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
C 3 H 6 O.HF
C 3 H 7 FO
55
....
Landolf
C. R, 96, 580
44, 655
dihydrofluoride
C 3 H 6 O.2HF
C 3 H 3 F 2
15 to 12
)i
)
JJ
Difluobenzoic acid
C 6 H 3 F a .COOH
C 7 H 4 F 2 2
232 u. c.
Jackson & Harts-
B., 18, 1993
48, 1224
horn
Benzoyl fluoride .
C 6 H 5 .CO.F
C 7 H 5 FO
161-5 (745)
Borodine
A., 126, 60
ii., 671
Fluobenzoic acid
C 6 H 4 F.COOH=1.2
C 7 H 5 F0 2
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
C 6 H 4 F.COOMe=1.3
C 8 H 7 FO 2
192-194
Liquid
Patern&
G. I., 11, 90
40, 598
)
192-194
Liquid
Paternd & Oliveri
G. I. [1882], 85
42,614
Fluotoluic acid
C 6 H 3 .Me.F.COOH= ?
....
160-161
,,
)1
,
Fluoanisic acid
C 6 H 6 .OMe.F.COOH=l.?.4
C 3 H 7 F0 3
204
,,
I
42, 615
Ethylic fluobenzoate
C 6 H 4 F.COOEt=1.4
C 9 H 9 FO 2
cf. G.I. 11,90
Cryst.
Schmitt & Gehren
J. p. [2], 1, 400
vii., 164
(2.) CHClBr and CHC1I.
1
Chlorobromoform
....
CHClBr 3
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
C 2 HClBr 2
141-142 (734
L 20
Denzel
B., 11, 1741
36, 213
a-Chlortetrabromethane
CHBr 2 .CBr 2 Cl
C 2 HClBr 4
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
C 2 HCloBr 3
215-220
L 20
),
B., 11, 1740
36, 213
Trichlordibromethane
....
C 2 HCl 3 Br 2
200 (760) p.d
....
Patern6
G. I., 1, 590
vii., 308
,,
....
93-95 (14)
jy
j,
a-Chlorbromethylene
CHj : CClBr
C 2 H 2 ClBr
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
?
....
(C 2 H s ClBr).
140
Solid
Demole and Diirr
B., 11, 1304
34, 846
a-Chlortribromethane
CH 2 Br.CBr 2 Cl
C 2 H 2 ClBr 3
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
CH 2 Br.CBrCl s
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
CCl 3 .CH 2 Br.
C 2 H 2 Cl 3 Br
151-153
Liquid
Henry
C. E., 98, 370
46, 978
a-Chlordibromethane
CH 3 .CClBr 2
0,,H. 1 ClBr 2
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
C s H 3 ClBr 2
162-5-163
1. 20
Denzel
B., 11, 1739
36, 213
o-Dichlorbromethane
CH 3 .CCl. 2 Br
CjHjCljBr
98-99 (758)
1. 20
B., 11, 1740
n
P-
CH,Br.CHCl 2 (?)
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 ...
CH 3 .CHClBr
C,H 4 ClBr
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
....
C 3 HClBr 2 (?)
a. 150
....
Pinner
B., 8, 1324
29, 554
Dichlorbromallylene
C 3 HCl 2 Br
143
....
B., 5, 205
26, 495
143
A., 179, 45
29, 549
Dichlortribrom propylene ....
C 3 HCl 2 Br 3
....
207
B
11
1
....
C 3 H 2 ClBr
100-110
n
B., 8, 1325
29, 554
Dichlordibrom propyleue ....
C 3 H 2 Cl 2 Br 2
190 p. d.
Kramer and Pinner
A., 158, 37
24, 558
Dichlorbrom propylene
a. C 3 HCl 2 Br
C 3 H 3 Cl 2 Br
143
Pinner
A., 179, 45
Dichlortribrom propane
Of. C 3 HCl 2 Br 3
C 3 H 3 Cl 2 Br 3
207
I!
Chlorbrom propylene
C 3 H 4 ClBr
105
....
A. 112, 237
.,,
CH,.CCi:CHBr
)>
100-110
Friedel
A. C. [4], 16, 343
vii., 1019
orCH 2 :CCl.CH 2 Br.
a-Bromallyl chloride
CH 2 : CBr.CHjCl
120
Liquid
Henry
B., 5, 186, 482
vii., 50; 25,686
a-Chlorallyl bromide
CH 3 .CCl.CH,Br
II
121
C. E., 95, 849
44, 173
Chlorbromglycide
CHC1 : CH.CH 2 Br
JI
126
....
....
As., 6, 375
ii., 899
i)
136-127
Eeboul
As., 1, 230
vii., 1020
Chlortribrompropane
3 H 4 ClBr 3
238 p. d.
....
As., 1, 231
ii., 899
Allylenedichlordibromide ....
....
C 3 H 4 Cl 2 Br 2
190
....
....
J. [1872], 323 ;
A., 179, 44
Dichlordibrotnpropane
CH 2 Br.CClBr.CH 2 Cl
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
,,
CH 2 Cl.CBr 2 .CH 2 Cl
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
CH 3 .CClBr.CH 2 Br
C 3 H 5 ClBr 2
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
CH a .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
OH 2 Cl.CHBr CH 2 Br
.,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
C 3 H 5 Cl 2 Br
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
....
C i H D Cl 2 Br
abt. 176
J. [1857], 477
i., 894
;>
180-187
....
Simpson
P. E. S., 27, 118
38, 456
a-Chlorbrompropane
Me.CClBr.Me
C 3 H 6 ClBr
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.CH 2 .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.CH 2 Cl
j>
120
B., 7, 1037
vii., 1019
7- .
>
v
121
....
A. C. [5], 14, 453
36, 128
>-
Me.CHCl.CH 2 Br
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
-
CH a 01.CH 2 .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
?
C 5 H 8 Cl 2 Br 2
C 5 H Cl 2 Br 2 (?)
232-236
Pinner
B., 8, 1326
29, 554
Dichloramylene dibroruide ....
....
C s H 8 Cl 2 Br 2
230-240
A., 179, 37
Methylchlordibrompropyl-
CHMeBr.CClBr.CHMeCl
))
140-145 (31)
....
Thurnlackh
A., 223, 149
46, 1118
carbinyl chloride
Dichlortribrombenzene
Cl s .Br 3 =1.3.2.4.6
C 6 HCl 2 Br 3
....
121
Langer
B., 15, 1332
Trichlordibrombeuzene
Br a .Cl,=
C 6 HCl 3 Br 2
149
M
B., 15, 1330
42, 1058
,,
=
J
....
119
....
A., 215, 119
Chlortribrombenezene
Br 3 .Cl=1.3.5.6
C 6 H 2 ClBr 3
....
80
Silberstein
J. p., 27, 116
44, 661
5
)J
....
82
Langer
B., 15, 1065
42, 954
Chlorbrombenzene
Cl.Br=1.4
C 6 H 4 ClBr
196-3(756-12)
67-4
Kbrner
G. I., 4, 305
29, 215
=1-3
JJ
196
....
j
29, 220
Chlordiallyltetrabromide ....
C 6 H 9 ClBr 4
....
Liquid
Henry
C. E., 87, 171
36,34
Chlorhexylene dibromide ....
....
C 6 H u ClBr 2
218-220
....
Destrem
B., 16, 229
Chlorbenzyl bromide
C 6 H 4 .Cl.(CH s Br)=1.4
C 7 H 6 ClBr
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.C 3 H 4 Br 2 Cl
C 9 H 9 ClBr 2
96-5
Grimaux
C. E., 76, 1598
26, 1139
o-Trichlordibromnaphthalene
C 10 H 3 Cl 3 Br.,
....
166
....
iv., 13
a-Dichlordibromnaphthalene
....
C 10 H 4 Cl 2 Br 2
170
....
0-
....
M
....
166
....
Dichlorbromnaphthalene ....
....
C 10 H 5 Cl 2 Br
80
Beilstein
Org. Chem. 1205
iv., 11
Chlordibromnaphthalene
CioHsdsBrj
....
150
5J
Org. Chem. 1206
iv., 10
tetrachloride
Chlorbromnaphthalene
a l> "2
C 10 H 6 aBr
....
115
....
B. S., 26, 540
Ohlorbromnaphthalene tetra-
C 10 H 6 ClBr 5
110
Beilstein
Org. Chem. 1205
bromide
Dichlornaphthalene tetrabro-
C 10 H 6 Cl 2 Br 4
....
a. 100+
j)
Org. Chem. 1206
iv., 10
mide
Dibromnaplithalene tetra-
....
C-ioH 6 Cl 4 Br 2
....
abt. 155
>
)1
cliloride
Bromnaphthalene dichloride
....
C 10 H 7 CI 2 Br
165
Gerhardt
....
iv., 8
Trichlorbromisocymene
Me.PrJS.Cl 3 .Br.=1.3.(?) 4
C 10 HioCl 3 Br
65
Kelbe
B., 16, 619
Dichlordibromanthracene ...
....
C 14 H 6 Cl 2 Br 2
251-252
Schwarzer
B., 10, 377
32,493
Diclilorbromanthracene
....
C 14 H 7 Cl 2 Br
168
)J
Di(bromphenyl )dichlorethy-
CCl 2 :C(C c H 4 Br).,
C 14 H 8 Cl. 2 Br 2
119-120
Zeidler
B., 7, 1180
28, 148
lene
Dichloranthracene tetrabro-
....
C 14 H 8 Cl 2 Br 4
166
Schwarzer
B., 10, 376
38, 493
mide
Di(bromphenyl)-trichlor-
CCl 3 .CH(C 6 H 4 Br) !i
C lt 'EL t ClJBt t
139-141
Zeidler
B., 7, 1180
28, 148
ethane
Di(bromtolyl)trichlorethane
C01 3 .CH(C 6 H. i BrMe) 2
C 16 H 1 .,Cl 3 Br 2
148
Fischer
B., 7, 1192
28, 154
a-Tetrachlortribromdinaph-
C 10 H 4 Cl 2 Br 2 .C 10 H 5 C] 2 Br
C 20 H 9 Cl 4 Br 3
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
CHC1 3 I
131
Liquid
....
A., 22, 229; 126,
i., 913
239
Methylene chloriodide
....
CH 2 C1I
109-109-5
Liquid
Sakurai
47, 198
(760-4)
jj jj
....
JJ
129
jj
41, 362
Chloriodoethyleue
CH 3 :ccn
C 2 H 2 C1I
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
C 2 H 3 C1 2 I
171-172 s. d.
Liquid
C. R, 98, 518
46, 719
(774)
Ethylidene chloricxlide
CH 3 .CHC1I
C 2 H 4 C1I
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
C 3 H 4 C1I
150 (760)
Eomburgh
R. T., 1, 233
44, 449
jj
JJ
92-95 (40)
B., 16, 393
0-
CHOI : CH.CH 2 I
JJ
162 p. d.
i
B., 16, 392
(760-4)
Dichloriodopropane
....
C 3 H 5 C1 2 I
SOS
Liquid
Henry
B., 4, 702
24,907;vii.,320
j
JJ
205-210
Simpson
P. R S., 13, 540
vi., 92
Ohloriodopropane
CH 3 .Cai.CH 3
C 3 H 6 C1I
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,H 4 .C1.I=1.2
C 6 H 4 C1I
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
C 7 H 6 C1I
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)
CC1 3 .COH
C 2 HC1 3 O
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
CHC1 2 .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
CH 2 C1.CO.C1
C 2 H 2 C1 2
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
CHC1 2 .COH
89-90
Paterud
G. S. P., 5, 123
vi., 76
,, .... ....
88-90
....
Paternd and Pisati
G. I., 1, 461
24, 1190
Paradichloracetaldehyde
....
(C S H,CLO).
....
129-130
Jacobsen
B., 8, 87
28, 631
Metadichloracetaldehyde ....
....
n.f. 200
Friedrich
A., 206, 253
40, 407
Dichloracetic acid
CHC1 2 .COOH
CjHjCljO,
189-191
s.
Wallach
B., 9, 1212
31, 59
195
Manmene
J., 17, 316
vi., 19
Chlorethylene oxide
CHC1.CH 2 .0
C 2 H 3 C10
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)
(CH 2 Cl.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.CH 2 C1
C 2 H a C10 s
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
CH 2 C1.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
C 2 H 3 C1,0
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
CC1 3 .CH(OH) 2
C 3 H,C1,0 2
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
CC1 3 .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.H 4 (a 2 o
105
Eegnault
A. C. [2], 71, 398
Dicliloracetaldehyde hydrate
CHCL.CH(OH) 2
C 2 H 4 Clj0 2
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
CH 2 C1.O.CH 3
C S H 5 C10
79-5 (759)
....
Friedel
C. E., 84, 247
32, 424
Ethyleue hydroxychloride ....
CH 2 C1.CH 2 .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
CH 3 .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
....
C 2 H 7 C1O
2
Liquid
Friedel
C. E., 81, 152
28, 1245
|3-Dichloracrylic chloride
cci 2 :cH.coci
CjHCljO
a. 145
....
Wallach & Hunaiis
B., 10, 569
32, 591
Trichloracetyl carboxylic acid
CC1 3 .CO.COOH
C 3 HC1 3 3
89
Hofferichter
J. p. [2], 20, 195
38, 35
Pentachloracetone
CHC1 2 .CO.CC1 3
C 3 HC1 6 O
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
+4H 2 ....
....
....
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+4H 2 O ....
....
C 3 H 2 C1 4 O
....
35
Bouis
A. C. [3], 21, 111
i., 30
>
JJ
177-180
38-39
Bischoff
B., 8, 1342
29, 559
Hexachloracetone hydrate ....
CO(CC1 3 ) 2 .H 3 O
C 3 H 2 C1 6 2
15
A., 122, 120
a-Chloracrylic acid
CH 2 :CC1.COOH
C 3 H 3 C10 2
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
C 3 H 3 C10 4
....
133
Conrad & Guthzeit
B., 15, 605
42,946
a-Dichlorpropionyl chloride....
CH 3 .CC1 2 .COC1
C 3 H 3 C1 3 O
105-115
Beckurts and Otto
B., 11, 388
34, 488
Trichloracetone
CH 3 .CO.CC1 3
))
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
+2H 2 ....
)>
....
43
u
B., 8, 1338
+2H 2 ....
n
44
Kramer
B., 7, 257
27, 676
Trichlormethylic acetate
CH 3 .COO.CC1 3 (?)
C 3 H 3 C1 3 2
145 d.
Laurent
A. C. [2], 73, 25
i., 23
Methylic trichloracetate
CCl 3 .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
CC1 3 .CH(OH).COOH
C 3 H 3 C1 3 3
105-110
Bischoff and Pinner
B., 5, 208
25, 485
>i it
)1
f}
105-110
A., 179, 79
29, 555
Isotriclilorglyceric acid
CC1 3 .C(OH) 2 .COOH
C ;1 H 3 C1A
102
Claisen & Antweiler
B., 13, 1938
40, 154
Dichlorvinyl methyl oxide ...
a-Chlorpropionyl chloride ...
CC1 S : CH.O.CH 3
CH 3 .CHCI.CO.C1
C 3 H 4 C1 2
109-110
109-110 (744)
Liquid
Denaro
Henry
G. I., 14, 117
C. E., 100, 114
46, 1283
48, 372
ft-
ft.
CH 2 C1.CH 2 .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
CH 3 .CO.CHC1 2
C 3 H 4 C1 2
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.C 2 H 4 C1
C 3 H 4 C1 2 2
150-160
Liquid
Nemirowsky
J. p. [2], 31, 173
48, 741
Methylic dichloracetate
CHClj.CO.OCH 3
11
143-144
....
Wallach
A., 173, 299
28, 351
11
J)
11
144
....
Henry
C. E., 101, 250
48, 1122
Dichlormethylic acetate
CH 3 .CO.OCHC1 2
))
145-148 p. d.
Malaguti
A. C. [2], 70, 379
i., 23
a-Dichlorpropionic acid
CH 3 .CC1 2 .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-
CH 2 a.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
CHC1 2 .CH(OH).COOH
C 3 H 4 C1 2 O 3
219-231
75-78
Grimauz and Adam
B., 10, 903
29, 65
11
)
n
....
76-5-77
....
B. S., 34, 29
CH 3 .CO.CH 2 C1
C 3 H 6 C10
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
CH 2 a.CH.CH 2 .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
CH 2 C1.CH.CH 2 .O
Q,H 5 C1O
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
CH 2 :CC1.CH 2 .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 ....
CH 2 C1.CH S .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
C 3 H 5 C1O 2
94
....
Dumas
A. C. [2], 54, 230
i., 916
Chlormethylic acetate
CH 3 .COO.CH 2 C1
115-116
Henry
B., 6, 740
vii., 807;
26, 1117
Methylic chloracetate
CH 2 C1.COO.CH 3
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
CH 3 .CHC1.COOH
180-185
....
C. R., 1203, 1258
28, 443
a-
,,
186
L 18
Buchanan
Z. C. [2], 4, 523
vi., 960
ft' 11 >
CH 2 C1.CH 2 .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
CH 2 (OH).CHC1.COOH
C 3 H 5 C10 3
Liquid
Melikoff
B., 13, 273, 956
38, 627
"- ,,
,,
Liquid
B., 13, 2153
40, 154
ft- 11 II
CH 2 C1.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
CCl 3 .CHMe.OH
C 3 H 5 C1 3 O
150-160
49-2
Thurnlackh
A., 210, 78
42,295
Propylphycite trichlorhydrin
....
)J
172-173
Wolff
Z. C., 12, 465
Chloral methylate
CCl 3 .CH(OH)(OMe)
C 3 H 6 C1 3 2
98
50
Bartholdy & Martius
B., 3, 445
vii., 314
II ,) ....
106
50
Jacobsen
A., 157, 244
24, 257
Allyl alcohol dichloride
CH 2 C1.CHC1.CH 2 OH
C 3 H 6 C1 2
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
CH 2 C1.CH(OH).CH 2 C1
"
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
CH 2 01.CH(OH).CH.,C1
C 3 H B C1 2
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
CH 3 .CH(OH).CH 2 C1
C 3 H ; 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
)) >!
CH 2 (OH).CH 2 .CH. ! a
)>
160 c.
....
Eeboul
C. E., 79, 169
27, 1154
)
160-162
....
A. C. [5], 14, 491
36, 128, 133
a-Glycerol chlorhydrin
CH 2 C1.CH(OH).CH 2 (OH)
C 3 H-C10 2
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-
CH 2 (OH).CHC1.CH 2 (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
....
C 4 HC1 7 O 2
....
b. 100
Leblanc
i., 22
Maleyl chloride
C 2 H 2 (CO.C1) 2
C 4 H 2 C1 2 O 2
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
....
C 4 H 2 C1 2 3
....
125
Schmeltz& Beilstein
As., 3, 280
iv., 764
,, ....
....
JJ
125
Bennett and Hill
B., 12, 656
Trichlorerotonyl chloride ....
CC1 3 .CH:CH.COC1
C 4 H 2 CI 4 O
162-166
Liquid
Judson
Z. C. [2], 7, 40
vii., 398; 24,
233
?
....
)!
196
Paternd
G. S. P., 5, 123
vi., 77
Tetrachlorethyl oxide
(C 2 HC1 4 ) 2
0^,0,0
189-7 (857-5)
Pa tern 6 and Pisati
G. I., 2, 333
26, 158
Chlorsuccinic anhydride
CH 2 .CHC1.CO.O.CO
C 4 H 3 C10,
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
4 H 3 C10 4
abt. 190 d.
178
Bandrowski
B., 15, 2695
44, 313
J)
....
191
Kander
J. p. [2], 31, 1
48, 652
Chloromaleic acid
C 2 HC1(COOH) 2
))
....
171-172
Carius
B., 3, 334
vi., 798
Trichlorcrotonic aldehyde .. .
CC1 3 .CH : CH.COH
C 4 H S C1 3
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
CC1 3 .CH:CH.COOH
C 4 H 3 C1A
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.CH 2 .COO.CH.CC1 3 (?)
C 4 H 3 C1 3 S '
....
41-42
....
A., 193 ; 36
n-y-dichlorcrotonaldehyde ....
CH 2 C1.CH : CC1.CHO
C 4 H 4 C1 2
86-87
s. in C0 2 and
Natterer
M. C., 4, 539
44,965
snow
a-Chlorcrotonyl chloride ....
CH 3 .CC1 : CH.COC1 or
>
142
Liquid
Sarnow
B., 4, 731
24, 1047
CH 3 .CH : CC1.COC1
3 A
362
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Billing
Point.
Melting
Point.
Authority.
Reference.
'Watts' Diet.
& J. Ch. Soc.
Tetrolyl chloride
C 4 H 4 CLO
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
C 4 H 4 Cl 2 Oj
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 ..
....
C 4 H 4 C1 4
....
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 ...
3 H 4 C1 3 .COC1
162-166
Judson
B., 3, 787
Tetrachlorethylic acetate ...
CH 3 .COO.CHC1.CC1 3
C 4 H 4 C1 4 O 2
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
(\H 3 C1 4 .COOH
140
Pelouze and Gelis
A. C. [3], 10, 449
i., 694
Hexachlorethyl oxide
CHC! 2 .CH 2 .O.CC1,,CH 2 C1 or
c 4 H 4 a 6 o
250
....
Paterno
G. S. P., 5, 123
vi., 77
.
CHC12.CHC1.O.CHC1.CHC12
ii
....
-
250
....
Z. C. [1869], 394
a-Crotouic chloride
CH 3 .CH:CH.CO.C1
C 4 H 5 C10
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. CH 2 :CMe.COOH
C 4 H 6 C10 2
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
CH a : CC1.CH 2 .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
CH 3 .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
CH 3 .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
C 4 H 6 C10 3
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.CH 2 .COOH
CH 3 .COO.CHC1.CHCL
C 2 H 5 .CC1 2 .COC1
C 4 H 6 C10 4
C 4 H 5 C1 3 2
C 4 H 5 C1 3
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 ....
)
CC1 8 .CH 2 .CH 2 .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
CH 2 C1.CHC1.CHC1.CHO
CCl 3 .COOEt
CH 3 .COO.CH 2 .CC1 3
C 4 H"ci 3 2
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....
CH 3 .COO.CHC1.CHC1 2
fr. (CH 3 ) 2 .CH.COOH
fr. CH 3 .CH 2 .CH 2 .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-
CC1 3 .CH:CH.CH(OH) 2
C 4 H 5 C1 3 2
....
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 ...
CC1 3 .CH 2 .O.CH 2 .COOH
C 4 H 5 C1 3 3
....
69-5
Thurnlackh
A., 210, 72
42, 295
Pentachlorethyl oxide
CC1 3 .CC1 2 .O.C 2 H 5
C 4 H 5 C1 5
190-210 p.d.
Liquid
Busch
B., 11, 446
34, 487
i ji
)J
*
Liquid
Jacobsen
B., 4, 217
24, 515
1>
CC1 3 .CHC1.O.CH 2 .CH 2 C1
JJ
235
....
Henry
B., 7, 763
27, 979
Dichlorbutyric aldehyde
C 3 H 5 C1 2 .COH
C 4 H 6 CLO
200
....
i., 689
GH 2 Cl.CH 2 .Cn 2 COH
JJ
225-230
Saytzeff
A., 171, 251
27, 570
d-Chlorbutyryl chloride
CH 3 .CH 2 .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
CH 3 .COO.C 2 H 3 C1 2
c 4 H e ci 2 o 2
110
Malaguti
A. C. [2], 70, 368
....
)1 J5 ""
JJ
JJ
125
....
Curie and Millet
C. B., 83, 745
31, 188
>J )
CH 3 .COO.CHC1.CH 2 C1
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 ....
CH 2 C1.COO.CH,.CH 2 C1
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
CHCl 2 .CMe(OH).COOH
C 4 H 6 C1A
82-83
Bischoff
B., 8, 1334
29, 558
acid
(CH 2 C1),,C(OH),COOH
JJ
90-92
Grimaux and Adam
C. JJ., 90, 1252
38, 801
Tetrachlorethyloxide
CC1 3 .CHC1.0.C 2 H 5
C 4 H C1 4
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
C 4 H 7 C1O
122-123
....
Geuther
Z. C. [2], 7, 128
24, 515 ; vii., 8
Ethylidene acetochloride ....
CH 3 .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 CaCl 2
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
CH 3 .CH 2 .CH 2 .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
C 3 H 6 C1.COH
JJ
141
i., 689
3- 11
CH 3 .CHC1.CH 2 .COH
JJ
....
96-97
Kekul6
Z. C. [2], 5, 57i
vi., 513, 25, 616
A., 162, 100
Ethylene chloracetin
CH 2 Cl.CH 2 .OAc
C 4 H 7 C10 2
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
C 4 H 7 C1O 2
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
CH 3 .COO.CHC1.CH 3
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...
CH 3 .CHCl.COOMe
130-131
A., 208, 342
)
j
ISM
....
Kahlbaum
B., 12, 344
36, 521
' ft- n
CH 2 Cl.CH 2 .COOMe
)>
155-157
....
Henry
C. R, 100, 114
48, 372
a-Chlorisobutyric acid
(CH 3 ) 2 .CCl"cOOH
j>
abt. 190
B. S., 25, 23
30, 397
7
ji
C 3 H 6 C1.COOH
230-235 p. d
106-107
Melikoff
B., S., 41, 311
40, 1301
/3-Chlorbutyric acid
CH 3 .CHC1.CH 2 .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
CH 2 Cl.CH(OH).COOMe
C 4 H 7 C10 3
185-187
....
Frank
A., 206, 347
40, 417
Chlorhydroxybutyric acid ...
C 3 H 5 C1(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
}
CH 3 .C 2 H 2 C1(OH).COOH
....
85
))
J)
)
M "
....
)
m. p. error
98-99
Jt
B., 15, 2586
44, 311
for 82-83
Acetone chloroform
CMe 2 .CCl 3 .OH
C 4 H.C1 3
167 u. c.
96-97
Willgerodt
B., 14, 2456
42, 492
)
JJ
)>
cf. B 15,2305
96
B., 16, 1585
44, 1079
+|H 2 O
)
))
80-81
D
Trichlorbutyl alcohol
C 3 H 4 C1 3 .CH 2 OH
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
CCl 3 .CH(OH)(OEt)
C 4 H 7 C1 3 2
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
C 3 H 4 C1 3 .CH(OH) 2
)
v.t. 100 (860)
....
Cngel & Moitessier
U. E., 90, 1075
40, 407
Dichlorethyl oxide
(CH 3 .CHC1) 2 O
C 4 H 8 C1 2 O
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
)?
CH 2 C1.CHC1.O.C 2 H 6
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
C 4 H r Cl(OH)Cl
43-5-(764)
jiquid
Ecominedes
G E., 92, 1235
40, 793
Erythrol dichlorhydrin
C 4 H 6 C1 2 (OH) 2
C 4 H 8 C1 2 2
....
45?
)e Luynes
A. C. [4], 2, 385
vi., 583
n
CH 2 C1.[CH(OH)] 2 .CH 2 C1
....
25-125-5
rzybytek
B., 17, 1092
46, 979
)> H
5)
....
24-125
M*l
J. E., 13, 171
Chloraldehyde hydrate
(CH 2 C1.CHO) 2 +H 2 O
C 4 H 8 C1 2 3
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,
C 4 H 9 C1O
7-98
....
acobsen
B., 4, 215
vii., 481 ; 24,
513
05
jiquid
lenry
C. E., 100, 1007
48, 883
,.
CH 2 C1.CH 2 .O.C 2 H 5
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
(CH 3 ) 2 .CC1.CH 2 .OH
C 4 H 9 C1O
128-130
.<>
Henry
B. S., 25, 23
30, 397
11 II
))
1)
137
....
Butlerow
A., 144, 26
vi., 376
Chloraldehyde alcoholate ..
CH 2 Cl.CH(OHXOEt)
C 4 H 9 C10 2
95-96
....
Jacobsen
B., 4., 216
vii., 481 ; 21,
514
ii 11
*1
93-95
....
A., 164, 219
Hydroxychlorethyl oxide ..
CH 3 Cl.OH(OH)OEt
))
151-152
Abeljanz
A., 164, 197
26, 156 ; vii.,
482
Butenylglyceryl chlorhydrin
C 4 H 7 C1(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..
....
C 4 H 10 C1 2 2
25 (40)
....
Hanriot
C. R, 92, 302
40, 404
Chloralide
CC1 3 .CH.O.CO.O.CH.CC1 3
C 5 H 2 C1 6 3
....
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
C 4 H 3 O.COC1
C 5 H 3 C10 2
170
...
Lies-Bodart
....
iv., 765
)J
160-180
Liquid
Wallach
B., 14, 753
40, 715
Chlorpyromecenic acid
C 5 H 2 C10.0H+H 2
MM
174
Hilacbein
J. p. [2], 32, 129
48, 1208
Chlorcitraconic anhydride ...
....
C 5 H 3 CI0 3
212
98-100
....
J., 1873, 583
11 ii
>1
....
100
Gottlieb
J. p. [2], 8, 73
27, 358
Trichlorphenomalonic acid ...
CC1 3 .CO.CH : CH.COOH
C 5 H 3 C1A
131-132
Kekule & Stfecker
A., 223, 181
46, 1122
)J
))
....
131-132
Carius
A., 140, 317; 142,
129
)>
C 6 H 3 C1 3 2 (?
Krafft
B., 10, 798
Mesaconyl chloride
C 3 H 4 (COC1) 3
C d H 4 Cl 2 2
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 ....
CCl 3 .CH.O.CHMe.COO (?)
C 5 H 5 C1 3 3
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.C 5 H 7 Cl 3 O 3
140
n
A., 179, 99
29, 556
Acetyl trichlorlactic acid ....
Ca 3 .CH(OAc).COOH
C 5 H 5 C1 3 4
....
65
Pinner and Fuchs
B. 10, 1061
Pentinic chloride
....
C 5 H 6 C1 2
189-191
....
Demarjay
B. S. [2], 33, 575
40, 255
11 ii
)
189-192
....
11
C. R, 88, 126
36, 458
Ethylic #-dichloracrylate ....
OC1 2 : CH.COOEt
C 5 H 6 C1 2 3
173-175
Liquid
Wallach & Hunaus
B., 10, 569
32, 591
Glutaryl chloride
COC1.(CH 2 ) 3 .COC1
M
216-218
Liquid
Eeboul
C. R, 82, 1502 ;
30, 508; 36,
A. C. [5], 14, 501
134
Pyrotartryl chloride
COC!.CH 2 .CHMe.COCl
H
190-195
Liquid
Hjelt
B., 16, 2624
46, 297
Allyl tetrachlorethyloxide ...
CC1 3 .CHC1.OC 3 H 5
C 5 H 6 C1 4
195d.
....
Oglialoro
G. I, 1874, 463
28, 878
Tetrachlorvaleric acid
C 4 H 5 C1 4 .COOH
C 5 H 6 C1 4 2
b.-15
Dumas and Stas
A., 35, 145
v., 978
a-chlorallylic acetate
CH 2 :CCl.CH 2 .OAc
C 5 H 7 C10,
140-145
Henry
B., 5, 454
a- ,, 11
145
ii
C. E., 95, 849
44, 173
- 11 ii
CHCi:CH.CH 2 .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 ...
CH 3 .CH : CCl.COOMe
60-8
....
Kahlbaum
B., 12, 344
36, 521
j3-chlor-/3-crotonate
CH 2 :CCl.CH 2 .COOMe
))
42 c.
jiquid
Frohlich
Z. C. [2], 5, 274
vi., 512
Chlormethylcrotonic acid ...
r. CH 3 .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
CH 3 .CCi: CMe.COOH
V
....
9-5
Friedrich
B., 15, 218
12, 945
Chlorangelic acid
Me.CCl : CH.CH 2 .COOH
03-104
Pinner and Klein
B., 11, 1499
36, 43
Ethylic malonyl chloride ..
COCl.CH 2 .COOEt
C 6 H 7 C10 3
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 ...
...
C 5 H 7 C10<
....
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
....
C 6 H 7 C10 S
....
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
CCl 3 .CO.Pr
C 5 H-C1 3 O
186 (753)
....
Grabowsky
B., 8, 1439
29, 557
Methyl trichlorpropy 1 ketone
CH 3 .CHC1.CC1 2 .CO.CH 3
>
192
....
Thurnlackh
A., 223, 149
46, 1118
Trichlorhydroxy ethyl allyl
CC1 3 .CH(OH).OC 3 H 5
C^CIA
116
20-5
Oglialoro
G. I. [1874], 463
28, 878
oxide
Propylic trichloracetate
CCl 3 .COOPr
))
187
Clermont
C. R, 96, 437
44, 729
Trichlorvaleric acid ....
C 4 H 6 Clj.COOH
))
....
b. 18
Dumas and Stas
A., 35, 145
v., 978
Ethylic trichlorlactate
CCl 3 .CH(OH).COOEt
C 5 H 7 C1 3 3
66-67
Bischoff and Pinner
B., 5, 218; A.,
25, 485 ; 29,
179, 83
555
Trichlorvalerolactic acid
CH 2 C1.(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
C 3 H 6 .Cl 2 (OAc)
C 5 H 8 C1A
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....
CH 3 .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-
CH 2 Cl.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-
CH 2 C1.CH 2 .COO.C 2 H 4 C1
))
210-215
Liquid
Henry
C. R., 100, 114
48, 372
pionate
Ethylic dichlorlactate
....
C 6 H 8 CI S 3
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
CH 2 : CCl.CH 2 .OEt
C 6 H 9 C1O
110
Friedel and Silva
C. R., 75, 81
26, 805
11 11 11
H
11
110
....
Henry
vii., 1020
"" 11 11 11
CHC1 : CH.CH 2 .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 ....
CH 3 .CH : CCl.CHMe.OH
))
158
Liquid
Thurnlackh
A., 223, 149
46, 1118
Acrolein+ethyl chloride ....
CH 2 : CH.CClEt.OH
))
115-120
....
As., 3, 182
Isovaleryl chloride
(CH 3 ) 2 .CH.CH 2 .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
CMe 3 .COCl
j
105-106
Liquid
Butlerow
A., 173,373; B.,
27, 1084; 28,
7,728
250
Chlorvaleric aldehyde
CHMe 2 .CHCl.CHO
)i
134- 135
....
Schroader
B., 4, 402
24, 560; vii.,
-
1195
Chlorruethylisopropyl ketone
CH 2 Cl.CO.CHMe 2
jj
120 p. d.
Etard
C. R., 84, 951
32, 427
Methylchlorpropyl ketone ....
CH,.CO.CHC1.C.,H 5
))
130
....
Wislicenus and
B., 8, 1038
29, 371
Conrad
n n
jj
130
Liquid
Conrad
A., 186, 242
32, 436
Ethylidene propioehlorhydrin
Propylene acetochloride
CH 3 .CHC1.(O.C 8 H 5 0)
CH 3 .CH(OAe).CH,Cl
C 5 H 9 C1O 3
"(1)
135 u. c.
151 c.
Kiibenchamp
Morley and Green
A., 225, 267
47, 132
48, 136
Isobutylic chlorocarbonate ....
Cl.COO.CH,,CHMe 2
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
CH 2 Cl.COOPr
n
161 (740)
....
....
A., 197, 8
11 11
Ethylic a-chlorpropionate ....
J)
CH 3 .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 ....
CH 3 CHCl.COOEt
C 5 H 9 C10 3
150
....
Wurtz
A., 107, 193,
iv., 736
-0-
CH 2 Cl.CH,.COOEt
)
150-160
....
vi., 960
,, -0- 11
))
162-163(765)
Henry
C. R, 100,114
48, 372
Glycerol aceto-ehlorhydrin ....
CH 2 (OAc).CHCl.CH 2 .OH
C 5 H 9 C1O 3
230
11
J. p. [2], 10 > 185,
28, 346
11 11
1?
aht. 250
....
i., 25
Ethylic /3-chlorIactate
CH 2 Cl.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
C 5 H 9 CI 3 O
123 (41)
50-5
Thurnlackh
A., 223, 149
46, 1118
Allylethyl clichlorhydrin ....
....
q,H 10 01 2
165
Markownikoff
J. [1865], 492
vi.. 99
/3-dichlorpropionic aldehyde
CILCl.CH01.eH(OH)(OEt)
C5H 10 C1 2 O 2
150-155
As., 3, 192
alcoholate
Amylene chlorhydrin
....
C 5 H,,C10
155
....
Carius
A., 126, 19
vi., 121
Dariv. of chlorinated ether....
^)
117-118
Liebeu and Bauer
J., 15, 394
Methylethyl chloracetal
C.;H 3 Cl(OEt)(OMe)
C 5 H n C10 2
abt. 137
Lieben
J., 20, 546.
vi., 598
Glycerol ethoxychlorhydrin
C 3 H 5 Cl(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
....
C 5 H H C10 3
225-230
Liquid
Conrad & Guthzeit
B., 17, 2287
48,43
Trichlorquinone
C 6 HC1 3 2
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
C 6 C1 6 .OH
C 6 HC1 6 O
....
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,a 4 (oa)(OH) =1.3
C 6 HC1 5 2
92-5
Steuhouse
P. B. S., 20, 78
26, 298 ; vii.,
1042
?
....
65
....
A., 160, 265
Pentachlorphenol dichloride
c 6 ci 6 (OH) : ci 2
c 6 na r o
....
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
C 6 H 2 C1 2 2
....
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
4 H 2 O(COC1) 2
C 6 H 2 C1 2 3
sb. 100
80
Klinkhardt
J. p. [2], 25, 46
42, 498
Dichlorcomanic acid
C 5 HC1A.COOH
C 6 H 2 C1 2 4
217
Ost
J. p., 27, 293
44, 796
11 11
}
)
217
11
J. p., 29, 57
48, 49
Trichloroehloroxybenzene ....
C 6 H 2 C1 3 .OC1
C 6 H 2 01 4
....
119
Benedikt
M. C., 4, 233
44,985
Tetrachlorquinol
C,C1 4 .(OH), =6.5.3.2. 4.1
C 6 H,,C1 4 2
a. 220
....
iii., 216
Chlorquinone ...
C 6 H,C1 : 0, = i
CH,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
C H 3 C10 4
....
247
Ost
J. p. [2], 29, 57
48, 49
Trichlorphenol
OH.Cl a 1
C 6 H 3 C1 3
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.C1 3 =1.2.4.6
C 6 H 3 C1 3
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 .C1 3 =1.3.4 (?) s
C 6 H 3 C1 3 2
....
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 .C1 3 =1.2.3. 4.5.6
C 6 H 3 C1 3 3
177 d.
Webster
45, 206
i, -i-3H 3 O
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.C1 2 =1.2.4
c 6 H 4 ca 2 o
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
C 6 H 4 C1 2 2
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
C 6 H 4 C1 2 4
w.m. 260 p.d.
Bell
B., 12, 1272
36, 917
Malic chloranilide chloride....
C 6 H 4 C1 4 4
a. 200
....
A., 193, 44
Chlorphenol
OH.C1=1.2
C 6 H 5 C10
....
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
C 6 H 5 C1O
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
C 6 H 5 C10 2
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.
C 6 H 5 C1 3 6
215
150
137-138
St. Evre
Wallach
J., 1, 529
B., 9, 1215
31,60
?
Tritetrachloracetone + 6H 2 O
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(CC1 3 ).O
))
Me.CCl 2 .CO.O.CO.CO.Me
C 3 H 5 .COO.CHC1.CH 3
C 2 HCl(COOMe) 2
CC1 3 .CH : CH.COOEt
CCl 3 .CH(OAc) 2
CH3.CC3j.COO.C3H5
c 6 H 8 o 2 .ci 2
OH 3 .CO.CCl 2 .COOEt
C 2 H 2 (OCl) 2 (OAc) 2
COOH.CClMe.CClMe.COOH
CCl 2 :C(OEt)(OC 2 H 3 Cl,,)
C 3 H 4 C1 3 .COO.CHC1.CH 3
fr. CH 2 :CMe.COOEt
CH 2 :CCl.CH 2 .COOEt
ii
fr. CH 2 :CH.CH 2 .COOEt
fr.CHj.CH: CH.COOEt
CH,Cl.CH:CH.CH 2 .OAc
C^CIA
C 6 H 5 C1 7 2
11
C 6 H 6 C1 2 O 4
C 6 H 6 C1 4 3
C 6 H 7 C10 2
C 6 H 7 C10 4
C 6 H 7 C1 3
C 6 H 7 C1 3 O 2
c 6 H 7 ci 3 o 4
C 6 H 7 C1 3 S
0^0,0
(W3A
)
C 6 H 8 C1 2 3
C 6 H S C1 2 4
})
C 6 H 8 C1 4 O 3
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
CH 2 :CCl.CMe 2 .COOH
C 6 H 9 C10 2
....
63-64
Demarcay
C. R., 84, 1087
32, 591
acid
Chlorethyl-crotonic acid
C,H 4 C1.C 3 H 4 .COOH
74-75
Ethylic acetochloracetate ...
CH 3 .CO.CHCl.COOEt
c 6 H 9 ao 3
193-195
Liquid
Allihn
B., 11, 569
34, 566
Trichlorcaproic aldehyde ...
C 6 H 3 C1 3 .CHO
C 6 H 9 C1 3
212-214
Liquid
Pinner
B., 10, 1053
32, 586
215-220
B., 8, 1321
29, 554
Isobutylic trichloracetate ...
CCl 3 .COO.CH 2 .CHMe 2
C 6 H 9 C1 3 2
187-189
....
Judson
B., 3, 784
vii., 10
Trichlorbutylic acetate
C 3 H 4 Cl 3 .CH 2 .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
C 6 H 8 C1 3 .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
CCl 3 .CH(OEt)(OAc)
C 6 H 9 C1 3 3
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
CCl 3 .CH(OEt)(OC 2 H 3 Cl 3 )
C 6 H 9 C1 5 2
186-189
Friedel
C. C. [1875], 514
30, 66
?- alcohol
(CH 2 ) 2 .CH(CH 2 C1).CC1.CH 2 .
C 6 H 10 C1 2
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.CH 2 .CHMe 2
C,H 10 C1 2 2
182-184
Wallach
A., 173, 300
28, 351
Metacrolein dihydrochloride
C 6 H 8 2 -2HC1
(?)
....
50
Geuther&Cartmell
i., 57
Ethylic dichlorhydroxyiso-
CHCl 2 .CMe(OH).COOEt
C 6 H 10 C1 2 3
208-215 p.d.
....
Bischoff
B., 8, 1336
29, 558
butyrate
(CH 2 C1) 2 : C(OH).COOEt
225-230
Liquid
Kelly
B., 11, 2223
36, 306
Chlorhexylene alcohol
C 6 H 10 C1.0H
c 6 H u ao
165-168
Liquid
Natterer
M. C., 5, 567
48, 498
,.
CH 2 C1.CH(OH).CH S .C 3 H 5 or
183-187
Liquid
Lopatkin
J. p. [2], 30, 389
48, 497
CH 2 Cl.CH(C 3 H 6 ).CHj.OH
185-187
Destrem
B., 16, 228
Allylethyl chlorcarbinol
C 3 H 6 .CClEt.OH
133-135
....
....
A., 162, 99
Capronyl chloride
CH 3 .(CH 2 ) 4 .COC1
136-140
..-.
A., 130, 364
Diemethylethylacetyl chlo-
CMe 2 Et.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
CH 2 C1.CH 2 (O.C 4 H 7 O)
C 6 H n ClO,
190
....
Simpson
A., 113, 119
ii., 571
Ethylidene
CH 3 .CHC1.(O.C 4 H,O)
149 u.c.
....
RUbencamp
A., 225, 267
48, 136
Isoamylic chlorocarbonate ....
Cl.COO.C 5 H n
154-3 c.
....
Rose
A., 205, 230
40, 252
Ethylic a-chlorbutyrate
CH 3 .CHj.CHCl.COOEt
156-160
Markownikoff
A., 153, 241
ft-
CH 3 .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 ....
Me 2 Ca.COOEt
148-5-149-5
Liquid
M
G. I., 8, 371
36, 615
c. (749)
Chloraldehyde ethylateacetate
CH 2 Cl.CH(OEt)(OAc)
C 6 HuClO 3
170
....
....
A., 134, 176
Dulcitol chlorhydrin
C 6 H 7 (OH) 4 C1
CA.CIO,
90
....
A. C. [4], 27, 178
Quereitol chlorhydrin
C 6 H 7 (OH) 4 C1
M
198-S02
Prunier
A. C. [5], 15, 54
36, 241
it
n
....
198-200
C. R., 86, 338
34,400
Trichloracetal
CCl 3 .CH(OEt) 2
C,H U C1 S 2
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?) ....
Ca 3 .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
....
C 6 H 12 C1 2 O
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 . ....
CHCl 2 .CH(OEt) 2
C 6 H,oCLO
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 ....
c 6 H 10 a 2 o 3
230-235
jr t Ji *
A. C. [3], 67, 303
Mannitol dichlorhydrin
C 6 H 8 C1 2 (OH) 4
C 6 H 12 C1 2 4
174 d.
Bouchardat
C. R., 75, 1187 ;
vii., 774 ; 26,
A. C. [4], 27, 174
161
Hexylene chlorhydrin
C,;H 12 CLOH
C 6 H 13 C10
Liquid
Domac
M. C., 2, 319
40, 1114
a-chlorhydrin
CHMe(OH).CHCl.CH 2 .Et
abt. 170
Liquid
Henry
C. R., 97, 261
46, 34
/3-
CHMeCl.CH(OH).CH 2 .Et
.,
170-171(761)
Liquid
Tetramethylethylene chlor-
CMe 2 a.CMe 2 .OH
....
55
Eltekoff
B., 16, 399
44, 567
hydrin
Ethylchlorbutyl oxide
Et.O.C 2 H 3 Cl.Et
ji
137
Lieben and Bauer
J., 15, 393
vi., 597
,,
JI
141
A., 123,133; 133,
288
Chloracetal
CH 2 Cl.CH(OEt) 2
C 6 H 13 C1O 2
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
C 2 H 4 Cl.O.C 2 H 4 .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
....
C 6 H 13 C10 3
222-223
A. C. [3], 67, 292
Diglycerol chlorhydrin
....
C 6 H 13 C10 4
270
A. C. [3], 67, 303
Trichlorbenzoyl chloride
C 6 H 2 C1 3 .COC1 =5.4.3.1
C 7 H 2 C1 4 O
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.C1 4 =1.2.3.4.6
C 7 H 2 C1 4 O 2
187
A., 152, 245
33
Chlormeeenic acid
HO.C 5 C10(COOH) 3
C 7 H 3 C10 6
+H 2
165 d.
Hilsebein
J. p. [2], 32, 129
48, 1202
Dichlorbenzoyl chloride
C 6 F 3 C1 2 .COC1 =4.3.1
c 7 H 3 a 3 o
242
Beilstein and Kiihl-
A., 152, 228
vi., 312
berg
=6.2.1
5)
244
Liquid
Schultz
A., 187, 273
32, 782
/3-Trichlorbenzaldehyde
C C H 2 C1 3 .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.C1 3 = 2
c 7 H 3 a 3 o 2
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
C 7 H 3 C1 6
193
Beilstein and Kiihl-
A., 152, 246
vi., 335
berg
Pentuchlororcin
....
C 7 H 3 C1 5 2
....
120-5
Stenhouse
P. R. S., 20, 72 ;
25, 297 ; vii.,
A., 163, 175 ;
878.
169, 265
Chlorbenzoyl chloride
C e H 4 Cl.COCl =1.4
C 7 H 4 C1 2 O
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
C 6 H 3 C1 2 .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
C 6 H 3 Cl 5 .CHO =5.3.1
C-H 4 C1 3 O
65-65-5
Gabriel
B., 15, 2001
Dichlorsalicylaldehyde
C 6 H 2 Clj.OH.CHO =(?) 2 .2.1
C 7 H 4 C1 2 3
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
C 7 H 4 C1 2 3
....
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 : O 2 = ?.C0 2 .1.2.5
JJ
....
157
Steuhouse & Groves
B., 13, 1306
Chlorbenzotrichloride
C 6 H 4 C1.CC1 3 ==1.4
c 7 H 4 a 4 o
240-260
Ml
Klepl
J. p., 28, 193
46,447
Tetrachlorcresol
CH 3 .OH.CI 4 = 1.3.2.4.5.6
150
Lallemand
J. [1856], 621
v., 795
Pentachlororcinhypochlorite
C 7 H 3 C1 !) O 2 .HC1O.
C 7 H 4 C1 6 3
....
140-5
Stenhouse
P. R, 20, 72
25, 297
A., 163, 181
vii., 878
Benzoyl chloride
c 6 H 5 .coci
C 7 H 6 C10
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
C 6 H 4 C1.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
r ackson and White
B., 11, 1043
34, 729
Chlorbenzoic acid
COOH.a = 1.2
C.H 5 C10 2
....
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
C 7 H 5 C1O 2
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
C 7 H 5 C10 3
....
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
Hubne r 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.C 5 H 2 C10(COOH) 2
c,H 5 ao 6
....
145 p.d.
Hilsebein
J. p. [2], 32, 129
48, 1203
Trichlorcresol
CH 3 .OH.C1 3 =1.3.(?) 3
C.H 5 C1 3
270
96
....
J., 1856, 620
Trichlororcinol
Me.(OH),.Cl 3 = ?
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 ....
C 6 H 4 .OH.CHC1 2 =1.2
C ; H 6 C1 2 O
82
Henry
Z. C. [2], 5, 371
vi., 507
Dichlorbenzyl alcohol
C 6 HjClj.CHO=1.4.6
)J
....
77
A., 147, 351
vi., 335
C 6 H2.Me.OH.a 2 =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
C 6 HCl,,Me.(OH) s
c 7 H 6 a 2 o 2
119-121
Southworth
A., 168, 274
27,62
-m- jj
JJ
)J
167-169
A., 168, 271
Trichlorvalerolactinic chloral-
....
C 7 H 6 C1 6 3
295-299
87-88
....
A., 193, 37
ide
Trichlorlactic-butyrchloralide
....
)>
106-107
....
A., 193, 47
Chlorbenzyl alcohol ....
C 6 H 4 .(CH,OH).C1=1.4
C 7 H 7 C1O
....
66
Beilstein and Kiihl-
A, 147, 344
vi., 335
berg
)>
n
....
70-5
Jackson and Field
A. C. J. [2], 88
40, 806
Chlormethoxybenzene
C 6 H 4 CI.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
C 6 H 3 Me.OH.Cl:=1.4.?
abt. 240
56
Biedermann
B., 6, 326
26, 898
Chlorterebilic acid
CMe 2 .O.CO.CCl : C.COOH
c 7 H 7 ao 4
200-203
Roser
A., 220, 254
46, 460
i i
Methylic malic chloralide ....
c 7 H 7 a,o 6
....
85
....
A., 193, 45
Oxyheptic dichloride
....
C 7 H 8 C1 S
21 d. (sic)
Demarcay
C. E., 86, 1138
34,662
Chlorterebic acid
....
C 7 H 8 C1O 4
....
168 d.
Frost
A., 226, 363
48, 393
jj jj
....
)>
....
160-170
Eoser
B., 15, 296
CMe 2 .COO.CH 2 .CCl.COOH
JJ
189-5-190
Williams
B., 6, 1097
27,72
i i
,, ,, ....
jj
JJ
191
Eoser
B., 15, 296
Acetchloral allylate
CCl 3 .CH(OAc).O.C 3 H 6
C 7 H 9 C1 3 O 3
105-107
Liquid
Oliveri
G. L, 14, 13
46, 1118
Lactic butyrchloralide
....
J>
260-262
....
....
A., 193, 47
Acetyltrichlorvalerolactinic
C 4 H 6 Cl 3 (OAc).COOH
C 7 H 9 C1 3 4
+H 2
84
Pinner and Klein
B., 11, 1492
acid
Pimelic chloride
C 5 H 10 (OOC1) 2
C 7 H 10 C1 3 S
210 p.d.
....
Kachler
A., 169, 173
27, 155
Acrolein acetyl chloride
C 3 H 4 0.2C 2 H 3 OC1
C 7 H 10 C1 2 3
140-145
....
Arontein
As., 3, 184
vl., 56
Methylchlorallylcarbinol
CHMe : CCl.CHMe.OAc
C 7 H U C10 3
172
....
Thurnlackh
A., 223, 149
46, 1118
acetate
Ethylchlormethyl crotonate
fr. CH 3 .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 ...
C 4 H 9 C10.COOEt
C 7 H U C10 3
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
,
>
221292
Liquid
Conrad & Bischoff
B., 13, 600
38, 629
Glycerol diacetochlorhydrin
C 3 H 5 .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 ...
....
C 7 H,,C1 3
228-229
Liquid
Barbaglia & Gucci
B., 13, 1571
40,34
Amylic trichloracetate
CC1 3 . COOCjH ! i
C 7 H n Cl 3 2
217
Clermonfc
C. R., 96, 437
44, 729
Methyltrichlorpropylcarbinol
CHMeCl.CCl 2 .CHMe.OAc
)I
227
Liquid
Thurnlackh
A., 223, 149
46, 1118
acetate
Ethylic trichlorhydroxy-
C 4 H 5 Cl 3 (OH).COOEt
c 7 H u a 3 o 3
225
40
Pinner and Klein
B., 11, 1492
36,42
valerate
Dichlordiisopropyl ketoue ....
