
369-3
358-4
334-8
731-2
642-0
Dalion, New System, 2, 476 ; cf.
Eaoult, C.B. 87, 169 ; 36, 4 :-
423-2
411-8
384-1
771-5
748-1
677-8
Storer, Diet. Sol. 452 :—
O
mm.
458-7
445-7
416-4
'
*
100
758-3
1 W.
508-0
491-9
459-7
100"56
•Hk
.
4"9
Tammann W 9il isi --Ri- is 9i<*--
581-0
5647
527-4
57-48 W.
86-86 W.
101-11
10'5
Tension of
Tension of Solutions.
660-4
760-9
641-1
738-9
599-2
690-7
34-1
mm.
28-7
mm.
24-9
101-66
103-33
M
14'9
19-3
pure H2O.
13-09 W.
35-97 W.
39-5
33-2
28-7
104-44
24'2
mm.
mm.
mm.
57-65 W.
64-43 W.
50-5
42-2
36-7
106-66
30-5
37-1
36-3
34-6
mm.
mm.
72-3
60-3
52-3
109-44
35-7
60-2
59-0
56-2
41-8
33-5
31-2
84-3
70-7
61-0
112-22
M
41-6
77-5
76-0
72-4
63-0
51-1
49-2
92-0
777
67-0
115-56
D
47-9
98-0
95-7
91-2
84-8
69-1
66-7
108-9
91-3
79-0
118-89
M
52-4
107-3
104-8
99-8
1207
99-3
95-9
125-6
105-2
91-3
123-89
58-2
132-4
....
123-6
150-6
124-8
119-5
138-2
115-9
100-3
129-44
m
65-5
158-8
154-3
147-4
183-1
152-9
1457
155-2
129-9
112-5
135-56
75-1
250-9
245-3
2327
209-9
173-5
167-8
181*3
151-8
131-6
143-33
n
87-6
295-5
289-3
274-3
253-6
207-2
202-8
217-3
181-6
158-3
160
104-5
343-4
335-0
316-9
290-5
240-9
233-0
240-2
201-0
174-1
188-22
y
131-5
410-9
401-9
380-7
326-4
270-8
262-0
265-2
2217
192-2
215-56
1747
529-6
518-2
490-7
369-3
307-5
296-6
296-7
247-5
214-3
315-56
262-3
601-8
589-2
558-4
423-2
352-4
340-0
360-2
300-9
261-1
red heat
n
525-0
676-2
628-5
458-7
381-5
369-1
392-1
327-8
284-0
778-1
759-0
720-0
508-0
4217
408-2
430-9
359-7
312-3
Cf. also Wullner, P.A. 110, 566,
•ifil •(!
xao.q
4fi7-7
47OQ
3927
341-3
568, where a large number of data
66-61 W.
96-34 W.
UO1 \J
660-4
550-3
531-8
re < U {7
529-2
442-7
384-9
are given.
37-1
mm.
327
mm.
30'6
760-9
634-3
613-4
582-3
643-6
485-7
537-7
422-8
468-4
* Of K2O to 100 pts. water.
60-2
77-5
98-0
52-8
67-4
84-6
48-9
62-4
77-9
Sodium iodide, Nal.
Kremers, P.A. 97, 14 ; v., 340 :—
693-5
731-2
771-5
578-7
609-1
643-0
503-0
529-3
560-8
Sodium hydroxide, NaOH.
Griffiths, Q.J.S. [1825], 18, 91 :—
o ats.
107-3
93-2
85-9
o
ats.
216
i
sat.
132-4
158-8
250-9
115-5
137-1
2157
106-5
125-8
198-2
141 1 sat.
Tammann, W. 24, 539 ; B.r. 18, 313 :—
Tension of Tension of Solutions.
Ammonia, NH3.
Dalton, New System, 2, 422.
Osann, v., 339 ; cf. Storer, Diet. Sol.
454 :— *
0 ats. W.
295-5
343-4
253-9
293-5
233-3
269-6
pure H2O.
o
— 3-3
ats.
1
W.
54-5
130
i
58-2
13-22 W.
43-97 W.
410-9
351-9
323-2
mm.
mm.
mm.
+ 3-3
"
48-3
Dalton, New System, 2, 496 ; cf.
529-6
451-2
415-4
50-5
48-6
44-5
10-0
42-6
Storer, Diet. Sol. 454 :—
601-8
5117
471-0
72-3
69-7
63-9
16-6
37-6
0
ats.
W.
676-2
578-5
530-4
84-3
81-5
74-5
23-3
32-8
100-56
1
4'9
778-1
663-8
92-0
89-5
817
30'0
28-5
101-11
..
97
108-9
105-4
96-2
36-6
24-7
102-78
»
14-9
Lithium iodide, Lil.
125-6
....
110-6
43-3
21-1
104-44
»
19-0
Tammann, ibid. : —
138-2
134-0
132-1
50-0
17-8
106-66
»
23-4
Tension of
Tension of Solutions.
155-2
181-3
150-2
176-2
137-9
160-0
56-6
fi'V'l
»
147
11-7
108-89
11278
;;
29'9
35;1
pure H2O.
11-16 W.
32-7 W.
217-3
211-0
191-4
oo o
70
9-0
116-66
•
40-8
mm.
mm.
mm.
240-2
233-5
212-0
78-3
6-6
120-00
N
44-9
41-3
40-0
37-1
265-2
258-2
234-1
86'1
4-3
123-89
»
51 '5
63-0
60-9
56-4
296-7
288-2
261-3
Ql-l
129-44
„
58-2
84-8
82-4
76-4
360-2
350-3
318-6
• ' 1 1
"
137-78
M
70-1
1207
117-1
108-8
392-1
381-8
346-1
148-89
,)
87'3
5c 2
748
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES:
Sodium hydroxide (continued) : —
Sodium chlorate, NaC103.
Sodium chlorate (continued) : —
Potassium bromate, KBrO:i.'
o
ats.
W.
Kremers, P.A. 92, 499 ; 97, 21 :—
Tammann, W. 24, 543 ;
Kremers, P.A. 92, 500 ; 97, 5, 21 :—
204-44
1
116-5
0
ats.
B.r. 13, 313:—
o
ats.
315-56
.,
174-7
a. 125
1
sat.
Tension of
Tension of Solution.
102
1
sat.
red heat
,,
350-5
132
T)
sat.
pure H2O.
24-66 W.
53-15 W.
104
,,
sat.
135
,,
supersat.
106
„
supersat.
Cf. also Wullner, P.A. 110, 571,
mm.
mm.
mm.
573, where a large number of data
Wullner, P.A. 110, 579 :—
166
15-4
13-8
are given.
* Of Na2O to 100 pts. water.
Tension of
Solution.
24-9
33-7
23-0
30-8
21-2
27-8
Sodium bromate, NaBr03.
Kremers, P.A. 97, 5 :—
Tension of
Aff.-t
1-1 .Q
17-8
Barium chlorate, Ba(C103-)2.
Temp.
pure H20.
12-5 W.
66-9
61-6
O 1 O
56-1
o
109
ats.
1
sat.
Kremers PA 99 43 •-
mm.
mm.
83-3
76-7
69-9
37°4
48-73
47-58
104-1
95-5
87-1
0
ais.
i
sat.
39-75
54-16
54-56
111-8
102-6
93-6
Potassium iodate, K103.
i.
41-0
57-91
56-16
132-5
122-1
110-8
Kremers, P.A. 94, 271 ; 95, 121 ;
43-2
64-20
62-25
153-2
140-9
128-2
97, 5 ; iii., 303 : —
Perchloric acid, HC104.
45-7
73-98
71-80
172-3
159-0
144-4
0
ats.
Serrullas, A.C. [2], 46, 296 :—
47-5
81-14
78-95
197-0
181-9
165-4
102
1
sat.
ats.
SD ffr
49-4
89'21
86'76
219-3
202-4
183'5
o
200
1
1-65*
51-2
97-62
94-77
246-8
227-5
205-9
Sodium iodate, NalO,.
* Most concentrated solution.
53-3
55-65
108-75
120-89
105-50
117-29
275-9
292-8
255-0
269-2
231-4
244-9
' a
Kremers, 97, 5, 8 ; 99, 444 ; iii.,
306:—
57-45
131-73
127-73
312-6
288-5
263'6
ats.
W.
Potassium chlorate, KC103.
59-3
144-69
140-59
342-8
316-3
286-9
O
102
1
34 sat.
Griffiths, Q. J.S. [1825], 18, 90 :—
62-7
169-25
164-50
374-3
345-8
314-4
o
103-3
ats.
1
W.
66 '6 7 sat.
64-25
65-1
180-37
187-79
175-07
182-39
409-2
496-0
378-8
459-6
344-1
416-1
Silver sulphate, Ag2S04.
67-6
209-89
203-59
541-9
500-6
453-9
Kremers, P.A. 92, 499 :—
Kremers, P.A. 97, 19 :—
69-4
217-12
210-27
585-9
539-1
490-3
o
ats.
o
ats.
71-07
244-09
236-69
645-3
591-9
539-7
100
1
sat.
105
1
sat.
70.9
2K7-42
OKQ.AO
*7("lQ.y<
fiQQ'A
Legrand, A.C. [2], 59, 43^
1 • iii 89 •
ION
75-3
291-17
— • 1.7 \J£l
283-12
/Ut7 T:
OO{7 t
Aluminium sulphate, A12(S04)3.
0
ats.
W.
78-2
329-53
319-13
86-41 W.
136-79 W.
Tammann, W. 24, 558; B.r. 18,
101
1
14-64
81-62
378-34
367-34
313:—
102
„
29-28
84-5
424-61
412-61
mm.
mm.
Tension of
Tension of Solutions.
103
„
43-92
25 W.
16'6 irv
....
pure H2O.
10-54 W.
20-81 W.
1O4.
KQ-K«
24-9 17'7
AV±
104-2
*'
OO U\J
61-50
39-75
54-16
51-26
33-7 23-7
....
mm.
mm.
mm.
41-0
57-91
54-41
45-1
31-6
66-6
65-7
65-7
Eaoult, C.E. 87, 169 ; 86, 4 :—
43-2
64-2
60-15
66-9
46-9
....
83-6
82-5
82-2
0
mm.
W.
45-7
73-98
69-62
83-3
58-4
99-3
97-8
97-6
100
758-18
1
47-5
81-14
76-49
104-1
73-4
126-4
124-7
124-1
Tammann, 1
ff. 24, 53S
; B.r. 18,
49-4
89-21
84-31
111-8
78-6
....
149-7
147-8
147-1
313:—
51-2
97-62
92-22
132-5
92-8
....
175-4
173-6
172-6
Tension of
Tension of Solution.
53-3
108-75
102-40
153-2
107-5
99-0
208-7
206-6
205-2
55-65
120-89
113-14
172-3
120-9
113-8
230-8
228-4
227-2
pure H2O.
11-41 W.
16-58 W.
57-45
131-73
124-23
197-0
136-9
126-0
286-7
284-6
282-8
mm.
mm.
mm.
59-3
144-69
136-54
219-3
153-4
141-0
302-9
300-7
298-6
183-5
180-9
....
62-7
169-25
159-70
246-8
173-0
158-2
346-9
344-7
342-7
203-5
200-2
200-0
64-25
180-37
169-77
275-9
193-1
176-4
372-4
370-1
368-2
243-6
238-6
....
65-1
187-79
177-39
292-8
204-6
186-9
422-3
418-7
416-5
275-3
270-2
270-0
67-6
209-89
197-74
312-6
219-6
200-4
507-6
503-0 •
298-4
292-9
292-4
69-4
217-12
204-27
342-8
239-9
219-5
567-2
562-4
558-4
344-3
337-5
337-1
71-07
244-09
228-79
374-3
262-2
240-5
634-6
629-8
624-9
377-5
368-3
367-3
73-2
267-42
251-52
409-2
286-5
261-7
689-0
684-8
678-6
432-3
421-6
420-1
75-3
291-17
274-47
496-0
346-6
317-0
765-7
759-5
754-0
488'2
476-3
474-8
78-2
329-53
309-53
541-9
379-6
347-0
45-24 W.
72-18 W.
553-9
540-6
538-3
81-62
378-34
356-84
585-9
410-1
374-5
605-9
590-3
588-4
84-5
424-61
388-61
645-3
451-5
412-7
mm.
mm.
677-1
660-7
657-1
763-6
535-6
•*••
66-6
62-5
61-0
771-6
751-2
746-8
83-6
78-8
76-3
99-3
93-2
90-2
126-4
119-0
115-0
MIXED LIQUIDS AND SALINE SOLUTIONS.
749
Aluminium sulphate (continued) : —
Beryllium sulphate (continued) : — •
Copper sulphate (continued) : —
Sulphuric acid (continued) : —
Tension of
pure H2O.
Tension of Solution.
Tension of
pure H20.
Tension of Solution.
Tension of
pure H3O.
Tension of Solution.
B.P.
Sp. gr. at
15°'56.
%so,
45-24 W.
72-18 W.
43-89 W.
64-01 W.
23-16 W.
33-19 W.
mm.
mm.
mm.
mm.
mm.
mm.
mm.
mm.
mm.
o
182-33
1'67
60
149-7
140-8
136-0
347-6
318-2
305-9
408-8
399-6
394-8
1'684
61
175-4
165-8
159-3
401-9
369-0
356-0
463-2
449-2
190'0
1'699
62
208-7
196-5
189-2
444-8
409-6
394-7
519-5
509-2
503-1
194-44
1715
63
230-8
218-3
210-8
502-3
461-6
444-6
573-1
561-4
555-2
199-44
173
64
286-7
272-9
263-8
540-7
498-0
479-8
627-9
613-9
607-4
204-44
1-744
65
302-9
288-0
278-2
589-6
544-0
524-0
682-6
669-7
661-3
210'0
1'757
66
346-9
330-4
319-0
637-6
588-4
566-8
759-5
744-9 736-6
216'33
1'769
67
372-4
356-1
343-2
775-0
7171
692-5
422-3
402-4
389-1
223'89
1-78
68
507-6
482-8
466-5
Ferrous sulphate, FeS04.
230"56
1-791
69
567-2
541-5
524-3
Cobalt sulphate, CoS04.
Griffiths, Q.J.S. [1825 ],18, 90 :—
237-78
1-801
70
634-6
689-0
765-7
606-9
661-2
734-5
588-4
639-1
710-4
Tami
Tension of
pure H2O.
nann, ibid. : —
Tension of Solution.
o
102-2
Nicol, P.M. [
ats.
1
5], 18, 367 ;
W.
177-78 sat.
48, 331 :—
245
252-78
260-56
268-33
1-81
1-819
1-827
1-833
71
72
73
74
33-04 W.
63-86 W.
mm.
~
1
~ — ~ •
f
1 CK»'7 T
276'66
1'838
75
mm.
mm.
mm.
GK J
loo 7 1
3(1 1.
24-7
24-0
22-8
1
169-9 /
285
1-842
76
Beryllium sulphate, BeS04.
39-4
....
37-1
75 {
259-3 \
293-33
1-845
77
Tammaun, W. 24, 558; B.r. 18,
61-9
59-6
56-4
>•
J
301-66
1-847
78
313: —
79-4
76-4
73-2
85 |
392-7 \
394-7 /
„
310
1-848
79
Tension of
Tension of Solutions.
107-6
104-2
997
95
587-8
318-33
1-849
80
pure H2O.
14-96 W.
33-0 W.
154-0
188-1
150-2
182-3
143-6
174-9
Tammann, W. 24, 557 ; B.r., 18,
326-66
1-85
81
mm.
mm.
mm.
220-5
213-5
203-8
313:—
Lunge, B 11, 373,374:—
17-4
....
16-1
261-6
253-7
243-0
Tension of
Tension of Solution.
B.P.
%H3S04.
345
....
296-8
288-4
277-3
pure H2O.
26-47 W.
58-47 W.
51 "8
50'6
48'1
344-1
333-6
321-7
o
ats.
76-1
74-0
71-6
399'6
388-1
373'8
mm.
mm.
mm.
101
1
5
85-4
126-3
83-0
123-2
79-9
118-7
459-1
528-6
444-9
512-9
428-8
494-6
76-2
112-0
73-7
108-7
70-7
104-2
102
103-5
"
10
15
142-9
163-3
200-1
228-8
139-1
159-8
195-7
223-7
135-0
154-5
189-9
216-9
604-9
682-4
763-1
587-5
665-6
743-4
567-9
644-2
720-7
122-9
144-6
176-6
177-0
119-1
140-5
171-5
172-0
114-1
134-6
165-3
165-5
105
106-5
108
110
»
20
25
30
35
255-3
249-3
242-7
207-1
201-1
193-6
114
n
40
296-3
347-6
401-9
289-0
339-5
393-9
281-1
330-3
383-5
Copper sulphate, CuS04.
Griffiths, Q.J.S. [1825], 18, 90 :—
234-4
275-6
323-6
226-8
267-8
314-5
219-4
259-3
304-4
118-5
124
128-5
»
45
50
53
444-8
436-6
425-5
o
102-2
ats.
1
W.
81-82 sat.
361-0
349-6
339-0
133
jj
56
502-3
491-2
478-7
408-8
397-1
385-2
141-5
jj
60
540-7
529-1
516-2
Brandes and Gruner, Archiv, 22,
463-2
450-6
437-4
147
„
62-5
589-6
563-7
169:—
519-5
505-0
489-7
153-5
„
65
637'6
609 -8
0
ats.
W.
573-1
559-0
541-3
161
„
67-5
775-0
759-4
740-0
103-7
1
130-4 sat.
627-9
610-2
593-9
170
„
70
Tammann, W. 24, 557 ; B.r., 18,
682-6
663-6
645-9
174-5
„
72
31 3 : —
759-5
740-1
719-3
180-5
jj
74
43-89 W.
64-01 W.
Tension of Solution.
189
„
76
17-4
mm.
15-7
mm.
14-7
Tension of
pure H2O.
Sulphuric acid, H2S04.
199
207
»
78
80
23-16 W.
33-19 W.
34-5
30-3
29-2
mm.
Tnm.
1 i 1 1 i i.
Dalton, New System, 2, 404; of.
218-5
jj
82
51-8
45-9
43-8
76-2
73-9
73-1
Storer, Diet. Sol. 581 :—
227
i
84
76-1
68-6
65-0
112-0
108-8
107-6
B.P.
Sp. gr. at
%S03.
238-5
„
86
85-4
77-4
72-9
122-9
119-5
117-7
15°'56.
251-5
„
88
126-3
114-3
108-8
176-6
172-4
170-0
o
262-5
„
90
142-9
129-3
123-5
177-0
172-9
170-8
103-33
1-10
10
268
„
91
163-3
148-2
141-9
207-1
201-7
199-6
106-66
1-20
20
274-5
„
92
200-1
182-2
174-4
234-4
228-9
227-6
115-56
1-30
30
281-5
„
93
228-8
208-1
199-6
275-6
269-1
265-9
126-66
1-408
40
288-5
jj
94
255-3
232-7
223-9
323-6
317-1
313-3
143-33
1-52
50
295
„
95
296-3
270-5
259-7
361-0
352-3
48-0
176-66
1-65
58-6
750
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES
Sulphuric acid (continued) : —
Eegnault, A.C. [3], 15, 179:—
Tension of H2SO4.
Temperature.
+HS0
+ 2H3O
+3HSO
+4H20
+5H2O
+7H20
+9HSO
+ 11H20
+ 17H2O
o
mm
mm.
mm.
mm.
mm.
mm.
mm.
mm.
mm.
5
0-105
0-388
0-861
1-294
2-137
3-168
4-120
4-428
5-478
6
0-106
0-409
0-922
1-399
2-296
3-398
4-416
4-787
5-879
7
0-108
0-430
0-985
1-510
2-464
3-643
4-728
5-164
6-300
8
0-110
0-452
1-053
1-628
2-641
3-902
5-059
5-562
6-745
9
0-112
0-476
1-125
1-753
2-829
4-176
5-408
5-980
7-216
10
0-115
0-501
1-200
1-885
3-029
4-466
5-777
6-420
7-712
11
0-118
0-527
1-280
2-025
3-240
4-773
6-166
6-883
8-237
12
0-121
0-556
1-364
2-173
3-463
5-098
6-578
7-371
8-790
13
0-124
0-586
1-454
2-331
3-699
5-443
7-013
7-885
9-374
14
0-127
0-617
1-548
2-498
3-950
5-808
7-473
8-425
9-991
15
0-131
0-651
1-648
2-674
4-215
6-194
7:958
8-995
10-641
16
0-135
0-687
1-753
2-861
4-495
6-603
8-471
9-592
11329
17
0-139
0-725
1-865
3-059
4-793
7-036
9-014
10-222
12-054
18
0-144
0-765
1-983
3-270
5-107
7-495
9-586
10-885
12-820
19
0-149
0-808
2-108
3-492
5-440
7-980
10-191
11-583
13-628
20
0-154
0-853
2-241
3-728
5-792
8-494
10-831
12-317
14-482
21
0-159
0-901
2-380
3-977
6-166
9-039
11-506
13-090
15383
22
0-165
0-952
2-528
4-243
6-561
9-615
12-220
13-904
16334
23
0-171
1-006
2-684
4-523
6-979
10-226
12-974
14-760
17338
24
0-177
1-064
2-849
4-820
7-422
10-872
13-771
15-661
18-397
25
0-184
1-125
3-024
5-135
7-892
11-55,7
14tfl3
16-610
19-516
26
0-191
1-190
3-209
5-469
8-388
12-282
15-503
17-608
20-697
27
0-199
1-258
3-405
5-822
8-914
13-050
16-443
18-659
21-944
28
0-207
1-331
3-611
6-197
9-471
13-862
17-436
19-765
23-260
29
0-216
1-408
3-830
6-594
10-060
14-723
18-485
20-929
24-650
30
0-225
1-490
4-061
7-014
10-684
15-635
19-594
22-154
26-117
31
0-235
1-577
4-305
7-459
11-345
16-600
20-765
23-443
27-666
32
0-245
1-670
4-564
7-933
12-045
17-622
22-003
24-800
29-300
33
0-256
1-767
4-838
8-432
12-785
18-704
23-311
26-228
31-025
34
0-268
1-871
5-127
8-962
13-569
19-850
24-692
27-732
32-847
35 0-280
1-981
5-432 9-524
14-400
21-063
26-152
29314
34-770
Potassium sulphate, KjSO^.
Potassium sulphate (continued) : —
Potassium sulphate (continued) : —
Wiillner, P.A. 103, 546 :—
Kremers, P.A. 99, 43 ; v., 608 :—
Brandes and Brunner ; Brandes,
Tension of
Tension of Solution.
o ats.
103 1
sat.
Archiv, 22, 1
o ats.
17 •
Temperature.
pure H20.
IW.
10W.
4 1 .
W.
5 W.
100-38 1 1
o
mm.
mm.
mm.
mm.
100-63 „ 2
28
28-10
27-976
27-51
26-82
100-75 „ 3
32-2
35-76
35-589
34-87
34-08
Griffiths, Q.J.S. [1825],
18, 90 :—
100-88 „ 4
34-9
41-59
41-392
40-60
39-61
o ats.
W.
101 „ 5
36-7
45-94
45-702
44-75
43-56
101-7 1
21-21 sat.
101-12 „ 6
39-3
52-79
62-563
51-59
50-59
101-25 „ 7
40-1
55-21
54-972
54-02
52-83
101-25 „ 8
42-7
63-35
63-101
62-17
60-79
101-38 „ 9
45-6
73-74
73-398
72-05
. 70-27
Penny, P.M. [4], 10,
406:—
101-5 „ 10
47-2
79-91
79-554
78-13
76-35
o ats.
W.
102-88 „ sat.
49-5
89-73
89-341
87-85
85-77
102-8 1
29 sat.
61-6
99-59
99-202
97-62
95-74
Eaoult, C.E. 87, 169 ; 36, 4 :—
63-1
107-16
106-739
104-99
103-01
W
56-0
123-24
122-818
121-16
118-99
Gerlach, Sp. gw. Salzlosungen, 21 : —
o mm. " •
100 758-47 1
57-6
60-3
133-06
150-90
132-620
150-413
130-90
148-53
128-62
145-96
° ats.
W.
61-5
159-50
158-966
154-16
100-3 1
9-9
See also Pauchon, C.E., 89, 754 ;
63-4
173-95
173-398
171-19
168-43
38, 211.
65-7
192-93
192-305
189-87
186-62
68-5
220-29
219-547
216-64
212-79
MIXED LIQUIDS AND SALINE SOLUTIONS.
751
Potassium sulphate (continued) : —
Magnesium sulphate (continued) : —
Sodium sulphate (continued) : —
Tension of
Tension of Solutions.
Tension of
Tension of Solutions.
Gerlach, Sp. gw. Salzlosungen, 104 : —
,mper
pure H2O.
1 W.
5 W.
10W.
pure H2O.
23-67 W.
31-63 W.
o
, 100-3
ats.
1
W.
5-26
O
mm.
mm.
mm.
mm.
mm.
mm.
mm.
100-8
„
11-1
69-3
226-14
225-436
222-59
219-14
246-0
238-7
235-8
73-5
270-88
270-025
266-54
262-40
299-7
291-7
287-7
Lowel, A.C. [3], 49, 32 ; v., 612 :—
76-3
304-66
303-730
300-12
295-29
346-5
336-8
333-1
O
1037
ats.
1
sat.
77-7
322-84
321-795
317-62
312-39
409-8
398-5
393-9
See also Pouchon, C.R. 89, 759 ; 38,
80-4
360-49-
359-390
355-08
349-39
453-3
440-6
436-5
211:—
81-4
375-34
374-280
370-33
364-44
523-2
508-2
504-2
83-6
403-81
402-516
397-21
391-00
576-2
560-7
Brandes and Gruner. Brandes's
88-5
496-15-
494-725
489-35
481-37
649-4
632-4
626-9
Archiv [1827], 22, 148 :-
89-4
513-56
512-105
505-99
499-30
770-0
750-0
743-2
Parts
90-9
543-72
542-230
536-33
528-76
Na,S04.
95-1
636-12
634-405
627-75
618-78
10H20 to
100-8
782-08
780-274
773-08
763-98
100 parts
100-9
785-12
783-280!
775-62
767-02
Manganese sulphate, MnS04.
0
ats.
water.
Tammann, W. 24, 533 ; B.r. 18,
Lithium sulphate (continued) : —
Brandes, P.A. 20, 575 :—
100-5
100-62
1
1
2
313 :—
Tension of
Tension of Solutions.
102-1
1
sat. (?)
100-62
n
3
Tension of
pure H2O.
lension 01 solutions.
pure H2O.
11-42 W.
14-09 W.
Nicol, P.M. [5], 18, 367;
48 331 •
10075
100-75
„
4
5
11-92 W.
14-68
W.
mm
mm.
mm.
°
11.1111.
100-87
6
mm.
mm.
mm.
305-
2
293-4
290-3
65
167-2
sat.
100-87
7
183-5
179-9
179-4
325-0'
312-0
309-4
75'
256-5
>i
101
g
203-5
196-6
199-2
360-9
346-7
343-3
85
394-7
H
101
"
9
243-6
238-6
238-2
416--
1
399-9
396-3
95
5&1-8 „
101
10
275-3
298-4
292-4
269-
291-
5
2
476-1
531-0
458-2
511-8
453-6
505-7
Tammann, W. 24, 556 ; B.r, 18,
31 3 • —
101-12
101-12
H
11
12
344-3
377-5
337-5
369-8
336-8
367-5
582-5
559-9
555-0
Tension of
Tension of Solutions.
101-25
101 "25
13
432-3
423-0
420-0
pure H2O.
42-15 W.
85-12 W.
101-25
"
15
488-2
477-8
474-9
Magnesium sulphate,. MgS04.
101 "25
16
553-9
542-7
S3&-4
Griffiths ,Q,J.S. [1825], 18, 90:—
mm.
58-9
mm.
56-5
mm.
51-9
101-25
17
605-9
677-1
593-1
664-1
589-6
659-3
o
105-5
ats.
1
W.
135-52
65-9
88-9
63-2
85-3
57-3
78-5
101-37
101-37
»
18
19
771-6
753-3
74&-7
Tammann, W. 24, 554 ;
B.r. 18,313: —
103-6
99-5
91-7
101-37
„
20
Tension of
Tension
of Solutions.
140-9
135-5
127-8
101-37
M
21
Lithium sulphate, Li^O^..
pure H2O.
10-55 W. 22-16 W.
155-3
148-5
138-9
101-5
"
22
Kremers, P.A. 99. 43 : —
'
200-0
192-5
180-8
101-5
»
23
mm
mm.
mm.
241-0
231-7
217-2
101-5
„
24
0
ats.
72-3
71-0
69-8
244-1
235-0
220-3
101-5
25
105
i
sat.
117-2
115-7
113-7
281-9
271-7
255-2
101-5
B
26
Tammann, W. 24, 548 ; B.r. 18,
144-4
142-5
140-5
303-7
293-0
275-4
101-63
;1
27
313
: —
177-2
174-6
171-9
242-7
330-9
311-0
101-63
„
28
Tension of
pure H2O.
Tension of Solutions.
211-2
246-0
299-7
208-6
242-9
296-0
204-9
239-0
292-2
400-5
430-1
473-0
386-6
415-9
456-9
367-1
393-3
436-1
101-63
101-75
105-12
1)
29
30
sat
5-20 W.
8-74 W.
mm.
187-6
258-7
mm.
183-9
253-5
mm.
182-1
250-9
346-5
409-8
453-3
342-5
404-9
448-6
337-4
399-8
442-3
526-9
575-5
620-0
510-5
557-0
600-6
485-2
529-1
572-5
Tammann, W
Tension of
24,540; B.r. 18, 313: —
Tension of Solutions.
305-2
300-5
296-9
523-2
517-7
—
684-6
663-7
639-5
pure H3O.
13-31 W.
20-22 W.
325-0
319-9
316-2
576-2
569-5
562-0
766-4
743-0
720-1
360-9
354-8
350-8
649'^
6
640-5
633-9
mm.
mm.
mm.
60'2
58 "5
57 '0
416-1
409-3
404-8
770-0
760-3
751-4
Rfi'A
476-1
468-6
463-1
70'3
683
DD 1
85'8
83'2
81 -3
531
582-5
522-5
573-2
515-9
566-7
23-67 W.
mm.
31-63 W.
mm.
Sodium sulphate, NaaS04.
Griffiths, Q.J.S. [1825], 18, 90:—
94-8
126-5
91-7
122-9
90-0
120-4
72-3
69-4
68-8
O
ats.
W.
139-5
135-2
132'4
11-42 W.
14-09
W.
117-2
113-4
111-8
100-6
1
45-98 sat.
149-6
145-1
142-3
mm.
mm.
144-4
139-8
138-5
Kremers, P.A. 99, 43 :—
186-5
180-3
177'0
187-6
179-4
177-0
177-2
171-7
169-2
o
ats.
218-8
211-7
207-8
258-7
247-8
245
•7
211-2
204-4
202-1
105
1
sat.
239-7
232-7
228-1
752
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES:
Sodium sulphate (continued) : —
Sodium sulphate (continued) : — Sodium sulphate (continued) : —
Ammonium sulphate,
Tension of
Tension of Solutions.
Tension of
Tension of
Solutions. Tension of Tension of Solutions.
(NH4)2S04.
pure H2O.
13-31 W. 20-22 W.
pure H2O.
37-34 W.
48-84 W. Pure HA 37-34 W. 48'84 W.
Eaoult, C.R. 87, 169 ; 36, 4 :—
„, ~nr
mm.
mm. mm.
mm.
mm.
mm. mm. mm. mm.
o
100
LL1111.
758-25
1
293-4
284-0 278-7
60-2
54-8
537 293-4 266'4 261 '6
328'8
319-1 313-5
70-3
63-9
62-5 328-8 299'8 294'0
368-8
357-4 351-2
85-8
77-9
76-0 368-8 335-3 3291
Tammann, W. 24, 545 : B.r. 18,
414-2
400-6 393-3
94-8
86-1
83-8 414-2 376-5 369'4
313:—
457-9
444-0 436-1
126-5
115-4
113-0 457-9 416-9 409'4
Tension of
Tension of Solutions.
504-9
489-1 480-8
139-5
127-0
124-4 504-9 460-0 451 '3
pure H2O.
13-93 W. 32-89 W.
548-5
531-3 522-2
149-6
136-2
132-9 548-5 500'2 490'2
mm.
mm.
mm.
602-2
585-3 574-8
186-5
169-3
166'0 602-2 550-3 539'4
35-6
34-6
32-9
691-4
669-7 657-8
218-8
198-4
195-0 691-4 630-3 619'3
48-3
47-1
44-7
769-5
744-6 732-2
239-7
218-1
213-7 769-5 702'6 6897
58-7
56-5
54-0
66-0
....
60-7
Wiillner, P.A. .103, 543 :—
75-8
73-5
70-0
Tension of Solutions.
89-2
85'6
81-8
rp • f
1 ng-n
QQ.Q
QQ-Q
Temperature.
xension ot
pure H2O.
1 W.
5 W.
10
W.
15 W.
20 W.
25 W.
lU_i U
117-4
yo o
113-2
t7t> t7
107-8
— —
"
133-6
129-0
122-1
o
mm.
mm
mm
mm.
mm.
mm.
mm.
155-3
150'3
142-6
26-3
25-43
25-35
25-03
24-73
24-23
23-83
....
172'6
166'5
158-2
27'9
27-93
27-843
27-08
26-58
....
28-7
29'57
29-17
28-68
28-19
27-69
27-29
26-90
204-3
197-6
187-3
235 '8
227-4
216"!
32-2
35-76
35-65
35-07
34-57
33-98
33-49
32-99
262 "6
253-7
241'6
35-7
43-43
43-29
42-69
41-99
41-30
40-71
40-21
281"2
271"8
258 "6
39-5
53-46
53-303
52-68
51-89
51-09
50-19
49-50
305-3
295-4
281-2
40-2
54-50
54-345
52-02
51-53
50-84
344-4
333-9
316"7
42-7
63-35
63-195
62-47
61-67
60-88
60-09
59-25
373'1
360'6
343"!
44-7
70-31
70-112
69-23
68-23
67-33
65-49
402 '0
387'9
370'0
45-4
72-58
72-377
70-50
69-31
68-52
6773
441'3
426 '7
407'1
47-2
79-90
79-684
78-80
77-80
76-90
75-90
75-00
482'7
468 "2
445-7
47-6
81-53
81-315
80-35
79-35
78-36
77-27
76-18
543-5
527'0
501'6
49-6
90-18
89-i
»5
MM
85-48
84-54
IM
589-g
569'7
543-2
50-6
93-88
93-639
....
90-22
89-13
87-84
630"0
609"0
580"9
52-5
104-01
103-739
102-63
101-14
99-95
98-67
97-28
683 '9
659'9
630'5
55-1
118-04
117715
116-46
114-84
111-53
109-89
57-1
129-88
129-571
128-30
126-81
125-22
123-64
122-36
762-3
738-0 704-H
58-4
138-14
137-731
136-66
135-08
133-39
131-91
130-43
60-6
152-61
152-249
150-83
148-99
146-98
145-39
143-81
33-20 W.
40-91 W.
61-7
160-96
160-54
158-99
156-76
154-57
152-51
....
mm.
mm.
63-9
177-92
177-49
....
173-38
171-20
169-62
167-54
35-6
32-7
32-1
65-8
193-74
193-231
....
,
...
185-84
183-66
181-74
48-3
44-7
43-6
67-3
205-13
204-63
202-66
199-98
197-42
195-04
192-68
587
53-7
52-6
69-8
231-10
230-547
....
,
...
222-61
220-04
217-48
66-0
60-6
59-9
72-5
259-57
258-929
256-12
253-15
250-09
246-74
243-77
75-8
69-9
68-2
73-9
275-47
274-849
269-26
266-00
263-04
260-08
89-2
81-9
79-9
76-2
303-37
302-672
300-02
296-07
292-69
289-45
286-21
102-0
94-0
91-7
78-7
336-38
335-61
....
...
324-36
320-90
317-45
117-4
107-8
105-0
79-5
347453
346-724
343-43
339-25
335-31
331-76
327-42
133-6
121-8
118-9
81-1
370-79
369-912
366-49
362-03
357-59
353-15
....
155-3
142-7
139-1
84-0
416-29
415-365
406-84
401-81
398-27
393-44
172-6
158-6
155-1
86-5
459-21
458-085
....
447-99
442-18
436-81
430-81
204-3
187-2
183-4
86-8
464-64
463-529
459-14
453-44
447-92
442-50
235-8
216-6
211-4
87-1
470-04
468-865
....
459-12
453-70
448-68
443-26
262-6
241-4
236-1
89-9
623-45
522-
232
517-35
511-57
504-85
499-05
491-95
281-2
258-4
253-2
91-0
545-78
544-57
....
533-63
527-68
521-68
515-48
305-3
281-4
274-9
93-2
592-82
591-
43
585-98
578-47
571-97
564-87
558-31
344-4
317-3
309-9
95-8
657-73
656-205
649-59
642-50
634-73
628-83
619-69
373-1
343-7
336-1
96-5
679-55
678-02
671
75
664-35
....
....
402-0
369-8
362-2
100-1
761-40
759-519
...
732-70
723-80
714-40
441-3
407-4
398-2
100-2
764-80
762-963
755-27
746-43
736-41
728-25
482-7
446-1
436-5
100-6
776-71
774-877
...
758-05
749-21
740-37
731-04
543-5
502-5
491-5
MIXED LIQUIDS AND SALINE SOLUTIONS.
753
Ammonium sulphate (continued) : —
Nickel sulphate (continued) : —
Sodium thiosulphate,
Potassium chr ornate, KoCr04.
Tension of
Tension of Solutions.
Tammann, W. 24, 555 ; B.r. 18,
Na2S203.
Kremers, P.A. 99, 43 :—
pure H2O.
33-20 W.
40-91 W.
616 : —
Tammann, ibid. : —
0
ats.
Tension of
Tension of Solution.
Tension of
Tension of Solutions.
107
1
sat.
mm.
589'6
mm.
544-2
mm.
531-6
pure H.,0.
31-07 W.
62-17 W.
pure H»O.
19-35 W.
32-44 W.
Raoult, C.E. 87, 169 ; 36, 4 :
630'0
581-0
568-5
rani.
mm.
mm.
mm.
mm.
mm.
683-9
629-9
617-1
24-7
24-2
22-6
53-2
50-1
48-3
0
mm.
W.
100
758'38
1
762-3
704-7
691-5
39-4
38-5
36-6
72-6
69-0
66-8
61-9
60-5
57-3
86-6
82-2
79-3
79-4
77-4
73-4
104-5
99-1
95-5
Tammann, W. 24, 533 ; B.r. 18,
107-6
105-0
100-4
125-5
119-6
115-0
313:—
Nickel sulphate, NiS04.
154-0
1 QQ*1
151-1
1 QO.Q
143-2
1 hre .ft
145-5
138-5
133-4
Tension of Tension of Solutions.
Griffiths, Q.J.S. [1825], 18, 90 : —
loo 1
220-5
ioz o
213-8
175 O
204-5
173-9
203-1
164-8
193-4
158-5
186-2
pure H2O.
25-35 W. 38-04 W.
o
ats.
W.
261-6
254-4
244-9
228-4
217-6
208-8
mm.
mm.
mm.
112-5
1
185-71 sat.