C 7 H 12 C1 2 O
175-176
Liquid
Barbaglia & Gucci
B., 13, 1571
40, 34
Glycerol butyro-dichlorhydrin
C 3 H 5 C1 2 (OC 4 H 7 0)
7 H 12 C1 2 2
226-227(738
Truchot
A., 138, 298
....
Isobutylica-diehlorpropionate
CH 3 .CCl 2 .COOBu3
)J
183-185
....
Backunts and Otto
B., 9, 1879
32, 181
Chlordi-isopropyl ketoue ...
....
c 7 H: l3 cio
141-142
Liquid
Barbaglia and Gucc
B., 13, 1570
40, 34
Chlorethylic valerate
C 4 H 9 .COO.CHC1.CH 3
C 7 H 13 C10 2
118-128 d.
....
Simpson
P. E. S., 27, 120
38, 459
Ethylidene valerochlorhydrin
CH 3 .CHC1.O.C 5 H 9 O
It
162 u. c.
Eubencamp
A., 225, 267
48, 136
Chloral iso-amylate
CC1 3 .CH(OH)(OC 5 H,,)
C 7 H 13 C1 3 2
143
s. 25
Bartholdy & Martius
B., 3, 443
vii., 314
)>
....
14S-147
50
Jacobsen
A., 157, 244
24, 257
Heytylene chlorhydrin
C 7 H 14 C1.OH
C 7 H 15 C10
206-208
Clermoiit
B. S. [2], 13, 404
vii., (544, 868
Glycerol diethyl chlorhydrin
C 3 H 5 Cl(OEt) 2
C,H 15 C1O 2
184
Eeboul & Loureii9o
A., 119, 237
Trichlor-phthalic anhydride
o : (co) 2 : c 6 HCi 3 =i.2.3.4 ?
CgHCl 3 3
157
Claus and Kautz
B., 18, 1370
48, 972
>
)>
....
157
Atterberg& Widman
B., 10, 1843
34, 322
t
/
C 8 HC1 13 4
115-120
Cahours
A., 67, 29
v., 463
Dichlor-phthalic anhydride
o : (co) 3 : c 6 H 2 ci 2 =i.2.(?) 2
C 8 H 2 C1 2 3
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 .C1 4 =1.2.3.4.5.6
C S H. 2 C1 4 4
250
Claus and Spruck
B., 15, 1404
Chlorphthalic anhydride
o : (C0 2 ) : c 6 H 3 ci=i.2.4
C 3 H 3 C1O 3
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
C 6 H 4 (COC1) 2 =1.2
C 8 H 4 CL0 2
268
s.
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 .... .
C 6 H 3 C1 2 .O.CO.CHO
C 8 H 4 C1 2 3
90
A., 159, 147
Dichlorphthalic acid
C 6 H 2 C1 2 .(COOH) 2 =(?) 2 .2.1
C 8 H 4 C1 2 4
....
183-185
Faust
A., 160, 64
25, 76; vii., 978
)>
!>
J
183
Claus and Kautz
B., 18, 1370
48, 972
/3-phthalide chloride
C 6 H 4 .CC1 3 .COC1=1.2
C 8 H 4 C1 4
262 p.d.
47
Gerichten
B., 13, 419
38, 474
-
c 6 H 4 :(cci 2 ) 2 : 0=1.2
))
275 p.d.
88
))
B., 13, 418
38, 473
Dichlorpiperonal chloride ....
C 6 H 3 C1 2 .O.CO.CHC1 2
C 8 H 4 C1 4 3
abt. 280 d.
Liquid
A., 159, 147
vi., 948
Tartaric chloralide
[.CH.COO.CH(CC1 3 ).O] 2
C 8 H 4 C1 6 6
122-124
Wallach
B., 9, 1215
31, 60
Chlorphthalic acid
(COOH) 2 .C1=1.2.4
C 8 H 5 C1O 4
....
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.Cl 3 =1.2.4.6(?)
CsHsCljO,
261-262
As., 7, 184
Dichloracetophenone
C 8 H 6 C1 2
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
C H 5 .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.CCl 2 .COOH
OSH.CIA
50-55 d.
Claisen
B., 12, 631
JJ JJ JJ
1)
H
69
Radziszewski
B., 2, 209
vi., 1102
Dichloracetoxybenzene
OAc.Cl 2 =1.2.4
n
244-245
....
A., 23, 60; As., 7,
184
Dichlortoluic acid
Me.COOH.Cl 2 =1.3(?),
j
160-161
....
A., 144, 269
Dichlorxyloquinone
C 6 Me,Cl 2 :O 2
175
Carstanjeii
J. p. [2], 23, 432
42, 612
Methylic dichlorsalicylate ....
OH.COOMe.CL=1.2.(2) 2
C 3 H 6 C1 2 3
..:.
142
Smith
B., 11, 1226
....
Dichlormethsalicylic acid ....
OMe.COOH.Cl 3 =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.Cl 2 =1.4.(?)
))
196
Reincecke
B. S. [2], 7, 177
vi., 173
Tetrachlor-/3-oreinol
C 6 Me 2 Cl 2 (OCl) 2
C 3 H 6 C1 4 2
109 or 190
Stenhouse& Groves
A., 203, 291
37, 399
Tetrachlordimethylquinol ....
C 6 Cl 4 (OMe) 2
153-154
Habermaiin
B., 11, 1035
34,728
Chloracetophenone
Ph.CO.CH 2 Cl
C 9 H 7 C1O
246
41
Graebe
B., 4, 35
24, 222
jj
1)
344-245 u.c.
58-59
Staedel
B., 10, 1830
34, 419
Acetochlorpheaone
C 6 H 4 C1(CO.CH 3 ) = 1.4
J)
230-231
20
Gautier
B. S., 43, 602
48, 1061
Toluyl chloride
C c H 4 Me.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 (?)
....
C 8 H 7 C10 2
173
106
Boquillon
J. P. [5], 11,654
48, 962
Phenylic chloracetate
CH 2 Cl.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
C 6 H 4 .OMe.COCl = 1.4
>
262
....
Cahours
A. C. [3], 23, 351
i., 306
Chlora-a-toluic acid
C 6 H 4 C1(CH 2 .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
C e HMe 2 Cl : O 2
)
48
Carstanjen
J. p. [2], 23, 431
42, 612
Methylic chlorsalicylate
COOMe.OH.Cl. = 1,2.5
C 8 H ; C1O 3
....
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
C 8 H 7 C1O 4
93
Precht
B., 9, 1101
30, 506
(?)
CPhCl 2 .COH+HCl
C 8 H 7 C1 3
begins 265 d.
..*.
Combes
C. R., 98, 678
46, 837
Ethoxytrichlorbenzene
C 6 H 2 Cl 3 .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 = ?
c 8 H 8 a 3 o
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 ....
C 6 H 2 (OMe) 2 Cl 2 = 1.3.(?) 2
C S H 8 C1 2 2
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 .... ....
C 6 Me 2 (OH) 2 Cl 2
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,,.CH 2 Cl
C 8 H S C10
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,H 4 .OEt.Cl = 1.2
C 8 H 9 C1O
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
CjH 3 Me.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
C 8 H 9 C10 2
230
....
St. Evre
J., 1, 530
Chlordimethylreaorcinol
C 6 H 3 (OMe) 2 Cl = 1.3.?
....
118
Hbnig
B., 11, 1039
34, 727
Chlorxyloquinol
C 6 HMe 2 (OH) 2 Cl
....
147
Carstanjen
J. p. [2], 23, 43
42, 612
ii
n
148-150
....
A., 151, 166
Acetotrichlorethylidene
....
C 8 H 9 C1A
154-158
Liquid
Mathews
43, 203
acetic ether
(24-26)
Crotonic chloral diacetate ..
C 3 H 2 Cl 3 .CH(OAc) 2
C 3 H 9 C1 S 4
240-250 p.d.
Liquid
Pinner
A., 179, 21
29, 549
Ethylic malic chloralide
....
C 3 H 9 C1 3 5
45-46
....
A., 193, 45
Diethylic chlormaleate
C 2 HCl(COOEt) 3
c 8 H n ao 4
843-845
....
Glaus
A., 191, 80
34,857
ii 11
It
250-260
....
Henry
A., 156, 179
Action of HC1 on aldehyde...
C 8 H 12 CJ 2
100
....
Hanriot
C. R., 92, 302
40, 404
? acetate
(CH 2 ) 2 .CH(CH S C1).CC1.CH 2 .
C 8 H 12 C1 2 O S
122-123
Liquid
Natterer
M. C., 5, 567
48, 498
1 ' OAc
Diethylic maleate diehloride
C 8 H 12 C1 2 4
243-245(735)
MM
Glaus and Franck
B., 10, 928
33, 740
? acetate
CH 2 Cl.CH(OAc).CH s .C 3 H 5
C 3 H 13 C10 2
203-207
Liquid
Lopatkin
J. p., 30, 389
48, 49
or
CH 2 Cl.CH(C 3 H 5 ).CH 2 .OAc
Ethylic ethylacetochlor-
CClEtAc-COOEt
C 3 H I3 C10 3
215-220 d.
....
Wislicenus and
A., 186, 241 ; B.,
29, 370
acetate
Conrad
8, 1034
Diethylic chlorsuccinate
COOEt.CH 2 .CHCl.COOEt
c 8 H l3 ao 4
234-235
Anschiitz
B., 18, 1952
Diglycerol acetrichlorhydrin
.*..
C 8 H 13 C1 3 3
190 (20)
Z. C., 1866, 513
Glycerolisovalerodichlorhy-
C 3 H 5 .(OC S H 9 )OC1 2
C 8 H 14 C1 2 2
245 (737)
Truchot
A., 138, 298
v., 980
drin
Hexylene acetochlorhydrin ...
C 6 H 12 C1.0Ac
C 8 H 1S C10 2
188-190
Liquid
Senry
C. R., 97, 260
46,34
Triethoxydichlore thane
C 2 HCl 2 (OEt) 3
C 8 H 16 C1 2 3
205
..
J., 1864 and 1873
?
0(C 2 H 3 C1.0Et) 2
11
163-165
Abeljanz
A., 164, 220
26, 156
?
O[CH(OEt).CH 2 Cl] 2
ii
abt. 165
Jacobsen
B., 4, 216
vii., 481; 24,
514
Octylenechlorhydrin
...
C 8 H 17 C10
204-208
Clermont
iv., 173
Glycerol isoamyl chlorhydrin
C 3 H 5 (OC 5 H n )(OH)Cl
C 8 H 17 C10 2
235
Reboul
J., 13, 464
ii., 884
Tetrachlorcoumarin
....
C 9 H 2 C1 4 2
144-145
Perkin
24, 45
vi., 500
a-Chlorcoumarin
....
C 9 H 5 C10 2
....
122-123
11
24, 44
ft'
....
j(
162
Saisecke
A., 154, 84
Chlortrimesic acid +H 2 O
C 6 H 2 C1(COOH) 3 =6.5.3.1
C 9 H,,C10 6
278
J. p. [21 15, 310
J)
a-Trichlorcinnamic acid
C 6 H 2 C1 3 .CH I CH.COOH
....
200-201
Seelig
r L Jj 7 "*"
B., 18, 425
48, 770
P- ii ,,
n
185
Trichloracetophenone benzoic
acid
C 6 H 4 (CO.CC1 3 ).COOH =1.2
C9H 6 C1 3 3
144
Jabriel & Michael
B., 10, 1556
34, 430
Salicylic chloral
....
j j
124-125
A., 193, 41
Dichlorethylene protocate-
O.C 2 H 2 Cl 2 .O.C f H 3 .COOH
C 9 H 6 C1 2 4
118-121
....
A., 168, 109
chuic acid
=43.1
Cinnamyl chloride
C 6 H 5 .CH:CH.COC1
C 9 H 7 C10
262
....
Cahours
A., 178, 214
.,990
Chloratropic acid
a-Chlorcinnamic acid
Fr. C 6 H S .C(COOH) I CH 2
Ph.CH:CCl.COOH
9)
C 9 H 7 C1O 2
170-171 (58)
r. water
35-36
85
137-138
^laisen & Antweiler
jadenburg
3 erkin
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
?
C 9 H 7 C10 2
....
132
....
A., 70, 7
i., 987
Acetylic chlorsal icy late
C 6 H 3 a(OH).COOAc =?.2.1
C 9 H 7 C10 4
....
149
Smith
B., 11, 1227
Chlormethylnoropianic acid
C c HCl.OMe.OH.CHO.COOH
C 9 H 7 C1O 6
206
Prinz
J.p., 24, 370
42, 403
Ethylic chlormecenate
HO.C,.C10(COOH)(COOEt)
C 9 H 7 C10 6
....
148
Hilsebein
J.p. [2], 32, 129
48, 1202
From polyporic acid
....
C 9 H 7 C1 2 2 (?)
....
108
Stahlschmidt
A., 195, 365
36, 383
Ethylic trichlorbenzoate ....
Cl 3 .COOEt =6.4.2.1
C 9 H 7 C1 3 !!
....
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....
CI 3 .(O.C 3 H 5 0) =6.4.2.1
*
262-5-264-5
Liquid
Daccomo
B., 18, 1163
48, 889
u.c.
Phenyl dichlorpropionic acid
Ph.CHa.CHCLCOOH
C 9 H 3 C1 2 O 2
....
162-164 d.
Erlenmeyer
B., 14, 1867
Dichlorbenzylic acetate
C 6 H 3 Cl 2 (CH 2 .OAc) =1.4.?
1
259
....
Beilstein and Kiihl-
A., 147, 350
vi., 336
berg
Ethylic dichlorbenzoate
C 6 H 3 CLCOOEt =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
C 6 H 2 Cl 2 .OH.COOEt =(?),.2.1
C 9 H 8 C1A
47
Smith
B., 11, 1226
Xylylic chloride
Me.Me.COCl =1.2.4
c 9 H 9 ao
234-236
25-5-26-5
Ador and Meier
B., 12, 1970
38, 252
Methylic phenylchloraeetate
Ph.CHCl.COOMe
C 9 H 9 C1O 2
248 c. ; p.d.
Liquid
Meyer and Boner
B., 14, 2392
Chlorethylic benzoate
Ph.COO.C 2 H 4 Cl
>
260-270
....
A., 113, 121
n-Chlorhydratropic acid
CH 2 Cl.CHPh.COOH
5J
....
78-74
Merling
A., 209, 20
40, 1143
ft- 11 11
CH 3 CClPh.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.(CH 2 .CH 2 .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
C 6 H 4 Cl(CIL,.OAc)=1.4
J
240
....
Neuhof
Z. C. [2], 3, 467
vi., 336
Phenyl chlorlactic acid
....
C 9 H 9 C10 3
....
104
....
A., 147, 79
11 11 11
....
J
+H 2
78-80
11
Chlortropic acid
CH s (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
C 6 H 4 .Me.OH + CC1 3 .COH
Og-tlgC/ljjOj
....
52-56
Mazzara
G. I., 13, 269
46, 187
Trichlorvalerolactic bntyr-
....
C 9 H 10 C1 6 6 3
300-310
84-86
....
A., 193, 48
chloralide
Phenyl chlorcarbinol ethyl
Ph.CHCl.OEt
C 9 H n ClO
210-212
Hubner and Bente
B., 6, 805
27, 152
oxide
Chlorbenzyl ethyl oxide
C 6 H 4 Cl(CH 2 .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
C 6 H 3 MeCl.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
....
C 9 H U C10 4
....
130
Kachler & Spitzer
M. C, 6, 173
48, 808
Diethylic trichlorethylidene-
CC1 3 .CH : C(COOEt) 2
C 9 H U C1 3 4
160-164 (23)
Liquid
Kommenos
A., 218, 145
46, 423
malonate
Diethylic chlorethenyltricar-
COOH.Ca(COOEt).CH 2 .
C 9 H 13 C1O 6
205-215 (160)
Bischoff
A., 214, 44
44, 45
boxylate
COOEt
Isobutylic chlorangelacetate
....
C 9 H 15 C10 3
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
C 9 H 15 C10 4
Liquid
Guthzeit
A., 209, 232
42,39
)J
228
Liquid
Conrad
B., 14, 618
Diethylic itachlorpyrotarta-
C 3 H 5 Cl(COOEt) 2
250-252 d.
Liquid
....
Z. C., 1866, 722
vi., 980
rate
Parachlorpropaldehyde
....
C 9 H 15 CI 3 3
170-175
33-5
Grimaux & Adam
C. B., 92, 300
40, 406
(12-15)
Pelargonpyl chloride
C 8 H 17 .COC1
C 9 H 17 C1O
220
....
Cahours
A. C. [3], 39, 207
iv., 371
Tetrachlornaphthaquinone ....
C1 4 ; O 2 =a! a 2 ft $ 2 ; a, a 3
C 10 H 2 C1 4 O 2
160 u. c.
Claus and Lippe
B., 16, 1018
44, 921
Trichlornaphthaquinone
CioH 3 Cl 3 . Oj
C 10 H 3 C1 3 2
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
c 10 H 4 ci 2 :o 2
C 10 H 4 C1 2 O 2
....
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
c 10 H 5 a : o 2
C 10 H 5 C10 2
109-111
Plagemann
B., 15, 485
Chlorhydroxynaphthoqui-
C 10 H 4 C1(OH) : O 3
C 10 H 5 C10 3
200
....
....
vi., 853
none
Dichlor-a-naphthaquinol
C 10 H 4 C1 2 (OH) 3
10 H 6 C1 2 2
....
135-140 d.
Grsebe
A., 149, 6
vi., 857
Diacetyltetrachlorquinol
C 6 Cl 4 (OAc) 2 =(?) 4 .4.1
C 10 H 6 C1 4 4
....
245
A., 146, 20
vi., 988
a-naphthoic chloride....
C 10 H 7 .COC1
C 10 H 7 C10
297-5
Solid
Hofmann
: vl., 851
Chlornaphthol
Ci H 6 .Cl.OH=aj ; o 2
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(CCl 3 )O
C 10 H 7 C1 3 3
305-310 p. d.
59
Wallach
B., 9, 1215
31,60
>
....
n
305-310 d.
82-83
A., 193, 40
Diacetyltrichlorquinol
C 6 HCl 3 (OAc) 2 =(?) 3 .4.1
C 10 H 7 C1 3 4
153
Grsebe
A., 146, 28
vi., 988
1
....
C 10 H 8 C1 2 2
195-196
....
J. [1872], 424
Diacetyl dichlorquinol
<OAc) r Cl s =1.4.2.5
C 10 H 8 C1 2 4
....
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,H 4 .OMe.(C,,H,,.COCl)=1.4
C 10 H 9 C10 2
abt. 50
Perkin
J. [1877], 792
31, 410
Diacetyl chlorquinol
(OAc) 2 .Cl=1.4. 2 or 5
C 10 H 9 C10 4
....
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
C 6 H.(COH).Cl.(OMe) 2 .COOH
C 10 H 9 C10 5
210-211
Prinz
J. p., 24, 367
42, 403
Butyryl trichlorphenol
(O.C 4 H 7 0).C1 3 =1.2.4.6
C 10 H 9 C1 3 2
272-275 u. c.
Liquid
Daccomo
B., 18, 1163
48, 889
Pentachlorthymol
....
C 10 H 9 C1 6
98
Lallemand
A. C. [3], 49, 158
v., 795
Dichlornaphthalene aceto-
C 10 H 6 Cl 2 .Cl 3 .OAc
C 10 H 9 C1 6 2
195
Widmann
B., 12, 1714
38, 47
chloride
Ethylic phenyldichloracetate
Ph.CCl 2 .COOEt
^ioSi Cl 3 O 3
263-266
Claisen
B., 12, 630
36, 648
Glycerol benzodichlorhydrin
C 3 H 5 Cl 2 (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,,
C 6 Me.COOEt.(OH) 2 Cl 2
C 10 H 10 C1 2 4
)
107
162
Stenhouse
Hesse
23,6
A., 117, 315
vi., 989
iv., 237
Deriv. of Valeral
....
C 10 H IO C1 4
208-210
....
Schroeder
B., 4, 401
24, 560; vii.,
Diethyl tetrachlorquinol ....
QA(dBt),
C 10 H 10 C1 4 2
112
Grtebe
A., 146, 19
1195
vi., 988
Chloranethol
C 6 H 4 .C 3 H 4 C1.0Me=1.4
C^H^CIO
258
6
L/adenburg
Z. C. [2], 5, 575 ;
vi., 157 ; vii.,
As., 8, 91
72
" >i
Cuminyl chloride ! C 6 H 4 .Pr.COCl
Benzylchlormalonamide ... CCl(CH 2 Ph)(CONH 2 )
u
CioH n C10 2
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
C 10 H U C10 2
260-265
A., 144, 267
Chlortolylpropionic acid
(CH 2 .CH 2 .CO 2 H)ClMe=1.2.
)>
122-123
Gerichten
B., 11, 365
34, 570
Benzochlorhydrin
C 3 H 5 (OH).C1.(OC 7 H 6 0)
Ci HiiC10 3
40
Berthelot
A. C. [3], 41, 302
i., 547
Chlorhydroxythymoquinone
C 6 MePr.OH.Ci:O 2
j>
....
122
Ladenburgand En
B., 10, 1222
34,' 60
gelbrecht
Trichlorthymol
Me.Pi-.OH.Cl 3
C 10 H U C1 3
250
45
A. C. [3], 49, 157
61
jj
v., 795
Diethyltrichlorquinol
C 6 H(OEt) 2 Cl 3 =1.4.(?) 3
Ci H n Cl 3 02
68-5
Grsebe
A., 146, 28
vi., 988
?
....
c )0 H 12 a 2 o
98-99
Auwers
B., 17, 2978
48, 381
Diethylic dichlormuconate ...
C 4 H 2 Cl 2 (COOEt) 2
C 10 H 12 C1 2 4
95-96
Bell
B., 12, 1273
Deriv. of Valeral
....
C 10 H 12 C1 6 O
203-204
Schroeder
B., 4, 401
a*, 559
Trichlorcamphor
Ci H 13 Cl 3 O
....
54
Cazeneuve
C. R, 99, 609
48, 59
Dichlorcamphor
....
C 10 H 14 C1 2
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
....
C 10 H 15 C10
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),
C 10 H 5 C10 4
140 (20)
Liquid
Natterer
M. C., 5, 567
48, 498
Triethylic chlormethintricar-
CCl(COOEt) 3
C IO H 16 C10,
210 (140)
....
Conrad
B., 14, 618
40, 577
boxylate
Camphor dichloride
....
C 10 H 16 C1 2 O
....
70
Pfaundler
B., 11, 364
34, 586
,,
150-155
Spitzer
)>
,, ,, ....
)
155-155-5
B., 11, 1819
36, 168
Campholic chloride
C 9 H| 7 .COC1
C 10 H 17 C10
222-226
....
A., 126, 265
1
CioHisCljOj
98
Kekulo
A., 162, 102, 309
vii.,34;25,617
Capryl chloride
C 9 H 19 .COC1
C 10 H 19 C10
200-220
Liquid
Grimm
A., 157, 272
24, 361 ; vii.,
249
Hydrochloride of worm seed
C 10 H 1S O.HC1
5)
30-35
Hell and Eitter
B., 17, 1977
46, 363
oil
Octylene acetochlorhydrin ....
C 8 H 16 Cl.OAc
C 10 H I9 C1O 2
225
Clermont
A., 152, 322
vi., 880
Isovaleraldehyde +2HC1 ....
(C 5 H 10 C1) 2
C 10 H 20 C1 2
180
Bruylants
B., 8, 414
Terpenehydratedihydrochlor-
C 10 H 20 C1 2 0(?)
49
Flavitzky
B., 12, 2355
38, 403
ide
Diglycerol diethylchlorhydrin
O : (C 3 H 5 )(OEt) 3 (OH)Cl
C 10 H 21 C10 4
285
....
Reboul & Lourengo
C. R, 52, 401
ii., 894
Dichlor-j3-naphthoic acid ....
C 10 H 5 C1 2 .COOH
CiiH Cl 2 O 2
....
291
Ekstrand
B., 17, 1605
46, 1361
a-Naphthoyl chloride
C 10 H-.COC1 = a
C,,H 7 C1O
297-5
Liquid
Hofmann
B., 1, 41
-
=
)J
304-306
43
Weith
A., 180, 317
30,86
Dichloroxysacchulmide
C n H 8 Cl 2 6
d.w.m. 200
Sestini
G. I. [1882], 292
42, 1182
Ethylic acetylchlormecenate
AcO.C 6 ClO (COOH) (COOEt)
C n H,C10 7
70
Hilsebein
J. p. [2], 32, 129
48, 1203
Diacetyltrichlortoluquinol ....
C 6 MeCl 3 (OAc) 3
C n H 9 Cl 3 4
....
114
Borgmann
A., 152, 253
vi., 1106
Diacetyl-ru-dichlortoluquinol
C 6 HMeCl 2 (OAc) 2
CiiHioCl 2 O 4
122-124
Southworth
A., 168, 271
27, 62
Valeryltrichlorphenol
(O.C 5 H 9 0).C1 3 = 1.2.4.6
CnH u Cl g O,
281-284 u.c.
Liquid
Daccomo
B., 18, 1163
48, 889
Isobutylic dichlorsalicylate....
COOBuP.OH.Clj = 1.2.(?) 2
C H H 12 C1 2 O 3
188
Smith
B., 11, 1226
Diethyltrichlortoluquinol ....
C 6 MeCl 3 (OEt) 2
3irH M Ca,O|
107
Borgmann
A., 152, 254
vi., 1106
Camphocarboxy lie chloride ....
C 10 H 14 .OH.COC1
CnH.^lO,
44
Kachler and Spitzer
B., 13, 1413
38, 892
Triethylic chlorethenyltricar-
C 2 H 2 Cl(COOEt) 3
C U H 17 C10 6
290 p.d.
Bischoff
B., 13, 2162
40, 156
boxylate
Glycerolchloracetyltriacetin
C 3 H 5 (OAc) 3 .AcCl
C n H 17 C10 7
240 (20)
Z. C. [1866], 513
Triglycerolacetotetrachlorhy-
2 (C 3 H 5 ) 3 (OAc)Cl 4
CnH 18 Cl 4 O 4
230 (20)
drin
Diethylic isobutylchlormalo-
C 4 H 9 .CCl(COOEt).,
c ll a ll cio 4
845
Conrad and Bischoff
B., 13, 600
38, 629
nate
!) !>
jj
245-247
Guthzeit
A., 209, 237
42,40
Octochlordiphenol
C 12 C1 8 (OH) 3
C 12 H 2 C1 8 2
233-5-234-5
Weber & Sollscher
B., 16, 884
Tetrachlor-y-diphenol
C 6 H 2 C1 2 (OH).C 6 H 2 C1 2 (OH)
C 12 H 6 C1 4 2
233
Magati
B., 13, 227
38, 644
Tetrachlorquinhydrone
C 12 H 6 C1 4 4
120
....
A., 69, 316
+2H 2
From naphthalene
C 10 H 6 CI 2 (OAc).Cl.,
C 12 H 9 C1 6 2
195
Widmann
B., S. [2], 28, 507
32,900
Diethylic tetrachlorphthalate
C 6 (COOEt) 2 .Cl 4 = 1.2.3.4.5.6
C 12 H 10 C1 4 4
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,,Cl 4 .COO.C(OEt) 2 = 1.2.(?) 4
C 12 H 10 C1 4 4
124
Graebe
B., 16, 861
Cumenylacrylcliloride
C 6 H 4 .Pr(C 2 H 2 .COCl
C 12 H 13 C10
....
abt. 25
Perkin
J. [1877], 790
31, 399
Diethylic chlorisophthalate...
(COOEt) 2 .Cl= 1.3.5
C 12 H 13 C10 4
....
abt. 45
Baeyer
J. p. [2], 25, 514
42, 1296
Thymol chloral
C 6 H 3 .Me.Pr.OH + OC1 3 .COH
C 12 H 15 C1 3 O 2
130-134
Mazzara
G. I., 13, 269
46, 187
?
C 12 H 25 C10 4
275-285
....
A. C. [3], 67, 310
Lauryl chloride
0] 1X123.0001
C 12 H 23 C1O
142-5 (15)
17
Krafft and Burger
B., 17, 1378
46, 1125
Dichlordiphenylene ketoue ...
C.H 3 Cl.CO.CjH 3 Cl = 1.4.5 ;
C I3 H 6 CL,0 (?)
....
103-104
Hodgkinson and
43, 171
5.4.1
Matthews
>l
!I
158
?
43, 170
Benzoxytrichlorpheuol
OBz.Cl 3 = 1.2.4.6
C 13 H 7 C1 3 2
70
Daccomo
B., 18, 1164
48, 889
Chlordiphenyl ketone
Ph.CO.C c H 4 Cl
C 13 H 9 C1O
a. 300
75-5-76
Kollarits and Merz
B., 6, 547
vii., 939 ;
26, 1036
Benzoxychl orbenzene
C 6 H 4 C!.OBz
C 13 H 9 C1O 2
87
A., 53, 96
i., 554
Ethylic dichlor-/3-naphthoate
C 10 H 6 Cl 2 .COOEt.
C 13 H 10 C1 2 2
66
Ekstrand
B., 17, 1605
46, 1362
Benzyloxychlorbenzene
C 6 H 5 .CH 2 .O.C 6 H 4 .C1
C 13 H U C1O
...
70-71
A., 161, 345
vii., 180
....
JJ
71-71-5
Sintenis
B., 4, 700
24, 909
Ethylic chlor-a-naphthoate ....
C 10 H 6 Cl.COOEt
CuHudo,
42
Ekstrand
B., 17, 1604
46, 1361
Chlorhydrin of ethylic aceto-
OHPhCl.CHAc.COOEt or
C 13 H 15 C10 3
41
Claisen & Matthews
A., 218, 170
46, 443
benzilidene acetate
CH 2 Ph.CAc01.COOEt
n
j
>?
...
71
!>
tt
Penta-chloranthraquinone ....
....
C 14 H 3 C1 5 2
w.m.
Diehl
B., 11, 181
34, 430
Tetra-
....
C 14 H 4 C1 4 2
320-330
j
B., 11, 180
34, 429
n
c 6 a 4 :(co) 2 :c 6 H 4
191
Kircher
B., 17, 1167
46, 1039, 1040
Tetrachloralizarin
C 14 H 2 C1 4 (OH) 2 :0 2
C H H 4 C1 4 4
260
Diehl
B., 11, 189
Trichloranthraquinone
....
c 14 H 5 a 3 o 2
....
284-290
)>
B., 11, 180
34, 429
Pentachloroxytolidene
....
C 14 H 5 C1 5 2
....
187-190
A., 153, 128
Dichloranthraquinone
C 14 H 6 C1 2 2
261
Kircher
B., 17, 1169
46, 1040
Dichloralizarin
c, 4 H 4 ci 2 (OH) 3 :o 2
C 14 H 6 C1 2 4
...
208-210
Diehl
B., 11, 188
34, 428
Acetyloctochlordiquiuol
C 6 Cl 4 (OH) J .C 6 Cl 4 (OAc)(OH)
C 14 H 6 C1 8 S
230
Hesse
A., 114, 294
iii., 216
Ohloralizarin . ..
C 14 H 5 C1(OH) 2 :0 2
C 14 H 7 C10 4
244-248
Diehl
B., 11, 187
34, 428
Trichlorxytolidene
....
C 14 H 7 C1 3 2
87
*
A., 153, 128
Anthraquinone dichloride ....
C { H 4 .CO.C 6 H 4 .CC1 2
C 14 H 8 CL,0
132-133
Thorner and Zincke
B., 10, 1479
34, 231
Phenanthradichlorketone ....
C 6 H 4 .C 6 H 4 .CO.CC1 2
H
165
Lachowicz
B., 16, 331
44, 667
Octochlorethyldiquinol
C 6 Cl 4 (OH) 2 .C 6 Cl 4 (OEt)(OH)
Cijifajo.
236
Hesse
A., 114, 292
iii., 216
Chlorphenanthrene
....
c 14 H 9 ao
....
122-123
Lachowicz
J. p. [2], 28, 168
46,82
Chloroxytolidene
....
C J4 H 9 C1O 2
57-58
A., 153, 127
Benzoylbenzenyl trichloride
C 6 H 4 .Bz.C01 3 = 1.4
C 14 H 9 C1 3 O
....
107-107-5
Thorner
B., 9, 483
30, 198
)!
))
111-111-5
j)
A., 189, 92
34, 68
Benzoylbenzylene dichloride
C f ,H 4 .Bz.CHCl 2 = 1.4
C 14 H 10 C1 2
....
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
C 10 H 4 Cl 2 (OAc) 2
C 14 H 10 C1 2 4
236
Grsebe
A., 149, 7
vi., 857
Benzoylbeuzyl chloride
C 6 H 4 .Bz.CH 2 Cl = 1.4
C^HuClO
....
97-98
Thorner
B., 9, 482
30, 197
)>
)
>j
a.a. 93-94
A., 189, 89
34, 68
Chlorbenzilic acid
....
C 14 H U C10 2
270
Cahours
A. C. [3], 23, 350
i., 915
Diphenoltrichlorethane
CC1,.CH(C 6 H 4 .OH),
C 14 H n Cl 3 3
202 d.
Meer
B., 7, 1201
28, 158
Tetracetoxydichlorbenzene ....
C 6 Cl 2 (OAc) 4
C 14 H 12 C1,0 8
235
Grsebe
A., 146, 34
vi., 990
Diaeetoxydichlordihydro-
C 10 H 6 Cl(OAc) 2
C 14 H 14 C1 2 4
130-131
Grimaux
B. S. [2], 18, 208
26, 69
naphthalene
Diethylic benzylchlormalo-
nate
(Ph.CH 2 .CCl(COOEt) 2
C 14 H 17 C10 4
305 p.d.
Liquid
Conrad
B., 13, 2159
40, 168
Chlorthymyldiacetate
C 6 HClMePr(OAc) 2
))
87-88
Schulz
B., 15,657
42, 838
Ostruthin hydrochloride
Anthraquinone carboxyl
chloride
C 14 H 17 O 2 .HC1
c 14 H 7 :o.,.coci
C^H^CIO^O
c ls H 7 eio 3
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
C 1S H 13 C10
quick heat
slow heat
119-120
110-112
Claisen and Clapa-
rede
B., 14, 2464
42, 512
Trichlorsantonin
TT
C 15 H 15 C1 3 O 3
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
....
C 15 H 19 C10 3
....
139
Cannizzaro and
G. I., 8, 309
36, 331
Valente
Santonic chloride
....
}J
....
170-171
n
Alantic chloride
C 14 H 20 (OH).OOC1
C 15 H 31 C10 2
....
140 d.
Kallen
B., 9, 156
29, 917
Myristyl chloride
C 14 H 2 -.COC1
C 1S H 27 C10
168 (15)
1
Krafft and Burger
B., 17, 1379
46, 1125
Ciruicyl chloride
....
JJ
....
abt. 44
Carius
A., 114, 154
I., 964
Dichlordiphthalyl
....
C 16 H 6 C1 2 4
....
248
Ador
A., 164, 245
26,68; vii., 980
Dicacetoxyoctochlordipheuyl
C,Cl 4 (OAc).C 6 Cl 4 (OAc)
C 16 H 6 C1 8 4
193-194
Weber & Sollscher
B., 16, 885
Dichlor-n-naphthylene pheu-
fr. C,H 4 .O.C I H.
C 16 H 8 C1 2
245
Arx
B., 13, 1727
40, 282
ylene oxide
1 '
Diphthalyldichloride
(.CC1.C 6 H 4 .CO.O) 2 =(1.2)
C 16 H 8 CI 2 O 4
...
245
Grsebe and Schmal
A., 228, 126
48, 798
p i
zigang
1
C 16 H 9 C1 3 5
17
Ador
A., 164, 229
26,69; vii., 981
Hydropiperom chloride
C 7 H 5 2 .CHC1.CHC1.C 7 HA
C 16 H 12 C1 2 4
....
198
Kemsen and Fittig
A., 159, 132
vi., 949 ; 24,
935
1
..
C 16 H 12 C1 4 O 2
....
109-110
....
A., 195, 371
Ethyloxanthranyl chloride ....
C 6 H 4 .CO.C 6 H 4 .CClEt
C 16 H 13 C10
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.e e H 4 .C 2 HCl 3 .C 8 H 4 .COOH
C 16 H 13 C1A
173-174
Fischer
B., 7, 1192
28, 155
chlorethane
Dichlorhydrocoerulignone ....
C 12 H 2 Cl 2 (OMe) 4 (OH) 2
C 16 H 16 C1 2 6
220
Hayduck
B., 9, 929
30, 516
Dulcitol aceto-chlorhydrin ....
....
CuB-aClO.,,
160
....
A. C. [4], 27, 154
Tetrethylic chlorethyl acetyl-
(COOEt) 2 CCl.CEt(COOEt) 2
C 16 H 25 C10 8
d.
Liquid
Bischoff and Each
B., 17, 2786
48, 244
ene tetracarboxylate
Palmityl chloride
C 15 H 31 .COC1
C 16 H 3 ,C10
192'5(15)s.d
12
Krafft and Burger
B., 17, 1379
46, 1125
....
50
Villier
B., 9, 1932
Cetene chlorhydrin
C 16 H 32 C1(OH)
C 16 H 33 C10
abt. 300
b. 15
Carius
A., 126, 201
vi., 421
Leucogallol +2H 2 O
....
C 18 H,,C1 12 O 12
....
104 d.
Stenhouse & Grove
A., 179, 240
28, 709
C, a H,Cl,,O, n
109 p.d.
A., 179, 237
28, 707
Phthalyltrichlorphenol
c 6 H 4 :o 2 :(o.c 6 H 2 ci 3 ) 2 =i.2
is 7 H 10
C 18 H 8 CLp 4
>.
193-194
Daccomo
B, 18, 1164
48, 889
(1.2.4.6) 2
Chlordehydrobenzoylacetic
cci : c : cph.o.GPh : C.COOH
C 18 H U C10 3
....
150-151
Perkin
47, 293
acid
Tetrachlorhydropolyporic
....
C 18 H 14 C1 4 4
....
108
A., 195, 372
acid
Diacetoxyphenyltrichlor-
CCl 3 .CH(C 6 H 4 .OAc) 2
C 18 H 15 C1 3 4
....
138
Fischer
B., 7, 1202
28, 158
ethane
From benzoic ether ....
....
C 18 H 16 Cl e O 3
188-190
*
Malaguti
A. C. [2], 70, 374
i., 567
Isobutyl oxanthranyl chloride
C 6 H 4 .CO.C 6 H 4 .CClBu/3
C I8 H 17 C10
....
78
Liebermann
A., 212, 87
42, 862 .
,1 I!
....
78
Liebermann and
B., 14, 463
40, 610
Walder
?
....
C 18 H 17 C10 3
....
57
Limpricht and
A., 160, 177
25, 137
Schwanert
Tetrachlorcarotin
....
C 13 H =0 C1 4
....
120
A., 117, 228
Dichlorole'ic acid
....
C 13 H 32 C1 2 O 2
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
C 6 H 4 .CO.C 6 H 4 .CC1.C 6 H U
c, 9 H 19 ao
....
85
Liebermann and
B., 14, 459
40, 609
i p
Landshoff
Dichlor-a-dinaphthaleue
....
C 20 H 10 C1 2 O
....
150-151
Knecht & Unzeitig
B., 13, 1725
oxide
--
....
....
245
B., 13, 1726
40, 281
Fluorescein chloride
c 6 H 4 :(co.c (i H 3 ci) 2 :o
C 2 ,H 10 C1 2 O 3
....
252
Baeyer
A., 183, 18
31, 198
,, ....
n
252 u.c.
Fischer
B., 7, 1212
28, 159
Dibenzoyltetrachlorquinol ....
C 6 Cl 4 (OBz) 2 =1.2.4.5.3.6
C 20 H 10 C1 4 O 4
....
230
Levy and Schultz
B., 13, 1429
38, 888
!, .
....
233
A., 210, 156
42,510
trichlororesorcinol
C 6 HCl,(OBz), =(?) 2 .4.3.1
C 20 H n Cl 3 4
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,H 4 (CO.C 6 H 4 C1) 2
C 20 H 12 C1 2 2
....
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(C 6 H 3 C1) 2 : CH.C 6 H 4 .COOH
C 20 H 12 C1 2 3
....
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 .Cl 2 =1.4.3.5
C 20 H 12 C1 2 4
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
C 20 H 13 C10 4
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,H 4 .CH.
C 2U H 14 C1 2 O
....
56
Baeyer
A., 202, 97
38, 656
ride
CfffZ
Dichlortriphenylmethane car-
(C,H 4 C1) 2 CH.C 6 H 4 .COOH
C2oHi 4 01 2 O 2
....
195
i)
A., 202, 84
38, 655
boxylic acid
>
)>
....
205-206
)>
j)
i
....
C 20 H 15 C1 3 O 2
137
Liebermann
B., 6, 953
26, 1242 ; vil.,
1061
Dichloracetyl-hydroccerulig-
C 12 H 2 Cl 2 (OMe) 4 (OAc) 2
C 20 H 20 C1 2 O 8
172
Hayduck
B., 9, 929
30, 516
none
Arachidyl chloride
j g Jj-gg. OOO1
CjoH^ClO
....
66-67
Tassinari
B., 11, 2031
36, 307
Benzene resorcinphthale'in
C 6 H 3 (OH) 2 CPh.C 6 H 4 .COO
C2iH 15 Cl 3 O 4
Cryst.(fr.
113-114
Pechmann
B., 14, 1860
+CHC1 3
CHC1 3 )
Glycerol stearochlorhydrin ....
C,H 5 (C 1 A,0)a(OH)
C 21 H 4I C10 3
28
Berthelot
A. C. [3], 41, 225
v., 425
Dithymol trichlorethane
CCl 3 .CH(C 6 H 2 Me.Pr.OH) 2
C 22 H 27 C1 3 O 2
+C 3 H 6
194
Jager
B., 7, 1197
31, 262
Naphthalfluorescem dichlo-
....
C 24 H 12 C1 2 O 3
....
283
Terrisse
A., 227, 133
48, 667
ride
Dibenzoxydichlortetrahydro-
C 10 H 4 .H 4 .(OBz) 2 .Cl 2
C.yH^CLO,
....
148-150
....
B. S., 18, 208
naphthalene
Dibenzoyldichlorthymoquinol
C 6 Cl 2 Me.Pr.(OBz) 2
C 24 H 20 C1 2 4
....
190-191
Schulz
B., 15, 658
42, 838
Dibenzoylchlorthymoquinol
C 6 HCl.Me.Pr.(OBz) 2
C 24 H 21 C10 4
116-118
1
C 24 H 25 C10 4
184-186
Liquid
Boquillon
J. P. [5], 11, 654
48, 962
Dithymoltrichlorethane
CCl 3 .CH(C 6 H 2 MePr.OH).,
C 2 .iH 33 Cl 3 O 3
....
194
Jager
B., 7, 1197
31, 262
+C 2 H 6
Lignocerylchloride ....
CggH.^' COC1
C 24 H 47 C1O
48-50
Hell and Hermann
B., 13, 1720
40, 250
Diacetyl dichlorcatechin
C 21 H 16 Cl 2 7 (OAc) 2
C 25 H 22 Cl 2 O n
....
169
Liebermann and
B., 13, 695
40,53
Tauchert
Heptachlorcholesterin
....
C 26 H 37 C1 2
....
60
A., 59, 110
Octochlorlepidine
....
C 28 H 12 CI 8 O
97
Dorn
Z. C. [2], 5, 597
vi., 781
Hexa-
....
c*a l4 cif)
80-90
A., 155, 356
)}
Penta-
....
C M H 1S C1 5
186
A., 155, 355
Chloride of diphenic anhy-
....
cH 16 aA
....
128
Graebe and Men-
B., 13, 1304
38, 812
dride
sching
Dichlorlepidine
....
C 28 H 1S C1 2
....
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
....
CWH 19 C10 2
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
C 23 H 24 C1 2 0(!)
....
87(?)
)) JT
)1
)
From quassin
C 32 H 39 C1 5 O 3
119d.
Oliver! and Denaro
G. I., 15, 6
48, 907
Glyceroklipalmitochlorkydrii
C 3 H 5 .C1.(O.C 16 H 31 0) 2
C 35 H W C10 4
44
Villier
B., 9, 1933
Tetrachlorabictic acid
....
C^4H 60 Cl4O 5
124
J., 1861, 391
Chlorobastin ....
f 1 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
C 4 H 2 C1 2 S
170
Weitz
B., 17, 795
46, 1130
Octochlorethyl sulphide
(C 2 HC1 4 ) 2 S
C 4 H 2 C1 8 S
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
....
C 4 H 3 C1S
130
....
Weitz
B., 17, 794
46, 1130
Hexachlorethyl sulphide ....
(C 2 H 2 C1 3 ) 2 S
C 4 H 4 C1 6 S
189-192
....
Eiche
A., 92, 359
ii., 545
Tetrachlorethyl sulphide ....
(C 2 H 3 C1 2 ) 2 S
C 4 H 6 C1 4 S
167-172
....
A. C., 43, 297
!
Chlorphenylsulphhydrate ....
C 6 H 4 C1.SH
C 6 H 5 C1S
53-54
Glutz
A., 143, 109
vi., 919
Dichlor-;3-ethylthiophene ...
C 4 SHCL..Et
C 6 H 6 C1 2 S
235-237C
Liquid
Bonz
B., 18, 551
48, 767
Chlorbenzyl sulphhydrate ....
C 6 H 4 C1(CH 2 .SH)=1.4
C 7 H 7 C1S
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(C 4 H 3 S) 2
CioH 6 CI 2 S 2
Liquid
Peter
B., 17, 1343
46, 1001
trichlorethane ....
CC1 3 .CH(C 4 H 3 S) 2
C 10 H 7 C1 3 S 2
76
B., 17, 1342
)1
?
....
^10^20^*2^2
240-250
....
Guthrie
A, 121, 108
v., 1077
Dichlorphenyl sulphide
(C 6 H 4 C1) 2 S
(_y| 2 -D. 8 01 2 O
88-89
Krafts
B., 7, 1165
28, 153
Dichlorphenyl disulphide ....
(C 6 H 4 C1) 2 S 2
C 12 H 9 C1 2 S 2
71
Glutz
A., 143, 111
vi., 919
Chlorbenzyl sulphide
(C 6 H 4 C1.CH 2 ) 2 S=?
C 14 H 13 01 2 S
Liquid
Pauly
A, 167, 187
i
=(1-4),
....
42
Jackson and White
B., 13, 1217
38, 879
disulphide
(C 6 H 4 C1.CH 2 ).,S 2 =(1.4) 2
C 14 H, 2 C1 2 S 2
....
59
A. C. J., 2, 166
40, 807
Dichlorthionessal
....
C 23 H 19 C1 2 S
....
219
Dorn
A., 153, 351
vi., 1087
Dimethyl selenio-dichloride
Me 2 Sea 2
C 2 H 6 Cl 2 Se
d. 70
59-5
Jackson
B., 8, 110
28, 553
Dimethyl telluro-dichloride ...
MejTeCL,
C.,H 6 Cl 2 Te
....
97-5
Wohler and Dean
A., 93, 233
iii, 992
(5.) CHC1N.
Triehlorguanidine
CH 2 C1 3 N 3
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.NH 2 +HC1
CH 5 C1N.,
....
81
Gautier
A, 145, 118
)J
....
81
Claisen & Matthews
B., 16, 310
41, 266
Methylamine hydrochloride .
NH 2 Me+HCl
CH.C1N
abt. 100
Wurtz
C.E.,28,223&322
iii., 997
Dichloracetonitril
CHC1 2 .CN
C 2 HC1 2 N
112-113
....
Bisschopinck
B., 6, 732
26, 1128
....
....
(C 2 HC1 2 N),
....
69-70
Weddige & Korner
J. p. [2], 31, 176
48, 739
Chloracetonitril
OH 2 C1.CN
C 2 H 2 C1N
126-127 p.d.
....
Engler
B., 6, 1003
27,76
.... ....
))
123-124
....
Bisschopinck
B., 6, 732
26, 1128
Ethyl nitrogen dichloride ....
C 2 H 5 .NC1 2
C 2 H 5 01 3 N
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
CH 2 C1.CHC1.NH 2
)J
....
136
Abeljanz
B., 4, 986
25, 607
Hydrogen cyanide sesqui-
2HCN+3HC1
C 2 H 5 C1 3 N 3
....
180 d.
Claisen & Matthews
B., 16, 309
hydrochloride
Acetamidine hydrochloride....
NH:CMe.NH,+HCl
2 H 7 C1N 2
....
164-165
Pinner
B., 17, 178
46, 723
Ethylamine hydrochloride ....
NHjEt+HCl
C 2 H,C1N
abt. 80
Kohler
B., 12, 1871
)
315-320
76-80
Wurtz
C. B., 28, 223, 323
ii., 557
?
HCN+(CN) 2 Clj
C 3 HC1 2 N 3
20
....
i)
A, 44, 308; 79,280
ii., 280
a-Dichlorpropionitril
CH 3 .CC1 2 .CN
C 3 H 3 C1 2 N
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
>!
....
(C 3 H 3 C1 2 N) 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
CH 3 .CHC1.CN
C 3 H 4 C1N
121-122
Liquid
Backunts and Otto
B., 9, 1592
31, 298
Propionitril hydrochloride ...
C 2 H 5 .CN+HC1
C 3 H 6 C1N
....
121
Gautier
C. R., 63, 921
vi., 524
Propionamidine hydrochlo-
NH:CEtNH 2 +HCl
C 3 H 9 C1N 2
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.NMe 2 +HCl
JJ
....
168-169
*?
B., 16, 1650
44, 1090
hydrochloride
Propylamine hydrochloride...
Me(CH 2 ) 2 .NH 2 +HCl
C 3 H 10 C1N
....
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
....
C 4 HC1 4 N
....
110 d.
Ciamician & Silber
B., 16, 2391
46, 292
a-Chlorcrotonitril
CH 3 .CH:CC1.CN
C 4 H 4 C1N
136
Liquid
Sarnow
B., 5, 470
25, 690
Chloroxalmethyline
C 4 H 5 C1N 2
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
CCl 3 .CH 2 .CH i ,CH:NH
C 4 H 6 C1 3 N
d. 192
164-165
Pinner and Klein
B., 11, 1491
36,42
ji ...
i)
1J
169-170
Schiff
B., 11, 2167
36, 452
Dichloracetethylimidechlo-
CHCl 2 .CCi:NEt
JJ
161-164
Wallach and
B., 13, 517
38, 547
ride
Kamenske
Hydropyrroline hydrochlo-
C 4 H 7 :N+HC1
C 4 H 8 C1N
...
173-174
Ciamician & Denn-
B., 16, 1539
44, 1142
ride
stedt
Butylamine hydrochloride ....
CH 3 .(CH 2 ) 3 .NH 2 +HC1
C 4 H 12 C1N
....
195
Linnemann & Zotta
A., 162, 3
vii., 222; 25,
475
Isobutylamine hydrochloride
CHMeEt.NH 2 +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 ....
CMe 3 .NH 2 +HCl
Jl
....
a. 250
Linnemann
A., 162, 7
vii., 223; 25,
477
!>
M
....
270-280
Brauner
A., 192, 65
34, 779
Trichlorpyridine
....
C 6 H 2 C1 3 N
48
Konigs and Geigy
B., 17, 594
46, 1195
i)
....
))
.$9-50
B., 17, 1834
46, 1369
?
....
C 5 H 2 C1 4 N 2
....
212
Pechmann & Stokes
B., 18, 2291
48, 1202
Dichlorpyridine
..,,
C 5 H 3 C1 2 N
....
66-67
Konigs and Geigy
B., 17, 1833
46, 1369
?
C 6 H 3 C1 3 N 2
157-5
Pechmann & Stokes
B., 18, 2291
48, 1202
Chlorpyridine (cf. B., 15, 1179)
N.C1=1.2
C 5 H 4 C1N
14S (743-5)
....
Ciamician & Denn-
B., 14, 1154
40, 826
stedt
Chloroxalmethylethyline ....
J
1)
C 5 H,C1N 3
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-
NEt 2 .CH : NH+Ha
C 5 H 13 C1N 2
125
Pinner
B., 17, 180
46, 724
chloride
Piperylhydrazine hydrochlo-
C 6 H 10 N.NH 2 +HC1
j;
162
Knorr
B., 15, 860 ; A.,
42, 1115 ; 46,
ride
221, 297
467
Hexachlor-a-picoline
C 5 HC1 3 N.CC1 3
C 6 HC1 6 N
....
60
Ost
J. p., 27, 277
44, 793
i)
))
60
Bellmann
J. p. [2], 29, 1
46, 841
Pentachloraniline
C 6 C1 6 .NH 2
C 6 H,C1 5 N
....
235
Langer
B., 15, 1331
42, 1058
)>
1)
232
A., 215, 120
Trichlormethylpurine
C 5 N 4 MeCl 3
C 6 H 3 a s N 4
174
Fischer
B., 17, 331
46, 996
Tetrachloraniline
NH 2 .C1.,=1.2.3.4.6
C 6 H 3 C1 4 N
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
NH 2 .C1 3 =1.2.3.4
C 6 H 4 C1 3 N
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
NH 2 .C1 3 =1.2.4.6
C 6 H 4 C1 3 N
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
C 6 H 2 C1 2 .NH.NH
C 6 H 4 C1 2 N 2
124 d.
Krause
B., 12, 48
i i
Tetrachlor-diaruidoboizene....
(NH ) 2 .C1 4 =1.4.2.3.5.6
C 6 H 4 C1 4 N 2
p. d. 200
218 u. c.
u
B., 12, 51
36, 462
NH 3 on (trichloracetonitril) n
C 6 cf 7 N 3 (NH 2 ) 2
C 6 H 4 C1 7 N 5
....
165
Weddige
J. p. [2], 28, 188
46, 35
Dichloraniline
NH 2 .C1 3 = 1.2.3
C 6 H 6 C1 2 N
252 c.
23-24
Beilstein and Kur-
B., 10, 2090 ; 11,
34, 299; 36, 143
batow
1861 ; A., 196,
217
f j ....
=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
NH 3 .C1 = 1.2
C fi H fi ClN
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
(NH 2 ) 2 .C1 2 = 1.2.3.5
C 6 H 6 C1 2 N 2
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
C 6 H 7 C1N 2
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
C 6 H 5 .NH 2 + HC1
n o ^^y t
C 6 H 8 C1N
....
192
Pinner
G. J. C., 1881
Picoline
C 6 H.N.HC1
....
160
Ramsay
P. M. [5], 2, 271
36, 263
Chlorcyanmethine
....
C 6 H 8 C1N 3
+ 3H 2 O
165 u. c.
Baeyer
B., 4, 176
Chlorcyanmethine dichloride
C 6 H 9 C1N 3 .C1 2
C 6 H 8 C1 3 N 3
s. b. 200
Keller
J. p. [2], 31, 363
48, 961
Chloroxalethyliue
....
C 6 H 9 C1N 2
217-218
s. f. m.
Wallach
B., 7, 327
27, 985
....
217-218
ord. temp.
A., 184, 40
32, 184
Di(chlorallyl)amine
(C 3 H 4 C1) 3 NH
C 6 H 9 CLN
194 d.
....
Engler
B. S. [2], 9, 134
vi., 95
hydrochloride
+ HC1
C fi H 10 d 3 N
b. 100
a-methylpiperidine
C 6 H 13 N + HC1
C 6 H 14 C1N
189
Ladenburg & Roth
B., 18, 48
48, 557
Capronamidine hydrochloride
NH : C(C 5 H U ).NH 3 + HC1
C 6 H lb ClN 3
106-107
Pinner
B., 17, 178
46, 723
Isobutylbiguauide
NH(CH 2 Pr0).C(NH).NH.
C 6 H 16 C1N 6
....
216
Smolka
M. C., 4, 815
46, 288
C(NH).NH 2 + HC1
dihydrochloride
+ 2HC1
C 6 H 17 C1 3 N 5
....
194
M
1)
Chlorbenzonitril
C 6 H 4 C1.CN = 1.2
C 7 H 4 C1N
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:CCl 2
C 7 H 6 C1 3 N
211-212
Liquid
Sell and Zierold
B., 7, 1229
28, 270
,i i)
212
....
Hofmann
B., 12, 1127
36, 805
Trichlortoluidine
Me.Cl : ,.NH 2 =1.2.4.6.3
C 7 H 6 C1 3 N
....
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.Cl 2 .NH 2 =1.2.4.6
C 7 H 7 C1 2 N
*259
88
Wroblewsky and
Z. C. [2], 6, 164
vii., 1167, 1177
Pirogow
,.
259
88
Wroblewsky
A., 168, 213
27, 56
Trichlordiamidotoluene
Me.Cl 3 .(NH 3 ) 2 =1.2. 4.5.3.6
C 7 H 7 C1 3 N 2
....
196
Seelig
B., 18, 423
48, 770
=1.2.3.4.5.6
195-207 d.
n
,,
Chlormethylaniline
Cl.NHMe=1.3
C 7 H S C1N
240
Liquid
Coste and Bodewig
B., 18, 431
48, 793
Chlorbenzylamine
C1.(CH 2 .NH 2 )=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.NH 2 =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
C 7 H,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.CH 2 .NH 2 +HCl
C 7 H 10 C1N
235-240
Spica
G. I., 10, 515
40, 262
Glyoxalisoamyline
C 7 H 13 N 3 +HC1
C 7 H 13 C1N 2
135-136
ladziszewsky & Szul
B., 17, 1291
46, 985
a-y-hydrolutidine
C 7 H 16 N + HC1
C 7 H 1B C1N
235
Ladenburg & Roth
B., 18, 919
48, 816
Phenyldichloracetonitril
C 6 H 5 .CC1.,.CN
223-224
Claisen
B., 12, 626
Chloroxiiidole chloride
C s H 4 .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,H 4 C1(CH S .CN)=1.4
C 8 H 6 C1N
....
Liquid
Neuhof
A., 147, 347
40, 806
....
29
Jackson and Field
A. C. J., 2, 85
40, 803
Tolyldichlorcarbimide
CH 3 .CNC1 =1.2
C 8 H 7 C1 2 N
218
Lachmann
B., 12, 1349
36, 935
Trichlordimethylaniline
NMe 2 .Cl 3 =1.2.4.6(?)
C S H 8 C1 3 N
257
32
Krell
B., 5, 879
26, 279
l)ichlordimethylaniline
NMe. 2 .Cl 2 =1.2.4(?)
C 8 H 9 C1 2 N
234
Liquid
Acetanilide chloride
Ph.NH.CCl 2 .CH 3
b. 50
Wallach and Hof-
B., 8, 1570 ; A.,
29, 604
niaim
184, 88
Chlordimethylaniline
NMe 2 .Cl=?
C 8 H 10 C1N
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.
Hofmann
A., 74, 143
iv., 451
Chlorxylidine
Me 2 .NH 2 .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.C 2 H 4 Cl + HCl
C 8 H,,C1 2 N
158
Nemirowsky
J. p. [2], 31, 173
48, 741
hydrochloride
Phenylethylamine hydio-
Ph.CH 2 .CH 2 .NH 2 +HCl
C 8 H 12 C1N
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.C 6 H 4 .CH 2 .NH 2 +HCl
185
Pieper
A., 151, 129
vi., 1132
11 )>
J! "
a. 230 d.
Colombo and Spica
G. I., 1875, 124
28, 895
Chloroxalpropyline
C 8 H 13 C1N S
235
....
Wallach & Schulze
B., 13, 516
38, 547
,,
236
....
B., 14, 423
40, 572
Di(chlorallyl)ethylamine
(C 3 H 4 Cl) 2 N.Et
C S H 13 C1 2 N
s.a. 200
Engler
B. S. [2], 9, 134
vi., 95
Hydro-a-isopropylpyridine
....
C 3 H 14 C1N
....
208-210
Ladenburg
B., 18, 1589
48, 992
hydrochloride
a-isopropylpiperidine hydro-
CTT XT _L TirM
8 17 ll -f-ilv^l
C 8 H 18 C1N
206
B., 17, 1679
46, 1386
chloride
Coniiue hydrochloride
,.
C 8 H, 6 C1N(?)
218
Copellidine ,,
....
171
Diirkopf
B., 18, 923
48, 817
Trichlorquinoline
C 9 H 4 C1 3 N
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., ;
C 9 H 5 C1 2 N
....
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 ; 8 2
U 9 H 6 C1N
256
Liquid
B., 15, 559
11
=meta
264-266
Liquid
Coste and Bodewig
B., 17, 926
46, 1197
_ ai) 3 i .
M
266-267
37-38
Friedlander and
B., 15, 334
42,732
Ostermeier
Anhydroamidotolyloxamic
11 * j
C B H,Me.N : CC1.CC1 : N
i 6 ; i
C,H 6 C1 2 N 2
114-115
Hinsberg
B., 16, 1533
44, 1129
chloride
=1.3.4
Methylchloroxindole
C,H 4 .Ca : CCl.NMe=1.2
C 9 H 7 C1 2 N
....
58-59
Baeyer
B., 15, 786
42, 1103
Tetrachlorcyanconine
C 9 H 10 C1 3 N 2 C1
C 9 H 10 C1 4 N 2
Liquid
Riess
J. p. [2], 30, 145
48, 236
Dimethylbenzamidochloride
Ph.CCl 2 NMe,
C 9 H,,C1 2 N
36
Hallmann
B., 9, 846
30, 418
Tetrahydroquinoline hydro-
CaHnN + HCl
C 9 H 12 C1N
180-181
Hoffmann and
B., 16,729
44, 1143
chloride
Konigs
Trichlorcyanethine ....
C,H 12 C1 3 N 3
....
110
Riess
J. p. [2], 30, 145
48, 236
Propyl|)henylamine hydro-
C 6 H 4 .Pr.NH 2 =1.4
C 9 H 14 C1N
203-204
Francksen
B., 17, 1221
46, 1007
chloride
C'uniidiiie hydrochloride
C,H 4 .Pr0.NH 2 =?
....
62
Schaper
Z. C. [2], 3, 12
vi., 516
Triacetonamine hydrochloride
CMe 2 .CH 2 .CO.CH 2 .CMe 2 . NH
C 9 H 18 C1N
293
Fischer
B., 16, 650
44, 790
Methyltrichlorquinoline
C 9 NH 3 MeCl 3
C 10 H 6 C1 3 N
134
Rugheimer and
B., 17, 741
46, 1023
Hoffmann
/3-dichlornaphthylamine
C 10 H 6 C1 2 .NH 2
C 10 H 7 C1 2 N
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
C 10 H 6 C1 2 .NH 2
C 10 H 7 C1 2 N
94
Cleve
B. S. [2], 29, 500
34, 736
Chlornaphthylamine
NH 2 .Cl=a,a,, ;
C ia H 3 ClN
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
C 10 H 8 C1 2 N 2
204-205
A16n
B. S. [2], 36, 433
42, 410
Quinoliue methochloride
C 9 H 7 N.MeCl + H 2 O
C 10 H 10 C1N
126
Ostermeyer
B., 18, 593 ;
48, 672
C.C., 1884, 970
Tetrahydroquinoline metho-
C 9 H n N.MeCl+H,0
244
3)
chloride
Chlor-a-naphthonitril
C 10 H 6 C1.CN
C U H 6 C1N
145
Ekstrand
B., 17, 1604
46, 1361
Tetrachlordispoline (tetra-
....
C n H 7 Cl 4 N
135
Zorn
J. p. [2], 8, 304
27, 484
chlorcryptidine)
?
CPh : N.CCl.CH.CMe : N
C U H 9 C1N
71
Pinner
B., 17, 2520
48, 159
i j'
Ethylchlorquinoline
N.Cl.Et=a l S 1 /3 2 ;
CnH^CIN
72-73
Baeyer & Jackson
B., 13, 120
38, 407
|3-naphthiniidoamide hydro-
C 10 H 7 .C(NH 2 ) : NH+HC1
CnHjjClNj
224-226
Pinner and Klein
B., 11, 1486
36, 48
chloride
Quinoline ethochloride
C 9 H 7 N.EtCl+H 2
C n H 12 ClN
92-5
Claus and Tosse
B., 16, 1278
44, 1009
Octochlorcarbazole
C 6 C1 4 .NH.C 6 C1 4
C 12 HC1 8 N
275
Knecht
A., 202, 29
38, 661
L. J
Hexachlorcarbazole
C 12 H 3 C1 6 N
225 d.
A., 202, 28
Dichlorazophenylene
Fr.C,H 4 .]fc 6 H 4 N
C 12 H 6 a 2 N 2
144
Claus
B., 8, 604
28, 899
i i
Trichlorcarbazole
C 12 H 6 C1 3 N
180
Knecht
A., 202, 28
38, 660
Tetrachlordiphenylamine ....
NH.(C 6 H 3 C1 2 ) 3
C 12 H 7 C1 4 N
133-134
Gnehm
B., 8, 1040
29, 265
Azoaraidodichlorbenzene
C 6 H 3 C1 2 .N 2 .C 6 H 2 C1 2 .NH 2
C 12 H 7 C1 4 N 3
126-5
Griesa
A., 121, 275
iv., 460
Dichlorazobenzene ....
C 6 H 4 C1.N 2 .C 6 H 4 .C1=(1.3) 2
C 12 H 8 C1 2 N 2
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(C 6 H 4 C1) 2
C 12 H 9 C1 2 N
80 u.c.
Claus and Schaare
B., 15, 1286
Azoauiidod ichlorbenzene
C,H 3 C1.N 2 .C 6 H 4 C1.NH 2
C 12 H 9 C1 2 N 3
124-5
Griess
A., 121, 271
if., 460
Chloramidodiphenyl
C 6 H 3 .Ph.NH 2 .Cl=1.2.?
C 12 H IO C1N
48
Liiddens
B., 8, 872
Di-chlorhydrazobenzene
(C1.C 6 H 4 .NH.) 2 =(1.3) 2
C 12 H 10 C1 2 N 2
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
(C 6 H 3 C1.NH 2 ) 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-
C 10 H 7 .NHEt+HCl
C 12 H 14 C1N
....
235
Henriques
B., 17, 2669
48, 168
drochloride
Trimethylquinoline
C 9 NH 4 Me 3 +HCl
n
260
Pfitzinger
J. p. [2], 32, 240
48, 1246
p-dimethamidoquinoline
C,NH s .NMej+MeCl
C 12 H" 5 C1N 2
+H 2
244
Ostermeyer
B., 18, 596; C.C. 48, 672
methochloride
1884, 970
Hydro- p-dimethamidoquino-
C 9 NH 10 .NMe 2 +Mea
C 12 H 19 C1N 2
+2H 2 O
220
B
M
(j
line methochloride
Chloroxalisoamylene
....
C 12 H 21 C1N 2
267-870
Liquid
Wallach
A., 214, 316
44,49
)!
....
265-270
Liquid
Wallach & Schulze
B., 13, 516
38, 547
Methyltetrachlordiphenyl-
NMe(C 6 H 3 Cl !! ) 2
C 13 H 9 C1 4 N
96-97
Gnehm
B., 8, 1041
29, 265
amine
Benzanilideimide chloride
Ph.CCl:N.Ph.
C 13 H 10 C1N
abt, 310
39-40
Wallach & Hofmann
B., 8, 313
28, 1031
Diehlordiphenylguanidine ...
C 13 H n Cl 2 N 3
140-141
B. S., 32, 170
a-amidotolyl-phenylhydro-
chloride
Fr. C 6 H 4 PhMe=1.4
C 13 H 14 C1N
280-283 p.d.
Carnelley
29, 21
?-
....
200
Jackson
B., 10, 961
32, 606
Benzylidene plienyldiamine
NHPh.CHPh.NH 2 +HCl
C 13 H I5 C1N 2
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(CH 2 .U 6 H 4 C1) 2 = ?
Oj 4 iij301 2 ^
Liquid
Berlin
A., 151, 141
40, 806
zylamine
" >!
=(1.4) 2
....
29
Jackson and Field
A. C. J., 2, 94
40, 805
Trichlorethylidene diphenyl
CCl 3 .CH.(NHPh) 2
C 14 H 13 C1 3 N 2
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,H 4 Cl) s =(1.4) 2
C 14 H 14 C1 3 N
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-
C01 3 .CH(NHPh) 2 +HCl
C 14 H 14 C1 4 N 2
196
Amato
G. I., 5, 461
30, 638
diamine hydrochloride
CCl 3 .CH(NHPh) 2 +2HCl
C 14 H 16 C1 5 N 2
w.m.
))
Dibenzylamine hydroohloride
(C 6 H 6 .CH 2 ) 2 HN+HC1
C 14 H 16 C1N
250
Limpricht
A., 144, 304
vi., 337
)
V
255-256
Spica
G. I., 10, 515
40, 262
?
....
C I6 H 9 a 2 N
162-1C3
Gabriel
B., 18, 2450
48, 1231
Cinnamaldehyde anilide hy-
Ph.CH:CH.CH : NPh+HCl
C 15 H 14 01N
149
Peine
B., 17, 2117
46, 1345
drochloride
Methy lacridine methochloride
C 13 H 8 NMe+MeCl
C 15 H 16 C1N
....
130-135 d.
Bernthsen
A., 224, 1
46, 1356
Ainidomethyl dihydro anthra-
C 14 H 10 Me.NH 2 -)-HCl
C 15 H 16 C1N
....
245
Roemer
B., 16, 1633
44, 1137
cene hydrochloride
? hydrochloride
C 16 H 16 N 6 +HC1
C 16 H 17 QN 6
....
252
Berger
M. G, 5, 451
48, 387
Dimethylphenylbenzylam-
(Ph.CH 2 .NPhMe 2 )Cl
C 15 H 18 C1N
+H 2
110
Michler& Gradmaim
B., 10, 2079
moniutn chloride
Dibenzylguaiiidine hydro-
NH : CCNH-CHsiPh^+HCl
C 15 H 19 C1N 3
176
Strakosch
B., 5, 696
vii., 182, 582
chloride
Triarnylamine hydrochloride
(CVH^N+HCl
C 15 H 34 C1N
b. 100
Plimpton
C. R., 91, 433
40,34
Quinoline benzylchloride ....
?
C 6 H 4 .CH : OH.C : NCl.CH 2 Ph
C 16 H 14 C1N
1
+ 2H 2 O
170
129-130
Clauss and Tosse
i)
B., 16, 1277
44, 1009
i) :i
i)
) JJ
J1
))
130
)>
j>
>i "
JI
+3H 2 O
65
D
)
i) >i
11 I!
J
)
65
Glaus & Himmel-
B., 13, 2046
mann
I
Ph.N:CMe.CH 2 .OCi:NPh
C 16 H 15 C1N 2
116-117
Wallach & Hof maun
B., 8, 1570; A.,
29,604;32,188
184, 95
Trichlorethylidene di-p-tolyl-
Cl 3 .CH(NHC 6 H 4 Me) 2
C 16 H l; a 3 N 2
114-115
Wallach
B., 5, 252; A.,
vii., 311,1179;
amine
173, 279
25, 611 ; 28,
350
From Zu-ethide on benzo-
C 16 H 18 N 2 +HC1
C K H 19 C1N 2
257
Frankland & Evans
....
37, 565
nitril
'
Diphenylethylamine hydro-
(Ph.CH 3 .CH 2 ) 2 NH+HCl
C 16 H 20 C1N
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.C 6 H 4 CH 2 ) 2 NH + HC1
)
198
Pieper
A., 151, 129
vi., 1133
Butylacridine hydrochloride
13 H 8 N.0 4 H 9 +HC1
C 17 H 18 C1N
191
Bernthsen & Traube
B., 17, 1509
46, 1183
Tetramethylbeuzidineiuetho-
Me 2 N.C 6 H 4 .C 6 H 4 .NMe 3 Cl
C 17 H 23 C1N 2
....
228
Michler& Pattinson
B., 17, 117
46, 747
chloride
=(1.4) 2
Acutamide on pheuylcyan-
C 18 H 17 N 6 +HC1
C 18 H 18 C1N 5
softens 240
256-264 u.c.
Berger
B., 14, 1256
40, 810
araide
Base from aceto-o-toluide ...
....
C 18 H 19 C1N 2
....
52-53
Wallach
A., 214, 208
44, 48
J-
71-72
D
B., 9, 1214
31, 92
Trichlorethylidene dixylyldi-
CCl a .CH(NH.C 6 H 3 Me 2 ) 2
C 18 H 21 C1 3 N 2
95-99
j>
A., 173, 283
28, 350
amine
Ethylene dipheuyldimethyl-
C 2 H 4 (NClMe 2 Pli) 2
C 18 H 26 C1 2 N 2
124
Hiibner, Tolle, and
A., 224, 331
46, 1318
auimoninm chloride
Athenstadt
?
C 19 H 13 N+HC1
C, 9 H 14 C1N(?)
a. 220
Bernthsen
A., 192, 1
34, 789
Dichlorbenzenyldiphenyl-
NPh 2 .CCl 2 .Ph
C 19 H 15 C1 2 N
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
CH 2 (C 9 H 6 N) 2 +2HC1
C 19 H 16 C1 2 N 2
168
llhousopoulos
B., 16, 2005
44, 1150
chloride
Benzenylisodiphenylamidine
NPhj-CPhiNH+HCl
C 19 H 17 C1N 2 (
223d.
Beruthsen
A., 192, 1
34, 788
hydrochloride
Triphenylmethylamine hy
CPh 3 .NH 2 +HCl
C 19 H 18 C1N
....
244
Elba
B., 16, 1276
44, 1000
drochloride
Triphenylguanidine hydro
PhN : C(NHPh) 2 +2HCl
C 19 H 19 C1 2 N 3
207
Sell and Zierold
B., 7, 1231
28, 270
chloride
Cinchonine chloride
....
C 19 H 21 C1N 2
52
Koenigs
B., 13, 287
38, 674
....
)>
....
72
B., 14, 1854
Diquiuoline methochloride ..
C I8 N 2 H 12 +2MeCl
C 20 H IS 01 2 N 2
+ 6H 2 O
260
Osteruieyer
C. C., 1884, 970
48, 672
Triphenylethylamine hydro
CPh 3 .CH 2 .NH 2 +HCl
C^H^CIN
....
247
Elbs
B., 17, 700
46, 1031
chloride
Chlorhydrobenzamide
isomeric
C 21 H I7 C1N 2 (?
183
A., Ill, 158
jj
., (
186
A., Ill, 146
Lophine hydrochloride
C 21 H 16 N 2 +HC1.
160
Kiihn
....
iii., 735
!) )!
....
)
155
Brunner
A., 151, 135
vi., 793
Trichlortribenzylamine
N(CH 2 .C fi H 4 Cl) 3 =(1.4) 3
C 21 H 18 C1 3 N
S8-89
Berlin
A., 151, 139
vi., 338
n
)
78-5
Jackson and Field
A. C. J., 2, 92
40, 805
hydro-
N(CH 2 .C 6 H 4 C1) 3 +HC1
C 21 H 19 01 4 N
abt. 196
>
chloride
=(1-4),
i
)i
)J
170-175
Berlin
A., 151, 139
vi., 338
Tribenzylamine hydrochlo-
(C 6 H 6 .CH 2 ) 3 N+HC1
C 21 H 22 C1N
....
227-228
Spica
G. I., 10, 515
40, 262
ride
?
....
C-^H^CIN,
....
162-163
Berlin
A., 151, 136
Phenylbenzo-3-naplithacri-
C 6 H 4 .CPh.C 10 H 6 .N + HCl
C 23 H 16 C1N
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.CH 2 .CH 3 ) 3 N+HCl
C^HjjCON
>...
137-138
Spica
G. I., 9, 555
38, 241
chloride
Trixylylamine hydrochloride
(Me.C 6 H 4 .CH 2 ) 3 N+HCl
))
212
5 ieper
A., 151, 129
vi., 1133
Triphenylmethylbenzyl-
Ph.CH 2 .NH.CPh 3 +HCl
C 26 H 24 C1N
....
249
Elbs
B., 17, 703
46, 1031
amine hydrochloride
Hydrocinnamide hydrochlor-
(Ph.CH:CH.CH 2 ) 3 N 2
C 27 K, 5 C1N 2
+3H 2 O
220-221
'eine
B., 17, 2111
46, 1344
ide
Benzylamarine ethochloride
C 21 H l; (CH 2 Ph)N 2 +EtCl
C 30 H 29 C1N 2
125 u.c.
Glaus & Kohlstock
B., 18, 1854
48, 1133
Ethylbenzylamarine hydro-
C 21 H 16 Et(CH 2 Ph)N 2 +HCl
)
135 u.c.
i
j)
1)
chloride
Benzylamarine benzochloride
C 21 H 17 (CH 2 Ph)N 2
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
PEtCl 4
PPrfCl,
C 2 H 5 C1 4 P
O.HyCljP
135
100 d.
Liquid
Michaelis
B., 13, 2175
40, 158
Phenylphosphodichloride ...
PPhCl,
C 6 H 5 C1 2 P
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 ....
PPh01 4
PEt.,( 1,
)
C,H 5 C1 4 P
C B H, 5 C1,,P
224-6 (763-6)
73
100
Thorpe
Michaelis
37, 347
B., 6, 817
27, 168
iv., 611
Tolylphosphodichloride
C 6 H 4 Me.PCl.= 1.2
v ^6 16 2
C.H 7 C1 2 P
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
C 6 H 4 Me.PCl 2 =1.4
C 7 H 7 C1 2 P
245
25
Michaelis & Panek
A., 212, 212
42, 959
>! !)
1)
240
Liquid
Michaelis
B., 12, 1009
36, 721
Tolylpliosphotetrachloride ...
C 6 H 4 Me.PCl 4 =1.2
C-H 7 C1 4 P
....
Solid
Michaelis & Panek
A., 212, 216 ; B.
38, 641; 48, 900
13, 653
)
= 1.4
i)
....
42
D
Phenylmethylphosphochlo-
PPhMeCl
C 7 H 8 C1P
160
KShler & Michael i
B., 10, 814
32, 451
ride
Xylylphosphodichloride
C 6 H 3 Me. 2 PC',,
C 8 H 9 C1 2 P
260-290 (?)
Liquid
Michaelis & Panek
A., 212, 236
42, 964
....
C 6 H 3 Me 2 .PU 4
C 8 H 9 C1 4 P
270
Liquid 18
1
D
Naphthylphosphodichloride
C IO H r .PCl 2
C 10 H 7 C1 2 P
a. 360 p. d.
Kelbe
B., 11, 1500
1
11
a. 250
B., 9, 1051
Diphenylphosphocliloride ....
PPh 2 Cl
C 12 H 10 C1P
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...
PPh 2 C1 3
CijHiQUljF
....
Solid
Michaelis
B., 10, 627
32, 453
Triphenylbenzylphosphochlo-
PPL 3 (CH 2 Ph)Cl
CjjHMpLP
+H 2
287
Michaelis & Soden
A., 229, 334
48, 1135
ride
Tetrabenzy Iphosph ochloride
P(CH 2 Ph) 4 Cl
C^H^CIP
224-225
Letts and Collie
T. E., 30, 181 ;
40, 722; 42,
P.E.S.E., 11, 46
724
Methylarsendichloride
AsMeCl 2
CH 3 Cl 2 As
133
Baeyer
A., 107, 279
i., 401
Ethylarsendichloride
AsEtC'l 2
C 2 H 5 Cl 2 As
156
Coste
A., 208, 34
Dimethylarsenchloride (caco-
AsMejCl
C 2 H 6 ClAs
a. 100
b. 45
Bunsen
A., 37, 31 ; 42, 22
i., 405
dylchloride)
Phenylarsendichloride
AsPhCl 2
C 6 H,,Cl 2 As
252-255
Liquid
Michaelis
B., 9, 1567
31,311
n
*
249
B., 8, 1317
29, 610
Phenylarsentetrachloride ...
AsPhCl 4
C 6 H 6 Cl 4 As
cf. B., 9, 1568
45
B., 10, 622
32, 452
Tolylarsendichloride....
C 6 H 4 Me.PCl 2 =1.2
C 7 H 7 CLAs
264-265
Liquid
Coste and Michaelis
B., 11, 1889; A.,
36, 1(53
201, 248
,, ....
= 1.4
J)
267
31
)
Naphthylarsendichloride
C 10 H 7 .AsCl 2
C 10 H 7 Cl 2 As
....
63
Michaelis & Schulte
B., 15, 1954
Phenyldiethylarsendichloriile
AsPhEt 2 Cl 2
C 10 H 15 Cl 2 As
Crystalline
Michaelis
B., 10, 626
32, 453
Diphenylarsenchloride
AsPhjCl
C 12 H 10 ClAs
333
Liquid
Coste and Michaelis
B., 11, 1885; A.,
36, 162; 38, 396
201, 215
11
11
330
Michaelis
A., 207, 195
Diphenylarsentrichloride ....
AsPh 2 Cl 3
C 12 H 10 C1 3 A S
cf.A.,201,222
174
B., 9, 1569
31, 311
Ditolylarsenchloride ....
(C 6 H 4 Me) 2 AsCl=(1.4) 2
C 14 H 14 ClAs
340-345
Coste
A., 208, 18
Diphenylethylaraendichloride
AsPh 2 EtCl 2
C 14 H 15 Cl 2 As
....
137
Michaelis
A., 201, 235
Triphenylarsendichloride
AsPh 3 Cl 3
P TT PI A a
^18- LJ -15^- 1 2"- a
cf.A.,201,242
171
Coste and Michaelis
B., 11,1888
36, 162
Tritolylarsendichloride
As(C 6 H 4 Me) 3 Cl 2 =(1.4) 3
C 21 H 21 C1 2 A 8
....
214
Coste
A., 208, 27
40, 905
Triethylstibine dichloride ...
SbEt 3 Cl 2
C 6 H 16 01 2 Sb
b. 12
A., 88, 323; 97,
i., 342
332
Tritolylstibine dichloride ...
Sb(C 6 H 4 Me 3 )Cl 2 =(1.4) 3
tvgj ji gjv/laO D
....
156-5
Hichaelis &Genzken
B., 17, 925
46, 1136
Ethylbismuthdichloride
BiEtCl 2
C 2 H,,Cl s Bi
....
Crystalline
A., 92, 376
(7.) CHBrl.
Dibromiodomethane
CHBrJ
6
....
A, 22, 233
i., 680
Dibromiodethylene
CIBrlCHBr
C 3 HBr,I
....
66
Homolka and Stolz
B., 18, 2285
48, 1198
a- Bromiodethylene ....
CH 2 : CBrI
C 2 H 2 BrI
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
CjH 2 BrI
162
Reboul
vii., 491
-
jj
u
150 p.d.
25
Lagermark
B., 6, 1211
JJ
lode thy lenedibromide
CH 2 Br.CHIBr
C-jH^Br^
170-180 d.
Simpson
P. R. S., 22, 51
27, 564
Ethylidene iodobromide
CH 3 .CHIBr
C 2 H 4 BrI
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 ,,
CH 2 Br.CH 2 I
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
CH 3 .CBrI.CH 3
C 3 H 6 BrI
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 ....
CH 3 .CBr CH 2 I(2)
JJ
160-168 p.d.
Liquid
Simpson
P. R. S., 22, 51
27, 564
Tribromiodobenzene
Br 3 .I=1.3.5.6
C 6 H 2 Br 3 I
....
103-5
Silberstein
J. p. [2], 27, 119
44,661
Bromidobenzene
C 6 H 4 BrI=1.4
C 6 H 4 BrI
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.Br 2 .I 2 =1.3.5.2.4
C 7 H 4 Br 2 I 2
...
68
Wroblewsky
B., 9, 1055
30, 511
Dibromiodtoluene
Me.Br 2 .I=1.3.5.4
C 7 H 5 Br s I
270
86
jj
A., 168, 190; 192,
27, 54 ; 34, 978
209
lodobenzyl bromide
C 6 H 4 I.CH 2 Br=1.2
C 7 H 6 BrI
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
C 1() H 6 BrI=a^ 2 ;
3 10 H 6 BrI
....
68
Meldola
47, 523
jj
=aja 2 ;
jj
83-5
jj
jj
jj
=a 1 /3 l . ;
jj
....
94
jj
?j
(8.) CHBrO.
Tribromacetaldehyde
CBr 3 .COH
C i! HBr 3 O
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
....
C 2 HBr 3 O
200 p.d.
67
Cloez
A., Ill, 178
iv., 340
Dibromacetyl bromide
CHBr 2 .COBr
194
....
Gal
B. S., 5, 172
vi., 21
Tribromaeetic acid
CBr 3 .COOH
C 2 HBr 3 2
....
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
CHBr 2 .COH
C 2 H 2 Br 2
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
CHBr 2 .COOH
C 2 H 2 Br 2 O 2
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
CH 3 .COBr
C 2 H 3 BrO
81
Gal
B. S., 5, 172
vi., 20
JJ
81
Hitter
J., 8, 504
Bromethylene oxide
CHBr.O.CH 2
89-92
Demole
B., 9, 51
29, 693
Bromacetic acid
CH 2 Br.COOH
C 2 H 3 Br0 2
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
CBr 3 .CH.(OH) 2
C 2 H 3 Br 3 O 2
53-5
Schaffer
B., 4, 366
24, 558; vii.,
209
Dibromethyl alcohol
CHBrj.CHj.OH
CTT "D_ f\
nl,J&ln\J
179-181
....
Demole
B., 9, 49
29, 692
?
Me.CBr(OBr)OH
C 2 H 4 Br 2 O 2
....
36-37
Hell & MUlhauser
B., 10, 2105
34, 289
Ethylene Bromhydrin
CH 2 Br.CH 2 .OH
C ; H 6 BrO
147
Henry
A. C. [4], 27, 243
11 11
145-150
Demole
B., 9, 48
?
....
C 2 H 7 BrO 3
89-91
40-45
B., 9, 50
Tribromacrylic acid
CBr 2 :CBr.COOH
C 3 HBr 3 O 2
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
CBr 3 .CO.COOH
C 3 HBr 3 3
....
90
Grimaux
C. R, 78, 974
27, 887
i) 11
J)
+ 2H 2
104
11
B. S., 21, 393
27, 888
Pentabromacetone
CHBr 2 .CO.CBr 3
C 3 HBr 6 O
75
Mulder
J. p., 91, 472
vi., 27
76
Benedikt
C. C. [1878], 101
34, 499
Pentabromomethylic .acetate
CH 2 Br.COOCBr 3
C 3 HBr 5 2
....
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
CBr 2 :CH.COOH
C 3 H 2 Br 2 2
....
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
CHBr 2 .CO.COOH
C 3 H 2 Br 2 O 3
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
CBr a .(COOH) 2
C 3 H 2 Br 2 O 4
....
126-128
Petrieff
B., 7, 402
27, 787
Tetrabromacetone ....
....
C 3 H 2 Br 4 O
+2H 2
42-43
Mulder
J. p., 91, 472
vi., 27
Tetrabrompropionic acid
CHBr 2 .CBr 2 .COOH
C 3 H~Br 4 2
....
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
CBr 3 .CHBr.COOH
118-120
Mabery
A. C. J., 5, 251
46, 664
'S-Bromaerylic acid
....
C 3 H 3 BrO 2 .
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
CH 3 : CBr.COOH
C 3 H 3 Br0 3
....
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
CH 2 Br.CO.COOH
C 3 H 3 Br0 3
....
Liquid
Wichelhaus
B., 1, 265
vi., 980
Tribrompropionic acid
CBr 3 .CH 2 .COOH
C 3 H 3 Br 3 2
....
53
Fittig and Petri
A., 195, 73
40, 800
CH 2 Br.CBr 2 .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
CHBr 3 .CHBr.COOH
....
118
Hill and Andrews
A. C. J., 4, 177
42, 1187
I! >!
....
118
Hill
A. C. J., 4, 273
Tribromlactic acid
CBr 3 .CH(OH).COOH
C 3 H 3 Br 3 3
141-143
Wallach & Eeinckt
B, 10, 2129
34, 403
Dibromacetone
CH 2 Br.CO.OH 2 Br
C 3 H 4 Br 2
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 ....
CH 2 Br.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 ....
CH 3 .CBr 2 .COOH
C 3 H 4 Br 2 O 2
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
,, ,,
+7H 2
s. 5
Linnemann & Penl
B., 8, 1098
29, 64
Dibromlactic acid
...
C 3 H 4 Br z 8
....
98
B., 8, 1101
Propionyl bromide
CH 3 .CH 2 .COBr
C 3 H 5 BrO
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
CH 2 Br.CH.CH 2 .0
138
Berthelot & DeLuca
J., 9, 600
i., 668
139
....
ii., 898
M
138-140
Henry
A., 154, 363
vii., 210
Bromacetone ...
CH 3 .CO.CH 2 Br
1 Aftl A*** H
Eiche
,
a-Bromallyl alcohol
CH 2 1 CBr.CH 2 .OH
"
155
Henry
B., 5, 453 .
vii., 50, 1018
,, ,,
M
152 (776)
B., 14, 404
25, 686
Methylic bromacetate
CH 2 Br.COOMe
C 3 H 5 BrO 2
144 d.
....
Perkin and Duppa
11, 22
i., 065
a-Brompropionic acid
CH 3 .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-
CH 2 Br.CH 2 .COOH
9)
it..
6V5
Bichter
Z. C. [1868], 450
n
61-62
Beckurts and Otto
B., 18, 227
48, 506
/3-Bromlactic acid
CH 2 Br.CH(OH).COOH
q,H.BrQ,
89-90
Melikoff
B., 13, 958
38, 800
Dibrompropyl alcohol
CH 2 Br.CHBr.(JH 2 .OH
C 3 H 6 Br 2 O
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
C 3 H 5 Br 2 .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
CH 2 Br.CH 2 .CH 2 .OH
C 3 H 7 BrO
98-112(185)
Liqviid
Fruhling
M. C., 3, 697
44, 42
drin
Pn.pylene
OH 3 .CHBr.CH 2 .OH
145-148
Z. C. [1870], 423
a-Glycerol-bromhydrin
CH 2 Br.CH(OH).CH.,(OH)( ?)
C 3 H 7 BrO 2
180 (10)
Berthelot and Luca
A. C. [3], 48, 304
i., 668
**' )i
CH 2 (OH).CHBr.CH 2 (OH)(?)
160 (66)
L. 15
Veley
C. N., 47, 39
1
C 3 H 8 Br 4
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
C 4 HBrO 3
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
C 4 HBr 3 O 2
....
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
C 4 H 2 Br 2 O
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
C 4 H 3 Br 2 O 2
88
Tonnies
B., 12, 1203
36, 918
Isodibromosuccinic anhydride
CBr .CH 3 .CO.O.CO
C 4 H 2 Br 2 O 3
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
C 2 Br, ! (COOH) 3
C 4 H 2 Br 2 O 4
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.,.CH 2 .CO.CBr 3
C 4 H 2 Br 6 O
89-90
Demole
B., 11, 1712
36, 220
a-Dibromfurfurane tetrabro-
CH Br.CBr 2 .O.CBr 3 CHBr
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-
CH 2 Br.COO.CBr 2 .CBr 3
C 4 H 2 Br 6 2
195-198
Liquid
Kessel
B., 11, 1923
36, 1.38
tate
Octobromethyl oxide
(CBr 3 .CHBr) 2
C 4 H 2 Br 8 O
132-135
B.. 10, 1668
34, 128
(450-470)
?
....
C 4 H 3 Br0 2
84
Limpricht
A., 165, 292
vii., 1032 ; 26,
625
Bromsuccinic anhydride
CH 2 .CHBr.CO.O.CO
C 4 H 3 BrO b
137(11)
26-31
Anschiitz & Bennert
B., 15, 643
42, 828
i " i
?
)
....
109
....
J. p. [2], 23, 441
Acid from mucobromic acid
C 4 H,Br0 4
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
Io-
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
C 4 H 3 Br s O 4
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,,
C 4 H 3 Br 5 2
175-177
Liquid
Kessel
B., 11, 1921
36, 138
tate
Dibromomethacrylic acid ....
fr. CH,:CMe.COOH
C 4 H 4 Br 2 2
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
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.CH 2 .CBrj.COOH
J)
....
160
Kekule
As. 2, 89
v., 459
Tetrabrombutyric acid
C 3 H 3 Br 4 .COOH
C 4 H 4 Br 4 O 2
....
115
Limpricht
A., 165, 296
vii.,828;26,(;2.-,
Bromomethacrylic acid
CHBr I CMe.COOH
C 4 H 5 BrO,.
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
CH s :C(CH 2 Br).COOH
)
65-66
Krusemark
A., 206, 12, 22
40, 416
0-Bromcro tonic acid
CH 3 .CBr:CH.COOH
))
....
90
....
J. p. [2], 25, 388,
394
ft-
>
)J
92
Michael & Norton
A. C. J., 2, 15
40, 799
- >i 11
CH 3 CH: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.
C 4 H 5 Br0 3
abt. 150
....
Kichter
C. C., 1875, 446
36, 139
Bronisucciuic acid
COOH.CHBr.CH 2 .COOH
C 4 H 5 BrO 4
159
A.
11 .... ....
>
....
160
Anschiitz & Bennert
B., 15, 643
11 11 .... ....
>
))
....
160
Fittig
B., 9, 122
29, 898
Aldehyde broraal
CBr 3 .CHO+OH 3 .CHO
C 4 H s Br 3 O 2
abt. 175
Liquid
Schiitzenberger
B. S. [2], 19, 8
26, 487
Ethylic tribroinacetate
CBr 3 .COOEt
JJ
225
Gal
B. S., 5, 172
vi., 21
Tribrombutyric acid
C 3 H 4 Br 3 .COOH
))
....
111
Michael & Norton
A. C. J., 2, 162
40, 799
,1 ....
J)
114
i?
ji
)J
n-Bromisobutyric bromide ....
CMe 2 Br.COBr
C 4 H fi Br 2 O
162-164
Kaachirsky
C. C., 1881, 287
42,37
a-Brombutyric
CH,.CH 2 .CHBr.COBr
j
172-174
11
1)
i
Ethylic dibromacetate
CHBr s .COOEt
C 4 H 6 Br 2 2
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 ....
CH 2 Br.COO.OH 2 .CH, ! Br.
J
230-240 d.
....
Demole
B., 9, 557
30, 283
11 11
CH 2 Br.COO.CHBr.CH 3
)J
180-240 d.
Kessel
B., 10, 1995 ; 11
34, 133
(o.p.);130-
1917
135 (360)
Dibromethylic acetate
CH 3 .COO.CH s .CHBr 2
193-195 u.c.
Demole
B., 9, 51
Methylic-a-a-dibrompro-
CH 3 .CBr 2 .COOMe
T
175-179
....
Philippi
A., 171, 323
pionate
Methylie-a-/3-dibrompro-
CH 2 Br.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} 7 ric 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
CH s .O.C 3 H 4 Br
C 4 H.BrO
115-116
Henry
Z. C. [2], 6, 575 ;
vii., 50 ; 25,
B., 5, 455
687
Isobutyric bromide ....
CHMe 2 .CX)Br
Jl
116-118
Kaschirsky
C. C., 1881, 273
42,37
Butyric bromide
CH 3 .CH 2 .CH 2 .COBr
)J
126-127
i
i>
D
11 )) . ....
M
I
128
J., 1857, 344
Bromisobutyric aldehyde ....
....
(0 4 H 7 BrO) n
128-129
A., 211,353
Bromethylic acetate....
CH 3 .COO.CHBr.CH 3
C 4 H 7 BrO 2
135-145 p.d.
....
Tawildarow
B., 7, 731
27, 1080
11 11
CH 3 .COO.CH 2 .CH.,Br
i)
161-163
....
A., 171, 121
Ethylic bromacetate
CH 2 Br.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:H 3 .CH 2 .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 ....
CH 3 .CH 2 .CHBr.COOH
C 4 H 7 BrO 2
214-217
>
Kaschirsky
C. C. [1881], 278
42, 37
i3-Bromisobutyric acid
CH 2 Br.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 ....
C 3 H 5 Br(OH).COOH
C 4 H 7 BrO 3
90
Melikoff
B. S., 43, 115
48, 650
11 11
3J
100-102
....
J. R., 7, 179
Bromhydroxyisobutyric acid
CH 2 Br.CMe(OH).COOH
....
100-101
Kolbe
J. p. [2], 25, 376
44, 573
>! 11
....
101
Melikoff
B. S., 43, 115
48, 650
Acetone bromoform ....
COMe 2 +CHBr 3
C 4 H.Br 3 O
....
167
Willgerodt
B., 14, 2458
42, 492
11 11
11
....
175
Willgerodt&MUller
C. C. [18S4], 808
48, 648
n i
+xH 2
165-167
11
V
Bromal alcoholate
CBr 3 .CH(OH)(OEt)
C 4 H 7 Br 3 2
....
44
Schaffer
B., 4, 367
24, 558 ; vii.,
209
Glycerol methyldibrom-
C 3 H 5 Br 2 (OMe)
C 4 H 8 Br 2
185
Henry
B., 5, 455
25, 687
hydrin
Ethylene oxybromide
....
C 4 H 8 Br 2 2
95
65
....
A. C. [3], 69, 317
ii., 580
Erythrol dibromhydrin
C 4 H 6 Br 2 (OH) 2
....
130
Champion
C. R., 73, 114
24, 811 ; vii.,
471
Bromethyl oxide
CH 2 Br.CH 2 .OEt
C 4 H 9 BrO
127-128(755)
Liquid
Henry
C. R., 100, 1007
48, 882
Diethyleneglycol bromhydrin
CH 2 Br.CHj.O.CH 2 .CH,.OH
C 4 H 9 BrO 2
205
....
....
A. C. [3], 67, 286
?
(C 2 H 4 O 2 ) 2 .Br 2 .HBr.
C 4 H 9 Br 3 4
....
8d.
Steiner
B., 7, 184
27, 566
Ethyl oxide + bromine
Et 2 O+Br 3
C 4 H 10 Br 3
....
22
A., 167, 86
Tribrompyromucic acid
O.CBr I CBr.CBr : C.COOH
i j
C 5 HBr 3 3
218-219
Hill and Sanger
B., 17, 1763
43, 1306
Dibrornpyromucic acid
O.CBr : CH.CBr : C.COOH
C 5 H 2 Br 2 3
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-
CBr 3 .CH.O.CH(CBr 3 )COO
C 5 H 2 Br 6 3
158
Wallach & Reiucke
B., 10, 2129 ; A.,
34, 404
lactate (Bromalide)
i j
193, 52
Bromcitraconic anhydride ....
C 3 H 3 Br.CO.O.CO
C 5 H 3 Br0 3
....
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.
+H 2
d. 120
....
J. p. [2], 23, 441
8-Brompyromucic acid tetra-
O.CBr 2 .CHBr.CHBr.CBr.
C 5 H 3 Br 6 3
....
170 d.
Hill and Sanger
B., 17, 1763
46, 1306
bromide
i i
COOH
Itadibrompyrotartaric anhy-
C 3 H 4 Br 2 .CO.O.CO
C 5 H 4 Br 2 3
50
Petri
B., 14, 1637
40, 1032
dride
r' " J
Pyromucic acid tetrabromide
O.CHBr.CHBr.CHBr.CBr.
C 5 H 4 Br 4 0,
159-160 d.
Tonnies
B., 11, 1086
34,786
i i
COOH
Bromitaconic acid
....
C 5 H 5 Br0 4 .
....
164 d.
....
J., 1873, 584
Tribromethylidene lactate ....
CBr 3 .CH.O.CHMe.COO
C 5 H 6 Br 3 3
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
CBr 3 .CO.COOEt
95-97
....
J. R., 8, 125
Tribrompyrotartaric acid ....
CTT T>_ //"1/^/~\TT\
1 Ll-,L>T'A \..'\J\J fl l.y
C 5 H 6 Br 3 O 4
w.m. 240
Lagermarck
Z. C. [2], 6, 303
vii., 1034
Ethylic /3-dibromacrylate ....
CBr 2 : CH.COOEt
<; 5 H 6 Br 2 2
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
....
C 5 H 6 Br 2 2
....
81
Wolff
A., 229, 24!)
48, 1121
Dibromlevulinic acid
....
C 5 H 6 Br 2 3
d. 130-140
112-113
Hell and Kehrer
B., 17, 1982
46, 1298
Methylic dibromsuccinate ...
COOMe.CHBr.CHBr.COOH
C i H.Br i 4
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.(CH 2 ) 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
C 5 H 7 Bi-0 2
155-158-5
Wagner and Tollenb
A., 171, 350
27, 681
Bromallylic acetate ....
CH 2 : CBr.CH 2 .OAc
163-164
Henry
B., 5, 453
25, 686 ; vii.,
50, 1018
Bromvalerolactone
))
....
1.-15
Messerschmidt
A., 208, 101
42, 35
Bromlevulinic acid
....
C 5 H ; Br0 3
59
Wolff
A., 229, 249
48, 1124
Bromethylmalonic acid
CH 2 Br.CH 2 .CH(COOH) 2
C 5 H 7 BrO 4
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....
C 3 H 5 Br(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,H 4 Br(OH)(COOH) 3
C 5 H 7 Br0 5
....
156 d.
Scherks
A., 227, 233
48, 513
acid
Ethylic tribromlactate
CBr a .OH(OH).COOEt
C 5 H 7 Br 3 3
....
44-46
Wallach
A., 193, 52
34,403
Ethylic u-dibrompropionate
CH 3 .CBr 2 .COOEt
C 5 H 3 Br 2 2
190-191
Philippi and Tollens
B., 6, 517
vii., 1011; 26
1019
i) ?)
))
191-192
Tollena
A., 171, 324
,, o/3-
CH 2 Br.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. CH S .(CH 2 ),.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
C 2 H 4 Br.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
CH 3 .CHBr.CBrMe.COOH
86-5
Schmidt
B., 12, 255
) "
)
)
....
86-86-5
Pagenstecher
A., 195, 123
36, 456
Broiuallylethyloxide
CH 2 :CBr.CH,,.OEt
C 5 H 9 BrO
130-135
Liquid
Henry
B., 5, 189
vii., 50
Isovaleric bromide
CHMe 2 .CH 2 .COBr
)}
143
Buchamp
C. E., 42, 224
v., 979
Ethylic a-brompropionate ....
CH 3 .CHBr.COOEt
C 5 H 9 Br0 2
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.CH 2 .CHBr.COOMe
|]
165-172
Duvillier
C. E., 88, 598
36, 523
a-Bromisovaleric acid
CHMe 2 .CHBr.COOH
226-230
Gahours
As., 2, 78
v., 978
Q-Broni-ni6thylethylacetic
( 1 W PIT PTLf^U nr\/^TT
^n 3 .^n 2 .OJMer>r.(JOOM
))
66-66-5
Pagenstecher
A., 195, 110
36, 455
acid
Glycerol acetobromhydrin ....
C 3 H s Br(OAc)(OII)
C 5 H 9 Br0 3
175 (100)
J., 1878, 523
ethyldibromhydrin
C 3 H 5 Br 2 (OEt)
CsHjoBijO
193-195
Morkownikoff
Z. C., 1865, 554
vi., 99
Tribromquiuone
G,HBr,:0,
C 6 HBr 3 2
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 ....
C 6 Br 3 (OH) : 2
C 6 HBr 3 3
..
206-207
Barth and Schreder
M. C., 5, 589
48, 520
Bromoxytetrabrombenzene ...
C 6 HBr 4 .OBr
C 6 HBr s O
121
....
M. G, 1, 361
Pentabromphenol
C 6 Br 5 .OH
....
225
Korner
A., 137, 210
vi., 908
Pentabromresorcinol
C 6 Br 4 OH.OBr 6 5.4 2 3.1
C 6 HBr 5 O 2
113-5
Stenhouse
P. E., 20, 72; A.,
25, 298; vii.,
163, 184
' > J
1042
Phlorobromin
C c HBr O
152
Benedikt
A., 189, 166
34, 499
Brom. deriv. of Bromanil-
C 6 HBr, 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
C 6 H 2 Br 2 6
+3H S
d. 105
J. p. [2], 26, 467
Bromoxytribrombenzene ....
C H Bi 3 .OBr
C 6 H 2 Br 4
....
109
Benedikt
A., 199, 128
J)
118
M. C., 1, 360
38, 246
Tetrabromphenol
C 6 HBr,.OH=6. 4.3.2.1
120
Korner
A., 137, 209
vi., 908
Tetrabromresorcinol.. .
C c Br 4 (OH) 2 =6.5.4.2.3. 1
C 6 H 2 Br 4 2
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
C 6 H 3 Br:0
C 6 H 3 BrO
....
195
Marker
A., 124, 250
v., 161
Bromqumone . ....
C,H 3 Br I O 2 =5.4.1
C 1 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
C 4 HJBr(NH 2 )(COOH) 2
C,H,Bi0 4
....
176
Pechmann
B., 17, 2397
48, 175
Di bromeitraconimide
C 4 H 2 Br 2 :(CO) 2 :NH
C 6 H 3 Br 2 2
....
142-144
Mendini
G. I., 15, 182
48, 1126
Tribromphenol
C 6 H 2 Br 3 .OH=6. 4.2.1
C 6 H 3 Br 8
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
C 6 HBr 3 (OH) 2 =('0 2 4.3.1
C 6 H 3 Br,0 2
+xH 2
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
C 6 Br 3 (OH) 3 =6. 4.2.5.3.1
C 6 H 3 Br 3 3
148 u.c.
Webster
47, 424
Bromeitraconimide
C 4 H 3 Br:(CO) 2 :NH
C 6 H 4 Br0 2
....
179-182
Mendini
G. L, 15, 182
48, 1126
Dibromphenol
C 6 H 3 Br 2 .OH=4.2.1
C 6 H 4 Br 2
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 ...
C 6 H 2 Br 2 (OH) 2 =?.?.3.1
C 6 H 4 Br 2 2
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
(=C 6 H 3 Br.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
C 3 HBr 2 O.COOAc
C 6 H<Br.0 4
53-54
Jackson and Hill
B., 11, 1673
36, 224
Broniphenol . . .