296-8
288-8
277-9
261-9
248-5
240-2
64-8
617
59-7
344-1
334-3
322-2
307-9
293-3
282-2
77-9
73-4
70-8
Wullner, P.A. 110, 578 :—
399-6
388-8
375-2
336-4
319-5
309-5
91-2
86-4
83-4
459-1
446-3
430-9
369-5
352-1
338-9
131-9
124-5
120-4
Tension of
Tension of
528-6
514-4
496-5
429-4
409-0
394-3
144-0
137-2
132-2
Temperature.
pure H2O.
Solution.
604-9
588-5
569-4
478-0
455-5
439-0
165-2
157-2
152-0
10 W.
682-4
665-6
643-4
5167
491-3
474-3
187-3
177-5
171-6
o
'Mill
in ni
763-1
742-9
723-1
561-3
533-5
514-5
215-1
204-7
197-5
48-69
86-21
84-48
619-6
588-4
567-0
231-3
219-6
211-9
51-70
100-07
98-44
690-0
654-7
630-9
259-2
OQK«O
246-6
O*7A'Q
239-1
oci .n
58-63
140-06
137-09
759-2
723-5
697-8
zoo 2,
Z/(J y ^.ui a
60-80
153-29
150-37
311-9
296-2 286-8
62-28
65 "64
165-45
191-07
162-19
187-12
Zinc sulphate, ZnSO4.
50-66 W.
76-71 W.
393-0
423-2
372-7 360-8
402-1 389-5
68-45
217-90
213-71
Griffiths, Q.J.S. [1825], 18, 90 :—
mm.
mm.
473-5
437-8
70-60
239-27
235-13
0
ats.
W.
17-2
15-0
12-4
484-9
459-8 446-0
74-38
281-90
277-67
104-4
1
81-81 sat.
32-7
28-3
24-0
516-1
490-9
475-0
78-80
337-74
332-03
43-4
37-7
32-1
558-0
530-3
513-5
82-63
84-80
393-83
429-51
386-43
421-46
Tammann, W. 24, 556 ; B.r. 18,
53-2
72-6
45-9
62-9
39-1
54-0
600-5
645-7
572-2
614-6
555-3
596-1
86-50
459-21
450-56
313:—
86-6
74-7
65-0
' 754-3
715-5
695-2
104-5
89-8
77-3
89'93
524-15
514'82
Tension of
Tension or solutions.
125-5
108-1
93-7
92-20
571 "03
560-51
pure H2O-
39-34 W.
84-49 W.
145-5
125-7
109-1
48'9 W.
67 '83 W.
94-65
625-63
614-32
173-9
149-8
129-9
mm.
mm.
96-85
99-30
678-31
741-28
666-00
728-08
mm.
58-9
65-9
mm.
56-5
63-4
mm.
53-6
59-3
203-1
228-4
175-8
196-9
153-5
172-4
64-8
77-9
Ol *0
57-1
69-1
SI -9
....
88-9
84-9
79-8
261-9
225-6
197-5
yi z
Oi fi
...»
20 W.
103-6
99-2
93-5
307-9
266-0
233-8
131-9
117-2
....
Him
140-9
135-3
127-5
336-4
290-5
255-1
144-0
128-7
—
48-69
86-21
83-09
155-3
148-9
140-2
369-5
318-7
280-6
165-2
147-6
....
51-70
100-07
96-12
200-0
192-4
182-2
429-4
372-1
3287
187-3
166-5
....
55-63
140-06
134-26
241-0
232-4
220-2
478-0
413-6
365-1
215-1
191-9
....
60-80
153-29
147-49
244-1
235-6
223-3
516-7
445-3
394-9
231-3
206-3
62-28
165-45
158-98
281-9
271-5
258-2
561-3
485-7
429-1
259-2
231-3
65-64
68-45
70-60
191-07
217-90
239-27
183-36
209-90
230-64
303-7
342-7
400-5
293-2
330-9
386-5
278-9
315-3
368-6
619-6
690-0
759-2
535-1
595-6
659-3
473-5
527-3
585-9
285-2
311-9
393-0
423 '2
255-3
279-5
350-9
377-8
265-3
332-9
358-3
74-38
281-90
272-24
430-1
416-0
396-3
473-5
424-6
406-1
78'80
337-74
326'10
473-0
457-8
436-8
484'9
434-8
412-9
82-63
84-80
393-83
429-51
379-58
413-64
526-9
575-5
510-3
556-5
488-1
531-7
Barium dithionate, BaS206.
516-1
rr;Q.f»
461-9
499-9
438-8
474-8
86-50
459-21
443-20
620-0
599-7
574-7
Baker, C.N. 36, 203; 34, 112:—
UUO \J
600'5
540-2
514-1
89-93
524-15
505-10
684-6
663-8
636-2
0
ats.
6457
580-2
550-5
92-20
571-03
550-38
766-4
743-5
714-4
102
1
sat.
754-3
675-5
642-4
94-65
625-63
603-01
96-85
678-31
653-60
99-30
741-28
715-38
5D
754
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES:
Potassium dichromate,
Calcium nitrate (continued) : —
Calcium nitrate (continued) : —
Potassium nitrate (continued) : —
K3O307-
0
ats.
W.
Tension of
Tension of
Faraday, Storer Diet. Sol. 390 :—
Kremers, P.A. 92, 499 :—
117
»
130-0
Temperature.
pure H2O.
Solution.
0
ats.
118
„
136'1
40 W.
115-6
1
sat.
o
ats.
119
142-1
104
1
sat.
120
148-1
o
mm.
mm.
Legrand, A.C. [2], 59, 434 ; iii., 89 :—
™
43-2
64-20
55-95
Alluard, A. 133, 292 ; vi., 453 :—
122
»
160-1
45-7
73-98
64-89
0
101
ats.
W.
12'2
124
172-2
ats.
103-4 1
sat.
126
184-5
47-5
81-14
71-14
102
„
26-4
128
197-0
49-4
89-21
78-35
103
„
42-2
130
209-5
51-2
97-62
85-70
104
„
59-6
Sodium borate, NaJB4O7.
132
"
222'2
53-4
108-75
95-75
105
78-3
Griffiths, Q.J.S. [1825], 18, 90 :—
134
))
235-1
55-65
120-89
105-89
106
„
98-2
0
ats.
W.
136
248-1
57-45
131-73
115-34
107
„
119-0
105-5
1
110-54 sat.
138
"
261'3
59-4
144-69
127-21
108
,,
140-6
i if\
•J
62-8
169-26
149-38
109
163-0
Silver nitrate, AgN03.
Kremers, P.A. 92, 499 :—
140
142
144
146
V
274-7
288-4
302-6
317-4
64-22
65-1
67-6
180-37
187-79
209-89
159-22
165-96
184-08
110
111
112
»
185-9
209-2
233-0
o
a. 125
ats.
1
sat.
148
H
333-2
69-4
227-12
199-07
113
„
257-6
150
351-2
114
„
283-3
Raoult, C.R. 87, 169 ; 36, 4 :—
151
^
362-2 sat.
Copper nitrate, Cu(N03)z.
115
..
310-2
O
mm.
W.
Griffiths, Q.J.S. [1825], 18, 91 :—
115-9
»
335-lsat.
100
758*78
Wulluer, P.A. 110,579:—
0
ats.
Guthrie, P.M. [5], 18, 113, 116 :—
Tension of
173
1
eat.
o
ats.
W.
Barium nitrate, Ba(N03)2.
Griffiths, Q.J.S. [1825], 18, 90 :—
Temperature.
Tension of
pure H2O.
Solution.
20 W.
Nitric acid, HN03.
101-5
102-83
1
25-0
33-3
o
ats.
W.
o
mm.
mm.
Roscoe, A. 116, 204 ; B. 3, 973 :—
103-41
„
42-9
101-1
1
36-05 sat.
25-0
23-55
22-05
0
mm.
% HNO>
104-02
„
53-9
27-62
26-45
24-65
70
75
66-7
104-5
„
66-7
Kremers, P.A. 99, 43 :—
29-8
31-14
29-14
?
150
67-6
106-56
„
81-8
0
102-5
ats.
1
sat.
31-8
33-6
35-00
38-62
32-66
36-27
120-5
735
1220
68-0
68-6
107-22
108-85
• ';;
100-0
122-2
Raoult, C.R 87, 169 ; 36, 4 :—
36-0
44-20
41-11
Storer, Diet. Sol. 374 :—
110-16
„
150-0
O
mm.
W.
37-43
48-73
45-64
o
ats.
% N A-
110-81
„
185-7
100
758-96
I
39-75
54-16
50-82
— 1-11 1
1
100
113-0
„
233-3
41-0
57'91
54"18
+ 3778 2
82-7
114-92
„
300-0
Calcium nitrate, Ca(N03)2.
43-2
45-7
64-20
73-98
59-55
69-28
79-44
98-89
»
72-5
68-0
Nicol, P.M. [5], 18, 367 ;
48, 33 :—
Kremer
a, P.A. 99, '
13:—
47-5
81-14
7614
115-56
„
58-4
0
65
mm.
152-9
sat.
o
152 p.d.
ats.
1
sat.
49-4
51-2
89-21
97-62
83-88
91-66
120
119-44
n
54-4
51-2
75
f 221-0 1
* 231-5 I
Berzelius, Lehrbuch : —
53-4
108-75
102-20
116-66
N
44-3
f 3147 "1
0
ats.
W.
55-65
120-89
113-34
113-33
i>
37-4
85
I 341-7 J
"
151
1
362-8 sat.
57-45
131-73
123-33
111-11
.,
32-3
f 427-1 1
Legrand, A.C. [2], 59, 439 ; iii., 89 :—
59-4
62-8
144-69
169-25
135-95
159-12
109-44
107-78
"
28-5
25-4
95
* 499-3 /
"
o
101
ats.
1
W.
15-0
64-22
180-37
169-45
106-11
<.
23-0
Raoult, C.R. 87, 169 ; 36, 4 :—
65-1
187-79
176-53
105
»
21-0
0
mm.
W.
103
**
34-4
67-6
209-89
196-79
104-44
„
19-3
100
757-87
1
104
42-6
69-4
227-12
212-71
103-89
»
17-8
See also Pauchon, C.R. 89, 753 ;
103-89
..
16-6
OQ Oil
105
H
50-4
oOj zil.
106
107
"
57-8
64-9
40 W.
Potassium nitrate, KN03.
Tammann, W. 24, 532 ; B.r. 18,
31 3 •—
108
109
110
"
71-8
78-6
85-3
25-0
27-62
29-8
23-55
26-45
31-14
20-25
22-60
26-74
Griffiths, Q.,
o
114-5
J.S. [1825],
ats.
1
18, 90 :—
W.
284-61 sat.
Tension of
pure H2O.
Tension of Solutions.
12-68 W.
41-08 W.
111
H
91-9
- 31-8
35-00
30-35
Graham Otto : —
mm.
mm.
mm.
112
„
98-4
33-6
38-62
33-50
o
ats.
187-0
181-0
174-9
113
„
104-8
36-0
44-20
38-20
116
1
sat.
210-1
202-8
195-7
114
5)
111-2
37-43
48-73
42-63
Kremers, P.A. 97, 19 :—
231-5
223-4
215-4
115
I!
117-5
39-75
54-16
47-39
0
ats.
265-3
255-9
247-1
116
n
123-8
41-0
57-91
50-64
118
1
sat.
289-3
279-7
270-1
MIXED LIQUIDS AND SALINE SOLUTIONS.
755
Potassium nitrate (continued) : —
Potassium nitrate (continued) : —
Potassium nitrate (continued) : —
Lithium nitrate, LiN03.
Tension of Tension of Solutions.
Tension of
Tension of
Solutions.
Tension of
Tension of Solutions.
Storer, Diet. Sol. 385 :—
pure H2O. 12.68 w.
41-08 W.
pure H2O.
86-03 W.
115-64 W.
pure H2O.
86-03 W.
115-64 W.
o
200
ats.
1
sat.
mm. mm.
322-6 310-9
mm.
300-2
mm.
187-0
mm.
160-0
mm.
151-1
mm.
509-5
mm.
430-0
mm.
403-6
Tammann, W. 24, 548 ; B.r. 18, 313 :—
366-4 354-8
342-5
210-1
179-4
168-4
557-6
469-3
440-0
Tension of
Tension of Solutions.
414-5 400-3
386-8
231-5
197-4
185-2
641-5
540-0
506-2
pure H2O.
15-92 W.
35-01 W.
457-1 442-0
427-1
265-3
225-7
212-1
723-8
604-3
565-0
509-5 491-3
474-0
289-3
246-0
231-6
759-0
636-3
596-1
mm.
33-2
mm.
29-2
mm.
24-6
557-6 537-6
518-5
322-6
273-2
256-7
49-8
44-6
37-4
641-5 617-2
597-6
366-4
310-6
291-5
78-1
71-0
60-9
723-8
671-1
414-5
351-1
329-2
94-1
85-7
73-5
759-0
705-3
457-1
387-1
363-0
120-2
109-9
94-5
146-0
132-6
114-3
174-7
159-3
137-0
Wiillner, P.A. 103, 547 :—
205-7
188-0
161-9
Tempera-
Tension of
Tension of Solutions.
271-4
248-2
213-8
ture.
pure H2O.
1 W.
5 W.
10W.
15 W.
20 W.
25 W.
SOW.
361-9
331-3
286-0
o
mm.
mm.
mm.
mm.
mm.
mm.
mm.
mm.
391-2
357-8
308-9
38-4
50-38
50-28
49-89
49-39
48-90
48-50
48-00
....
479-2
438-2
378-6
42-4
62-33
62-20
61-64
61-04
60-25
59-66
59-06
571-9
523-1
452-1
46-7
78-07
77-91
77-18
76-29
75-40
74-70
74-11
....
777-9
710-3
615-5
47-0
79-09
78-92
78-10
77-31
76-61
75-72
74-63
....
59-06 W.
83-53 W.
50-7
95-29
95-05
94-01
92-82
91-53
90-84
53-1
107-16
106-92
105-88
104-69
103-40
102-70
101-31
mm.
mm.
53-9
111-41
111-18
110-13
109-15
107-56
107-17
105-78
33-2
20-2
15-7
60-9
155-13
154-80
153-25
151-57
149-89
148-61
146-82
49-8
29-6
22-9
61-3
158-62
158-24
156-94
155-26
153-28
152-19
150-51
78-1
48-3
38-1
. 61-6
160-06
159-68
158-09
156-11
153-93
152-94
....
94-1
58-3
45-6
61-7
160-94
160-58
157-38
153-58
149-97
120-2
75-4
59-2
65-2
188-64
188-21
184-10
179-68
175-99
146-0
90-8
71-3
65-8
193-74
193-30
191-62
189-25
186-83
185-05
182-58
174-7
109-3
86-0
65-8
193-74
193-29
191-47
189-20
186-53
185-25
205-7
129-2
102-0
69-6
229-13
228-61
223-60
218-86
213-43
271-4
170-8
135-4
70-3
234-18
233-65
231-42
228-76
226-13
224-16
221-33
310-7
196-0
155-6
70-6
239-45
238-90
236-79
234-32
230-37
361-9
229-3
182-7
72-3
257-37
256-81
254-51
252-04
248-59
246-12
243-46
391-2
247-3
196-6
72-7
263-77
263-15
260-42
258-06
253-81
251-63
248-20
479-2
304-1
242-9
75-9
299-60
298-99
296-15
293-39
289-05
286-63
282-69
571-9
364'6
76-3
304-64
303-96
300-90
297-93
294-29
291-34
287-78
777-9
....
78-6
334-97
334-21
....
327-59
....
312-12
Sodium nitrate, NaN03.
81-0
369-28
368-47
364-85
361-40
356-18
353-28
349-68
....
Griffiths, Q.J.S. [1825], 18, 90 :—
81-6
378-36
377-52
374-13
368-91
364-76
362-40
358-17
....
0
ats.
W.
82-6
393-72
392-74
388-80
383-87
378-94
....
119
1
150 sat.
83-0
86-3
400-10
455-68
399-14
454-68
450-37
390-45
445-44
439-73
436-48
431-52
371-33
Kremers, P.A. 97, 19, 21 ; iv., 105 :—
o
ats.
87-9
484-81
483-70
....
473-99
....
....
451-05
122
1
sat.
91-4
554-09
552-87
....
542-78
....
516-61
123
supersat.
93-3
595-09
593-71
588-21
581-32
574-64
567-36
560-37
94-2
615-29
613-76
600-34
566-98
Legrand, A.C. [2], 59, 435; iii., 89:—
95-3
640-83
639-35
626-09
618-22
611-42
0
ats.
W.
101
1
9'3
97-0
682-03
680-41
665-52
....
....
633-78
102
18-7
100-6
776-48
774-33
765-19
755-27
744-27
736-02
....
....
103
28-2
100-8
782-04
779-88
760-42
.
104
ii
37'9
105
„
47-7
106
„
57-6
107
„
67-7
*
108
„
77-9
109
„
88-3
110
M
98-8
111
„
109-5
5D2
756
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES:
Sodium nitrate (continued) : —
Sodium nitrate (continued) : —
Lead nitrate, Pb(N03)3.
o
ats.
W.
Wullner, P.A. 103, 544 :—
Griffiths, Q.J.S. [1825], 18, 90 :—
112
113
114
1
14
120-3
131-3
142-4
Temperature.
Tension of
pure H20.
1 W.
Tension of Solutions.
30 W.
o
102*2
ats.
1
W.
110-53 sat.
10W.
20 W.
115
B
153-7
Kremers, P.A. 92, 499 : —
o
mm.
mm.
mm.
mm.
mm.
116
»
165-2
23-1
21*01
20-955
20-51
19-82
19-42
o
ats.
117
„
176-8
27-1
26*66
26-597
26-06
25-32
24-77
103*5
1
sat.
118
„
188-6
29-1
29-95
29-873
29-16
28-41
27-62
119
„
200-5
31-5
34-36
34-256
33-27
32-28
31-28
Eaoult, C.E. 87, 169 ; 36, 4 :—
120
„
212-6
37-5
48-25
48-106
46-86
45-37
43-88
o
mm.
W.
121
»
224-8 sat.
39-4
53-14
52-979
51-46
49-87
48-38
100
759-16
1
Nicol, P.M. [5], 18, 364 ; 48, 331 :-
41-5
59-48
59-298
57-69
55-76
54-03
0
mm.
44-0
67-79
67-570
65-66
63-33
61-22
65
129-9
sat.
47-3
80-33
80-051
77-56
7474
71-96
75
179-5
49-1
87-93
87-649
85-25
82-28
79-41
Strontium nitrate, Sr(N03)2.
85
256-4
n
51-5
99-10
98-771
95-83
92-57
89-20
Griffiths, Q. J.S. [1825], 18, 90 :—
95
362-8
n
55-1
118-04
117-649
114-19
110-26
106-24
o
ats.
W.
Eaoult, CJ
0
100
I. 87, 169 ;
mm.
757-1
36,4:—
W.
1
56-5
58-5
62-5
126-24
138-76
166-98
125-829
138-321
166-387
122-18
134-40
160-85
117-93
130-06
154-92
113-92
125-50
149-58
106*5
Kremers, P.
1
A. 92, 499 ;
112-98 sat.
99, 43 :—
64-5
182-12
181-473
175-60
169-08
162-85
0
ats.
See also Pauchon, C.E. 89, 753 ; 38, 21 1.
65-6
201-07
200-385
194-30
187-34
180-42
107-5
1
sat.
Tammann, W. 24, 544 ; B.r. 18. 313 :—
68-9
222-29
221-525
214-69
206-79
199-48
108-0
»
"
Tension of
Tension of Solutions.
70-5
72-5
238-24
260-60
237-375
259-717
229-56
251-72
220-97
242-83
212-28
234-24
pure H3O.
15-2 W.
26*34 W.
75-4
78-7
293-00
336-33
291-944
335-154
281-76
324-41
271-69
312-57
261-82
301-42
Potassium carbonate, K3C03.
mm.
35*0
mm.
33-7
mm.
32*4
81-5
376-85
375-480
363-05
349-15
336-15
Poggiale, A.C. [3], 8, 468 :—
53-4
51-1
48-0
83-4
406-57
405-063
391-50
376-24
361-55
o
ats.
70-2
67*0
63*8
86-0
450-34
449-694
433-80
417-35
401-11
135
1
sat.
118-7
112*5
108-3
88-7
499-98
499-184
481-38
463-96
446-83
Gerlach, Sp. gw. Salzlosungen : —
141-7
134*6
129-0
92-6
579-67
577-593
559-21
537-77
517-41
o
ats.
W.
175-7
166*6
159-6
94-9
631-44
629-237
609-34
586-74
566-06
100-8
1
11*1
219-9
208*1
199-2
100-3
768-20
765*524
740-92
714-00
689-13
102-2
,5
25*0
254-0
240*1
230'7
104'5
42 -9
303-9
367-9
391-7
468-4
287*3
347*9
370*5
442*9
275-1
333-4
355-9
424-7
Ammoniuir
Griffiths, Q.
o
182
L nitrate (
J.S. [1825],
ats.
1
N"H4)N03.
18, 91 :—
sat.
Ammonium
o
119
120
nitrate (con
ats.
1
tinned) : —
W.
256-8
275-3
108-6
115-2
Dalton, Ne
w System, i
66*6
100*0
!, 481 :—
529-1
500*0
480-0
122
314-0
o
ats.
W.
580-1
548*1
525-2
Eaoult, C.E. 87, ] 69 ; 36, 4 :—
124
"
354-0
100-56
1
4-93
642-3
767-3
606*5
725*9
581-6
694-9
0
100
mm.
757-26
W.
1
126
128
11
»•>
396-0
440-2
100-56
101-11
„
9-89
15-21
JI
101*11
20'19
Legrand, A.C. [2], 59,
435 :
130
„
487-4
101-66
"
25-78
52*47 W.
91-11 W.
o
101
ats.
1
W.
10
132
»
537-3
102-22
31-58
mm.
mm.
102
TJ
20-5
134
i *}fi
"
590-0
645'Q
102-78
„
37-55
35-0
29-6
25*8
103
„
31-3
loo
"
705'5
103-33
»
43-88
53-4
44-3
39*0
104
„
42-4
1 J/t
"
770'5
104-44
i,
50-60
70-2
58-0
51-2
105
V
53-8
14-J
TJ
840'6
105-56
H
56-74
118-7
98-0
86*7
106
65-4
J)
915-5
107-22
a
63-93
141-7
117-5
103*8
107
n
77-3
1 Afi
"
995-5
108-33
„ '
71-53
175-7
145-9
128*7
108
89-4
1-*D
1 A.R
J)
1081-5
109-44
»
76-36
219-9
182-0
159*8
109
V
101-9
1-4:0
JJ
1173-5
111-11
H
84-50
254-0
209-9
187*3
110
JJ
114-9
5
"
1273
112-78
•
95-31
303-9
250-3
219*8
111
128-4
"
1383
114-44
i.
108-8
367-9
303-7
267*1
112
J)
142-4
i f-.fi
"
1504
116-11
J)
127-3
391-7
323-2
283*4
113
156-9
lob
i *"»ft
))
1637
117-78
..
152-5
468-4
385-5
338*3
114
J'
172-0
lOo
"
1775
119-44
».
190-7
529-1
436-0
383*3
115
188'0
loO
»
122-22
„
254-6
J,
-1 ftQ
1923
580-1
477-6
418-9
116
1)
.204-4
ibz
"
2084
125-56
j)
380-8
642-3
528-0
464-0
117
221-4
164
"
129-44
„
762-1
767-3
632-3
556-3
118
J)
238-8
180
"
00
137-78
»
00
MIXED LIQUIDS AND SALINE SOLUTIONS.
757
Potassium carbonate (continued) : —
Potassium carbonate (continued) : —
Sodium carbonate (continued) : —
Sodium carbonate (continued) : —
Legrand, A.C. [2], 59, 438
;iii.,89:-
Tension of
Tension of Solutions.
Gerlach, Sp. gw. Salzlosungen,
Tension of
Tension of Solutions.
0
ats.
W.
pure H2O.
24-43 W.
48-7 W.
108 : —
pure H2O.
10-16 W.
21-86 W.
101
1
13
o
ats.
W.
102
22-5
mm.
mm.
mm.
100-5
1
5-26
mm.
mm.
mm.
103
31-0
234-1
217-2
196-2
101-1
„
11-1
398-9
385-8
369-3
104
11
38-8
264-3
244-5
221-3
101-8
H
17-6
450-3
435-5
416-8
105
106
11
46-1
53-1
280-3
305-4
259-7
282-9
235-0
255-5
Kremei
o
-a, P.A. 99,
ats.
43:—
510-3
580-7
491-5
560-9
471-5
537-0
107
1)
59-6
326-2
302-5
273-9
106
1
sat.
669-2
645-6
619-3
108
fi<VQ
363-9
338-0
306-4
762-1
733-7
704-6
109
"
\)O tj
71-9
398-6
370-4
336-2
Payen, A.C. [3], 43,
233 :—
110
)!
77-6
429-8
399-7
362-8
o
104
ats.
1
sat.
27-73 W.
34-76 W.
111
83-0
477-9
444-7
403-6
- — -
112
110
-
88-2
QO-O
511-8
559-8
476-5
521-0
432-8
473-2
Poggiale,
o
A.C. [3], 8,
ats.
468:—
W.
29-5
mm.
26-3.
mm.
25-3
l io
IT
• '•> ~
GQ-A
628-7
585-2
532-2
104-6
1
48-5 sat.
39-1
35-0
33-8
11
yo U
49-2
43-8.
42-1
115
„
102-8
756'2
638-1
Dalton, New System,
2, 501 : -
55-9
49-7
48-0
116
n
107-5
0
im •! i
ats.
i
W.
IQ'fi
70-9
63-4
60-7
117
11
112-3
85-9 W.
136-3 W.
I'M 1 1
i
Ii7 \t
88'1
79"!
75"8
110
102-78
29-4
118
yi
117"!
mm.
mm.
104-44
40-45
103-9
93-3
89-7
119
»
122'0
18-1
11-8
8-6
"
121-7
109-1
105-6
120
•
127-0
27-5
177
12-9
Legrand, A.C. [2], 59, 433; iii., 89 :—
140-7
126-0
122-3
121
II
132-0
35-3
23-0
16-6
0
ats.
W.
156-9
V40-7
135-4
122
11
137-0
49-7
33-0
23-4
100-5
1
7-5
175-6
K7-7
153-3
123
11
142-0
57-9
38-3
27'6
101
»
14-4
196-8
177-5
171-5
124
„
147-1
71-9
47-9
34-7
101-5
»
20-8
226-8
203-6
197-3
125
„
152-2
91-2
61-0
44-3
. 102
»
267
258-4
232-4
225-6
126
„
157-3
102-0
68-6
49-9
102-5
»
32-0
286-3
257-3
249-7
127
„
162-5
115-2
77-6
56-6
103
»
36-8
325-5
292-7
284-5
128
„
167-7
130-2
88-3
64-3
103-5
»
41-0
360-7
324-8
315-8
129
„
172-9
145-0
98-4
72-7
104
»
44'7
398-9
358-9
349-2
130
„
178-1
165-0
112-5
82-9
104-5
»
47'9
450-3
406-2
395-2
131
11
183-4
188-0
128-5
95-4
104-63 „
48-5
510-3
4597
445-9
132
>,
188-8
217-8
149-6
111-2
Nicol, P.M. [51, 18, 367 ; 48, 331 :—
580-7
522-4
509-1
133
H
194-2
234-1
161-0
120-4
0
mm.
669-2
604-4
589-9
134
,,
199-6
264-3
1-81-8
136-0
65
154-9
sat.
762-1
689-5
671-1
135
))
205-0 sat.
280-3
193-6
145-3
75
239-5
»
Nicol, P.M. [51, 18, 367 ; 48, 331 :—
305-4
210-8
158-2
85
364-4
»
o
mm.
326-2
226-0
169-9
95
536-8
»
Potassium aluminium
75
85
95
Tammann,
123-5
172-7
244-8
W. 24, 534
313:—
sat.
; B.r. 18,
363-9
398-6
429-8
477-9
511-8
252-9
278-8
3017
335-4
359-5
190-9
211-2
229-6
256-5
Tammann,
Tension of
pure H2O.
W. 24, 541 ; B.r. 18,
313:—
Tension of Solutions.
sulphate
Griffiths, Q
0
104-4
[Alum), A
J.S..[1825],
ats.
1
K(SOt)3.
18, 90 :—
W.
108-33 sat.
10-16 W.
21-86 W.
Tension of
Tension of Solutions.
559-8
628-7
393-2
443-8
mm.
29-5
mm.
28-1
mm.
26-9
Copper potassium sulphate,
pure H2O.
24-43 W.
48-7 W.
756-2
536-1
....
39-1
37-4
36-1
CuK2(SO4)3,
mm.
mm.
mm.
49-2
47-3
45-5
Griffiths, ibid. :-
18*1
16'8
15"!
55-9
54'1
51 '3
0
ats.
W.
27-5
25-7
22-9
70-9
68-7
65-3
102-8
1
66-67 sat.
35-3
32-8
29-3
Lithium carbonate, Li2C03.
88-1
84-7
81-2
49-7
45-7
41-2
Kremers, P.A. 92, 499 ; 99, 43, 48 ;
103-9
100-2
95-9
57-9
52-6
47-6
J. [1856], 294 :—
1217
118-1
112-2
Hydrogen potassium sulphate,
71-9
65-9
59-2
0
ats.
W.
140-7
135-8
130-0
HKS04.
91-2
83-8
75-9
100
1
0-66 sat.
156-9
151-3
144-7
Griffiths, ibid. : —
102-0
93-6
84-8
102
»
0'78
175-6
170-3
162-2
o
ats.
115-2
105-8
95-2
196-8
190-8
182-6
105-5
•J
sat.
130-2
119-9
108-2
226-8
219-0
209-6
145-0
133-8
120-8
Sodium carbonate, Na^COg.
258-4
249-8
238-8
Kremer
i, P.A. 92, 4
ats.
99:—
165-0
153-0
138-2
Griffiths, Q.J.S. [18251, 18, 90 :—
286-3
276-2
264-2
108
1
sat.
188-0
217-8
174-6
9O1-8
157-6
189-Q
o
ats.
i
325-5
o.fla.7
314-5
348-4
300-7
333-6
758
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES:
Hydrogen disodium
Formic acid (continued) : —
Acetic acid (continued) : —
Ethylalcohol (continued) : —
phosphate, NaH^POi.
Konovaloff, W. 14, 45 ; 4o, 1093 :—
o
mm.
W.
Sp. gr. of
Griffiths, Q.
o
J.S. [1825],
ats.
18, 90 :—
o
18-9
mm.
15-3
W.
29-3
80-55
100-0
352-5
750-2
22-2
Boils.
alcohol at
15°'56.
105-5
1
sat.
42-35
58-0
51
16-45
12-5
100-4
61-35
147-4
49-95
85-0
o
ats.
Legrand, A.C. [2], 59, 433 ; iii., 89 :—
80-8
343-6
80-2
335-6
|J
82-44
1
•9420
o
ats
W.
"
83-33
•9516
100-5
i
11-0
100-0
719-8
M
100-0
724-0
n
84-11
•9600
101
M
21-0
16-95
11-7
100-1
16-0
11-8
405-5
85-33
•9665
101-5
31-0
31-8
29-1
n
49-85
78-2
»
87-22
•9729
102
40-8
42-9
51-7
„
80-0
300-7
n
88-78
•9786
102-5
50-3
54-9
102-7
„
100-05
645-7
»
91-33
•9850
103
59'4
70-1
166-9
„
Melts at 16°.
94-44
•9920
103'S
68'1
80-95
309-4
„
104
I)
76'4
90-7
457-85
„
Ethylalcohol, C2H60.
Casoria, J. Chim. M6d. [1846], 467;
104-5
84-2
99-65
644-0
„
Groaning, Brand's Archiv, 6, 200 : —
cited by Pohl, and by Storer : —
105
91-5
18-0
14-5
394-5
% by vol. of alcohol.
Boils.
Sp.gr.
105-5
106
»
98-4
105-0
42-15
61-05
54-5
130-5
»
Temp, of
vapour.
o
75-8
ats.
1
•7939
In still.
In distil-
late.
106-5
111-4
59-9
123-3
„
75-5
„
•8034
106-6
M
112-6
80-7
290-9
„
o
77'2
92
93
75-8
5,
•8118
80-8
292-1
^
tlHtK
rti-v
76'1
•8194
Benzene
o
(and Wate
mrn.
r), C6H6.
oT
99-8
5
590-7
lelts at 7°.
»
77 5
77-81
78-12
y(J
85
80
SI
90-5
78
78-6
"
•8265
•8332
10-10
54-92
78-75
75
90
79-4
M
•8397
10-53
56-03
^1
Methylalcohol, CH40.
79-38
70
89
80-5
»
•8458
12-38
61-93
PL!^
Konovaloff, W. 14, 40 ; 40, 1093 :—
80
65
87
81 "7
»
•8518
15-26
72-34
*r^
o
mm.
W.
81-25
50
85
82"8
j)
'8630
18-01
83-00
1°
17-25
30-15
32-5
82-5
40
82
84
53
•8765
19-88
91-49
gjOO
29-9
62'6
83-75
35
80
86-1
„
•8875
22-53
104-28
F
43-2
126-2
11
85
30
78
87-8
n
•8892
KO.O
Ofl^.OK
Rft-9^
„_
•7ft
90
•9013
Carbon hexachloride (and
Water), CaCl8.
64-9
84-25
17-0
ZUl ~->
345 '7
750-8
44-5
M
-97-1
87-5
88-75
90
20
18
15
/ O
71
68
66
917
92'8
94
T)
it
•9126
•9234
•9335
o
mm.
7-79
11-39
63-49
75-37
29-9
43-3
90-6
177-3
"
91-25
92-50
12
10
61
55
Pohl, W.
A. [1851], 2, 12 :—
16-75
97-25
^
53-5
284-0
H
93-75
7
50
- »
ep. gr. at
i K0
20-49
115-69
jp
65-5
479-9
„
95
5
42
15 ; sp. gr.
of H.,O at
25-66
146-58
"3
-rt
76-7
747-6
»
96-25
3
36
Boils.
29-12
170-77
(3
12-55
39-8
175-4
97-5
2
28
34-42
214-67
I
29-75
104-2
„
98-75
1
13
0
ats.
38-59
256-42
43-7
206-2
»
Storer, Diet. Sol. S3 : —
90-27
1
•9814
44-59
328-38
54-0
330-2
tt
% absolute
90-83
»
•9827
65-7
543-45
91-4
•9840
Carbon disulphide (and
18-65
, 29-25
63-7
112-8
261-0
alcohol of
gp.gr. 0-791
at 20°.
92-03
92-7
»
•9854
•9868
W
ater), CS3
43-2
224-6
93-43
•9883
0
8-85 "
mm.
196-81
53-5
357-8
11
75-72
720
94
94-21
„
•9898
12-07
225-93
65-5
591-7
5)
75-74
•
95
95-02
„
•9913
14-10
247-43
J
71-15
747-7
J)
75-68
H
96
95-9
»
•9930
18 "85
9QQ
*
75-60
„
97
96-85
j,
•9947
22-43
26-87
31-80
347-17
412-28
1
00
5T
M
Oxalic acid, C2H304.
Griffiths, Q.J.S. [1825], 18, 91 :—
75-60
75-65
75-78
"
98
99
100
97-82
98-79
"
•9964
•9982
49o 74
ats.
Konovaloff, W. 14. 34 : 40, 1093 :—
38-35
634-60
112 and rises
to^ O1 n\-i
1
sat.
Tire, Diet, of Arts, Boston, 1853,
o
mm.
W.
Izl so.
quoted from P. J. 7,
17'4
4/V7
35'9
133'3
599'3
Formic acid, CHoO^.
Eoscoe, B. 3, 974 ; A. 116, 204 :—
Acetic acid, C2H403.
Boils.
top. gr. or
alcohol at
15°-56.
*fj 1
60-45
346-35
„
107-1
mm.
760
W.
344
Konovaloff, W. 14, 34 ; 40, 1093 :—
70-2
79-65
532-5
782-9
"
o
mm.
w.
o
ats.
124-1
1350
400
16-65
13-35
22-2
81-44
1
•9200
79-95
789-5
„
134-6 1830
495
49-85
87-7
82-08
M
•9821
18-1
34-2
213-0
MIXED LIQUIDS AND SALINE SOLUTIONS.
759
Ethylalcohol (continued) : —
Propyl alcohol (continued) : —
Butyric acid, C4H803.
Isobutyl alcohol (continued) :—
o
mm.
W.
0
mm.
W.
Konovaloff, W.A. 14, 45 ; 40,
o
mm.
W.
40-45
123-0
213-0
33-0
54-6
56-0
1093 :—
95-1
784-0
1580
60-65
327-8
jj
42-35
91-8
JJ
o
mm.
W.
18-1
18-9
6-5
70-35
509-7
jj
50-65
141-75
JJ
18-3
15-15
34-2
40-3
71-7
„
80-5
768-7
„
60-5
231-5
„
49-85
90-4
59-4
193-9
„
15-3
27-4
101-6
70-9
368-8
)J
80-5
364-9
_
70-9
331-3
„
15-5
27-7
„
80-3
546-0
JJ
99-7
766-4
B
81-55
516-15
„
40-6
117-5
„
88-0
745-3
JJ
15-0
14-2
100
91-0
746-05
,,
59-65
295-7
„
19-65
24-5
111-8
31-25
35-6
12-1
14-3
J3 - <u '
60-05
301-4
jj
32-35
52-9
JJ
42-75
65-5
jj
41-65
82-2
11*1
M >-, W 0
70-15
470-7
jj
40-15
82-6
JJ
52-25
109-4
jj
46-8
107-9
~ -_j ~
70-3
473-4
„
51-55
149-8
JJ
60-35
152-3
jj
59-9
207-6
13 ^ cc eS
80-5
720-0
„
60-95
237-5
JJ
70-3
237-3
jj
71-4
355-6
•ill!
80-55
720-9
„
71-4
382-8
n
79-6
350-8
jj
71-5
356-15
o >
21-15
85-1
49-5
81-4
579-8
j;
99-0
741-1
80-85
530-8
O 03 „. 5 '2
40-9
107-1
J)
877
749-9
JJ
19-45
16-4
234-4
81-2
537-4
jjj aji g g,
60-45
281-6
JJ
19-4
25-1
164-9
50-2
90-8
jj
81-6
550-0
•0-2.S a;"^
70-4
436-7
„
33-0
56-8
jj
80-45
351-3
jj
88-55
722-4
* sj| |
80-25
654-0
JJ
427
94-8
jj
100-0
740-8
„
88-75
728-3
1 §,> 1 6
51-05
148-7
163
748-1
nnrfi acid
89-1
738-6
f
Propionic acid, C3H602.
Konovaloff, ibid.: —
o mm. "W\
60-5
71-43
81-4
234-8
384-1
586-0
jj
Diethyl oxide, C4H100.
Itegnault, C.K. 39, 401 ; P.M. [4J
16-65
40-8
19-0
78-8
11
16-85
14-1
33'2
87-6
749-0
,j
9, 19 :—
59-9
207-0
.M
46-85
76-6
19-4
19-4
792-9
Tension of
Tension of
71-78
360-5
"Ji
62-9
167-7
32-55
42-7
»
pure water.
mixture.
81-6
548-0
^2
81-25
99-25
15-95
46'35
370-8
746-9
12-8
73'2
97'5
42-2
51-2
61-35
70-85
74-1
119-2
195-0
295-5
»
o
15-56
20-40
24-21
13-16
17-83
25-30
89-0
97-2
731-6
991-9
|'£ls
362-95
440-32
510-08
64"0
173'8
M
80-65
455-8
26-73
26-09
562-79
Citric acid, C6H807.
70"2
229-5
»j
89-4
649-6
27-99
27-58
589-38
Gerlach, Sp. gw. Salzlosungen,
81-5
379-3
jj
90-55
751-2
H
33-08
28-08
710-02
111:—
90-0
99-5
17-3
528-6
739-6
13-7
jj
311-2
IsobutyL alcohol, C4H10O.
Konovaloff, W. 14, 43 ; 40, 1093 :—
O mm ~\W
o
101-8
105-8
ats.
1
W.
30-4
91-4
46-7
63-4
69-6
151-4
"
Gerlach, C.C. [1884], 884; Jour.
16-9
4/V1
17-6
65 '5
1580
Camphoric acid, C10H1604.
81-45
336-7
jj
Chem. Ind. 7, 277; B.r. 17, 523;
rtw O
59-9
176-5
jj
Brandes, Sch. J. 38, 276:—
99-6
139-0
676-3
741-5
pure acid
48, 499 :—
o
100-9
mm.
760
% glycerol.
10
71-4
81-5
299-9
457-6
o
96-25
ats.
1
W.
12 sat.
Propyl alcohol, C3H80.
101-8
102-8
JJ
20
30
Sugar, C12H22On.
Konovaloff, ibid.: —
104
JJ
40
Wullner, P.A. 103, 548 :—
o
17-65
40-3
mm.
20-8
79-4
W.
6-6
106
109
113-3
JJ
JJ
50
60
70
Tempera- Tension of
ture. pure H2O.
Tension of Solutions.
1 W.
50 W.
100 W.
150 W.
51
138-7
,,
121
JJ
80
o mm.
mm.
mm.
mm.
mm.
59-8
214-2
n
138
JJ
90
29-2 30-13
30-103
28-64
27-45
26-16
69-35
334-1
jj
164
JJ
95
34-9 41-59
41-552
39-71
37-82
36-03
80-85
540-3
290
100
39-3 52-89
52-850
90-81
88-92
86-74
88-5
740-4
jj
40-1 55-20
55-154
52-82
50-54
48-35
16"25
19-0
27-8
42-7 63-35
63-303
61-07
58-59
56-16
32-6
51-2
JJ
44-2 69-59
69-532
66-92
64-14
61-36
42-9
91-2
JJ
Tartaric acid, C.tLO,,.
47-2 79-91
79-848
76-94
73-67
70-50
51-45
52-1
144-2
149-0
"
' 4 0 o
Gerlach, Sp. gw. Salzlosungen,
111.
51-6 99-58
53-8 110-88
99-505
110-808
95-72
92-35
103-66
88-29
99-89
61-4
235-1
Jj
'
W
56-0 123-24
123-141
118-20
113-49
108-20
70-55
357-2
jj
102-2
1
33-3
61-5 159-50
159-379
153-57
147-54
141-01
80-75
547-5
JJ
106-7
100-0
66-8 202-60
202-457
195-59
188-67
181-06
88-6
747-0
69-3 226-14
225-978
217-95
210-34
201-26
16-25
19-2
56-0
73-1 266-29
266-115
257-31
249-30
239-62
760
VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES:
Sugar (continued) : —
Dipotassium tartarate (cont.) : —
Potassium thiocyanate (cont.) : —
Tempera-
Tension of Tension of Solutions.
Legrand, A.C. [2], 59, 438 ; iii., 89 :-
Tension of
Tension of Solutions.
ture.
pure HjO. ^ ^y
50 W.
100 W.
150 W.
o
101
ats.
1
W.
26-9
pure H2O.
51-38 W.
81-53 W.
o
mm. mm.
mm.
mm.
mm.
102
„
47-2
mm.
mm.
mm.
77-7
322-84 322-621
311-48
300-86
290-40
103
„
65-0
112-1
93-1
83-8
80-4
360-49 360-244
348-64
336-44
322-64
104
„
82-3
130-0
107-7
96-7
81-4
375-34 375-100
363-60
350-84
339-44
105
„
100-1
151-8
126-3
112-9
83-6
409-81 409-540
396-51
382-91
369-03
106
„
118-5
190-9
158-6
141-2
88-5
496-15 495-837
....
464-95
449-20
107
„
137-3
218-1
181-0
160-9
•90'9
543-72
527-29
509-58
491-87
108
11
156-5
256-7
212-8
1887
951
636-12
596-92
575-66
109
„
176-1
305-1
253-2
224-6
96-7
674-60
653-48
630-87
606-29
110
fli
196-2
391-6
323-3
286-2
100-9
784-83
761-07
735-04
704-98
111
„
216-8
488-1
402-1
355-9
112
„
237-9
554-4
457-3
404-2
113
„
259-5
780-3
639-7
—
A TYI TV* rt-l*» ^ i"1 *v» ^w<a 1 at.£*
Potassium a^^^0^"** ^nrt«tiT»iia/i\.
114
m
281-6
fUMMMf
Griffiths,
(NH4)3C204.
Q.J.-S. [1825], 18,90:-
o
120
121
ats.
1
W.
136-9
143-8
114-67
11
296-2 sat.
Potassium ferricyanide,
K3Fe(CN)6.
0
103-3
ats.
1
w.
40-83 sat.
122
„
150-8
Hydrogen potassium tartarate,
Wallace, 7, 80 :—
123
„
157-9
KHC4H4Ofl.
o ats.
W.
124
165-1
Griffiths, Q.J.S. [1825],
1 ft, OO •
104-4
1
82'6 sat.
Copper acetate, Cu(C2H302)2.
125
172-5
0
ats.
W.
Griffiths, ibid.:—
126
180-1
101-1
1
10-497 sat.
Eaoult, C.E. 87, 169; 36, 4:—
o
ats.
W.
1 QQ-A
mm TjP
101-1
i
128
1 OQ
„
loo U
196-1
Potassium sodium tartarate,
100
lillll.
758-75
1
Mercuric cyanide, Hg(CN)2.
129
130
„
204'4
213-0
Griffiths, ibid. : —
Sodium acetate, NaC0H302.
Griffiths, ibid. : —
132
V
230-6
o
ats.
W.
Griffiths, Q.J.S. [1825], 18, 90:-
0
ats.
W.
134
•11
248-7
115-5
1
900 sat.
Q
ats
W.
101-1
1
53-85 sat.
136
11
267-5
124-4
i
1 SO sat.
138
287"3
Eaoult, C.E. 87, 169 ; 36, 4 :—
d40
"
308-3
Potassium oxalate, K3C20,,..
Brandes ; Brandes, Archiv, 22, 147: —
100
11-1111.
759-34
1
142
,,
330-8
Griffiths, ibid. : —
o
ats.
W.
(144
n
354-9
o
1 ft A' A
ats.
i
W.
CC-ft7 ant-
100-18
1
1-20
.146
n
380-6
lU^t **
1 W W t O<A\J.
100-2
1-51
Potassium cyanide, KCN.
148
H
407-9
100-3
»1
2-01
Griffiths,
Q.J.S. [1825], 18, 90 :—
150
„
436-9
Potassium thiocyanate, KCNS.
100-4
15
3-01
o
IOS'3
ats.
J
W.
1 22-2 sat.
152
,i
467-6
Tammann, W. 24, 530 ; B.r. 18,
100-8
H
6-03
154
11
500-0
313:—
101-7
)i
12-06
156
1 r^Q
"
534-1
Tension of
lension of Solutions.
103'6 „ 30'io
Potassium acetate, KC2H302.
Legrand, A.C. T21 59. 440 : iii.. 89 :—
loo
160
n
569'9
607-4
pure H2O.
20-48 W.
45-09 W.
Legrand, A.C. [2], 59, 439; iii., 89 :—
o
ats.
W.
162
n
646-6
mm.
mm.
mm.
0
ats.
W.
101 •
1
10-5
164
687-6
48-7
46-1
42-5
101
1
9-9
102
11
20-5
166
730-4
63-7
59-9
55-0
102
11
17-6
103
11
28-6
168
.
775-0
89-6
84-0
76-5
103
»
24-1
104
n
36-4
169
798'2sat.
112-1
104-9
65-4
104
1>
30-5
105
«
43-4
130-0
121-3
110-5
105
i /w>
n
36-7
A £\,(\
106
107
-11
49'8
55-8
151'S
190-9
142-f
179-5
129-5
162-8
lUo
107
n
»
4z y
49-3
108
11
61'6
Dipotassium tartarate,
218-1
204-5
185-6
108
11
55-8
109
11
67-4
KsjC^Ofl.
256-7
240-6
218-2
109
11
64-2
110
11
73-3
Berzelius, Lehrb., 3, 168 : —
305-1
285-1
259-0
110
u
69-2
111
•i
79-3
0
ats.
W.
391-6
365-0
331-2
111
»i
76-2
112
11
85-3
114-7
1
296-2 sat.
488-1
454-4
412-2
112
11
83-4
113
91-4
554-4
517-0
469-0
113
90-9
114
11
97-6.
Griffiths, Q.J.S. [1825], 18, 90 :—
780-3
724-8
660-7
114
jj
98-8
115
103-9
O
ats.
W.
115
107-1
116
11
11
110-3
112-2
1
212-5 sat.
51-38 W.
81-53 W.
116
„
115-8
117
11
116-8
Faraday; Storer, Diet. Sol. 683 :—
47-8
41-5
37-5
117
D
125-1
118
11
123-4
o
ats.
63-7
53-7
48-4
118
,.
134-9
119
11
130-1
116-7
1
sat.
89-6
75-3
67-0
119
11
145-2
MIXED LIQUIDS AND SALINE SOLUTIONS.
761
Sodium acetate (continued) : —
Lead acetate, Pb(C2H302)2.
Miscellaneous.
o
120
ats.
1
w.
156-1
Griffiths, Q.J.S. [1825],
18, 90 :—
Guthrie, P.M. [5], 2, 221 ; 31, 6 :-
o
121
H
167-4
o
ats.
W.
Gum arabic .... 20 %, boils 100
122
179-3
101-7
1
70-94 sat.
Gelatine 20%, „ 99'9
123
**
191-6
„ 45 %, „ 97-5
, 50 %, „ 97-5
124
124-37
"
204-5
209 sat.
20 % Gelatine + 20 % Gum arabic
+ 60 % H20 boils 97°'7.
Albumen decomposes.
B.— VAPOUR TENSIONS OF SOLUTIONS OTHER THAN THOSE IN WATER.
Mixtures of carbonic and
Mixtures of ethyl bromide and
Mixtures of chloroform and carbon-
Mixtures of diethyloxide and carbon-
hydrochloric acids.
ethyl iodide (continued) : —
disulphide (continued) : —
disulphide (continued) : —
°/ CO,
% ethyl
mm. at
70CHC13
0
mm.
o
ats.
bromide.
13°-8.
by weight.
4-72
207-58
0
27-84
17-18
0
mm.
0
9-31
252-33
a
15
40-66
D
16-7
276-4
30
13-8
202-3
80
12-60
288-96
cS
27
54-22
„
306-4
40
N
214-0
70
17-00
344-14
O O
37-5
70-28
H
„
332-3
50
n
227-8
60
20-54
395-52
O ^
46
82-26
H
„
360-9
60
H
235-0
50
24-07
451-79
47-2 c.t.
92-21
)j
„
380-4
70
n
240-6
40
2719
506-63
*& to
*w 'o
0
28-86
19-37
„
405-2
80
n
245-4
30
30-79
575-90
0 £
0) --,
13-8
39-86
„
428-2
90
„
248-6
20
33-28
627-82
Is
25-5
52-77
„
„
452-2
100
n
250-3
15
36-01
688-73
_y
38-0
44-0
67-36
76-23
»
Solution of sulphur in
;;
251-5
2557
10
5
39-44
772-49
45-5 c.t.
80-52
carbon disulphide.
..
251-6
0
0
33-17
25-48
Cossa, B.
o
i, loa ; vi.,
ats.
KJOI : —
W.
mm. at 16°.
O
8-01
mm.
253-76
1
25-4
63-98
„
55
1
181-34 sat.
16-0
169-2
100
f\r\
9-46
11-17
268-81
288-55
CD
>O
34-0
77-02
„
Mixtures of carbon hexa-
"
901 -A
90
12-88
309-50
1
43-2
90-03
»
chloride, (C2C16) and CS2.
i)
__ 1 t
234-6
70
16-22
353-33
8 •
45*1 c.t.
0
19-0
25-6
31-89
51-93
60-46
42-44
jj
Eegnault, '.
o
8-75
P.M. [41 9,
39, 404 :—
mm.
151-24
21 ; C.E.
CD
»
243-7
254-0
259-7
60
50
40
18-62
21-12
23-68
26-89
388-42
434-88
478-38
538-77
|-8
^H
39-5 c.t.
80-28
n
13-32
183-32
o
3
"
"
30
30-09
603-93
•M
O
0
32-72
45-67
18-84
229-15
a
0
"
9ftfi-R
i PI
32-65
659-45
§
17-5
26-6
50-73
63-31
"
22-81
26-44
267-53
307-41
1
O4
j>
^DD O
266-1
10
10
35-61
38-18
730-33
795-80
£
35-0
76-64
i)
30-64
358-81
y
"
70
37-6
79-14
n
33-78
400-47
o
»
9«6.2
38-0 c.t.
81-35
QfJ.EO
1 I 1-*J 1
E
»»
^ o
Oi-itTivia "P "^ rci i o Kt o .
0
18-8
25-5
34-56
55-79
65-68
74-18
GO OO
42-35
48-43
444 o4
542-21
661-95
1
i
Mixtures of diethyloxide
and carbondisulphide.
Kegnault,P.M.[4],9, 19; C.E.39,402:
^jruunriej r
o
mm. at
18°-88.
%EtsO
by weight.
33-5 c.t.
77-69
„
11-98
143-82
£
0
mm.
18-88
284-5
0
0
34-65
82-14
13-16
149-97
o O
—16-71
80-59
„
346-3
10
18-8
56-44
18-70
188-39
—11-36
105-26
O
374-3
20
24-9
67-27
21-09
206-71
1 i^'
—11-02
107-67
2
M
387-3
30
32-4 c.t.
77-23
35-12
349-23
-id ^
— 8-94
119-18
3
'53
410-1
40
Ansdell, P.E. 34, 116.
41-50
436-52
S3
— 8-53
Q-AA
121-77
199.170
V
1q
B
419-3
50
fin
Mixtures of ethyl bromide
and ethyl iodide.
Guthrie, P.M. [5], 18, 517 :—
Mixtures of chloroform and
carbondisulphide.
— 7-15
- 7-14
— 4-01
i _~ it?
130-40
130-82
151-76
Is
a oo"
If
429-8
433-0
432-5
DU
70
80
90
% ethyl
Guthrie, P.M. [5], 18, 513, 514 :—
0
182-92
•go
432-1
100
mm.
bromide.
mm. at
%CHC13
+ 8-93
271-38
CO
"
O
16-7
163-2
0
o
13°*
by weight.
8-94
271-26
•M
X
„
214-8
10
13-8
158-4
100
8-96
270-92
i
„
246-9
20
190-4
90
9-07
274-02
5E
762
-VAPOUR TENSIONS AND BOILING POINTS OF MIXED SUBSTANCES.
Mixtures of methylcyanide
Mixtures of amylene and
Mixtures of methylcyanide
Mixtures of chloroform and
and methylalcohol.
ethylalcohol.
and ethylalcohol.
diethyloxide.
Vincent, O.K. 90, 747 ; 38, 525 :—
Guthrie, P.M. [5], 18, 517 :—
Vincent, C.E. 90, 747 ; 38, 525 :—
Guthrie, P.M. [5], 18, 511 :—
0
ats.
% MeCN.
mm. at
by weight.
0
ats.
% MeCN.
mm. at
19°-02.
% CHC13
by weight.
81 '6
1
100
o
81-6
1
100
o
74-0
90
-18-4
41-9
0
76-8
90
19-02
190-7
100
69-2
80
,,
124-1
10
74-8
•
80
..
196-0
90
67-1
"
70
„
227-4
20
73-8
70
))
211-7
80
65'7
60
„
277-3
30
73-2
n
60
»
226-4
70
"
309-0
40
179.17
v»
u
233-1
63
64"8
50
i £1 t
j»
mj
64'2
"
40
,,
323-7
50
72-6
44
»
236-4
61-76*
63-8
.
30
n
330-0
60
72-7
•
40
»
241-4
60
63 '7
20
„
334-5
70
73-2
30
»
278-2
50
64-0
10
i»
334-8
80
74-1
)(
20
»
312-2
40
64-8
"
o
„
338-1
90
75-4
10
»
344-8
30
"
„
356-5
100
75-4
5
„
377-9
20
78-4
„
0
»
408-8
10
I!
437 '8
0
Manganous chloride in ethyl-
alcohol.
Brandes, P.A. 22, 271 :—
Mixtures of benzene and
ethylalcohol.
Kegnault, P.M. [4], 9, 21 ; C.E.
39, 405 :—
»=(C4H100+CH3C13).
Suberic acid, C8HUO4.
Brandes, Sch. J. 32, 409, 410 :—
-
%MnCl2.
0
mm.
Mixture of benzene and di-
(a) In diethyloxide.
o
76-25
ats.
1 36-2*
7-22
9-98
43-17
50-22
a
ethyl oxide (equal weights).
0
35
ats.
1
w.
16-6
87-5
32-21-
13-11
59-66
.2 *
Eamsay, P.E. 31, 194 ; 43, 136.
(6) In turpentine.
* Absolute alcohol.
16-05
69-43
S3 -2
o
ats.
W.
t Alcohol of 75 %.
18-59
79-35
8 ^
174-44
1
100
763
III.— FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING
CRYOHYDRATES.
I. placed after a freezing point indicates that ice separates; ch., that a cryohydrate separates; sch., that 'a subcryo hydrate separates; S., that only
the substance itself separates. W = number of parts of the substance to 100 parts of the solvent, p.c. = percentage of substance in 100 parts of
the mixture. Sat. = saturated. A number placed before the symbol H2O in the 3rd column indicates that so many molecules of water are
present to 1 molecule of the substance. By " Temperature of Cryogen " is meant the lowest temperature which can be produced by mixing the
substance with the solvent.
A.— MIXTURES WITH WATER, H2O.
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Sodium fluoride
NaP
?
—5-63
—3-2
Guthrie
P. M. [5], 6, 40
36, 428
Aluminium chloride
Barium chloride
A12C16
BaCl2
1 W.
23'2 p.c.
—0-481
—Sch.
—7-2
Kaoult
Guthrie
G E., 99, 324
P.M. [4], 49, 267;
46, 1248
29, 336; 36, 429;
5 B.C.
—0-9 I.
[5], 6, 105
P. M. [5], 2, 211
viii., 1005
31,36
,, „
J)
10,,
15 „
—2-2 I.
—4-0 I.
»
))
M
20,,
—6-0 I.
21-83 p.c.
—7-5 ch.
— 7-3
23'98 „
0'OS+H,O
30
+25 „
1 W.
—0-233
Kaoult
C. E., 98, 1047
46, 808
•Calcium chloride
CaCl2
21-8 „
Saturated
—10
—21
....
Eudorff
P. A., 114, 63
v., 1012
1 W.
—0-42
Eaoult
C. E., 98, 1047
20 p.c.
—15
Guthrie
P. M. [5], 1, 50
viii., 1006
1
—0-2 I.
P.M. [5], 1,361, 455
30, 169
2 .
—0-5 I.
H
3 ,
—1-1 I.
1)
4 ,
—1-6 I.
M
5 .
—2-1 I.
»
7 .
—3-3 I.
M
10 „
—5-5 I.
)»
„ ,,
»
15 „
20 „
— 10-5 I.
—17-5 I.
....
»
»)
H
n
28 „
—27-5 ch.
»
36-45 p.c.
—37? hydrate
—33
1)
)»
39 p.c.
0 CaCl2.6H2O
»»
,, ,, .... .... ....
N
-fH90
45 „
33'3 to 50 p.c.
-15-5 „
—17
»
)>
P. M. [5], 1, 51
»
»
, +3H.O
61 '5 p.c.
—33
P. M. [5], 1, 50
if
+6H,0
8'45 H2O
?
—54-9
Hammerl
W. A., 78, 59
36, 689
Cadmium chloride
CdCl2
?
2
—8-3
Guthrie
P. M. [5], 6, 44
36, 428
Cobalt
CoCl2
?
?
—15-35
ii
n
Chromic „ (violet)
Ccesium „
Cr2016
CsCl
1 W.
1 W.
—0-408
—0-211
Eaoult
C. E., 99, 324
C. E., 98, 510;
46, 1248
46, 701
Cupric „
CuCl2
1 W.
—0-36
B.r. 17, 196
C. E., 98, 1047
46, 808
Ferric „
Hydrochloric acid
Fe2Cl6
HC1
1 W.
1 W.
1 W.
—0-396
— 1-006
—1-071
....
i>
j>
C. R, 99, 324
»
A. C. [6], 2, 66
46, 1248
jj
46, 953
Mercuric chloride
HffCL
1 W.
—0-048
C. E., 87, 169
36,4
„ ,,
D
1 W.
3'24 p.c. (sat)
—0-076
—0-2 ch.
—0-2
jj
Guthrie
C. E., 98, 1047
P. M. [4], 49, 268
46, 808
29, 336; viii.,
Potassium chloride
,, „
>» « •••• •••• "••
KCl
»
H
1 W.
1W.
20-03 p.c.
— 0-446
— 0-451
—11-4 ch.
B.r., 17, 196
»*..
Eaoult
»»
Guthrie
C.E., 87, 169
C.E., 98, 509
P.M. [4], 49, 17,
212
1005
36, 4
46, 701
28, 531 ; viii.,
1005
5 E 2
764
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Lithium chloride
Magnesium „
LiCl
MgCL
MnCl2
NaOl
»
»«
))
»
)J
»
»
»
M
))
»
i)
j>
»
»
»
»
j>
)»
»
»j
»
»
»
(NH4)C1
»
n
n
»
n
»
n
»
»
j)
»
»»
i)
)>
T>
)»
)>
)>
))
NiCl2
SnCl4
SrCl2
»
1 W.
1 W.
?
10 p.c.
1 „
5 „
10 „
15 „
20 „
25 „
1 W.
23'6 p.c.
1 „
2 „
3 „
4 „
7 „
10 „
13 „
15 „
16 „
19 „
20 „
22 „
23-6 „
25 „
26-27,,
26-5 „
26-8 „
10 p.c.
1 W.
1 W.
19-27 p.c.
1 „
3 „
5 „
7 „
10 „
13 „
15 „
16 „
17 „
18 „
19 „
19-27 „
20 „
22 „
23-2 „
25 „
30 „
?
1 W.
1 W.
27-57 p.c.
— 0-866
— 0-514
?
- 6
— 0-76
— 3-78
— 7-44
—10-99
—14-42
—17-77
— 0-6
—22
— 0-3 I.
— 0-9 I.
— 1-5 I.
— 2-2 I.
— 4-2 I.
— 6-6 I.
- 9-1 I.
—11-0 I.
—11-9 I.
—15-5 I.
—17-0 I.
—20-0 I.
—SS-0 ch.
—12-0 sch.
o-o s.
+ 25 -OS.
+40-0 S.
— 6-5
— 0-639
— 0-650
—15 to— 16
— 0-4 I.
— 1-6 I.
- 3-1 I.
— 4-6 I.
- 7-1 I.
— 9-9 I.
—12-0 I.
—13-0 I.
—14-0 I.
—15-01.
—15-8 I.
— 16-0 ch.
— 15 S.
— 5S.
OS.
+ 8S.
+32 S.
?
— 0-37
— 0-32
—17
B.r., 17, 196
—28
B.r., 17, 196
-23
B.r., 17, 196
—16
—10-35
—18
Eaoult
)j
Guthrie
Rudorff
Karsten
»
51
»
»
)>
Raoult
Guthrie
»
»
»
»
»
)»
j)
)»
5»
»*
»1
>»
»
})
»
Poggiale
»
Rudorff
Raoult
»
Guthrie
j>
»
n
»
j»
H
)»
l>
jj
)»
>j
1}
))
j>
))
)»
j>
j»
Raoult
»
Guthrie
C.R., 98, 510
C.R., 98, 1047
P.M. [5], 6, 44
P. A., 114, 63
C.R., 87,169; 98,
510 ; 99, 324
P.M. [4], 49, 9
P.M. [5], 1, 359
)i
»
»
»
)!
»»
>!
*'
Jl
))
)>
J>
)I
))
JJ
n
P.A., 114, 63
C.R., 87, 169
C.R., 98, 510
P.M. [4], 49, 13,
211
P.M. [5], 1, 360,
455
»
)>
!>
M
»
J»
1)
»
)»
>!
J»
))
»
)>
)J
))
P. M. [5], 6, 44
C. R., 99, 324
C. R, 98, 1047
P. M. [4], 49, 267
46, 701
46, 808
36, 428
v., 1012
v., 337
))
)'
))
»
»
36, 4 ; 46, 701,
1248
viii., 1005
28, 334, 531
M
j)
»
»)
u
»
T)
»I
)>
)>
)»
»
i»
)>
)»
»
v., 1012
36, 4
46, 701
viii., 1005
|
28, 531
»
»
)>
)>
»
)>
)>
u
»)
j>
5)
))
))
))
?J
*)
36, 428
46, 1248
46, 808
29, 336
Sodium „
„ ,,
„ ,,
,, „
„ „
,j ,, .... ....
„ „
„ „
Nickel chloride
Stannic ,, .... ....
Strontium chloride ....
» »
Potassium bromide ....
KBr
1 W.
— 0-295
B.r., 17, 196
Raoult
C. R., 87, 169 ; 98,
510
36, 4 ; 46, 701
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHTDRATES.
765
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Potassium bromide
j) »
KBr
»
3215 p.c.
10 „
20 „
— 13
- 3-0 I.
— 7-1 I.
MM
Guthrie
»
P. M. [4], 49, 17,
211
P. M. [5], 1, 363
viii., 1005
28, 531
30
—12-0 I.
32-15 „
—13-0 ch.
—13
») » •••• ••••
M
33 „
34 „
- 9-8 S.
— 5-0 S.
)>
J)
»
35-03 ,.
OS.
39-7 „
+20 S.
Kremers
43'2 „
+40
Sodium „
NaBr
41-33 „
—24
—28
P.M. [4], 49, 214
Ammonium „
NH<Br
32-12 „
-17
-17
M
P. M. [4], 49, 213
viii., 1005
Barium iodide
BaI2
1 W.
— 0-13
Eaoult
C. R., 98, 1047
46, 808
Potassium iodide
KI
1 W.
— 0-215
C. E., 87, 169
36, 4
1 W.
— 0-212
B.r., 17, 196
C. E., 98, 510
46, 701
52-07 p.c.
—23
—22
Guthrie
P. M. [4], 49, 17,
viii., 1005
10
— 2-2 I.
211
P. M. [5], 1, 363
28, 531
20
— 5-1 I.
30 „
— 9-0 I.
40
—14-4 I.
52-07 „
—22 ch.
55-93 „
OS.
,, ,,
)>
58-9 „
61-4 „
+ 20 S.
+40 S.
....
Kremers
»
ji
Sodium iodide
Nal
59-45 „
— 15 ch.
—26-5
Guthrie
P.M. [4], 49, 214
viii., 1005
5
— 0-7 I.
P. M. [5], 1, 452
28, 531
10
— 2-1 I.
15 „
— 3'9 I.
20
— 6-0 I.
25
— 8-5 I.
30
—11-8 I.
35
—15-2 I.
40
—20-5 I.
45
—26-0 I.
49-2 „
—30-0 ch.
—26-5
50
and — 15 ch.
—29'5 sch.
55
— 20'0 sch.
60
— 14'7 sch.
61-6 „
O'OS.
63-6
+ 13-0 S.
NH4I
55'49 „
—27 to— 28
—27
P. M. [4], 49, 213
28, 531 ; viii.,
ch.
1005
Arsenic trioxide
As,O,
|
—0-5
—0-3
Guthrie
P. M. [5], 6, 44
36, 428
Sulphur dioxide ....
SO2
?
—1-5
u
»
Ammonia
NH3
1 W.
—1-117
B., 15, 1749;
Eaoult
C. E., 94, 1518 ;
44, 7, 952 ; 46,
1 p c.
— 0-8 I.
16, 3054
Guthrie
97, 941 ; A. C.
[3], 28, 133
P. M. [5], 18, 23
255
48, 337
3 ,
— 3-2 I.
)»
M
5 „
— 5-6 I.
?»
n
10 „
—12-8 I.
»
M
15 ,
—21-4 I.
)>
..
20 „
—43-4 I.
»
»i
33-3 „
L.-80
>»
»
766
FREEZING (AND MELTING) POINTS OP MIXTURES, INCLUDING CRYOHYDRATES.
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Barium and strontium chlorides ....
Cupric and potassium chlorides
Mercuric and ammonium chlorides....
Potassium and magnesium chlorides
Potassium and sodium chlorides ....
Potassium and ammonium chlorides
Sodium and platinum chlorides
Mercuric and potassium iodides ....
BaSrCl4
CuK2Cl4
Hg(NH4)2Cl4
K2MgCl4
KNaCl2
K(NH4)C12
Na.,PtCl6
K2HgI4
1 W.
1 W.
1 W.
?
23-57 p.c.
1 W.
1 W.
-18 ch.
-0-412
-0-181
-0-480
-21 ch.
-17 ch.
-0-119
-0-065
-167
-21
-18
Guthrie
Eaoult
Guthrie
11
Baoult
P. M. [5], 1, 55
C. B., 99, 915
P. M. [5], 1, 53
P. M. [5], 1, 55
C. R, 99. 915
30, 170
48, 122
30, 169
11
48, 122
Barium hydrate BaH2O2
„ „ .... .... .... „
Calcium „ CaH2O2
11
Ccesium „ CsHO
Potassium „ KHO
Lithium „ LiHO
Sodium „ NaHO
Rubidium „ BbHO
Strontium hydrate SrH2O3
II •••• •••• •••• i:
Thallium , T1HO
Sodium sulphhydrate NaHS
Ammonium „ (NHJHS
Sodium hypochlorite NaCIO
Barium chlorate Ba(C103)2
Potassium „ KC1O3
.... .... „
Ammonium perchlorate (NH)4C1O4
Sodium iodate NaI03
Potassium permanganate KMnO4
11 ii — • •••• i)
Potassium sulphite K2SO3
Aluminium sulphate A12(SO4)3
Chromium „ (violet) .... Cr2(SO4)3
Copper „ .... ' CuSO4
„ ,,
Ferrous sulphate FeSO4
Ferric sulphate Fe2(S04)3
Sulphuric acid H2SO4
Potassium sulphate K2SO4
ii 11
« ii
Magnesium „ MgS04
11 .... .... ....
ii
I!
1 W.
1-65 p.c.
0-362 p.c.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
0-46 p.c.
1 W.
1 W.
1 W.
-0-290
-0-5
-0-15
-0-648
-0-237
-0-630
-1-558
-0-905
-0-360
-0-396
-0-1 ch.
-0-150
-0-648
-0-703
B., 16, 3054
—0-5
—0-18
B., 16, 3054
Baoult
Guthrie
11
Kaoult
-0-09
B., 16, 3054
B.r., 17, 196
Guthrie
Baoult
C. R, 97, 941
P. M. [5], 6, 35
)>
C. R, 97, 941
46, 255, 1248
36, 428
))
46, 255
P. M. [5], 6, 36
C. B., 97, 941
C. B., 98, 510
36, 428
46, 255
46, 701
1 W.
1 W.
1 W.
2-93 p.c.
1 W.
1 W.
1 W.
2-836 p.c.
-0-454
-0-145
-0-215
-0-5 ch.
-0-252
-0-153
-0-197
-0-57 ch.
B.r., 17, 196
—0-7
B.r., 17, 196
11
II
—0-52
Baoult
!»
II
Guthrie
Baoult
ii
11
Guthrie
C. B., 98, 510
C. B., 98, 1047
C. R, 87, 169
P. M. [4], 49, 15
C. B., 98, 509
P. M. [5], 6, 37
46, 701
46, 808
36, 4
28, 334; viii.,
1005
46, 701
36, 428
1 W.
1 W.
1 W.
1 W.
16-89 p.c.
16-92 „
5-0 „
10-0
14-5
14-9
1 W.
1 W.
1 W.
1 W.
7-8 p.c.
21-86 p.c.
5-0 „
10 „
15 „
20 „
21-86 „
21-9 „
11
25
—0-285
—0-129
—0-115
—0-113
— 2ch.
—2-2 ch.
—0-2 I.
—0-8 I.
—2-0 ch.
OS+7H2O
—0-115
—0-390
—0-210
— 0-224
—1-2
— 6ch.
—0-6 I.
—1-5 I.
—3-0 I.
—4-8 I.
—5-0 ch.
0 S+7H2O
+ 15-0 „
B.r., 17, 196
, O
-1-7
Baoult
Guthrie
A. C. [6], 2, 66 ;
B.r., 17, 196
—1-5
—5-3
Baoult
Guthrie
C. B., 98, 510
C. R, 99, 324
J>
C. R, 98, 1047
P. M. [4], 49, 15
P. M. [4], 49, 267
P. M. [5], 2, 212
C. B., 99, 324
1>
C. R, 87, 169
C. B., 98, 510 ;
99, 324
P. M. [4], 49, 217
P. M. [4], 49, 14
P. M. [5], 1, 365
46, 701
46, 1248
»
46, 808
28, 334 ; vlli.,
1005
29, 336
31,36
46, 1248
11
36,4
46, 701, 952,
1248
28, 532 ; viii.,
1005
28, 334
viii., 1005
FREEZING (AND MELTING) POINTS OP MIXTURES, INCLUDING CRTOHTDRATES.
767
Name.
Magnesium sulphate
Sodium sulphate
Ammonium sulphate
Zinc sulphate..
Sodium thiosulphate
Barium dithionate ..
Ammonium selenate.
Potassium chromate.,
„ dichromate K2Cr2O7
Magnesium chromate MgCrO4
Sodium tungstate Na2WO4
Boracic acid H,BOa
Silver nitrate AgNO3
„ .... .... .... ....
„ „
„ .... .... ....
Aluminium nitrate A12(NO3)6
Barium nitrate Ba(N03)2
Formula.
MgSO4
Na2S04
(NH4)2S04
ZnSO4
BaS2O6
NH4)2SeO4
K2Cr04
Composition,
30p.c.
1 W.
1 W.
Sat. at 5°
4-55 p.c.
1 W.
1 W.
41-7 p.c.
10 p.c.
20 „
28-6 p.c.
40 p.c.
41 -7 p.c.
41-9 „
43-2 „
30-84 p.c.
1 W.
1 p.c.
2 „
3 „
5 „
6 „
10 „
15 „
20 „
30 „
30 „
33-55 p.c.
41 p.c.
1 W.
1 W.
1 W.
1 W.
36-27 p.c.
5-3 p.c.
1 W.
1 W.
1 W.
Freezing
Point.
+31-08.
+H20
—0-160
—0-249
—1-85
—0-7 ch.
—0-273
—0-280
—17 ch.
—2-6 I.
—6-0 I.
— 10-81.
— 16-0 I.
—77-0 ch.
OS.
+ 19-OS.
-7
—0-112
—0-1 I.
—0-4 I.
—0-65 I.
-1-2 I.
—1-5 sch. ?
-2-5 „
-3-9 „
-5-45 „
—9-5 to 11-0
sch.?
— 11 ch.
OS+5H20
+20 „
—0-252
—0-075
—0-215
—0-200
— 11
— 1-0
0-146
0-139
0-148
Temperatur
of Cryogen.
B.r., 17, 196
-0-7
A. C. [6], 2, 6'
B.r., 17, 196
—5
-10
B.r., 17, 196
B.r., 17, 196
B.r., 17, 196;
A. C. [6], 2, 66
—10-2
—1-0
B.r., 17, 196
B.r., 17, 196
Authority.
Guthrie
Raoult
»
Coppet
Guthrie
Eaoult
?>
Guthrie
Eaoult
Guthrie
Kremers
Eaoult
ruthrie
Raoult
Reference.
P. M. [5], 1, 36E
C. B., 98, 1047
C. E., 98, 510
A. C. [4], 23, 37
P. M. [4], 49, 1
217
C. E., 87, 169
C. E., 98, 510
P.M. [4], 49, 21
P.M. [5], 1, 364
P.M. [4], 49, 14
C.E., 98, 1047
P.M. [5], 6, 41
I.E., 98, 510
C.E., 98, 1047
!.E., 98, 510
'.E., 87, 169;
98, 510
P.M. [4]> 49, 267
P.M. [4], 49, 16
I.E., 98, 510
O.E., 98, 1047
C.R., 98, 510
Watts' Diet.
& J. Ch. Soc.
viii., 1005
46, 808
46, 701
28, 334, 532 ;
vlil., 1005
36, 4 ; 46, 952
46, 701
28, 532
viii., 1005
28, 334; viii.,
1005
46, 808
36, 428
46, 701
46, 808
46, 701
36, 4 ; 46, 701,
952
29, 336; viii.,
1005
28, 334; 29,
336; viii., 1005
46, 701
46, 808
46, 701
-0-7
—0-8
Guthrie
P.M.
[5^6,44
36, 428
1 W.
1 W.
10 p.c.
20 „
30 „
40 „
48-3 p.c.
JO p.c.
>3 „
55 „
69-4 p.c.
. W.
W.
1 W.
0-145
0-174
0-8 I.
2-7 I.
4-7 I.
6-0 I.
6-5 ch.
5-5 S.
2-2 S.
S.
+ 19-5 S.
—0-458
—0-145
—0-155
B.r., 17, 196
—6-5
ilaoult
ruthrie
remers
Eaoult
C.E., 87, 169
!.E., 98, 509
'.M. [5], 1, 367
P.M. [5], 1, 455
P.M. [5], 1, 367
C.E., 99, 324
C.E., 87, 169
C.E., 98, 1047
36,4
46, 701
viii., 1007
6, 1248
6,4
6, 808
768
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Barium nitrate
Ba(N03)2
02(N03)6
HNO3
KN03
JJ
JJ
JJ
H
u
jj
JJ
JJ
JJ
1)
Jl
JJ
JJ
JJ
»J
JJ
JJ
Jl
J)
JJ
NaN03
JJ
JJ
)J
JJ
J»
JJ
JJ
JJ
JJ
)J
JJ
(NH4)N03
JJ
JJ
51
JJ
JJ
1)
I]
J)
JJ
JJ
JJ
Pb(N03)2
5)
JJ
JJ
JJ
JJ
JJ
5-3 p.c.
3-0 „
1 W.
1 W.
Saturated
1 W.
1 W.
t
11-2 p.c.
11-2 „
1 ,,
2 „
3 „
4
5
7 „
8'5 „
10 „
11-2 „
12 „
13 „
15 „
20 „
25 „
35 „
40 „
+7H2O
1 W.
1 W.
40'8 p.c.
6 p.c.
10
15
20
25
30
35
40-8
42-34
Sat.
1 W.
1 W.
437 p.c.
10 p.c.