O r ,H 4 Br.OH=1.2
G-H-BrO
236-238
Liquid 10-12
Fittica
J. p. [2], 28, 176
46, 55
Vy 6 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.
C 6 H 4 Br.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 .
C 6 H,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
C 3 HBr 2 O.COOEt
C 6 H 6 Br 2 3
....
50-51
Jackson and Hill
B., 11, 1672
36, 224
Tetrabromadipic acid
C 4 H 4 Br 4 (COOH) 2
C 6 H 6 Br 4 4
....
200-211
Limpricht
A., 165, 271
vii., 29 ; 26,
623
Methylic brommaleate
C 2 HBr(COOMe) 2
C 6 H 7 Br0 4
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
C 4 H 6 Br 3 (COOH) 2
C 6 H 7 Br 3 4
....
177-180
A., 165, 269
vii., 28 ; 26,
623
Dibromallyl oxide
(C 3 H 4 Br) 2
C 6 H 8 Br 2
212-215
....
Henry
B., 6, 729
26, 1123
Allylic a-^-dibrompropionate
CH 2 Br.CHBr.COO.C 3 H s
C 6 H 8 Br 2 3
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
C 6 H 8 Br 2 4
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 ....
C 3 H 5 Br,,CH(COOH) 2
....
119-121
Hjelt
B., 15, 624
42, 947
Dibromadipic acid
C 4 H 6 Br 2 (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
C 5 H 7 Br 4 .COOH
C 6 H 8 Br 4 O 2
....
178-179
Barringer & Fittig
A., 161, 325
vii., 1091
i
))
))
183
....
A.,168,277; 200,58
Etliylic bromomethacrylate
fr.CH 2 :CMe.COOH
C 6 H 9 BrO 3
192-193
Liquid
Cahours
As., 2, 349
vi., 511
Hemibromhydriu
....
D
b. 200
Berthelot and Luca
A., 101, 72
i., 669
Propylic a-dibrompropionate
CH 3 .CBr 2 .COOPr
C 6 H ln Br,O s
200-204
....
Philippi
A., 171,324
-0-
CH 2 Br.CHBr.COOPr
H
233
Weger
A., 221, 61
46, 11
Ethylic dibrombutyrate
C 3 H 6 Br 2 .COOEt.
fj
191-193
....
vi., 380
Dibromcaproic acid ....
C 5 H 9 Br 2 .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.CH 2 .CHBr.CHBr.COOH
j
....
77
Markownikoff
B., 6, 1176
. ....
ij
80-5
Fittig and others
A., 200, 35
38, 376
) )) ' ....
C 2 HBr 2 MeEt.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 ....
Me 2 .CBr.COOEt.
C 6 H n BrO 2
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
C 2 H 5 .CHBr.COOEt
C 6 H n Br0 2
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 ,,
3 H 6 Br.COOEt
11
abt. 185 p.d.
Schneider
A., 119, 115
vi., 379
Bromcaproic acid
CH 3 .(CH 2 ) 3 .CHBr.COOH
11
abt. 240
Cahours
As., 2, 78
vi., 395
11 55
C 2 H 4 Br.CHEt.COOH
11
Liquid 18
Fittig
B., 9, 121
29, 897
,, ,, ....
11
11
Liquid 18
Fittig and others
A., 200, 42
38, 377
C 3 H 5 EtBr.COOH
11
....
25
A., 200, 24
38, 375
jj
C 5 H 10 Br.COOH
11
85-86
J. B., 11, 128
Mannitol bromhydrin
C 6 H 8 Br(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
C 6 H n Br 2 .OH
C 6 H 12 Br 2
252-254
....
Destrem
B., 16, 228
Mannitol dibromhydrin
C 6 H 8 Br 2 (OH) 4
C 6 H 12 Br 2 4
....
178 d.
Bouchardat
A. C. [5], 6, 120 ;
vii., 774;
C. E., 75, 1181
26, 161
Hexylene bromhydrin
Me.CHBr.CHPr.OH
6 H 13 BrO
188-190(769)
Liquid
Henry
C. E., 97, 260
46, 34
Bromacetal .... ....
CH 2 Br.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
C 6 H 13 Br0 3
250
....
A. C. [3], 67, 286
drin
Pentabrombenzoic acid
C 6 Br 6 .COOH
C 7 HBr b O.,
234-235
Eeinecke
Z. C. [2], 5, 110
vi., 310
Tribrombenzoic acid
C 6 H 2 Br 3 .COOH = ?
C 7 H 3 Br 3 2
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
C 6 Me.Br 3 : O 2 = 1.3.4.6.2.5
11
235-236
Canzoneri & Spica
G. I., 12, 469;
44,330
B., 16, 793
Tribromdihydroxybenzoicacid
COOH.(OH) 2 .Br 3 = 1.3.5.2.4.6
C 7 H 3 Br 3 O 4
183
Barth and Senhofer
A., 159, 225
vii., 433
Pentabromorcinol
....
C 7 H 3 Br 5 2
....
126
Stenhouse
P. E. S., 20, 72;
25, 297 ; vii.,
A,, 163, 180;
879
169, 252
Dibrombenzoic acid
COOH.Br.Br= 1.2.3
C 7 H 4 Br 2 2
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 .... .*
C 6 HMe.Br 2 : (X,
C 7 H 4 Br 3 O 2
...
85
Canzcmeri & Spica
G. I., 12, 469 ;
44, 331
B., 16, 793
Dibromsalicylic acid
COOH.OH.Br 2 =1.2.(?) 2
C 7 H 4 Br 3 3
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 .Br 3 =1.2.6.3.4
C 7 H 4 Br 2 O 4
....
214 d.
Zehenter
M. C., 2, 475
42, 193
aci
Dibromgallic acid
COOH.(OH) 3 .Br 2 =1.3.4.5.2.
C 7 H 4 Br s 5
+H 2
140
Grimaux
As., 5, 235
ji
J J
jj
150
Etti
B., 11, 1882
Tetrabromcresol
Me.OH.Br 4 =1.4.2.3.5.6
C 7 H 4 Br 4
....
108-110 d.
Baumann & Briege
B., 12, 804
36, 789
Benzoyl bromide
C 6 H 5 .COBr
C 7 H 5 BrO
218-219
Claisen
B., 14, 2473
42, 514
Brombenzaldehyde ....
C 6 H 4 Br.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
C 7 H 5 BrO,,
....
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
C 7 H 5 BrO s
....
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
7 H 5 Br0 3
....
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 ....
C 6 HMe.Br.(OH).:0 2
196-197
Spica & Magnanimi
G. I., 13, 312
46, 175
Bromdihydroxybenzoic acid
COOH.(OH).j.Br =1.2.6. ?
O.H 5 BrO 4
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.
C 7 H 5 BrO 5
....
a. 200 d.
Grimaux
B. S. [2], 7, 479
vi., 628
Tribrommethoxybenzene ....
C 6 H s Br 3 .OMe
C 7 H 5 Br 3
87
Eeinecke
B. S..[2], 7, 177
vi., 173
Tribromomethoxyphenol ....
OMe.OH.Br 3 =1.2.(?) 3 .
C 7 H 5 Br 3 O 2
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 .Br 3 =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 ....
C 5 H 3 BrO 2 .COOMe
C 7 H 6 Br0 4
....
134
Pechtnann
B., 17, 2379
48, 176
Dibrommethoxybenzene
OMe.Br.Br =1.2.4
C 7 H 6 Br 2
54
Cahours
A., 52, 331
i., 305
11 11
11 11
))
272
59
KSrner
A., 137, 206
vi., 908
Bromomethoxybenzene
OMe.Br =1.4
C 7 H 7 BrO
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
(CH 2 .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.?
C 7 H 7 BrO 5
....
135
Lamparter
A., 134, 258
iv., 213
Ethylic pyromucate tetrabro-
CHBr.(CHBr) .O.CBr.COOEt
i " i
C 7 H s Br 4 3
46-48
Tonnies
B., 11, 1086
34, 786
mide
Bromterebic acid
C.H 9 BrO 4
151 d.
Frost
A., 226, 363
48, 393
Methylic ethylic dibrom-
COOMe.(CHBr)j.COOEt
C 7 H 10 Br 2 4
62-5 u. c.
Glaus
B., 15, 1846
succinate
Ethylic bromlevulinate
C 4 H 6 BrO.COOEt
CjE.^^
240 p. d.
Conrad & Guthzeit
B., 17, 2286
48, 43
Glycerol dicetobromhydrin ....
C 3 H 6 Br(OAc) 2
CVH.^rO^?
170-180(100)
Hanriot
A. C. [5], 17,62
36, 1030
Isobutylic a-dibrompropio-
CH 3 .CBr 2 .COOBu3
C 7 H 12 Br 2 O 2
213-218
Philippi
A., 171, 324
nate
Ethylic dibromvalerate
fr. CHMeEt.COOEt
ji
185
Jaff6
A., 135, 298
Bromamylene ethylate
C 6 H 8 Br.OEt.
C 7 H 13 BrO
177-180
Bauer
Z.C.P.(1861),673
vi., 1-20
11 11
is
J>
177-180
Eeboul
A., 133, 84
Isoamylic bromacetate
CH 2 Br.COOC 5 H n
CyH^BrO.,
207
.i.*
Perkin and Duppa
11,22
i., 666
Ethylic a-bromvalerate
CH 3 .(CH 2 ) 2 .CHBr.COOEt
190-192
Liquid
Juslin
B., 17, 2504
4:8, 137
a-bromisovalerate ...
CHMe 2 .CHBr.COOEt
190-194
....
Borodine
A., 119, 121
v., 978
Bromoenanthic acid
250
....
....
As., 2, 83
(ilycorol diethylbromhydrin
C 3 H,Br.(OEt) 2
C 7 H 14 Br0 2 -
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
C 6 HBr 3 :(CO) 2 : 0=14.3.2.1
C 8 HBr 3 O 3
....
157
Flessa
B., 17, 1484
46, 1186
Dibromphthalic
C 6 H 2 Br 2 :(CO) 2 :0=(?) 2 .2.1
C 8 H.Br 2 3
207-5-208
Guareschi
A., 222, 262
46, 842
>.
11 11
....
SOS
Bliinileiu
B., 17, 2491
48, 163
Tetrabromphthalic acid
C 6 Br 4 (COOH) 2 =6.5.4.3.2.1
C 8 H 2 Br 4 4
266 d.
B., 17, 2494
48, 164
Bromphthalic anhydride
C 6 H 3 Br:(CO) 2 : O=3.2.1
C 8 H 3 BrO 3
....
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. C 8 H 2 Br 2 O
207-5-208
Guareschi
G. I., 7, 24 ; G. I
31, 712; 42,
[1881], 542
734
Tribromphthalic acid
(COOH) 2 .Br 3 =1.2.3.4.?
C 8 H 3 Br 3 4
....
190-191
Flessa
B., 17, 1484
46, 1186
Dibromphthalide
....
C 8 H 4 Br 2 2
....
188-189
Guareschi
A., 222, 262
46, 842
Dibromphthalic acid
(COOH) 2 .Br 2 =1.2.(?) 2
C 8 H 4 Br 2 4
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,H 4 .CH : CH.O
C 8 H 6 BrO
....
36
Ebert
A., 226, 347
48, 391
r i
Brompiperonal
C 6 H 2 Br(COH).O.CH 2 .O
C 8 H 6 Br0 3
129
Fittig and Mielck
A., 152, 49
vi., 948
=?.1.3.4
Bromphthalic acid
(COOH) 2 .Br =1.2.3
C 8 H 6 Br0 4
....
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. C 8 H 3 BrO 3
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
C 6 H,,Br(COOH).O.CH 2 .O
....
204-205
Fittig and Mielck
A, 172, 158
27, 899
=?.1.3.4
Tribromresorcinol acetate ....
OH.OAc.Br 3 =1.3.(2) 3
C 8 H 6 Br 3 3
114
Claassen
B., 11, 1442
Pentabromethylphenol
C 6 H 4 .OH.(CBr 2 .CBr 3 )
C 8 H 6 Br 6
....
103-106 d.
....
A., 216, 284
Dibromacetophenone
Ph.CO.CHBr 2
C 8 H 6 Br 2
....
36
Eunnius
B., 10, 2010
34, 147
.,
.;..
36-37
A., 195, 161
Dibromethylenephenol
HO.C 6 H 4 .C 2 HBr 2
240-250 s.d.
37-38
A., 216, 283
?
d.
68-69
Jannasch
Z. C. [2], 7, 453
25, 241
Coumarone dibromide
C 6 H 4 .O.CHBr.CHBr
"
....
86
Fittig and Ebert
A., 216, 169
44, 474
Dibromphenyl acetic acid ....
C 6 H 3 Br 2 (CH 2 .COOH)
C 8 H 6 Br 2 2
114-115
Bedson
37,97
Dibromtoluic acid
COOH.Me.Br 2 =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
C 6 Me 2 Br 2 :0 2 =1.3.(?) 4
174
....
A., 195, 273
ii
=1.4.(?) 4
184
J. p. [2], 23, 434
Methyldibromsalicylic acid ....
OOOH.OMe.Br 2 =1.2.(?) 2
C 8 H 6 Br 2 3
145
Cahours
A. C. [3], 10 339
v., 163
Dibromanisic acid
COOH.OMe.Br 2 =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 ....
C 6 Br 2 (OMe) 2 :0 2
C 8 H 6 Br 2 4
175
lofmann
B., 8, 67
28, 56!)
ii 11
n
.75
n
B., 11, 332
34, 418
Tetrabromethylphenol
....
C 8 H 6 Br 4
58-59
....
A., 216, 283
" "
i
105-106
....
A., 156, 255
138
lantzch
A., 215, 51
44,84
Teti'abrom-/3-orcinol
C: 6 Me 2 Br 2 (OBr) 2
C 8 H 6 Br 4 2
....
101
Stenhouse and
A., 203, 293
37, 401
'
Groves
'
....
C 8 H 7 BrO
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.CH 2 Br
C 8 H,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
C s H-BrO 3
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
(CH 2 .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
C 6 H 4 Br.O.UH 3 .COOH
C 8 H 7 BrO 3
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. C 6 H 3 (OH):0 2 :C 2 H 4
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. CH 2 Ac.C : CH.C(COOH) : C.
1 1
>J
C 8 H 7 Br0 4
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
+ H 2
192-193
Matsmoto
B., 11, 139
34, 503
Ethylic bromcomenate
C 6 HBrO 2 (OH)(COOEt)
C 8 H 7 Br0 6
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
C 6 H 2 Br 3 .OEt
G 8 H 7 Br 3
72-5
Mohlau and Oeh
J. p., 24, 484
48, 396
michen
Ethyltribromphenol
C 6 HBr 3 Et.OH.
11
53-5-55
....
A., 156, 256
Tribromxyleuol
Me 2 .OHBr 3 = ?
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
C 6 H 3 Br 2 .OEt=1.3.5
G 8 H 8 Br,0
268
Liquid
Mohlau and Oeh
J. p. [2], 24, 483
42,396
michen
Dibromxylenol
Me 2 .OH.Br 2 =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 .Br 2 =1.2.(?) 2
C 8 H 8 Br 2 O 2
....
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.Br 2 =1.3.5.6.(?)
146
Tiemann & Streng
B., 14, 2002
42, 52
Dibrom-|8-orcinol
Me 2 .(OH) 2 .Br 2 =?
155
Stenhouse & Grove
A., 203, 296
37, 402
Dibromxyloquinol
184
Carstanjen
J. p. [2], 23, 421
42, 612
?
C 8 H 6 Br 4 0(?)
C 8 H 8 Br 4
....
138
Hantzsch
A., 215, 51
44,84
Phenylbromethyloxide
Ph.O.CH 2 .CH 2 Br
C 8 H 9 BrO
350-260 p. d
39
Henry
C. B., 96, 1233
44, 802
Ph.O.C 2 H 4 Br
n
240-250 p. d.
39
Weddige
J. p., 24, 241
40, 1137
Bromhydroxystyrolene
C 6 H 5 .C 2 H 3 Br(OH)
H
265
Liquid
Suida and Plohu
W. A., 81, 245
40, 268
Ethoxybrombenzene
C,H 4 Br.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 .... . .
Me 2 .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
C 2 HBr(COOEt) 2
C^ErO,
56(o.p.),u.c.
Anschiitz
B., 12, 2284
143 (30-40)
Brommalophthalic acid
....
C 8 H n Br0 5
....
d. 180
A., 166, 353
Tribromdipropylacetolactone
....
C 8 H n Br,O s
f. A., 216, 76
Liquid 13
Hjelt
B., 15, 628
42,946
1
C 8 H n Br 3 3
....
42-43
Spatzky
J. E. [1885], 61
48, 512
Diethylic dibromsuccinate ....
COOEt.(CHBr) 2 .COOEt
C s H 12 B r!! 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
C 6 H 10 Br 2 (COOH) 2
72-173
Gantter and Hell
B., 15, 149
42, 716
Bromdipropylacetolactone ....
....
C 8 H 13 BrO 2
f. A., 216, 73
jiquid 13
Hjelt
B., 15, 628
42,946
Diethylic bromsuccinate
COOEt.CH 2 .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
....
J 9 H 20 Br 6 O 2
Od.
. 22
Schiitzenberger
B. S. [2], 19, 8
26, 487
Xanthogallol ....
C 18 H 4 Br 14 6 (?)
C 9 H 2 Br 7 3 (?)
22
Stenhouse
C. N., 29, 96
27, 586; vii.,
1031
Tribromumbelliferone
C 6 Br 3 (OH).CH.CH.COO
C 9 H 3 Br 3 8
94
'osen
B., 14, 2746
42, 839
Tribromoesculetin
=(?) 3 .1.2. ?
C 9 H 3 Br 3 4
240 d.
jieberruann and
B., 13, 1592
40, 108
Knietsch
0-Dibromcoumarin
fr. C 6 H 4 .CH : CH.COO=1.2
C 9 H 4 Bf n O 2
176
'erkin
24,42
vi., 500
' ~ |
"'
C 6 H 3 Br.C 2 HBr.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-
....
C 3 H 4 Br 2 O 2
173
Kronfeld
B., 17, 721
46, 1037
imicle
Dibromoesculetin
C 9 H 4 Br 2 4
233
Liebermann anc
B., 13, 1594
40, 108
Knietsch
a-bromcoumarin
fr. C fi H 4 .CH : CH.COO=1.2
i i
C 9 H 5 Br0 2
110
Perkin
23, 371 ; 24, 37
vl., 499
(3-
C 6 H 3 Br.C 2 H 2 .COO=1.2
M
160
Ebert
A., 226, 349
i i
8-
i 11
)
>
160
Perkin
24,42
vi., 500
Bromomethylenephthalyl ...
C 6 H 4 :(CO) 2 :CHBr.=1.2
11
132-133
Gabriel andMicha
B., 11, 1011
34, 734
Bromocoumarilic acid
fr. C 6 H 4 .CH I C(COOH).0
i i
C 9 H 5 Br0 3
a. 250
Perkin
24,48
vi., 498
=1.2
11 11
....
250-251
Ebert
A., 226, 350
Bromomethylenephthalyl
C 9 H 5 Br 3 2
117-5-118-5
Gabriel andMichae
B., 11, 1007
34, 735
dibromide
u. c.
Tribromacetophenone car-
C,H 4 (CO.CBr 3 ).COOH=1.2
C 9 H 5 Br 3 3
159-5-160
11
B., 10, 1555
34, 229
bonio acid
Coumarin dibromide
....
C 9 H 6 Br 2 2
abt. 100 p. c
Perkin
23, 369
vi., 499
i> 11
C 6 H 4 .CHBr.CHBr.COO=l.
)>
105
A., 216, 163
Methylene phthalide dibro-
C 6 H 4 .COO.CBr.CH,Br=1.2
))
98-99
Gabriel
B., 17, 2523
48,164
i i
mide
Bromcinnamic aldehyde
Ph.CBr:CH.COH
C 9 H 7 BrO
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
C 9 H 7 Br0 2
....
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 .... ....
C 6 H 4 Br.(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.C 6 H 4 .(CH 2 ) 2 .CO.O=1.2
11
106
Hochstetter
A., 226, 355
48, 390
Phenoxybromacrylic acid ....
CHBr:C(OPh).COOH
C 9 H 7 BrO 3
....
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. C 6 H 4 (COH).O.CH 2 .COOH
C 9 H 7 Br0 4
....
163
Rossing
B., 17, 2992
48, 388
acetic acid
a-phenyltribrompropionic
Ph.CBr 2 .CHBr.COOH
C 9 H 7 Br 3 O 2
132
Glaser
A., 143, 335
acid
0- 11
Ph.CHBr.CBr 2 .COOH
>
45-48
u
A., 143, 338
0- 11
Ph.C 3 HBr 3 .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 ....
C 6 H 2 Br 3 (O.C 3 H 5 0)
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.C 6 H 4 Me.Ac=1.4
100
Vlichaelis
B., 15, 186
42,970
Dibromhydratropic acid
Ph.CBr(CH 2 Br).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.Br 2 =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.Me 2 Br 2 1 3.5.2.4.or6
94-195
iussencfuth
A. 215 249
4, 470
}>
Dibromatrolactic acid
CHBr 2 .CPh(OH).COOH
C 9 H 3 Br 2 3
....
67
Jottinger
B., 14, 1236
40, 815
Phenyldibromlactic acid
Ph.C 2 HBr 2 (OH).COOH
1)
....
84
Cinnicuttand Pal-
A. C. J., 5, 583
46, 603
mer
Methylic dibromanisate
COOMe.OMe.Br a =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,..
(CH 2 .CH 2 .COOH).OH.Br 2
C 9 H 8 Br 2 O 3
107
Stohr
A., 225, 57
46, 1350
' I)
..
....
115
Zwenger
A., 25, 116
vi., 716
Dibrommethoxytoluic acid ...
COOH.OMe.Me.Br 2
193-194
Paternd and Can-
G. I., 10, 233
38, 884
=1.2.4.(?) s
zoneri
Methylacetophenone bromide
C 9 H 9 BrO(?)
C 9 H 10 Br 2 0(?
55
Bottinger
B., 14, 1598
40, 1036
Phenylbromallyl oxide
Ph.O.CH 2 .CBr:CH 2
240 s.d.
Liquid
Henry
C. E., 96, 1233
44, 803
a-Bromhydratropic acid
CH 2 Br.CHPh.COOH
C 9 H 9 BrO 2
....
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.CH 2 .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.(CH 2 .CH 2 .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
C 6 H 4 Br.(CH 2 OAc)=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.Me 2 .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.Me 2 .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.C 2 H 2 Br(OH).COOH
C 9 H 9 Br0 3
125
Glaser
A., 147, 83
>.
+H 2
120-122
a-Bromphenoxypropionic acid
CH 3 .CH(O.C 6 H 4 Br).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.CH a .COOH)=1.2
....
141-142 d.
Hochstetter
A., 226, 355
48, 390
Bromveratric acid
COOH.(OMe) 2 .Br=1.3.4. ?
C 9 H 9 Br0 4
183-184
Matsmoto
B., 11, 136
34, 502
Isopropoxytribrombenzene ....
C 6 H 2 Br 3 .OPr/s
C 9 H 9 Br 3 O
....
93
Silva
B. S. [2], 13, 27
vi., 917
Methoxytribromxylene
Me 2 .OMe.Br 3 1.3.4.2.5.6
120
Jacobsen
B., 11, 26
Bromacrolein ....
IT "
' ' . ,
B. S. [21 36 136
40 1029
Stycerin dibromhydrin
Ph.C 3 H 4 Br 2 .OH
C 9 H 10 Br 2
...
74
Grimaux
C. E., 74, 1598
26, 1139
Methylacetophenone bromide
C 9 H 9 BrO (?)
55
Bottinger
B., 14, 1598
40, 1036
Dibrompseudocumenol
Me 3 .OH.Br 2 =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 .Br 2 =1.3.5.2.4or6
C 9 H 10 Br 2 O 2
K.I
160
Tiemannand Streng
B., 14, 2001
42, 51
Dimethyldibrommethylpyro-
Me.(OMe)j.OH.Br 2 =?
C 9 H 10 Br 2 3
....
126
Hofmann
B., 12, 1375
38, 249
gallol
Dibromnono-dilactone
(CH 2 Br.C.COO.CH 2 ) 2
C 9 H 10 Br 2 4
130
Hjelt
B., 14, 627; 15, 625
40, 577; 42, 946
Isopropoxybrombenzene
C 6 H 4 Br.OPris=1.4
C 9 H n BrO
236 (760)
Liquid
Silva
Z. C. [1870], 250
vi., 917
Brompseudocuminol
Me a .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
(CH 2 .OH) 2 .Me.Br=1.3.5.2
C 9 H u Br0 2
126
C'olson
C. E, 97, 177
46, 57
or 4
Phorone tetrabromide
(Me 2 CBr.CHBr) 2 CO
C 9 H l4 Br 4 O
88-89
Claisen
A., 180, 12
29, 896
Me 2 CBr.CHBr.CBrMe.
86-88
B., 7, 1168
28, 161
CHBrAc
Diallylcarbinolacetate tetra-
(CH 2 Br.CHBr.CH 2 ) 2 CH.OAc
C 9 H 14 Br 4 O 2
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
....
C 9 H 15 BrO 4
270-275 p.d.
....
Z. C. [1866], 722
vi., 981
?
....
C 9 H 16 Br 2 2
42
Fittig
B., 17, 3014
48, 376
Ethylic a-bromoananthylate....
C 5 H u .CHBr.COOEt
C 9 H 17 BrO 2
220-225 p.d.
Liquid
Hell and Schiile
B., 18, 625
48, 757
Tetrabrom-a-naphthaquinone
....
C 10 H 2 Br 4 2
....
265
Bliimlein
B., 17, 2489
48, 163
-~ D
164
Flessa
B., 17, 1482
46, 1186
Pentabrom-n-naphthol
C 10 H 2 Br 5 .OH
C 10 H 3 Br 6
....
238-239
Blumlein
B., 17, 2488
46, 163
.. -#-
237
Flessa
B., 17, 1481
46, 1186
Dibrom-a-naphthaquinone ....
Br^Oj^fta^;
C 10 H 4 Br 2 2
....
149-5 ; a.s
Diehl and Merz
,B., 11, 1065
34, 736
151 ; 5
.,
=^ l /3 1 a i2 :
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
C 7 H 3 Br 4 .OH.
C 10 H,Br 4 O
156
Smith
i 35,"791
Bromhydroxy-a-naphthoqui-
HO.Br: 05=3,^0,;
C 10 H 6 BrO 3
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
C 10 HjBrO.
Cry st&ll in6
Fischer
A. 211 227
42 500
Phthalylbromacetic acid
C 6 H 4 :(CO) 2 :CBr.COOH=1.2
...
232-235
Gabriel & Michael
B., 10, 2200
34, 426
Pentabromsafrol
....
C 10 H b Br 5 2
169-170
Grimaux & fiuotte
A., 152, 90
vi., 1014
Dibrom-a-naphthol
C 19 H 6 Br 2 .OH
C 10 H 6 Br 2 O
....
111
Biedermann
B., 6, 1119
27, 161
-a-
111
Meldola
C. N., 47, 536
44, 536; 45, 161
Br on diamidonaphthol
C 1( ,H 6 Br 2 3
175
Diehl and Merz
B., 11, 1068
34, 737
Tetrabromresorcinol .diacetate
(OAc) 2 .Br 4 =1.3.2.4.5,6
C 10 H 6 Br 4 4
169
Claasen
B., 11, 1441
34, 868
Furil octobromide
....
C 18 H,Br 8 4
....
185 d.
Fischer
B., 13, 1338 ; A.,
38, 798; 40, 500
.an, 214
Brom-/3-naphthol
C lp H 6 Br.OH=a 1 /3 1 ;
C 10 H 7 BrO
84
Smith
B., 12, 6bO
35, 790
.,
84
Armstrong
B.,'l5, 202
36, 722
3-Brompropionic coumarin ...
....
C 10 H 7 Br0 2
....
146
Perkin
Ji [1875], 591
28, 13
Methoxybromphenylpropiolic
C,H 3 Br (OMe)C i C.COOH
C 10 H,Br0 3
abt. 168 d.
39, 419
acid
=1.2.1
Phenoxymucobromic acid ....
CHO.CBr : C(OPh).COOH
C 10 H 7 Br0 4
....
104-105
Hill aoid Stiven
A. C. J., 6, 187
48, 532
Bromhydroxy-(3-methylcou-
HO.C.H 2 Br.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 ....
C 2 Br(OPh)(COOH) 2
C 10 H 7 Br0 6
....
103-104
Hill and Stiven
A, C. J., 6, 187
48, 532
Tribromresorcinol diacetate
(OAc) 2 .Br 3 =1.3.4.(?) 2
C 10 H 7 Br 3 4
108
Claasen
B., 11, 1439
34, 867
Benzoyldibrompropionic acid
Bz.CHBr.CHBr.COOH
C lo H 8 Br 2 3
....
135
Pechmann
B., 15, 888
42., 1074
Carboxylphenyldibrompro-
COOH.(CHBr.CHBr.COOH)
C 10 H 9 Br.,0 4
....
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 .Br 2 =1.4.5.2
159-5 ; 161
Schula
B., 15, 654, 655
Dibromphenylene dioxyacetic
C 6 H 2 Br 2 (O.CH 2 .COOH)j
C )0 H 9 Br 2 6
249-25o'd-
Gabriel
B,, 12, 1640
38, 34
acid
=(?) 2 .3.1
2
C 10 H 8 Br 4 2
183
Fittig & Barriuger
A w 161, 307
25, 488
Methoxydibromphenyldi-
(CHBr.CHBr.COOH).OMe.
C 10 H 8 Br 4 3
200-202
Perkin
39, 421
brompropionic acid
Br 2 =1.2.()) 2
Methoxyphlenylbromacrylic
(C 2 HBr.COOH).OMe.Br
C 10 H 9 BrO 3
169/5-171
39 % 423.
acid
=1.2.?
J 1)
169
39, 426
Methylic bromterephthalate
(COOMe) 2 .Br=1.4.5
C 10 H 9 Br0 4
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 ....
CH 2 :O 2 :C 6 H 2 Br(CH 2 ) 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
CioH 9 BrO 5
....
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.
C lo H 9 Br 3 3
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
C 10 H 10 Br 2
....
124-125
Claisen & Claparede
B., 14, 2462
42, 512
ide
Methylic phenyldibrompro-
Ph.CHBr.CHBr.COOMe
C 10 H 10 Br.,Oj
....
117
Anschiitz and Kin-
B., 11, 1220; 12,
34,981; 36,645
pionate
nicutt
538
Phenyldibrombutyric acid ....
Ph.CHBr.CHBr.CH 2 .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.Br 2 =1.4.(?) 3 or
....
152-153
Claus and Wimmel
B., 13, 903
38, 632
dibrom toluene propionic acid
(CH 2 .CH 2 .COOH).Me.Br 2
Dibrommethylbenzylacetic
....
w
....
135
A., 193, 316
acid
Dibromeugenol
(CH : CHMe).OMe.OH.Br 2
is
59
Chasanowitz & Hell
B., 18, 824
48, 779
=1.4.3.(?) s
Dibromthymoquinone
Me.Pr : O 2 .Br 2 =1.4.2.3.5.6
73-5
Carstanjen
J. p. [2], 3, 55
24, 351 ; vii.,
1156
Methoxyphenyldibrompro-
(CHBr.CHBr.COOH).OMe
C 10 H 10 Br 2 O 3
....
abt. 156 d.
Perkin
A., 216, 160
39, 420
pionic acid
=1.2
Ethylic dibromanisate
COOEt.OMe.Br s =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.Br 2
C 10 H 10 Br 2 4
144
A., 117, 315
iv., 237
Dibromeugenol dibromide ....
(CHBr.CHBrMe).OMe.OH.
Ci H 10 Br 4 O 2
118-119
Chasanowitz & Hell
B., 18, 824
48, 779
Br.,=1.4.3.(?) 3
Brompropylphenylketone ....
Ph.CO.CHj.CH 2 .CH 2 Br
C 10 H n BrO
37-39
Perkin
47, 843
Phenylbrombutyric acid
Ph.CHBr.CH5.CHj.COOH
Ci H,,BrO 2
69
Jayne
A., 216, 102
44, 472
Ethylic bromtoluate
CH 3 .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.?
C 10 H n BrO.,
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
C 6 H 4 Br.O.CH 2 .COOEt
59
....
J. p. [2], 20, 298
?
....
83
Magatti
B., 12, 1863
38, 250
Anethol dibromide
(CHBr.CHBr.Me).OMe=1.4
C, H 12 Br,,0
abt. 65
Ladenburg
As., 8, 95
vi., 157; vii., 72
Bromcamphoric anhydride ....
C 8 H u Br:(CO),:0
C 10 H 13 BrO 3
215
Wreden
A., 163, 330
25, 896
Tribromcamphor
....
C 10 H 13 Br 3
64
Swarts
B., 15, 1625
42, 1300
....
63-64
Royere
B., 15, 1621
a-Dibromcamphor
C 10 H 14 Br s O
....
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
C 10 H 15 BrO
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.CH 2 .
C 10 H I3 Br s 2
,.,.
135 u.c.
Hell and Schoop
B., 12, 194
36, 521
COOH or BuP.CHBr.CBr
PrP.COOH
?
C, H 18 0+HBr
C 10 H 19 BrO
33-35
Hell and Bitter
B., 17, 2610
48, 172
Tetrabrom-u-naphthoic acid
C 10 H 3 Br 4 .COOH
C n H 4 Br 4 2
....
239
Hausemann
B., 9, 1523
31, 321
~P" !> "
H
259-260
M
)
n
Tetrabromacetyldaphnetin ....
C 6 Br 2 (OH)(OAc).CBr : CBr.
C u H 4 Br 4 5
.*
290 d.
Stilnkel
B., 12, 113
36,469
i
co.o
Tribrom--naphthoie acid ....
C 10 H 4 Br 3 .COOH
C n H 5 Br 3 2
269-270
Hausemann
B., 9, 1522 .
31, 320
Brom -a-
C 10 HjBr.COOH
C n H.BrO 2
242
M
B., 9, 1517
31, 318, 319
,, -P- >! ))
....
11
....
256
)
B., 9, 1518
31, 319
Couuiaroxyacetic anhydride
C 6 H 4 .(CHBr) 2 .COO.CO.CH 2
C n H 8 Br 2 4
213
Bossing
B., 17, 3002
48, 389
dibromide
=1.2
Methyl /3-methylbromumbel-
MeO.CeHjBr.CBrMe.
C u H 9 Br 3 3
233-235
Pechmann & Cohen
B., 17, 2134
46, 1332
liferone dibromide
CHBr.COO=U.4.5
Tribromorcinol diacetate
Me.(OAc) 2 .Br 3 =1.3.5.2.4 l 6
C n H 9 Br 3 4
...i
143
Claassen
B., 11, 1440
Bromphenylmethylfurfuraue
fr.Ph.CBr.(CHBr) 2 .CBrMe.O
C u H 9 Br 5
bl^kens 200
208-210
Paal
B., 17, 2760
48, 249
tetrabromide
Coumaroxyacetic acid dibro-
COOH.(CHBr) 2 .C 6 H < .O.CH 2 .
CiiH 10 Br 3 O 5
219-220
Bossing
B., 17, 2999
48, 389
mide
COOH=1.2
Dibrommethoxyphenyl di-
C 6 H 2 Br 2 (OMe)(CHBr.
C u H 10 Br 4 3
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
CnH n BrO 3
164
Perkin
39, 428
acid
Dibromallylacetophenone ....
Ph.CO.(CH 8 ) 2 CHBr.CH 2 Br
Ci.H.jBrp
121-122
45, 189
Ethylic phenyldibrompro-
PLCHBr.CHBr.COOEt
C 11 H 12 Br 2 !
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.C 3 H 4 Br 2 .OAc
)1
85-86
Grimaux
C. B., 76, 1598
26, 1 139
Methylic /3-methoxyphenyl
MeO.C 8 H 4 .C 2 H 2 Br 2 .COOMe
CuHjjBrgOa
68
Perkin
39, 425, 427
dibrompropionate
=1.2
a ~
....
125
39,425 426
Ethoxyphenyldibrompro-
EtO.C 6 H 4 .C 2 H 2 Br 2 .COOH
H
....
155 d-
Ebert
A., 216, 158
44,472
pionic acid
=1.2
Methylbromeugenol
(CH:CHMe)(OMe) 2 .Br
C u H ls BrO 2
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)
CnH 14 Br 2 O 3
108-109
Hofmann
B.,8, 67; 11,331
gallol
Bromcamphocarbonic acid ...
C, H 14 BrO.COOH
^llH|5 Br O3
109-110
Silva
B., 6, 1093
27,70
Dibromundecylenic acid
10 H 19 Br 2 .COOH
CnHjoBr/X
38
Becker
B., 11, 1413
34, 853
, ,1
38
Kraflft
B., 10, 2035
34, 292
Dibromdiphenylene oxide ....
....
C,,H 6 Br 2 O
185
A., 159, 215
....
)
....
185
Kreysler
B., 18, 1721
Bromrosoquinol
C 12 H 4 Br 4 (OH) 2
C 12 H 6 B ri 2
264
Baeyer & Schraube
B., 11, 1301
34, 869
T etiubrom-y-diphenol
(.C 6 H 2 Br 2 .OH) 2 =[l.(?) J .4] :!
....
264 u.c.
Magatti
B., 13, 225
88, 643
Didromphenyl oxide
C, 2 H 8 Br 2 O
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
C 12 H 8 Br 2 4
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
CH 2 : (O a ) : C 6 H 2 Br.CHBr.
C I2 H 8 Br 2 6
....
181-182-5
Fittig and Mielck
A., 172, 156
27, 899
CH : C(OH).CH.COO or
i 1
CH 2 : (O) : C 6 H 2 Br.CHBr.
CH(OH).CH : C.COO
i_ |
Bromnaphthalic acid
C 10 H 6 Br(COOH) 2
C 12 H.BrO;
....
210
Blumenthal
B., 7, 1095
Benzofuril tetrabromide
....
C^H.BrA
....
127^128 p.d.
Fischer
A., 211, 230
42, 500
Bromphenylphenol oxide ...
C,H 4 Br.O.C 6 H 4 .OH
C 12 H 9 BrO 2
....
Liquid
Bohmer
J. p. [2], 24, 473
42, 398
Brom-yS-acetonaphthol
C 10 H 6 Br.OAc
>J
215 (20)
Liquid
Canzoneri
G. I., 12, 424
44, 68
Bromoxypiperide
CH a : O 2 : C 6 H 3 .CHBr.CH :
C 12 H 9 BrO 6
....
131-5-132
Fittig and Mielck
A., 172, 144
27, 898
C(OH).CH.COO or
1 1
CH 2 : O 2 : C 6 H 3 .CHBr.
CH(OH). CH : C.COO
L. 1
Tetrabrompiperonic acid
C 12 H 10 Br 4 4
....
160-165 d.
>>
A., 172, 137
Tetrabromoxypiperonie acid'
....'
C 12 H 10 Br 4 6
d. 100; 155 d.
u
A., 172, 154
Ethyl brom-a-naphth6'l
C 10 H,(Br.OEt
C 12 H u BrO
48
Machetti
G. I., 9, 504
38, 261
~P~
j
....
96
Koelle
B., 13, 1954
40, 178
Brom-S-hydropiperic acid ....
....
C 12 H n BrO 4
170-171
Buri
A., 216, 177
44, 485
Cinnamenylvinylmethylke-
Ph-C^Br^CO-Me
C 12 H 12 Br 2 O
....
173-5 d.
Diehl and Einhorn
B., 18, 2323
48, 1221
tone dibromide
Diethylic dibromterephtha-
(COOEt) 2 .Br 2 =1.4.3.6
C l2 H 12 Br 2 4
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-
C c H 2 Br 2 (OMe)(CHBrV
C 12 H 12 Br 4 3
abt. 159 d.
Perkin
39, 437
brom valeric acid
CEtBr.COOH)=(?) 2 .1.2
Phenylhomoparae'onic acid
C 12 H 1S BKV
....
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*
C 12 H 14 Br 2 0,
....
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
C 3 H 6 ;OMe.OEt.Br=1.4.3.?
>
48
Wassermann
A., 179, 386
29, 707
Ethylbromeugenol dibromide
C 3 H 5 Br 2 .OMe.OEt.Br
C 12 H 16 Ur 3 O 2
....
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
6 HBr 3 .C 6 Br' 4 .CO'
C 13 HBr 7 O
...
136
Salzmann and
B., 10, 1402
34,80
ketone
1 1
"Wichelhaua
Hexabromdiphenylene
C 6 HBr 3 .C 6 HBr 3 .CO(?)
C 13 H 2 Br 6
black 225
nf. 280
)>
ketone
i : 1
Dibromdipheuylene ketone....
fr. C,-H 4 .C 6 H 4 .CO=2
C 13 H 6 Br 2
....
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
)
C 13 H 6 Br 2 2
....
210
Perkin
43, 190
oxide
" ;>
i>
))
....
211-212
Behr and Dorp
B., 7, 399
27, 798
Tetrabromdihydroxybenzo-
CO.(C 6 H 2 Br 2 OH) 2
^i3H 6 Br 4 O a
213-214
Baeyer and Bur-
B., 11, 1299
34, 887
phenone
kardt
)J
>
....
213-214
Baeyer
A., 202, 131
38, 658
Bromdiphenylene ketone ....
C 6 H 3 Br.C 6 H 4 .CO=!.1.2 ; 1.2
C 13 H 7 BrO
....
104
Hodgkinson and
B., 16, 1103
43, 165
Matthews
Benzoyltribromphenol
OBz.Br 3 =1.2.46
C 13 H 7 Br 3 2
81-5
Daecomb
B., 18, 1168
48, 890
Diacetyltribromcesculetin ....
C 8 HBr 3 O,,(OAc),,
C 13 H.Br 3 6
180-182
Liebermann and
B., 13, 1592
40, 108
Knietsen
Dibromphenylbenzoic acid ....
....
C 13 H 8 Br 2 3
212
Holm
B., 16, 1082
44,922
a ~
C 6 H 4 Br.C 6 H 3 Br.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
C 6 H 4 Br.C 6 H 3 Br.COOH
C la H 8 Br 2 2
....
232 ; af. 231
Carnelley and
47, 589
=1.4 ; l.(3 or 2).4
Thomson
Diacetyldibromoesculetin ....
C 9 H 2 Br 2 O 2 (OAc) 2
C l3 H 8 Br 2 O 6
177
Liebermann and
B., 13, 1595
40, 108
Knietsen
Tetrabromdihydroxydi-
CH 2 (C 6 H 2 Br 2 OH) 2
C 13 H 8 Br 4 2
225
Beck
A., 194, 326 ;
34, 421 ; 36,
phenylmethane
=[1.(?) 2 .4] 2
B., 10, 1839
325
Bromdiphenyl ketone
6 H 4 Br.CO.Ph
C 13 H a BrO
81-5
Kollaritzand Merz
B., 6, 547
vii., 939 ; 26,
1036
Phenylio brombenzoate
COOPh.Br.=1.3
C 13 H 9 BrO 2
65
J. [1879], 676
Dibrombenzhydrol
fr. Ph.CH(OH)Ph
C u H 10 Br/)
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.CH 2 .O.C 6 H 4 Br
C ls HuBrO
....
59-59-5
Sintenis
B., 4, 700; A.,
24, 909 ; vii.,
161, 344
180
Bromdiethyloesculetin
fr. C 6 H 2 (OEt) 2 .CH : CH.COO
C 13 H 13 Br0 4
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
Ci 3 H 14 Br 2 O 3
97
Claisen
B., 14, 347
40, 405
propionate
Benzylidene mesityl oxide
....
C, 3 H 14 Br 4
118
Claiseu and Cla-
B., 14, 2461
tetrabromide
pare"de
Ethylic ethoxyphenyldi-
C 6 H 4 (OEt)[(CHBr)2.COOEt]
Ci 3 H 16 Br 2 O b
78
Perkiu
39, 428
brom propionate
=1.2
Isoamylic dibromresellinate
....
C I3 H 16 Br 2 Q 4
73-8
A., 139, 40
A cetyldimethylpropyldi-
C 6 Br 2 Pr(OMe) 2 (OAc)
n
....
101-5-102-5
Hofmann
B., 11, 331
34, 417
brompyrogallol
Hydrobromcumenyl crotonic
C 6 H 4 .Pr(CH 2 .CHBr.CH 3 .
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 ....
....
C 14 H 3 Br 6 O 2
....
w.m.
Diehl
B., 11, 183
34, 430
Tetrabromauthraquinbne ....
....
C 14 H 4 Br 4 2
295-300
jj
B., 11, 182
i
....
n
....
nf. 370
Hammerschlag
B., 10, 1213
34, 76
Tribromanthraquinone
....
C 14 H 6 Br 3 2
186
Diehl
B., 11, 181
34, 430
...;
....
365
Hammerschlag
B., 10, 1213
34, 76
Tribromflavopurpurin
....
C 14 H 5 Br 3 6
284 d.
Schunck & Roemer
B., 10, 1823
34, 322
Peiitabromoxytolidene
.._
C 14 H s Br 5 2
....
206
......
A., 153, 127
a-Dibromanthraquinone
....
C 14 H 6 Br 2 2
....
145
Perkin
37, 555
0-
)>
174-175
n
37, 555
-
....
))
....
236 u.c.
Diehl
B., 11, 181
?-
....
''
....
270-272
Auerbach 1 -
B., 15, 2918
Dibromphenanthrene qui-
fr. CO.C 6 H 4 .C 6 H 4 .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-
C 6 H 4 ,:(CO) s :C 6 HBr a .OH
C I4 H 6 Br 2 3
....
207-208
Baeyer
A, 202, 136 ; B.,
31, 308
quinoue
=2.1 ; 1.2.3.5.4
9, 1231
Dibromalizarin
....
C 14 H 6 Br 2 4
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
C 14 H 8 Br 2 4 (?)
197-1 98 u.c.;
Carnelley&Thomson
47, 592
201-202 c.
Tetrabromoxytolidene
t*
C, 4 H 6 Br 4 2
150
A., 153, 127
Bromanthraquinone
C 6 H 4 :(CO) 2 :C 6 H 3 Br
C 14 H 7 BrO 3
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 ....
C 14 H 5 Br(OH) 2 O 2
C, 4 H,BrO,
a. 280
Diehl
B., 11, 190
34 49S
Brompurpurin
^14 7*^ ^^4
C 14 H 7 BrO 5
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 ....
....
C 14 H 8 Br 2 2
121
A., 153, 125
Dibromdiphenylene glycollic
....
C I4 H 8 Br 2 3
abt. 225
Friedliinder
B., 10, 537
32, 493
acid
Fr. dibrom-o-p-ditolyl
v. C 14 H 6 Br 2 4
O^ilyDl'gO 4
....
....
....
414
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference,
'Watts' Diet.
& J. Ch. Soc.
Dibromdiphenic acid
C 12 H 6 Br 2 (COOH)j
C 14 H 8 Br 2 4
....
295-296
Ostermayer
B., 7, 1091
Bromsalicylic anhydride ...
[C 6 H 3 Br(OH).CO] 2 O=(..2.1) 2
C I4 H 8 Br 2 6
....
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
C c H 4 (COOH).C 6 H 3 Br.COOH
C 14 H 9 BrO 4
....
208u.c.;215c
Carnelley & Thom-
47, 591
=4.1; 1.4.2
son
Pentabromcurcumin dibro-
C 14 H 9 Br 7 4
cf. B., 16, 573 abt. 120 d.
Jackson and Menke
A. C. J., 4, 360
44, 482
mide
Dibromdeoxybeiizoin
C 14 H 10 Br 2
....
87
Zinin
A., 126, 221
vi., 332
ii
110-112
Limpricht and A., 155, 70
vii., 174
Schwanert
Tetrabromethylene phenyl-
....
Ci 4 H 10 Br 4 O 2
....
b. 100
....
Z. C. [1869], 447
oxide
Bromdeoxybenzoin
....
C 14 H u BrO
...
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
C 14 H n Br0 2
69-70
Claisen
B., 14, 2475
42, 514
Benzoxydibromtoluene
Me.OBz.Br 2 =1.4.3.5
C 14 H n Br 2 2
....
91-91-5
Schall and Dralle
B., 17, 2532
48, 146
Ethylene diphenol tetabro-
....
C, 4 H 14 Br 4 O 2
....
a. 100
vi., 917
mide
Curcumin tetrabromide
....
C 14 H 14 Br 4 4
cf. B., 16, 573
185 d.
Jackson and Menke
A. C. J., 4, 360
44, 481
Dibromthymoquinol diace-
C 6 Br 2 MePr(OAo) 3
C 14 H 16 Br 2 4
MM
121-122
Schulz
B., 15, 658
tate
Diacetyl dibrompicomar
C 6 Br 2 Pr(OAc) 2 .OMe
C M H le Br 2 6
....
78
.,..
M. C., 4, 185
Bromthymoquinol diacetate
C 6 HBrMePr(OAc) 2
C, 4 H 17 BrO 4
91
Schulz
B., 15, 658
42, 838
Tetrabrommorin
....
C,,H 6 Br 4 7
+2JH S O
258
Benedikt & Hazura
M. C., 5, 667
48, 554
Brombenzylidene phthalide
C 6 H 4 .COO.C. CBrPh=1.2
C 15 H 9 BrO 2
160
Gabriel
B., 18, 2444
48, 1230
From ethobromcodeine
121; 121-122
Gerichten and
B., 15, 1485, 2179
42, 1113; 44,
Schrotter
222
Methylbromhydroxyanthra-
C 6 H 4 ;: (C0)j.. C 6 H.Me.OH.Br
C 16 H 9 BrO s
305
Fraude
A,, 202, 165, B.,
36, 635
quinone
Br.OH.Me=1.2.3
12, 237
Benzylidene phthalide di-
C 6 H 4 .COO.CBr.CHBrPh
C 16 H. Br 2 2
146
Gabriel
B., 17, 2521
48, 165
bromide
=1.2
Tetrabromphloretin
...
C 16 H 10 Br 4 5
205-210 d.
Hlasiwetz
A., 119, 104
iv., 492
Bromcresolphthalein
C 6 H 2 BrMe(OH).OC.C 6 H 4 .
C 15 H,,Br0 4
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(C a H 4 .OMe) 2 =(1.4) 2
C.sHuBrA
....
181
Bosler
R, 14, 329
40, 422
none
Dibromhydrocotoi'n
C 15 H 12 Br 2 4
95
Jobst and Hesse
A., 199, 59
38, 328
Tetracetyldibromgallic acid
C 6 Br 2 (OAc) 3 .COOAc
C 15 H 12 Br 2 9
+ 2H 2
91
t
B., 3, 643
=6.2.5.4.3.1
Bromlapachic acid
C lo H 4 (C 8 H 9 );0 2 .OBr
C 16 H 13 Br0 3
cf.B., 16, 801
139-140
Paterno
G. I., 12, 337
44, 211
Bromhydrocotoin
....
C 15 H 13 Br0 4
147
Jobst and Hesse
A., 199, 59
33, 328
Dibromoesculin
C 15 H 14 Br 2 9
....
193-195 d.
Liebermann and
B., 13, 1594
40, 108
Kuietsch
Brompicrotoxin
C 15 H 15 Br0 6
....
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
C 16 H 16 Br 2 3
....
184
Cannizaro and Car-
G. I., 10, 461
40, 286
neluti
~P~
....
186
Brom-/3-metasantonin
Ci 5 H 17 BrO.,
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
....
Ci 5 Hi 9 BrO 3
145-5
Cannizaro and
G. I., 8, 31)9
36, 331
Valente
Dibrora-a-naphthylene phe-
....
C 16 H 8 Br,0
cf. A., 209, 144
284
Arx
B., 13, 1727
40, 282
nylene oxide
Diphthalyl dibromide
C 6 H 4 .COO.CBr i CBr.C 6 H 4 .
Cl 6 H 8 Br 2 O 4
4:
begins 220 d.
Greebe & Schmal-
B., 15, 1674
48, 1298
COO=(I.2) 2
zigang
Dibrom-m-acetoxyanthaqui-
C 6 H 4 : (00), : C 6 H(OAc)Br 2
t
cf. A., 202, 137
189-190
Baeyer
B., 9, 1231
81, 308
none
Dibromocampheride
....
C 16 H IO Br 2 6
224-225 d.
Jahns
B., 14, 2389
42, 209
Diacetyltetrabrom-y-diphenol
(C 6 H 2 Br 2 .OAc),=(l.U4) 2
C 16 H 10 Br 4 4
245
Magatti
B., 13, 225
38, 643
Tetrabromlecanoric acid
....
C 16 H 10 Br 4 7
abt. 157
Hesse
A., 139, 28
vi., 778
Ethylic dibromdiphenylene
fr. C 6 H 4 .C 6 H 4 .C(OH).COOEt
C 16 Hi 2 Br 2 O 3
150-151
Friedlander
B., 10, 537
32, 493
glycollate
Dibromhsematoxylin
....
C,,H 12 Br 2 6
d. a. 120
Dralle
B., 17, 373
48, 1043
Dibromlecanoric acid
....
C 16 H 12 Br 2 7
175 ; 179 c.
Hesse
A., 139, 28
vi., 778
Diacetyldibromrhamnetin ....
C 13 H,Br,O s (OAc),
211-212
Liebermann and
B., 11, 1621 ; A.,
36, 272
Hermann
196, 322
?
C 14 H 10 Br.Ac
C 16 H 13 BrO
107
Limpricht and
....
vii., 1163
Schwanert
Bromdioxyretistene
....
C I6 H 13 Br0 2
210-212
Z. C. [1869], 74
Fr. tolane dibromide
C 14 H 10 Br.OAc
....
107
Limpricht and
B., 4, 380
Schwanert
Dibromethyl deoxybenzoin....
fr. Ph.CH 2 .CO.C 6 H 4 Et=1.4
C 16 H l4 Br 2
113
Sollscher
B., 15, 1681
42, 1292
Methylic diphenyl dibrom-
Ph.CHBr.CBrPh.COOMe
Ci 6 H 14 Br 2 O 2
105-108
Cabella
G. I., 14, 14
46, 1348
propionate
Tetrabromhydrocoerulignone
C 12 Br 4 (OMe) 4 (OH) 2
C 16 H 14 Br 4 6
217-218
Hayduck
B., 9, 930
30, 517
Dibromhydrocoerulignone ....
C 12 H 2 Br 2 (OMe) 4 (OH) 2
C 16 H 16 Br 2 O 6
....
262
5
)1
Brompalmitolic acid ,.,
C l5 H 26 Br.COOH
C 16 H 27 Br0 2
31
Schroeder
A., 143, 31
vi., 896
Bromhypogceic acid
C^H^Br.COOH
C 16 H 29 Br0 2
....
19-23
)5
A., 143, 26
vi., 727
Tribrompalmitic acid
CjsHjsBrj.COOH
C 16 H 29 Br 3 2
39
A., 143, 27
Dibrompalmitic acid
C 15 H J9 Br 2 .COOH
C 16 H 30 BrA
29
>
A., 143, 24
vi., 726
Ethyl tetrabrommorin
C 15 H,,Br 4 EtO 7 + 3H 2 O
C 17 H 10 Br 4 7
135
Benedikt & Hazura
M. G, 5, 667
48, 551
From bromcinnamic acid ....
....
C 17 H 12 Br 2 2
a. 340
Leuckart
B., 15, 19
42, 615
Tetrabromevernic acid
....
C 17 H 12 Br 4 O 7
161
Stenhouse
P. R S., 17, 222
vii., 496
Bromdehydracetonebenzil ....
....
C 17 H 13 Br0 2
172
Japp and Miller
47, 29
Pentabromdurylbenzoyl
....
C 17 H 13 Br 5
224-225
J. [1879], 372
Dibenzylidene-acetone tetra-
CO(CHBr.CHBrPh) 2
C 17 H 14 Br 4
206-208
Claisen and Clap-
B., 14, 2461
42, 511
bromide
ardde
Benzylidenephthalidebromide
Ph.C 2 HBr(OEt).C 6 H 4 .COO
Ci7H 15 BrO 3
149
Gabriel
B., 17, 2527
48, 165
ethoxide
> 1
=1.2
Acet.ylbromhydrocoto'in
....
C 17 H 15 BrO 3
166
Jobst and Hesse
A., 199, 61
38, 328
Brom a-ditolylpropionic acid
f r. (Me.C 6 H 4 ) 2 .CHMe.COOH
C| 7 Cj 7 BrO 2
143-144
Haiss
B., 15, 1478
42, 1071
=(1.4) 2
Ethylic phenyldibrompro-
CHBrPh.CHBr.CO.CEt 2 .
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
C 18 H,Br I0
139 d.
Stenhouse
A., 177, 197
28, G ; vii., 1029
Xanthogallol
....
C 18 H 4 Br 14 O c
122
,,
A., 177, 193
28, 6; vii., 1031
?
C 18 H 7 Br n 9
130
D
n
28, 4; vii., 1031
Dibromchyrsoquinoiie
C 18 H s Br 2 2
....
160-165
Adler
B., 12, 1892
38, 263
Dibromethylenebenzoyl car-
C 6 H 4 : (CO), : CH.CBr 2 .OC.
C 18 H 10 Br 2 O 5
285-287
Gabriel & Michael
B., 10, 1561
34, 230
bonic anhydride
C 6 H 4 .COOH=(1.2) 2
Dibromethylene dibenzoyl
fr. (.CH 2 .CO.C 6 H 4 .COOH). 2
C 18 H 12 Br 2 O 6
270-272
u
B., 10, 2209
24, 428
carbonic acid
=(1.2),
Tribrompyrogiiajacol
Ci 8 H 13 Br 3 O 3
172
Wieser
M. C., 1, 601
40, 813
Phenyldibrompropylic cin-
Ph.CH:OH.COO.CH.
C 18 H 16 Br 2 2
151
Miller
B., 9, 275
29, 939
namate
(CHBr) 2 .Ph
Dibromhexmethoxyd iphenyl
fr. (MeO) 3 C 6 H 2 .C 6 H 2 (OMe)3
C^BrA
138-140
Ewald
B., 11, 1623
36, 253
Dibromoleic acid
cf. A., 140, 56
C 18 H 3! ,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
C 17 H 31 Br 4 .COOH
C| 8 H 32 Br 4 O 2
cf. A., 140, 56
abt. 70
Marasse
Z.C. (2), 5, 571
vi., 1038
Broraoleic acid
C 17 H 32 Br.COOH
C.sH^BrO,
cf. A., 140, 47
35-36
Overbeck
J. p., 97, 159
vi., 881
Dibromoelai'dic acid ...
C^H^Br^COOH
C 18 H 34 Br 2 2
cf.A.,140,6
27
Burg
B. S. (2), 3, 191
vi., 550
Bromstearie acid
CjjH^Br.COOH
C 18 H 35 BrO 2
....
41
Oudemanns
J. p., 89, 1957
v., 419
From isoamyloxanthranol ..
....
C 19 H 18 Br 2
120 d.
....
A., 212, 95
Dibromdiacetylpicrotoxide
....
19 IS 2 8
180
Paternd & Oglialorc
G. I., 9, 57
36, 729
or Diacetylpicrotoxide di-
or
bromide
C 19 H 2(1 Br 2 8
Ethyl brompodocarpic acid ..
....
C 19 H 25 BrO 3
....
158
A., 170, 237
Pentabromquinol phthale'in
fr.C.H 4 :[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.C 6 H 2 Br(OH).CO.C : (C 6 H
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
....
20 H JO Br 2 O 5
260-270
A., 183, 38
81, 200
Tetrabromphenol phthale'in...
C 6 H 4 (CO.C 6 H 2 Br 2 .OH) 2 =1.2;
C 20 H lo Br 4 4
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
C 6 H 2 Br 2 (OH).CPh.C 6 H 4 .COO
i i
CH It Br,Q,
196
Pechmaim
B., 13, 1615
40, 96
pntnalide
Dibromphenylresorcinphtha-
fr. C 6 H 3 (OH) 2 .CPh.C 6 H 4 .COO
CsoH 12 Br 2 4
219
B., 14, 1861
42, 184
lein
i i
=1.3.7; 1.2
Tetrabromphenolphthalin ....
C 6 H s Br 2 (OH).CH(OH).C 6 H 4 .
C 20 H 12 Br 4 O 4
140
Baeyer
R, 9, 1233
31, 308
CO.C 6 H 2 Br.,OH
j>
....
J"
205
,,
A., 202, 85
38, 655
Tetrabrompurpurogallin
C 20 H 12 Br 4 9
202-204
Clermont ftdbautan
C. E., 94, 1362
42, 1066
Hexabromdiresorcinoltetra-
C 6 Br 3 (OAc) 2 .C,Br 3 (OAc) 2
C'., H 12 Br 6 O 8
259
....
M. C., 1, 356
acetate
Tetrabrom-/3-diresorcinol-
C 6 HBr 2 (OAc) 2 .C 6 HBr 2 (OAc) 2
C 20 H 14 Br 4 O s
195
....
M. C., 1, 353
tetracetate
Tribromerythrol
C 20 H 19 Br 3 1 ,
+ 1^H 2 O
139
A., 117,310
Dibromdiacetylhydroccerulig-
C 12 H 2 Br i .(OMe) 4 (OAc) 2
C^H^BrijO,
178
Hayduck
B., 9, 930
30, 516
noue
a-Dibenzoyldithymol
....
C 20 H 24 Br 2 O 2
....
215
Dianin
J. E. [1882], 130
42, 624
Hexabromresocyauin
....
C2iH 12 Br 6 O 6
250 d.
J. p., 24, 127; 25, 83
Bromphthalacene oxide
C 21 H 13 BrO
200
Gabriel
B., 17, 1398
46, 1190
Brombenzylcurcumin
C 14 H 13 (CH 2 .C 6 H 4 Br)0 4 =1.4
C 21 H 19 Br0 4
cf.B.,15,1761
78 ; sf. 76
Jackson and Menkt
A. C. J., 4, 77
42, 1108
Alcoholate of ethylbrompodo-
....
C 21 H 31 Br0 4
....
a, 80
A., 170, 213
carpinic acid
Acetyl tetrabromfluovescein
....
C 22 H 10 Br 4 6
278
Baeyer
A., 138, 1
31, 203
7 bromhydrin dibromide
C 22 H 12 Br(OH).Br 2
C 22 H 13 Br 3
d.w.m. 280
Rousseau
A. C. (5), 28, 145
46, 180
Dibromacetoxydiphenyl -
"! 6 H 2 Br 2 (OAc).CPh.C 6 H 4 .COO
C 22 H 14 Br 2 O 4
....
170-172
Pechmann
B., 13, 1616
phthalide
i .--i
Tribromcotoin
....
C 22 H 15 Br 3 O 6
114
Jobst and Hesse
A., 199, 26,
38, 326
Dibromorthocresolphthalein
fr. C 6 H 4 (CO.C 6 H 3 Me.OH) 2
C 22 H 16 Br 2 O 4
cf.A.,202,158
255
Fraude
B., 12, 239
36, 635
= 1.2 ; (7.1.2),
Dehydroacetophenonebenzil
....
C 22 H 16 Br 4 2
....
110-115
Japp and Miller
47,36
tetrabromide
Dibrom-o-cresolpbthaliu
....
C 22 H ls Br 2 4
236
A., 202, 170
Dibromerucic acid .... . ...
....
46-47
Hausknecht
A., 143, 44
vi., 257
Tetrabrombehenic acid
C 22 H 40 Br 4 O n
77-78
A., ] 43, 45
Bromerucic acid
C 22 H 41 BrO 2
33-34
A., 143, 50
vi., 581
Tribrombehenic acid....
31-32
1}
Brassidic acid dibromide ..
C 22 H, 2 Br 2 O.,
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
C 19 H 8 Et 2 Br 4 3
C 2 3H ls Br 4 O 3
110-115
Ackermann
B., 17, 1627
46, 1340
Tetrabrornphthalfluorescem
C 24 H 10 Br 4 5
a. 310
Terrisse
A., 227, 133
48, 667
(naphthaleosin)
Tetrabromfluorescein diace-
....
C 24 H l2 Br 4 0-
278
....
A., 183, 53
tate
Tetrabromquercetin
fr.C 24 H 14 9 :(O.C 6 H 12 4 ) 2 :0
C 24 H 12 Bi-,O n
218
Liebermann and
B., 12, 1185
Hamburger
Diacetyldibromfluorescem ....
....
C 34 H 14 BrA
208-210
Baeyer
A., 138, 1
31,200
Dibromfluorescein diacetate
...
C 24 H 14 Br,0 7
208-210
A., 183, 38
Diacetyltetrabromphenol-
C 6 H.,Br,(OH).6!c 6 H 4 .C
C 24 H l4 Br 4 5
....
256
Baeyer
A., 202, 95
38, 656
phthalidin
1
r
(OH).C 6 HBr s .OAc
Diacetyltetrabromphenol-
....
C 24 H 14 Br 4 6
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. C 6 H 2 Br 2 (OH).CH(OH).
C 24 H 16 Br 4 O|.
....
165-166
B., 9, 1234 ; A.,
31, 309 ; 38,
phthalin
C 6 H 4 .CO.C 8 H 2 Br 2 ,OH
202, 36
655
Tetrabromtetracetylbrazilin
C 16 H 6 Br 4 5 Ac 4
C 24 H I9 Br 4 9
220-222
Buchka and Erck
B., 18, 1141
48, 907
Tribromtetracetylbrazilin ....
C 16 H ; Br 3 O i Ac 4
C 24 H 19 Br 3 O,,
145-147
B., 18, 1140
?
C 6 H 4 (CH 2 .O.CHBr.C 6 H 4 ,
C 24 H 20 Br 2 4
80
Low
B., 18, 2073
48, 1208
COH) 2 =1.4;(1.4) 2 (?)
Diethylic tetrabromrosolic
QwH 10 Et 2 Br 4 O.,
C 24 H 20 Br 4 3
110-115
Ackermann
B., 17, 1627
46, 1340
acid
Bromtetracetylbraziliii
C 16 H 9 Br0 6 Ac 4
C 24 H 21 BrO 9
203-204
Buchka
B., 17, 685
46, 1044
Diacetylbromcaitechin
C 21 H 17 Br0 7 (OAc) 2
C 2i H 23 BrO H
....
120
Liebermaim and
B., 13, 696
40,53
Tauchert
Pentacetyldibronicesculin ....
C 15 H 9 Br 2 4 (OAc) s
C 25 H 24 Br 2 14
203-206
Liebermaim and
B., 13, 1594
40, 108
Knietsch
Fr. benzophenone
....
C 26 H 15 Br s O 2
125
Linnemann
A., 133, 6
iv., 478
Pentacetylbromhsematoxylin
C 16 H 8 BrO 6 .Ao 6
CjuHaBrO,,
210
Buchka
B., 17, 684
46, 1043
Tribrombaphinitone ....
C 26 H 23 Br 3 O fi
180-2 c. ; ,d.
Anderson
....
30, 585
Br-deriv. of styrogenin
C 26 H 39 Br 3 (?)
C. 6 H 37 Br 3 0(?)
260
Myhus
B., 15, 945
Cholesterin dibromide
C 26 H 44 Br 2
113-114
Liebermaim
B., 18, 1807
48, 1075
Tetrabromdiacetylquercetin
C 24 H IO Br 4 11 Ac : .
C M H 16 Br 4 O 13
....
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 ! | 8 Br 2 O 2
222
....
J. [1876], 425
239
Tetracetyldibromgallein
....
CjgH^BrjO,,
234
Buchka
A., 209, 266
42, 61
Dibromdiacetylquercetin
O 24 H 12 Br ; Ac 2 O 11
O^HigBrgOj-j
218
Liebermann and
B., 12, 1184
36, 945
Hamburger
a-Tribrompyrocressol
C 28 H 23 Br 3 O 2
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
....
C 30 H 47 Br0 2
116
A., 178, 63
Bromoquassiin
....
C 31 H 4 ,- I BT- I O 9
75
Christensen
A. P. [3], 20, 481
42, 1302
Dibrompalmitone
.....
C 31 H m Br 2
55
Herez
A., .186, 257
32, 427
,, hydrobro-
....
C 31 H 6 ,Br 3 O
5-5
J)
>!
inide
Tetrabromdibenzoylhydro-
C 32 H 28 Br 4 O 8
....
84
Jobst and Hesse
A., 199, 56
38, 327
cotin
Dibromdibenzoylhydrocotin
....
C 32 H 30 Br 2 O s
147
A., 199, 55
Fr. quassin
C 32 H 41 Br 3 9
155 d.
Oliveri and Denaro
G. I., 14, 1
46, 1192
Bromechitin ....
C 32 H 51 Br0 2
100
A., 178, 68
Tetrabromleucotin ....
....
C 34 H 28 Br 4 O 10
157
Jobst and Hesse
A., 199, 42
38, 326
Tetrabromoxyleucotin
....
C^H^Br.O,,
....
159
n
A., 199, 51
38, 327
Dibromleucotin
...
34 H 30 Br 2 1( ,
187
A., 199, 41
38, 326
Dibromoxyleucotin
....
C 34 H 30 Br 2 12
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.... .
....
U M H w Br 3
C 40 H 31 Br 4 5
C^Hc-Br-jO.
....
72
234-235
150
Ekstrand
J. [1855], 517
A., 185, 102
A., 176, 72
v., 425
32, 498
Dibromabietic acid ....
....
C 44 H, 2 Br s 5
134
Emmerling
B., 12, 1443
38, 265
(9.) CHBrS, CHBrSe, and CHBrTe.
Tribromthiophene
C 4 HBr 3 S
259-260 c. j 29
Rosenberg
B., 18, 1774
48, 1051
Dibromthiophene
S.Br 2 =1.2. ?
C 4 H 2 Br 2 S
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
....
C 4 H 3 BrS
149-151 u. c.
....
B., 16, 1472
?)
,, ....
....
J>
149-151
....
Meyer and Stadler
B., 18, 1490
48, 972
Diethylene dithiotetrabro-
C 2 H 4 :SBr 2 :SBrj:C 3 H,
C 4 H 8 Br 4 S 2
....
96 d.
Husemann
A., 126, 287
vi., 607
mide
Tribrom-thiotolene
S.Me,Br 3 = ?
C 6 H 3 Br s S
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.Br 2 =1.2.(?) 2
C 5 H 4 Br 2 S
227-229
Liquid
Meyer and Kreis
B., 17, 787
--
*) 5)
JJ
227-229 n. c.
Liquid
Meyer
B., 16, 2970
46, 586
Brombenzene sulphhydrate
O 8 H 4 Br.SH=l,4
C,H 6 BrS
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.Br 3 =1.3.2.4.5
C 6 H 5 Br 3 S
....
108
Bonz
B., 18, 550
48,766
Dibromthioxylylbromide ....
S i Me.Br 2 ,CH,,Br=1.2.3.4.5
)
142-144
Paal
B., 18, 2253
48, 1206
Dibrom-|3-ethylthiophene ....
S,Et.Br 2 =1.2.(?) 2
C 6 H 6 Br 2 S
Liquid
Bonz
B., 18, 550
48, 766
Dibromthioxylene
S.Me 2 .Br 2 =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.Me 2 .Br=1.2.5.3
C 6 H 7 BrS
193-1 94 u. c.
Liquid
Messinger
B., 18, 1637
48, 1052
Brombenzylsulphhydrate ....
C 6 H 4 Br,(CH 2 .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 ....
CBr 2 :C(C 4 H 3 S) 2
CioHfiBr.jS,,
Liquid
Peter
B., 17, 1344
46, 1001
Dithienyltribromethane
CBr,,.CH(C 4 H 3 S) 2
C 10 H ; Br 3 S 3
101-102
jj
Dibromphenyl sulphide
S(C G H 4 Br) 2
C^HgBr^S
109-110
Krafft
B., 7, 1164
28, 153
disulphide ....
S 2 (C 6 H 4 Br). 2 =(1.4) 2
C 12 H s Br 2 S.j
....
93
Nbtling
B., 8, 1310
28, 264
?
....
C I4 H 6 Br 2 S 2
n. f. 250
Limpricht
B., 6, 534
26, 1032
Brombenzyl sulphide
(U 6 H 4 Br.CH :: ), ! S=(1.4) 2
C 14 H 12 Br 2 S
59
Jackson and Harts-
A. C. J., 5, 264
46, 665
horn
disulphide
(C 6 H 4 Br.CH 2 ) 2 S 2 =(1.4) 2
C 14 H 12 Br 2 S 2
87-88
u
J)
1*
Bromtolyl disulphide
(C,H 3 MeBr) 2 S 2 =1.2.3 or 5)
,,
56-58
Hubner and Poat
A., 169, 42
27, 59
Bromphenylmercaptole of
CMe 2 (S.C 6 H 4 Br) 2 =(1.4) 2
C 15 H l4 Br 2 S 2
89-90
Baumann
B., 18, 888
48, 749
acetone
Bromphenylmercaptal of
Ph.CH(S.C 6 H 4 Br) 2 =(L4.) 2
C igf H 14 Br 2 S 2
79-80
B., 18, 885
J)
benzaldehyde
Bromphenylmercaptal of
Ph.CH :CH.CH(S.C 6 H 4 Br) 2
C 21 H 16 Br 2 S 2
105-107
,,
)
p|
cinnamaldehyde
=(l-4) 3
Tribromthionessal
C 2s H 17 Br 3 S
....
265-270
Fleischer
A., 144, 194
vi., 1087
Dimethylselenio-dibromide....
Me 2 SeBr 2
C 2 H 6 Br a Se
cf. A., 179, 5
82 d.
Jackson
B., 8, 110
28, 553
Diniethyl-telluro-dibrotnide
Me. 2 TeBr 3
C,H 6 Br,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
C 2 HBr 2 N
142
Van t'Hoff
B., 7, 1571
Bromacetonitril hydro-
CH 2 Br.CN+HBr.
C 2 H 3 Br 2 N
sb. 65
65
Engler
A., 133, 139; 142
vi., 523
bromide
69
Acetonitril cKhydrobromide
CH 3 .CN+2HBr.
C 2 H i Br 2 N
sb. 49
47-50
?)
II
t)
Tribromglyoxalin
C 3 HBr 3 N 2
214 d.
Wyss
B., 10, 1371
Brompropionitril hydrobro-
C 3 H 4 BrN+HBr
C 3 H 5 Br 2 N
64
Engler
A., 142, 65
vi., 524
mide
1
Propionitril dihydrobromide
Me.CH 2 .CN+2HBr
C 3 H 7 Br 2 N
....
50-55
jj
Tribromomethlyglyoxaline ....
C 3 Br 3 N.NMe
C 4 H 3 Br 3 N 2
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.Cl a =1.2.?
C 6 H 3 Br 3 N
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
C 5 H 4 BrN
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
....
C 6 II 4 Br 6 N 2
120
Beiiedikt
C. C. [1878], 101
34, 499
?
....
....
124
....
A., 189, 167
Tribromethylglyoxaliue
(C 3 Br 3 N)NEt
C 5 H b Br 3 N 2
....
61-62
Wallach
B., 16, 537
44, 911
....
61
Wyss
B., 10, 1372
Tribronidiazobenzenimide ....
C H 2 Br 3 .N.N : N=1.3.5.6
C 6 H 2 Br 3 N 3
....
59
Silbersteiu
J. p., 27, 116
44,661
Peutabromaniline
C e Br 6 .NH 2
C 6 H 2 Br 5 N
Not b. 220
Korner
G. I., 4, 305
29, 218
)i
**8
....
J. [1875], 344
Tribronidiazobenzenimide
C 6 H 2 Br 3 .NBr.NBr 2 = 1.3.5.6
C 6 H 3 Br 6 N 2
....
98-5
Silberstein
J. p., 27, 118
perbromide
Diazodibromphenylimide ....
C 6 H 2 B 2 .N 2 .NH
C 6 H 3 B ri N 3
....
62
Griess
P. T. [1864], 700
iv., 484
Tetrabromaniline
Br 4 .NH 2 =1.2.3.5.6
C 6 H 3 Br 4 N
115-3
Korner
G. I., 4, 305
29, 212
)1
....
116-117
Wiirster & Nolting
B., 7, 1564
29, 389
p-Diazobromphenylimide ....
C 6 H 3 Br.N 2 .NH
C 6 H 4 BrN 3
20
Griess
P. T. [1864], 700
iv., 483
Trbiromaniline
Br 3 .NH 2 =1.3.5.6
C 6 H 4 Br 3 N
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
NH 2 .Br 2 =1.2.5
=1.3.5
C s H s Br 2 N
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
NH 2 .Br 2 =1.2.4
11 n
i )i
11 i
11 i
1 11
1 34
C 6 H 5 Br 2 N
11
i
J5
)1
fi
; *)
n
11
C 6 H 6 Br 4 N
))'
1
C 6 H 6 BrN
j^
jf
11
11
si
f1
1
51
J
Jf
11
>1
51
rt
si
11
i)
*;
11
)i
i>
*:
i
11
11
C 6 H"Br 3 tf
C 6 H 7 BrN 2
C 6 n"BrN
C c H 8 BrN 3
C 6 H 8 -Br 2 N 2
C 6 H 14 BrN
CyH.BrN
C 7 H 4 Br 2 N 3
C 7 H 3 BrN 2
241'5
241-5
241-5
251
229
cf. 28, 147
cf. 29, 212
+3H 2 O
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
(NH 2 .Br 3 =1.3.5)+HBr
NH 2 .Br = 1.3
1) 1
)) 1)
J)
1 11
> 1*
NH s .Br=l,2
!>'
l '
!) II 1
NH 2 .Br =1.4
)>
)
n
)> )
)') >>
'
>'
i) n
>^ n
!<
)t
1>
I )1
JJ >*
)>' H
if i*
*)
NHj.NH 2 .Br =1.2.4
*j
C 6 H 7 N.HBr.
fr,C 3 H 2 MeN.NEt
C 6 H 4 Br.CN =L3
C 6 H 3 Br.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.NH 2 .Br, =1.3.2.4.5.6
C ; H 3 Br 4 N
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.NH 2 .Br 3 = ?
C 7 H a Br 3 N
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
C 6 H s .CN + 2HBr.
C 7 H 7 Br,N
70
Engler
A., 149, 307
vi., 525
Dibromtoluidine
Me.NH 2 .Br 3 =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
C ll H 4 Br(CH, ! .NH. ! )=1.2
C-H 8 BiN
....
Liquid
Jackson and White
B., 13, 1219
38, 879
i
=1.4
11
Liquid
Jackson & Lowery
A. C. J., 3, 247
42, 170
Brommethylaniline
C 6 H 4 Br.NHMe=1.4
11
259-260
Liquid
Wiirster & Scheibe
B., 12, 1817
38, 107
Bromtoluidine
Me.NH 2 .Br=1.2.3
)
....
Liquid
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.NH 2 .Br 1.4.5
C 7 H 8 BrN
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.(NH 2 ) 2 =1.4.2.3
C 7 H 9 BrN 2
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 ...
C 7 H 9 Br 3 N 2
....
216-217
Kadziszewski and
B., 17, 1293
46, 986
Szul
Luticline hydrobromide
C 7 H 9 N+HBr
C r H 10 BrN
d. 230
Ladenburg & Roth
B., 18, 1592
Dibromglyoxalisoamyline ....
....
C 7 H 10 Br 2 N 2
....
157-158
Badziszewski and
B., 17, 1293
46, 986
Szul
Glyoxalisoamyline hydro-
C 7 H 12 N 3 +HBr
C 7 H 13 BrN 2
100
H
B., 17, 1292
46, 985
bromide
Bromdiazobenzene cyanide....
C 6 H 4 Br.N 2 .CN+HCN=1.4
C 8 H 5 BrN 4
127-5
Gabriel
B,, 12, 1638
38,41
Phenylbromacetic nitril
Ph.CHBr.CN
C 8 H 6 BrN
d. 150
Liquid
Beimer
B., 14, 1798
Brom-a-toluic nitril
C 6 H 4 Br.(CH 2 .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
6 H 3 Br.NH.CH 2 .CH : N
C^BrNj
206
Bemmers
B., 7, 348
27, 696
=11.2
Bromformanhydroisodi-
C 6 H 2 MeBr.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
C 8 H 7 Br 2 N
...
200 d.
Reimer
B., 14, 1797
42, 169
mide
Dibroiuiiaphthylamine
NH 2 .Br 2 =a,/3 s ; a
I)
101-102
yieldola
47, 514
jj
=ao3, ; /5
)1
105
D
47, 511
Bronidimethylaniiine
C 6 H Br.NMe 2 =1.3
C 3 H 10 BrN
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
C 6 H 4 Br.NMe 2 =1.4
C 8 H 10 BrN
SfT (722)
55
Merz and Weith
B., 10, 763
32, 603
i
)
264 c.
55
Wiirster and Beran
B., 12, 1820
38, 108
Bromxylidine
Me 2 .NH 2 .Br=1.3.4.5
96-97
Genz
B., 3, 225
vii., 1210
Fr. dimethyl-p-diamidoben-
....
C s H u BrN 2
146
Wiirster and
B., 12, 1803, 2071
88, 110
zene
Sendtners
Bronicyanmethethiue
....
C 3 H 12 BrN 3
155 d.
Eiess and Meyer
J. p. [2], 31, 112
48, 646
Hydro-a-isopropylpyridine
....
C 8 H M BrN
230-233
Ladenburg
B., 18, 1589
48, 992
+HBr
a-isopropylpiperidine + HBr
....
C 8 H 19 BrN
216
s
B., 17, 1679
46, 1386
Coniine+HBr
C 8 H 16 BrN(?)
,, (?)
207
Copellidine+HBr
....
165
Diirkopf
B., 18, 923
48, 817
Tetrethylammonium tri-
NEt 4 .Br s
C 8 H 20 Br 3 N
78
Marquart
J. p. [2], 1, 429
vii., 485
bromide
Hexabromquinoline
....
C 9 HBr,N
88-89
Weidel
A., 173, 95
28, 88
Tetrabromquinoline
....
C 9 H 3 Br 4 N
119 u.c.
Clauss and Istel
B., 15, 820
42, 1110
Tribromquinoline
....
C 9 H 4 Br 3 N
173-175
Lubavin
Z. C. [2], 5, 690
vi., 430 ; vii.,
A., 155, 318
307
....
....
))
173-175
Hoffmann & Konigs
B., 16, 737
Dibromquinoline
N.Br s =l ; 1.3
C 9 H 6 Br 2 N
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=?
C 9 H 6 BrN
270
Coste
B., 14, 916
40, 741
=1 ; 3
11
276-278
....
)>
B., 15, 558
42, 978
Amidobromquinoline
)i >
C 9 H r BrN 2
164
i
B., 15, 1920
44,91
Propenyltribromphenylene
C 6 HBr 3 .NH.CEt:N=(?) 3 .1.2
C 9 H 7 Br 3 N 2
257-262
Smith
A. C. J., 6, 172
48, 525
diamine
i i
Quinoliue tetrabromide
....
C 9 H 7 Br 4 N(?)
cf. B. S., 38,
88
Grimaux
C. E., 95, 85
124
Propenyldibromphenylene
C 6 H 2 Br 2 .NH.CEt:N=(?) 2 .1.2
C 9 H Br 2 N 2
224-226
Smith
A. C. J., 6, 172
48, 524
diamine
Quiuoline dibromide+HBr
C 9 H 9 Br 3 N
cf. B. S., 38,
86
C. E., 95, 85
42, 1215
124
Dibromtetrahydroquinoline
C 9 H 9 Br 2 N
05-66
Clans and Istel
B., 15, 823
42, 1110
Bromtetrahydroquinoline
....
C 9 H n Br 2 N
192 d.
Hoffmann and
B., 16, 737
44, 1145
+ HBr
Konigs
Ethylmethylbromaniline
C 6 H 4 Br.NMeEt=1.4(?)
C 9 H 12 BrN
265
s. b.
Clans and Howitz
B., 17, 1327
46, 1006
Dimethylbromtoluidine
Me.NMe 2 .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 ....
....
C 9 H 12 Br 3 N 3
126
Riess
J. p. [2], 30, 145
48, 236
Propylphenylamine+HBr ....
C 6 H 4 .Pr.(NH 2 .HBr)=1.4
C 9 H 14 BrN
213
Francksen
B., 17, 1222
46, 1008
Bromcyanethine
C 9 H 14 BrN 3
152-153
Meyer
J. p. [2], 26, 339
44, 353
j) ....
)
153
Riess
J. p. [2], 30, 145
48, 235
Methylcopellidine-fHBr ....
C 8 H 16 MeN+HBr
C 9 H 20 BrN
151
Diirkopf
B., 18, 926
48, 817
Dibromnaphthylamine
NH 2 .Br 2 =a 1 o 2 3 1 ;
C 10 H 7 B r2 N
118-119
Meldola
B.,12, 1961
38, 260 ; 43, 4
....
=ft
121
Laws on
B., 18, 2424
48, 1239
Bromnaphthylamine
NH 2 .Br=a.^, ;
C 10 H 8 BrN
62
Meldola
47, 510
,> =0ii ;
M
63
j
43, 5
47, 523
j) ...
D
)i
63
Cosiner
B., 14, 59
40, 606
,,
=a 1 ; 0! or /3 2
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.(CH 2 .CN)=l.?.4
C 10 H 9 BrN 2
127-129
Gabriel
B., 15, 840
42, 1070
cyanide
Bromam idoacenaphthal ide ....
(NH 2 ) 2 .Br=a 1 a 2 1 ;
)
222
Meldola
47, 501
Quinoline dibromide metho-
CaNHjEr^MeBr
C w H w Br I N
123
Ostermeyer
C.C. [1884], 970;
48, 672
bromide
B., 18, 594
Pyridine dibromide hydro-
(C 6 H 5 Br 2 N) 2 .HBr
C 10 H ll Br 6 N 2
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 ....
C 6 H 4 Br.NEt 2 =1.4(?)
C 10 H 14 BrN
270
33
Glaus and Howitz
B., 17, 1324
46, 1006
Brom-a-naphthoic nitril
....
C n H 6 BrN
147
Hausamann
B., 9, 1516
31, 318
-ft-
....
JJ
....
148-149
B., 9, 1517
Quinoline ethobromide
C 9 H 7 N.EtBr+H 8
G,,H 12 BrN
80
Glaus and Tosse
B., 16, 1277
44, 1009
Decabromdiphenylamine
NH(C 6 Br 6 ) 2 (?)
C 12 HBr 10 N
a. 310
Gessner
B., 9, 1512
31, 301
Octobromdiphenylamine
C 12 H 3 Br 8 N
302-30o
31, 302
Hexabromdiplienylamiue ...
....
C 12 H 3 Br 6 N
218
Gnehm
B., 8, 926
29,83
Hexabromdiazoamidoben-
C 6 H.,Br 3 . Nj. NH.l'sH.Br.,
C 12 H 6 Br 6 N 3
....
158 d.
Silberstein
J. p. [2], 27, 120
44, 661
zene
=1.3.0.6; 6.5.3.1
Tetrabromazobenzene
C 12 H,Br 4 N 2
320
Werigo
A., 165, 200
26,385;vii.,148
Azimido-dibromdiphenyl ...
C 12 H 7 Br 2 N 3
206
Schultz
B., 17. 466
46, 903
Tetrabromdiphenylamine ....
NH(C 6 H 3 B, 2 ) i
C, 2 H 7 Br 4 N
cf. A., 132,166
182
Gnehm
B., 8, 925
29, 83
Diazoamidodibrombenzene ....
....
C 12 H 7 Br 4 N 3
167-5
Griess
A., 121, 273
iv., 460
Bromcarbazole
....
G 12 H 8 BrN
199
Ciamician & Silber
G. I., 12, 272
42, 1104
Dibromazobenzene
C 6 H 4 Br.N 2 .C 6 H 4 Br=(1.3) 2
C 12 H 8 Br 2 N 2
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
C 6 H 2 Br 3 .N 2 .NHPh=1.3.r>.6
C 12 H 3 Br 3 N :i
104
Silberstein
J. p. [2], 27, 121
44, 661
Tetrabrbmbenzidine
G 12 H 8 Br 4 N 2
284-286
Glaus and Risler
B., 14, 86
40, 605
Phenanthroline octobromide
CHBr.(CHBr) 1 ,.N : G.C ;
C,.H.Br s N,
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-
C 10 H 5 Br.NH.CMe:N
C 12 H 9 BrN 3
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.C B H 4
Phenanthroline hydrobro-
>...
);
....
278-280
Skraup & Vortmann
M. C., 370
44,87
mide
Dibromdiphenyilamine
NH(C 6 H 4 Br) i!
C 12 H 9 Br 2 N
107
Lellmami
B., 15, 830
42, 1060
Dibromaniidoazobenzene
C I2 H 9 Br 2 N 3
145
Griess
A., 121, 269
iv., 460
!,
..,,
cf. B.,17, 1403
152
Berju
C. C. [1884], 871
46, 11 48; 48, 660
Dibromhydrazobenzene
C 6 H 4 Br.(NH) 2 .C 6 H 4 Br
C 12 H 10 Br 2 N 2
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
,,
(.C 6 H 3 Br.NH 2 ) 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-
C 6 H 3 Br.N : CPh.N
C 13 H 9 BrN 2
200
Johnson
B., 10, 1710
1 i
ume
Tctrabrommethyldiphenyl-
NMe(C 6 H 3 Br 2 )_,
C 13 H 9 Br 4 N
129
Gnehm
B., 8, 926
29,83
amine
Tribrommethyldiphenyl-
C 6 H 3 Br 2 .NMe.C 6 H 4 Br
C 13 H 10 Br 3 N
98
amine
Oxaldipropylisoamyline bro-
(XH.|Pi*N^Pf"Br
C 13 H 23 BrN,
162-163
Radziszewski and
B., 17, 1295
46, 986
mide
Szul
Pheuyldibromanilidoacetic
C 6 H 3 Br,(NH.CHPh.CN)
G 14 H 10 Br 2 N..
92
Tiemann and Piest B., 15, 2032
44, 198
nitril
=1.3.4
Benzylidene dibronitoluidine
C 14 H u Br 2 N
160-165 d.
J. [1880], 566
Tetrabroin-p-ditolylamine
(Me.C 6 H 2 Br 2 ) 2 NH
C 14 H n Br 4 N
162
Lehue
B., 13, 1545
40, 41
Diniethamidoazotribromben-
C,H s Br,.N s .C,H 4 .NMe s
C 14 H 12 Br 3 N : ,
..'.
161
Silberstein
J. p. [2], 27, 124
44, 662
zene
= 1.3.5.6; 1.?
Bromazotoluene
Me.C 6 H 4 .N 2 .C 6 H 3 Br.Me
C H BrN
136
Petrieff
B., 6, 557
26, 1027
Dibromdibenzylamine
(C 6 H 4 Br.CH 2 ) 2 NH=(1.2) 2
C H H M Br,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
(C 6 H 5 .CH 2 ) 3 NH+HBr
C 14 H 16 BrN
266
Limpricht
A., 144, 304
vi., 337
Quinoline amylbroniide
C 9 H 7 N.C 5 H n Br
C 14 H 19 BrN
....
140
Claus and Tosse
B., 16, 1278
44, 1009
j> i>
11
))
+.rH 2 O
87
*
?
....
C 14 H 18 Br 2 N :
57-5
Werigo
Z. C. [1865], 631
vi., 285
Picoline ethylene dibromide
(C 6 H 7 N) 3 .C 2 H 4 Br 2
)
27,6
Ramsay
P. M. [5], 2, 279
36, 263
/3-Lutidine dibromide + HBr
(C 7 H 9 NBr 2 ) 2 +HBr (?)
C 14 H 19 Br 5 N 2
64
Grimaux
C. K., 95, 85
42, 1216
Bromphenylquinolinamine ....
N.(NH.C 6 H 4 Br)=1.2 ; (1.4)
C 16 H n BrN 2
146
Friedlander and
B., 18, 1533
48, 990
Weinberg
Phenylhydrazine f Bromcin-
Ph.CBr:C 2 H 2 :N 2 HPh
C 15 H 13 BrN 2
....
129-130
Zincke and Hagen
B., 17, 1815
46, 1344
namaldehyde
Tetrabrom-/3-naphthyl-
fr. C 10 H 7 .NHPh
C^H^r^N
cf. A., 209, 15!
19.8
Streiff
B., 13, 1853
40, 177
phenylamine
Tribrom-a-naphthylpheny.l-
. J)
C 16 H 10 Br 3 N
cf. A., 209, 155
137
u
B., 13, 1852
40, 176
amine
Dibrom-/3-naphthylpl'enyl-
i)
C 16 H u Br 3 N
cf.A.,209,15f
140
n
B., 13, 1853
40, 177
amine
Methyldiphenylbrompyr-
C 3 N 2 BrMePh 2
C 16 H 13 BrN 3
....
75
Knorr and Blank
B., 18, 316
48, 556
azene
Brombenzylquinoline dibro-
C,H 7 N.C 7 H 7 Br.Br s
C 16 H 14 Br 3 N
100 u. c.
Glaus
B., 18, 1306
48, 908
raide
Dixylylamine Ijydrobromide
(Me.C 6 H 4 .CH 3 ) s NH+HBr
C 16 H 20 BrN
.... |
195-19,6
Pieper
A., 151, 129
vi., 1133
Tetrabrpnxtolyjnaphthyl-
fr. C 10 H..NH.C 6 H 4 Me
C 17 H n Br 4 N
168-169
i Friedlander
B., 16, 2080
46, 80
amine
=; 1-4
?
C 9 H 6 N.CHBr.CHBr.Ph
C 17 H 13 Br 3 N
173-174
Wallach & Wiisten
B., 16, 2009
44, 1097
Dibromdiquinoline
(C 9 NH 6 Br) 2 =a 1 ; /3 2 -a, ; a,
C 18 H )0 Br 2 N.,
n.f. 280
Fischer
M. C., 6, 546
48, 1247
Bromdiquinoline
C 18 H n Br^ 2
....
150-155
Ostermeyer and
B., 17, 2149
48, 174
Henrichsen
Dibromtetramfthyldiamido-
Me 2 N.MeBrC 6 H 2 .C 6 H 2 BrMe.
C 18 H 33 Br 2 N 3
,117
Michler and Sam-
B., 14, 2173
48, 177
ditolyl
NM ej =1.2.('0 2 ;(?) 2 .2.1
paio
Methylphenam,idoazotri-
G 6 H 2 Br,.N 2 .C 6 H 4 .NMePh
C 19 H 14 Br 3 N
.I? 8
Silberstein
J. p. [2], 27, 98
44, 662
brombenzene
=1.3.5.6 ; 1.?
Pentabromazonaphthalene ....
....
C 20 H 9 Br 5 N 2
a. 320
Klobukowski
B., 10, 576
32, 623
Tribromtribenzylamine
(C 6 H 4 Br.CH 2 ) 3 N=(1.4) 3
C 3l H 18 Br 3 N
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
C 21 H 19 Br 4 N
270
Jackson & Lowery
B., 10, 1211
34, 65
Brom-deriv. of phenanthroline
C 24 H l6 Br 3 N 4
176-178
Skraup & Vortmanu
M. C., 3, 581
n
....
C 24 H 17 Br 3 N
176-178
i
M. C., 3, 581, 583
5> I)
C 12 H 8 N s Br 2 +C 12 H s N 2 .HBr
C 24 H 17 Br 3 N 4
....
178
5)
M. C., 3, 370
44,87
Tetrabromtetrimidazoan-
[C 6 H 4 :(C:NH) 2 :C 6 HBr 2 ] 3 :N 2
C 28 H 14 Br 4 N 6
....
233
Glaus &Dierufellnei
B., 14, 1336
42, 523
thracene
Tetrabromdibenzylene di-p-
(Ph.CH) 3 (N.C 6 H 2 Br 3 Me) 3
C^Bir.N,
....
160-165, d.
Mazzara
G. I., 10, 370
38, 879
tolylamine
Diphenyldiisoindolazotri-
( CH.CPh.N.C 6 H 4 .Nj.
C 40 H 34 Br 6 N 6
....
149-^50
Mohlau
B., 15, 2491
44, 342
brombenzene
C,HjBr 3 ),=L2;. 6.5.3.1
(11.) CHBrP, CHBrAs, and CHBrSb.
Phosphenyl dibromide
Ph.PBr 2
C 6 H s Br 2 P
255-257
Liquid
Michaelis & Kohler
B., 9, 519
30, 4-20
tetrabromide ....
Ph.PBr 4
C 6 H 5 Br 4 P
....
207
M
B., 9, 521
u
hexabromide ....
Ph.PBr 6
C 6 H 6 Br 6 P
sb. a. 110
solid
11
*>
Bromethyltriethylphosphon-
PBrEtj.C,H 3 Brj
G 8 H l9 Br 2 P
235 d.
Hofmann
As., 1, 154
iv., 618
ium bromide
Bromethy [dimethyl phenyl-
PBrMe 3 Ph.C 3 H 4 Br
C 10 H 16 Br 2 P
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-
C a H 4 (PMe 2 PhBr) 2
Cj.HJBr.P.
a, 300
Gleichmann
B., 15, 199
42, 958
pheiiylphosphonium di-
broraide
Tetrabromide of above
C 2 H 4 (PMe !! PhBr). ! .Br 4
Ci S H 26 Br 6 P 2
171
B., 15, 200
Triphenyl benzylphosphon-
Ph.CH 2 .PPh 3 Br
C 25 H S2 BrP
274
Michaelis & Soden
A., 229, 334
48, 1135
ium bromide
Tetrabenzyl phoaphonium
(Ph.CH 2 ) 4 PBr
CjsHjgBrP
216-217
Letts and Collie
T. E., 30, 181
42, 724
bromide
Ethylene di(triphenylphos-
C 2 H 4 (PPh 3 Br) 2
C 38 H 34 Br 3 P 2
a, 300
Michaelis & Gleich-
B., 15, 804
42, 1062
phonium bromide)
mann
Arsenpheuyl dibromide
Ph.AsBr 2
CeHsBrjAs
285 s.d.
Liquid
Michaelis
A., 201, 203; B.,
32, 452
10, 625
Arsendiphenyl bromide
Ph 2 AsBr
C 12 H 10 BrAs
356 in CO,
Liquid
Coste and Michaelis
A., 201, 230 ; B.,
36, 162
11, 1886
Stibtriethyl dibromide
Et 3 SbBr 2
C 6 Hi 5 Br 2 Sb
....
s. 10
Lowig & Schweitzer
J. [1850], 475
i., 342
Stibtritolyl
(C 6 H 4 Me) 3 SbBr 2 =(1.3) 3
C 51 H 21 Br 2 Sb
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
C S HI 3 O
25-115
iii., 280
110
....
Johnson
P. M. [3], 2, 415
Tetriodmethyloxide
(CHI,)/)
C 2 H 2 I 4 O
181-182
s. 6
Bruning
J., 10, 434
CH 3 .COI
C 2 H 3 IO
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
CH 2 I.COOH
C 2 H 3 I0 2
82
Perkin and Duppa
P. M. [4], 18, 55
iii., 279
Methyl iodide hydrate
(CH 3 I) 2 ,H 2
C 2 H 9 I 2
....
4
Fourcraud
C. E., 80, 1491
40, 32
lodopropargylic acid
CI : C.COOH
C 3 HI0 2
....
140
Baeyer
B., 18, 2274
48, 1199
,,
J)
J)
140
Homolka and Stolz
B., 18, 2282
Triiodacrylic acid
CL/CLCOOH
C 3 HI 3 2
207
H
B., 18, 2286
48, 1198
3-diiodacrylic acid
CI S :CH,COOH
C.HAO.
....
133
11
B., 18, 2284
H
<i-/3-
CHI : CI.COOH
,,
106
H
lodacrylic acid
CHI : CH.COOH
C 3 H 3 I0 2
139-140
Bandrowsky
B., 15, 2703
48, 510
Diiodacetone . , ...
CHjI.CO.CHJ
C 3 H 4 I O
,>, ... fjo.e
Viilkov
Ai ' t ' vi
^_
....
DJ. O~Oi O
V 1 H Kt I
., 1 ' . OC7
*5^) iOL
Propionyl iodide
CH 3 .CH 2 .COI
C 3 H 5 IO
127-128
Sestini
B.S. [2], 11, 469
vi., 963
lodallyl alcohol
C 3 H 4 I.OH
....
160
Hiibner and Lell-
B., 13, 461
38, 5.38
mann
160
B., 14, 208
40, 242
Epi-iodhydrin
O.CH 2 .CH.CH.,I
..
160-180
Liquid
Reboul
As., 1, 227
Methylic iodacetate
CHjI.COOMe
C 3 H S I0 2
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
CH 3 .CI(OH).COOH
C 3 H 5 I0 3
84-85
Glinsky
B., 6, 1257
8-
CH 2 I.CH(OH).COOH
100-101
Melikoff
B., 14, 937
40, 712
Glycerol diiodhydrin
C 3 H 5 I 2 .OH
C 3 H 6 I 2
d. 70-76
s. -16 to -20
aaus
A., 168, 25 ; B.,
25, 684 ; 26,
5, 355
1122
Diiodopropyl alcohol
CjH 3 Ij.CH,OH
,,
....
45 d.
Hubner and Lell-
B., 14, 207
40, 242
mann
Propylene gtycol iodhydrin....
C 3 H.IO
106 (60)
....
Z. C. [1870], 424
lodofumaric acid
COOH.CH : CI.COOH
C 4 H.IO 4
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
C 3 H 2 I.O.Me
C 4 H 5 IO
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.CH 2 .CH 2 .COI
C 4 H 7 IO
146-148
Cahours
J., 10, 344
i., 699
Ethylic iodacetate
CH 2 I.COOEt
C 4 H 7 IO 2
178-180
cf. A., 112,
Butlerow
B., 5, 479
127
Methylic /3-iodopropionate ....
CH 2 I.CH 2 .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
CH 2 I.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.CH 2 .OEt
C 4 H 9 IO
154-156
Liquid
Baumstark
B., 7, 1173
28, 141
J)
154-155
....
Demole
B., 9, 744, 746
lodopyromeconic acid
C 5 H 3 IO 3
cf. A., 92, 321
a. 100
Brown
P. M. [4], 8, 201
iv., 761
Ethylic iodopropargylate ....
ci ; c.cooEt
C 5 H 5 I0 2
....
68
Baeyer
B., 18, 2274
48, 1199
Itaiodopyrotartaric acid
C 6 H 7 IO 4
....
135
Z. C. [1866], 722
vi., 981
Isovaleric iodide
CHMej.CHj.COI
C 6 H 9 IO
168
....
Cahours
C. E., 44, 1252
v., 980
Propylic iodacetate
CH 2 I.COOPr
C 6 H 9 I0 2
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
Me 2 .CI.CH 2 .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
C 6 H 2 I 2 :0 2 =?.U.4
C 6 H 2 I 2 2
178
Seifert
J. p. [2], 28, 437
46, 431
Triiodophenol
OH.I 3 =1.2.4.6
C 6 H 3 I 3
150
Schiitzenberger
A., 120, 307;
vi., 909
131, 232
156
Korner
A., 137 214
vii., 929
Triiodoresorci ii ol
(OH) 2 .I 3 =1.3.4.6.?
C 6 H 3 I 3 O 2
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.I 2 =?
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
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
*>
....
O7
907
lodoresorcinol
(OH) 2 .I=1.3.?
C 6 H 6 I0 2
67
Stenhouse
P. E., 22,53; A.,
27, 586
171,311
Ethylic a-iodobutyrate
CH 3 .CH 2 .CHI.COOEt
C 6 H n I0 2
190-192 d.
*
Hell
B., 6, 30
26, 495
Triiodosalicylic acid
COOH.OH.I 3 =1.2.(?) 3
C 7 H 3 I 3 O a
157 d.
Lautemann
A., 120, 306 ;
v., 158
174, 104
Diiodosalicylic acid ....
COOII.OH.I 2 =1.2.(?) 2
C 7 H 4 I 2 3
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.I 2 =1.2.(?) 3
C 7 H 4 I S S
220-230 d.
Demole
B., 7, 1439
lodobenzaldehyde
COH.I=1.4
C 7 H 6 IO
73
Jackson and White
B., 11, 1043
34, 729
lodobenzoic acid
COOH.I=1.2
C 7 H 5 I0 2
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-
Glassner 1
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,?
C 7 H 5 IO :)
160
Peltzer
A., 146, 288
vi., 900
lodosalicylic acid
=1.2.5
mixture ?' :
184
Liechti 1
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.I 2 =1.4.3.S
C 7 H 6 I 3
61-61-5
Schall and Dralle
B., 17, 2534
48, 146
lodobenzyl alcohol
(CH 2 OH).I=1.4
C,H 7 IO
cf. A. C. J.,
71-75
Mabery & Jackson
B., 11, 56
34, 421
2, 251
lodorcinol
Me.(OH) 2 .I=1.3.5.?
C 7 H 7 IO S
.... '
86-5
Stenhouse
P. R., 22, 53;
vii., 879; 26,
C. N., 26, 279 ;
275 ; 27, 585
A.,- 171, 310
Acetyldiiodophehol'
C 6 H 3 I 2 .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
C 8 H 7 I0 2 "
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
C 6 H 4 I.(CH 2 .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
C 8 H 7 IO 3
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
C 8 H 9 IO
237-238 '
Liquid
Schall and Dralle
B., 17, 2533
48, 146
Iodo-j3-orcinol ....
C 6 HIMe 2 (OH) 2
C 8 H 9 I0 2
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
C 9 H 9 IO S '
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.C 2 H 3 I.COOH
C 9 H 9 I0 2
....
119-120 d.
Fittig and Binder
B., 9, 1195; A.,
31, 61 ; 36, 378
147, 97; 195, 133
lodohydrocinnamic acid
C 6 H 4 I.(CH 2 .CH 2 .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.I 2 =1.4.3.5
C 9 H 9 T 2 O 3
62-62-5
Schall and Dralle
B., 17, 2534
48; 146
lodonaphthol.... .... ..
OH.I=?