20
30
40
43-7
47
51
541
66-5
1 W.
1 W.
5 p.c.
10 „
15 „
20 „
26-23 „
—0-8
-0-4
—0-115
—0-568
—2-8
—0-245
—0-305
—2-5 S.
2-7 ch.
2-6 ch.
—0-1 I.
—0-3 I.
-0-7 I.
—1-1 I.
—1-5 I.
—2-2 I.
—2-6 I.
—2-9 I.
—3-0 ch.
OS.
+2-0 S.
6S.
14 S.
21 S.
358.
41 S.
-15-7
—0-347
—0-396
-17-5 ;
—16-5 ch.
—21.
—4-2 I.
—6-3 I.
—8-4 I.
—10-8 I.
— 131.
—15-5 I.
— 17-5ck.
0 S or sch.
— 16-7
— 0.378
— 0-400
-17-2
— 3-5 I.
- 7-0 I.
—11-5 I.
—17-0 I.
—17-2 ch.
—12-0 S.
— 5-7 S.
OS.
+ 18-1 S.
— 0-104
— 0-113
— 0-3 I.
— 0-5 I.
- 0-71.
- 1-2 I.
- 2-5 ch.
B., 2, 70
B.r., 17, 196
—3-0
m.p. — 15
B.r., 17, 196
—16-5
B., 2, 70
B.r., 17, 196
-17-2
—2-5
Guthrie
>j
Eaoult
»
Kudorff
Raoult
»
Guthrie
»
»)
)j
j>
j>
i»
n
»
>i
«
»
»
ji
)j
i»
)j
H
)>
Ditte
Eaoult
H
Guthrie
»»
i)
jj
j»
i»
»>
n
»
!)
Rudorff
Eaoult
)>
Guthrie
it
»
M
»
)>
1)
)j
11
))
Eaoult
»
Guthrie
»»
j»
is
»>
P.M. [4], 49, 17,
267
P.M. [5], 2, 214
C.E., 99, 324
>j
P.A., 122, 341
O.E., 87, 169
C.R, 98, 509
P.M. [4], 49, 14
»
P.M. [4], 49, 218
P.M. [5], 1, 361
»
)J
11
I)
r>
H
»
P.M. [5], 1, 455
P.M. [5], 1, 361
H
»
))
))
»
»
B., 8, 699
C.B., 87, 169
C.R, 98, 509
P.M. [4], 49, 218
P.M. [5], 2, 213
j>
»)
»
»
j>
»»
u
jj
P. A., 122, 341
C. K., 87, 169
C. R, 98, 509
P. M. [4], 49. 217
P. M. [5], 1, 365
u
1J
1)
JJ
))
)>
J)
JJ
C. R, 87, 169
C. R, 98, 1047
P. M. [5], 2, 214
>j
jj
jj
jj
29, 336
viii., 1005
46, 1248
)>
36, 4
46, 701
viii., 1005
28, 334, 532
JJ
J1
JJ
JJ
J)
J)
J1
JJ
J)
J>
J>
JJ
JJ
J1
J1
JJ
36, 4
46, 701
28, 532 ; viii.,
1005
31,36
JJ
J)
JJ
JJ
JJ
JJ
J)
JJ
36, 4
46, 701
28, 532
viii., 1005
u
jj
jj
jj
j)
j)
u
jj
36,4
46, 808
viii., 1008
j»
»
Nitric acid
Potassium nitrate
„ ,,
Sodium nitrate
Ammonium nitrate
,, „
,, „
„ ,,
„ ,,
,, ,,
,, ,,
,, »
„ „
,» „
„ ,,
u jj
,, j)
Lead nitrate ....
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
769
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
1
Watts' Diet.
& J. Ch. Soc.
Pb(N03)3
29-89 p.c.
OS.
Guthrie
P. M. [5], 2, 214
viii., 1008
Strontium nitrate
Sr(N03)2
1 W.
- 0-195
Raoult
C. R, 98, 1047
46, 808
„ ,,
)>
25-99 p.c.
- 6-0 ch.
—6-0
Guthrie
P. M. [4], 49, 26
20, 336
„ „ "«
>,
5 „
— 0-5 I.
....
„
P. M,[5], 2, 214
31,36
,, „ .... ....
„
10 „
- 1-2 I.
„
,, ,, .... ....
„
15 „
- 2-3 I.
„
H
M
„ „
„
20 „
- 3-8 I.
....
„
n
M
,, „
„
26 „
- 6-0 ch.
„
*
„ „
„
29-62 „
OS.
....
,,
'
viii., 1005
Trisodium phosphate
Na3P04
1 W.
— 0-298
B.r., 17, 196
Raoult
C. R, 98, 510
46, 701
Tetrasodium pyrophosphate
Na4P2O7
1 W.
- 0-172
»
»
»
»
Potassium carbonate
K2CO3
1 W.
— 0-303
A. C. [6], 2, 66
Raoult
C. R, 98, 510
46, 701 ; 952
B.r., 17, 196
Sodium „
Na,CO3
Sat.
- 2-0 ch.
B., 2, 70
Rudorff
P. A., 122, 341
„ „
„
8 W.
— 2-8
...
Coppet
A. C. [4], 23, 373
„ „
„
1 W.
- 0-380
B.r., 17, 196
Raoult
C. R 98, 510
46, 952
„ „
,,
?
- 2-0 ch.
....
Guthrie
P. M. [4], 49, 17
20, 336
„ „
»
5-97 p.c.
- 2-0 ch.
— 2-2
»
P. M. f4], 49, 26
viii., 1005
Potassium hydrogensulphite
KHSO3
1 W.
- 0-270
B., 17, 196
Raoult
C. R, 98, 510
46, 701
Aluminium ammonium sulphate ....
A1(NH4)(S04)2
4'7 p.c.
- 0-2 ch.
—0-7
Guthrie
P. M. [4], 49, 26
20, 336; viii.,
1005
„ potassium „
A1K(S04)3
1 W.
- 0-159
....
Raoult
C. R, 99, 915
48, 122
Chromium „ „
CrK(S04)2
1 W.
- 0-147
....
„
„
n
Copper „ „
CuK2(SO4)2
1 W.
- 0-175
....
„
n
Ferrous „ „
FeK2(S04)2
1 W.
- 0-173
O
„
„
„
Ferric „ „
FeK(S04)2
1 W.
- 0-148
....
„
„
M
Hydrogen potassium sulphate
HKS04
1 W.
— 0-334
B.r., 17, 196
ft
C. R., 98, 510
46, 701
Magnesium „ „
MgK2(S04)2
1 W.
- 0-196
....
„
C. R., 99, 914
48, 122
Zinc „ ,,
ZnK2(S04)2
1 W.
— 0-173
„
„
„
„ » i)
„
8-25 p.c.
- 1-25 ch.
- 1-01
Guthrie
P. M. [5], 6, 38
36, 428
Sodium ammonium „
Na(NH4)S04
12-24 p.c. (NH4)2
- 7-0 ch.
—16-0
„
P. M. [5], 1, 57
30, 170
SO4 ; 4-84 Na^S
04 ;
82-92 H2O
1
Potassium sodium nitrate ....
KNa(N03)3
,
— 7to— 17ch.
—16-8
Guthrie
P. M. [5], 1,' 53
30, 169
Barium strontium „
BaSr(NO3)4
?
—4-3 ch.
— 5-8
„
P.M.; [5], 1,55
30, 170
„ hypophoaphite
Ba(H2PO2)2
1 W.
—0-190
....
Raoult
C. R.; 98, 1047
46, 808
Disodium phosphite
HNajPOj
1 W.
—0-327
B.r., 17, 196
„
C. R, 98, 510
46, 701
Mono-sodium „
H2NaPO3
1 W.
-0-307
„
„
„
„
Disodium phosphate
HNa.,PO4
1 W.
—0-260
„
„
„
„
„ „
„
1-83 p.c.
— 0-9 ch.
— 1-0
Guthrie
P. M. [5], 2, 213
31, 36
Monosodium „ H2NaPO4
1 W.
—0-225
B.r., 17, 196
iaoult
C.R., 98, 510
46, 701
Mouopotassium arsenate H2KAaO4
1 W.
-0-168
»
»
JJ
»
Sodium chloride and potassium sul-
NaCl.K2S04
,
-10 ch.
Guthrie
P. M. [5], 1, 59
30, 171
phate
„ „ „
2NaCl.K2SO4
2
—12-5 ch.
....
„
„
N
Sodium nitrate and potassium sul-
•2NaNO3.KjSO4
?
— 5ch.
„
M
„
phate
Potassium nitrate and sodium sul-
2KN08.Na2S04
?
— 5ch.
....
„
fh
„
phate
CH2O2
1 W.
-
B., 15, 1749
laoult
C. R, 94, 1518 ;
44, 7, 952
A. C, [3], 28, 133
Methyl alcohol
CH4O
1 "W
— 0-541'
C2H2O4 + 2,kq
1 W.
— 0'182
™
— 0'5 ch.
"
Guthrie
P. M. [4], 49, 17
Ethvl aldehyde
c HO"
0-779 D.C.
—0-32
Paterno
B., 19, 2529
5 F
770
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Ethyl aldehyde
CMI4O
3'229 p.c.
—1-38
Paterno
B., 19, 2529
3'249 „
—1-39
9'887 „
—4-32
1 W.
—0-426
C2H,O»
100 pts. HAc
—7-4
Rudorff
B., 3, 392
24, 1093
+ 24pts. H2O
21
—5-1
—2-6
15
—0-2
12
+ 27
11
3-6
„ 10 „
4-3
q
5-3
Q
6'25
7
7-1
8'2
r
9-4
4
10-5
q
11-95
a
13-25
1-5
14-0
I'O
14-8
0'5
15-65
0
16-7
P. J. [2], 2, 241
0 p.c.
+ 0-8
Grimaux
C. R, 76, 486
26, 614
16'21
— 5'4
B., 6, 566
IS'll .
— 6-2
20'78
— 7'2
23'77 .
— 8'3
30'77 „
—10-8
38-32
—14'5
43'46 ,
—16-4
50'62
— 19'8
55'50
—22-3
61-86 „
—24-0
66-44
—20-5
68'82 ,
—18-9
, .
J»
76-48 „
86"75
-11-7
— 1-4
ii
»>
51
92'69
+ 5-4
lOO'O
+ 16-7
1 W
— 0'317
B., 15, 1749
Kaoult
C. R, 94, 1518 ;
44, 7, 952
Ethyl alcohol
C2H60
50 p.c.
20
—30 viscid
— 8
Melsens
Marchand
A. C. [3], 28, 133
P.M. [4], 49,274
J. p., 25, 253
29, 337
30
— 13
40
— 16
50
—17-5
jj 5, .... .... ....
«
60 „
70
—19
—21
»
»
90
—22
5
— 2 begins
Guthrie
P.M. [4], 49, 273
29, 337
10
— 4-3
)) ,, ....
)j J, .«.
))
»
15 „
20 ,.
25
- 7-2 „
-10-7 „
—14-7 „
....
»
*>
J)
J5
jj
j»
30
— 19'4
35
—23-3
), ,,
))
40 „
45
-27 „
—31
)>
11
»
») „
1»
50 „
-37
i?
»
»
FREEZING (AND MELTING) POINTS OP MIXTURES, INCLUDING CRYOHYDRATES.
771
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Ethyl alcohol
C.H.O
n
11
11
11
H
11
»1
11
M
))
11
11
11
11
11
11
n
11
11
i)
11
»1
11
i»
11
i»
11
JI
11
11
11
31
j»
11
11
11
11
11
CaH60
C3H603
C3H803
11
11
?>
IJ
11
11
11
31
u
11
C4H605
C4H606
i)
»,
»
55 p.c.
60 „
65 „
70 „
39-07 p.c.
1 W.
ow.
1-32 W.
2-65 W.
3-97 W.
5-50 W.
6-62 W.
7-95 W.
9-27 W.
10-60 W.
11-90 W.
13-00 W.
15-30 W.
17-80 W.
19-80 W.
21-90 W.
23-60 W.
27-60 W.
31-30 W.
35-10 W.
39-00 W.
42-80 W.
46-60 W.
50-60 W.
54-80 W.
59-20 W.
64-60 W.
70-00 W.
48 p.c.
60 „
80 „
Hollands gin
French brandy
Extra strong
whisky
1 W.
1 W.
1 W.
9-8 p.c.
19-6 „
29-4 „
39-2 „
44-1 „
49-0 „
58-8 „
68-6 „
78-4 „
88-2 „
98-0 „
1 W.
1 W.
5 p.c.
10,,
15,,
— 42 begins
-45 „
-53 „
—65 (not)
—34 ch.
— 0-376
0
- 0-5
— i-o
— 1-5
— 2-0
— 2-5
- 3-0
— 3-5
- 4-0
— 4-5
— 5-0
- 6-0
- 7-0
— 8-0
— 9-0
-10-0
—12-0
—14-0
—16-0
-18-0
—20-0
—22-0
—24-0
—26-0
—28-0
—30-0
—32-0
-32
—52
-75
-47
-47
-52
-0-294
—0-213
—0-186
—1-25
—2-5
—6-25
-17-5
—26-25
—31-25 to
—33-75
L.— 35
L.— 35
L.— 35
L.— 35
L.— 35
-0-139
—0-130
-0-7 I.
-1-41.
—2-5 I.
B., 15, 1749
B., 15, 1749
11
11
B., 15, 1749
»
Guthrie
11
)j
)»
M
Raoult
»
si
»
»»
»
)i
?j
i)
»
i)
»
»j
?>
)»
»
>»
»
»
7>
I>
JJ
»
1)
n
»
i>
i)
PictSt
Coleman
j»
»
)>
it
Raoult
u
n
Fabian
j)
»»
»
51
)J
?)
»
J>
»)
)»
Raoult
»
Guthrie
•
»)
)j
P.M. [4], 49, 273
ii
n
ji
P.M. [4], 49, 274
C.R., 94, 1518
A. CL [5], 20, 207
B., 13, 1883
C. R., 90, 866
11
?»
»
)»
it
51
)1
))
T»
11
91
11
)1
)1
M
Jl
n
51
n
>i
Ji
11
)i
n
C. N., 51, 174
11
11
11
Jl
11
C. R., 94, 1518 ;
A. C. [3], 28, 133
n
11
D. P., 155, 347
51
11
»!
'1
11
11
11
»
11
11
C. R., 94, 1518
A.C. [3], 28, 133
P. M. [5], 2, 218
!»
11
29,337
!>
11
)!
11
44, 7,' 952
38, 523
11
11
n
11
11
11
»
ji
D
M
11
11
11
M
11
n
11
!>
11
'>
!»
11
)!
31
11
11
44, 7, 952
11
Jl
44, 7, 952
'>
31, 36
»
)»
,, ,, .... .... .... ....
„ (cf. Storer, Diet. Sol. 291)
Malic acid
Tartaric acid ....
5 F 2
772
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Tartaric acid ....
C.H6O6
20 p.c.
- 3-7 I.
Guthrie
P. M. [5], 2, 218
31,36
25 „
- 4-7 I.
30 „
- 6-3 I.
35 „
- 7-6 I.
40 „
— 10-1 I.
45 ,.
— 13-0 I.
46'6 p.c.
-8ch.
—8
50 p.c.
16-5 ?
55 „
—17-6 s.
E thy lie acetate ....
C.HoO,
1 W.
—0-202
B., 15, 1749
Baoult
A. C. [3], 28, 133
44, 7, 952
Butyric acid ....
1 W.
-0-212
C. R., 94, 1518
CjH.nO
1 W.
—0-232
C. R, 94, 1518
Diethyl oxide .... ..;.
1 W.
—0-224
1
—2-0 ch.
Guthrie
P. M. [4], 49, 276
Phenol
C.HfiO
1 W.
—0-165
B., 15, 1749
Raoult
A. C. [3], 28, 133
44, 7, 952
Pyrocrallol
C.H.O.
1 W.
—0-129
C. R., 94, 1518
C6H8O7 +H3O
1 W.
—0-092
i) ,,
C6H807
10 p.c.
20 ,
— 1-1 I.
—2-8 I.
....
Guthrie
P. M. [5], 6, 42
36, 428
30 ,
—5-0 I.
40 „
—8-5 I.
42 '62 p.c.
—9-2 ch.
—9-3
?) j* *"* •••• **** ••••
»
45 p.c.
45-93 p.c.
—11-3
—11-7
At these tempe-
ratures ord.
47-06 „
—12-2
hydrate, sch.,
„
50'7 „
—13-7
or even ice
51-5
—15-0
maybe formed
Paraldehyde ....
2-469 W.
—0-36
Paterno
B., 19, 2529
4-957 W.
—0-75
1 W.
—0-1485
Dextrose
C.H.,,OK
1 W.
—0-107
B. 15, 1749
Eaoult
C. R., 94, 1518;
44, 7, 952
Mannitol
C«H,.O,
1 W.
—0-099
A. C. [3], 28, 133
Saccharose
1 W
—0-054
5 D.C.
—0-3 I.
Guthrie
P. M. [5], 2, 216
31, 36
10 „
—0-5 I.
viii., 1008
15 „
—0-9 I.
20 ,,
—1-3 I.
25 „
—1-8 I.
30 „
—2-4 I.
35 ,,
—3-2 I.
40 „
—4-1 I.
45 „
—5-4 I.
50 „
—7-0 I.
51 "4 p.c.
—8'5 ch.
67'33 ,,
OS.
Lactose (A. C. [3], 28, 133)
Salicine „
))
^IsHssOy
1 W.
1 W.
—0-050
-0-060
B., 15, 1749
!>
Eaoult
»
C. R, 94, 1518
»
44, 7, 952
Hydrocyanic acid
CHN
1 W.
—0-718
B., 15, 1749
Raoult
C. R, 94, 1518
44, 7, 952
Cyanamide
CH2N2
0-9803 W.
—0-38
Paterno
B., 19, 2529
1 W
—0-3876
Metliylamine
CH,N
1 W.
—0-638
B., 16, 3054
Raoult
C. R., 97, 941
46, 255
Acetonitril
C2H3N
2-489 W
—1-13
Pateruo
B., 19, 2529
2-952 W
—1-28
7-824 W
—3'30
1 W
— 0-4364
Dicyandiamide
C3H4N4
1-57 W.
1 W.
—0-29
-0-185
»
»
}J
1)
Ethylamine (A. C. [3], 28, 133)
C2H7N
1 W.
—0-411 (
B., 15, 1749 ; )
16, 3054 '
Raoult
(C. R.,94, 1518;
( 97, 941
44, 7, 952; 46,
255
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
773
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Ethylamine (b.p. 18°)
C2H7N
11
0'99 p.c.
5-0 „
10- „
15- „
20- „
20-64 „
25- „
30' „
32-4 „
35- „
40- „
50- „
1 W.
1 W.
5 p.c.
10 „
15 „
20 „
21 „
22 „
22-5,,
23 „
25 „
30 „
35 „
40 „
45 „
50 „
60 „
70 „
1W.
(?)
0-6553 W.
0-6651 W.
1-1095 W.
1-6528 W.
2-1684 W.
3-7103 W.
4-1646 W.
7-6970 W.
13-8540 W.
5 p.e.
10,,
15 „
18 „
19-1 p.c.
20 „
30 „
40 „
50 „
70 „
80 „
1 W.
- 0-4 I.
- 2-01.
- 4-7 I.
- 8'4 I.
—13-3 I.
—13-9 ch.
—9-5 sch.
—8-1 sch.
—8-0 sch.
—8'2 sch.
— 10-1 sch.
—16-4 sch.
—0-342
—0-312 j
-1-1 I.
-2-9 I.
—5-2 I.
-8-4 I.
—9-1 I.
—9-9 I.
—11-0 ch.
— 9'9 sch.
- 9-1 sch.
— 8-3 sch.
— 8"0 sch.
- 8-2 sch.
— 8'6 sch.
- 9-1 sch.
—12-2 sch.
—23-4 sch.
-0-164
—0-7 ch.
—0-04
—0-04
-0-07
—0-13
—0-16
—0-26
—0-28
—0-42
—0-64
-1-0 I.
—2-0 I.
—2-9 I.
-3-4 I.
—3-8 ch.
—3'5 sch.
— 4"! sch.
—5-1 sch.
—6-7 sch.
—13-6 sch.
—20-6 sch.
—0-124
B., 16, 3054
B., 15, 1749 ; \
16, 3054 J
pure
B., 16, 3054
B., 16, 3054
Guthrie
i,
„
»
,,
,,
,,
,,
,,
,,
„
,,
Eaoult
,,
Guthrie
,,
»,
„
,,
,,
,,
,,
,,
j,
,,
j,
,,
J!
,,
,,
Eaoult
Guthrie
Paterno
,,
,,
,i
,,
,,
,»
,,
»
Guthrie
»
,,
,?
,,
,,
,»
„
,,
»
,,
Eaoult
P. M. [5], 18, 24
M
»
»)
>t
)T
))
»
JJ
t)
)»
C. B., 97, 941
fC.R,94, 1518;
t 97, 941
P.M. [5], 18, 27
H
11
»
»
n
j»
»i
»»
)»
jj
»»
n
»)
»»
j)
C. R, 97, 941
P. M. [5], 18, 105
B., 19, 2529
n
)»
i)
n
»
n
»
))
P. M. [5], 18, 28
))
»)
J)
J)
11
»
))
))
11
J>
C. E., 97, 941
44, 337
)>
11
11
11
i»
»
»»
)>
»j
11
j)
46, 255
44, 7, 952 ; 46,
255
48, 337
n
»
n
ti
n
»>
11
11
11
11
11
11
11
yi
11
46, 255
48, 337
48, 337
j>
»
11
11
11
11
11
11
11
11
46, 255
11
11
11
5t
11
»
J)
11
C3H9N
»
C4HUN
))
))
11
)J
))
»)
11
)»
)»
)}
»)
1)
11
)»
C6H7N
C6H9N3
))
1)
1)
11
i)
)'
11
C6H15N
»»
JJ
Propylamine (A. C. [3], 28, 133) ....
Diethylamine (b.p. 54°)
11 •••• •"*
Triethylamine (b.p. 88°)
}»
>J
»
1)
»
II
C10H14N,,
C2H3C13O2
C2H5C1O
C6H8C1N
»»
,,
,j
1 W.
+4H20
1 p.c.
4 „
5 „
6 „
—0-114
—11 to— 17
—0-2 I.
—1-0 I.
—1-3 I.
-1-6 I.
B., 15, 1749
CH2C1.CH2OH
Eaoult
Bouchavdat
Guthrie
,,
,,
,5
C. E., 94, 1518
C. E., 100, 454
P. M. [5], 18, 105
n
»)
11
44, 7, 952
48, 499
48, 337
11
11
11
Aniline hydrochloride
11 n
11 "
»i n
774
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Aniline hydrochloride
j» »j
„ „ ....
jj jj •••• *••
jj jj **" **'
jj jj •••* •••
jj >j
jj jj "••
Trimethylethylammoniumiodide ....
C6H8C1N
J)
JJ
JJ
JJ
JJ
J)
JJ
C6HUIN
CH4ON2
7 p.c.
8 „
9 „
10 „
*•*- JJ
12 „
13 „
20 „
25 „
30 „
31-86 p.c.
35
40-35 „
46-72 „
1 W.
1 W
—1-9 I.
-2-2 I.
—2-5 I.
—2-8 I.
—3-0 I.
—3-3 I.
—3-6 I.
-5-7 I.
—7-2 I.
-9-0 I.
— 10-7 ch.
—8-0 S.
OS.
+ 13-1 S.
— 0-J60
—0-286
—10-5
MM
B.r., 17, 196
B 15 1749
Guthrie
jj
jj
Raoult
P. M. [5], 18, 105
»
C. R, 98, 510
C. R, 94, 1518
48, 337
46, 701
44, 7, 952
„ nitrate
CH504N3
C2H-ON
8-57 p.c.
1 W
—4-0 ch.
— O'SOl
-4-5
B 15 1749
Guthrie
Raoult
P. M. [5], 6, 39
C. R., 94, 1518
36, 428
44, 7, 952
Diammoninm oxalate
Tetramethylammonium hydroxide
Trimethylethylammonium „
C2H804N2
C4H13ON
C5H1SON
CaHsCsN.,
2-8 p.c.
1 W.
1 W.
2 p c
—0-2 ch.
—0-404
—0-353
— 0'4 I
B., 16, 3054
Guthrie
Raoult
Guthrie
P. M. [4], 49, 268
C. R, 97, 941
jj
P. M. [5], 18, 106
46, 255
48, 337
4
—0-8 I
R
—1-1 I
"
g
—1-5 I
10
— 2'0 I.
10-61
—2-2 ch
—2-2
10-94
OS.
"
15-58
+ 13-1 S
Ditetramethylanimonium oxide
Aniline salicylate
C,,H,,O,N
10 „
0*24
—16
— 0-06 ch.
»
P. M. [5], 18, 501
P. M. [5], 18, 108
48, 337
0*28
OS
0*65
+ 6'2 S
0*77
+ 16-8 S.
V
Dianiline oxalate
C H"O N
0'14
— 0'4 ch.
P. M. [5], 18, 107
14 16 4 2
0*29
OS.
l-OQ
+ 14-5 S
Aniline pyrogallate ....
Q*OQ
—1-0 I.
P. M. [5], 18, 109
» ua „
20'00 „
23-98 „
oo.r»K
—2-7 I.
—4-6 ch.
OS
—4-6
»
JJ
JJ
dfi-fWl
+ 17-8 S
Dianiliue sulphate ....
C H O SN
O'l I
Guthrie
P. M. [5], 18, 107
48 337
0'2 I
jj
A-f^
— 0'6 I
jj
-I.QO
0'9 ch
—0-8
iOtJ „
4'Q1
0 S
"
"
^ »i „
K-QA
+ 13"! S
"
0 S4 „
T V*^
+ 100 S
"
"
Silver potassium cyanide
Barium formate
„ acetate
AgK(CN)2
Ba(CHO2)2
Ba("C H O "1
1 W.
1 W.
1 W
—0-156
—0-215
0"193
....
Raoult
C. E., 99, 915
C. R, 98, 1047
48, 122
46, 808
„ malate
BaC H O
1 W
A.A7F:
"
„ cobalticyanide
Calcium acetate
Ba3(CoCy6)2
CaCC H OH
1 W.
—0-063
—11-8
Guthrie
C. R., 98, 1048
P M. [5] 6 44
36 428
Copper „
CufC H CM
1 W
O-1 71
Raoult
C. R, 98, 1047
46 808
Mercuric cyanide
HeYCN1)
o-AFi ,*h
—0'6
Guthrie
P. M. [5] 6, 40
36, 428
1 "W
/vn^o
Raoult
C R 87 169
36 4
"
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
775
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Gryogen.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Mercuric cyanide .. .
Hg (ON).
1 W.
—0-069
Raoult
C R 98 1047
4ft sos
,, potassium cyanide
Potassium oxalate
HgK2(CN)4
KjC.O4
1 W.
1 W.
—0-150
—0-271
B.r., 17, 196
ji
C. R., 99, 915
(j R gg 5iQ
48, 122
46 7O1
17'62 p.c.
— 6'3 ch.
— 6'2
P M [5] 6 40
36 4.9ft
„ cyanide
KCN
1
—33-0
—21-1
P M [5] 6 44
1 W.
—0-495
B r., 17 196
Eaoult
0 R 98 510
»
46 701
„ formate ....
KCHO2
1 W.
—0-419
C R 98 509
„ acetate
KC.H,O,
1 W.
—0-352
tartarate
K,C,H.OC
1 W.
—0-160
C R 98 510
>}
„ thiocyanate
„ methylic sulphate
)> »)
» »
» .. i)
» i» ••••
j» j)
» »
» »
„ ethylic sulphate
jj »
» »)
H I»
„ ,,
»> »J •—
?? ))
)» »
„ amylic sulphate
„ „
„ „
„ „
» „
„ „
„ cobalticyanide ....
„ ferricyanide
5) )J
„ „
„ ferrocyanide
i) »
,, antimonious tartarate ....
KCSN
KCH304S
I)
))
)»
»
»
»1
KCSH,04S
))
))
>»
)5
»)
»J
KC6Hn04S ,
)»
»»
»J
))
K3CoCy6
K3FeCy6
))
K4FeCy6
KSbC4H407
Mg (C,H,O,),
1 W.
10 p.c.
15 „
20 „
30 „
39-84 p.c.
40p.c.
47-08 p.c.
54-8
10 p.c.
20 „
30 „
40 „
45-01 p.o,
50 p.c.
53-71 p.c.
62-35 „
10 p.c.
20 „
24-03 p.c.
25 p.c.
33-44 p.c.
59-46 „
1 W.
1 W.
1 W.
19-8 to 24 p.c.
11-9 p.c.
1 W.
1 W.
1 W.
—0-342
—2-3 I.
-3-6 I.
—5-0 I.
—8-0 I.
— 11-8 ch.
—11-5 S.
OS.
+ 12-3 S.
- 2-2 I.
— 4-9 I.
- 8-2 I.
—12-1 I.
—14-2 ch.
-6-0 S.
OS.
— 15-0 S.
—1-9 I.
—4-3 I.
—5-4 ch.
—4-8 S.
OS.
+ 17-3S.
—0-146
-0-146
-0-144
—3-9 ch.
— 1-7 eh.
—o-iio
—0-055
—0-344
)>
—11-3
—13-9
—5
B.r., 17, 196
B.r., 17, 196
-3-9
—1-61
B.r., 17, 196
»
Illingworth
j>
i)
»
u
j»
»i
»»
V
»»
»»
»
)1
»»
n
j)
H
)»
»
)»
)>
Eaoult
)»
»)
Guthrie
»
Raoult
i)
»
P.M. [5], 18, 125
V
1)
))
»
M
n
»
>»
ii
»»
»)
n
»t
»i
>5
H
H
»
>i
»»
C. E., 98, 510
C. E., 87, 169
C. E., 98, 511
P. M. [5], 6, 39
»
C. E., 98, 511
C. E., 98, 1047
»
j)
48, 1339
»?
»
»
j»
;i
»
))
)»
?»
»)
))
»5
»1
)1
)»
)>
»»
)*
)J
>1
46, 701
36, 4
46, 701
36, 428
»
46, 701
46, 808
„ succinate
malate ... .... .. .
MgC4H404
MsrC^H.O.
1 W.
1 W.
-0-171
—0-124
»i
ji
)»
, citrate ....
Mg,(C8H,O,)2
1 W.
—0-022
C. E., 98, 1048
NajCjO4
?
—1-7 ch.
Guthrie
P. M. [5], 6, 44
36, 428
NaCHO2
?
viscid — 14
—14-3
NaC-jHaO,,
5 p.c.
— 2-2 I.
P. M. [5], 2, 215
viii., 1008
10 „
- 5-1 I.
15 „
- 9-1 1.
20 „
—14-0 I.
„ „
,, „ .... -... ....
)»
))
22 „
23-3 p.c.
26-6 „
—16-0 I.
—18-0 ch.
OS+2H.,O
—18
)>
n
»
>1
!»
»
1 W.
—0-390
B.r., 17, 196
Raoult
C. R., 98, 509
46, 701
Monosodium tartarate
NaC4H606
NaC6H7O7
1 W.
1 W.
—0-181
—0-125
»)
»
C. R., 98, 510
)>
»»
»>
Disodium citrate
Na,C6H6O-
1 W.
—0-161
»
JJ
Na,UBH,O-
1 W.
—0-186
»
))
?
—11-3
Guthrie
P. M. [5], 6, 44
36, 428
Sodium nitroprusside
Na.FeCy^NO)
Pb(C2H;,O2).,
1 W.
1 W.
—0-179
-0-068
B.r., 17, 196
Eaoult
C. E., 98, 510
C. E., 98, 1047
46, 701
46, 808
776
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CBTOHTDEA.TKB.
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Lead acetate
Zinc
Pb.(C2H302).!
Zn(C2HA)2
18-0 p.c.
23-0 ,
-1-4 ch.
-5-9 ch.
— 17
Guthrie
P. M. [5], 6, 38
P. M. [5], 6, 41
36, 428
Gum arable
Gelatine
Albumen
20 p.c. gelatine-)- 20 p.c. gum arable
+ 20 p.c. H2O
1 to 30 p.c.
35 p.c.
45 „
5 to 20 p.c.
5 p.c.
10 „
13'37 p.c.
01.
0 to— 0-5 I.
—1-2 I.
01.
0 to 0-2 I.
0 to 0-3 I.
0 to— 0-5 I.
0
Guthrie
P. M. [5], 2, 220
P. M. [5], 2, 222
P. M. [5], 2, 221
P. M. [5], 2, 222
31, 36
B.— MIXTURES WITH BENZENE, C6H6.
(See Eaoult, C.R., 95, 1031 ; 102, 1307 ; A.C. [6], 2, 66 ; Jour. Chem. Soc., 44, 278 ; 46, 952 ; 50, 763.)
Hexane C6H14
Naphthalene (46, 952) C10H8
Terebenthene C10H16
Anthracene CUH10
Carbon tetrachloride CC14
„ disulphide .... .... .... CS2
Trichlormethane CHC13
Ethylene dichloride C2H4C12
Ethyl bromide C2H8Br.
Methyl iodide (46, 952) CH3I
Ethyl „ C2H5I
Formic acid CH2O3
Methyl alcohol CH4O
Ethyl aldehyde C2H4O
Acetone C3H6O
Ethylic formate (46, 952) C3H6O2
Dimethylic oxalate C4HfiO4
Diethyl oxide C4H10O
Benzoic aldehyde ... C7H6O
Ethylic valerate C7H14O3
Methylic methylsalicylate C9H10O3
Valerone C9H,8O
Camphor C10H16O
Lapachone Ci5H14O3
Lapachic acid.... .... .... .... „
Santonide ClbH18O3
Glycerol tributyrate C15H26O6
„ trioleate C57H104O,
Diethyl sulphide C4H10S
Ethyl cyanide C3H5N
Chloral C3HC13O
Methylic nitrate OH3O3N
Trinitroglycerol C3H5O9N3
Nitrobenzine C6H6O2N
Allyl thiocarbimide ! C4H5SN
I
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1-796 W.
1-096 W.
2-182 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
1 W.
-0-597
—0-391
—0-366
—0-287
—0-333
—0-654
—0-428
—0-491
—0-461
—0-335
-0-331
—0-504
—0-791
—1-107
—0-850
—0-666
—0-417
—0-671
—0-473
—0-384
—0-339
—0-359
—0-338
—0-32
—0-21
—0-42
—0-161
—0-056
—0-576
—0-938
—0-342
—0-640
—0-220
—0-390
—0-519
A. C. [6], 2, 66
A. C. [6], 2, 66
A. C. [6], 2, 66
Raoult
Paterno
Eaoult
C. R., 95, 188
A. C. [6], 2, 66
)>
C. R., 95, 188
B., 19, 2529
C. R., 95, 188
42, 1260
46, 952
42, 1260
42, 1260
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
777
C.— MIXTUEES WITH NAPHTHALENE, C10H8.
(See Raoult, C. R, 102, 1307 ; A. C. [6], 2, 66 ; Jour. Chem. Soc., 46, 952 ; 50, 763.)
Name.
Formula.
Composition.
Freezing
Point.
Temperature
of Cryogen.
Authority.
Reference.
Watts' Diet.
& J. Gh. Soc.
C2H4O2
1 W.
—0-306
Baoult
A. C. [6], 2, 66
46 952
Stearic acid ...
100 acid
56
Courtoune
C. R., 95, 923
44, 177
„ + 7'5
53-5
CIOHS
„ + 15 „
51-5
„ + 22-5,,
50-0
„ + 40 „
47-0
» + 45 ,,
47-5
47-6
» + 79 „
55-6
58-5
„ +135 „
66-0
„ +270 „
73-0
0 „ +100 „
79-0
D.— CARBON BISULPHIDE AND ETHYL ALCOHOL.
Carbon disulphide and ethyl alcohol
C2H60
5-06 p.c.
clear — 18'4
Guthrie
P. M. [5], 18,504
» »
15
10-46 „
turbid — 14'4
....
»
)V
,, D
ii
15-11 „
» -15-9
jj
J)
„ »
*5
20-04 „
„ -16'1
»
»)
,, 11 •••
)>
34-89 „
» -1"
jj
»1
„ ))
i,
40-42 „
clear —20
»
»>
j> >i
»
50-09 „
»» j»
»
1)
,» )*
j>
60-04 „
» )»
....
ii
)»
„ i)
J*
70-08 „
» »
»»
)1
E.— MIXTURES WITH ETHYLENE DIBROMIDE, C2H4Br2.
(See Raoult, C. E., 95, 1030 ; 102, 1307 ; A. C. [6], 2, 66 ; Jour. Chem. Soc., 44, 278 ; 46, 952 ; 50, 763.)
F.— MIXTURES WITH FORMIC ACID, CH202.
(See Raoult, C. R., 95, 1031 ; A. C. [6], 2, 66 ; Jour. Chem. Soc., 44, 278 ; 46, 953.)
G.— MIXTURES WITH ACETIC ACID, C2H402-
(See Eaoult, C. R, 95, 1031 ; A. C. [6], 2, 66 ; Jour. Chem. Soc., 44, 278 ; 46, 952.)
Hydrochloric acid *
Sulphuric acid . .
HCl
H2S04
1 W.
1 W.
—0-471
—0-189
Raoult
A. C. [6], 2, 66
»)
46, 952
n
0-5 W.
+ 16-4
Riidorff
B., 3, 393
Methyl iodide
CH3I
1 W.
—0-273
Baoult
A. C, [6], 2, 66
46, 952
Formic acid
CH2On
1 W.
—0-793
JJ
»
M
Ethyl alcohol ....
C,H6O
1-8 W.
+ 15-25
Kudorff
B., 3, 393
Picrotoxide hydrate
Ci5H18O7
1-0339 W.
1-2106 W.
—0-15
—0-16
Pateruo
)j
B., 19, 2529
»
O TT O
0-9926 W.
—0-18
»»
»
or C12H14O5
1-046 W.
—0-19
1.1*
»
H
C6H9N3
1-342 W.
—0-26
j»
»i
5 G
778
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
H.— MISCELLANEOUS MIXTURES.
Name.
Formula.
Composition.
Melting
Point.
Melting
Point.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Thymol and various compounds ....
Details not given
Raoult
C. R, 102, 1307
50, 763
/3-Naphthol and iodoform
C10H8O & CHI3
pure CHI3
119
....
BrUgelmann
B., 17, 2363
,, ,,
„
from 10 to 90 p.c.
102
„
„
CHI3
„ „
u
pure C10H8O
122
....
„
„
Suberic and azelaic acids
C8H1404&C9H1604
pure C9H16O4
106
....
Gauttner & Hell
B., 14, 1547
„ „
„
95 p.c. „
104
....
„
„
„ „
,,
90 „ „
103-5
....
„
„
„ „
„
86 „ „
98-5
11
,,
„ „
„
81 i, ,1
98
„
„
,, „
„
76 „ „
96
„
„
,, „
„
72 „ „
98-100
....
„
11
„ „
„
66 „ „
99-101
„
„
„ „
11
62 „ „
106-109
....
)J
„
„ „
„
57 „ „
108-109
„
„
„ ,,
„
51 u i)
115
„
„
„ „
„
42 „ „
123
„
„
„ „
„
**•*• » M
124-128
....
11
„
„ „
„
21 „ „ '
125-130
„
„
„ .,
n
10 „ „
135-136
....