C 10 H ; IO
88
Ostermeyer-
C. C.' [1884], 937
48,672
.. ^ /J, (1 J
94-5
Meldola'
47, 525
DiacetyltriioJoresorcinol
(OAc) 2 .I 3 =1.3.4.(i) 2
n
CioHyl-jO,
....
170
Claesson
B., 11, 1443
34, 868
lodomeconin ....
C ln HJO 4
112
Anderson 1
A., 98, 49
iii., 863
HI on Cantharidiu
i.*.
10 9* 1 V 4
^loHiJjlO.,
131
Piccard
B., 12, 577
36, 655
lodocamphor
C 10 H 15 IO
....
43-44
Haller
C. B., 87, 695
36, 329
Diiododiphenylquinol
C 6 H 3 I(OH).C 6 H 3 I(OH)
C 12 H 8 I S 2 >
abt. 150
Kammerer & Ben-
B., 11, 557
34, 574
zinger
Bsnzoyldiiodophenol
C 6 H.,I 2 OBz
C 13 H 8 I 2
95-96
Schall
B., 16, 1903
44, 1109
Diiododipheuic acid ....
(C 6 H 3 I.COOH) 2 =(1.4.2) 2
C 14 H 8 I 2 O 4 ,
....
abt. 260
Schultz
B., 11, 217
34, 511
i) 11
I> )>
>i
262
)J
B., 12, 236
36, 653
Benzoxydiiodotoluene
Me.OBz.I 2 =1.4.3.5
C 14 H n IA
....
129-5-130
Schall and Dralle
B., 17, 2534
48, 146
Santonic iodide
....
C,,H lf IQi.
136
Cannizzaro and
G. I., 8, 309 '
36, 331
Valente
Benzaldide oxyiodide
C 2 iH 13 I 4 O ;
....
28
Geuther&Cartmell
A., 112, 22
1., 572
(13.) CHTS, CHISe, and CHITe.
Diiodothiophene
C 4 H 2 I 2 S
40-5 ::
Meyer and Kreis
B., 17, 1558
46, 1131
lodothiophene
....
C 4 H 3 IS
182 u.c.
Liquid
)!
B., 17, 1559
))
Diethylene disulphotetriodide
(C 2 H,) 2 S 2 I 4
C 4 H 8 I 4 S 2
132-133 d.
Husemann
A., 126, 289
vi., 607
Iodo-^-ethylthiophene
C 4 SH 2 IEt
C 6 H 7 IS
....
Liquid
Bonz
B., 18, 551
48, 767
lodothioxylene
C 4 SHIMe 2
)>
....
Liquid
Messinger
B., 18, 1638
48, 1052
Triethyl sulphuro-iodide
SEtJ
C 6 H 15 IS
a. 100
Dehn
As. -4, 95
v., 882
Diiodophenylsulphide
S(C 6 H 4 I) 2
tt| 2 H 8 I 2 S
....
138-139
Krafts
B.,- 7, 1165
28, 154
Triethyl seleno-iodide
SeEt 3 I
C 6 H, 5 ISe
w.m. 80-126
Pieverling
A., 185, 333
34, 130
Benzyldimethyl seleno-triio-
Ph.CH 2 .SeMe 2 I 3
C,H 13 I 3 Se
65
Jackson
A., 179, 19
29, 581
dide
Diethyltellurod iiod ide
TeEt 2 I 2
C 4 H 10 I 5 Te
50
Maleet
A., -79, 223
ii., 550
Triethyltelluroiodide
TeEt,!
C 6 H 16 ITe
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).NH 2 + HI
C 3 H ln IN 3
...i
149 d.
Letnii
B., 8, 767
29, 911
Tetriodopyrroline
C 4 I 4 :NH
C 4 HI 4 N
....
d.w.m. 140-
Ciamician & Denn-
B., 15, 2584
44, 351
150-
stedt
Pyridiue periodide
C 5 H S N.HI.I 4
C 6 H 6 I 6 N
....
89
Dafert
M. 0., 4, 496
44, 980
Trimetliylethylammonium
NEtMe 3 I 3
C 6 H 14 I 3 N
64
Muller
A.; 108, 1
iii., 1000
triiodide
>! 11
J)
))
....
64
Dafert
M. C., 4, 496
44, 978
Trimethylethylamnionium
NEtMe 3 I 5
C 6 H 14 IiN:
....
68'
'
11
11
pentiodide
11 11
)t
'
68
MUller
A., 108, 3
iii., 1000
Triiodaniliue ...
NH n .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.
NH 2 .I 2 =1.2.4.
C 6 H 5 I 2 N
95-95-5
Michael & Norton
B., 11, 111
34, 406
M
96
Rudolph
B., 11, 79
34, 422
lodaniline .... .... ...
NH 2 .I=1.3
c 6 n"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....
(C 3 H 3 N)NEt.MeI
C 6 H n IN 2
....
74-75
Wallach
B., 16, 535
44, 911
Methylhydropyrroline meth-
C 4 H 6 MeN.MeI
C 6 H 12 IN
286 d.
Ciamician & Denu-
B., 16, 1542
44, 1142
iodide
stedt
Pipecoline hydriodide
NH.(CH 2 ) s .CHMe.CH 2 +HI
C 6 H 14 IN
131
Hesekiel
R, 18, 912
48, 812
L J
Triethylazonium iodide
C 6 H 17 IN 2
74-78
Fischer
B., 11,2208
36, 451
lodobenzonitril
C,H 4 I.CN=1.3
C 7 H 4 IN
....
41
Griess
B., 2, 370
vii., 427
Diiodotoluidine
Me.NHj.I 2 =1.4.3.5
C 7 H 7 I,N
124-5
Michael & Norton
B., 11, 115
34,407
lodobeuzylamine
C 6 H 4 I.(CHj.NH 2 )=1.2
C 7 H 9 IN
Liquid
A. C. J., 4, 101
=1.4
Liquid
A. C. J., 2, 257
lodotoluidine....
Me.NH 2 .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
C 6 H 7 N.MeI
C 7 H 10 IN
226-5-227u.c.
Ramsay
P. M. [5], 2, 277
36, 263
Picoline methiodide diiodide
C 6 H 7 NIs,.MeI
C 7 H 10 I 3 N
129
P. M. [5], 2, 278
J)
Methyltriethylammonium
NEtjMeL,
C,H 18 I 3 N
62
Muller
A., 108, 1
ill., 1000
triiodide
lod-a-toluic nitril
C,H 4 L(CH,.CN)=1.4
C 8 H 6 IN
50-5
Mabery & Jackson
B., 11, 56
34, 422
Dimethyliodaniline
C,H 4 LNMe 2
C 8 H 10 IN
79
Merz and Weith
B., 10, 757, 765
32, 603
Picoline ethiodide
..
C 8 H 12 IN
b. 100
Anderson
A., 94, 361
Hydro-a-isopropyl pyridine
....
C 8 H U IN
242-243
Laden burg
B., 18, 1589
48, 992
+HI
Tropidine periodide
C 8 H 14 I 3 N
92-93
B., 14, 232
lodotrimethylpiperidine
MM
C 8 H 16 IN
....
60
Fischer
B., 17, 1796
46, 1291
Trimethylpiperylium iodide
(CsHgMey'Me^I
C 8 H 18 IN
200
Hofmann
B., 14, 663
40, 621
Trimethy lamylammoni um
NMe.CQ.HJLI,
C 8 H 20 I 3 N
80
Muller
A., 108, 1
lli., 1001
triiodide
Tetrethylammonium triiodide
NEt 4 I.I 2
Jj
142
Dafert
M. C., 4, 496
44, 978
lodoquinoline
N.I= ai /3, ;
C 9 H 6 IN
52-53
Friedlander and
B., 18, 1531
48, 990
Weinberg
= '
JJ
300+
62-63
La Coste
B., 18, 782
48, 815
Quinoline diiodide
C 9 H 7 I 2 N(?)
67
Dafert
M. C., 4, 496
44, 980
J!
jj
90
Claus and Istel
B., 15, 824
42, 111
lodocyanethine
C,H 14 IN 3
152
Riess
J. p. [2], 30,145
48, 236
Trimethylphenylammouium
NMe 3 PhI.I 2
C 9 H 14 I 3 N
116
Dafert
M. C., 4, 496
44, 978
triiodide
,,
Trhnethylphenylammonium
NMe 3 PhI.I 4
C,H 14 I S N
87
pentiodide
J)
Oxalmethylisoauiyline meth-
C 7 H, 1 MeN 1 ,MeI
C,H, 7 IN S
169-170
Radziszewski and
B., 17, 1294
46, 986
iodide
Szul
lodotetramethylpiperidine ...
C 9 H 18 1N
90
Fischer
B., 17, 1792
46, 1290
Iod-o-methyl quinoline
C 9 NH 5 MeI
C 10 H 8 IN
73-74
La Coste
B., 18, 785
48, 815
Quinoline methiodide
C 9 NH ; .MeI
C 10 H 10 IN
72
B., 15, 192
Dimethylethylphenylammo-
NPhMe 2 EtI
C 10 H 16 IN
72
124-5
Ostermeyer
Claus & Rautenberg
B., 18, 594
B., 17, 1325
48, 672
46, 1005
nium iodide
126
Claus and Howitz
Dimethylconylammonium
iodide
C 8 H 16 1 NMe 2 I
C 10 H 22 IN
100
Hofmanu
JJ
B., 14, 708
40, 745
Dimethylcopellidinium iodide
C 8 H 16 Me 2 NI
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-
C 10 H,N.MeI
C,,H 13 IN
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
C n H 15 IN 2
192 d.
Fischer & Kuzel
A., 221, 261
46, 442
Ethylanhydracetdiamido-
C 6 H 3 Me.N : CMe.NHEtI
)1
+H.O
141-5-143-5
Hiibner
A., 210, 328
42, 505
toluene iodide
i i
Diethylaniline methiodide ...
NPhEt 2 MeI
C,,H I3 IN
....
102
Clans and Howitz
B., 17, 1326
46, 1006
Methylamylpiperylammo-
C 6 H 10 N(C 5 H u ).MeI
C,,H 24 IN
195
Schotten
B., 15, 422
42, 982
nium iodide
Diiodoazobenzene ...
C 6 H 4 I.N 2 .C 6 H 4 I=(1.3) 2
C 12 H 8 I 2 N 2
150
Gabriel
B., 9, 1410
81, 307
=(l-4) 2
ij
237
!>
B., 9, 1409
?
Diiodohydrazobenzene
C 6 H 4 I.N 2 H 2 .C 6 H 4 I=(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-
C u H u N.MeI
C 12 H 14 IN
203
Ntilting and Wein-
B., 18, 1342
48, 978
line methiodide
gartner
Ethyltetrahydroquinoline
C 9 H 10 EtN.MeI
C 12 H 18 IN
179 u.c.
Clausand Stegelitz
B., 17, 1331
46, 1051
methiodide
Trimethylpropylphenylam-
C 6 H 4 Pr.NMe 2 +MeI=1.4
C 12 H 20 IN
168
Glaus and Howitz
B., 17, 1328
46, 1006
monium iodide
Triethylphenylammonium
NEt 3 PhI.I 2
C 12 H 20 I 3 N
....
81
Dafert
M. C., 4, 496
44, 978
triiodide
Triethylpheuylainmonium
NEt,PhI.I 4
C.sH^N
....
68
?>
>r-
u
pentiodide
Tetramethyldiamidotoluene
Me.(NMe i ) 2 =1.2.5
C 12 H 21 IN 2
160
Wurster and Riedel
B., T2;'J802
38, 109
methiodide
Ethvlmethylquinoline meth-
N.Et.Me=a,/3 1 /3 2 ;
I3 H I6 IN
196 p.d.
Dobner and Miller
B., 17," 17 15
46, 1375
iodide
E ih eny Idiethyltoluy leneami-
C 13 H 19 I 3 N 2
Ill
A., 210, 376
dine triiodide
Methylbenzylpiperyl ammo-
C 5 H 10 N.C 7 H 7 +Met
C 13 H 20 1N
145
Schotten
B., 15,423
42, 982
nium iodide
Triethylbenzylamine perio-
NEt 3 (CH 2 Ph)I 3
C 13 H., 2 I 3 N
87
Ladenburg& Struve
B., 10, 46
dide
/3-Naphthoquinoline methio-
C 13 H 9 N.MeI
C 14 H 12 IN
200-205
Skraup & Cobenzl
M. C., 4, 436
44, 1011
dide
Diiododibenzylamine
(C 6 H,I.CH 2 ) 2 NH=(1.4). 2
C 14 H 13 I 2 N
76
Mabery & Jackson
B., 11, 58
34, 422
Uibenzylamine hydriodide ....
(C 6 H 5 .CH 2 ) 2 NH.HI
C 14 H, r .IN
....
224
Limprieht
A., 144, 304
vi., 337
Dimethykliethyldiamidoben-
C 6 H 4 .NMe 2 .NEtj+2MeI
C 14 H S6 I 3 N 2
218
Lippmann &Fleiss-
M. G, 4, 788
46, 178
zene dimethiodide
3*1.4
ner
Methylacridine methiodide ..
C 13 H 8 NMe.MeI
C 15 H 14 IN
185 d.
Bernthsen*>
A., 224, 1
46, 1356
Dimethylanhydrobenzodi-
C 6 H 4 .N : CPh.NMe.,1
15 H 15 IN 2
280
Hiibner.-
A., 201, 365
42, 505
amidobenzene iodide
1 1
Diiuethylanhydrobeuzodi-
C' r ,H 4 N : CPh.NMe,I 3
*--i5Hi 5 I 3 N 2
140-5
ii
)>
11
amidobenzene triiodide
1 ___ 1
Azobenzenetrimethylam mon -
Ph.N 2 .C 6 H 4 .NMe 3 I
C 16 H 18 IN 3
173-174
Berjiv
B., 17, 1402 ;
46, 1148 ; 48,
mm iodide
C.C. [1884], 871
660
3-Methylquinoline amyl-
C 10 H 9 N.C 5 H U I
C 15 H M IN
....
215
Dobner and Miller
B., 18, 1643
iodide
Benzenyldimethdiamidoto-
....
<' 16 H 17 I 3 N 2
101
Hiibner
A., 210, 368
luene triiodide
Flavoline methiodide
N.Ph.Me=n,3 1 n 2 ;
C 17 H 16 IN
185 d.
Bernthsen an d Hess
B., 18, 34
48, 559
Methyldiphenylpyrazene
C 3 HN 2 Ph 2 Me+MeI
C 17 H 17 IN,,
187
Knorr and Blank
B., 18, 315
48, 556
methiodide
lao-methyldiphenylpyrazene
)T
....
192
i
B., 18, 935
48, 811
methiodide
Trimethylanthrammonium
C 14 H 9 Me 3 NI
C 17 H 18 IN
....
215 d. ; u. c.
Bollert
B., 16, 1637
44, 1139
iodide
Diethylanhydrobenzoyldi-
C.H 4 .NEt 2 I.CPh : NI,
C 17 H 19 I 3 N 2
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
Me s N.C H 4 .C 6 H 4 .NMe. J T=
C 17 H 23 IN 2
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-
....
C 19 H 21 I 3 N 2
128-129
A., 210, 373
amidine triiodide
Diethylene-ethyldiamidodi-
....
c 19 H B m,
100
J. [1858], 353
iv., 456
phenyl iodide
?-Diquinoline luethiodide ...
(.C 9 NH 6 ) 2 =/3 2 ;,-,-.,;,
C 19 H 15 IN 2
126 ; sf. 83
Fischer
M. C., 6, 546
48, 1247
-
= '
280-286 d.
Weidel
M. C., 2, 499
46,70
Dimethylbenzoylpseudo-
(C,HMe 3 Bz.NMe 2 +MeI
C 19 H 2 JN
187 d.
Frohlich
B., 17, 2675
48, 154
cumidine methiodide
= 1.3.4.2.6
Diquiuoliue dimethiodide ..
C )8 H I2 N 3 .2MeI
C 20 H lb I 2 N 2
a. 290
Fischer
M. C., 5, 417
48, 399
>i
(.C 9 NH 6 ) 2 =(/3 2 ; ,),
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
(C IO H 14 N 2 ) 2 I 3
CsoH^N,
100
Wertheim
iv., 47
Triiodotribenzylamine
(C 6 H 4 I.CH 2 ) 3 N=(1.4) 3
U 21 H 13 I 3 N
....
114-5
Mabery & Jackson
B., 11, 57
34, 422
Dimethylcyanine iodide
C 19 N 2 H 13 Me 2 I
C ?1 H 19 IN 2
291
Hoogewevff& Dorp
R. J., 2, 317
48, 674
Phenylbenzaldehydine ethio-
C 6 H 4 (NC 7 p s ) 2 +EtI=1.2
C 22 H 21 IN S
....
211-213
Ladenburg and
B., 11, 1654
36, 235
dide
Engelbrecht
Tolubenzaldehydine methio-
C 6 H 3 Me(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- *
Ph 2 CH.C 6 H 4 .NMe 2 + Mel
C 22 H 24 IN
....
184-185
Fischer and Roser
B., 13, 675 ; A.,
38, 661 ; 40,
methane methiodide
206, 115, 157
588
Benzenyldiisoamylphenylene-
....
C 23 H 21 I 3 N 2
111-112
A., 210, 363
ainidine triiodide
Tolubenzaldehydine ethio-
C 6 p 3 Me(NC 7 H 6 ) 2 +EtI=
C 23 H 23 IN 2
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
C 19 jN 2 H 13 Et 2 I
)
271-273
Hoogewerff & Dorp
R. X., 2, 317
48, 674
Tolubenzaldehydine ethio-
C 6 H 3 Me(NC 7 H 6 ) 2 +EtI,I 2 =
^23 "23 ^3^ 2
123-135
Ladenburg
B., 11, 593
34, 572
dide+I 2
J.3.4
Ethyltribenzylamine iodide
(C 6 H 5 .CH 2 ) 3 N.EtI
C 23 H 26 IN
....
190
Vasca-Lanza ,
B.,-7, 82
Diamylanhydrobenzoylami-
C 6 H 4 .N(C 5 H 11 ). ) I.CPh:NI 2
C23H 31 I 3 N 2
....
111-112
Hiibnerand Simon
B., 10, 1720 ;
34, 145; 36,
dobenzene triiodide
i i
B., 12, 1344
923
TetramethdiamidotripheTiyl-
Ph.CH(C 6 H 4 .NMe 2 ) 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(C 9 H.NI) S
28 H 22 I 3 N 3
65
Rhoussopoulos
B., 16, 202
44, 600
Quinoline iodooyaniae
i
28 H 35 IN 2
100 d.
Nadler and Merz
J. p., 100, 129
vi., 430
Tetramethdiamjidopropyltri-
Pr.C 6 H 4 .CH(C 6 H 4 .NMe.) 2
a s H 39 T 2 N 2
200
Zeigler
B., 13, 787
38, 640
phenylmethane methiodide
- + MeI
Benzylamarine methiodide
C 21 H l? (CH 2 Ph)N. ! .MeI
C 29 H 27 IN 3
....
130 u. c.
Clans & Kohlstock
B., 18, 1855
48, 1133
,, ethiodide
C 21 H 17 (CH 2 Ph)N 2 .EtI
CaoHoglN.j
182 u. e.
n
B., 18, 1854
(15.) CHIP, CHI As, and CHISb.
Tolylphosphonium iodide ...
C 6 H 4 Me.(PH 2 .HI)=1.4
C 7 H 10 IP
340inCO 2 (?)
Michaelis & Paneck
A., 212, 235
43, 963
Trimethylphenylphosphon-
NMe 3 PhI
C 9 H 14 IP
205
Ananoff
A., 181, 363
ium iodide
Dimethylethylpheuylphos-
....
C 10 H J6 IP
>.
137
,
A., 181, 362
phonium iodide
Trimethyltolylphosphonium
C; 6 H 4 Me.(PMe J l) = 1.4
255
Czimatis
B., 15, 2015
44, 57
iodide
Methyldiethylphenylphos-
PMeEtjPhI
C H H 18 IP
95
Ananoff
B., 8, 49 ; A.,
28, 1204
phoiiium iodide
181, 358
TriPthylphenylphosphoniuni
PEt,,PhI
C IS H 20 IP
....
115
.
>
H
iodide
Methyldiethyltolylphospho-
C fi H 4 Me.(PEt,M t -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-
C 6 H 3 Me 2 .(PEtjMeI)
C 13 H 22 IP
SO
Czimatis
B., 15, 2016
44, 58
ium iodide
Diphenyldimethylphosphon-
PMejPhJ
C 14 H 16 IP
241
Michaelis and Link
A., 207, 210
42, 306
ium iodide
!) !!
n
*J
245
Michaelis and Coste
B., 18, 2117
Triethylxylylphosphonium
C 6 H 3 Me a .(PEt 3 I)
C 14 H 24 IP
....
136
Czimatis
B., 15, 2016
44, 58
iodide
Ethylene hexethyldiphos-
C 2 H 4 : PEt 6 I. :
Ci4H 34 I 2 P 2
....
231
As., I, 188
iv., 622
plionium iodide
Diphenylmethylethylphos-
PMeEtPh 2 I
C 15 H 13 IP
....
181
Michaelis and Link
A., 207, 212, 215
42, 306
phonium iodide
Diphenyldiethylphosphon-
PEt,Pli 2 I
C 16 H 2( ^P
204
ji
A., 207, 214
n
ium iodide
Naphthyltriethylphosphon-
PEt/C..!!.)!
C 16 H 22 IP
....
209
Kelbe
B., 11, 1502
36, 68
ium iodide
Triphenylphosphonium
PHPh 3 I
C I8 H 16 IP
cf. B., 15,
215 p. d.
Michaelis & Soden
A., 229, 334
48, 1134
iodide
803
Triphenylmethylphosphon-
PMePh 3 I
C 19 H 18 IP
165-166
Michaelis & Gleich-
B., 15, 803
42, 1062
ium iodide
mann
Triphenylethylphosphonium
PEtPh 3 I
C 20 H 20 IP
....
165
'Michaelis & Soden
A., 229, 334
48, 1134
iodide
Triphenylpropylphosphon-
PPr'Pli,!
PnH M IP
201-5
j
48, 1135
ium iodide
Triphenylisopropylphosphon-
PPr^PhjI
*
+2ILjO
191
i
J)
ium iodide
Tripheny] isobutylphosphon-
PBu0Ph. t I
^H 24 IP
176
~*i
Ji
i)
ium iodide
Triph eny lisoamylphosphon-
P(C 5 H u )Ph 3 I
^tflnff
174
i>
i
ium iodide
Triphenylbenzylphosphon-
P(CH 3 Ph)PhJ
C-J5-H.J2IP
253
ij
ium iodide
Methylenehexaphenylphos-
CH. 2 (PPh 3 I) 2
C3:H 32 I 3 P 2
230-231 d.
Michaelisi& Gleich-
B., 15, 804
42, 1062
phonium iodide
mann
Arsemnethyldiiodide
AsMeI 2
CH 3 I 2 As
a. 200
25
Baeyer
A., 107, 285
i., 401
Arsendimethyliodide(caeodyl
AsMe 2 I
C 2 H 6 IAs
a. 100
b. 10
Bunsen
A., 37, 35; 92,
i., 407 .
iodide)
362 .
Tetramethylarsenium iodide
AsMe 4 I+AsI,,
C 4 H 12 I 4 As. 2
170
....
Cahours
C. R, 49, 87
i., 410
+AsI 3
Arsenphenyl diiodide
AflPhI 2
C 6 H 5 I 2 As
....
Liquid
Michaelis & Schulte
B., 14, 913 ; 15,
40, 723
1953
Phenyltrimethylaisenium
AsMe 3 PhI
C 9 H 14 IA
....
244
Michaelis and Link
A., 207, 205
42, 306
iodide
Diidoarsenobenzene
C 6 H 5 .AsI.AsI.C 6 H 5
C 12 H W I 2 A8 3
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
AsMe 2 Ph 2 I
C 14 H 16 IAs
109
Michaelis and Link
A., 207, 204
42, 305
iodide
Diphenylethylmethylarsen-
AsMeEtPh 2 I
C 15 H 18 IAs
170
A,, 207, 196
>
ium iodide
Uiphenyldiethylarsenium
AsEt 2 Pb 2 I
C 16 H M IA 8
....
184
....
A., 201, 236
iodide
Stibtriethyl diiodide
SbEt 3 I 2
C 6 H 16 I 2 Sb
cf. A., 97, 331
70-5
Buckton
13, 116
1., 342
>J
1
....
70-5
Lowig& Schweitzer
J., 75, 339
Stibtritolyl
(C 6 H 4 Me) 3 SbI,=(1.4) s
C 21 H 21 I 2 Sb
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
CH 2 OS
cf. A,, 91, 125
120
Limpricht
A., 97, 361
v., 778
Methylsulphonic acid
CH 3 .S0 3 H
CH 4 3 S
d. 130
Richter
R. K. T.
Methylic hydrogen sulphate
MeHSO 4
CH 4 O 4 S
....
Liquid 30
Claesson
J. p. [2], 19, 240
36, 776
Thiacetic acid
Me.CO.SH
C 2 H 4 OS
95
....
....
v., 771
)J
93
....
Ulrich
J., 12, 355
Sulphacetic acid
HO 3 S.CH 2 .COOH
C S H 4 6 S
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
c 2 H 4 :(so 3 ) 2
C 2 H 4 6 S 2
80
Magnus
P. A., 47, 509
ii., 523
Dimethyl sulphoxide
Me 2 SO
C 2 H 6 OS
Solid
Saytzeff
A., 144, 148
vi., 827
sulphone
Me 2 SO 2
C 2 H 6 2 S
238
109
i)
D
vi., 827
Dimethylic sulphite
Me 2 SO 3
O 2 H 6 O 3 S
121-5
Carius
A., 110, 219
v., 556
,, sulphate....
Me 2 SO 4
C 2 H 6 4 S
188
Dumas and Peligot
A. C. [2], 58, 32
v., 626
Ethylene disulphonic acid ...
HSO 3 .CH 2 .CH 2 .SO 3 H
C 2 H,0 6 S 2
....
94
Husemau
A., 126, 272
v., 566
trisulphonic acid ...
HS0 3r CH 2 .CH(S0 3 H) 2
C 2 H 6 9 S 3
80-1 10 pd.
Monari
B., 18, 1346
48, 970
dithiocarbonate ...
C 2 H 4 ;COS 2
C 3 H 4 OS,,
31
A., 126, 269
Mythylic thiacetate
....
CjH t OS
62-68
B. S., 25, 562
>
CH 3 .(X).SMe
)
95-86
Wallach&Bleibtreu
B., 12, 1062
36, 786
Trimethylene oxysulphide ...
....
C 3 H 6 OS 2
+iH 2
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
CH 3 .CH(SH).COOH
C 3 H 6 2 S
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.SO 2 .Et
C 3 H 8 2 S
....
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 ...
C 2 H 5 .S0 3 Me
197-5-200-5
....
J. [1870], 728
Isopropylsulphonic acid
Me 2 .CH^O 3 H
....
b. 100
Claus
B., 5, 660
Thiosuccinyl ....
CO.CH 2 .CH 2 .CO.S
C 4 H 4 O a S
31
Wesilsky
B., 2, 521
vi., 1042
Thiophene sulphiuic aeid ....
C 4 SH 3 .S0 2 H
C 4 H 4 2 S 2
....
67
Weitz
B., 17, 800
46, 1131
/3-thiophene sulphonic acid ....
C 4 SH 3 .SO,3
C 4 H 4 3 S S
....
Cryst.
Langer
B., 18, 554
48, 765
Thioglyoxylic acid
...
C 4 H 4 6 8
....
78-82
A., 198, 212
j8-thiophene disulphonic acid
C 4 SH 2 (S0 3 H) 2
C 4 H 4 6 S 3
....
Cryst.
Lauger
B., 18, 553
Sulphethylic ether
....
C 4 H 6 OS 3
....
120-123
Malaguti
A. C. [2], 70, 338
a, 541
Thiacetic anhydride
(Me.CO) 2 S
C 4 H 6 2 S
121
....
Kekulo
A., 90, 311
v., 772
>i
)1
))
121
....
Saytzeff
Z. C. [2], 4, 642
vi., 20
Acetyl disulphide
(Me.CO) 2 S 2
C.HeO^,
....
20
Kekul6 and Lin-
A., 123, 278
v., 772
nemann
Thiodiglycollic acid
S(CH a .COOH)5 I
C 4 H 6 4 S
....
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
S 2 (CH 2 .CX)OH) 2
C 4 H 6 4 S 2
....
100
Claesson
B., 14, 409
40, 580
Sulphoue diacetic acid
SO 2 (CH 2 .COOH) 2
C 4 H 6 6 S
d. 200
182
Lov^n
B., 17, 2819
48, 241
Ethylic thiacetate
CH 3 .CO.SEt
C 4 H S OS
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
C 3 H-.CO.SH
j)
130
Ulrich
A., 109, 280
i., 694
Aldehyde + thioaldehyde
C 2 H 4 0+C 2 H 4 S
35 d.
2
Pinner
B., 4, 258
24, 383; vii., 37
Ethylic methylic dithiocar-
....
C 4 H 8 OS 2
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
CH 2 (SH).COOEt
C 4 H 8 2 S
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.
C 4 H 8 O 2 S
145
Couerbe
A., 40, 297
Ethylic sulphonacetic acid ...
Et0 2 S.CH 2 .COOH
C 4 H 8 4 S
Liquid
Claesson
B. S. [2], 23, 144
29, 568
Thiodiethylene glycol
HO.C 2 H 4 .S.C 2 H 4 .OH
C 4 H 10 2 S
....
60
Carius
A., 124, 263
ii., 582
Diethyl sulphone
EtjSO 2
)
2J#
70
Oefele
A., 127, 370
ii., 968 ; vi.,
598
!>
n
.
70
Frankland and
B., 12, 845
35, 246
Laurance
Ethylic thioethylsulphonate
Et.SO 2 .SEt
C 4 H 10 O2S 2
130-140 d.
Liquid
Otto
R, 15, 122
42,832
Diethylic sulphite
(EtO) a SO
C 4 H 10 3 S
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
C 4 H 10 4 S
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
C 5 H 4 OS
-
Liquid
Peter
B., 18, 537
48, 765
n- acid
S.CH : CH.CH : C.COOH
C 5 H 4 2 S
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
CH 3 .CO.SPr"
CjH.oOS
135-137
....
Wallach & Bleibtreu
B., 12, 1062
36, 786
Isopropylic
CH 3 .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
C S H 10 O.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
CH 3 .CH(SH).COOEt
1)
150-160
....
Lov6n
B., 16, 790
|3-Thienylglyoxylic acid
C 4 SH 3 .CO.COOH
C 6 H 4 3 S
....
86 ; sf. 78
Peter
B., 18, 537
48, 764
Thiophene dicarboxylic acid
C 4 SH 2 (COOH) 2 = ?
C 6 H 4 O 4 S
....
n. f. 295
Bonz
B., 18, 2307
11 11
=1.2.5
))
w. m. 350
Messinger
B., 18, 567
48, 767
Phenol sulphhydrate
C 6 H 4 .OH.SH =1.2
O.H.OS
216-217
5-6
Haitinger
M. C., 4, 170
44, 989
(750-7)
Acetothienone
C 4 H 3 S.CO.Me
1>
213-5 c.
1. 15
Peter
B., 17, 2644
48, 141
Benzene sulphinic acid _ ..
Ph.SO 2 H
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-
2 (CS 2 Et) 2 (?)
C 6 H, O 2 S 4
....
28
....
A., 72, 5 ; 82, 253
bonate
thioxalate
COOEt.CO.SEt
C 6 H 10 3 S
211u.c.;217c.
....
Morley and Saiut
43, 401
Thiodilactic acid
S(C 2 H 4 .COOH) 2
C 6 H 10 4 S
Mf
125
Lovuii
B., 16, 790
Sulphone dipropionic acid ....
SO 2 (CHMe.COOH) 3
C 6 H 10 6 S
..
155-156
51
B., 17, 2822
48, 241
Isobutylic thiacetate
CH 3 .CO.SBuP
C 6 H 12 OS
148-150
....
Wallach & Bleibtreu
B., 12, 1062
36, 786
Isoamylic xanthogenate
C 5 H n S.CO.SH
C 6 H, 2 OS 2
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
C 6 H 12 2 S
187-189
Liquid
Claesson
B., 8, 121
29, 567
?
+H 2
C6Hi 2 O,>S 4
180-185
80-82
A. C. [5], 17,307
Dipropyl sulphone
(CH 3 .CH 2 .CH 2 ) 2 SO 2
C 6 H 14 2 S
....
29-30
Spring&Winssinger
B., 16, 329
Di-#-isopropyl sulphone
(Me 2 CH) 3 .SO 2 .
)
36
Beckmann
J. p. [2], 17, 459
36, 38
Ethylene diethyl
C 2 H 4 : S0 2 Et 2
136-5
j)
J. p. [2], 17, 469
36, 39
,, sulphoxide
C 2 H 4 (SOEt) 2
C,H 14 OA
170
Ewerlof
B., 4, 717
24, 1189
Glyceric sulphaldehyde
(C 3 H 6 S 2 0) 2 H 2 0.
C 6 H 14 3 S 4
180-185
sf. 80-82
Benard
C. R., 82, 562 ;
30, 64 ; 38, 25
A. C. [5], 16, 289
n-Thiobenzoic acid
C 6 H 5 .COSH
C 7 H 6 OS
....
24
Engelhard t,
Z. C. [2], 4, 3.^3
vi., 324
Latschinoff, and
Malyscheff
Hydrothiobenzoic acid
C 6 H 4 .SH.COOH =1.3-
C 7 H 6 2 S
146-147
Frerichs
B., 7, 793
27, 9iX)
Sulphobenzoic acid
C 6 H 4 (S0 3 H)(C0 2 H)=1.3
C 7 H 6 6 S
....
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.S0 3 H=1.2.?
C 7 H 6 6 S
120
Mendius
A., 103, 39
v., 525
Sulphohydroxybenzoic acid....
= 1.3..?
)J
208
Senhofer
A., 152, 102
vi., 890
Disulphobenzoic acid
COOH.(S0 3 H) 2 =1.2.4
C 7 H 6 8 S 2
a. 285
Fahlberg
A. C. J., 2, 188
40, 818
Methylphenyl sulphone
CjH5.SOj.Me
C 7 H 8 2 S
88
Michael & Palmer
A. C. J., 6, 253
48, 536
J1
)r
....
88-89
Otto
B., 18, 156
48, 536
Toluene sulphinic acid
C 6 H 4 Me.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
C 7 H 8 3 S
sf. 152
150-162
Norton and Oppen-
B., 10, 703
heim
Toluene sulphonic acid
C,H 4 Me.SO,H=I.2
....
91-92
Hiibner and Miiilei
Z. C., 14, 299
24, 1055
Cresol sulphonic acid
Me.OH.SO 3 H=1.2.4
C 7 H 8 4 S
....
80-81
J. [1879], 758
it ,,
=1.4.6
n
anhydrous
187-188 ;
Jenssen
A., 172, 237; B.,
27, 480; 28, 77;
+5H 2
98-5
7,57
vii., 932
Toluene trisulphonic acid ...
Me.(S0 3 H)=?
C 7 H 8 9 S 3
+6H 2 O
145
Claessou
B., 14, 308
40, 429
2
....
C 7H 12 O 3 S 2
165
Cech and Steiuer
C. R., 81, 155
28, 1255
Isobutylic ethylic xantho-
EtS.CS.OBuS
C 7 H 14 OS 2
227-228
....
Mylius
B., 5, 975
26, 266
genate
Ethylic isobutylic thiocar-
Bu0S.CO.OEt
C 7 H 14 2 S
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(C 5 H u )SO
C 7 H 18 OS
s. 16
Saytzetf
A., 139, 354
vi., 123, 599
-isoamyl ethyl sulphone ....
(Me 2 CH.CH 2 CH,).S0 2 .Et
C 7 H 16 2 S
270
13-5
Beckmann
J. p. [2], 17, 450
36, 38
Ethylic amylic sulphite
Et(C 5 H n )S0 3
C,H 16 3 S
210-225 p. d.
C'arius
A., 106, 291
v., 555
Thiophthalic anhydride
C 6 H 4 .CO.OCS=1.2
L J
C S H 4 O 2 S
284
114
Grsebe & Zschokke
B., 17, 1176 46, 1025
Isophthalosulphonic acid
(COOH),,SO 3 H=1.3.4
C 8 H 6 7 S
....
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 .S0 3 H=1.3.4
C 8 H 6 7 S
....
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 ....
C 6 H s .SAc
C 3 H 8 OS
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.CH 2 .COOH
C 8 H 8 O 2 S
....
43-5
Claesson
B. S. [2], 23, 441
29, 567
1
)
61-62
Gabriel
B., 12, 1639
,, sulphinacetic acid ....
Ph.SO.CHj.COOH
C 8 H 8 3 S
74
Claesson
B. S. [2], 23, 446
29, 568
sulphonacetic acid ....
Ph.S0 2 .CH. 2 .COOH
C 8 H 8 4 S
....
109
u
i
ij )>
J
)>
110-111
Gabriel
B., 14, 834
40, 716
Dimethylic thiophene dicarb-
C 4 SH 2 (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.SO 3 H=1.4.2
C 8 H 8 5 S
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
C 4 SHMe 2 Ac=1.2.5.3
C 8 H 10 OS
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
C 6 H 4 Me.(SO 2 .Me)=1.4
)
....
86-87
B., 18, 161
48, 537
Xylene sulphinic acid
Me 2 .S0 2 H=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
Me 2 SO 3 H=1.3.4
C 8 H I0 : ,S
....
53 Limpricht
B., 18, 2188
Diethylic dithiosuccinate ....
(.CH,.COSEt) 2
C 8 H 14 OjS 2
270-271
Liquid
Seifert
J. p. [2], 31, 462
48, 1057
Ethylene ethyl xanthate
C 2 H 4 (S.CS.OEt) z
C 8 H 14 3 S 4
....
42
Welde
B., 9, 1047 ; J. p
30, 624 ; 32,
[2], 15, 55
137
Diethylic thiodiglycollate ....
....
C 8 H 14 4 S
240-250
....
Schulze
Z. C. [1865], 78
11 11
....
?J
267-268 <:
....
Wisliscenus
Z. C. [1865], 261
v., 777
dithioglycollate ....
(.S.CH 2 .COOEt) 3
C 3 H 14 4 S 2
280 d.
Liquid
Claesson
B., 14, 411
40, 581
Sulplioue dibutyric acid
SO 2 (CHEt.COOH)j
C,H 14 6 S
....
152
Loven
B., 17, 2824
48, 241
diisobutyric acid ....
SOj(CMe.,.COOH) 2
Jj
188
n
B., 17, 2825
Dibutyl oxysulphide
(Me.CH 2 .CH 2 .CH 2 ).,SO
C 8 H 1S OS
cf.B.,7, 1650
32
Grabowsky
A., 175, 349
28, 629, 1 1 75
Diisobutyl oxysulphide
(Me 2 CH.CH 2 ) 2 SO
r
....
41
Saytzeft' and Gra-
A., 171, 257
27, 565
bowsky
i >-
68-5
Beckmann
J. p. [2], 17, 439
36, 37
aulphone....
(MejCH.CH 2 ) 2 SOj
C 8 H 18 3 S
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"
C 9 H 8 OS
250 p.d.
....
Engelhardt, Latschi-
Z. C. [2], 4, 359
vi., 470
notf, & MalyschefF
Sulphocinnamic acid
(S0 3 H)(CH:CH.COOH)
C 9 H 9 5 S
+5H 2 O
100
Rudneu
A., 173, 12
28, 76
=1.4
Ethylic thiobenzoate
Ph.CO.SEt
C 9 H 10 OS
242-243
Liquid
Engelhardt, Latschi-
Z. C. [2], 4, 356
vi., 325
noff, & Malysclieff
Benzylthioglycollic acid
Ph.CHj.S.CHj.COOH
C 9 H 10 0.,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
C 9 H 10 3 S
v. 100
87
Baumann
B., 18, 263
48, 514
piouic acid
Toluene sulphonacetic acid ....
Me.(SOj.CH 2 .COOH)=1.4
C 9 H 10 O 4 S
117-118-5
Gabriel
B., 14, 834
40, 716
i
n
117-119
Otto
B., 18, 161
48, 537
Phenylpropyl sulphone
Ph.S0 2 .Pra
C-yH^OgO
....
45
Michael & Palmer
A. C. J., 7, 65
48, 986
Tolylethyl sulphone
CH 3 .C 6 H 4 .S0 2 .Et=1.4
))
55-56
Otto
B., 18, 161
48, 537
,, ....
*> )
5
....
56
B., 13, 1276
38, 811
Mesitylene sul]>hinic acid ....
Me 3 .SO 2 H= 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.C 2 H 4 .SO. .C 6 H 4 Me= 1 . 4
C 9 H 12 3 S
54
Otto & Damkohler
J. p. [2], 30, 321
48, 538
phone
Ethylic toluene sulphonate ...
C 6 H 4 Me.SO 3 Et
M
....
32
....
v., 860
Mesitylene sulphonic acid ...
Me 3 .SO 3 H 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 ...
Me 3 .SO 3 H=1.3.5.6
C 9 H 12 3 S
abt. 100
Jacobsen
A., 145, 85
vii., 787
Sulphocamphoric acid
....
C 9 H 16 6 S
160-165
Walter
A. C. [3], 9, 177
v., 490
Diisobutylic xanthate
Bu0O.CS.SBu0
C,H 19 OS 2
247-250
....
Mylius
B., 5, 975
26, 266
Ethylic isoatnylthioglycollate
C 6 H 11 S.CH 2 .COOEt
C 9 H 18 2 S
230
cf. B., 8, 122
Claesson
B. S., 23, 446
29, 568
a-Naphthalene sulphinic acid
C 10 H 7 .S0 2 H
C 10 H 8 2 S
High temp.
Gessner
B., 9, 1500
31, 315
/3- sulphonic acid
JJ
105
11
B., 9, 1502
31, 316
"- 11 11
C 10 H 7 .S0 3 H
C 10 H 8 O 3 S
85-90
....
....
v., 560
a-Naphthol sulphonic acid ...
C 10 H 6 (OH).SO S H
C 10 H 8 4 S
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 ...
C 6 H 4 (S.CH 2 .COOH) 2 =1.3
C 10 H 10 O 4 S 2
....
127
Gabriel
B., 12, 1639
38, 33
Trimethylic thiophentricar-
C 4 SH(COOMe) 3 =1.2.3.?
C 10 H 10 6 S
118
Messinger
B., 18, 2303
48, 1205
boxylate
Ethylic phenylthioglycollic
PhS.CH 2 .COOEt
C 10 H 12 2 S
275-285
....
Claesson
B. S. [2J 23, 441
29, 567
acid
11 11 11
S76-278p.d.
M
Ethylic methylthiosalicylate
C 6 H 4 .OMe.COSEt=1.2
197-198 (80)
Liquid
Seifert
J. p. [2], 31, 462
48, 1058
Phenylsulphonethylic acetate
Ph.SO 2 .C 2 H 4 .OAe
C, 10 H, 2 O 4 S
....
1. -12
Otto & Damkohler
J. p. [2], 30, 171
48, 262
Ethylic phenylsulphonacetate
Ph.SO 2 .CH 2 .COOEt
45
Michael & Comey
A. C. J., 5, 116
46, 319
Diethylic thiophendicarboxy-
C 4 SH 2 (COOEt) 2 = 1.2.5
....
46
Messinger
B., 18, 1639
48, 1052
late
a-Cymene sulphonic acid
Me.Pr.SO 3 H=1.4.2
C 10 H 14 O 3 S
50-51
Spica
B., 14, 654
40, 602
n * 11 11 11
= 1.4.3
86-87
11
B., 14, 635
?-
Me.Pr.SO 3 H=1.3.2
86-87
B., 16, 792
P~ >) >j
Me.PrP.SO 3 H=1.3.?
....
88-90
Kelbe
A., 210, 26, 31
42,300
a ~ )1
Me.Pr.SO 3 H=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
-H3H 2 O
78-79
M
11 11 n
Me.Pr0.S0 3 H=1.4.2
n
270
Fittica
....
40, 602
Isodurene sulphonic aeid ...
Me 4 .SO 3 H = 1.2.3.5.6
,,
+^H 2 O
100
Bielefeldt
A., 198, 381
38,37
Thianissic acid
C 10 H 14 O 4 S
+2H 2
b. 200
Stiidler & Waehter
A., 116, 163
v., 774
Tsobutylic isoamylie xanthate
Bu0O.CS.SC 6 H n
C 10 H 20 OS 2
265-270 p. d.
c. f. B., 5, 975
Mylius
B. S., 19, 221
26, 266
Diisoamyl sulphoxide
(C 5 H n ) s SO
C 10 H 22 OS
....
37-38
Satyzeff
A., 139, 355
vi., 116
sulphone
(Me 2 CH.CH 2 .CH 2 ) 2 SO 2
CjoH^OjS
295 p. d.
31
Beckmaiin
J. p. [2], 17, 441
36, 38
Diamylic sulphite
(C 5 H n ),S0 3
C 10 H 23 O 3 S
230-250
Carius
A., 106, 291
v., 553
Phenyl thienyl ketone
Ph.CO.C 4 H 3 S
C n H 9 OS
abt. 300
55
Comey
B., 17, 791
46, 1168
y-Sulphonaphthoie aeid
S0 3 H.COOH=a ;
C n H 8 6 S
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
C U H 12 OS
250 d.
MM
Z.C. [1868], 359
Toluene dithiacetic aeid
Me.C B H 3 (S.CH 2 COOH),,
C U H 12 O 4 S 2
....
151-151-5
Gabriel
B., 12, 1640
38,33
Ethylic benzylthioglycollate
Ph.CH 2 .S.CH 2 .COOEt
275-290
>. ii
B., 12, 1641
38, 34
Diethylic sulphosalicylate ....
OH.COOEt.SO 3 Et=1.2.?
C n H 14 O 6 S
MM
56
Mendius
A., 103, 62
v., 526
Isobutyltoluene sulphonic
Me.Bu0.SO 3 H=1.3.?
C,,H 16 O 3 S
75-76
Kelbe and Baur
B., 16, 2559
46, 300
acid
Diisoamylic dithiocarbonate
CO(S.C 5 H n ) 2
C n H 22 OS 2
281
Liquid
Schmidt and Glutz
B., 1, 169
Diphenylene sulphone
C 6 H 4 .S0 2 .C f H 4
C 12 H,AS
....
230
....
A., 156,334; 174,
188
Diphenylene disulphone
c a H 4 :(so 2 ) 2 :c 6 H 4
C 12 H S O 4 S 2
....
a. 300
Grwbe
A., 179, 182
29, 579
Phenyl sulphone
Ph.SO2.Ph
C 12 H 10 O 2 S
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
....
C 12 H 10 2 S
....
230
Stenhouse
P. R. S., 18, 543
vi., 277; vii.,
941
Dipheny] sulphinic acid
C 6 H 5 .C 6 H 4 .S0 2 H
11
....
d. 70
Gabriel & Deutsch
B., 13, 388
38, 477
Phenol sulphide
S(C 6 H 4 .OH) 2
i>
143-144
Krafft
B., 7, 1165
28, 154
Phenylic thiobenzene sulpho
Ph.S0 2 .SPh
C 12 H 10 O 2 S 2
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
S 2 (C 6 H 4 .OH) 2 =(1.2) 2
11
a. 200 d.
Liquid
Haitinger
M. C., 4, 166
44, 988
Phenylic phenylsulphonate...
C,H s .S0 3 Ph
C 12 H 10 O 3 S
....
35
Schiaparelli
G. I., 11, 65
40, 602
Oxysulphobenzide
S0 2 (C 6 H 4 .OH) 2
C 12 H 10 4 S
....
293 or 239
Annaheim
A., 172, 28
27, 796
Diphenj'l disulphonic acid ....
(.C 6 H 4 .S0 3 H) 2
C 12 H 10 O 6 S 2
....
72-5
Fittig
A., 132, 209
v., 565
Benzyl sulphone .... m .
(CeH^CH^O,
C 12 H U 2 S
150
Vogt & Henninger
A. C. [4], 25, 129
25, 1097
Ethylic thioisophthalate
C 6 H 4 (COSEt) 2 =1.3
C 12 H 14 2 S 2
....
easily
Luckenbach
B., 17, 1428
46, 1158
Isoamylic thiobenzoate
Ph.COSC 5 H u
C] 2 H 16 OS
271 p. d.
Liquid
Engelhardt, Lats-
Z. C. [2], 4, 356
vi., 325
chinoff, and Maly-
scheff
Ethylic ethylpheuylsulphon-
Ph.SOj.CHEt.COOEt
Ci 2 H 16 O 4 S
....
62
Michael & Palmer
A. C. J., 7, 65
48, 986
acetate
Toluylene amylene disul-
C 6 H 10 :(S0 2 ) 2 :0 6 H 3 Me
C 12 H 16 O 4 S 2
35-36
Otto
A., 143, 223,
vi., 1060
phone
?
C 12 H,,O 6 S 2
78-79
11
A., 143, 224
1
Dipropylbenzene sulphourc
Pr 2 .S0 3 H=1.4.5
Ci 2 H 18 O 3 S
....
62
Korner
B., 11, 1864
36, 142
acid
Ethylic acetoacetate sul-
S(CHAc.COOEt) 2
CuHi 8 O 6 S
....
80-81
Buchka
B., 18, 2092
48, 1200
phide
Diisoamyldisulphocarbonic
(C 6 H U 0) 2 CS 4
C 12 H 2 _,O 2 S 4
187
....
Johnson
5, 142
v., 496
sulphide
Ethyleue diisoamyl sulphone
C 2 H 4 (S.00 6 H n ) 2
C 12 H,, 6 O 2 S 2
....
14&-150
Ewerlof
B., 4, 717
24, 1189
Benzophenoue sulphone
C,H 4 .OO.C 6 H 4 .S0 2
C] 3 H 8 O 3 S
....
174-175
Beckraann
B., 8, 992
29, 583
11
)
i
186-187
11
B., 6, 1112
27, 157
Phenylic thiobenzoate
C 6 H 5 .COSPh
C 13 H 10 OS
._.
56
Schiller and Otto
B., 9, 1634
31, 468
Sulphobenzid carbonic acid....
Ph.SO 2 .C 6 H 4 .COOH=1.4
Ci 3 Hi O 4 S
a. 300
Michael and Adair
B., 11, 119
34, 415
Phenyl tolylsulphone
C 6 H 4 Me.(S0 2 .Ph)=1.4
<AsH, a O 3 S
124-5
11
B., 11, 116
11
i i'
>i 11
11
124-125
Beckurts and Otto
E., 11, 2068
36, 243
Diphenylmethane disul-
C 13 H 10 (S0 3 H) 2
C 13 H 12 O 6 S 2
59
Doer
B., 5, 796
26, 170
phonic acid
Ethylic allylphenylsulphon-
Ph.SO 2 .CH(C 3 H 6 ).COOEt
G U H, 6 O 4 S
....
64-5
Michael & Palmer
A. C. J., 7, 65
48, 986
acetate
Erythrohydroxyanthraqui-
c 6 H 4 :(co) 2 :c,H 2 ^o 2 .o
C J4 H 6 6 S
d. b. 100
Lifschutz
B., 17, 900
46, 1189
none sulphonic anhydride
1
Thiobenzoic anhydride
(Ph.CO) 2 S
C 14 H 10 O 2 S
....
48
Jngelhardt, Latschi-
Z. C. [2], 4, 357
vi., 325
noff, & Malyscheff
Benzoyl disulphide
(Ph.CO) 3 S 2
CiiH 10 OjSj
...
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 ....
S 2 (C 6 H 4 .COOH) : ,=(1.3) ;I
Ci 4 H 10 4 S 2
....
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
S0 2 (C 6 H 4 COOH) 2 =(1.4) 2
CuHi O 6 S
a. 300
Michael and Adair
B., 11, 121
34, 415
Benzylic thiobenzoate
C 6 H 5 .COS.CH 2 Ph
C 14 H Ia OS
....
39-5
lichter
R. K. T.
Tolylic thiobenzoate
C 6 H 6 .COS.C 6 H 4 Me=1.4
n
....
75
Schiller and Otto
B., 9, 1636
31, 469
Diphenyl sulphacetic acid ....
Ph.C 6 H 4 .S.CH 2 .COOH
C 14 H 12 O 2 S
....
169-170
Gabriel & Deutsch
B., 13, 389
38, 477
Phenylmercaptane-benzoyl-
PhS.CPh(OH).COOH
C 14 H, 2 O 3 S
....
68-5
iaumaun
B., 18, 891
48, 749
forraic acid
Benzyl oxysulphide
(Ph.CH 2 ) 2 OS
C 14 H 14 OS
....
130
Marcker
A., 136, 90
v., 859
ii ii
)>
))
....
33
Otto and Luders
B., 13, 1284
38, 811
Benzyl sulphone
(Ph.CH,) a SOj
14 H u O a S
50
11
B., 13, 1277, 1284
)
)
?
....