„
JJ
„ „
„
pure C8H14O4
140
....
„
„
Benzoic and cinnamic acids
C7H602 & C9H8O2
pure C,H8O2
133-3
....
Kachler
B., 2, 515
„ „
„
99 p.c. „
131-8
....
„
„
,, „
„
90 „ „
126-6
„
„
„ „
„
80 „ „
118-0
„
„
„ „
1)
70 „ „
108-2
„
„
„ „ ....
„
60 „ „
98-7
....
„
„
„ „
„
^ J> JJ
84-3
i,
„
„ „
„
40 „ „
87-1
„
51
„ „
„
30 „ „
101-4
„
„
„ „
„
20 „ „
106-4
....
„
„
„ ,,
„
10 „ „
111-5
....
„
„
„ „
„
*- 11 11
118-2
„
„
„ „
„
pure C7H6O2
123-3
....
„
„
Phenylacetic and hydrocinnamic
C8HA&C9H1002
pure C8H802
melts com-
....
Salkowski
B., 18, 323
48, 602
acids
pletely 77
>. >i
11
90 p.e. „
„ 71-5
....
„
„
„
„ „
„
80 „ „
„ 65-5
„
„
„
„ „
„
70 „ „
„ 58
....
„
11
„
„ „
„
60 „ „
» 50
»
„
„
n 11
11
50 „ „
„ 39-5
„
•„
„
„ „
„
47-6,, „
„ 37-5
„
„
„
» »
„
40 „ „
„ 26-5
„
„
11
I! >!
„
37-5,, „
„ 25-5
....
„
u
„
„ „
„
35 „ ,,
„ 21-0
....
„
n
11
» 11
„
32"5,, „
„ 25-5
....
„
„
„
11 11
„
30 „ „
„ 27-0
„
„
„
11 51
„
20 „ „
33-0
....
„
H
„
11 11
„
10 „ „
„ 41-5
„
„
„
„ „
„
pure C9H10O2
„ 47-5
„
„
„
Nitrobenzene and various compounds
A. C. [6], 2, 66
....
C. R, 95, 1030 ;
44, 278 ; 46,
1-2 & 1-3
1-2 & 1-4
1-3 & 1-4
102, 1307
953 ; 50, 763
m.p.
m.p.
m.p.
Mixtures of nitrobenzoic acids
proportion 10 '. 10
92-98
200
165-205
Widnmanu
B.. 10, 1159
32, 783
„ 11
1015
125
142-190
127-185
„
„
M
u 11
11 10:i
140
141
130-155
„
„
„
11 11
lo:0-5
144
145
132-133
„
n
JJ
ii 11
„ 10:0-2
146
147
134-135
„
„
J)
FREEZING (AND MELTING) POINTS OF MIXTURES, INCLUDING CRYOHYDRATES.
779
Name.
Formula.
Composition.
Melting
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
1-2 and 1-3.
1-2 and 1'4.
1-3 and 1'4.
m.p.
m.p.
m.p.
Mixtures of nitvobenzoic acids
proportion 10 !0'1
146
145
135-136
Widnmann
B., 10, 1159
32, 783
„ »
„ o-i : 10
132-135
233-237
236-238
»
)J
»
!> V
„ 0-2 : 10
132-134
228-235
232-237
»
J»
n
)) »
„ 0-5:10
132-140
222-235
215-234
j»
))
u
)> 11
i : 10
132-133
200-225
205-230
)5
»1
n
» II
5:10
112
210-216
195-208
)»
»)
)>
)1 11
pure acid
140-141 (m)
238 (p)
149 (o)
IJ
JJ
»
Sodium acetate and nitrate
C2H3NaO2
pure C2H3NaO.2
319
....
Briigelmann
B., 17, 2364
1, 11
ii
50 p.c. NaNO3
complete 100
....
»
J)
)> 11
n
pure NaNO3
310-330
....
j?
7J
Acetic and sulphuric acids and water
100 pts. HAc
+ 10 pts. H3O
5-8
Eudorff
B., 3, 393
+ 2 pts. H,SO4
11 11
100 pts. HAc
+10 pts. H2O
10-7
j)
»
+20 pts. H2SO4
Chlorethyl alcohol, hydrochloric
2(CHsCl.CHjOH)
+8H2O
10-6
Bouchardat
C. R, 100, 454
48, 499
acid, and water
+HC1
5 G 2
780
IV.-MISCELLANEOUS MELTING AND BOILING POINT DATA
(FATS, OILS, &c.).
m.p. = melting point, s.p. = solidifying point, b.p. = boiling point, r.s. = resolidifies, sp. gr. = specific gravity.
Name.
Melting, Boiling, and
Solidifying Point.
Remarks.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Hatchettine
Picropodophyllin
Sikimine
m.p. 54-64
m.p. 200-210
m.p. 175
Mineral
Comp. unknown
Dewalque
Podwissotsky
Eykmann
Jahr. f. Mineralogie
B., 15, 337*; P.J. [3], 12,
1011
B., 14, 1721; P.J. [3], 11,
48, 220
42, 976
40, 919
1046
Paraflin oil
„ wax
i> »
» i»
)> »
Petroleum ....
a.p.— 35
m.p. 38—52 ; b.p. 350-390
m.p. 52-56 ; b.p. 390-430
m.p. 49-6-53-2 ; r.s. 49'6-53
m.p. 49'5
s.p.— 52
sp. gr. 0-810
soft ; sp. gr. 0-87-0-88
hard ; sp. gr. 0'88-0'93
sp. gr 0'790
Coleman
Landolfc
»
Riidorff
Wolff
Coleman
C. F., 51, 174
Phys.-Chem. Tabellen, 139
» ii
P. A., 145, 279
D. P., 217, 411
C. N., 51, 174
26,238 ;vii.,605
viii., 937
b.p. 40-70
sp. gr. 0'65-0"66
Laudolt
Phys.-Chem. Tabellen, 139
Ligroin (for lamps)
Photogen „
Solar oil „
Gasolin (for oil extraction)
Benziu
b.p. 110-120
b.p. 170-245
b.p. 245-310
b.p. 70-90
b.p. 90-110
sp. gr. 0-7-0-73
sp. gr. Q'76-0-8
sp. gr. 0-80-0-83
sp. gr. Q-66-0'69
sp. gr. 0'69-0-70
D
»
)»
?>
» )!
» )>
» ))
»*• »
Putzol, Lackol
Schmierol
b.p. 120-170
b.p. 310-350
sp. gr. 0-73-0-76
sp. gr. 0-83-0-87
)»
j-i
» >;
)) »
Cider
s.p.— 2-0
— 4*8 p c alcohol
Raoult
C. E., 90, 867; A. C. [5],
38, 523
•Beer
Vin ordinaire (rouge)
„ „ (blanc)
Beaujolais .... ....
s.p.— 2'8
s.p.— 27
s.p.— 3'0
S D. — 4'4
= 6-3 „ „
= 6-8 „ „
= 7-0 „ „
— 10-3
»
)»
n
20,207; B., 13,1883
» )»
jy »
»» , >»
»
»)
»
j)
Bordeaux rouge
Bourgogne rouge
Roussillon rouge
Marsala
s.p.— 5-2
s.p.— 5-7
s.p.— 6-9
s.p.— lO'l
= 11-8 „ „
= 13-1 „ „
= 15-2 „
= 207 „ „
ij
»•>
»
5)
j» n
)» »
)? »
») »
u
»
»
)i
Palm oil (fresh, soft)
„ (fresh, hard)
„ (old)
Tea oil
m.p. 30 ; r.s. 21
m.p. 38 ; r.s. 24
m.p. 42 ; r.s. 38
does not solidify — 13'3
sp. gr. 0-905
sp gr G'9175 at 15'5°
Wimmel
»
D
P. A., 133, 121
)}
M
P J [3], 15, 634
48, 1022
Wood oil
— 13-3
sp gr 0'9401 at 15'5°
Cabbage oil
Spermaceti....
s.p.— 12
m.p. 44—44*5 ; r.s. 44
sp. gr. 0-914 at 15'5°
sp <T 0'88 0'94
»
jj
P. A., 133, 121
)J
m.p. 43-5-44-3 ; r.s. 43'4-44'2
Riidorff
P. A., 145, 279
26,238 ;vii.,605
m.p. 45'2
Wolff
D. P., 217, 411
viii., 937
Beeswax (yellow)
(white)
„ (yellow)
„ (white) „
„ (yellow)
„ (white)
Ceresin
m.p. 62-62-5 ; r.s. 62
m.p. 63-63-5 ; r.s. 63
m.p. 63-4 ; r.s. 61'5-62'6
m.p. 61'8; r.s. 61 '6
m.p. 64
m.p. 62-8
m.p. 71'35
sp. gr. 0-96-0-965
sp. gr. 0-96-0-969
Wimmel
»?
Rudorff
Wolff
, »
P. A., 133, 121
D
P. A., 145, 279
>J
D. P., 217, 411
JJ
f
26,238 ;vii.,605
ii
viii., 937
)•)
Japan wax
m.p. 53-5-54-5 ; r.s. 40'5-41
sp gr 0"992
Wimmel
P. A., 133, 121
„ >, ....
m.p. 50-4-51'Q
m.p. 41'3
RUdorff
Wolff
P. A., 145, 279
D. P., 217, 411
vii., 605
viii., 937
Butter (fresh)
m.p. 31-31-5; r.s. 19-20
sp. gr. 0-865-0-868
Wimmel
P. A., 133, 121
MISCELLANEOUS MELTING AND BOILING POINT DATA.
781
Name.
Melting, Boiling, and
Solidifying Point.
Bemarks.
Authority.
Reference.
"Watts' Diet.
& J. Ch. Soc.
Butter (tub)
m.p. 32-5; 32-37; r.s. 24
m.p. 26'4 ; r.a. 23'8
sp. gr. 0'94
Gives 87'5-88 per cent, of insoluble
Wimmel
Dubois and Fade
P. A., 133, 121
B. S., 43, 207
48, 844
,, (P"re)
r.s. 34
r.s. 37
r.s. 40
fat acids ; s.p. 37"5
+ 10 p.c. horse fat
+20 „
MUnzel
»
B., 14, 1125
»
r.s. 44
+30 „
r.s. 40
+ 10 p.c. sebum tabulat
r.s. 43
+ 20 „ „
r.s. 46
r.s. 38
+ 10 p.c. adeps suillus
r.s. 41
+ 20 „ „
r.s. 43
+30 „ „
» - ••** •••• *•*•
r.s. 40
r.s. 48
+25 p.c. margarin butter
)>
»
Margarin butter
Nutmeg „
„ j,
Beef fat (fresh)
„ (old)
>t
r.s. 56
m.p. 43-5-44 ; r.s. 33
m.p. 70-80
m.p. 43 ; r.s. 33
m.p. 43-5 ; r.s. 34
m.p. 43-5-45 ; r.s. 27-35
m.p. 42-2; r.s. 41 -5
sp. gr. 0-968
Gives 94'2 per cent, of insoluble
»
Wimmel
Riidorff
Wimmel
it
Riidorff
Dubois
»
P. A., 133, 121
P. A., 145, 279
P. A., 133, 121
»
P. A., 145, 279
B. S., 43, 207
vii., 605
vii., 605
48, 844
Mutton fat (fresh)
(old)
,, .... ....
„
„
Veal fat
m.p. 47 ; r.s. 36
m.p. 50-5 ; r.s. 39'5
m.p. 46-5-47-4 ; r.s. 32-36
m.p. 45-6
m.p. 46'6 ; r.s. 44
m.p. 37'2 ; r.s. 3.V9
fat acids ; s.p. 44'2
sp. gr. 0-92
Gives 94-5 per cent, of insoluble fat
acids; s.p. 49'4
Gives 94-54 per cent, of insoluble
Wimmel
»»
Kudorff
Wolff
Dubois
P. A., 133, 121
))
P. A., 145, 279
D. P., 217, 411
B. S., 43, 207
vii., 605
viii., 937
48, 844
»»
Lard
m.p. 33-2 ; r.s. 33
m.p. 41-5-42 ; r.s. 30
fat acids ; s.p. 42 7
Gives 93-4 per cent, of insoluble fat
acids ; s.p. 42
sp. gr. 0-92-0-94
»
Wimmel
))
P. A., 133, 121
))
Margarin
Cocoa butter
si )>
J) 5)
„ ))
Cocosol
m.p. 39-6 ; r.s. 38'4
m.p. 33-5-34 ; r.s. 20'5
m.p. 33-5
m.p. 31-8
m.p. 31-6; r.s. 30'2!
m.p. 24-5 ; r.s. 20-20-5
Gives 95'6 per cent, of insoluble fat
acids; s.p. 95'6
sp. gr. 0-89-0-91
Gives 94-73 per cent, of insoluble
fat acids ; s.p. 48 '8
Dubois
Wimmel
Eudorff
Wolff
Dubois
Wimmel
B. S., 43, 207
P. A., 133, 121
P. A., 145, 279
D. P., 217, 411
B. S., 43, 207
P. A., 133, 121
48, 844
vii., 605
viii., 937
48, 844
Illipe fat
m.p. 32-8 ; r.s. 31
Gives 95'64 per cent, of insoluble
Dubois
B. S., 43, 207
48, 844
Nitromolasses
b.p. 180-200
fat acids ; s.p. 50'6
Explodes 220-250
Gilles
D. P., 255, 337
48, 852
782
V.— VOLUMES AND CORRESPONDING YEARS OP ISSUE OF THE MORE
IMPORTANT CHEMICAL AND PHYSICAL PERIODICALS.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Philosophical Transac-
ions of the Royal Society
of London.
1833
1834
1835
1836
123
124
125
126
Proceedings of the Royal
Society of London.
Journal of the Chemical
Society of London.
1869
1870
1871
1872
19,20
21,22
23,24
25,26
2nd
1827
1828
Series.
1, 2
3, 4
1837
127
1832
1
1849
1
1873
27,28
1829
5, 6
1781
71
1838
128
1833
2
1850
2
1874
29, 30
1830
7, 8
1782
72
1839
129
1837
3
1851
3
1875
31,32
1831
9,10
1783
73
1840
130
1843
4
1852
4
1876
33,34
1832
11
1784
74
1841
131
1851
5
1853
5
1877
35,36
1785
75
1842
132
1854
6
1854
6
1878
37,38
3rd Series.
1786
76
1843
133
1856
7
1855
7
1879
39,40
1832
1
1787
77
1844
134
1857
8
1856
8
1880
41,42
1833
2, 3
1788
78
1845
135
1859
9
1857
9
1881
43,44
1834
4, 5
1789
79
1846
136
1860
10
1858
10
1882
45,46
1835
J "
6, 7
1790
80
1847
137
1862
11
1859
11
1883
47,48
1836
8, 9
1791
81
1848
138
1863
12
1860
12
1884
49,50
1837
1 v
10,11
1792
82
1849
139
1864
13
1861
13
1885
51,52
1838
12,13
1793
83
1850
140
1865
14
1862
14,15
1886
53,54
1839
14,15
1794
84
1851
141
1867
15
1863
16
1887
55
1840
16,17
1795
85
1852
142
1868
16
1864
17
1841
18,19
1796
86
IRfi^
1 A**
1869
17
1865
18
1797
87
AOUO
1854
Ito
144
1870
18
1866
19
1842
1843
20, 21
22,23
1798
88
1855
145
1871
19
1867
20
The Philosophical
1844
24,25
1799
89
1856
146
1872
20
1868
21
Magazine and Journal
1845
26,27
1800
90
1857
147
1873
21
1869
22
of Science {London).
1846
28,29
1801
91
1858
148
1874
22
1870
23
1847
30 31
1802
1803
1804
1805
92
93
94
95
1859
1860
1861
1862
149
150
151
1*19
1875
1876
1877
1878
23
24
25,26
27
1871
1872
1873
1874
24
25
26
27
1798
1799
1800
1, 2
3- 5
6- 8
AO1* /
1848
1849
1850
32,33
34,35
36,37
1806
1807
96
97
1863
1864
&mn
153
154
1879
1880
28,29
30
1875
1876
28
29,30
1,801
1802
9-11
12-14
4th Series.
1808
98
1865
i ^
1881
31,32
1877
31,32
1803
15-17
1851
1, 2
1809
99
1866
iOO
1 ^fi
1882
33
1878
33,34
1804
18-20
1852
3, 4
1810
100
1867
iO\j
1 fi7
1883
34,35
1879
35,36
1805
21-23
1853
5, 6
1811
101
1868
i • ' '
1 f^fl
1884
36,37
1880
37,38
1806
24-26
1854
7, 8
1812
102
1869
At)O
I^IQ
1885
38,39
1881
39,40
1807
27-29
1855
9,10
1813
103
1870
1«J<7
1 fiO
1886
40,41
1882
41,42
1808
30-32
1856
11,12
1814
104
1871
i\J\J
161
1887
42
1883
43,44
1809
33,34
1857
13,14
1815
1816
1817
1818
1819
105
106
107
108
109
1872
1873
1874
1875
1876
162
163
164
165
166
NOTE. — Vols. 1-3 are
abstracts of the papers
printed in The Philo-
sophical Transactions,
1884
1885
1886
1887
45,46
47,48
49,50
51,52
1810
1811
1812
1813
1814
35,36
37,38
39,40
41,42
43,44
1858
1859
1860
1861
1862
15,16
17,18
19,20
21,22
23,24
1820
110
viz. : —
1815
45,46
1863
25, 26
1821
1822
1823
111
112
113
1877
1878
1879
1 RQA
167
168, 169
170
1800-1814
1815-1830
1830-1837
1
2
3
Chemical News.
Ed. by W. Crookes.
1816
1817
1818
47,48
49,50
51,52
1864 •
1865
1866
27,28
29,30
31,32
1824
114
looU
1881
m"
Vols. 4-6 are abstracts
1860
1, 2
1819
53,54
1867
33, 34
1825
115
1882
.
173
of papers communicated
1861
3, 4
1820
55,56
1868
35,36
1826
116
1883
174
to the Koyal Society.
1862
5, 6
1821
57,58
1869
37,38
1827
117
1884
175
1837-1843
4
1863
7, 8
1822
59, 60
1870
39,40
1828
118
1885
176
1843-1850
5
1864
9,10
1823
61, 62
1871
41,42
1829
119
1886
177
1850-1854
6
1865
11,12
1824
63, 64
1872
43,44
1830
120
1866
13,14
1825
65,66
6*7 £»Q
1873
45,46
1831
121
1867
15,16
1826
/, 08
1874
47,48
1832
122
1868
17,18
1875
49,50
VOLUMES AND YEARS OF ISSUE OF CHEMICAL AND PHYSICAL PERIODICALS.
783
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
5th S
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1887
ieries.
1, 2
3, 4
5, 6
7, 8
9,10
11, 12
13,14
15,16
17,18
19,20
21,22
23
1875-78
1878-80
1880-82
1882-84
1884-86
9
10
11
12
13
2nd
1860
1861
1862
1863
1864
1865
1866
1867
1868
1869
1870
3rd
Series.
1
2
3
4
5
6
7
8
9
10
11
Series.
1886
1887
25
26
1822
1823
1824
1825
1826
1827
1828
1829
1830
1831
1832
1833
1834
1835
1836
1837
1838
1839
1840
1841
1842
1843
1844
1845
2nd
1846
1847
1848
1849
1850
1851
1852
1853
1854
1855
1856
1857
1858
1859
1860
1861
1862
1863
1864
1865
1866
1867
1868
1869
1870
3rd
1871
1872
1873
1874
1875
1876
1877
1878
1879
4,5
6
70
;8
9
10,11
12
13,14
15,16
17,18
19,20
21,22
23, 24
25-27
28,29
30,31
32,33
34,35
36,37
38,39
40,41
42,43
44,45
46,47
48,49
Series.
1, 2
3, 4
5, 6
7, 8
9,10
11,12
13,14
15,16
17,18
19,20
21,22
23,24
25,26
27,28
29,30
31,32
33,34
35,36
37,38
39,40
41,42
43, 44
45,46
47,48
49,50
Series.
~ 1, 2
3, 4
5, 6
7, 8
9,10
11,12
13,14
15,16
17,18
1880
1881
1882
1883
1884
1885
1886
19,20
21, 22
23, 24
25,26
27,28
29,30
31, 32
The Analyst.
(Ed. by Wigner & Muter,
London.)
Journal of the Society of
Chemical Industry.
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1887
1
2
3
4
5
6
7
8
9
10
11
12
Memoirs of the A merican
Academy of Arts and
Sciences. (Boston.)
1882
1883
1884
1885
1886
1887
1
2
3
4
5
6
1833
1846
1848
1849
1855
1857
1860
1861
1867
1868
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1887
1
2
3
4
5
6
7
8
9 n.s.
10
11
12
13
14
15
16
17
18
19
20
21
22
Transactions of the Royal
Society of Edinburgh.
1871
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1887
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
Quarterly Journal of
Science (Royal Institution,
London).
1788
1790
1794
1798
1805
1812
1815
1818
1823
1826
1831
1834
1836
1839
1844
1845
1848
1849
1853
1857
1861
1864
1867
1869
1872
1876
1879
1880
1882
1883
1884
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16,17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
1816
1817
1818
1819
1820
1821
1822
1823
1824
1825
1826
1827
1828
1829
1830
1831
1
2, 3
4, 5
6, 7
8, 9
10,11
12,13
14,15
16,17
18,19
20,21
22,23
24,25
26,27
28,29
30,31
American Chemical Jour-
nal. (Ed. Remsen, Boston.)
1879-80
1881
1882
1883
1884
1885
1886
1887
1
2
3
4
5
6
7
8
Proceedings of the Man-
chester Literary and
Philosophical Society.
Journal of the American
Chemical Society. (New
York.)
Annalen der Chemie und
Pharmacie, continued
from Vol. 169 [1873]
under the titta "Jus-
tus Liebig's Annalen
der Chemie und Phar-
macie."
1857-60
1862
1864
1865
1866
1867
1868
1869
1870
1871
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
Pharmaceutical Journal
and Transactions.
(London.)
!lst
1877
2nd
1879
1880
1881
1882
1883
1884
1885
1886
Series.
1
Series.
1
2
3
4
5
6
7
8
1st
1841-2
1842-3
1843-4
1844-5
1845-6
1846-7
1848
1849
1850
1851
1852
1853
1854
1855
1856
1857
1858
1859
Series.
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
1832
1833
1834
1835
1836
1837
1838
1839
1840
1841
1842
1843
1844
1845
1846
1847
1848
1- 4
5- 8
9-12
13-16
17-20
21-24
25-28
29-32
33-36
37-40
41-44
45-48
49-52
53-56
57-60
61-64
65-68
Proceedings of the Roy a
Society of Edinburgh.
American Journal of
Science and Arts
(Silliman's Journal).
1832-44 1
1844-50 2
1850-57 3
1857-62 4
1862-66 5
1866-69 6
1869-72 7
1872-75 8
1st
1818
1820
1821
Series.
1
2
3
784,
VOLUMES AND CORRESPONDING YEARS OF ISSUE OF THE
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
1849
1850
1851
69- 72
73^ 76
77- 80
Berichte der Deutschen
Chemischen GeselUchaft.
(Berlin.)
Poggendorf
1824
1825
's Annalen : —
1,2
3- 5
1874
1876
1878
6
7
8
1854
1855
1856
61- 63
64- 66
67- 69
1877
1878
1879
16
17
18
1852
81- 84
1857
70- 72
1880
19
1853
85- 88
1826
6- 8
Registers: —
1858
73- 75
1881
20
1827
9- 11
1845
1- 60
1854
89- 92
1868
1
1859
76- 78
1882
21
1855
93- 96
1869
2
1828
12- 14
1854
61- 90
1860
79- 81
1883
22
1856
1857
97-100
101-104
1870
1871
3
4
1829
1830
1831
15- 17
18- 20
21- 23
1865
1875 |
91-120
Sach-Reg.,
121-150
1861
1862
82- 84
85- 87
1884
1885
23
24
1858
1859
105-108
109-112
1872
1873
5
6
1832
24- 26
1875 \
Nam. -Reg.,
1-150
1863
1864
88- 90
91- 93
1886
1887
25
26
1833
27— 30
1860
1861
113-116
117-120
1874
1875
7
8
1834
31- 33
Wiedemann's Annalen : —
1865
1866
94- 96
97- 99
Registers : —
1862
121-124
1876
9
1835
34- 36
1877
1, 2
1867
100-102
1872
1-10
1863
125-128
1877
10
1836
37- 39
1878
3- 5
1868
103-105
1882
1-20
1864
129-132
1878
11
1837
-| QOQ
40- 42
1879
6- 8
1869
106-108
1865
133-136
1879
12
1838
43- 45
1880
9-11
1866
137-140
1880
13
1839
46- 48
1881
12-14
Registers: —
Dingler's Polytechnisches
1867
141-144
1881
14
1840
49- 51
1882
15-17
1844
1- 30
Journal.
isfifi
145-148
1882
15
1841
52- 54
1883
18-20
1854
31- 60
icuu
1869
1870
1871
1872
149-152
153-156
157-160
161-164
1883
1884
1885
1886
16
17
18
19
1842
1843
1844
1845
1846
55- 57
58- 60
61- 63
64- 66
67- 69
1884
1885
1886
1887
21-23
24-26
27-29
30
1865
1871
Kolbe's ,
1870
61- 90
91-108
Tournal : —
1, 2
1820
1821
1822
1823
1- 3
4- 6
7- 9
10- 12
1873
165-170
1887
20
1847
70- 72
Beiblatter :—
1871
3, 4
1824
13- 15
1874
1875
171-174
175-179
Register : —
1848
1849
73- 75
76- 78
1877
1878
1
2
1872
1873
5, 6
7, 8
1825
1826
16- 18
19- 22
1876
180-183
1880 1-10
1850
79- 81
1879
3
1874
9,10
1827
23- 26
1877
1S7R
184-189
1QO IQd.
1851
82- 84
1880
1 ftftl
4
1875
!R7ft
11,12
TO -I A
1828
27- 30
1O 1 O
A J7W — ly±
1852
85- 87
lool
1O i D
1O, l^t
1829
31- 34
1879
195-199
1853
88- 90
1882
6
1877
15, 16
1830
35- 38
1880
200-205
Annalen der Phi/sik und
1854
91- 93
1883
7
1878
17,18
1831
39- 42
1881
206-210
Chemie.
1855
94- 96
1884
8
1879
19,20
1832
43- 47
1882
211-215
l R^fi
Q7 QQ
1885
9
1880
21,22
1833
48- 50
1883
1884
216-221
222-226
Gilbert's Annalen : —
1O<JO
1857
1858
o i — {/y
100-102
103-105
1886
1887
10
11
1881
1882
23,24
25,26
1834
1835
51- 54
55- 58
1885
227 231
1799
1 3
1883
27,28
1836
59- 62
1886
1887
232-237
238-
1800
1801
1802
4- 6
7- 9
10-12
1859
1860
1861
1862
106-108
109-111
112-114
115-117
Journal fur Pratt ische
Chemie. (Leipzig.)
1884
1885
1886
29,30
31,32
33, 34
1837
1838
1839
63- 66
67- 70
71- 74
Supplements : —
1803
13-15
1863
118-120
1887
35
1840
75- 78
1861/2
i
1804
16-18
1864
121-123
Erdmann's Journal : —
1841
79- 82
1862/3
1864/5
1865/6
1867
i
2
3
4
5
1805
1806
1807
1808
19-21
22-24
25-27
28-30
1865
1866
1867
1868
124-126
127-129
130-132
133-135
1834
1835
1836
1837
1- 3
4- 6
7- 9
10-12
Zeitschrift fur Analy-
tische Chemie. (Fre-
zenius, Wiesbaden.)
1842
1843
1844
1845
83- 86
87- 90
91- 94
95- 98
IfifiR
1809
31-33
1869
136-138
1838
13-15
1846
99-102
1OUO
1870
7
1810
34-36
1870
139-141
1839
16-18
1862
1
1847
103-106
1872
i
g
1811
37-39
1871
142-144
1840
19-21
1863
2
1848
107-110
1812
40-42
1872
145-147
1841
22-24
1864
3
1849
111-114
Registers : —
1813
1814
43-45
46-48
1873
1874
148-150
151-153
1842
1843
25-27
28-30
1865
1866
4
5
1850
1851
115-118
119-122
1843
1- 40
1815
49-51
1875
154-156
1844
31-33
1867
6
1852
123-126
1855
40- 76
1816
52-54
1876
157-159
1845
34-36
1868
7
1853
127-130
1861
1-100
1817
55-57
1877
160
1846
37-39
1869
8
1854
131-134
1861
101-116
1818
58-60
1847
40-42
1870
9
1855
135-138
117-164
1819
61-63
Erganzungbander : —
1848
43-45
1871
10
1856
139-142
and
1820
64-66
1842
1
1849
46-48
1872
11
1857
143-146
Spl. 1-8
1821
67-69
1848
2
1850
49-51
1873
12
1858
147-150
1885
165-220
1822
70-72
1853
3
1851
52-54
1874
13
1859
151-154
1823
73-75
1854
4
1852
55 57
1875
14
1860
155-158
1824
76
1871
5
1853
58-60
1876
15
1861
159-162
MORE IMPORTANT CHEMICAL AND PHYSICAL PERIODICALS.
785
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume. Year.
Volume.
1862
18G3
1864
1865
1866
1867
1868
1869
1870
1871
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1887
Regis
1843
1850
1860
163-166
167-170
171-174
175-178
179-182
183-186
107 i an
1852
1853
1854
1856
1857
1858
1859
1860
1861
1862
1863
1864
1865
1866
1867
1868
1869
1870
1871
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1887
Kegi
1870/81
23
24
25
26 n.s.
27
28
29
30
31
32
33
34
35
36
37
38
39
40 n.s.
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
ater : —
1-12
1883
1884
1885
1886
1887
3
4
5
6
7
1868
1869
1870
1871
1872
1873
1874
1876
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1887
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
1861
1862
1863
Engelbad
1864
1865
1866
1867
Strt
1868
1869
Nau
1870
1871
1872
1873
1874
Fif
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
Kegi
1847/56
1857/66
1867/76
14
15
16
i and Will.
17
18
19
20
scker.
21
22
maim.
23
24
25
26
27
tica.
28
29
30
31
32
33
34
35
36
37
38
39
sters : —
1- 9
10-19
20-29
1851
1854
1859
1861
1864
1850
5
6
7
8
9
Suppl.-bd.
Jenaische Zeitschrift fiir
Medicin und Naturwis-
sensuhaft. (Leipzig.)
191-194
195-198
199-202
203-206
207-210
211-214
215-218
219-222
223-226
997 9^ft
Neues Handworterbuch
der Chemie. (Fehling.)
1864
1866
1867
1868
1870
1871
1873
1874
1875
1876
1877
1878
1879
1880
1881/2
1882/3
1884
1884/5
1885
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
1871
1875
1878
1886
1
2
3
4,5
231-234
235-238
239-242
243-246
247-250
Sitzungsberichte der Kai-
serlichen Akademie der
Wissenschaftenzu Wien,
Math.-Natw. Classe.
Jahresbericht der Reinen
Chemie. (Staedel, Tu-
bingen.}
255-258
259-262
263
ters : —
1- 78
79-118
119-158
1848
1849
1850
1851
1852
1853
1854
1855
1856
1857
1858
1859
1860
1861
1862
1863
1864
1865
1866
1867
1868
1869
1870
1871
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1
2, 3
4, 5
6, 7
8, 9
10,11
12-14
15-18
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1
2
3
4
5
6
7
8
9
10
11
12
13
^itzungsberichte d. Malh.-
Phys. Classe d. Kgl.
Bair. Akad. d. Wiss.
zu Miinchen,
19-21
22-27
28-33
34-38
39-42
43
44,45
46-48
49
50-52
53,54
55,56
57,58
59,60
61,62
63, 64
65,66
67,68
69,70
71,72
73,74
75,76
77,78
. 79, 80
81,82
83, 84
85,86
87,88
89,90
Chemisches Centralblatt.
(Leipzig.)
Up to Vc
entitled '
tisches Ce
1830
1831
1832
1833
1834
1835
1836
1837
1838
1839
1840
1841
1842
1843
1844
1845
1846
1847
1848
1849
1850
1851
1. 20 (1849),
' Pharnjaceu-
ntralblatt."
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21 71.8.
22
1871
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1887
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
Zeitschrift fiir Physiolo-
gische Chemie. (Hoppe-
Seyler, Strassburg.)
Chemiker-Zeitung.
(Krause, Cothen.)
Jahresbericht der Reinen,
Pharmaceutischen vnd
Technischen Chemie.
(G lessen.)
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1887
1
2
3
4
5
6
7
8
9
10
11
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1
2
3
4
5
6
7
8
9
10
Liebig
1847/8
1849
1850
1851
1852
1853
1854
1855
1856
Kopp
1857
1858
1859
1860
and Kopp.
1
2
3
4
5
6
7
8
9
and Will.
10
11
12
13
Handworterbuch der
Chemie. (Liebig, Pog-
gendorff, and Wo/tler.)
Repertorium der A naly
tischen Chemie. (Skal-
weit, Hannover.)
Carl, Repertorium der
Experimental- Phi/sit.
1865
1866
! 1867
1
2
3
1842
1848
1849
1,2
3
4
1881
1882
1
2
fi H
780
VOLUMES AND CORRESPONDING YEARS OF ISSUE OF THE
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Monatshefte fur Chemie
zu Wien.
1878
1879
1880
86, 87
88, 89
90, 91
1828
1829
1830
37-39
40-42
43-45
1877
1878
1879
10-12
13-15
16-18
Journal de Pharmacie
et de Chimie. (Paris.)
1857
1858
1859
31, 32
33, 34
35, 3(i
1881
92, 93
1831
46-48
1880
19-21
1860
37, 38
1880
1
1882
94, 95
1832
49-51
1881
22-24
1st Series.
1861
39, 40
1881
2
1883
96, 97
1833
52-55
1882
25-27
(Bulletin de Pharmacie.)
1862
41,42
1882
3
1884
98, 99
1834
56,57
1883
28-30
1809
1
1863
43,44
1883
4
1885
100, 101
1835
58-60
1810
2
1864
45, 46
1884
5
1886
102, 103
1836
61-63
6th Series.
1811
3
4th Series.
1885
6
1887
104
1837
64-66
1884
1-3
1812
4
1886
1887
7
8
Supplements : —
1856 1
1838
1839
67-69
70-72
1885
1886
4-6
7-9
1813
1814
5
6
1865
1866
1, 2
3, 4
1861
2
1840
73-75
1887
10
1867
5, 6
3rd Series.
2nd Series.
1868
7, 8
Comptes rendus de VAca-
Table gfinerale: —
1815
1
1869
9, 10
demie des Sciences.
1853 | 1-31
1841
1- 3
Repertoire de Chimie
1816
2
1870
11, 12
(Paris.)
1842
4- 6
pure. ( Wurtz, Paris.)
1817
3
1871
13, 14
1843
7- 9
1818
4
1872
15, 16
Annales de Chimie et de
1844
10-12
1819
5
1873
17, 18
1835
1
Physique. (Paris.)
1845
13-15
1859
1
1820
6
1874
19, 20
1836
2, 3
1846
16-18
1860
2
1821
7
1875
21, 22
1837
4, 5
1847
19-21
1861
3
1838
6, 7
1st Series.
1848
22-24
1862
4
1822
8
1876
23,24
1839
1840
1841
1842
8, 9
10, 11
12, 13
14, 15
IK 17
1789
1790
1791
1792
1- 3
4- 7
8-11
12-15
1849
1850
1851
1852
1 Qro
25-27
28-30
31-33
34-36
1863 5
Continued in the
following : —
1823
1824
1825
1826
1827
9
10
11
12
13
1877
1878
1879
5th
25,26
27,28
29,30
Series.
184.5
ID, 1 I
1793
16-18
1853
37-39
1828
14
1844
18, 19
1797
19-24
1854
40-42
Bulletin de la Sodete
1829
15
1880
1, 2
1845
1846
20, 21
22, 23
1798
1799
25-27
28-31
1855
1856
43-45
46-48
Chimique de Paris.
1830
1831
16
17
1881
1882
3, 4
5, 6
1847
24, 25
1800
32-34
1857
49-51
1832
18
1883
7, 8
1848
26, 27
1801
35-39
1858
52-54
New Series.
1833
19
1884
9,10
1849
28,29
1802
40-43
1859
55-57
(See above.)
1834
20
1885
11,12
1850
30,31
1803
44-47
1860
58-60
-
1 0
1835
21
1886
13,14
1851
32,33
1804
48-51
1861
61-63
I QftK
i, -
3 A
1836
22
1852
34,35
180*1
52 55
1862
64-66
1ODO
, *±
1837
1853
1854
1855
1856
36, 37
38,39
40,41
42, 43
lOVyU
1806
1807
1808
56-60
61-64
65-68
1863 67-69
Tables des Matie'res: —
1851 1-30
1866
1867
1868
1869
5, 6
7, 8
9,10
11,12
1838
1839
1840
24
25
26
Revue Scientifique et
Industrielle. (Paris.)
1 ft**1?
1809
69-72
1866
31-69
1870
13, 14
1841
27
loo/
1858
46, 47
1810
73-76
1871
15,16
Tables des Matie'res : —
1859
48, 49
1811
77-80
4th Series.
1872
17,18
1831
1-16
1st Series.
1860
1861
1862
1863
50, 51
52,53
54, 55
56, 57
1812
1813
1814
1815
81-84
85-88
89-92
93-96
1864
1865
1866
1867
1- 3
4- 6
7- 9
10-12
1873
1874
1875
1876
19,20
21,22
23,24
25,26
1842
3rd
1842
17-27
Series.
1, 2
1840
1841
1842
1- 3
4- 6
7-11
1864
58, 59
2nd Series.
1868
13-15
1877
27,28
1843
3, 4
1843
12-16
1865
1866
60, 61
62,63
1816
1- 3
1869
1870
16-18
19-21
1878
1879
29,30
31,32
1844
1845
5, 6
70
> 6
2nd Series.
1867
1868
1869
1870
64, 65
66,67
68,69
70,71
1817
1818
1819
1820
4- 6
7- 9
10-12
13-15
1871
1872
1873
22-24
25-27
28-30
1880
1881
1882
1883
33,34
35,36
37,38
39,40
1846
1847
1848
1849
9,10
11,12
13, 14
15,16
1844
1845
1846
1- 3
4- 7
8-11
1871
72,73
1821
16-19
Tables des Matie'res : —
1884
41,42
1850
17,18
1847
12-15
1872
74,75
1822
20,21
1874 1-30
1885
43,44
1851
19,20
3rd Series.
1873
76,77
1823
22-24
5th Series.
1886
45,46
1852
21,22
1874
78, 79
1824
25-27
1887
47
1853
23, 24 ; 1848
1, 2
1875
80, 81
1825
28-30
1874 "
1-.3
1854
25, 26
1849
3, 4
1876
82, 83
1826
31-33
1875
4-6
~
1855
27, 28
1850
5, 6
1877
84, 85
1827
34-36
1876
7-9
1856
29,30 1851
7- 9
MORE IMPORTANT CHEMICAL AND PHYSICAL PERIODICALS.
7S7
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
Year.
Volume.
4th
1852
Follow
Series.
1
ed bv : —
1867
1868
1869
1870
3rd
1871
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
9
10
11
12
Series.
13
14
15
16
17
18
19
20
21
22
23
24
25
26
Journal de Physique
thfor. et applique publ.
par d' Almeida,
(jazzetta Chimica Italiana.
(Paterno, Palermo.)
Recueil des Travaux
Chiiniques des Pays-
Bus. ( Van Dorp and
others, Leide.)
1871
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
1871
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
1882
1883
1884
1885
1886
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
1st
1872
1873
1874
1875
1876
1877
1878
1879
1880
1881
2nd
1882
1883
1884
Series.
1
2
3
4
5
6
7
8
9
10
Series.
1
2
3
Moniteur Scientifique.
(Paris.)
1882
1883
1884
1885
1886
1
2
3
4
5
1st!
1857
1863
2nd
Series.
1
2
3
4
5
Series.
Journal of the Russian
Chemical Society. (St.
Petersburg.)
1864
1865
1866
6
7
8
1869
1870
1
2
5 H 2
788
VL-ALPHABETICAL INDEX OF THE ROOT COMPOUNDS OF CARBON.
Compounds with the prefixes iso, pseudo-, alpha-, beta-, ortho-, meta-, para-, dextro-, leevo-, &c., will be found under the primitive name, unless the}' are
non-isomeric with the compound indicated by the latter, in which case they are given under their proper letter. Broni-conipouuds and iodo-
compounds will be found under the corresponding chlor-compounds.
Abietic acid, C44H64O5.
Abietin, C44H60 ; C63H76O8-
Absinthin, C^H^O, ; C40H68O9-
Absinthol, 010H16O.
Acecaffe'ine, C6H11OilN3.
Aceconitic acid, C6H6O6 ; CgHjOj.
Acenaphthene, C12H10.
Acenaphthylene, C12H8.
Acetal, C6H14O.
Acetic acid, C2H4O2.
Acetoglyceral, CdHluO3.
Acetoguanamine, C4H7N5.
Acetone, C3H6O.
Acetone ether, C17H16O4.
Acetonine, C9H18N2.
Acetonitril, C2H3N.
Acetonuramic acid, C6H10O3N2.
Acetonyl carbamide, C5H8O2N2.
Acetophenine, C24H19N.
Acetophenone, C8H8O.
Acetotannic acid, C17H20O9.
Acetothienone, C6H6OS.
Acetoxime, C3H7ON.
Acetoximic acid, C3H6O2Nj.
Acetulmic acid, C17H12O2.
Aceturic acid, C4H7O3N.
Acetylene, C2H2.
Acetylglycine, C4H703N.
Acetylide, C16H1804.
Achillem, C^H^O^N,,.
Achilletin, CUH17O4N.
Achrodextrin, C6H10O6.
Achroglycogen, Z. P. C., 6, 74.
Aconic acid, C5H4O4.
Aconine, C26H39OnN.
Aconitanilic acid, C12H9O4N.
Aconitdianil, C18H14O3N,,.
Aconitic acid, C6H6OC.
Aconitine, C30H47O7N ; C33H43012N.
Acridine, C12H9N.
Acridinic acid, CnH704N.
Acrole'in, C3H40.
„ ammonia, C6H9ON.
„ resin, C3H4O.
Acropinacone, C6H10O2.
Acrothialdine, C9H13S2N.
Acrylcolloid, C3H4O3.
Acryldiure'ide, C5H10O2N4.
Acrylic acid, C3H4O2.
Adipic acid, C6H10O4.
Adipornalic acid, C6H10O5.
Adipotartaric acid, C6H,0O6.
Aescigenin, Ci2H20O2.
Aescinic acid, C24H40O12.
Aescioxalic acid, C7H604.
Aescorcei'n, C9H7O6N.
Aescorcin, C9H8O4.
Aesculetin, C9H6O4.
Aesculetic acid, C9H1207.
Aesculin, C15H16O9 ; C21H24013.
Aesthesin, O35H69O3N.
Agaricic acid, C16H30O5 ; CxHjO,.
Agaricin, CiHyOz.
Agarythrin, B., 16, 244.
Agoniadin, C10H14O6.
Alacreatinine, C4H7ON3.
Alanine, C3H7O2N.
Alantic acid, C15H22O3.
Alantol, 010H16O.
Alban, C10H160 ; C20H30O.
Albumin, C72H112O22SN18 ;
C,o4H322066S2N62.
Aldehyde green, C22H27OS2N3.
„ ammonia, C4H,,O2N.
Aldehydine, C8HnN.
Aldehydocollidine, C8HnN.
Aldol, C4H8O2.
Alizarin, C14H8O4.
Alizarin blue, C17H9O4N.
Alkannin, C15H14O4.
Allanic acid, C4H5O5N6.
Allanto'in, C4H6O3N4.
Allantoic acid, C4H8O4N4.
Allantoxaidine, C3H3O2N3.
Allan toxanic acid, C4H3O4N3.
Allanturic acid, C3H4O3N2.
Allituric acid, C6H6O4N4.
Allocaffeiine, C8H,O5N3.
Allophanic acid, C2H4O2N2.
Alloxan, C4H2O4N2.
Alloxanic acid, C4H4O5N2.
Alloxantin, C8H4O7N4.
Alluranic acid, C'6H4O4N4.
Allylene, C3H4.
Allylene digallein, C16H12O6.
Aloeresiuic acid, C7H3O6N; C15H16O;.
Aloeretinic acid, C30H34O15.
Aloctinic acid, C7H2O5N2.
Aloexanthin, C15H,0O6.
Aloin, C15H1607 ; C16HI8O- ;
(C15H170),,.
Aloisol, C6H803 ; C6H16O3.
Alorcinic acid, C9H10O3.
Alpinin, C17H1206 ; C17H12O6.
Alstonidin, CaHbOcNd.
Alstonin, C^H^N,,.
Amalic acid, C12H14O8N4.
Amanitin, C6H15O2N.
Amaric acid, C46H42O6.
Amarine, C21H18N2.
Amarone, C,6HUN.
Amasatin, C;6H1403N4.
Ambrai'n, C25H48O.
Amenthic acid, C7H14O2.
Amisatin, C48H39O9Nn.
Ammelide, C6H9O3N9.
Ammelin, C3H6ON6.
Amydecylenic acid, CtoSlsOf
Amygdalin, C20H27O,,N.
Amygdalinic acid, C20H26012.
Amylan, C6H10O5.
Amylene, C6H10.
Amylin, C8H18O3.
Amylenguanamine, C8H16N5.
Amylodextrin, C36H62O31.
Amylum, C24H38O19.
Amyrin, C20H34O ; C25H42O ;
C47H78O£.
Anacardic acid, C22H32O3 ; C44H6407.
Anamirtic acid, C35H-0O4.
Anamirtin, C19H24O10 ; C19H36O2.
Andromedotoxin, B., 16, 429, 798.
Anchoic acid, C9H16O4.
Anemonin, CJ5HJ.JO5.
Anemonic acid, C15H14O7.
Anethenol, C10H16O.
Anethol, Cj0H12O.
Angelic acid, C5H8O2.
Angelin, C10H13O3N.
Anhydrodiacetylacetamidil,
Anhydrolupinin, Cjj^jgON,,.
Anhydrotolylketamine, C27H180N4.
Aniline, C6H7N.
Aniline black, C30H2SN6.
Aniline blue, C38H31NS.
Aniline brown, J. [1863], 785; [1865],
857.
Aniline gray, J. [1866], 906.
Aniluvitonic acid, CuB^C^N.
Anisamine, C8HUON ; C16H]9O3N.
Anishumin, C18H14O3.
Anishydi'amide, C24H24O3N2.
Anishydroxamic acid, C8H9O3N.
Anisic acid, C3H8O3.
„ camphor, C10H16O.
Anisidine, C7H9ON.
Anisil, ClfiH14O4.
Anisilic acid, Ci6H16O6.
Anisine, C24H24OaN2.
Anisoic acid, C^H,^,;.
Anisoi'n, C10Hj,,0; Ci6H16O4.
Anisol, C7H8O.
Anisolquinine, CjdHd^jN..
Anisuric acid, C10HnO4N.
Anisuramic acid, C9H15O4N2.
Anol, C'9H10O.
Anthemol, C10H16O.
Anthracene, C14H10.
Anthracene orange, CaHbOcNd.
Anthrachrysone, C14H8O6.
Anthracylamine, C14HnN.
Anthraflavic acid, C14H8O4.
Anthragallol, C14H8O5.
Anthramine, C14HnN.
Anthranil, C7H5ON.
Anthranilic acid, C;H7O2N.
Anthi'anol, C14Hi0O.
Anthrapurpurin, 0,411(^04-
Anthraquinoline, Cj-HnN.
Anthraquinone, C14H8O2.
Anthrarufin, C14H8O4.
Anthrol, C14H10O.
Anthropocholic acid, C18H2SO4.
A nthropodyslysin, C18H26O3.
Anthroxauic acid, C8H5O3N.
Antiarin, C14H20O6.
Antiar resin, C16H24O.
Antronol, C16H14.
Apachoic acid, C15H14O3.
Aphrodascin, C52HS2Oj3.
Apigenin, C15H10O6.
Apiin, C24H;8013 ; C2.H32O16.
Apiol, C12H14O4.
Apoaconitine, G^H^O^N.
Apoatropine, C17H21O2N.
Apocaffeine, C.H;O5N3.
Apochinine, C1SH17O2N.
Apocinchene, C18H17ON.
Apocinchonicine, Ci9H22ON2.
Apocinchonidine, C19H22ON3.
Apocinchonine, C19H22ON2.
Apocode'ine, Cj8H19O2N.
Apocolchicei'ne, M. C., 4, 163.
Apocouquinine, C19H2.,O2N2.
Apocynei'n, B., 16, 255.
Apocynin, B., 16, 255.
Apoglucinic acid, C9H10O5; C18H2COU.
Apomorphine, C17H,-O2N.
Apophyllic acid, CSH.O4N.
Apopseudaconine, C27H39O8N.
Apopseudacoiiitine, C36H47OUN.
ALPHABETICAL INDEX OF THE ROOT-COMPOUNDS OF CARBON.
780
Apoquinamine, C19H22ON2.
Apoquinine, C19H22O2N2.
Aposorbic acid, C5H3O7.
Apotheobromine, C6H5O5N3.
Arabin, C12H22On.
Arabinose, C6Hi2O6.
Arabinic acid, C12H22On.
Aracliidic acid, C20H40O2.
Araliin, B., 14, 1112; 15, 2746.
Arbutin, C12H16O7.
Arcyldiglycollic acid, CnH^Oj.
Argyraescetin, C21H30O6.
Argyraescin, C2;H42O12.
Aribine, C23H20N4.
Aricine, C23H26O4N2.
Arnicin, CSOH30O4.
Arsenobenzene, C12H10As2.
Asarin, C20H26O5.
Asarone, C12H16O3 ; C20H26Ob.
Asclepione, C20H34O3.
Asebotoxin, C,Hj,Cv
Aserpetin, C15H2.jO4.
Asparagine, C4HSO3N2.
Asparagiuic acid, C4H7O4N.
Aspidosamine, C22H28O2N2.
Aspidospermatine, C^H^OoNj ; not
CaftAN,.
Aapidospermine, C22H30O2N2.
Assamar, A., 49, 3.
Athamantii), C24H30O7.
Atherosperma resin, C21H32O5.
Atisine, C46H;4OiN2.
Atractyligenin, CxHyO,.
Atractylin, C20H30O6.
Atractylic acid, C30H54O18S2.
Atraic acid, C]6H18Ob.
Atrauoric acid, C19H18O8.
Atranorinic acid, C9H10O4.
Atraric acid, C,0H16O8 ; C10H10O5.
Atroglyceric acid, C9Hj0O4.
Atrolactic acid, C9H10O3.
Atrolactyltrope'ine, Ci-H23ON.
Atrolinic acid, C16H18O6.
Atronic acid, C17H14O2.
Atronihe sulphone, C16H10O2S.
Atronol, C16H14.
Atronylene, C16H12.
Atropatrope'ine, C17H21O2N.
Alropic acid, C9H8(X
Atropine,C17H23O3N; not C,;H23ON.
Atroxindole, C9H9ON.
Aurantia, C)2HSO12N7.
Aurautiin, C^H^O^.
Aurin, C19H14O3.
Auatralene, C10H16.
Austrapyrolene, C10H16.
Axiuic acid, C18H22O2.
Axlepione, C20H34O3.
Azelaic acid, C9H16O4.
Azimidobenzene, C6H5N3.
Azobenzeue, C^H^N^
Azobenzoi'lide, C42H33N5.
Azobenzoyl, C22HJ6Nj.
Azodioxiiidole, C8H602N2.
Azodiphenyl blue, C18H15N3.
Azoerythrin, A., 39, 40.
Azolitmin, A., 39, 57.
Azoncarbonic acid, C6H3O5N.
Azopheiiine, C36H29ON6 ; not
C36HMN5.
Azoxindole, C8H6ON2.
Azuline, C26H22O2N2.
Azulmic acid, C4H5ON5.
Azulmoxine, C4H3O2N5.
Azurine, C35H32O3N4.
Balata, C10H16.
Baphie acid, C24H22O10.
Baphiin, C12Hi0O4.
Baphinitin, C4H4O.
Baphinitone, C26H26O6.
Barbalo'in, C16H18O7.
Barbatic acid, C19H20O;.
Barbituric acid, C4H4O3N2.
Basilicum camphor, C10H22O.
Bassorin, C6H10O5.
Bebirine, Cj9H21O3N.
Beech wax, C^H^C^.
Behenic acid, C22H44O2.
Belladonine, C17H23O3N.
Benylene, C^H^.
Benolic acid, C22H4002.
Benomargarie acid, C15H30O2.
Benostearic acid, C^H^Cy
Benzacine, C32H27ON3.
Benzacrylic acid, C8H6O2.
Benzamarone, C-0H6(1O4.
Benzamil, C^H^C-jN,, (?).
Benzamsuccinic acid, CnHn
Benzaurin, C19H]4O2.
Benzcreatine, C9H,,O2N3.
Benzcyanidine, C24H19O2N.
Benzdioxyanthraquinone, C14H804.
Benzene, C6H6.
Benzeneresorcinphthalei'n, C20H)4O4.
Benzenylamidoxirae, C7H8ON2.
Benzenylazoximecarbinol,C8H6O2N2.
Benzerythrene, C24H18.
Benzfuril, C12H8O3.
Benzfurilic acid, C12H10O4.
Benzfuroi'n, C12H10O3.
Benzglycocyamine, C8H9O2N3.
Benzhydramide, C22H18ON2.
Benzhydrol, C13H12O.
Benzhydrolene, C13H10.
Bsnzhydroxamic acid, C7H7O2N.
Benzhydrylpropionic acid, C10H12O3.
Benzidine, C1S.H12N2.
Benzil, C14H10O2.
Benzilani, C42H32O2N2.
Benzilamine, C14H9N.
Benzilic acid, C14H12O3.
Benzilimide, C14HnON; C^H^N.,;
C42H3304N.,
Benzimide, C23H18O2N2.
Benzoic acid, C7H6O2.
Benzoicin, C24H20O6.
Benzoin, C14H12O2.
Benzoinamide, C21H18N2.
Benzoinamine, C28H24ON2.
Benzoinimide, Ci4HnN.
Benzolone, C21H15O2 ; C22H,6O2.
Benzonaphthoue, C9H4O.
Benzophenone, C13H10O.
Benzostearicacid,C21H42O2;C22H44O2.
Benzostilbene, C14Hi0O ; C3iH22O2.
Benzosuccinin, C14H14O6.
Benzotannic acid, C2-H44O9.
Benzoylarnmeline, C10H9O2N5.
Benzoylglyceral, C10Hi2O3.
Benzoylazotide, C15H12N2.
Benzoylhyperoxide, C14H1004.
Benzpinacolin, C26H20O.
Benzpinacone, C26!L202.
Benzylaldoxime, C.H7ON.
Benzylidenebenzidine, C26H20N2.
Berberine, C20H17O4N.
Berberic acid, C8H8O4.
Berberonic acid, C8H506N.
Bergamot camphor (C3H6O2)B.
Bergapten, C9H6O3.
Bergenitol, C3H10O6.
Beronic acid, C-H5O4N.
Betaln, C5HnO2N.
Betaorcinol, C8H10O2.
Betulin, U36H60O3.
Betulinamaric acid, C36H52O16.
Betulinic acid, O36H64O6.
Betuloretinic acid, C36H66O6.
Bilianic acid, C26H36O9.
Bilic acid, C16H22O6.
Bilifuscin, C16H,0O4N2.
Bilihumin, A., 132, 341.
Bilineurin, C5H15O2N.
Biliprasin, C16H22O6N2.
Bilirubin, C9H9O2N : C32H36O6N4.
Biliverdin, C32H36O8N4.
Bitter almond oil green, C23H26ON2.
Biuret, C2H5O2N3.
Bixin, C28H34O5.
Boheic acid, C7H10O6.
Borneene, C10H16.
Borneocamphene, C10H16.
Borneol, C10H18O.
Borneodambose, C6H,2O6.
Bornesite, C7H14O6.
Branchite, C9H16.
Brasileln, C16H12O5.
Brasilin, C16H14O5.
Brassidic acid, C22H42O2.
Brassylic acid, CllH.10Ot.
Brean, C26H44O.
Bromdichroic acid, C^HjBr^O,!.
Bromanil, C6Br402.
Bromoxaform,
Bromocodide,
Bromrosoquinol, C12H6Br402.
Brucine, C23H26O4N2.
Bryoiidine, C20H3803.
Bryonine, CjsHgnO,,.
Bryoretine, Cj^jjOj.
Butane, C4H10.
Butine, C4H,.
Butylene, C4HS.
Butylidene, CnH^.
Butyline, C4H13N3.
Butyral, C4H8O.
Butyric acid, C4H8O2.
Butyrofuronic acid, C9H12O5.
Butyrolactone, C4H6O2.
Butyrone, C14H3002.
Butyropinacone, C14H30O2.
Buxin, C16H21O3N.
Cacodyl, C4H12As2.
Cacodylic acid, C2H7O2As.
Cacostrychnine, C21H22OnN6.
Cacotheline, C^Hj^OgN^
Caffeetannic acid, C15H18O8.
Caflfeie acid, C9HS04.
Caffeidine, C7H12ON4.
Cafieme, C8H10O2N4.
Caffeol, C8H10O2.
Caffoline, C5H9O2N3.
Caffuric acid, C6H9O4N3.
Ca'incaic acid, C40H64O18.
Camcetin, C22H34O3.
Ca'incigenin, C14H24O3.
Caincin, C40H64O18.
Cajeputene, 010H16 ; C10H2203.
Cajeputol, C10H18O.
Calamene, C10H16.
Calutannic acid, C14H14O9.
Calluxanthin, C14H10O7.
Calycin, C18H12O5.
Camellin, CyJ^^O^.
Camomillene, C,0H16.
Camphene, C10H16.
Campheride, C16H12O6.
Campheramic acid, C10H17O3N.
Campherimide, C,0H15O2N.
Campherol, C10H16O2.
Camphilene, C10H16.
Camphimide, C10H15N.
Camphine, C9H16 ; C10H13 ; C1SH32.
Camphinic acid, C10H16O2.
Camphocarbonic acid, C,,H16O3.
Camphocarbonyl chloride, CjoH^Clg.
Camphocarboxylic acid, C22H32O6.
Camphoglycuronic acid, C16H24OS.
Camphol, C10H18O.
Campholene, C8H,4 ; C9H16.
Campholic acid, C10H18O2.
Camphor, C10H16O.
Camphoranil, C16H19O2N.
Camphoranilic acid, C,6H21O3N.
Camphoric acid, Ci0Ht6O4.
Camphorone, C9H14O.
Camphoronic acid, C9H12O5; C9H14O6.
Camphoroxime, C10H17ON.
Camphorylchloride, C9H13C1.
Camphorylcode'ine, C28H35O6N.
790
ALPHABETICAL INDEX OP THE ROOT COMPOUNDS OF CARBON.
Camphorylmorpliine, C.,-H3.(O6N.
Camphorylsuperoxide, C10H14O4.
Camphoterebene, C20H32.
Camphoterpene, C20H32.
Camphrene, C9H14O ; C8H12O.
Camphrone, C30H44O.
Camphryl chloride, C9H13C1.
Cannabene, C9H10.
Cantharene, C8H12.
Cantharic acid, C1(IH12O4.
Cantharidine, C5H12O2 ; C10H12O4.
Cantharidic acid,C10H14O5; C10HleOfi.
Caoutchene, C4H8 ; C10H16; C^H^O,,.
Capnomor, dHyO,.
Capric acid, C10H20O3.
Caprinone, C19H38O.
Caproic acid, C6H12Oj.
Caprolactone, C6H10O2.
Caprone, CUH2,,O.
Caprylic acid, CSH16O2.
Caprylidene, C3H14.
Caprylone, C15H30O.
Capsaicin, C9H14O2.
Capsulsescie acid, C13H|2O8.
Caramelan, C12H43O9 ; C24H26O13.
Cararaelen, C66H50O25.
Caramelin, C6H4O2 ; C24H30O15.
Carbacetoxylic acid, C3H4O4,
Carbamide, CH4ON2.
Carbamic acid, CH3O2N.
Carbanil, C7H5ON.
Carbanilic acid, C,H7O2N.
Carbazole, C12H9N.
Carbazolic acid, CI3H9O2N.
Carbazoline, C12H15N.
Carbobenzonic acid, C^H^Oj.
Carbocamphoric acid, C20H32O6.
Carbocaprolacton ic acid, C-H10O4.
Carbocymolic acid, CnH14O2.
CarboisobutyraWine, CaH18S2N2.
Carbomesyl, C10H,,ON.
Carbonaphtholic acid, CnH8O3.
Carbopetrocene, C24H18 and (C5H2)n.
Carbopyrotritaric acid, CSH8O5.
Carbopyrrolic acid, C5HSO2N.
Carbostyril, C9H-ON.
Carbostyrilic acid, C9H7O6N.
Carbothialdine, C5H10S2N2.
Carbovaleraldine, CnHgjSjNj.
Carbovalerolactonic acid, C6H8O4.
Carbolic acid, C6H6O.
Carbusnetic acid, C18H16O7.
Carbusnic acid, C]9H16O8.
Carboxethy If urf urine, C18H, 6O6N2.
Carboxamidohippuric acid,
C19H1807N4.
Carboxylcornicularic acid, C19H14O5.
Carboxytartronic acid, C4H4O7.
Cardol, C21H30O2.
Carmine red, CUH12O7.
Carmine sugar, C6HIOO5.
Carminic acid, C17H18O10.
Carmufelic acid, C12H20O1C.
Carnine, C7H,O3N4.
Carotin, C1SHS4().
Carpene, C9H14.
Carthamin, C14H16O7.
Carvacrol, C10H14O.
Carvacrolic acid, CnH14O3.
Carvene, C1(IH16.
Carvol, C10H14O.
Carvoxime, C10H15ON ; C10Hj7ON.
Caryophyllin, C,,0H32O2.
Caryophyllic acid, CioH32O6.
Cascarillin, C12H18O4.
Cassonic acid, C5H8O7.
Catechin, C18H18O8 ; C21H18O8;
C2jH20O9 ; C40H38O16 ; C42H34O16 ;
k«-"-36O16 ! C42H38OI6.
Catechinazobeuzene, C30H26O8N4.
Catecholcarbouate, C7H4O3.
Catechuic acid, C15H14O7.
Catechutannic acid, C36H34Oj5.
Catechuretiu, C42H30O13.
Cattelagic acid, C14H,0O7.
Caulosterin, C26H44O.
Cedar camphor, C|5H26O.
Cedrene, C15H24 ; C16H34.
Cellulose, (C6H10O6).-
Cephalin, C42H79O13NP.
Cerasinose, C6H12O6.
Ceratophyllin, (\HrOv
Cerebrin, C17H33O3N ; C57H110O25N2 ;
C80H160016N.
Cerebrose, C6H1206.
Cerebrosic acid, C6H)2O6.
Cerin, C17H28O ; C,9H4804.
Cerinic acid, C13H20O4.
Ceropinic acid, C36HraO5.
Cerosin, C^HjgO.
Cerosinic acid, C24H4802.
Cerotene, C27HS4.
Cerotic acid, C2;H54O2.
Cerotinone, C53H106O.
Ceroxylin, C20H32O.
Cerylalcohol, C^H^O.
Cespitine, C5H13N.
Cetene, C16H32.
Cetic acid, C15TI30O2.
Cetin, C16H30.
Cetin, C32H64O2.
Cetraric acid, ClaHltOg.
Cetylide, C^H.A-
Cevadilline, C34H53O8N.
Cevadine, C32H49O9N.
Cevine, C27H43O8N.
Chairamidine, C22H2604N2.
Chairamine, C22IL-6O4N2.
Chamomile oil, C10H16O.
Chelamide, CbHsON.
Chelerythrine, C,7H15O4N.
Chelidonic acid, C7H4O6.
Chelidonine, C19H17O3N3.
Clielidoninic acid, C-H]0OC.
(Jhenocholic acid, C27H44O4.
Chenopodine, C12H13O8N.
China red, C12H14O7 ; C^H^O^.
Chiniiie, C^H^ONy
Chiuochromin, C26HS8O2.
Chinovatannic acid, C14H1SO8.
C'hinova red, C2SH2BO12.
Chinovic acid, C24H39O4.
Chinovin, C38H62On.
Chinvic acid, C32H4SOC.
Chiratin, C26H4SO1S.
Chiratogenin, C13H24O.,.
Chitenidine, C19H22O4]Sr.!. '
Chitenine, C19H22O4N2.
Chitine, C15H.,6O10N2.
Chlorhydrinimide C12H23C12O4N3.
Chloral, C2HC13O.
Chloralbin, C6H6C12.
Chloralcarbamide, C2H5C12ON3 ;
C5H6C1603N2.
Chloralhydratecamphor,C12H19Cl3O3.
Chloralide, C5H2C16O3.
Chloralimide, CSH2C13N.
Chlornicene, C6H5C1.
Chlorocodide, C18EL0C102N.
Chloroform, CHC13.
Chlorogenine, Co^jgO^N,.
Chloropicriu, CC13O3N.
Chlorothioform, C2CLS3.
Chloroxethide, C8C11(1O7.
Chloroxethose, C4C160.
Cholanic acid, C20H28O6 ; C24H36O7 ;
C28H36O7.
Cholecamphoric acid, C10H16O4.
Cholestenic acid, C25H40O4.
Cholesterilene, C.,6H43.
Cholesterin, C26H44O.
Cholesteric acid, C8H1()O5 ; C12H16O7.
Cholestrone, C.:6H42.
Cholestrophane, C5H6O3N2.
Choleteline, C15H18O6N2.
Cholic acid, C24H40O5.
Choline, C5HlbO2N.
Chologlycollic acid, C26H42O7.
Cholo'idanic acid, C17H25O7.
Chololdic acid, C^H^ ; C48H7809.
Cholphosphinic acid, C72H114O1SP2.
Chryiodme, C.,8H8O14N3.
Chrysamminic acid, C34H20O12N4.
Chrysaniline, C20H17Nj.
Chrysanisic acid, C7HSO6N3.
Chrysarobin, C3I)H26O7.
Chrystatinic acid, C24H20O19N6.
Chrysazin, C14H804.
Chrysazol, Cl4H10Oj.
Chrysean, C4H5S.,N3.
Chrysene, C18H12.
Chrysezarin, C18H10O4.
Chrysin, C15H10O4.
Chrysocyamminic acid, C18H6O12N6.
Chrysoidiue, C12H12N4.
Chrysophanic acid, C15HIOO4.
Chrysotoluidine, C21H21N8.
Cicutene, C10HJ6.
Cimic acid, C15H28O2.
Cinacrol, C'10H18O2.
Cinchamidiue, C19H24ON2 ;
C^H^ON,.
Cinchene, CuH^Nj.
Cinchocerotic acid, CJOH22O2.
Cinchocerotin, C.,7H48O2,
Cincholepidine, C,0H9N.
Cinchomeronic acid, C;HaO4N.
Cinchonamine, C19H,,4ON2.
Cinchonicine, C19H2.,ON2.
Cinchouidiue, C,,jH2,,ON2.
Cinchoniue, C19H22ON2.
Cinchonic acid, C7H6O6.
Cincnoninic aciil, C10H7O2N.
Cinchotenicine, C^HjuOjNj.
Cinchotenidine, C18H20O3N£.
Cinchoteniiie, C1SH20O3N2.
Cinchotine, C^Hj.ONy
Cinnoline, C8H6N3.
Cinnamene, C8H9.
Cinnamic acid, C9H9O2.
Cinnyl tribromide, C9H9Br3.
Cinosbene, C10H16.
Cincephene, Cyfl,.,.
Citracetic acid, C6H6O6.
Citraconic acid, C5H6O4.
Citramalic acid, C5H8O6.
Citramethane, C8HI4O6N.j.
Citratartaric acid, C5H8O6.
Citrazinic acid, C6H6O4N.
Citrene, C10H16.
Citric acid, C6H8O7.
Citromannitol, C12H14O7.
Citronellol, CJOH16O.
Cladonic acid, C18H18O7.
Cnicin, C42H56O15.
Cocaine, C17H2IO4N.
Coccinin, C14H12O6.
Coccognin, C^H^Og.
Cochlearin, C6H14O., (?).
Cocinin, C42H8nOfi.
Codamine, C19H23O,N ; C20H25O4N.
Codeine, C1SH21O3N.
Codethyline, C19H23O3N.
CoemleSn, C.,0H10O6.
Cterulignol, C10H14O2.
Ccerului, C20H12O6.
Colchiceme, C,7H1905N; C17H01O5N;
C35H42011NS.
Colchicine, C,.H19O5N ; C17H23O6N.
Colchicoresiu, C24H39O10lSr.
Colein, C10H10O5.
Collidine, C^^N.
Collinic acid, CuHjOj.
Colloidine, C^H^O^N,;.
CoUoturine, C.HbOcNd.
Colocynthein, C44H64O13.
Colocynthin, C^H^O^.
Colophanthrene, CZH,.
Colophene. C10H16.
Colopheue, C20H32O.
Colophonone, C,|H18O2.
Golophthaliri, CUH10.
ALPHABETICAL INDEX OF THE BOOT-COMPOUNDS OF CARBON.
791
Colophthalumina, C10H6O2.
Colophthaluminic acid, C10H6O4.
Columbin, C21H22O7.
Columbic acid, C21H22O5.
Comenic acid, C6H4O6.
Oouchairamidine, C22H26O4N.,.
Conchairamine, C22H26O4N2.
Concusconidine, C23EL6O.,N2.
Concuscoiiine, C23H26O4N2.
Conessin, C26H42ON2.
Conethylalkine, CJOH21ON.
Conhydrin, C3H17ON.
Coniferin, C,6H22O8.
Coniferyl alcohol, C10H12O3.
Coniine, 0SH15N ; C3H17N.
Coniinic acid, C7H15O2N.
Conilinephthamic acid, C!6H21O3N.
Conimene, Cj5H24.
Conquinamine, C19H24O2Nj.
Conquinine, C20H24O2N2.
Convallamaretin, Co0H36Og.
Convallamarin, C23H44O2.
Convallarin, C34H62Ou.
Convicine, C10H14O7N3.
Convolvulin, C34H60O16.
Convolvulinic acid, C31H52Oj7.
Convolvulinol, C26H50O7.
Convolvuliuolic acid, C13H2403.
Couylene, C8H14.
Conylene glycol, C8H16O2.
Copabeue, C10H16.
Copaibic acid, C20H30O2.
Copaibaol hydrate, C60H93O.
Corallin, C19H14O3 ; C40H38OU.
Corallinphthale'in, C20H14O4.
Coriamyrtin, C30H36O10.
Coridine, C10Hi5N.
Coriine, C6H10O3N2.
Cornicularic acid, C17H14O3.
Corticinic acid, C12IT10O6.
Corydalin, CI8H19O4N.
Cotarnine, C12H13O3N.
Cotarninic acid, CUH1204.
Cotogenin, C14H14O5.
Cotom, C21H2006 ; C22H18O6.
Coumaric acid, C9H8O3.
Coumarilie acid, 09H6O3.
Coamarin, C9H6O2.
Coumarone, C8H6O.
Crbatine, C4H9O2N3.
Creatinine, C4H7ON3.
Cressol, C8H10O2.
Cresol, C7H8O.
Cresolaurin, C22H.,0O3.
Cresolphthalem, C22H18O4.
Cresolphthalin, C22H20O4.
Cresorcinol, C7H8O2.
Cresorciunuorescein, C.,2HI6O5.
Cresylpurpuric acid, C9H7O6N5.
Crocetiu, C34H46OU.
Crocin, C16H1806 ; C6SH86O31.
Crocirihydrate, C32H38O13.
Croaonic acid, C5H2O6.
Crotaconic acid, C5H6O4.
Crotonic acid, C4HCO2.
Crotonyleue, C4H6.
Cryptidine, CnHnN.
Cryptophanic acid, C5HaO6N.
Cryptopine, C21H23O5N ; C23H25O5N.
Cubebic acid, C13H14O7 ; C14H16O4 ;
C28HS2O8.
Cubebin, C10H1003 ; C17H16O5.
Cubebs camphor, CJ5H28O.
Cumene, C9H12.
Cumidic acid, C10H10O4.
Cumidine, C9H13N.
Cuminic acid, C^H^Oj.
Cuminilic acid, C20H24O3.
Cuminyl, C20H22O2.
Cumin oil, C20H34O.
Cumiuom, C.0H24O2.
Cuminol, C10H12O.
Cuminuric acid, C12H15O3N.
Cumostyril, C12H13ON.
Cupreme, CnH-O3N.
Cuproiiine, C20H1306N2 ; C2lHi806N2.
Curarine, C18H35N.
Curcumine, C10H10O3 ; C14H1404.
Cuscamine, C,HbOcNd.
Cusconine, C23H26O4N2.
Cusparine, C19H17O3N.
Cyalbidin, C76H112O26SN22.
Cyanielide, CHON.
Cyameluric acid, C6H3O3N-.
Cyamidoamalic acid, C13H14O7N6.
Cyananiliue, C14H14N4.
Cyanbenzine, C24H21N3.
Cyancamphor, CHH16ON.
Cyanconiine, C9H,4N2.
Cyanethine, C9H15N3.
Cyanic acid, CHON.
Cyanilic acid, C3H3O3N3.
Cyanine, C30H39IN2.
Cyanmethiue, C6H9N3.
Cyanoform, C4HN3.
Cyanogen. C2N2.
Cyanuromalic acid, C6H6O4N4.
Cyanuric acid, C3H3O3N3.
Cyaphenine, C21H16N3 ; (C7H5N)n.
Cyclamin, C20H34O10 ; C32H54O18.
Cyclamiretin, C15H22O2.
Cyclopia red, C19H22O10.
Cyclopin, C25H28O,3.
Cyclopic acid, C7H8O4.
Cymene, C10H14.
Cymidine, C10H15N.
Cymophenol, C10H14O.
Cymothymol, C10H14O.
Cynanchin, C15H24O.
Cynanchocerin, C^H^O.
Cynanchol, C16H14O.
Cynene, C10H16 ; C12H18.
Cystine, C3H7O2SN.
Cytisine, C20H27ON3.
Damaluric acid, CuH^O., ; C7H12Cv
Dambonite, C4H803 ; C8H18O6.
Dainbose, C6H12O6.
Dammaran, C40H62O6.
Danimaranic acid, C40H62O7.
Damniaryl, C45H72.
Dammarylic acid, C45H-203.
Damolic acid, C12H22O».
Daphnetin, C9H6O4 ; C19H14O9.
Daphnin, C15H16O9 ; C31H34O19.
Datiscetin, C15H10O6.
Datiscin, C21H22O12.
Daturine, C^H^ON.
Decacrylic acid, C10H18O.j.
Decane, C10H22.
Decanaphtheue, C10H20.
Decarbusnem, C17H18O6.
Decarbusnic acid, C9H10O3 ; C15H16O5.
Decenyleue, C10Hi8.
Decin, C10H18.
Decone, C10Hi6.
Decylene, C10H20.
Behydracetic acid, C8H8O4.
Dehydrocamphor, C10H14O.
Dehydrocholalic acid, C25H36O5.
Dehydromucic acid, C6H4O5.
Belphinine, C22H35O6N ; C24H3502N.
Delphinoiidin, C42H68O7N2.
Delphisin, C27H46O4N2.
Deoxyamalic acid, C12H14O6N4.
Deoxyaniso'in, C16H16O3.
Deoxybenzo'inpinacone, C28H260._.
Deoxyphorone, C1SH2SO.
Desoxalic acid, C5H6O8.
Dextran, CCH10O5.
Dextrin, (C6H10O5)n.
Dextroglucose, C6H12O6.
Dextronic acid, C6H12O7.
Dextrose, C6H12O6.
Diacetonalkamine, C6H15ON.
Diacetonamine, C6H13ON.
Diacetonic alcohol, C6H12O2.
Diacrylic acid, C6H804.
Dialactamidic acid, C6HU04N.
Dialdane, C8H14O3.
Dialdanic acid, CSH14O4.
Diallyl, C6H10.
Diallylene, C6H8.
Diallylidenediphenamiue, C18H13N2.
Dialuric acid, C4H4O4N2.
Diamylene, C10H20.
Diamylin, C13H28O3.
Dianhydrolupinine, C21H36N,,.
Dianilinhydrin, C15H18ON2.
Dianishydroxamic acid, C16H15O5N.
Dianisotriure'ide, C19H24O5N6.
Diantipyrine, C22H2.,O2N4.
Diapocinchonin, C3SH44O2N4.
Diapotetramorphine, Ci36H148022N8.
Diarachin, C43H34O6.
Diarbutin, C2SH32O14.
Diaterebic acid, C7H1SO6.
Diaterpenylic acid, C8H14O5.
Diazoacetamide, C2H3ON3.
Diazobenzoimide, C7H,,O2N3.
Diazobenzoliniide, C6H3N3.
. Diazocamphor, C10H14ON2.
Diazoethoxan, C4H1(1O2N,,.
Diazoresorcin, C18HKIO6N2.
Diazoresorufin, C36H18O9N4.
Diazorosaniline, C20H U1N6.
Diazothymol, C10H12ON2.
Dibarbituric acid, C8H6O5N4.
Dibenzhydrylamine, CjjHjjN.
Dibenzyl, C14H14.
Dibutyllactiuic acid, CSH14O5.
Dibutyraldine, CSH17ON.
Dibutyril, C8H14O2.
Dicamphorilimide, C2I,H31O2N.
Dicarbocaprolactonic acid, C8H10O6.
Dicarbothionic acid, C2H2O4S.
Dicarboxethylainidamariue,
C27H2703N3.
Dichromatic acid, C20H34O3.
Diconchinine, C40H4603N4.
Diconic acid, C9H10O6.
Diconylene alcohol, C16H30O3.
Dicotoi'n, C44H34On.
Dicuminyl, C.,0H26.
Didenlactamidic acid, C6HU04N.
Diepinic acid, C2H4O4.
Diethoxalic acid, C6H12O3.
Diethylcarbobenzoic acid, C|8H18O2.
Diethyldaphnetilic acid, C13H14O5.
Diethylin, C7H16O3.
Diethylsemicarbazide, C15H]3ON3.
Diffluan, C3H4O3N2.
Difrangulic acid, C28H1809.
Digallic acid, CHH10O9.
Digitalacrin, CUH22O2.