50
Vogt & Henninger
A. C. [4], 25, 129
vii., 185
Benzyltolyl sulphone
Ph.CH 2 .SO.,.C 6 H 4 Me=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
(0 6 H 4 Me) 2 S0 2 =(1.4) 2
C 14 H 14 2 S
....
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.SO 2 .C 6 H 3 Me.
80
Bjckurts and Otto
B., 1 1, 2069
36, 243
Toluene disulphexide
C 6 H 4 Me.SO 2 .S.C 6 H 4 Me
C 14 H 14 O 2 S 2
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,,(C 6 H 4 .OMe) 2 =(1.2) 2
119c.
Haitinger
M. C., 4, 168
44, 988
Ethylic diphenylsulphonate
C 6 H 5 .C (i H 4 .SO 3 Et
C 14 H ]4 O 3 S
73-74
Gabriel & Deutsch
B., 13, 388
38, 477
Methyl oxysulphobenzide ....
SO 2 (C 6 H 4 .OMe) 2
C 14 H I4 4 S
130
Annaheim
A., 172, 45
27, 796
Ethylene diphenylsulphone....
C 2 H 4 (S0 2 .Ph) 2
C 14 H 14 O 4 S 2
....
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.CH 2 .C 6 H 4 Me=1.4
C' 14 H 14 O,;S 2
38
Zincke
B., 5, 685
25, 1005 ; vii.,
acid
183
Phenylcournarin .sulphouic
C 16 H 9 O 2 .S0 3 H
C 15 H 10 O 6 S
+ 2JH 2 O
262 d.
Curatolo
G. I., 14, 257
48, 539
acid
PhenylcouruariB tiisulphonie
C 16 H*0 2 (S0 3 H) 2
C 15 H 10 O 8 S. 2
+6H 2 O
18
11
n
acid
(i-Dithiophenyl propionic
(PhS) 2 CMe.COOH
c, 5 H 14 o 2 a,
....
113-114
Baumann
R, 18, 65
48, 514
acid
Plienylsulphonethyl benzoate
Ph.S0 2 .C 2 H 4 .OBz
C 15 H,,0 4 S
....
124-125
Otto & Damkfihler
J. p._[2], 30, 171
48, 262
Ethylene phenyltolylsul-
Ph.SO 3 .C 2 H 4 .SO 2 .C 6 H 4 Me
C 15 H 16 O 4 S 2
....
162
11
42,263
phone
=1.4
Atronine sulphene
....
C 16 H 10 2 S
193
Fittig
A., 206, 63
40, 427
o-Naphthyl phenyl sulphone
C 10 H 7 .SO 2 .Ph
C 16 H 12 O 2 S
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 ...
C 16 H U .SO 3 H
C, 6 H 12 O 3 S
258 p.d.
Fittig
A., 206, 61 ; B.,
38, 120; 40,
12, 1739
427
Atronol
C 16 H 13 .SO 3 H
Cj 6 H 14 O 3 S
130-131 p.d.
A., 206, 52
40, 427
Diphenyldisulphacetic acid ....
(.C 6 H 4 .S.CH 2 .COOH) 2
C 16 H 14 O 4 S 2
252
Gabriel & Deutsch
B., 13, 390
38, 477
Tolylsulphonethylic benzoate
i|Bzp.C 2 H 4 .S0 2 .C 6 H 4 Me= 1 .4
C 1B H 16 4 s"
175
Otto & Damkohler
J. p. [2], 30, 321
48, 538
Ethyl oxysulphobenzide
S0 2 (C 6 H 4 .OEt) 2
159
Annaheim
J.p. [2], 1,14; 2,
vii., 886 ; 27,
385; A., 172,52
797
Ethylene ditolyl sulphone ...
C 2 H 4 (S0 2 .C r ,H 4 Me) 2 =(1.4),
16 H 18 O 4 S 2
200
Otto & Damkohler
J. p. [2], 30, 321
48, 537
Diphenylsulphonethyl sul-
S(C a H 4 .SO a .Ph),
C 16 H 1S O 4 S 3
123
11
phide
,i oxide....
0(C 2 H 4 .S0 2 .Ph) 2
C 16 H,AS 2
69-70
J. p. [2], 30, 171
48, 263
11
....
88
B
J. p. [2], 30, 321
48, 537
Sulphocetenic acid
....
C 16 H 32 O 3 S
....
18
Lasarenko
B., 7, 125
Ethylic benzylphdiiyl sul-
PhSO 2 .CH(CH 2 Ph).COOEt
17 Hi 8 O 4 S
95-96
Michael & Comey
A. C. J., 5, 116
46, 319
phon acetate
?
Ph.S0 2 .C 6 H 4 .O.S0 2 .Ph
C 18 H 14 O;,S 2
123
Schiaparelli
G. I., 11, 65
40, 603
Ditolylsuphonethyl sulphide
(C 6 H 4 Me.S0 2 .C 2 H 4 ) 2 S
C^OA
150-160
Otto & Damkohler
J. p. [2], 30, 321
48, 538
Ditolylsulphonethyl oxide ....
(C 6 H 4 Me.S0 2 .C 2 F 4 ) 2
W>A
....
83
.i
11
?
CsoHjA +S0 3
OeHuOjS
140-150
Baeyer
A., 183, 1
31, 199
Dinaphthyl sulphoxide
SO(C 10 H 7 ) 2
C^OS
162 u.c.
Ekstrand
B., 17, 2603
48, 171
sulphone
(C 10 H 7 ) 2 S0 2
C 20 H 14 2 S
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) a CPh.COOH
C, H 16 O 2 Si
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. 20 H 21 3 N + H 2 S0 4
C 2( ,H 23 7 S(?)
+ 7H 2
15
K6rner& Bohringer
G. I., 13, 363
46, 341
Amyl oxysulphobeuzide
S0 2 (C 6 H 4 .OC 5 H n ) 2
GftHjoQJS
98
Annaheiin
A., 172, 55
27, 797
Methoxycymene sulphone ....
SO 2 (C 6 H 2 MePr.OMe) 2
1)
150-151
Paterud
G. I. [1875], 13
28,639
Diphenyl sulphone .... ^..
S0 2 (C 6 H 4 .C 6 H 5 ) 2
C^I^AS
214-216
Gabriel and Deutscli
B., 13, 387
38, 476
Ethylic dibenzylphenyl sul-
PhS0 2 .C(CH 2 Ph) 2 .COOEt
C 24 H 24 O 4 S
118
Michael and Comey
A. C. J., 5, 116
46, 319
phonacetate
/3-Naphthalene diuaphthyl-
C 10 H,:SO(C 10 H 7 ) 2
CvayU-OyOfe
....
111 u.e.
Ekstrand
B., 17, 2602
48, 170
sulphoxide
Carvol + H,S
(C,,H 14 0) 2 .SH Z
^ / 32-*"*3o^2"
....
187
Beyer
A. P. [3], 21, 283
46, 331
Meliiiointriaulphonic acid ....
C 34 H 17 3 (S0 3 H) 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.H b OA
168-180
Tscherniak
J.p. [2], 2, 258
vii., 1183
Phenol + SO 2
>
140
25-30
Holzer
J.p., 25, 462
44, 585
(17.) CHOSe.
Methyl selenious acid
Me.SeO.OH
CH 4 O 2 Se
122
A., 97, 6
Benzyl
Ph.CH 2 .SeO.OH
C 7 H 8 O 2 Se
....
85
Jackson
A., 179, 13 ; B.,
28, 154 ; 29,
7, 1278
581
1
....
-
....
88
M
B., 8, 111
28, 553
(18.) CHON.
Nitroform
CH(N 0j ) 3
CH0 6 N 3
15
Schischkoff
A., 103, 364
iv., 110
Methylazaurolic acid
CH 3 .N.O.N
CH 2 ON 2
....
d. a. 100
....
A., 214, 336
Methylnitrolic acid ....
HO.N:CH.NO,,
CH 2 O 3 N 2
G4, d.
Tscherniak
B., 8, 115; A.,
28, 561 ; 29,
180, 168
903
Formamide
H.CO.NH 3
CH 3 ON
192-195
Liquid
Hofmann
16,72
11., 681
(cf. A., 128, 335}
150 (i. v.)
....
J. [1863], 319
Methylic nitrite
Me.O.NO
CH 3 O 2 N
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.NO 2
CH 3 3 N
66
....
Dumas and Peligot
A. C. [2], 58, 37
iv., 109
Isuretine
CH 4 ON S
....
104-105 p. d.
Lessen & Schiffer-
A., 166, 295 ;
vii., 707; 25,
decker
Z. C. [2], 7, 594
500
Carbamide (urea)
CO(NH 2 ) 2
.,
....
120
....
v., 951
,, .... ....
n
n. v.
130
Michler
B., 8, 1664
29, 702
i, ), .... ....
133
Lubavin
G. J. C., 1870
Hydroxyl urea
NH 2 .CO.NH(OH)
CH 4 O 2 N 2
cf. A., 182,214
128-130
Dressier and Stein
Z. C. [2], 5, 202
vi., 725
Paracyanformic acid
....
(C 2 H0 2 N) n
....
a. 250 d.
J. p. [2], 10, 212
Cyanformamide
NC.CO.NH,
C 2 H 2 ON 2
60
J. E., 7, 99
Nitracetonitril
N0 2 .CH 2 .CN
C 2 H 2 O 2 N.,
abt. 40
Steiner
B., 9, 781
30, 289
v
...
( )n
216 d.
B
B., 9, 783
Methylic isocyanate
O I C : N.Me
C 2 H 3 ON
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 ....
CH 2 .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 (OHXNH 2 )
CO(NH 2 ).COOH
CH 3 .CH.KO.N
NH 2 .CO.NH.COH
H.CN(OH).CN(OH)H
CO(NH 2 ).CO(NH 2 )
CHrNO.O.NO.CH,,
2 H 3 ON 3
C a H 3 O 3 N
C 3 H 4 ON 2
C 2 H 4 O 2 N 2
)*
C 2 H 4 3 N 2
M
C 2 H 4 4 N 2
)>
C 2 H 5 ON
)
1)
1
5
5*
)>
)
>
1
C 2 H 6 2 N
1)
>
1J
1
)9
)>
))
)l
)
)
H
i
i)
>
C 2 H 5 O 2 N 3
?>
J)
U
C 2 H 5 3 N
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
+2H 2 0(?)
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
CH 3 .CO.N:O 2 ;NH(?)
CH 3 .C(N0 2 ):NOH(?)
O 2 N.CH 2 .CH 2 .NO 2
CH 3 .CH(NO !1 ) !
H.CO.NHMe
CH 3 .CO.NH 2
>
>1
>
CHMe:N,OHorCHMe.
i
NH.O
m.o.N;o
M
H
M
v>
H
Et.NO 2
)J
)
>1
NH 2 .COOMe
CH S (OH).CO.NH.
J
CH 2 (NH 2 ).COOH
)>
NH 2 .GO.NH.CO.NH 3
n
n
j
>
EtO.NO 2
)
)>
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
C 2 H 5 O 3 N 3
....
134
Dressier and Stein
Z. C. [2], 5, 202
vi., 725
Diraethylnitrosamine
NMe,,NO
C~H 6 ON 2
148-5 (724)
Liquid
Renouf
B., 13, 2170
40, 152
Methyl carbamide ....
NH 2 .CO.NHMe
1)
....
100-101
Hofmann
B., 14, 2734
42, 822
j,
))
)>
109
Fischer
B., 14, 1913
Ethenylamidoxime .... .;,.
NH 2 .CMe I N.OH
)J
135
Nordmann
B., 17, 2748
48, 239
Ethyl hydroxylamine
NHEtOH
C 2 H 7 ON
(58
Liquid
Gurke
A., 205, 274
40, 572
Ammonium aldehydate
)
100
70-80
Liebig
A., 14, 144
i., 107
Hydroxylamine acetate
(NH 2 .OHXC 2 H 4 O 2 )
C 2 H 7 O 3 N
....
87-88
Lossen
Z.C.[2]
vl., 723
Ethylenediamine hydroxide
C 2 H 4 (NH 3 .OH),
C 3 H 12 2 N 2
117
Hofmann
)>
))
118
10
ihouspolos & Meyer
A., 212, 251
48, 940
Ammonium acetate -{- am-
AcO(NH 4 )+3NH 3
C 2 H 16 2 N 4
18
Troost
C. E., 94, 789
42, 1162
monia
51 JJ
Ac.O(NH 4 )+6NH 3
C,H,0 S N 7
32
u
u
Acetyl cyanide
CH 3 .CO.CN
C 3 H 3 ON
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.CH 3 .COOH
C 3 H 3 3 N
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
C 3 H 3 6 N
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
C 3 H 4 ON 3
105
Van t'Hoff
B., 7, 1383
28, 251
Paracyanocarbomethylamide
....
( )n
250
Weddige
J. p. [2], 10, 217
28, 449
Glycolylcarbamide (hydan-
CH 2 .CO.NH.OO.NH
C 3 H 4 2 N 2
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)
(C 3 H 5 ON) 3 (?) q.v.
))
95
Hofmaun
B., 3, 766
Ethylene cyanhydrin
C 2 H 4 (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
CH 2 : CH.CH 2 O.NO
C 3 H 6 2 N
85 ; 93 (?)
Brackebusoh
B., 7, 226, 1142
27, 573
Nitropropylene
C 3 H 5 .N0 3
j
96 ; 107 (?)
j
J)
Nitrosoacetone
CH 3 .CO.CH 2 .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
CH 3 .CO.CO.NH 3
)>
124-125
Claisen & Shadwell
B., 11, 1566
36, 45
Allylic nitrate
C 3 H 5 .O.N : O
C 3 H b 3 N
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
CH 2 (NO 2 ).CH 2 .COOH
C 3 H b 4 N
66-67
Lewkowitsch
J. p. [2], ?0, 169
38,33
Tartronamic acid
CH(OH).CO(NH 2 ).COOH
....
160 d.
Menschutkin
A., 182, 82; J. E.,
30, 627 ; 32,
8, 177
323
Glyceryl trinitrite
C 3 H 6 6 N 3
150-154
cf. B,, 6, 1290
Masson
43, 350
(nitro
C 3 H 6 (N0 3 ) 3 .
C 3 H S 9 N 3
....
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
CH 3 .CH.NH.CO.NH
C 3 H 6 ON 3
154
A., 151, 204
1 __[
Propylazaurolic acid
*
1
. ...
127-5
Meyer and Coustam
A., 214, 334
44, 41
Methyloxamide
CONH 2 .CONHMe
C 3 H C 2 N 3
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 ....
CH 2 (CO.NH,),
C 3 H..OoN 2
168-170
Henry
C. R, 100, 943
48, 886
^^2\ ' *~*'2/z
3 o f^ z
770
J. [1875], 528
Acetylcarbamkle
))
NH 2 .CO.NHAc.
)
112
Moldenhauer
A., 92, 405
i., 753
,,
I
200?
Ziuin
A., 94, 100
)J
Acetoximic acid
OH 3 .CH(NO).CH 2 (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 .... ''.
CH 3 .CH 2 .C(NO 2 ) : N.OH
C,H 6 3 N 2
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 ...
CH 3 .C(NO)(NO 2 ).CH 3
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
CH 3 .CH 2 .CH(N0 2 ) 2
C 3 H 6 4 N 2
182-5 u.c. ;
1. -17
ter Meer
B., 8, 1080 ; A.,
29, 68 ; 30, 186
189 c.
181, 19
Dinitroisopropane
CMe 2 (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
C 3 H.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
CH 3 .CO.NHMe
1
207
26
?
B., 14, 2730
42, 822
)
)1
906
28
))
5)
Propionamide
CH 3 .CH 2 .CO.NH 2
>
75-76
Sestini
Z. C. [2], 7, 34 ;
24, 234 ;
Cimento 4, 21
vii., 1009
II
75-76
Hofmann
B., 15, 981
Dimethylacetoxime (acetox-
CMe 2 : 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-
CH 3 .CH 2 .CH5.NO (?)
J)
130-132
Liquid
Petraczek
B., 15, 2784
propane)
Propylic nitrite
CH S .CH 2 .CH.,O.NO
C 3 H ; O 2 N
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
(CH 3 ) 2 CH.O.NO
i
43-44
Kissel
J. E. [1882], 226
42, 936
. ...
))
n
45 (762)
Liquid
Silva
Z. C., 12, 637
vi., 966
Nitroisopropane
(CH 3 ) 2 CH.NO 2
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
CH V CH 2 .CH 2 .NO 2
?;
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
CH 3 .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)
NH 2 .COOEt
47-50
McOeath
B., 8, 384
" )>
H
49
Ponornareff
B., 15, 515
V
75
))
ISO
b. 100
i., 751
a-Amidopropionic acid (al-
CH 3 .CH(NH 2 ).COOH
abt. 200
Strecker
A., 75, 29
i., 63
anine)
0- ,, (fl-al-
NH 2 .CH 2 .CH 2 .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.CH 2 .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.CH 2 .COOH
C 3 H 7 O 2 N
....
210-220 d.
Meylius
B., 17, 286
46, 994
cosine)
Amidomalonamide ....
NH 2 .CH(CO.NH 2 ) 2
C 3 H 7 2 N 3
....
182
Conrad & Guthzeit
B., 15, G07
42, 946
Isopropylic nitrate ....
UHMe 2 .O.N0 2
C 3 H 7 0,N
100-102(760
Liquid
Silva
A., 154, 256
vi., 966
Propylic nitrate
CH 3 .CH 2 .CH 2 .O.NO 2
i)
110-5
....
Wallach & Schulze
B., 14, 422
40, 572
Ethyl carbamide .... ...
NH 2 .CO.NHEt
C 3 H 8 ON 2
....
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
CH 3 .CH(NH 2 ).CO.NH 2
)}
cf.A.,173,344
a. 250
Baumstark
B., 6, 883
26, 1243
Ethyl semicarbazide
....
C 3 H 9 ON 3
...
105-106
....
A., 199, 294
Dinitropyrroline
C 4 NH 3 (N0 2 ) 2
C 4 H 3 4 N 3
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
C 4 H 4 3 N 2
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
C 4 H 4 6 N 2
128-130 d.
M tiller
B., 16, 2986
46, 584
Cyanacetone ....
CH 3 .CO.CH 2 .CN
C 4 H 5 ON
120-125
I^tatthews and
B. 15 2679
Hodgkinson
(polymer)
166
J. p. [2], 1, 141
*
Allylic isocyanate
CO I N.C 3 H 5
i
82
Liquid
Cahours and Hof-
P. T. [1857], 555
ii., 195
mann
Propionic cyanide
CH 3 .CH 2 .CO.CN
)>
108-109
Claiaen and Moritz
37, 692
,,
5
)>
108-110
Liquid
B., 13, 2121
40, 154
Epicyanhydrin
: C 3 H 5 .CN
)5
....
162
Pazschke
J. p. [2], 1, 98
vii., 466
'?
....
11
d. 280
A., 213, 174
Ethylic cyanocarbonate
NC.COOEt
C 4 H 5 O 2 N
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 ....
CH 2 .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.CH 2 .CO.NH.CO.NH 2
C 4 H 5 2 N 3
200-210 d.
Mulder
B. S. [2], 29, 531 ;
34, 786; 36,
B., 12, 466
619
Diglycollimide
....
C 4 H 6 3 N
142
Wurtz
A. C. [3], 69, 342
vi., 642
Fumaramic acid
NH 2 .CO.C 2 H 2 .COOH
J>
217 d.
Michael and Wing
A. C. J., 6, 419
48, 968
Acetyl oxatnic acid ....
NHAc.CO.COOH
C 4 H 6 4 N
54
....
J. p. [2], 9, 299
Amidomaleic acid
C 2 H(NH 2 ).(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.C 2 H 2 (N.OH).COOH
C 4 H 6 5 N
d. 126
Ebert
A., 229, 45
48, 1123
Allanic acid ....
C 4 H 6 5 N 5
+H 2
d. 210-220
A., 159, 353
Nitrosopyrroline
C 4 H 6 N.NO
C 4 H 6 ON 2
37-38
Ciamician and
B., 16, 1543
44, 1142
Dennstedt
Diethylic dicyanate
C 2 N 2 O,Me 2
C 4 H 6 2 N 2
98
Hofmann
B., 3, 766
24, 136
Lactyl cyanamide
CH 3 .CH(OH).CO. NH.CN
212
Mertens
J. p. [2], 17, 34
34, 398
Fumaramide
NH 2 .CO.CH : CH.CO.NH 3
i)
232
Curtius and Koch
B., 18, 1298
48, 885
Glycocollimide anhydride ....
CH 2 .NH.CO.CO.NH.CH 2
....
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
CH 2 .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
CH 2 .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
C 4 H 6 (NO,,) 4 O 4
C 4 H 6 12 N 4
61
Stenhouse
P. T. [1849], 399
ii., 505
Isopropylic cyanate
....
C 4 H 7 ON
67
Hofmanu
B., 15, 756
vii., 1016
CHMe 2 .CNO
74
Silva
B. S. [2], 17, 97
26, 367
Hydroxyisobutyronitril
CMe 2 (OH).CN
abt. 120
Urech
A., 164, 257
26, 59
y-hydroxybutyronitril
CH,(OH).CH 2 .CH 2 .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.NH 2
159
B., 12, 2056
38, 99
Ethylleucazone
C 4 H 7 ON 3
158-158-5
) J
Meyer & Coustam
A., 214, 341
44, 40
Nitrobutylene
Me 2 C : CH.NO 2 or
C 4 H 7 2 N
154-158 p. d.
Liquid
Haitinger
W. A., 77, 428
36, 701
CH 2 : CMe.CH 2 .NO 2
Nitrosomethyl acetone
CH 3 .CO.CH(NO).CH 3
185-186 c.
74
Meyer and ZUblin
B., 11, 323
34, 487
1! ,,
JJ
11
....
74
Ceresole
B., 15, 1874
44,41
Methylio isonitrosoacetone ....
CH 3 .CO.CH:N.OCH 3
,,
115-116 u. c.
Liquid 15
B., 16., 833
Diacetamide ....
NHAc 2
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
CH 3 .CH 2 .CO.CO.NH 2
3)
116-117
Claisen and Moritz
B., 13, 2121
37, 693; 40, 154
Amidomaleic diamide
C 2 H(NH 2 )(CO.NH 2 ) 2
C 4 H 7 2 N 3
122
Clans and Voeller
B., 14, 152
40, 204
Ethylic oxamate (oxamethane)
NH 2 .CO.COOEt
C 4 H 7 3 N
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.CH 2 .COOH
....
206
Curtius
B., 16, 757 ; 17,
46, 1307
1667
! i,
M
Ml
d. 130
Kraut & Hartmann
A.. 133,105
Succinamic acid
NH 2 .CO(CH 2 ) 2 .COOH
300
....
A., 134, 136; 162,
175
n-Nitrosobutyric acid
CH 3 .CH 2 .CH(NO).COOH
n
151 d.
Wleiigel
B., 15, 1058
42, 944
/3-isomitrosobutyric acid
CH 3 .C(N.OH).CH 2 .COOH
140 d.
Westenberger
B., 16, 2996
46, 581
Ethylic nitro-acetate
CH 2 (NO ; ).COOEt
C 4 H 7 O 4 N
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.(CH 2 .CO.NH 2 ) 2
,,
....
a. 125
Heintz
A., 128, 141
vi., 645
Amidodiglycollic acid
NH(CH 2 .COOH) 2
d. a. 210
,,
A., 132, 276
vi., 644
Ethylic nitroglycollate
N0. 2 .CH(OH).COOEt
C 4 H 7 O 5 N
180-182
....
Henry
A. C. [4], 28, 424
Allyl carbamide
NH 2 .CO.NH.C 3 H 5
C 4 H 8 ON 2
....
85
And reasch
M. G, 5, 33
46, 732
ii ii
1)
....
141
Maly
Z. C. [1869], 261
Succinatnide
NH 2 .CO. (CH 2 ) 2 .CO. NH 2
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
NH 2 .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
C 4 H 4 (NH.OH) 2
C 4 H 8 2 N 2
....
173
Ciamician and
G. I., 14, 156
48, 246
Dennstedt
Amidosuccinuric acid
NH 2 .CO.CH 2 .CH(NH.CO.
C 4 H 8 2 N 3
137-138 d.
Guareschi
B., 10, 1747
34, 138
NH 2 ).COOH
Ethylazaurolic acid
ON.CHMe.N^.CHMe.NO
C 4 H 8 2 N 4
....
142 d.
Meyer & Constam
B., 14, 1457
40, 896
3-nitrosocreatinine .... .
....
195
Marcker
A., 133, 310
vi., 503
-
....
210 d.
A., 133, 306
Butylpseudonitrol
CH 3 .CH 2 .C(NO)(NO 2 ).CH 3
C 4 H S 3 N 2
58
Meyer and Locher
B., 7, 1509 ; A.,
28, 1183 ; 29,
180, 135
904
Ethylic allophanate
NH 2 .CO.NH.COOEt
190-191
Kichter
B. K. T.
Lacturamic acid
NH 2 .CO.NH.CHMe.COOH
,,
....
155 d.
Urech
A., 165, 99
vii., 723 ; 26,
380
Dinitrobutane
CH 3 .CH 2 .CH 2 .CH(NO. i ) 2
C 4 H 8 4 N 2
190 d.
Liquid
Ziiblin
B., 10, 2085
34, 284
197 p. d.
Chancel
C. B., 96, 1466
44, 915
CH 3 .CH 2 .C(N0 2 ) 2 .CH 3
n
199 c. ; p. d.
Liquid
Meyer
B., 9, 701
30, 288
C 4 H 8 (N0 2 ) 2
95-96
Beilstein and Kur-
B., 14, 1621
40, 1021
batow
Iso-diiiitrobutaue
CHMe 2 .CH(NO 2 ) 2
H
d.
Liquid
Ziiblin
B., 10, 2087
34, 284
Ethylene allophanate
NH 2 .CO.NH.COO.C 2 H 4 .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
C 4 H a ON
220
A., 149, 158
Ethylacetamide
CH 3 .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
CH 3 .CH 2 .CH 2 .CO.NH.,
....
115
Chancel
C. B., 18, 8J9
i., 690
216
A. 52, 294
Isobutyramide
CHMe 2 .CO.NH 2
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
CH 3 .CH,,CH 2 .CH 2 .O.NO
C 4 H 9 O.,N
76
Bertoni and Truffi
G. I., 14, 23
46, 1110
Isobutylic nitrite
CHMe 2 .CH 2 .O.NO
66-70
,,
J)
67
Chapman & Smith
J., 22, 153
Butylic nitrite
CMe 3 .O.NO
76-78
Liquid
Tscherniak
A., 180, 159
29, 902
Nitrobutaue ....
(CH 3 ) 3 .C.NOj
110-130
T ' 'fl
A. 180 155
Nitroisobutane
CHMe 2 .CH 2 .NO 2
137-140
Liquid
Demole
B., 7, 710; A.,
vii., 897 ; 27,
175, 142
984 ; 28, 561
Nitrobutane
CH 3 .CH 2 .CH(N0 2 ).CH 3
D
abt. 140
Liquid
Meyer and Locher
A., 180, 134
29, 904
n
CH 3 .CH 2 .CH 2 .CH 2 .NO 2
151-152 c.
Liquid
Zubliu
B., 10, 2083
34, 284
Propylic carbamate
NH 2 .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
Me 2 C(NH 2 ).COOH
....
sb. 220
Tieniannand Fried-
B., 14, 1972
lander
Ethylamidoacetic acid
NHEt.CH 2 .COOH
<*
a. 160 d.
Heintz
A., 129, 33; 132, 1
vi., 643
a-Methamidopropionic acid ....
CH 3 .CH(NHMe).COOH
brown 180
260 d.
Lindenberg
J.p. [2], 12, 244
29, 701
Ethylglycollamide
CH 2 (OEt).CO.NH a
225
b. 100
Heintz
A., 129, 42
Glycolethylamide
CH 2 (OH).CO.NHEt
250
Liquid
A., 129, 29
vi., 647
Guanoliu
C 4 H 9 O. N
1 \A 1 1 PL
J.p. [2], 17, 238
...
+H 2
1 L* i LO
100
"'.
Butylic nitrate
C 4 H 9 .O.NO 2
C 4 H 9 3 N
a. 130
Wurtz
J., 7, 575
Isobutylic nitrate
CHMe 2 .CH 2 .O.NO 2
123
Chapman & Smith
Z. C. [1869], 433
22, 153
Base from creatiuine
C 4 H 9 O 4 N
....
152
Marcker
A., 133, 314
vi., 503
448
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
?
....
C 4 H 1U ON 3
170-172
Linneitiann
vi., 63
Diethylnitrosamine
NEt 2 .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
NH 2 .CO.(CH.NH 2 ) 2 .CO.NH_,
C 4 H 10 2 N 4
160
Glaus and Helpen-
B., 14, 626
40, 578
steiu
Ethylene dicarbamide
C 2 H 4 (NH.CO.NH 2 ) 2
cf. A., 119,
192
Volhard
P. R., 11, 268
ii., 595
349
Ethylic methanedicarboxyl-
CH(CO.NH 2 ) 2 .COOEt
C 4 H 10 4 N 2
....
190-191
Amato
G. I., 1, 690
vii.. 9
amide carboxylate
Butaldehyde ammonia
CH 3 . CH 2 .CH 2 .COH +NH 3
C 4 H H ON
+ 5H,,0
30-31
Lipp
A., 211, 356
42, 709
Dimethylethj lalkine
....
n
130-134
Ladenburg
B., 14, 2408
42, 166
Acid ammonium acetate
CH 3 . COONH 4 + C 2 H 4 O 2
C 4 H U 4 N
....
76
....
....
i., 13
Furfuronitril ....
C 4 H 3 O.CN
C 5 H 3 ON
146-148
Liquid
Wallach
B., 14, 752
40, 715
147 (757-8)
Ciamician & Denn-
B., 14, 1058
40, 801
stedt
Nitropyromucic acid
C 4 H 2 O(N0 2 ).COOH
C 5 H 3 O 6 N
183
Klinkhardt
J.p. [2], 25, 51
42, 499
184
Priebs
B., 18, 1363
48, 971
Sarcine
C 5 H 4 ON 4
n. f. 150
Strecker
A.
v., 196
Suceinocyanimide
c 2 H 4 : (co)j : N.CN
C 5 H 4 2 N 2
....
138
Holler
J.p. [2], 22, 207
40, 259
Nitrocarbopyrrolic acid
....
C 5 H 4 4 N 2
144-146
Ciamician & Danesi
G. I., 12, 28
42, 875
Hydroxypyridine (chelamide)
C 5 H 4 N.OH
C 5 H 5 ON
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
,.
+ H 2
66-67
Ally lie cyanocarbonate
CN.COOC 3 H 5
CiHsO-jN
135
Liquid
Wagner & Tolleus
B., 5, 1045
26, 381
Pyromucamide
C 4 H 3 O.CO.NH 2
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
C 4 H 4 N.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
C 4 H 4 N.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
C 5 H 3 N(OH) 2
255 d.
KSnigs and Geigy
B., 17, 1836
46, 1369
Allylalcohol dicyanide
C 3 H 5 .(CN) 2 .OH
C 5 H 6 ON 2
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-
C 4 H 4 :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
NH 2 .C 5 NH 3 .OH+H 2
sb. a. 214
214
Krippendorff
J.p. [2], 32, 153
48, 1243
Diacetyl cyanamide ....
CN.NAc 2
C 5 H 6 2 N 3
d. 75
Mertens
J.p. [2], 17, 14
34, 397
Succinocyaminic acid
COOH.C 2 H 4 .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
C 6 H 6 3 N,
160
Mabery and Hill
B., 13, 740
40, 39
Malylureio acid
NH.CO.NH.CO.CH 2 .CH.
C 5 H 6 O 4 N 2
215-220 d.
Grimaux
C. E., 80, 828
28, 7. r .2
1 1
COOH
Isobutyryl cyanide
CHMe 2 .CO.CN
C 5 H 7 ON
117-120
Moritz
39,13
Butyryl
CH 3 .CH 2 .CH 2 .CO.CN
"
133-137
39,16
Furfurylamine
O.CH.CH : CH.C.CH,.NH 2
145-146(761)
Liquid
Ciamician and
B., 14, 1476
40, 898
i 1
Dennstedt
Ethylic cyanacetate ....
NC.CH 2 .COOEt
C 5 H 7 O 2 N
207
....
Van t'Hoff
B., 7, 1383
28, 251
Methyl succinimide
CO.(CH 2 ) 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.CH 2 .CO.NH
1)
280 d.
66
Arppe
A., 87, 231
iv., 775
Glutarimide
CO.(CH 2 ) 3 .C'O.NH
n
151-152
Bernheimer
G. I. [1882], 281
42, 1190
Acetonyl carbaminate
CMe 2 .O.CO.NH.CO
C 5 H ; 3 N
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
Me 2 HC 3 N 3 O 3
C 6 H 7 3 N a
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
C S H 4 (CO.NH 2 ) 2
176-5
Strecker
B., 15, 1641
42, 1281
Citraconamide
191 d.
11
B., 15, 1640
192
Dimethylic amidocyanurate
(C 3 N 3 )(OMe).,NH 2
)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
C 5 H 8 3 N 4
....
225 d.
Hill
B., 9, 1091
30, 50!)
Ethylic oxalurate
NH 2 .CO.NH.CO.COOEt
C 6 H 8 4 N 2
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
NH 2 .CO.NH.CO.(CH 2 ) 2 .
203-204
Pike
C. N., 28, 173
27, 49
COOH
11 n
....
203-205
B., 6, 1104
Isobutylic isocyanate
CHMe 2 .CH. 3 NCO
C 5 H 9 ON
110
Brauuer
B., 12, 1877
Butylic cyanate
CMe 3 .NCO
85-5 c.
Liquid
B., 12, 1875
38, 228
Hydroxyisovaleronitril
CHMe 2 .CH(OH).CN
ti
136 d.
1. -17
Lipp
A., 205, 26
40, 86
Ethylic diamidocyanurate ....
C 3 N(NH 2 ) 2 .OEt
C 5 H 9 ON 5
190-200
Hofmann and
B., 3, 275
vii., 410
Olshausen
Nitroamylene
C 6 H 9 .N0 2
C 5 H 9 2 N
160-170 d.
Haitinger
M. C., 2, 290
40, 1115
11
11
69-73 (14)
11
Nitrosoethyl acetone
CH 3 .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 ....
CH 3 .CO.CH : N.OEt
130
Ceresole-
B., 16, 834
Methylic isonitroso-methyl-
CH 3 .CO.CMe I N.OMe
125 u.c.
11
acetone
Methyl diacetamide
NMeAc 2
102
Liquid
Hofmann
B., 14, 2731
42, 822
0)
82-83
Brandes
Z. C. [1866], 459
vi., 829
Butyryl formamide ....
CH 3 .CH 2 .CH 2 .CO.CO.NH,
105-106
Moritz
39,16
Isobutyryl
CHMe 2 .CO.CO.NH s
,,
....
125-126
39, 13
vi., 13
Levulinamide
C 4 H 7 O.CO.NH 2
107
Wolff
A., 229, 249
48, 1124
Caffoline
CH(OH).NMe.C'O.N : C.
C 5 H 9 O 2 N,
cf. B., 15, 29
194-196
Fischer
B., 14, 1907
43, 217
NHMe
Ethylic acetylcarbamate
NHAc.COOEt
C 5 H 9 O 3 N
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.CH 2 .COOMe
C 6 H 9 3 N
254 (712)
58 4 5
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.
Wallach and West
B., 9, 265
30, 185
a-nitrosopropionate
CH 3 .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
CH 3 .(CH 2 ) 2 .C(N.OH).COOH
))
143-144-5 d
Furth
B., 16, 2181
46, 42
y~ i!
CH 3 .C(N.OH).(CH,) 2 .COOH
95-96
Miiller
B., 16, 1618
44, 112!)
Dimethyloxaluramide
NH 2 .CO.CO.NMe.CO.NHM
C 5 H 9 3 N 3
225 d.
Menschutkin
A., 178, 203
29, 379
Niti-ovaleric acid
C 4 H 8 (NO.,)COOH
C 5 H 9 O 4 N
m.a. 100
cryst.
Dessaignea
A., 69, 274
v., 97!)
Glutamic acid
C 3 H 5 (NH 2 )(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 ....
CH 2 (NO 2 ).OH 2 .COOEt
5)
161-165
Liquid
Lewkowitsch
J. p. [2], 20, 167
33, Z3
nitrolactate
C 5 H 9 5 N
178
Henry
B., 3, 532
Nitrosopiperidine
C 6 H 10 N.NO
C,,H 10 ON 2
218
Liquid
Schotten
B., 15, 425
42, 983
n
240 pd.
Liquid
Wertheim
A., 127, 81
vi., 947
Ethylacetyl carbamide
CO(N 2 H 2 EtAc)
C 5 H 10 2 N 2
120
....
J. p. [2], 21, 31
Butyryl carbamide
NH 2 .CO.NH.CO.C 3 H 7
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
CMe 2 (CONH 2 ) 2
)>
196-198, a.f.
Thome
39, 545
20-210
Pyrotartaramide
NH 2 .CO.CHMe.CH 2 .CO.NH 2
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
NH 2 .CO.NH.COOPr
C 5 H 1U S N 3
150-160
Cahours
C. R., 76, 1383
26, 872
Acetonyl uramic acid
NH 2 .CO.NH.CMe 2 .COOH
160, d.
Urech
A., 164, 274
vii., 18; 26,62
Glycerylic allophanate
C 3 H 5 (OH) 2 (O.C 2 H 3 N 2 2 )
5 H 10 5 N 2
160
Baeyer
A., 114, 160
i., 134
Diethylformamide
H.CO.NEt 2
C 5 H U ON
175-178
Liquid 20
Linnemann
W. A., 60, 44
vi., 619
7)
175-178
....
Wallach
B., 14, 744
Isobutylformamide
H.CO.NH.CH 2 .CHMe 2
)>
135
Schmidt & Sacht-
A., 193, 102
36, 139
leben
Isovaleramide
CHM e2 .CH 2 .CO.NH 2
....
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 ....
CHMe 3 .CMe : N.OH
157-158
....
'fiigeli
B., 16, 2984
46, 611
Isoamylaldoxime
CHMe 2 .CH 2 .CH : N.OH
160-162
3 etraczek
B., 16, 829
Isoamylic nitrite
CHMe 2 .CH 2 .CH.j.O.NO
C S H H 2 N
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
CH 3 .(CH 2 ) 3 .CH 2 .O.NO
T
97
Jertoni and Trutfi
G. I., 14, 23
46, 1110
Nitropentane ...
C 5 H U .N0 2
JT
150-160
VIeyer and Stxiber
B., 5, 204 ; A.,
25, 474; vii.,
171, 43
897
Ethylic dimethyl carbamate
NMe 2 .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
NH s .COO.CH 2 .CHMe,
20G-207
55
Vlylius
B., 5, 973
26, 266
a-ethylamidopropionic acid ....
C 2 H 3 Et(NH 2 ).COOH
M
w. m.
)uvillier
C. R., 99, 1120
48, 373
o-amidoisovaleric acid
CHMe 2 .CH(NH 2 ).COOH
?
w. m.
ustin
B. S. [2], 37, 3
42, 589
#-
(CH 3 ) 2 .C(NH S ).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
CH 3 .CH(OH).CO.NHEt
C 5 H U 2 N
200
48
Wurtz and Friedel
A. V. [3], 63, 110
ill., 453
Ethyl lactamide
CH 3 .CH(OEt).CO.NH 2
)*
219
62-63
Wurtz
A. C. [3], 69, 175
iii., 452
a-methoxybutyrumide
CH,.CH 2 .CH(MeO).CONH.,
;
77-78
Duvillier
C. R., 88, 598
36, 523
<i-hydroxyisovaleramide
CHMe 2 .CH(OH).CO.NH 2
104
Lipp
A., 205, 27
40, 86
y-hydroxyvaleramide
CH 3 .CH(OH.(CH 2 ) 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.N0 2
O i H 11 3 N
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.(NMe 2 ),
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
C 6 H 10 (OH).NH,
J)
157-159
Badziszewski and
B., 17, 839
46, 1190
Schramm
)> ....
t)
160
As., 7, 90
Hydroxypropylethylamiiie ....
C 3 H 6 (OH).NHEt
160
Liebermann & Paal
B., 16, 533
44, 910
Diethylsemicarbazide
Unsymmetiical
C 6 H 13 ON 3
149
A., 199, 312
Dimethylpropylglycoline ....
CH 2 (OH).CH(OH).C'H. 2 .
C 6 H 13 O a N
216-217
Liquid
Both
B., 15, 1153
42, 1195
Taurobetain .
NMe 2
C H O N
240
Z. P. C. 7 35
Bidimethylamidoearbanude
OO(NH.NMe 2 ) s
^'V^M^V 1
C 5 H 14 ON 4
220-
Renouf
B., 13, 2172
40, 152
Ammonium glutarate
COO(NH,)(CH 2 ) 3 .COO(NH.,)
C S H U 4 N 2
150
....
Bernheimer
G. I. [1882], 281
42, 1190
Dinitrodihydroxyquinone
C'(OH) 2 (NO 2 ) 2 :Oj
C 6 H 2 3 N 2
d.w.m. 170
Nietzki
B., 10, 2147
34, 426
(nitranilic acid)
!! >!
M
+ xII 2
a. 100 +
i)
))
Tetranitrodihydroxy benzene
C 6 (OH) 2 (N0 2 )<
C 9 H 2 10 N 4
166
Henriques
A., 215, 335
44, 329
Nitrophenylene oxide
C 6 H 3 (N0 2 ):0
CH,(NO),:O,=54.1
C 6 H 3 S N
C H O N
150
232
Etard
A., 124, 250
A. C. (5), 22, 273
v., 161
40, 583
Trinitrobenzeue
6 3\ /2 ~'2~~~"^ *
C 6 H 3 (N0 2 ) 3 =?
vg AJ. 3 v.' ^ J. '
C s H a O.N 3
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.(N0 2 ) 3 =?
C,,H 3 7 N :1
90-104
Zehenter
M. C., 6, 523
48, 1235
=1.3.4.6
>J
....
96 u.c.
Henriqus
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 .(NO 2 ) 3 =1.3.4.5.6 or
C.H 3 8 N :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 .(N0 2 ) 3 =1.3.5.2.4.G
C 6 H 3 9 N 3
....
158
Benedikt
B., 11, 1376
36, 58
>
JJ
159-160
Benedikt & Hazura
M. C., 5, 667
48, 554
m-nitrodiazobenzol imide
NOj.C' 6 H 3 .N : N.NH
C 6 H 4 2 N 4
....
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
C 6 H a (NO 2 ).N.NHN
C fl H 4 2 N 4
cf. A., 115, 25
211
Hofmanu
P. R., 10, 496
iv., 484
i i
Dinitrobenzene
C 6 H 4 (NCg 2 =1.3
C 6 H 4 4 N 2
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
NO 2 .C 4 H 2 O.CH : CH.N0 2
C 6 H 4 5 N 2
143-144
Priebs
B., 18, 1362
48, 971
Dniitropheiiol
HO.(NO S ) 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
C 6 HAN S
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 .(NO 2 ) 2 =1.4.5.?
C 6 H,0 6 N 2
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) ....
NH 2 .(NO,) 3 =1.2.4.6
C.H 4 6 N 4
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
C 6 H 5 ON
156
Proskauer and SeL
B., 9, 1264
31, 68
Nitrobenzene...,
C 6 H S .N0 2
C 6 H 5 2 N
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.N0 2 = ?
)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
C 6 H 6 2 N
T^
J
rt
i)
jj
6 H 5 3 N
^
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
C 6 H 6 O,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
C 4 H,O.CH:CH.NO,
N.COOH.OH=1.2.<
JI V
55 . )
= 1.3.6
J)
))
C (1 H 4 .NOj.NH(NO)= 1 . 2
(OH) 2 .NO,=1.2.3.
1.2.4
>
11
)J
)J
fj
)J
))
C 6 H 6 3 N 3
C 6 H 6 4 N
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
NH 2 (NO,), 1 2 6
CH C O,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 .NO 2 =1.2.3.?
OH.NH,.(NO,) S =1.2.4.6
W
) M
= 1.4.2.6
NH 2 .(NO 2 ) 2 ^consecutive
Me.CO.C 4 NH 2 (NO 2 ) 2
1
(OH) 2 .NH 2 .(NO.,). ! =1.3.(?) 3
(NH 2 ) 2 .(NO 2 ) 3 =1.3.2.4.6
C 5 N 4 H 2 Me.OH
(CH 3 CO.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,
C 6 H 6 ON 4
C 6 H 6 0,N 3
T
+H 8
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
,,
NH 2 .N0 2 =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).,.
C 4 H 3 O(CONH 2 )j
OH.NH 2 .N0 2 =1.2.6
= 1.2.4
i)
= 1.4.?
>; )i
Me.CO.C 4 NH 3 .NO 2
J
C 5 H 3 MeO 3 N 4
(OH) 2 .N0 2 .NH 2 =1.3.(?) 3
(NO^CNH^?
=(?)s.l.4
NH 2 (OH).C C H 2 .OH,(NO,) 3
C.H 6 2 N 2
>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
C 6 H 6 2 N 4
C 6 H 6 3 N a
JJ
J)
>I
I>
T
J>
H
)J
C 6 H 6 3 N 4
C 6 H,0 4 'N 2
C 6 H 6 4 N 4
C 6 HAN 4
C 6 H 6 8 N 4
285
cf. A, 205, 85
+ xH 2
+H 2 O
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)
C 6 H 4 .OH.NH 2 = ?
=1.2
1.3
C 6 H 6 12 N 4
C G H ; 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
C 5 H 4 MeON
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
C 4 H 4 N.COOMe
C 4 H 3 MeN.COOH
(NH 2 ),.NO 2 =1.2.4
=1.3.?
= 1.4.6
C 6 H ; 3 N 3
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 : C 4 H 3 CMe : N.OH
CO.C 2 H 4 .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.CH 2 .CO.NMe.CO. NMe
| |
123
Mulder
B., 12, 467
,,
CO.CMe 2 .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,H 8 5 N 2
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
C 6 H 2 .ONH 4 .NH 2 .(NO 2 ) a
C 6 H 3 (O.N0 2 ) 6
)1
n
NC.COO.CH 2 .CHMe s
CO.CH 2 .CH 2 .O.NEt
i " )
C 6 H 8 5 N 4
C 6 H 8 18 N 6
It
C 6 H 9 ON
C 6 H 9 0,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.CH 2 .CMe 2 .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
NAc 3
C 6 H 9 3 N
....
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
....
C 6 H 9 3 N 3
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
NH 2 .CO.CN 2 .CH 2 .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
(C 2 H 3 ON 3 ) 3
C 6 H 9 3 N 9
170 d.
Curtius
B., 18, 1290
48, 884
Ethylie aeetoxamate
NHAc.CO.COOEt
C 6 H 9 O 4 N
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
C 6 H 9 4 N 3
210-220 d.
Fischer
B., 14, 1909
42, 217
Ethylie oximidosuccinate ..
COOH.C 2 H 2 (N.OH).COOEt
C 6 H 9 6 N
110-111 d.
Ebert
A., 229, 45
48, 1122
Amidotriglycollic acid
N(CH 2 .COOH).,
C 6 H 9 6 N
a. 190, d.
Heintz
A., 122, 269
vi., 646
Citramic acid
C 3 H 6 0(CO.NH 2 )(COOH) 2
138
Behrmann ant
B., 17, 2687
48, 138
Hofmann
Xyloidin
C 6 H 9 (NO 2 \
C fl H 9 7 N
b. 180
v., 1060
Nitroisodulcitol
C 6 H 9 U N 3
b. 100
..>.
A., 127, 364
Mannitol pentanitrate
(C 6 H 8 (OH)(O.N0 2 ) 5
C 6 H 9 16 N 5
77-79
J. [1864], 583
Diethyl carbamine cyanide ...
NC.CO.NEtj
C 6 H 10 ON 2
219-220
Liquid
Wallach
B., 14, 737
40, 717
Ethylie ethyl cyanamido-
N(CN)Et.COOEt
C 6 H 10 2 N 2
abt. 213
Liquid
Bassler
J. p. [2], 16, 160
34,215
carbonate
Sarcosine anhydride
NMe.CH 2 .CO,NMe.CH,,CO
350
149-150
Mylius
B., 17, 287
46, 994
Dimethyl allantoin
C 6 H 10 3 N
225
Cloez
I. D., Paris, 1866
vi., 520
Ethylie amidomaleamate
NH^CO.CH :C(NH 2 ).COOE
C fi H 10 3 N 2
62 u.c.
Claus and Voeller
B., 14, 152
40, 254
imidosuccinamate ...
NH 2 .CO.CH.NH.CH.COOE
118
Lehrfeld
B., 14, 1821
42, 163
| |
a-|8-diisomtrasobuty-
CH 3 .C(N.OH).C(N.OH).
C 6 H 10 4 N 2
....
140 d.
Ceresole & Kockerl
E, 17, 821
46, 1121
rate
COOEt
dioarboxylamide car-
CH(CQNH 2 ) 2 COOEt
B
190-191
Amato
G. I. ?, 690
25, 401
boxylate
Citrodiamic acid
C 3 H 6 0(CO.NH 2 ) r COOH
C 6 H 10 5 N 3
158
Behrmaun and
B,, 17, 2685
48, 138
Hofmauu
Dinitrohexylic acid
CH 3 .C(N0 2 ) 2 .CMe 2 .COOH
C 6 H 10 6 N 2
215
Kachler
A., 191, 144, 155
34, 513
Tetranitrodulcitol
C 6 H 10 (NQ 2 ) 4 6
C H 10 14 N 4
130-140
Bechamp
C. E., 51, 257
ii., 351
Amylic cyanate
CHPr^Me.O.CN
C 6 H n ON
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),CH 2 .CN
v
173
Pinner
B., 12, 2053
38,99
11
)J
173-174
Einne
B., 6, 389
Ally] acetoxime
C 6 H 10 :N.OH
187-5 c.
Liquid
Nageli
B., 16, 496
14, 728
Mesityloxime....
J,
180-190 p.d.
Liquid
B., 16, 495
Ethyldiacetamide
NEtAc 3
C 6 H U 0,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 ....
....
C 6 H n O 2 N 3
10-112
Tischer
A., 215, 253
4i, 356
Ethylie acetamidoacetate ....
NHAc.CH 2 . COOEt
C 6 H U 3 N
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
NH 2 .CO.COOBu3
C 6 H n 3 N
....
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 ....
NMe 2 .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
NEt 2 .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.
C 6 H U 3 N 3
205-207
Menschutkin
A., 178, 210
39, 380
CO.NHMe
Diethylic carboxylocarba-
NH(COOEt) 3
C 6 H n 4 N
226 (760) ;
49-50
Wurtz &Henninger
C. R., 100, 1419
48,969
mate
144^146(20;
Ethylamidodiglycollic acid ....
NH(CH 2 .COOH)(CHEt.
200-220
Liquid
Heintz
A., 145, 214
vi., 646
COOH)
Nitrohexylic acid
CH 3 .C(N0 2 ).CMe 2 .COOH
)
....
116;ar.lll-5
Kachler
A., 191, 159
34, 514
Citramide .. .... ....
C 6 H S O 4 (NH 2 ) 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 ....
(NH 2 .CO.NH.CO.CH 4! ) 2 NH
C 8 H n 4 N 6
195-200
Mulder
B., 6, 1016
27,48
Oximido-ether
HN : C(OEt).C(OEt) : NH
C H 12 2 N 2
170
25
Pinner and Klein
B., 11, 1482
3S, 47
Propionylethylcarbamide ...
NHEt.CO.NH.C 3 H 5 O
U
....
100
Hofmann
B., 15, 754
42, 1052
Isovaleryl carbamide
NH 2 .CO.NH(C 5 H 9 O)
....
191
....
A., 94, 102
i., 753
Di-(acetamido)-ethylidene ....
CH 3 .CH(NHAc) 2
)
169
Tawildarow
B., 5, 477
26,58;vii.,3,32
laodiethyloxamide
NEt.,.CO.CO.NH 2
J
266-268 u.c.
126-127
Wallach
B., 14, 735
40, 717
Dimethylsuccinamide
NHMe.CO.(CH 2 ) 3 .CO.
1
....
175
Wallach&Kamenski
B., 14, 170
40, 285
NHMe
....
J
)1
175
Henry
C. R., 100, 943
48, 887
j, ...
NH 2 .CO.(CHMe) 2 .CO.NH 2
)1
....
n.f. 260
....
J. p. [2], 26, 359
NFT CO.(CH 2 ) 4 .CO.NH 2
220
Henry
C. R., 100, 943
J)
H
Diisonitroso-acetonyl acetone
HON : CMe.(CH 2 ) 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
C 6 H 1 AN 4 (?)
142
Meyer & Constam
A,, 214, 328
44, 40
Triaceto-diamide
N 2 H 3 Ac 3
C 6 H 12 3 N 2
212-217
Gautier
A., 150, 189
vi., 524
Sarcosiue anhydride
(NHMe.CH 2 .CO) 2 O
J
143-146
Traube
B., 15, 2112
44, 192
Oxalyl diethylnitrosohydra-
....