Digitale'in, C22H38O9.
Digitalin, C5H802 ; C21H2309 ;
C27H4bO15.
Digitaliretin, C16H26O3.
Digitin (C4H902)».
Digitonin, C3]H52O17.
Digitoxin, C21H32O7 (?).
Diguanide, C2H7N6.
Dihydrocarboxylic acid, CioHjO,,.
Diimidoisatin, C16H12O2N4.
Diisatogen, C16H8O4N2.
Diisoprene, C10H16.
Dimethylacetal, C4H10Oo.
Dimethylsulphone, C2H6O2S.
Dimetoxybenzoid, CHH10O5.
Dinaphthyl, C20H14.
Diuaphthylanthrylene, C22H12.
Dicenauthylidenediphenamiiie,
Dioxalethylin, C12H18N4.
Dioxindole, C8H7O2N.
Dioxymorphine, C17H19O2N.
Dioxyretistene, C16H14O2.
Diphenanthrenazotide, C28H16N2.
Diphenic acid, C14H10O4.
Diphenine, C12H14N4.
Diphenic phthalein, C26H1SO4.
792
ALPHABETICAL INDEX OF THE ROOT-COMPOUNDS OF CARBON.
Diphenylaminacrolei'n, C27H24N2.
Diphenylhydrazine, C12H12N2.
Diphenyline, C12H12N2.
Diphthalimidodiphenyl, C28H16O4N2.
Diphthalyl, C16HSO4.
Dipbthalylaldeliydic acid, C16H10O5.
Diphthalic acid, G16H10O6.
Dipiperyltetrazene, C10H,0N4.
Dipropargyl, C6H6.
Dipyridyl, C10H8N2.
Dipyrogallopropionic acid, C15HHO8.
Dipyrotetracetone, CSH12O2.
Dipyruvintriurei'd, C9HI2O6N6.
Diquinoline, C18H14N2.
DiquinolyliDe, C18H12N2.
Disacryl, C3H4O.
Disacryl resin (C10H1303)n.
Dispoline, CuHnN.
Distyrenic acid, C,7H16O2.
Ditaine, C22H28O4N2.
Ditamine, C19H19O2N.
Ditartrylic acid, C8H10On.
Dithiodiprussiatuic acid, C^HyS^Ng.
Ditolyl, C14H14.
Ditolylphthalid, C22H18O2.
Diureidbenzoic acid, C'9H10O4N4.
Divicin, C22H3809N20 ; C31H50O16N30.
Divinyl, C4H6.
Docosane, C22H46.
Dodecanaphthene, C12H24.
Dodecane, C12H20.
Doeglic acid, C19H36O2.
Drupose, C12H2008.
Dulcamaretin, C,6H26O6.
Dulcamarin, C22H34O10.
Dulcid, C6H12O4.
Dulcitol, C6HJ4O6.
Dulcitarnine, C6H15O5N.
Dulcitan, C6H12O5.
Dulcitotartaric acid, C14H20O15.
Dumasin, 06H10O.
Duodecane, C12H26.
Duodecine, C12H22.
Duodecylene, C12H24.
Duodecylic acid, C12H24O2.
Duplothiacetone, C6H12S2.
Durene, CJOH14.
Duorylbenzoic acid, Ci8H18O3.
Duric acid, C10H12O2.
Dyslysin, C24H36O3.
Dyslyte, C3H6O6N4.
Eogonine, C9H15O3N.
Echicautschin, C25H40O2.
Echiceric acid, C30H46O4.
Echicerin, C30H4SO2.
Echiretin, C35H56O2.
Echitamine, C22H28O4N,.
Echitein, O42H7(1O2.
Echiteuine, C20H27O4N.
Echitin, C32H52O2.
Eicosane, C20H42.
Eicosylene, C20H38.
Elaidic acid, C1SH34O.,.
Elaidin, C57H10406.
Elaldehyde (C2H4O)n.
Elaterin, C^HjA.
Elemic acid, C35H06O4.
Eleomargaric acid, C,7H30O2.
Eleostearic acid, C17H3t)O2.
Ellagene, C14H10.
Ellagentannic acid, C14H6O8 ;
CnH10O10.
Ellagic acid, C14H608 ; C14H8O9 ;
CuH^Ojo ; C14H16O8.
Emetine, C30H44O4N2.
Emodin, C,,,H10O5 ; C40H30O13.
Encephaline, C102H20(A9N14.
Endecanaphthene, CUH22.
Eosin, C20H8O5Br4.
Epiclilorhydrin, C3H5C1O.
Epicyanhydrin, C4H5ON.
Epihydriu alcohol, C3H6O2.
Epihydrincarboxylic acid, C4H6O3.
Epioxyphenylhydrin,C9H10O2.
Ergotinine, C35H40O6N4.
Ericinol, CIOH16O.
Ericinone, C24H24O9.
Ericoline, C34H66O2l.
Erlen red, CL3H22O8.
Erucic acid, C22H42O2.
Erythrin, C12H4O6 ; C20H22O10.
P- » C21H24O10.
Erythric acid, C20H22O,0 ; C28H30O14.
Erythrocentaurin, C27H24O8.
Erythrol, C4H10O4.
Erythroltartaric acid, C12H18O14.
Erythropyrocatechol, C18H2Br10O.
Erythroglucinic acid, C4H8Od.
Eserine, C15H21O2N3.
Ethal, C1(iH34O.
Ethane, C2H6.
Ethenylamidoxime, C2H6ON2.
Etherin (C2H4)n.
Etherol (C2H4)n.
Ethionic acid, C2H6O7S2.
Ethylaldoxime, C2H6O.N.
Ethylazaurolic acid, C4H8O2N4 ;
C6H1202N4.
Ethylcumazonic acid, C13H15O3N.
Ethylene, C2H4.
Ethylic carbamate, G3H7O2N.
Ethylisatoxime, C10H10O2N2.
Ethylleucazone, C4H7ON3.
Ethylperoxide, C8H20O3-
Ethylpicrazide, C8H9O6N5.
Ethylquinazole, C10H12N2.
Ethylsalidine, C27H30O3N2.
Ethylideneurethane, C8H16O4N2.
Ettidine, C15H19N.
Eucalyn, C6H12O6.
Eucalyptene, Ci0H16 ; C12H18.
Eucalyptolene, C12H1S.
Eucalyptol, C10H16O ; C12H18O8.
Enchroic acid, C12H4O8N2.
Eugenol, C10H12O2.
Eugetic acid, .CUH13O4.
Eulysin, C24H36O3.
Eulyte, C6H6O7N4.
Euodic aldehyde, CUH22O.
Euosmite, C34H53O2.
Euphorbone, 013H22O ; C15H24O.
Eupione, C6H12.
Eupittonic acid, C2SH26O9.
Euthiochronic acid, C6H4Oi0S2.
Euxanthic acid, C^H^O,,.
Euxanthone, C13H8O4.
Euxauthonic acid, C,3H10O5.
Everniin, C6HI4O7.
Everninic acid, C9H10O4.
Everuic acid, C17H16O7.
Excretin, C20H36O.
Felicic acid, C13H16O5.
Ferulic acid, C10H1UO4.
Fibroin, C15H2306N6.
Fichtelite, C40H70.
Filix acid, C14H18O5.
Fiscic acid, C,HyOz.
Fisetin, CJ6H10O6.
Flavaniline, C16H14N.,.
Flaveanhydride, C2H2SN2.
Flavenol, ClfiH13ON.
Flavol, C14H10O2.
Flavoline, C16H13N.
Flavopurpurin, C14H806.
Fluavil, C20H32O.
Fluorantheue, C15H10.
Fluorene, C13H10.
Fluorenic acid, C14H10O2.
Fluorenic alcohol, C,3H10O.
Fluorescein, C20H12OS.
Fluoresceincarboxylic acid, C^H^C
Fluorescin, CioH14O6.
Fluoresorce'in, C20H14O6.
Formic acid, CH2O2.
Formoguanamine, C3H5N6.
Formomelamine, C4H6ON6.
Formonetin, C24H20O6.
Frangulic acid, C14H8O4.
Frangulin, C20H20O10.
Fraxetin, C10H8O6.
Fraxin, C16H18O10 ; C21H22013 ;
C27H30017.
Fraxitannic acid, C13H16O7.
Fucusamide, C15H12O3N2.
Fucusine, C16H12O3N2.
Fucusol, C5H4O2 ; 05H10O2.
Fulminuric acid, C3H3O3N3.
Fulmiteti-aguanurate, C7H13O3N,,.
Fulmitriguanurate, C6HUO3N9.
Fumaric acid, C4H4O4.
Fumerol, CI9H»gO.
Furfuracrolein, C7H6O2.
Furfuracrylic acid, C7H6O3.
Furfuraldoxime, C5H5O2N.
Furfuramide, C15H12O3N2.
Furfurangelic acid, C9H10O3.
Furfuraniline, C17H18O2N2.
Furfurbenzidine, C22H16ON2.
Furfurbutylene, f'~
Furfurine, Cl;H12^3N2.
Furfurol, C5H4O2.
Furfurpropionic acid, C7H8O3.
Furfurtoluidine, C16H.,2O2N2.
Furfuryl alcohol, C5H6O2.
Furil, C10H604.
Furilic acid, C10H8O5.
Furo'in, C,0H8O4.
Furonic acid, C7H8O5.
Fu-icophlobaphene, C27H26O1:i.
Gai'dic acid, C16H30O2 ; CJ8H34O2.
Galactin, C6H10O5 ; C54H73O45N4.
Galactose, C6H12O6.
Galangin, CISH10O5.
Galbauum oil, C10H16O.
Galipeiue, C20H21O3N.
Gallacetonin, C9H1(IO3.
Gallacetophenone, C18H8O4.
Gallactucone, C14H24O.
Gallactic acid, C14H10O9.
Gallem, C20H10O7.
Gallic acid, C7H6O5.
Gallin, C2(1H14O7.
Gallol, C^H^Oe.
Gallomalotaiiuic acid, C14H10O9.
Gardenic acid, C14H10O6.
Gardenin, C14H12O6 ; C23H30O10.
Gaultheriline, C10H16.
Geisospermin, C19H24O2N2.
Gelsemine(C11H19O2N)n;C24H28O4N2.
Gentianin, C14H10O5.
Gentianose, C36H66O31.
Gentiogenin, G14H16O5.
Gentiopicrin, C20H30O12.
Gentisin, C14H10O5.
Gentisic acid, C7H6O4.
Geocera'in, C^H^O,;.
Geoceric acid, C28H56O2.
Geocerinone, C53H110O.
Geomyricin, C34H6SO2.
Georetinic acid, C12H22O4.
Geramene, C10H16.
Geraniol, C10H19O.
Gingkoic acid, C24H48O2.
Glaucohydroellagic acid, C14H10O7.
Glaucomelanic acid, C12H6O-.
Globularetin, C9H6O ; C12H14O3.
Globularin, €15H20O8 ; C30H44O14.
Gluciuic acid, C12H22O12.
Gluconic acid, O6H12O7.
Glucoprotein, C6HI2O4N2 ;
07H1404NS ; C8H1604N2.
Glucosan, C6H10O5.
Glucose, C6H12O6.
Glutamic acid, CSH9O4N.
Glutamine, C3H10O3N2.
Glutaric acid, C5H3O4.
Glutimide, C5H8O2N,,
Glutiniiuic acid, C5H,O3N'.
ALPHABETICAL INDEX OF THE ROOT-COMPOUNDS OF CARBON'.
793
Glutonic acid, C5H6O4.
Glyceric acid, C3H8O4.
Glycerol, C3^
Glycide, C3H602-
Glycidic acid, C3H4O3.
Glycin, C2H5O2N.
Glycocholic acid, C26H4306N.
Glycocholonic acid, C26H41O5N.
Glycocinimide anhydride, C2H3ON.
Glycocoll, CjHjOjN.
Glycocyamidine, C3H5ON3.
Glycodrupose, C24H36O16.
Glycodyslysin, C26H39O4N.
Glycogen, C6H10O5; C18H3iOI6.
Glycogenic acid, C6Hi2O7.
Glycol, C2H6O2.
Glycolignose, C30H46O21.
Glycoline, C6H10N2.
Glycollic acid, C2H4O3.
Glycollide, C5H2O2.
Glycoluril, C4H,O2N4.
Glycosamine, C6H13O5N.
Glycosanilide, C12H,7O5N.
Glycosine, C6H6N4.
Glycotannin, C^HjsOjj.
Glycuronic acid, C6H10Or
Glycuvic acid, CsH^Oj.
Glycyphyllin, C.jH,^
Glycyphyllic acid, C9H10O3.
Glycyrrhizinic acid, C44He3O18N.
Glyoxal, C2H2O2.
Glyoxaline, C3H4N2.
Glyoxalmethyline, C4H6N,.
Glyoxime, C2H4O2N2.
Glyoxylic acid, C2H4O4.
Gnoscopine, C34H36O11N3.
Granattannic acid, C20H,6Ora.
Graphitic acid, CUH4O6.
Gratioleretin, C^H^O,.
Gratioletin, C17H28O5.
Gratiolin, C20H34O3.
Gratiosoleretin, C^H^O,.
Gratiosoletin, C^H^O,,.
Gratiosolin, CiiSitOa.
Greenhartin, C30H26O6.
Guajacol, C7H8Oj.
Guajaconic acid, C19H20O5 ; CnHn03.
Guajaretic acid, C20HS6O4.
Guajene, C)2Hla.
Guajol,C6H80; C9H14O2.
Guanidine, CH5N3.
Guanamine, C3H5N6.
Guanine, C5H5ONS.
Guanoline, C4H902N3; C8H1804N6.
Gummie acid, C3H805 ; C6H1(iO10.
Gurjunic acid, C22H34O4.
Guyaquillite, C50H26O3.
Gyrophoric acid, CK~H.MOU.
Hsematem, C16H12O6; CmH.mOufi.
Haematin, C34H35O5N4Fe.
Heemathionic acid, C,,,H14O15S.
Haematoidin, C,4H18O,N2.
Hsematoline, C68H78O7N8.
Hsematoporphyrin, C34H37O6N4.
Hsematoxylin, C16H14O6.
Harmaline, C13H14ON2.
Harmalol, C,2H13ON2.
Harmine, C13H12ON,,.
Harminic acid, C10H8O4N2.
Hartin, C^H.jO; (C10Hl7O)n;
0>oH34o2.
Hartite, C6H10; (CBH5)B.
Hederic acid, C16H26O4.
Helenene, CraH.26.
Helenin, 06H8O; C16H14O5; C21H2603-
Helianthic acid, C14H18O8.
Helicin, C13H1CO7.
Helicoidin, C26H34O14.
Helleborem, C26H44O15.
Helleboresin, CjoH.,^.
Helleboretin, C14H20O3.
Helleborin, C36H42O6.
Hemialburaen, C24H40O10N6.
Hemibromhydrin, C6H9BrO.,.
Hemicolline, C47H70O19N4.
Hemimellithene, C9H12.
Hemimellitic acid, C9H606.
Hemipinic acid, C10H10O6.
Hemiproteidin, C24H42O12N6.
Heneicoaane, C21H44.
Hentriacontane, Oj,!!^
Heptacosane, C27H56.
Heptadecane, 017H36.
Heptane, C7H16.
Heptinic acid, C21H30OP
Heptolactone, C;HUO].
Heptone, C7H10.
Heptylene, C7H14.
Heptylic acid, C7H14Oj.
Heptylidene, C7H,2.
Heraclin, C^H^O,,,.
Hesperetic acid, G^H^O^
Hesperetin, C16H14O6.
Heaperetol, CgH^Oj.
Hesperidene, C10H16.
Hesperidin, C22H26O12 ; C23H26O12.
Heveene, C15H24 ; C^H^
Hexacosane, C26HS4.
Hexacrolic acid, C18H24Oe.
Hexadecane, C16H34.
Hexadeeylic acid, C16H3JO..
Hexadecylidene, Ci6H30.
Hexane, C6H14.
Hexepinie acid, C6H;2O9.
Hexerinic acid, C6H12O4.
Hexine, C6H10.
Hexic acid, C^H^O-
Hexone, C6H8.
Hexoylene, C6H10.
Hexylene, C6H12.
Hexylenic acid, CjHmO,
Hexylidine, C6H12.
Hipparaffin, C16H16O2Nj.
Hipparin, CSH9O2N.
Hippuric acid, C9H9O3N.
Homatropine, CI6H21O3N.
Homocerebrin, C80H,S,0UN2.
Homocinchonidine, C19H22ON2.
Homocreatine, C5HUO2N3.
Homocumaric acid, CWH10O3.
Homocuminic acid, CUH14O3.
Homoferulic acid, CUH12O4.
Homofluoreacein, C23H1SO5.
Homohydroapoatropine, C16H21O2N.
Homoitaconic acid, C6H8O4.
Homoiaophthalic acid, C9H804.
Homoprotocatechuic acid, C8H8O4.
Homopyrocatechol, C7H,O2.
Homopyrrol, C5H7N.
Homoquinine, C19H22O2N2 ;
Homosaligenin, C8H10Oa.
Homoterephthalic acid, C9H8O4.
Homovanillic acid, C9H,0O4.
Homoveratric acid, C10H12O4.
Hop-bitters, C16H26O4.
Hop-phlobaphene, C50H46O25.
Hop-red, C^HiijOu.
Hordeinic acid, C12H2402.
Humic acid, C24H,0O10 ; C60H64O27.
Hiuninic acid, 024H18O9.
Hysenic acid, C25H50O.j.
Hydantoin, C3H4O2N2.
Hydantoic acid, C3H6O3N2.
Hydrseaculetin, C18H14O8.
Hydrastin, C^H^OgN.
Hydrazoindol, CI6H13N3.
Hydraztine, C-jH.^t^N.
Hydrazulmine, C4H6N6.
Hydrimidotetrazoresorufin,
C36H2809N14.
Hydrindine, C32H22O5N4.
Hydrindic acid, C8H7O2N.
Hydrindonaphthaleue carboxylic
acid, C,0H10OP
Hydrisoalizarin, C28HWO8.
Hydrobenzamide, C21H18Na.
Hydrobenzuric acid, Ci8H2406N2.
Hydrobenzyluric acid, C16H21O4N.
Hydrobryotin, C21H3708.
Hydrocaflfurie acid, 06H9O3N3.
Hydrocarboxylic acid, Ci0H60)(|.
Hydrocarpol, Ci6H,.0O.
Hydrocellulose, 012H22On.
Hydrocholalic acid, C^H^Oj.
Hydrocinchonidine, C19H23O3N.
Hydrocinnamide, C27H24N.,.
Hydrocinnamocarbonic acid,
C10H10O3.
Hydrocosrulignone, Ci6HMO6 ;
CiSH18O6.
Hydrocotoln, C15HUO4.
Hydrocotone, C^H^O,.
Hydrocoumarinic acid, C19H18O6.
Hydrocoumarin, C18H14O4.
Hydrocuminamide, C30H36N2.
Hydrocuminoindichloride,C,0H24CL
Hydrocyanaldine, 09H13N4.
Hydrocyanbenzide, C23HI7N3.
Hydrocyanic acid, CHN.
Hydrocyaurosaniline, C20H18N4 ;
C21H20N4.
Hydrocyanrosolio acid, C21H17O3N.
Hydrocyansalide, C22H,6O3Nr
Hydrogratiosoleretin, C34HS6On.
Hydrokynurin, C1,H2(1O2N2.
Hydronaphthamide, C33H24N2.
Hydroosnanthamide, C21H42N2.
Hydrophthalide, C9H8O2.
Hydropiperoin, CI6H14O6.
Hydropolyporic acid (C9H9O2)n.
Hydroquinidine, C20HMO2N2.
Hydroquinizarol, C14H,,,O3.
Hydroquinoline, C18H,sN.j.
Hydroquinone, C6H6O2.
Hydroquinonequinoline,C24H20O2N2.
Hydroquinonephthale'in, CjjH^Oj.
Hydroquinonephthaleinic acid,
C20H,4O6.
Hydroquinonephthalin, C20H14O5.
Hydrosalicylamide, C21H18O3N2.
Hydrosantonamide, CuHjjOjN.
Hydrotarniu, C12H1503N.
Hydrotinic acid, C5H9O5N.
Hydrovanillo'in, C16H1806.
Hydroxonic acid, C8H10O7N6.
Hydroxybenzyluric acid, C16H210SN.
Hydroxyglutarilactone, C6H8O4.
Hydroxypentinic acid, CSH8O, ;
C7HI203.
Hydroxytetrinic acid, C4H60}.
Hydruvinic acid, C6H10O7.
Hydurilic acid, C8H6O6N4.
Hyocholic acid, C25H40O4.
Hyodyalyain, C^H^O^
Hyoglycocholic acid, C»7H43O5N.
Hyoscine, C^H^N; notC17H23ON.
Hyosciuic acid, C9H1003.
Hyoscyamine, C^HojOjN ; not
C^H-aON.
Hyotaurocholic acid, C27H4SO6SN
Hypocaffeine, C6H7O3N3.
Hypogo3ic acid, C16HMO2.
Hypoquebrachine, C21H2602Nr
Hypoxanthin, CSH4ON4.
Icacin,C45H740; C46H760 ; C47H78O.
Icican, C^H^O.
Idrialin, C80H54Oj.
Idrioline, C10H9N.
Idryl, C1SHI0.
Ilixanthin, C17H22On.
Imabenzil, C14H,,ON ; C42H32O4N2.
Imasatin, C,6HU03N3.
Imeaatin, C8H6ON2.
Imperatorin, Ci2H12O3 ; CitHI6O4.
Indazole, C7H6N2.
Indifulvin, C22H20O3N2,
Indifuscin, C24H20O9N2.
Imlifuscon, C22H20O5Nj.
Indiglucin, C6HWO6.
5 I
794
ALPHABETICAL INDEX OF THE ROOT-COMPOUNDS OF CARBON.
Indigo blue, C16H10O2N,,.
Indigopurpurin, 03H5ON.
Indigotin, C1CH10O2N2.
Indigwhite, C16H12O2N2.
Indigo white, C,6H14O2N2.
Indihumin, OlaH9O,N.
Indicanin, C20H23O12N ; C26H31O17N.
Indin, C16H10O2N2.
Indiretin, CI6H16O4N2 ; C18H17O5N.
Indirubin, CSH5ON ; C16H10O2N2.
Indom, C32H20O5N4.
Indole, C8H7N ; C16HUNS.
Indoline, C,6H14NS.
Indophane, <J22H10O4N4.
Indophenin, C20H15ON.
Indoxyl, CSH7ON.
Indoxylic acid, C9H7O3N.
Inosinic acid, C,0H14OnN4.
Inosite, C6H12O6.
luulin, C6H1005 ; C36H62O31.
Tmilold, C6H1005 ; C^H^O,,,
Inulol, C10H16O.
lodal, C2HI3O.
Ipecacuanhic acid, C14H18O-.
Ipomceic acid, C10H18O4.
Iridoline, C10H9N.
Iriscamphor, C8H16O2.
Isoethionic acid, C2H604S.
Isamide, C16H14O3N4.
laamic acid, C16H13O4N3.
Isatamidobenzoic acid, C,5H12O4N.,.
laatan, C32H26O6N4.
Isatide, C16H12O4Nj.
Isatilim, C24H16O5N4.
Isatimide, O24H17O4N5.
Isatin, C8H5O2N.
laatindiamide, Ci6H12O2N4.
Isatinic acid, C8H7O3N.
Isatochlorin, C32H24O5N4.
Isatogenic acid, C9H5O4N.
Isatoic acid, C8H5O3N.
laatone, C32H24O3N4.
Isatopurpurin, CjjH.jgO.jN.,.
Isatropic acid, C19H16O4.
Isobutylal, C16H32O4.
Isobutyraldin, C12H25S2N.
Isodibutol, C8H18O.
Isodibutolic acid, CSH16O2.
laodulcitic acid, C6H10O9.
Isodurenol, C10H14O.
Isoindileucine, Ci6HlsONj.
Isoline, C14H,7N.
Isophlorylchloride, C9H13Q.
Isopinic acid, C,4H,0O6.
Isoprene, C5H8.
Isoaaccharic acid, C6H10OS.
laovaleroglyceral, C8H16O3.
laovaleryloroaelin, C19H20O5.
lauretine, CHjON^
Itapyrotartaric acid, C4H6O3.
Itacoanilic acid, CnHuO3N.
Itaconic acid, C5H6O4.
Itamalic acid, C5H8O5.
Itatartaric acid, C5H8O6.
Ivain, C24H42O3.
Ivaol, C12H2U0 ; C24H40O2.
Jaborandin, C10H12O2S.
Jalapic acid, C^H^O^ ; C34H8()0I8 ;
CesHnsOss-
Jalapin, C34H56O16.
Jalapinol, C^H^O,.
Jalapinolic acid, C16H30O3.
Jambosin, C10H6O3N.
Japaconine, C26H41O10N.
Japaconitine, C^H^C^N,,.
Jervaic acid, C14H12O12.
Jervine, C2,H37O3N ; C26H43O2N ;
C30H4603N2.
Juglone, C18H12O5.
Jugloxime, C10H7O3N.
Kairine, CUH15ON.
Kairocoll, CnHnOjN.
Ketine, C6H8N2.
Ketolactonic acid, C8H10O4.
Kinoiin, C14H12O,;.
Kino-red, C^H^O,,.
Koenlite (CH)» ; (C6H6)n.
Kosin, C31H38O10.
Kusain, C26H44O6.
Kynuric acid, C9H705N ; C10H7O3N;
C20H1406N2.
Kynurine, C9H7ON ; C18H1402N2.
Lactic acid, C3H6O3.
Lactide, C6H8O4.
Lactocaramel, C6H10O5.
Lactoglucoae, C6H12O6.
Lactose, C12H22On.
Lactosetartaric acid, C17H26O19 ;
CMH4jO28.
Lactucerin, C20H32O2 ; C40H66O3.
Lactuceryl alcohol, C1SH30O.
Lactucone, C14H24O ; C15H240 ;
C40H66O3.
Lacturamic acid, C4H8O3Nj.
Lantanuric acid, C3H4O3N2.
Lanthopine, C23H25O4N.
Lanuginic acid, C,9H30O10N6.
Lapachic acid, C15H14O3.
Lapacone, C30H28O6.
Larixinic acid, C10H10O6.
Laaerol, C14H2aO4.
Laaerpitin, C16H22O4 ; C24H36O7.
Laudanine, C20H25O4N.
Laudanoaine, C21H27O4N.
Laurene, C10H14 ; CnHle.
Laurie acid, C12H24O2.
Laurin, C^EL^C^.
Laurone, C23H46O.
Lauroateric acid, C12H24O2.
Laurostearin, C27H50O4 ; C39H74O6.
Lauroxylic acid, C9H10O.j.
Lecanoric acid, C16H,4O7 ; C36H36O15.
Lecithin, C42H34O,JNP.
Ledum camphor, C25H44O2.
Leken, C,HT.
Lepamine, C20H32N2.
Lepargylic acid, C9H16O4.
Lepidene, C28H20O.
Lepidine, C10H9N.
Leucaniline, C19H19N3 ; C20H21N3.
Leucanisidine, C21H23O2N3.
Leucaurin, C]9H14O2.
Leucic acid, C6H12O3.
Leucine, C6H,3O2N.
Leucogallol, C,8H6C112O,2.
Leucoline, C9H7N.
Leucolinic acid, C9H9O3N.
Leuconic acid, C5H8O9.
Leucopetrin, C50H4203(2)=C50HS4O3
Leucophenylenaaffranin, C,SH18N4.
Leucopthal green, C^HjjON^
Leucoroaolic acid, C20H18O3.
Leucotin, C21H20O6 ; C^H^O,,,.
Leucotolylen blue, C15H20N4.
Leucoturic acid, C6H6O6N4.
Levinulin, C6H10O6.
Levulan, C6H10O5.
Levulin, C6H10O5.
Levnlinic acid, C5H803.
Levuloaan, C6H10OS.
Levuloae, C6H12O6.
Licarene, C10H16.
Licheniu, C6H10O6.
Lichenstearic acid, C14H24O8.
Lignin, C18H24O10.
Lignoceric acid, C24H48O2.
Lignoae, C^H-jjO,,.
Limettic acid, CnHgO,.
Limonin, C22H26O7 ;
C4»H50O13.C26H30O8.
Linoleic acid, C16HMOS.
Linoxyn, C^H^O,,.
Lipicacid,C5H604; C6H8O4.
Lithobilic acid, C30H58O6.
Lithofellic acid, C20H36O4.
Lithuric acid, C15H19O9N.
Lobaric acid, C17H16O6.
Locaetin, C9HSO5.
Loca'in, C2SH34O17.
Lophine, C2]H16N2.
Loturin, C.HbOcNa.
Loxoterygine, C^H.uO.jN.j.
Lupigenin, C17H12O6.
Lupiuine, C21H40O2N2 ; C29H8.iO16.
Luteolin, CiSH8O6 ; C20H14O9.
Luteic acid, C20H20OI2.
Lutidinbetam, CjHuOjN.
Lutidine, C7H9N.
Lutidinic acid, C.H5O4N.
Lutorcin, C7H8O2.
Lycoctonine, C36H49O12N.
Lycopodine, C^HjjOjNj.
Lycoresin, C9H16O.
Lycoatearone, C^H^O,,.
Macene, C1(IH16.
Machromin, C14HIOO5.
Macleyine, C2I,H19O5N.
Maclurin, C13H10O6.
Mairogallol, ClsH7ClnO1().
Malachite green, C23H26ON,,.
Malanil, C10H9O3N.
Malanilide, C16HlnO3N2.
Maleic acid, C4H4O4.
Malic acid, C4H6O5.
Malobiuric acid, O5HbO4N3.
Malonic acid, C3H4O4.
Maltic acid, C6H10O5.
Maltose, C12H22On.
Malylureide, C5H7O3N3.
Malylure'idic acid, CbH6O4N2
Mandelic acid, C8H8O3.
Mangostin, C20H22O5.
Mannide, C6H10O4.
Mannitane, C6H12O5.
Mannitic acid, C6H,,O7.
Mannitic ether, C12H26On.
Mannitine, C6H8N2.
Mannitol, C6H14O6.
Mannitolide, C41H39O11N6.
Mannitoae, C6H12O6.
Margaric acid, Ci-H34O2.
Margarolic acid, C17H3nO2.
Masopin, C12H18O2 ; C22H36O.
Matezite, C10H20O9.
Matezodambose, C6H12O6 ; C9H1SO9.
Maticocamphor, C12H20O.
Mauvaniline, C19H17N3.
Maveine, C27H24N4.
Maynoa resin, C14H18O4.
Meconidine, C21H23O4N.
Meconin, C10H10O4.
Meconinic acid, CIOH12O6.
Meconoisin, C8H10On.
Meconic acid, C7H4O7.
Medullic acid, C^H^O^.
Melam, C6H9Nn.
Melamine, C3H6N6.
Melaniline, C,,H13N3.
Melanine, C9H10O4N2.
Melanoximide, C15H],O2N3.
Melanic acid, C6H4O3.
Melanthin, C20H33O7(?).
Melanureuic acid, C3H4O2N4.
Melaasinic acid, C12H10O5.
Melene, C30H60.
Melezitoae, C12H22O,,.
Melidoacetic acid, C5H8O2N6.
Melilotic acid, CaH10O3.
Melilotol, C9H8O2.
Melilotic coumarin, C,SH16O3.
Melissene, CMH9).
Meliaaic acid, C^JI^O,,.
Melitose, C^H^O,,.
Mellitic acid, C12H6O12.
Mellone, C6H3N9.
Mellonhydride, C9H3N13.
Mellophanic acid, C,,,H6O8.
Melolonthin, QHuOaSNj.
ALPHABETICAL INDEX OF THE ROOT-COMPOUNDS OF CARBON-.
795
Meuaphoxiraide, CjjHuOjNj.
Menaphthylamine, CnHjjN.
Meiiisperraiue, C9H12ON ;
C18H2402N2.
Menthene, C10H13.
Menthol, C10H20O.
Menthone, C10H1SO.
Meuthyl alcohol, C10H20O.
Meuyauthin, C22H36OU.
Menyanthol, C3HSO.
Mercaptane, C2H6S.
Mesaconic acid, C5H6O4.
Mesarualic acid, C5HSO5.
Mesidic acid, 09H8O4.
Mesidine, C9H13N.
Mesitene, C6H24O3(?).
Mesitol, C9H12O.
Mesitonic acid, C7H12O3.
Mesityl alcohol, C9H12O.
Mesitylene, CgH12.
Mesitylenic acid, C9H10O2.
Mesitylene quinhydrone, C27H3.,O6.
Mesityl oxide, C6H10O ; C12H22O.
Mesityloxime, C6HuON.
Mesitylic acid, C8H13O3N.
Mesocamphoric acid, C10H16O4.
Mesorciuol, C9H12O2.
Meaoxalic acid, C3H4O6.
Mesotartaric acid, C4H6O6.
Metacamphretic acid, C10H10O5.
Metacetone, C6H10O.
Metacopaibic acid, C22H34O4.
Metadehydracetic acid, C14H14O7.
Metaldehyde, C4H8O2.
Metanapththalene, C45H72.
Metaphloretin, C33H32O14.
Metapurpuric acid, C7H5O4N3.
Metatemplene, C15H24.
Metaterebenthene, C20H,2 ; C20H32O.
Metatropine, C18H15ON.
Metaustraterebenthene, (C10H16),,.
Meteceric acid, C.HyO^
Methacrylic acid, C4H6O2.
Methane, CH4.
Methazonic acid, C2H4O3N2.
Methiutricarboxylic acid, C4H4O6.
Methylal, C^Oy
Methyl alcohol, CH4O.
Methylazaurolic acid, CH2ON2.
Methylchloracetol, C3H6C12.
Methylcodethylene, C.HbO,:Nd.
Methylenecafle'le acid, C10H8O4.
Methylenediphenylene, C,3H10.
Methyferiediquino'il, C19H14N,,.
Methylenehomocaffe'ic acid, CnIT10O4.
Methylenenitane, C7H14O6.
Methylene white, C32H40S2N6.
Methylethylpinacone, 08H13O2.
Methylisatoid, C17H12O4N2.
Methylketole, C9H9N.
Methylleucaurine, C20H18O3.
Methylnitrolic acid, CH2O3N2.
Methylphosphinic acid, CH5O3P.
Milk sugar, C12H22OU.
Morin, C12H10O6.
Morindin-, C14H8O3.
Morinic acid, C12H10O6.
Moriutannic acid, C13H10O6.
Morphine, C1?H19O3N.
Morphothebaiine, C17H17O3N.
Moschatine, C21H27O7N.
Mucic acid, C6H10OS.
Mucobromic acid, C4H2Br2O3.
Muconic acid, C6H6O4.
Munjistin, C15H8O6.
Murexan, C4H5O3Na.
Murexide, C8H6O6N5.
Murexom, C12H16O6N6.
Murrayetin, C,2H,,,O6 ; C24H24O10.
Murrayin, C18H22O10.
Muscarin, C5H15O3N.
Mustard oil, C4H5SN.
Mycomelinic acid, C4H4O2N4.
Mycoprotei'n, C25H42O9N9.
Mycose, C12H22On.
Myricin, C46H92O2.
Myricyl alcohol, C30H62O.
Myristic acid, C^H^O,,.
Myristicin, C10H20O3.
Myristicol, C,0H16O.
Myristin, C46H86O6.
Myristolic acid, C14H24O2.
Myristone, C27H64O.
Myristoxime, C^-H^ON.
Myronic acid, C10H19O10S2N.
Myroxocarpin, C24H34O3 ; C43H7l)O6-
Naphartannic acid, C56H5(iO37.
Naphthacoumaric acid, C13H1(1O3.
Naphthacoumarin, C13H8O2.
Naphthalene, C10HS.
Naphthaleosin, C24H10Br4O5.
Naphthalic acid, C12HSO4.
Naphthazarin, C10H6O4.
Naphthene alcohol, C10H12O4.
Naphthesic acid, C10H6O4.
Naphthocyaminic acid, CogH^OjNj.
Naphthoic acid, CUH8O2.
Naphthol, C10H8O.
Naphtholdiquinoue, C10H4O4.
Naphtholphthale'in, C23H16O.t.
Naphthoquinhydron, C20H14O4.
Naphthoquinol, C10H8O2.
Naphthoquinoline, C13H9N ;
Naphthoquinone, C10H6O2.
Naphthoquinonechlorimide,
C20H10C103N.
Naphthoxalic acid, C,0HSO6.
Narce'ine, C2SHJJO9N.
Narcotine, C22H23O7N.
Naringin, C23H;6O12.
Nartine, C.^H.AN,,.
Nartinic acid, C20H16O6N2.
Natolom, C26H28OU ; C34H38O15.
Neurin, C5HUON.
Neurostearic acid, C^HajOj.
Ngai borneol, C10H18O.
Ngai camphor, C10H,8O.
Nicotic acid, C6H5Os,N.
Nicotine, C,0H14NS.
Nigrosine, C36H2,N3.
Nithialin, C12H16OSN4.
Nitranilic acid, C6H2O8Na.
Nitrocarbole, CH3O2N.
Nitroforni, CHO6N3.
Nitroglycerin, C3H6O9N3.
Nonaue, C9H20.
Nonine, C9H16.
Nonodecane, C19H40.
Nonodilactone, C10H12O4.
Nonyldecoxylcarbamide,C20H4l)O2N2
Nonylene, C9H18.
Nonylic acid, C9H18O2.
Nornarcotine, C19H,7O7N.
Noropianic acid, C8H6O6.
Nucin, C18Hi2O5.
Nucleln, C29H49O22N9P3.
Nupharin, C18H24O2N2.
Nupharphlobaphen, CjjH^Ojs.
Nymphosaphlobaphen, C66H4SO36.
Nymphceataunic acid, C66H68O38.
Octane, C8H18.
Octine, C8H14.
Octocosane, C28H68.
Octodecane, C^Hj,.
Octodecene, C18H36.
Octodecylidene, C18H34.
Octooxybenzoiid, C66H340,r.
Octylene, C8H16.
CEnanthodiureide, C9H20O2N4.
CBnanthohexure'ide, CjjH^OjN^.
(Enanthol, C7H14O.
CEnanthone, C13H26O.
ffinanthotetrureide, C25H52O4N8.
(Enanthothialdin, C21H43S2N.
CEnanthylic acid, C7H14O2.
(Enanthylidene, C7H12.
(Enanthylidenebenzidin, C26H36N2.
CBnanthylidenedibenzamide,
C33H3402N,,
CEnoglucinol, C6H6O3.
(Enolin, C20H20O5.
Oleandrine, C.HbOcNd.
Olei'c acid, C18H34O2.
Olein, C67H10406.
Olibene, C10H,6.
Olivil, C14H1S06.
Ouocerin, C12H20O.
Ouonetin, C-aH^Oe ; C4SH44O13.
Onouin, C30H34O13 ; C^S^O^.
Onospin, CjjH^O,,, ; CjoH^O-js.
Ophelic acid, C, :iH2llO10.
Opiammon, C20H19O8N.
Opianic acid, C10Hi0O6.
Opiaiiine, C22H23O7N.
Opinic acid, C9H6O5 ; C14H10O8.
Opionine, CS2H:J307N.
Opoponax resin, C20H24O7.
Orcacetophenone, C9H10O3.
Orcem, C7H7O3N.
Orcendialdehyde, C9H8O4.
Orciuol, C7HSO2.
/3-Orcinol, C8H10O2.
Orcinaurin, C22H18O6.
Orcinphthalein, Cj,H,,O6.
Orcinphthalin, C22H1804.
Orcylaldehyde, C8H8OS.
Orcyldiglycollic acid, CnHls06.
Oruithin, C6H12O2N2.
Oruithuric acid, C19H20O4N2.
Oroselone, C14H12O4.
Orsellinic acid, C8H8O4.
Ostruthin, (C14H1702)Il.
Otobite, C24H2605.
Oxacetein, C18H1604.
Oxalantin, C6H6O6N4.
Oxalein, CjoH^Oj.
Oxalethyline, C6H10N2.
Oxalic acid, C2H2O4.
Oxalmethyline, C4H6Nj.
Oxalylnaphthalide, C22H16ON2.
Oxalylthiosinamin, C6H6O2SN2.
Oxamethane, C4H7O3N.
Oxamic acid, C2H3O3N.
Oxamide, C2H4O.jNj.
Oxamoidin, C14H23O10Nn.
Oxatolylic acid, C16H16O3.
Oxindole, C8H7ON ; C^H^O.N.,.
Oxoctenol, C8H,,O2.
Oxonic acid, C4H5O4N3.
Oxyacanthine, C^H^OgN ;
0,^,0,^,.
Oxybenzuric acid, C9H904N.
Oxycannabin, C6H6O2; C20H.j007Na.
Oxycellulose, C18H26O16.
Oxyconiceme, C8H15ON.
Oxycyclopin, C25H3(1O16.
Oxydimorphine, C34H:)606N2.
Oxyguanine, C10H14O9Ng.
Oxyheptinic acid, C21H32O7.
Oxyhexic acid, C,8H26O10.
Oxyidrialin, CgdH^On,.
Oxylepidenic acid, C28H22O3.
Oxypentaldin, C,0H16ON.
Oxypentic acid, ClbH.wOlo.
Oxypeucedauin, C,4H22O7.
Oxypurpurogallin, C-^S^O^
Oxysulphobenzide, C^H^O^S.
Oxytetric acid, C12H14O10.
Oxytolic acid, C7H6O,.
Oxytolideue, CltHwOf
Pachymose, C^H^On.
Palmitic acid, C16H32O.,.
Palmitin, C51H93O6.
Palmitolic acid, C16H23O2.
Palmitone, C31H6=O.
Palmitoxylic acid, C16H2804.
Panacone, C19H30O7.
Pauaquilone, C20H42O15.
5 I 2
796
ALPHABETICAL INDEX OF THE ROOT-COMPOUNDS OF CARBON.
Papaveric acid, <J10H13O-N.
Papaverine, C2iH21O4N.
Parabuxin, C26H49ONj.
Parabanic acid, CjHjOsN,,.
Paracajeputene, C20H32.
a-Paracatol, C15H24O.
£-Paracatol, C^H^Oj.
•y-Paracatol, C^H^O.,.
Paraconic acid, C6H6O4.
Paracopaiba oil, C15H24.
o-Paracotene, C,SH18; C45H72.
0-Paracotene, Cull,,,; C46Hr,.
Paracotoic acid, Ci9H14O7.
Paracotoin, C19H12O6.
Paracoumarhydrin, C9H8Oj.
Paradiconiine, C1BH27N.
Paradigitalin, C22H3)0;.
Paraffinicacid,C24H43O2 ; C13H2605N.
Paraglobularetin, C12H,6Or
Parahydrazotoluene, C28H30N4.
Paraldehyde, C6H12O3.
Paraldol, (C4H802)n: C3H16O4.
Param, CH2N2.
Paramorin, C12H8O5.
Paramylene, C^Hj,,.
Paramylum, C6H10O5.
Paranicene, C10H12.
Paraniline, C12H14N2.
Paraoxylophine, C^H^ONj.
Parapectin, C32H48O32.
Parapectic acid, C24H34O23.
Parapeptone, C144H2,,4O24SN36.
Parapicoline, C6H7N ; C12HHN2.
Parasaifranine, C20H18N4.
Parasalicyl, C14H10O3.
Paraxanthine, C|5H17O4N9.
Parazotoluene, (C^N^,.
Parellic acid, C9H6O4.
Paricine, Cl6H,3ON.j.
Paridin, CleH.KOr
Paridol, C36H46O9.
Parigenin, C2SH4204.
Pariglin, C18HroOr
Parillin, C40H70O13.
Paristyphnin, C.^H^O,,.
Parsley camphor, C12H14O4.
Parvoline, 09H13N.
Patchouli camphor, C16H26O;
CuH.0.
Patchoulin, CjSH24.
Patellaric acid, C17H20O10.
Paviin, C16H18Oi0.
Paytamin, C21H24ON2.
Paytin, C2iH24O2N2.
Pectic acid, C14H20O13 ; C^^O^.
Pectin, C6H805; C9H14O8;
Cj8H42O24; Cj-jH^Oj.,.
Pectin sugar, C6H12O6.
Pectolactinic acid, C8H806.
Pectosinic acid, C32H48O31.
Pelargonic acid, C9H18O2.
Pelletierine, C8H16ON.
Pellutein, C18H19O3N.
Pelosin, C18H21O3N.
Pentadecanaphthene, C,6HM.
Pentadecane, C15HS2.
Pentadecine, C^H^.
Pentadecylic acid, C16H3002.
Pentahiroline, C13H16N.
Pentane, C5H12.
Pentatriacontane, C35H72.
Pentethyleneglycol, C10H2206.
Pentic acid, C15H20O7.
Pentine, (C5H8),,.
Peppermint camphor, Cj|jH20O.
Perchlormesol, C4C16.
Perchlormecylene, C6C18.
Pereirine, C19H24ON2.
Perezonoxime, C15H21O3N.
Petinine, C4HUN.
Petrocene, C45H72.
Petrocin, (C12H8)n.
Petrolene, C15H24.
Petroleum acid, C11H20O2.
Peucedanin, C,2H12O3 ; C16H16O4 ;
C24H2406.
Phellanthrene, C,0H16.
Phellyl alcohol, C^H^O.
Phenanthrene, Ci4H10.
Phenanthrenebenzalquin, C35H24O.
Phenanthrene quinacetone, C,7H14O3.
Phenanthrene quinhydrone, C28H18O4.
Phenanthrenequinimidacetone,
Phenanthrenesulphe'inresorcinol,
Cj6Hl6O7S3.
Phenanthrol, C14Hi0O.
Phenanthroline, C19H8Nj.
Phenanthrone, C14H10O.
Phenenyltribenzoic acid, C3-H1806.
Phenetoil, C8H10O.
Phenocyanin, C6H5ON.
Phenoic acid, C6H4O2.
Phenol, C,H6O.
Phenolcorallin, C20H16O4.
Phenolglucinol, C6H6O3.
Phenolglucoside, C12H,6O6.
Phenolphthale'in, C20H14O4.
Phenolphthalidein, CajH,^.
Phenolphthalidin, C20H14O3.
Phenolphthalin, C20H16O4.
Phenolphthalol, C20Hlg03.
Phenoquinone, C18H,4O4.
Phenosaffranine, C18H16N4.
Phenose, C6H12O6.
Phenacetotrope'ine, C16H21O2N.
Phenylanisaldehydine, C^HjdO^N,,.
Phenylarabinosazone, C18H22O4N4.
Phenylazonitrolic acid, C12H10ON3.
Phenylbenzaldehydine, C20H16Nj.
Phenylcarbamidol, C19H19ONS.
Phenylfurfurazide, CnH,0ONr
Phenylgalactosazone, CjgHjjO^N^
Phenylglucosazoue, C18H22O4N2.
Phenyllactosazone, C24H32O9N4.
Phenylmaltosazone, C24H3,jO9N4.
Phenylsemicarbazide, C7H9ON3.
Phenylthiocarbizine, C7H6SN2.
Phenyltolylpinacone, C^HogO.;.
Phenylensaffranine, C18H14N4.
Phillygenin, C21H24O6.
Phillyrin, C27H34On.
Phloramine, C!6H7O2N.
Phlorem, C19HUO7N.
Phloretic acid, C9H1003.
Phloretin, C15H14O5.
Phloretol, C8H10O.
Phlorizem, C21H30O13N2.
Phlorizin, C2iH24O10.
Phlorizinanilide, 0^11340^2.
Phlorobromin, C6HBr9O.
Phloroglucide, C12H10O6 ; C^H^O,,
Phloroglucinol, C6H6O3.
Pliloroglucinphthalem, C20H12O7.
Phloroglucinphthalin, C20H14O7.
Phloroglucinvanillem, C20H1SO8.
Phlorol, C8H100.
Phlorone, C8H8O2.
Phlorose, C6H12O6.
Phorone, C9H14O.
Phoronic acid, C9H16O2 ; CnH18O6.
Phoronoxime, C9H15ON.
Phosene, C14H10.
Phosgene, CC12O.
Phosphenylic acid, C6H7O3P.
Phosphobenzene, C12H10P2.
Photosantonic acid, C15H20O4.
Photosantonin, C11H14O3.
Phrenosin, C4|H81O8N.
Phthalacene oxide, C21H14O.
Phthalamidothiophenol, C^H^SjN
Phthal green, C24H24O2Ns,.
Phthalic acid, C8H6O4.
Phthalidanil, C14HUON.
Phthalidanilide, C20H14ON2.
Phthalidchloride, C8H4OC14.
Phthalidine, C8H9N ; C8H7ON.
Phthalophenone, C^H^O,.
Phthalureide, C9H6O3N.j.
Phthaluric acid, C9H8O4N2.
Phthalylhydroxylamine, C8H6O3N.
Phthalylpinacone, C16H1SO4.
Phthalylpiperidine, C,8H24O2N2.
Phthalyltropeme, C24H32O4Nj.
Phycic acid, C,H7OZ.
Phylloescitannin, C26H24O13.
Phyllic acid, C36H6408.
Phylloretin, C8H10.
Physalin, C14H16O3.
Physetolic acid, C16H3002.
Physodem, C10H8O6.
Physodin, CioH.oO; ; C12H12O8.
Physostigmin, C15H21O2N3.
Phytosterin, C26H44O.
Picamar, C10H1403.
Picene, C22H14.
Picoerytliriu, C13H16O6.
Picoline, C6H7N.
Picolinic acid, C6H502N.
Picraconine, C24H41O8N.
Picramic acid, C6H5O6N3.
Picramide, C6H4O6N4.
Picric acid, C6H3O;N3.
Picroaconitine, C31H45O10N.
Picroerytlirin, C12H16O7.
/3-Picroerythrin, C13H6O6.
Picrolicheniu, C,2H20O6.
Picrorocellin, C'27H29O5N3.
Picrotin, C13H15O7 ; C21H24O10 ;
Picrotoxide, C15H16O6 ; C2:H28On.
Picrotoxin, C9H10O4 ; C12H14O5 ;
CisH16O6 ; C30H31O,3 ; C36H40O16.
Picrotoxinin, C1SH18O7.
Picrylamine, C12H6O12N7.
Pilocarpene, C10H16.
Pilocarpin, CnH16O2N2.
Pimaric acid, C20H30O2.
Pimelic acid, C7H12O4.
Pimento oil, C45H72.
Pinacolin, C12H26Oj.
Pinacone, C6H1402.
Pinipicrin, C22H36On.
Finite, C,H12O6.
Pennitanic acid, C7H8O4.
Piperethylalkamine, C7HiSON.
Piperhydronic acid, C12H14O4.
Piperic acid, C12H10O4.
Piperidine, C6HUN.
Piperidinic acid, C4HBO2N.
Piperine, C17H19O3N.
Piperonal, C8H6O3.
Piperonyl alcohol, C8H3O3.
PiperonyKc acid, C8H,O4.
Piperylene, C5H8.
Piperylhydrazine, CdH12N2.
Piperylsemicarbazide, C6H13ON3.
Pipitzaho'inic acid, C15H20O3.
Pirylene, C6H6.
Piscidine, CojE^Og.
Plumieric acid, C10Hj0O5.
Podocarpic acid, C17H22O3.
Podophylloquercetin, C,H7O,.
Poeonin, C5H4O.
Poley oil, C10H160.
Polyasparagincarbamide,
C34H40026N10.
Polychro'ite, C48H68O18.
Polydehydroazotoluene, C^H^Nj.
Polyethylene, C16H32.
Polyfurfurol, (C5H4O)n.
Polyporic acid, (C9H?O.!% ; ClaH14O4.
Polystyrolene, (Cfl)n.
Polythymoquinone, (Ci0H,..O2)0.
Populin, CjoHjjO,.
Porphyrine, C21H25O2N3.
Prehnitic acid, C10H608.
Prehnomalic acid, C10H8O9.
Primula camphor, CUH12O5 ;.
C22H24O10.
Propane, C3H3.
Propargylic acid, C3H2O2.
ALPHABETICAL INDEX OF THE BOOT-COMPOUNDS OF CARBON.
797
Prophetin, C23H36O7.
Propionic acid, C3H6O2.
Propylal, C3H6O.
Propylaldoxime, C3H7ON.
Propylene, C3H6.
Propylphycite, C3H8O4.
Protagon, C160H308O35N5P.
Protamine, CjH^OjNj.
Protocatechuic acid, C7H6O4.
Protopine, C20H190,,N.
Protoquinamicin, Ci^S^O^Sf
Pseudaconine, C27H41O9N.
Pseudoaconitine, C36H49Oi2N.
Pseudatropine, C17H23O3N ; not
CjjHaON.
• Pseudobenzopyrroline, CnH9ON.
Pseudocaproic acid, C6H12O2
Pseudocholoi'danic acid, C16H24O7.
Pseudocorallin, C26H38O10.
Pseudocumeue, C9H12.
Pseudocumenol, C9H12O.
Pseudocumidine, C19H3N.
Pseudocumolphthaloylic acid,
C17H1603.
Pseudodiazoacetamide, C6H9O3N9.
Pseudoheptyleue, C7H14.
Pseudojervine, C29H4;jO-N.
Pseudoleucaniline, C19H19Na.
Pseudolutostyril, C7H9ON.
Pseudonjauve'ine, Cj.tHjoN.,.
Pseudomorphine, C17H19O4N.
Pseudopelletierine, C9H15ON.
Pseudophenanthrene, Cj6HI2.
Pseudopurpurin, C15H8O7.
Pseudorosolic acid, C20H,4OS.
Pseudotoluidine, C7H9N.
Pseudotriacetonalkamine, C9H19ON.
Pseudotropine, C8H15ON.
Pseudoveratrine, C14H3BO3N2.
Pseudoxanthin, C5H4O2N4.
Psoronic anhydride, C20H14O9.
Psychosin, C^H^C^N.
Pterocarpin, C20H16O6.
Pulvamic, C18Hj3O4N.
Pulvic acid, O1SH12O5.
Purpuric acid, C8H5O6N5.
Purpurin, CMH8O6.
t-Piirpurin, C16H8O6.
Purpurogallin, C20H16O9.
Purpuroxanthin, C,4H8O4.
Pyrene, C16H10.
Pyridine, C6H5N.
Pyridine betaine, C7H7O2N.
Pyridone, C5H6ON.
Pyroamaric acid, C16H16O,,.
Pyrocamphretic acid, C10HHO4.
Pyrocatechol, C6H6O2.
Pyrochiuovic acid, C3|H48O4.
Pyrocholesteric acid. CnH16O5.
Pyrocinchonic acid, CjHjO^ ;
C10H10O6.
Pyrocoll, C10H6O2N2.
Pyrocomenaniic acid, C6H502N.
Pyrocressol, C^H^O.,.
a-Pyrocressoldioxide, C28H22O6.
Pyrocressoloxide, C28H22O4.
Pyrodextrin, C48H74O37.
Pyrogallinphthaleinic acid, C^H^C^
Pyrogallol, C6H6OV
Pyrogalloquinone, CiSH14O8.
Pyrogallolanhydride, C2IH14O7.
Pyrogallovanille'in, CjjH^Og.
Pyroglutamic acid, C5H7O3N.
Pyroglycide, C6H12O4.
Pyroguajacol, C^H^O, ; C19H52O3.
Pyroinulin, C6H10O5.
Pyroisomalic acid, C6HSO5.
Pyrolithofellic acid, C^H^Oj.
Pyrolivilic acid, C^H^O,,
Pyromaric acid, C20H30O2.
Pyromecazone, CSH3O3N.
Pyromecazonic acid, C5H6O3N.
Pyromeconic acid, C5H4O3.
Pyromellitic acid, C10H6O8.
Pyroruucic acid, C5H4O3.
Pyropapaveric acid, C,5H15O5N.
Pyrophotosantonic acid, C14H2002.
Pyrophthalone, C14H9O2N,
Pyroracemic acid, CjH4O3.
Pyroricinic acid, C18H30O2.
Pyrotartaric acid, C5H8O4.
Pyroterebic acid, C6H,0O2.
Pyrotritartaric acid, C7H8O3.
Pyrousuetic acid, C14H14O6.
Pyrouanic acid, C12H13O6.
Pyroxanthin,. C5H8O2 ; CJ5H12O3.
Pyrrol, C4H6N.
PyrroHc acid, C5H5O2N.
Pyrroline, C4H6N.
Pyrrol red, C12H14ON2.
Pyrrone, C,H8ON2.
Pyruvic acid, C3H4O3.
Pyruvin, C6H10O5.
Pyruvinurelde, C4H4O2N2.
Pyvuril, C6H8O3NV
Quartenylic acid, C4H6O2.
Quassiin, C10H12O3 ; C31H4209.
Quebracharaine, C,HbOcNd.
Quebrachine, C21H26O3Na.
Quebrachotannic acid, C26H27O10.
Quebrachol, C^H^O.
Quercetagetin, C-^HjjO^.
Quercetin, C24H16OU.
Quercetic acid, C16H10O7>
Querciglucinol, C6H6O3 ; C18H18O9.
Quercimeric acid, C8HSO6.
Quercite or Quercitol, C6HU05.
Quercitau, C6H10O4.
Quercitrin, C16H,9O9; C3,H38O20.
Quercitetartaric acid, C22H32O7.
Quinacetophenone, C8HSO3.
Quinaldine, C^HgN.
Quinamicine, C19H2402N2.
C^uinamidine, C19H24OSNS.
Quinamine, C19H24O2N2.
Quinanilide, C,3H17OSN.
Quindecone, C15H26.
Quindecylic acid, C15H30O2.
Quinethionic acid, CUH18O,.
Quinetum, dHyO,.
Quinhydrone, C12H10O4 ; C,^.,^,.
Quiiiic acid, C7H12O6.
Quinicine, C20H24O3N5.
Quinide, C7H10O6.
Quinidamiiie, C^H^OjN,;.
Quinidine, C20H24O2N2.
Quinine, C30H.UO^^.
Quininic acid, C,,H9O3N.
Quinisatiu, C9H5O3N.
Quinizarin, C14H804.
Quinol, C6H6OS.
Quinoline, C9H7N.
Quinolinebenzcarboxylic acid,
CIOH702N.
Quinolinebetai'ne, CnH9O2N.
Quinolinecyanine, C^H^NjI.
Quinolinic acid, C7H5O.,N ; C3H9O3N.
Quinoline yellow, C^H^QgN..
Quinolic acid, C9H6O4N2.
Quinone, CeH4O2.
Quinonamide, C^H^O^N.
Quinophenol, C9H7ON.
Quinophthalone, C17H9O2N.
Quinoxaline, CSH6N2.
Eacemic acid, C4H6O6.
Eaffinose, C6H4O7 ; C9H16O8.
Bangiformic acid, CnHlsO3.
Eatanhia red, CjgHjjOn.
Batanhin, C10Hj3O3N.
Begianic acid, C6H6O7.
Beichenbach's paraffin (CH2)n.
Besacetei'n, C16H12O4.
Besacetophenone, C8H8O3.
Besaurin, C19H14O6.
Besinein, C20H30O.
Besineone, C29H46O..
Beainone, CnE^O.
Besocyanin, Cj^^Oj.
Besoquinone, C12H10O4.
Besorcinol, C6H6OS.
Besorcinbenceiin,C19H14O4 ;
Besorcinindophan, C9H4O6N4.
Besorcinoxalei'n, Cx1:luOr.
Besorcinphthalein, C14H10O6 ;
C20H14O6.
Besorcinquinoline, C24H20O2N2.
Besorcyldialdehyde, C8H6O4.
Besorcylic acid, C7H6O4.
Betene, C18H18,
Betenic acid, C^HjgOj.
Betenindole, CSH8ON.
Betinic acid, C40H64O6.
Betinaphtha, C7H8.
Betinite, C40H62O3.
Betinol, C8PS,
Betinyl, C9H12.
Betistenequinoxime, Ci,H18O2.
a-Rhamnegin, C48H66O29.
Bhamnetin, C12H10O6.
Bhamnodulcitol, C6H14O,.
Bheumtannic acid, C26H26O14.
Bheumic acid, C20H1609.
Bhinanthin, CS9H52O20.
Bhodanin red, C9H603S6N3.
Bhodanic acid, C3H3OS2N.
Bhodizonic acid, C5H6O6.
Bhodotanic acid, C14H14O9.
Bhceadine, C21H21O6N.
Bhoeagenine, C21H21O6N.
Bicinedaldic acid, C1SH34O3.
Bicinelaidin, C39H72O7.
Bicinoleiic acid, C18H34O3.
Bicinostearolic acid, U18H3203.
Bicinostearoxylic acid, C1SH32O4.
Bobinin, C35H30O16.
Boccellinin, C18H16O7.
Boccellic acid, C17H32O4.
Bosaniline, C19H19ON3 ; CsoHjjO
Bose oil (CH,)n.
Bosolic acid, C20H16O3 ; CjeH^O,,
Bottlerin, CnH^Oj.
Bubeanhydride, C2H4S2N2.
Buberythric acid, C2(iH2aO14.
Bubidine, CnHJ7N.
Bubijervine, C26H43O2N.
Eubiretin, C7H6OS..
Buficarmin, C16H12O5.
Buficoccin, C16H10O6.
Bufigallic acid, C14H8O8.
Bufimoric acid, C16H140,.
Bufin, C21H20O8.
Bufiopin, C14H8O6.
Bufohydroellagic acid, C14HSO,.
Bufol, C14H10Oj.
Butin, C^HjsO^.
Butylene, C10H18.
Sabadilline, C20H26O6N2;
Saccharamide, C6H12O6Nj.
Saccharic acid, C6H12O6.
Saccharide, C6H10O5.
Saccharin, C6H10O5.
Saccharone, C6H10O2.
Saccharonic acid, C6H10O7.
Saccharose, C^H^O,,.
Saccharovanillic acid, C14HlflO9.
Saccacharumic acid, C14H180,,.
Safflower yellow, C24H30O16.
Saffranine, C21H20N4.
Safrene, C10H16.
Safrol, C10H100S.
Salicin, C13H13O7.
Salicylic acid, C7H6O3.
Salicylide, C.H4O2;. C14H8O4.
Salicylol, C7H6O2.
Salicyltropelne, C1SH19O,N.
Saligenin, C-H8O2.
Saliretin, C14H14O3; C.jHj.O,.
Saliretone, C14H12O3,
Salviol, C10HI80.
798
ALPHABETICAL INDEX OF THE ROOT-COMPOUNDS OF CARBON.
a- Salylic acid, C14H140S.
£- » » C21H22O8.
Samandariii, G,4HCOO6N2.
Sanguinarin, C17H15O4N.
Santal, CSH6O,.
Santalic acid, C15H14OS.
Santalin, C15H14O6 ; C17H16O6.
Santalol, C15H2BO.
Santaual, C15H,4O.
Santaiiol, C15H18O.
Santonic acid, Ci5H2004.
Santonide, C16H18O3.
Santonin, C15H18O3.
Santonous acid, C15H20O3.
Sapogenin, C14H22O2.
Saponin, C32HMO18.
Sappanin, C12H1004.
Sarcine, C6H4ON4.
Sarcosine, C3H7O2N.
Scheelite (CH4)B.
Scoparm, C21H2oO10.
Sebacic acid, C10H18O4.
Sebacin, C10H18; C1(1H30O8.
Semiglutin, C^H^O^TV
Senegin, C32H54O18.
Sequoiene, C10H16 ; C13H10.
Sericic acid, C16H30O7N4.
Sericine, C15H25O8N6.
Serin, C3H7O3N.
Sesquiterebene, C1^H.jf
Sesquiterpene, C1SH24.
Sikimine, B., 14, 1721 ; m.p. 175.
Sinalbin, C30H44O16S2NS.
Sinamine, C4H6N2.
Sinapic acid, CnH,sO6.
Sinapin, C18H23O5N.
Sincalin, C5H15O2N.
Sinistrin, C6H10O6.
Skatole, C9H9N.
Smilacin, C18H30O6.
Socotrinalo'in, C15H16O7.
Solanicine, C.26H39ON.
Solanidine, C26H41O2N.
Solanine, C42H75O15N.
Sorbic acid, C6H9O2.
Sorbin, C6H12<\
Sorbite, C6H1406 ; C12H30O13.
Sordidin,C13H1008; C16H18O7.
Sparteme, C15H26N2.
Spermine, C2H5N.
Sphingosin, C17H35O2N.
Starch, (C6H1006)n.
Staphisagrin, C22H33O6N.
Stearic acid, C18H36O2.
Stearidic acid, C18H34O2.
Stearin, C57H110O,
Stearcutic acid, Ca"H.aOt.
Stearolic acid, C18H32O2.
Stearone, Q,5H70O.
Stearoptene, C10H14O; C^H^O^.
Stearoxylic acid, C18H32O4.
Steraopteue, C45H72.
Stilbene, C14H,,.
Stilbous acid, C15H12O3.
Storesin, C36H58O3.
Strychnine, C21H22O,N2.
Stryphnic acid, C4H3O2N5.
Stycerin, C9H12O3-
Styphnic acid, C6H3O8N3.
Styracin, C^gH^O,.
Styrene, C8H8.
Styrogenin, G'26H40O3.
Styrolene, C8H8.
Styrolene alcohol, CSH10O2.
Styrolene pinacolin, CSH8O.
Styrone, C9H10O.
Suberancarboxylic acid, CSH14O2.
Suberconic acid, C8H12O4.
Suberencarboxylic acid, C8H12O2.
Suberic acid, CgH14O4.
Suberocarboxylic acid, C9H14O6.
Suberomalic acid, C8H14O5.
Suberone, C7H12O ; C14H24O2.
Suberotartaric acid, C8H14OP
Suberoxime, C7H13ON.
Suberylglycollic acid, C8H14O3.
Succincyamic acid, C6H6O3N2.
Succinic acid, C4H,.,O4.
Suceinimidine, C4H7N3.
Suocinylfluorescein, C6H12O6.
Succisterene, C15H19.
Sulphisantonous acid, C8H7O4SN.
Sulphohydroquinone yellow,
Sulphohydroquinine brown,
C,2H10O4Sr
Sulphuvinuric acid, C4H4O2SN2.
Sulphonediacetic acid, C4H6O6S.
Sycoeeryl alcohol, C13H30O.
Sylvan, C6H6O.
Sylvestrene, C10H1S.
Sylvic acid, C^H^O,;.
Sylvinolic acid, C2SH36O4.
Synanthrene, C14H10.
Synanthrose (Levulan), C6H10O6.
Syntonin, C144H224O24SN3,;.
Syringenin, C13H18O6.
Syringin, C^H^O,,,.
Taiguic acid, C4H4O.
Tampicin, C34H64Oi4.
Tampicinic acid, C34H60O17.
Tampicolic acid, C16H32O3.
Tanacetylhydride, C10H16O.
Tannic acid, C20H20O9.
Tannin, C14H10O9.
Tannomelanic acid, C6H4O3.
Tannoxylic acid, CyHgO,.
Tansol, C10H16O.
Tarconic acid, C10H7O3N.
Tarconin, CnH9O3N.
Tarconyl alcohol, C60H1020 ; C61H1MO.
Tarnin, C10H9O3N ; C^f)^.
Tartaric acid, C4H6O6.
Tai-tralic acid, CUO.
Tartrelic acid, C4H4O6.
Tartronic acid, C3H4O5.
Tartrophthalio acid, C8Hj2O6
Taurin, C£H7O3SN.
Taurocarbamic acid, C3H8O4SN2.
Taurobetain, CjH13O3N.
Taurochenolic acid, C29H49O6SN.
Taurocholic acid, C26H45O-SN.
Taurocyamiue, C3H9O:,SN3.
Tauroglycocyamine, O3H9O3SN3.
Taxin, C.HbOcNd.
Tectochrysin, C16H12O4.
Teloescin, C18H30O7.
Tekoretin, (C5H8)».
Templiu oil, C10H16.
Teracanic acid, C7H10O4.
Teracrylic acid, C7H12O2.
Terebanglene, C10H16.
Terebene, C10H16.
Terebenthene, C10H18.
Terebentilic acid, C8H10O.:.
Terebentinic acid, C9H14O6.
Terebenzic acid, C14H14O4.
Terebic acid, C7H10O4.
Terebilene, C10H,6.
Terebilenic acid, C7H8O4.
Terebilic acid, C8H8O4.
Terecamphene, C10H16.
Terechrysinic acid, C6H8O5.
Terecuuimic acid, C10Hi2O2.
Terelactone, CBHgO^
Terepentilin, C10H16.
Terephthalic acid, C8H6O4.
Terpene, C10H16.
Terpenylic acid, C8H12O4 ; C8H14O6.
Terpilene, C10H16.
Terpine, C^H^O..
Terpenine, C10H16.
Terpinol, C10H18O ; C20H34O.
Terpinylene, C10H16.
Tetrabutyraldin, C16H2SON.
Tetracetylquinide, Ci5HlsO9.
Tetrachlorglycide, C3H4C14.
Tetracodeine, C72H84O12N4.
Tetracosane, C24H50.
Tetradecanaphthene, C14S.^.
Tetradecane, C14H30.
Tetradecylene, C14H28.
Tetradecylidin, C14H26.
Tetrahiroline, C12H13N.
Tetramorphine, C63H76O12N4.
Tetramylene, C20H40.
Tetraphenol, C4H4O2.
Tetraphenyltetrazone, C24H20N4.
Tetrapyruvintetraureide,
C16H1608N8.
Tetraterebenthene, C40H64.
Tetrene urethane, C7H9O2N.
Tetric acid, C12H14O7.
Tetroenanthoxaldiu, C^H^ON.
Tetrol, C4H4O.
Tetrolcarbamide, C6H6ON2.
Tetrolcyaiiuramide, UliHlsN6.
Tetroldianil, C,6H14N2.
Tetrolditolyl, O18H19N2.
Tetrolic acid, C4H4O,,.
Tetrolmelamine, C)5H12N6.
Tetroxybenzo'ide, C28H19O13.
Tetrylendicarboxylic acid, C6H8O4.
Tetrylintriamine, C4HnN3.
Teucrin, C21H24OU.
Thallin, C1UH13ON.
Thaimouynphoein, C56H5,.O36.
Thapsic acid, C16H30O4.
Thebain, C19H21O3N.
Thebeuin, C^H^OjN.
Them, C8H10O2N4.
Theobromiue, C7H9O.,N4.
Theobromic acid, C6t"H.lsaOr
Theveresin, C48H70O17.
Thevetiu, C64H84O24.
Thiacetonin, C9H19S2N.
Thialdin, C,H13S,N.
Thiammeliii, C3H5SN.
Thianilide, C^HjjSN,.
Thiauissic acid, C10H1404S.
Thiobenzaldin, C21H19S2N.
Thiochronic acid, C6H4O17S5.
Thiodilactylic acid, C6H10O4S.
Thioisatyde, C6H12O3SN...
Thiolepidin, C^H^S.
Thionessal, C28H20S.
Thiopheiie, C4H4S.
Thiorufinic acid, C10H14O4S3.
Thiosiunamiu, C4H8SN2.
Thiosulphauiliue, C24H22S3N4.
Thionuric acid, C4HSO6SN3.
Thiuramdisulphide, C,H4S4N.,.
Thiuramsulphide, C2HJS3N2.
Thujetin, C14H1408.
Thujetic acid, CogH^O^.
Thujigenin, C14H1SOP
Thujin, C^H.,,,0,,
Thymene, C10H16.
Thymoil, C12H1602.
Thymoilol, C12H1SO2.
Thymol, C10H14O.
Thymoquinol, C10H14Oj.
Thymoquiuone, C10HI3Oj,
Thymotic acid, CUH14O3.
Thymotide, 0,^,^
Tiglic acid, C5H8O,.
Tolaue, C14H10.
Tolene, C10H1B.
Tolidine, C14H16N2.
Toluanisaldehydin, C23Ho2O2N,,.
Tolubenzaidehydin, C21H1SN2.
Toluene, C7H8.
Tolufurfuraldehydin, C17HJ4O3N2.
Toluic acid, C8H8O2.
Toluidine, C7H9N.
Toluidine black, C^HsiNs.
Toluquiuhydrone, C21H^0O,j.
Toluquinine, C,7H30O2N2.
Toluquinol, C7H8O2.
Toluquinoliue, C10H9N.
AI PHABETICAL INDEX OF THE ROOT-COMPOUNDS OF CARBON.
799
Toluquinone, O7H6O2.
Toluquinoxaline, C9H,N2.
Toluric acid, C10HnO3N.
Toluylene blue, C15H18N4.
Toluylene red, C15H16N4.
Tolylene, C;H6.
Tolylene dibromide, C8H8Brj.
Tolylene alcohol, C8H10O2.
Toi-mentill red, C^H^C*!,.
Trehalose, C13H22On.
Triacetonalkamine, C9H19ON.
Triacetonamine, C9H17ON.
Triacetonciiamiue, C9H20ON2.
Triacetylformidil, C8HnO3N3.
Triamylene, C15H30.
Trianilcesculin, C33H31O6N3.
Tricarballylic acid, C6H9O6.
Trichlorhydrin, C3H5C13.
Tricodeine, C54H63O9N3.
Tricosane, C^H^.
Tricnmylamine, C30H39N.
Tridecane, C^H.^.
Tridecylene, C13H26.
Tridecylic acid, C^H^O,,.
Triepinic acid, C3H6O5.
Triethylalkarnine, C6H15ON.
Triethylin, C9H,,0O3.
Trigenic acid, C4H7O.jN3.
Triglycerol, C9HMO7.
Triglycolamidic acid, C6H9O6N.
Trihydrocarboxylic acid, C10H10O10.
Trimellitic acid, C9H6O6.
Trimesic acid, C9H6O6.
Trimorphine, C51HS7O9N3.
Trinitropetrol, C8H7O,,N3.
Trinkerite, C.HbOcSd.
Triopianide, C^H^O,,,.
Triphloretide, C^H^O-.
Trisulphonediphenylnitric oxide,
C36H2-O.SSN.
Trivaleryleue, Ci5H24.
Tropic acid, C9H10O3.
Tropide, C9H8O2.
Tropidine, CSH13N.
Tropigenin, C-H13QN.
Tropilene, C7H10O.
Tropilidene, C7HS.
Tropinic acid, CSH13O4N.
Tropine, C8H15ON.
Tulucunin, C10H14O4.
Tunicin, C6H10O5.
Turmerol, C19H23O.
Turpentine, C,0H16.
Turpethin, C34H56O16.
Turpethinic acid, 034H60O,,.
Turpetholic acid, C1BH3.iO4.
Tyroleucine, C7HnO2N.
Tyrosine, C9HUO3N.
Ultraquiiiine, C19H22O2N2.
Umbellic acid, C9H10O4.
Umbelliferone, C9H6O3.
Umbelliferouic acid, CgHgOy
Umbellol, C3H12O.
Umbellulic acid, CnH22O,;.
Undecane, CUH24.
Undecolic acid, C,jHi8O2.
Undecylene, CuH22.
Undecylenic acid, CnH20O2.
Undecylic acid, OnH22O2.
Uramidobenzoic acid, CjHsOjNj.
Uramil, C4H5O3N3.
Uramilic acid, C8H9O7N5.
Urea, CH4ON2.
Urechitin, C29H4,,O3.
Urechitoxin, C13H20O5.
Urethane, C3H7O2N.
Urethanebenzoic acid, C10H11O4N.
Uric acid, C5H4O3N4.
Urinilic acid, CSH7O6N7.
Urobilin, C32H40O7N4.
Urobrohsemalin, C34H3,O7N4Fe.
Urobutylchloralic acid, C10H15C1307.
Urocanin, CUH10ON4.
Urocaniuic acid, C6H6O2N2 ;
C12H1204N4.
Urochloralic acid, C8HUC13O;.
Urofuscohrematin, C34H3.OiN4.
Uromelanin, C^H^OgNj,.
Uronitrotoluolic acid, C13H15O9N.
Urosulphinic acid, C5H4O2SNj.
Uroxanic acid, CSH8O8N4.
Ursone, C10H16O.
Usneol, CnH12O3.
Usnetic acid, C9H10O3.
Usnetol, C13H14O4.
Usnic acid, C1ST113O7.
Usnolic acid, CjjH^O,,,.
Uvic acid, C7H8O3.
Uvitic acid, C9H8O4.
Uvitonic acid, C9H14O9.
Uvitoninic acid, C8H7O4N.
Valeraldin, C16H31S2N.
Valeric acid, C5Hi0O2.
Valeritrine, C16H27N.
Valerol, C6H10O.
Valerolactide, C5H3Oj.
Valerolactone, C6H8O2.
Valerone, C9H18O.
Valerylene, C5H8.
Validine, C[BH21N.
Valylene, C5H6.
Vanillic acid, C8H8O4.
Vanillin, C8H8O3.
Veratralbin, C^H^OsN.
Veratric acid, C9H,0O4.
Veratroidine, C24H37O7N;
C^H-^N,.
Veratrol, C8H10O2.
Verine, C28H45O8N.
Vertivert oil, C45H72.
Vicine, C23H51021Nn.
Vinylbroniide, C2H3Br.
Violaniline, C18H15N3.
Violantin, C3H6O9N6.
Violuric acid, C4H304N3.
Viridine, C12H,9N.
Viscicaoutchin, C8H16O.
Viscin, C10H2404.
Viscose, C6H1(IO5.
Vulpic acid, C19H,4O6.
Walchovite, C40H62O3.
Waldivin, C18H24O10.
Xanthil, C4H20O3 ?
Xanthin, C5H4O2N4.
Xanthogallol, C9H2Br7O3 ;
C18H4Br1406.
Xanthoquinic acid, C10H-O3N.
Xanthorhamnin,
Xanthoroccellin, Cj
Xanthoxylene, C10H12O4; C10H160.
Xanthurin, C4H8O2S.
Xantinin, C4H3O.,N3.
Xeronic acid, CSH,2O4.
Xylene, C8H10.
Xylenol, C8H10O.
Xyletic acid, C9H10Oa.
Xylidine, C3HUN.
Xylic acid, CgH^O,,.
Xylidic acid, C9H8O4,
Xylite, O.HyO,.
Xylite naphtha, C,jHj3O3.
Xylite oil, C12H18O.
Xylitone, C12H18O.
Xyloidin, C6H9O7N.
Xyloquiuol, C8H10Oi,.
Xyloquinone, C8HSO2.
Xyloretin, C10H16O.
Xylyl alcohol, C8H10O.
Zeorin, C13H2aO.
HARRISON AKD SUNS, PRINTERS IN ORDINARY TO HER MAJESTY, ST. MARTIN'S LANE, LONDOX.
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