C 6 H 13 4 N 6
144-145 d.
A., 199, 298
zine
Acetyl diethylarnide
NEt 2 Ac
C 6 H U ON
185-186
Wallach
A., 214, 235
44, 49
Capro-amide ....
CH 3 .(CH 2 ) 4 .CO.NH 2
120
Hofmaun
B,, 15, 983
C 5 H,,.CO.NH 3
255
Henry
B., 2, 495
Isocaproamide
CHMe 2 .CH, i .CH 2 .CO.NH 2
Jt
J)
100
Hofmann
J * ^"*f
B., 15, 983
Oaproamide ....
CHMePr.CO.NH 2
95
Kelbe and Warth
B., 15, 311
42, 711
>V
Methyl butylacetoxime
CMe 3 .CMe : N.OH
1)
....
74-75
Janny
B., 15, 2780
44,580
Piperyl-semicarbazide
C 5 H 10 N.NH.CO.NH 2
C 6 H 13 ON,,
136
Knorr
A., 221, 297
46, 468
Isoamylic carbaraate
NH 2 .COO(C 5 H U )
C 6 H a OJi
220
66
....
A., 71, 106
i., 750
Ethylic propylcarbamate ....
NHPrCOOEt
>J
186
Schreiner
J. p. [2], 20, 125
38, 312
Methylaniidovaleric acid
CH Me 2 .CH(NHMe).COOH
J
w.m.a. 120
Duvillier
A. C. [5], 21, 433
40, 713
a-amidocaproic acid (Leucine)
CH 3 .(CH 2 ) 3 .CH(NH 2 ).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
Cn 3 .CH 2 .CH(OEt).CO.NH 2
68-70
A. C. [5], 17, 542
0-
CH,.CH(OEt).CH 3 .CO.NH 2
...."
71
Pinner
B., 12, 2057
38,99
a-hydroxycaproamide
C 4 H 9 .CH(OH).CO.NH 3
M
140-142
J. R., 12, 367
Hexylnitrous acid .... .' ....
C 6 H 13 .N0 2 (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.NH 2
CeH.AN
MM
76-5
....
Z. C. [1870], 168
IT
81-82
Pinner and Klein
B., 11, 1477
36,47
Isoamylcarbamide
NH,,.CO.NH(CH 2 ) 3 CHMe 2
C 6 H 14 ON 3
88-91
Ouster
B., 12, 1330
36, 913
Amyl carbamide
NH 2 .CO.NH.CH 2 .C 4 H 9
}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
NH 2 .CO.NH.CHMe.C 3 H 7
C 6 H 14 ON S
cf. A, 139, 328
151
Wurtz
B. S. [2], 7, 141
vi., 1116
Nitrosodipropylamine
O : N.NPr 2
200-205
Siersch
A., 144, 144
vi., 9C5
?
....
C 6 H 14 5 N 2
....
152
Ehrenberg
J. p., 32, 97
48, 1192
Aceto-ethyl-nitrate .... '
....
C 6 H U 7 N 2
84-86
....
Nadler
A., 116, 173
Hydroxypropylpropylauiine
NHPr.C 3 H 6 .OH
C 6 H 15 ON
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-
(C 2 H 3 ON 3 ) 3 .2NH 3
C 6 H 16 3 N U
....
155 d.
Curtius
B., 18, 1290
48, 884
amide
Acid ammonium propionate
(Et.COONH 4 +Et.COOH)
C 6 H 15 4 N
45
Sestini
Z. C. [2], 7, 34
24, 235 ; vii. ,
1010
Trinitrobenzoic acid
COOH.(NO 2 ) 3 =1 .2.4.6(?)
C 7 H 3 8 N 3
....
190
Tiemann & Judson
B., 3, 224
vii., 166
Triuitrohydroxybenzoic acid
COOH.OH.(NOj)s=1.3.(?) 3
C 7 H 3 9 N 3
+H 2
105
Schardinger
B., 8, 1491
29, 584
Nitrobenzonitril
CN.N0 2 =1.2
C,H 4 2 N S
....
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.N0 2 =1.3.?
C 7 H 4 O 3 N 2
182-183
Smith
J. p. [2], 16, 228
34, 72
Dinitrobenzoic acid
COOH.(NO 2 ) 2 =1.3.4
C 7 H 4 0,N 3
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 ....
CH 2 :0 2 :C 6 H 2 (N0 2 ) 2 =1.2.(?) 2
J
cf. A., 199, 75
101 u.c.
Jobst and Hesse
B., 11, 1034
34,733
Dinitrosalicylic acid
COOH.OH.(N0 2 ) 2 =1.2.(?) 2
C 7 H 4 7 N 2
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
C 7 H 6 ON
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
C 7 H S ON
....
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
C 6 H 4 .N : CH.O=1.2
)J
182-5
30-5
Ladenburg
B., 10, 1124
32, 752
1 1
Anthranil
C 6 H 4 .NH.CO or C 6 H 4 .N : C.
)I
210-215 d.
L. 18
Friedlander and
B., 15, 2105
44, 188
i iii
OH=1.2
Henriques
Nitrosoindazole
....
C ; H 5 ON 3
....
73
Fischer and Fafel
A., 227, 303
48, 541
Salicylimide ....
C 6 H..CO.NH.O=1.2
C,H,O,N
n.f. 200
Lirnpricht
A., 98, 261
v., 167
i i
V 7 5 z^ 1
Oxycarbanil ....
CO : N.C 6 H 4 .OH=1.2
136-138
Grenvik
B. S, [2], 25, 177
31, 473
Diazobenzoimide
C 6 H 4 .N 2 .NH.O.CO=1.2
C 7 HAN 3
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
C 6 H 5 .CO.N0 2
C 7 H S 0,N
Liquid
Lippmann and
B., 9, 1464
31, 315
Hawliczek
Nitrobenzaldehyde
COH.N0 2 =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 ....
NO 2 .C,H 3 .NH.CO.NH
C.H 5 3 N 3
n.f. 300
Hager
B., 17, 2625
48, 150
i i
Nitrobenzoic acid
COOH.N0 2 =?(4th)
C 7 H 5 O 4 N
....
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.N0 2 =1.3
C 7 H 6 4 N
....
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
,,
....
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.N0 2 =1.4
C 7 H 5 4 N
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.NO 2 =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,.C 6 .H 3 .O.CH 2 .O=?.1.2
cf. A. 199, 73
148 u. c.
Jobst and Hesse
B., 11, 1034
34, 733
" i
Nitrotoluquinone
C 6 H 2 Me.(N0 2 ):0 2
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.
Watts 1 Diet.
& J. Ch. Soc.
Pyridine dicarboxylic acid ....
N.(COOH) 2 =?
C 7 H 6 4 N
266-268
Gerichten
B., 13, 1637
40, 110
Acid from diquiiioline
....
ii
....
96 u. c.
Glaus
B., 14, 1942
42, 215
Nitre-salicylic acid +H 2 O ....
COOH.OH.N0 2 =1.2.3
C 7 H 5 6 N
....
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.NH 2 ).(N0 2 ) 2 =1.3.5
C 7 H 6 6 N 3
....
777
Z. C. [1870], 642
11
)
)J
183
Voit
A., 99, 105
i., 541
Trinitrotoluene
Me.(NO 2 ) 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.NH 2 .(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
C 4 HO(OH)(COOH) 2 (C:NOH)
C 7 H 6 7 N
+H 2
d. 190
Odernheimer
B., 17, 2083
46, 1302
Trin itroanisol
OMe.(NO 2 ) 3 =1.2.4.6
C 7 H 5 7 N 3
....
58-60
Cahours
A., 69, 238
i., 306
,, ....
)1 I!
-J
....
64
Post and Merteus
B., 8, 1552
Me.OH.(N0 2 ) 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.(NO a ) 3 =l. 3.2.4.6
C 7 H 6 7 N 3
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 .(NO 2 ) 3 =1.3.5.2.4.6
C 7 HAN 3
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 ...
C 6 H 2 (N0 2 ) 3 (NMe-.N0 2 )
C 7 H S S N 6
cf. 38, 108
127
Eomburgh
B. T., 2, 304
48, 660
Phenylene carbamide
C 6 H 4 :N.CO.NH 2 =1.2(?)
C 7 H K ON 2
....
12&-130
Bendix
B., 11, 2264
36, 314
jj jj
c 6 H 4 : (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
C 6 H,.CO.NH.NH=1.2
JJ
cf.B.,13, 681
242 d.
Fischer and Benou
A., 212, 333
42, 1069
i i
Nitrosoformanilide
C 6 H 5 .N(NO).COH
C Z H 6 2 N 2
....
39
Fischer
B., 1.0, 959
32, 607
NitrosoDi ethyl nitrobenzene
N0 2 .(CH 2 .NO)=1.2
C 7 H 6 3 N 2
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
N0 2 .CONH 2 =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
N0 2 .(NH.COH)=1.2
J)
....
122
HUbneB
A., 209, 369
42, 181
Nitrobenzaldoxime ....
NO 2 .(CH : NOH)=1.4
w
128-5
Herzberg
C. C., 1884, 35
48,662
Dinitrotoluene
Me.(NO 2 ) 2 =1.2.6
C ; H 6 O t N 2
...
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
CONH 2 .OHJST0 2 =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.NH 2 .N0 2 =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
Jt
....
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.NH 2 .NO 2 =1.3.5
=1.2.5
)3
> 3
=1.4.5
Me.(OH) 2 .(NO) 2 =l. 3.5.2.?
(CH 2 .O.NO 2 ).NO 2 =1.4
(CH 3 .O.NO s ).(NO s )j=1.4?
OMe (NO 2 ) 2 1 3 4
C 7 H 6 4 N 3
JJ
3)
35
33
33
)3
+H 2
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
CO 2 H.OH.NH 2 .NO 2 =1.2.3.5
OMe.OH.(NO 2 ) 2 =1.4.(2) 2
=1.2.3.5
Me.(OH) 2 .(N0 2 ),=1.3.5.2.?
1! !>
Me.NH 2 .(NO.,) 3 =1.3.2.4.6
C 6 H 5 .NH.COH
)>
)
C 6 H 5 .CO.NH
C 7 H 6 5 N 2
C 7 H 6 6 N 2
H
i)
j
C 7 H.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 .... .... ...
C 6 H 5 .CH : N.OH
NH 2 .COH=1.2
u
=1.3
Probably 2(C 7 H 7 ON)
NHPh.COOH
NH 2 .COOPh
Ph.CH 2 .NO 2
C 6 H 5 .0(OH):N.OH
Me.NO 2 =1.2
)J J
)J
t
J1
II
)
)1
C 7 H 7 2 N
))
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.NH 2 ).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
C 7 H 7 OjN
65
Lach
B., 16, 1785
44, 1104
Amidobenzoic acid (Anthra-
COOH.NH 2 =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.NH 2 =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 ....
C 4 H 3 NH.CO.Ac(?)
,, (?)
....
75 d.
Ciamician & Silber
G. I., 14, 162
48, 247
Acetoxypyridine ....
C 5 H 4 N.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
=
C 5 H 5 N.CH,.CO.O
CjHjOjN
1)
)
C.H 7 2 N 3
C 7 H 7 3 N
)?
))
>?
)
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
+H 2
Hex. plates
Needles
+H 2 O
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
C 6 H 5 .N:N.CH.,.NO S
N.(CO.NH 2 ) S =1.2.6
(CH 2 .OH).NO 2 =1.3
=1.2
=1.4
) Jt
)J >
) J)
OMe.NO 2 =1.2
) )?
J
)I )
.'I
=1-3
JJ
=1-4
J>
))
))
' )
) J)
Me.OH.NO 2 =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
C 4 H 4 N.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 : C 4 H 3 .COO.COMe
C 7 H 7 3 N
d.
75
Ciamician & Silbei
B., 17, 1154
46, 1044
Pseudacetyl a-carbopyrrolic
Me.CO.C 4 H 2 (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 ...
NO 2 .C 6 H 4 .C(NH 2 ) I N.OH
C 7 H 7 3 N S
174
Schopf
B., 18, 1064
48, 896
= 1.3
Amidonitrobenzamide
(CONH 2 ).NH 2 .NO 2 =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.N0 2 =1.4.?
C,H 7 O 4 N
....
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.N0 2 =1.3.5.?
115
Weselsky
B., 7, 442
27, 694
a-
=1.3.5.?
120
Gallamide
(CO.NH 2 ).(OH) 3 =1.3.4.5
"
d 245
243
"
Bio 400
"
11
ociiiit tLnci Jrons
., J-O, "iOO
Dinitromethylaniline
NHMe.(N0 2 ) 2 =1.2.4
C 7 H 7 O 4 N 3
....
175
Norton and Allen
B., 18, 1996
48, 1214
,,
178
Leymann
B., 15, 1234
42, 1057
Dinitrotoluidine
Me.NH 2 .(N0 2 ) 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
C 4 H 2 O(NO 2 ).COOEt
C 7 H 7 S N
107
Klinkhardt
J. p. [2], 25, 52
42, 499
Dinitroamidocresol
Me.OH.NH 2 .(N0 2 ) 2 =1.3.(?) 3
C 7 H 7 6 N 3
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
NH 2 .CO.NHPh
C 7 H 3 ON 2
144145
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
NH 2 .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
NH 2 .(CH : N.OH)=1.3
88
Gabriel
B., 16, 1998
44, 1105
....
=1.4
....
124
Gabriel & Herzberg
B., 16, 2001
44, 1104
Nitrosomethylamidobenzene
NH 2 .(CH.NO)=1.2"
"
124-5
132-133
Herzberg
Gabriel and Meyer
C. C. [1884], 35
B., 14, 2339
48, 662
42, 189
Amidobenzamide
NH 2 .(CO.NH 2 )=?
....
a. 100
Chancel
A., 62, 274
iv., 294
=1.2
,,
300 p.d.
108
Kolbe
J. p. [2], 30, 467
43, G66
=1.3
+H 2
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
C 5 H 2 ON 4 Me 2
C 7 H S ON 4
112
Fischer
B., 17, 334
46, 997
Nitromethylaniline
C 6 H 5 .NH.CH 2 .N0 2
149
Steiner
B., 7, 1245
28, 165
Hydroxyphenyl carbamide ....
HO.C 6 H 4 .NH.CO.NH 2 =1.2
154 d.
Kalehoff
B., 16, 375
44, 735
11 ii
,, =1.4
168 d.
B., 16, 376
Hydrazinbenzoie acid
NH 2 .NH.C 6 H 4 .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
NH 2 .NH.C 6 H 4 .COOH=1.4
C 7 H 8 O 2 N 2
220-225 d.
Fischer and Eenou
A., 212, 337
42, 1070
Diamidobenzoic acid
COOH.(NH 2 ) 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.NH 2 .N0 2 =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 x CH r
I CO.NMe.C . N /" J
C 7 H 8 2 N 4
....
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.NH 2 .NO 2 =1.2.3
C 7 H 8 3 N 2
76
Bantliu
B., 11, 2106
36, 238
= 1.3.4
129
Amidobenzylalcohol
)J
(CH 2 .OH).NH 2 =1.2
11
C 7 H 9 ON
82
Friedlander and
B., 15, 2110
Henriques
OMe.NH 2 =1.2
216
Liquid
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.NH 2 =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 '
C 4 H 3 Ac : NMe
n
ii
200-202
Liquid
Ciamician and
B., 17, 2952
48, 378
Dennstedt
Aeetylmethylpyrroline
C 4 H 3 Me : NAc
n
....
4-6
Weidel and Cia-
B., 13, 78
38, 404
mician
/5-ethoxypyridine
C 5 H 4 N.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
C 6 H 5 .NH.NH.CO.NH S
C,H 8 ON 3
....
170
Fischer
A.,190, 113
34, 307
Diamidobenzaniide
(CO.NH 2 ).(NH 2 ) 2 =1.3.5
177
Muretow
Z. C. [2], 6, 642
vii., 130
)
=
11
183
Voit
i., 541
Pyromucethylamide ....
C 4 H 3 O.CO.NHEt
C 7 H 9 0,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
C 6 H 4 .O(NH 4 ).COH=1.2
II
....
115
Ettling
A., 29, 310 ; 35,
v., 169
244
Tetrene uretbane
C 4 H 4 : N.COOEt
|9
180 (770)
Liquid
Ciamician & Denn-
G. L, 12, 84; B.,
42, 606; 44,
stedt
15, 943, 2579
350
Ethylic a-pyrrolate
C 4 H 4 N.COOEt
11
230-232
39
Ciamician and Sil-
G. L, 14, 162;
46, 1044; 48,
ber
B M 17, 1152
246
Ethylcarbopyrrolic acid
C 4 H 3 EtN.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.(NH 2 )j.NO 2 =1.2.4.6
C 7 H 9 2 N 3
....
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
C 7 H 9 O 3 N
26
....
C. R., 95, 235
Ammonium salicylate
C 6 H 4 .OH.COO(NH 4 )=1 .2
51
126
Procter
J. Ph. [3], 3, 275
v., 155
Hy poethyltli eobromine
C 7 H 9 3 N 3
142
Fischer
A., 215, 308
44, 357
Trihydroxydimethylpurin ...
C 6 N 4 Me 2 (OH) 3 ?
C 7 H 9 3 N 4 ?
....
Very high d.
B., 17, 337
46, 998
? acid
....
C 7 H 9 4 N
d. 135
84-87
Pinner
B., 14, 1070
40, 797
Nitrotoluidine nitrate
C 6 H 3 Me.NO,NHs + HNO 3
C 7 H 9 S N 3
185 d.
Beilstein & Kuhl-
Z. C. [2], 5, 280
vi., 1105
berg
Hydrazineaniso'il
C 6 H 4 .OMe.N 2 H 3 =1.2
C 7 H 10 ON 2
43
Reisenegger
A., 221, 314
46, 440
Dimethylcarbopyrrolamide...
4 H !! Me,,N.CO.NH 2
!!
89-90
Bell
B., 10, 1866
36, 525
Ethylsuccinylcarbamide
CO(CH 2 ),.CO.N.CO.NHEt
C ; H 10 3 N,
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
C 7 H 10 4 N 2
....
32-8
,Bassler
J. p. [2], 16, 134
34, 214
boxylate
Dtacetylmethylglyoxime
CMe(NOAc).CH(NOAc)
51
Schramm
B., 16, 2187
46, 52
Nitrodehydropiperylmethyl-
C 5 H 7 (NO 2 )N.GOOMe
)>
....
102-103
Schotten
B., 16, 647
44,811
urethane
Oxy-/3-dimethylurie acid
....
C 7 H 10 6 N 4
173-174
Fischer
B., 17,1781
46, 1309
Hydroxyheptamide
C 6 H 9 .(OH)(CO.NH 2 )
C 7 H n 2 N
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)
C 7 H U 3 N 3
....
173
Limpricht
A., 74, 208
ii., 293
Methylcaffuric acid ..
....
C 7 H,,0 4 N 3
....
167
Schmidt& Schilling
A., 228, 141
48, 995
Diethylic nitrosomalonate ....
ON : CH(COOEt) 2
C 7 H U 6 N
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
C 7 H M 7 N
45-46
Henry
A. C. [4], 28, 415
Diallyl carbamide
CO.N 3 H 2 (C 3 H 5 ) 2
C 7 H 12 ON 2
....
100
Eichter
B. K. T., 153
Amidoheptamide
....
....
251 d.
Demargay
C. B., 86, 1135
34, 662
Diethylic amidocyanurate ....
C 3 N,(OEt) a .NH a
C 7 H )2 3 N 4
...
97
Hofmann and
B.,3, 274;T.B.S.
vii., 410
Olshausen
18, 493
?
....
C 7 H,AN 3
147
Behrend
B., 16, 3027
46, 583
Ethylsuccinuric acid
NHEt.CO.NH.CO.(CH 2 ) 2 .
C 7 H 12 4 N 2
....
166'5-167
Menschutkin
A., 178, 206
29, 380
COOH
Dinitroheptylene
C 7 H 12 (N0 2 ) 2
>i
....
182
Morris
41, 176
Methylic cyanurate forma-
(CO)sN 3 Me3+ NHj.COH
C 7 H 12 4 N 4
....
-175
Gautier
,A., 149, 315
vi., 529
mide
Hexylic isocyanate
6 H 13 .N CO
C 7 H 13 ON
a.100
Pelouze &'Cahours
J. [1863], 526
C 7 Hj 2 : N.OH
Liquid
Na'geli
T3., 16, 497
'44, 728
Acetylpiperidine
C 5 H 10 N.Ac
)t
Jl
fff|
Liquid
Schotten
B., M, 426
)
42, 983
....
J)
226-227
Liquid
WaHach
A., 214, 238
Tropigenine .... .... ....
C 7 Hj 2 O : 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
CMe 2 (OH).O.CMe, ! .eN
C 7 H 13 O 2 "N
135-152
Urech
A., 164, 260
vii., 15 ; 26,60
Amidotrimethylbutyllactide
Me.C.(O.C : O)CH 2 .CMe 2 .NH,
J)
a. 180
Heintz
A., 189, 238,
32, 878
Nitrosoisobutylketone
CH 3 .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.CH 2 :eO0Et
(o.p.)
Piperylmethylurethane
C s H 10 N.COOMe
)
201
Liquid
Schotten
B., 16, 647
44, 814
Isoamylic oxamate
NH 2 .CO.COO(C 5 H U )
C 7 H 13 3 N
92-93
Wallacli and Lieb-
B., 13, 507
38, 557
mann
Ethylsuccinuramide
NH 2 .CO.(CH 2 ) 2 .CO.NH.OO.
C 7 H 13 0,N 3
..
195-196
Menschutkin
A., 178, 208
29, 380
NHEt
Ethylic grutamate
C 3 H 5 (NH 2 )(COOH)(COOEt)
C 7 H 13 4 N.
MM
164-165
Habermann
A., 179, 253
29, 907
Diethylic guanidodicafbonate
NH: C(NH.OOEt) s
C 7 H 13 4 N 3
....
162-u.c.
Nencki
B., 7, 1588
28, 755
Nitrobornesite
No. of nitre-groups ?
C 7 H 13 8 N(?)
,,
30-35
Girard
C. B., 73, 426
24, 915
Diethyhualonanride ;
CHj(CO.NHEt). 2
C 7 H 14 2 N 2
....
149
Wallach and 'Ka-
B., 14, 170
40, 285
menski
Dimethylpyrotartaramide ....
NHMe.CO.CHMe.CH s .CO.
)
MM
113-115
Henry
C. B., 100, 943
48, 887
NH.Me
laoamylic allophanate
NH 2 .CO. NH.COO.C 6 H U
C 7 H 14 3 N 2
a. 100
Schlieper
A., 59, 23
i., 133
<) i)
')
)
....
162
Hofmann
B., 4, 267
Propiodiacetodiamide
N 2 H 3 Ac 2 (C 3 H 6 0)
J)
220
68
Gautier
A., 150, 189
vi., 525
Ethylic j3-hydroxyainidoglu-
NH 2 .CO.CH 2 .G(OH)(NH.,).
C,-H 14 1D 4 N 2
....
86
Pechmann and
B., 18, 2291
48, 1202
tamate
CH,.COOEt
Stokes
Oxallyldiethylamine
NEt 2 .C 3 H 5
C 7 H 15 ON
160
Liquid
Eeboul
C. B., 97, 1556
46, 577
CEnanthaldoxime
j?
195 c.
50
Westenberger
B., 16, 2992
46, 581
CEnantharaide
C 6 H 13 .CO.NH 2
)>
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
CH 2 (OH).(CH 2 ) 5 .CO.NH 2
C 7 H 15 2 N
....
147
Helms
B., 8, 1170
29, 375
Methamido-a-caproic acid ...
Me.(CH 2 ) 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).CH 2 .COO
C 7 H 15 3 N
....
42-43
Kuckert
B., 18, 618
48, 750
droxybutyric acid
Et
Triethylcarbamide
NHEt.CO.NEt 2
C 7 H,,ON 2
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
NH 2 .CO.NH.C 6 H 13
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
....
C 7 H 16 2 N 2
72-73
Heintz
A., 185, 1
32, 428
Trimethylene diethylalkine
....
C 7 H 17 ON
189-5
Liquid
Behrend
B., 17, 512
46,1115
Diethylpropylalkine
....
158-159
Liquid
Ladenburg
B., 14, 2407
42, 165
Diethylpropylglycoline
NEt 2 .CH 2 .CH(OH).CH 2 .OH
O TT f~~\ XT
v^yJj. i V 2 -^
233-235
Liquid
Eoth
B., 15, 1151
42, 1195
Tetramethylallylalkine
C 3 H 6 (OH)Me 4 N 2
C 7 H 18 ON S
170-185
Liquid
Behrend
B., 17,510
46, 1114
Hydroxyallyldiethyldiamine
(NHEt) 2 .C 3 H 5 .OH
.
185
Liquid
Reboul
C. R, 97, 1488
46, 579
Nitrophthalic anhydride
C 6 H 3 (N0 2 ):(CO) 2 : 0=4.2.1
C 8 H 3 O 5 N
....
114
Miller
A., 208, 230
42, 404
Nitrobenzoic cyanide
N0 2 .(CO.CN)=1.2
C 8 H 4 3 N S
....
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
C 6 H 4 .CO.CO.N.NO,=1.2
C 8 H 4 O 4 N 2
226-230
BaeyeF
B., 12, 1313
36, 938
i i
K.I.
Nitroisatoic acid
C 8 H 4 5 N 2
220-230 d.
Kolbe
J. p. [2], 30, 467
48,666
Dinitrophthalic acid
(COOH) 2 .(NOJ 2 = 1.2.3.6
C S H 4 S N 2
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.(N0 2 ) 2 =1.4.(?) S
C S H 4 9 N 2
.*
178
Burkhardt
B., 10, 1273
34,73
acid
Benzoyl cyanide
C 6 H 6 .CO.CN
C 8 H 5 ON
206-208
31
Strecker
A,, 90, 62
i., 568
!> )
M
32-33
Hiibner & Buchka
B., 10, 480
Nitrophenylacetylene
C 6 H 4 (N0 2 ).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
C B H. '. (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
C 6 H 4 .lo.C.CHO=1.2
51
72-5
Schillinger and
B., 16, 2223
46, 60
Wleugel
Isatin ....
C 6 H 4 .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
C 6 H 4 .N.O.C.COOH=1.2
i i
C 8 H 5 3 N
190-191
Shillinger and
B., 16, 2224
46,60
Wleugel
Anthranilcarboxy lie acid (Is-
C 6 H 4 .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(C 8 H 4 2 ).OH
1?
....
230 u.c.
Cohn
A., 205, 295
40, 586
Nitrophthalic aldehyde
(COH) 2 .NO 2 =1.2.3 or 4
C 8 H 6 4 N
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 ...
C 6 H 4 (CO.COOH).NO 2 = 1 . 2
C 8 H 5 O 6 N
..
122-123
Claisen & Thompso
B., 12, 1945
n
JJ
ii
+xH 2
46-47
,,
ii
11 11
=1.3
-..
77-78
n
38, 254
Nitroterephthalaldehydicaeid
COH.COOH.NO 2 =1,4.6
....
160
Low
B., 18
48, 799
Nitropiperonal
CH 2 ; O 2 : C 6 H 2 (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 .NO 2 =L2.3
C 8 H 6 Q 6 N
....
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
CH 2 : 2 : C 6 H 2 (N0 2 ).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.(NO 2 ) 3 =1.2.4.6
C 8 H 5 8 N 3
....
75-76
Tommasi & David
A.,169,167;C.E.
vii., 910 ; 26,
77, 207
1238
Trinitrocresotic acid
C 6 Me.OH.COOH.<NO 2 ) 3
C 8 H 5 9 N 3
A., 64, 23
170-180
Liebermann,& Dorp
A., 163, 100
Anhydroformyl amidobenza-
C 8 H 6 ON.,
....
209-210
Weddige
J. p. [2], 31, 124
48,661
mide
Carbimidoamidobenzoyl
C 6 H 4 .CO.C(:NH).NH
JJ
....
214
Griess
B., 18, 2419
48, 1227
Hydroxycinneline .
c 6 H 4 .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
C 8 H 6 2 N 2
197
Falck
B., 18, 2469
48, 1217
H 1
Benzoylene carbamide
a. 350
Griesa
B., 2, 416
Nitrosoisophthalidine
C 6 H 4 .C(: N.NO).0:CH 2 =1.2
#i
....
156
Grsebe
B., 17, 2599
48, 166
1 _ 1
Dihyclroxyquinoxaline
G 6 H 4 :[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
C 6 H 4 .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
C 6 H 4 .N0 2 .(CH 2 .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
C 6 H 4 .N0 2 .(CH 2 .CN)=1.4
C 8 H 6 2 N 2
116
Gabriel
B., 14, 2342
42, 188
Nitrotoluic nitril
Me.CN.NO 2 =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
C 6 H 4 .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
C 6 H 4 .NH.CO.CH.N0 2 ==1.2
C 8 H 6 O,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.N0 2 =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 ....
C 6 H 4 (NO 2 )(CH:CH.NO 2 )= 1 . 2
C 8 H 6 O 4 N 2
....
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
C 6 H 4 (N0 2 )(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.(NO 2 ). ! =1.3.2.?
C 8 H 6 5 N 2
110-112
Bornemann
B., 17, 1473
46, 1163
Uiuitro-a-toluic acid....
(CH 2 .COOH)(NO 2 ) 2 =1.2.4
C 8 H 6 6 N S
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.(NO 2 ) 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.(NO 3 ) 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) ...
....
C 8 H 6 6 N 4
189 c.
Bassett
Z. C. [1871], 701
26, 100
Methylic dinitrosalicylate ....
CO<DMe.OH.(N0 2 ) 2 =1.2.(?).,
C 8 H 6 7 N 2
124-125
Cahours
A. C. [3], 25, 6
v., 164
I!
1>
127^128 !
Salkowski
A., 173, 43
28,71
Dinitranisic acid
COOH.OMe.(N0 2 ) 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
....
C 8 H 6 9 N 6
+4H 2
d. 120
Baeyer
A., ,127, 226
(violantin)
Pentanitrodimethylaniline ....
Ce-NMe^NO^
C 8 H 6 10 N 6
....
127
Michlerand Meyer
B., 12, 1793
38, 108
)>
)>
....
127
Michler & Salath6
B., 12, 1790
Phenoxyacetonitril
PhO.CH 2 .CN
C 8 H ? 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.CH 2 .CO
i 1
....
263
Meyer
B., 10, 1967
34, 294
Tolyl isocyanate
C 6 H 4 Me.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)
C 6 H 4 .OMe.CN=l,4
)
253-254 u.c.
56-57
Henry
B., 2, 667
vii., 81
Hydroxy-a-toluic nitril
C 6 H 4 (OH).(CH 2 .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
C 6 H 4 .O.CMe : N=1.2
))
200-201
Liquid
Ladenburg
B., 9, 1524
31, 302
Phthalidine
C 6 H 4 .C(:NH).O.CH 2 =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
C 6 H 4 .CH 2 .CO.NH or
C S H,ON
120
Baeyer and Knop
A., 140, 29
vi., 736
C 6 H 4 .C(OH) : CH.NH=1.2
i i .
^87
Methenylamidocresol
C 6 H 3 Me.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)
C 6 H 4 .NH.C(NH).G(OH) : N
C 3 H 7 ON 3
....
nf. 280
Bladin
B.,18,673;B.S.,
48, 257, T85
=1.2
42, 104
/3-Benzoyl formamide
Ph.CO.CO.NH 2
C S H 7 O 2 N
+ H 2
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
(C 8 H 7 2 N) 2
134-135
B., 12, 635
36, 649
Phenylnitroethylene
Ph.CH:CH.N0 2
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
C 6 H 4 (NO 2 )(CH : CH 2 )=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 **
C tl H 4 .O.CH 2 .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
C 6 H 4 .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
C 6 H 4 .C(OH):C(OH).NH
=1.2
Nitrophthalene
...
)J
280-320
48
Dusart
A. C. [3], 44, 332
iv., 113
Nitroamido-a-toluic nitri] ....
(CH S .CN).NH 3 .NO J =1.4,6
C 8 H 7 2 N 3
....
117-118
Gabriel
B., 15, 839
42, 1070
Phenylic oxamate
NH 2 .CO.COOPh
C 8 H 7 3 N
132
Wallach and 'Lieb--
B-i 13, 507
38, 558-
mann
Phenyloxamic acid (oxanilic)
NHPh.CO.CO0H
JJ
fr. C 6 H 6
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
CH 3 .CO.C 6 H 4 .N0 2 =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.NH 2 )=1,4
JJ
....
214
Sandmeyer
B., 18, 1498
48, 981
Amidobenzoyl formic acid ....
NH 2 .(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.NO 2 =1.3 !
C 8 H 7 O 4 N
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 .
(CH S .COOH).NO S =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.NO 2 =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-
C 6 H 4 (NO)(O.COOMe)
C 8 H 7 O 4 N
137
Walker
B., 17, 400
46, 1003
boxylate
Nitrotoluic acid
Me.COOH.NO 2 =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.NO 2 =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 .NH 2 =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.NO 2 =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
C 6 H 3 N(COOMe)(COOH)
,,
205
Anderson
A., 86. 196
5, 257 ; i., 350
11 11 "
*.*
S41-S42
Gerichten
B., 13, 1636
Nitromandelic acid
NO 2 .C 6 H 4 .CH(OH).COOH
C 8 H 7 6 N
....
120
Beyer
J. p. [2], 31, 382
48, 983
=1.3
Nitrophenoxyacetic acid ....
NO 2 .C 6 H 4 .O.CH 2 .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,N0 2 =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.NO 2 =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 .NO 2 .Ac=1.3.(?) 2
C S H 7 5 N
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.(NO 2 ) 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.N0 2
C 8 H.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.NH 2 .(N0 2 ) 2
C 8 H 7 O a N 3
....
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.(N0 3 ) 3 =?
))
Liquid
....
....
v., 1058
Triuitroxylene
Me 2 .(NO 2 ) 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. r 153, 276
24, 554
)J
....
137
Glinzer and Fittig
A, 136, 307
v., 857, 1058
,,
1> J
)>
....
137
Fittig and Ahrens
A V 147, 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
C 8 H 7 (N0 2 )3
)I
....
162
Bussenius and
A, 113,, 15L
iv., 382
Eisenstuck,
Ethylic nitrocomenate
C 5 HO s (NO 2 XOH).COOEt
C 8 H 7 7 N
....
147
Reibstein
J. p. [2], 24, 279
42,197
Trinitrophenetoil
OEt.(NO 2 ) 3 =1.2.4.6.
C 8 H 7 7 N 3
....
78
WJllgerodt
B., 12, 1278
36, 923
n ""
....
78-5
Miiller & Stenhouse
A, 141, 80
19, 236; vi.,
911
Trinitroethylresorcinol
OEt.OH.(NO 2 ) 3 =1.3.2.4.6
C 8 H 7 8 N 3
120-5
Stenhouse
19, 238
vi., 893
Trinitrodimethylquinol
((>Me) 2 .(NO 2 ) 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
C 6 H 3 (NH 2 ).CH 1 .CO.NH
CsHsONj
....
200 d.
Gabriel and. Meyer
B., 14, 832
40, 731
=1.4.5
Nitrosoacetanilide
C 6 H 6 .NAc.NO
C 8 H 9 2 N 2
....
40-41
Fischer
B., 9, 464
30, 205
Benzoyl carbamide
NH 3 .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
NH 2 .CO.CO.NHPh
A., 73, 184
224
Klinger
A, 184, 271
Phenylhydrazine glyoxylic
Ph.N 2 H::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 ....
C 6 H 4 (NH.CHO) 3 =1.3
....
155
Tobias
B., 15, 2447
44, 326
,, ....
=1.4
)
....
203-5-204
Wundt
B., 11, 828
34, 668
Formamidobenzamide
NH 2 .CO.C 6 H 4 .NH.CHO= 1.2
)
123
Weddige
J.. p. [2], 31,, 124
48, 661
Isophthalamide
C 6 H 4 (CO.NH 2 ) 2 =1.3
I)
265
Beyer
J, p. [2], 22, 352
40,96
Terephthalaldoxine ....
C S H 4 (CH : NOH) 2 =1.4
t
....
200
Westenberger
B., 16, 2995
46, 581
Nitrosophenylglycocoll
Ph.N(NO).CH 2 .COOH
8 H 8 3 N,
105 d.
Schwebel
B., 11, 1132
34, 795
Nitro-acetanilide
C 6 H 4 (N0 2 ).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
C 6 H 4 (NO 2 ).NHAc=1.4
C 8 H 8 3 N,
....
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
C 6 H 4 (NH.CO.NH 2 ).COOH
T
....
d. 200
Traube
B., 15, 2117
44, 194
=(1.3
Methyl nitrosomethylnitro-
C,H 4 .NO 2 .(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
C H 4 .N0 2 .(CMe:NOH)=1.3
H
....
131-132
n
B., 15, 3063
11
Benzenylamidoxime car-
C 6 H 4 .C0 2 H.[C(NH 2 ):NOH]
j)
a. 330
Miiller
B., 18, 2486
48, 1227
boxylic acid
=1.4
Nitro-a-toluamide
C 6 H 4 .N0 2 .(CH 2 .CO.NH 2 )
))
190-192
Gabriel
B., 14, 2342
=1.4
Nitrotoluamide
(CO.NH 2 ).Me.NO 2 =1.3.?
151
Beilstein and
A., 144, 175
Kreusler
Hydroisophthalajuide
(CO.NH 2 ) 2 .OH^=1.^.4
)>
....
250
Jacobsen
B., 11, 380
34, 583
Azophenylmethazonic acid ....
C 6 H 5 .N 2 .C 2 H 3 N 2 3
C 8 H a 3 N 4
164 .d.
Kimich
B., 10, 141
32, 325
/3-pyridine tricarboxylamide
N.(CO.NH 2 ) 3 =symmetrieal
?1
a. 280
Voigt
A., 228, 29
48, 813
Nitrophenylamidoacetic acid
NO 2 .[CH(NH 2 ).COOH]=1.3
C 8 H 8 4 N 2
172 d.
Plochl and Loe
B., 18, 1180
48, 899
Amidonitro-a-toluic acid
NH 2 .N0 2 .(CH 2 .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.(N0 2 ) 2 =?
))
Liquid
....
....
v., 1058
Dinitroxylene
Me 2 .(NO 2 ) 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-
N0 2 .C 4 NHj.(CO.Me),,
)
....
149
Ciamiciau & Silber
B., 18, 1468
48, 994
ketone
Diuitrophenetoil
OEt.(NO 2 ) 2 =1.2.6
C S H 8 5 N 2
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.(NO 2 ) 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).(NO 2 ) 2
C 8 H a 5 N 4
125
Gattermanu
B., 18, 1488
48, 976
idine
Dinitro-dimethylresonhnol ....
(OMe) 2 .(N0 2 ) 2 =1.3.(?) 2
8 H 8 6 N 2
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 .(N0 2 ) 2 =1.4.5.?
C 8 H 3 6 N 2
169-170
Habermann
B., 11, 1037
34, 728
Dinitroethylquinol ....
OEt.OH.(NO 2 ) 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
C 6 H 2 (N0 2 ) 3 .NMe 2
C 8 H B 6 N 4
....
115
Krell
B., 5, 880
26, 279
Trinitromethyltoluidine
C 6 HMe.NHMe.(N0 2 ) 3
137-138
Gattermann
B., 18, 1488
48, 976
Dinitroethoxydihydroxy-
C 6 H(OH) 2 (OEt)(N0 2 ) 2
QjH 8 O 7 N 2
cf, A., 215, 155
143d.
Nietzki
B., 11, 1449
34, 867
benzene
C 6 H 5 .NHAe
C 8 H 9 ON
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
C 6 H 4 .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.NH 2 )=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
C 6 H 4 .NH.,,(COMe)=1.2
"
I.
Liquid
Gevekoht
B., 15, 2085
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
? ..
C 4 H 3 O.C : N.CMe,
M
300-310
142
Tonnies and Staub
B., 17, 857
46, 1130
I 1
Tetrene urethane
C 8 H,O 3 N
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(NH 2 ).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.CH 2 .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 H 2 O
108
Norton and Tcher-
C. B., 86, 1332
34, 775
niak
55 ....
fr. cold H 2 O
98
B. S., 30, 104
n
Phenylhydroxyacetamide ....
CH 2 (OH).CO.NHPh
....
65-115
Tommasi
B. S., 22, 6
26, 627
Isonitrosophenylethyl alcohol
Ph.C(NOH).CH 2 .OH
....
70
Meyer and Nageli
B., 16, 1624
44, 1076
Phenoxyacetamide
Ph.O.CH 2 .CO.NH 2
,,
....
101-5
Fritzsche
J. p. [2], 20, 277
38, 319
Pheiiylglycollamide
Ph.CH(OH).CO.NH 2
"
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.NH s
Ph.C(OH) : N.OMe
Ph.C(OMe) : N.OH
NH 2 .COO.C 6 H 4 .Me (?)
NH 2 .(CH 2 .COOH) =1.3
=1.4
>! !)
OAc.NH 2 =1.2
=1.4
OKNHAc =1.4
=1.2
C 6 H 4 Et.N0 2 =1.2
= J
=1.4
OMe.(CO.NH 2 ) =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,.NO s =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) >!
Me s .OH.NO =1.4.3.6
"
C 4 H 2 Ac 2 NH
C 6 H S .N:N.C 2 H 4 .NO 3
C 8 H 9 3 N
)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
C 8 HAN 3
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
CH 2 Ac.C: CH.CfCO.NH,) : C
i i
C 8 H 9 3 N
....
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.N0 2 =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.NO 2 =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 ....
Me 2 .OH.NO 2 =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-
C 4 H 2 AcNH.COOMe
>
....
113
Ciamician & Silber
B., 17, 1156 ;
46, 1045 ; 48,
carbopyrrolate
G. I., 14, 162
247
Hydroxylutidine carboxylic
....
+H 2
246
Collie
A., 226, 294
48, 374
acid
Nitro-acetdiamidobenzene ....
NH 2 .NHAc.NO 2 =1.4.7
(VE^N,
....
184
Biedermann and
B., 7, 1531
Ledoux
))
186
Ladenburg
B., 17, 148
46, 738
Nitrodimethylquinol
(OMe) 2 .NO 2 =1.4.5
C 8 H,0 4 N
....
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.NO 2 =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 ....
C 4 HjEtN.COOH
....
w. m. 250
Bell
B., 10, 1865
36, 525
Dimetliylpyrroline dicar-
CO n H.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....
C 5 H(NH 2 )O.OH.OOOEt
I)
+2H 2 O
205
Eeibstein
J. p. [2], 24, 284
Ethylcomenamic acid
C,,H(NH 2 )O.OEt.COOH
If
)
210 d.
Mennel
J. p. [2], 32, 176
48, 1203
Dinitrodimethylaniline
NMe 2 .(NH 2 ) 2 =?
C 8 H 9 4 N 3
....
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.(NO 2 ) 2 =1.4.(?) 2
))
129
Thomsen
B., 10, 1584
34, 218
i ....
)>
)1
....
129
Gattermann
B., 18, 1487
48, 976
Dinitroamidoethylbenzene ....
Et.NH 2 .(N0 2 ) 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
Me 2 .NH 8 .(NO 2 ) 2 =?
C 8 H,0 4 N 3
....
105
Krell
B., 5, 879
26, 279
,,
' =?
))
....
191-192
Beilstein
A., 133, 45
v., 1059
Ethyl-nitropyrogallol
(OH) a .OEt.NO a =?
C h H 9 6 N
139
Weselsky & Bene-
M. 0., 2, 215
42,53
dikt
Allocaffeine
....
C 8 HAN,
....
198
Fischer
A., 215, 275
44, 355
Ethylpicrazide
C 2 H 6 .N 2 H 2 .C 6 H 2 (NO,,) 3
C 8 H 9 6 N 6
....
200 d.
D
A., 199, 299
Phenylethenylamidoxime ....
Ph.CH 2 .C(NH 2 ) : NOH
C 9 H 10 ON.,
67
Knudsen
B., 18, 1068
48, 897
Methylbenzenylamidoxime...
NH 2 .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(NH 2 ) 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.N 2 H 2 .CO.CH 3
)
128'5
Fischer
A, 190, 129
34, 309
Phenylglycocinamide
Ph.NH.CH 2 .CO.NH 2
1)
....
133
Meyer
B., 8, 1157
29, 373
Methylphenylcarbam ide
NHj-CO.NMePh
)>
....
82
Gebliardt
B., 17, 2095
46, 1321
Benzylcarbamide
NH 2 .CO.NH.CH 2 Ph
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.NH 2 )=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.NMe 2 =1.4
j>-
85-5
Wurster and Roser
B., 12, 1823
....
....
92
Baeyer and Caro
B., 7, 810, 963
28, 84
Amidoacetanilide
NH 2 .NHAc=1.4
....
161
Nietzki
B., 17, 344
46, 1016
Amidophenylacetamide
NH 2 .(CH.j.CO.NH 2 )=1.4
....
169-170
Einhorn
B., 17, 2014
p-Amidotoluamide
(CO.NH 2 ).Me.NH 2 =?
>
....
115
Beilstein & Kreuslei
A., 144, 181
?
>.*
)
....
90
j
A., 144, 177
Dipropionyl dicyanide
....
C 8 H 10 2 N 2
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(NH 3 ) nSTOH
JJ
....
140
Tiemann
B., 17, 126
46,, 734
doxime
)
.....
158-159
Gross
B., 18, 1075
48, 898
?
Ph.C( : N.OH).CH 2 .NH.OH
>
162-163.
Schramm
B., 16, 2183
46, 51
Phenylhydrazido-acetic acid
Ph.N 2 H 2 .CH 2 .COOH
....
157 d.
Elbers
A., 227, 340
48, 535
Methoxybenzene carbamide
OMe.(NH.CO.NH 2 ) =1.2
7>
146-5
Mulhauser
B., 13, 923 ; A,
38, 642; 42,
207, 244
302
Phenylene dicarbamide
(NH.CO.NH 2 )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
N0 2 .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
N0 2 .NMe 2 =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
NH 2 .[CH(NH 2 ).COOH]=1.3
....
214
Plochl and Loe
B., 18, 1181
48, 899
acid
Nitro-atnidoethylbenzene ....
Et.NH 2 .NO 2 =?
a
....
45-47
Paucksch
B., 17, 770
46, 1143
Nitromethyltoluidine
Me.NHMe.NO 2 =1.4.5
)>
84-85
Gattermann
B., 18, 1487
48, 976
Nitroxylidine
Me 2 .NO 2 .NH 2 =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
Me 2 .N0 2 .NH 2 =1.3.5.6
C 8 H 10 2 N 2
....
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.NH 2
C 8 H 10 3 N 4
77 d.
Fischer
A., 190, 165
34,311
carbazide
Pheuylene dicarbamide
C 6 H 4 (NH.CO.NH 2 ) 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...
C 6 H 4 .N0 2 .(O.C 2 H 4 .NH 2 )=1.2
C S H 10 3 N 3
72-73
Widdige
J. p. [2], 24, 247
40, 1137
=1.4
JJ
....
108-109
J. p. [2], 24, 254
40, 1139
Nitroamidoethoxybenzene ....
OEt.NH 2 .NO 2 =1.2.4
))
96-97
Andreae
J. p. [2], 21, 327
38, 466
Hydroxycaffe'ine
CgHN 4 Oj.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
?
C 4 H 3 O.CH.N 2 O 3 .CMe 2
C 3 H 10 4 N 2
d. 145-150
94
Tonnies and Staub
B., 17, 853
46, 1129
Hydrodinitroazobenzene
C 8 H 10 N 2 (N0 2 ) 2
C 8 H 10 4 N 4
....
220
Lermontoff
B., 5, 234
25, 503
Dinitrodiamidoethoxy ben-
OEt.(NH 2 ) 2 .(N0 2 ) 2 =1.4 (J),
C 8 H 10 5 N 4
cf. A., 215, 154
245 u. c.
Nietzki
B., 11, 1448
34, 867
zene
a-(3-diisonitrozobutyric anhy-
external anhydride-
C 8 H I0 7 N 4
....
132-133 d.
Ceresole & Kockert
B., 17, 823
46, 1121
dride
Hydroxyethylene aniline- ....
Ph.NH.C 2 H 4 .OH
C 9 H U ON
280
Liquid
Demole
B., 6, 1025
27, 77
Dimethamidophenol
OH.NMe 2 =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.NH 2 =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-
NH 2 .(C 2 H < .OH)=1.2
'
....
89-90
Weddige
J. p. [2], 24, 241
40, 1138
zene
Anisamine
OMe.(CH,.NH s )=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.NH 2 =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
Me 2 .OH.NH s =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 ....
C 4 H 2 Me 2 1 NAc
L. 20
Weidel & Ciamician
B., 13, 79
38, 404
Anhydrodiacety lacetamidil. . .
CMe : N.CMe : CH.CO.NH.
i
C 8 H n ON,
....
185
Pinner
B., 17, 174
46, 723
CMe:.N
Methylphenyl semicarbazide
NMePh.NH.CO.NH 2
....
133
Fischer
A., 190, 164
34, 311
Hydroxyethylene amido-
NH 2 .(O.C 2 H 4 .OH)=1.2
C 8 H 11 2 N
....
89-90
Wagner
J, p. [2], 28,. 199
46, 436
pheuol
Amidodimethyl quinol
(OMe) 2 .NH 2 =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
C 4 H 3 O.C(NH 2 ).CMe 2 .O
C 8 H U 2 N
215-220 d.
Liquid
Tonnies and Staub
B., 17, 857
46, ] 130
i " i
Nitrodiamidoxylene
M e2 ,(NH 2 ) 2 .N0 2 =1.3.(?) 3
C 8 H n 2 N 3
....
212-213
Fittig and Velguth
A., 148, 7
....
215
Bussenius and
A., 113, 160
iv., 382
Eisenstuck
Arnidocaffe'ine
C 9 H,NA.NH S
C 8 H n 2 N 6
....
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
....
C 8 H n 3 N s
>.**
224
Pinner
B., 17, 172
46, 723
Diethylic cyanoraalonate ....
CN.CH(COOEt) 2
C 8 H n 4 N
120-130 (25)
Liquid
Haller
C. R., 95, 142
42, 1189
Urethaue furfurol
C 4 H 3 O.CH(NH.COOEt) 2
N
169
Bischoff
B., 7, 1081
28, 146
Diethylic oxaloxamate
NH(CO.COOEt) 2
C 8 H n O 6 N
67
Salomon
J. p. [2], 9, 295
27, 791
?
C 8 H n N 2 .OH
C 8 H 12 ON 2
....
150
Riess and Meyer
J. p. [2], 31, 112
48, 646
Diallyloxamide
(CH 2 :CH.CH 2 .NHCO) 2
C 8 H 12 2 N 2
274 d.
154
Wallach & Strieker
B., 13, 513
38, 547
Amidopheuylurethane
NH 2 .(NH.COOEt)=1.2
....
86
Rudolph
B., 12, 1295
Diethylbarbituric acid
NH.CO.NH.CO.CEt-CO
i i
C 8 H 12 3 N 2
182
Conrad & Guthzeit
B., 15, 2849
44, 314
Phenylguanylguanidine ni-
NH:C(NHPh).NH.C(NH 2 )
C 8 H 12 3 N 6
+HNO 3
208-209
Bamberger
B., 13, 1583
40, 44
trate
:NH
Nitrodehydropiperylurethane
C 5 H,(NO 2 )N.COOEt
C 8 H 12 4 N 2
51-5
Schotten
B., 16, 644
44, 814
Trimethylic cyanurate difor-
C AN 3 Me 3 + NH(CHO) 2
C 8 H 12 5 N 4
168 (24)
163
Gautier
C. R., 67, 804
vi., 529
mamide
Ethylic nitrotartrate
CO 2 Et.(CH.O.NO.,) 2 .C0 2 Et
C 8 H 12 10 N 2
....
45-46
Henry
Z. C.,13,692;B.,
3,533
?
basic
C 8 H I3 ON
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.CH 2 .COOEt
C 8 H 13 2 N
225
64-65
Canzoneri and Spica
G. L, 14, 491
48, 750
ate
Mesityloxidehydrocyanicacid
....
C 8 H 13 3 N
....
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
....
C 3 H 13 3 N 3
106-107
Fischer
A., 215, 299
44, 356
Diethylic amidomaleate
CO 2 Et.CH : C(NH 2 ).CO 2 Et
C 8 H 13 4 N
....
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
C 2 H 2 : (CO.NHEt),
C 8 H 14 2 N 2
Ml
182-183
Wallach and
B., 14, 170
40, 285
Kamenski
Mesitylamide....
222
Pinner
B., 15, 577
42, 941
Hydroxycaprylonitril
C 6 H 13 .CH(OH).CN
C 8 H" a ON
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. C 9 H 15 ON
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
C 8 H,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.CHMe 2 ) 2
C 8 H 15 2 N
....
174
Hofmann
B., 15, 982
42, 950
Piperyl urethane
C 5 H 10 N.COOEt
211
Liquid
Schotten
B., 15, 425
42, 983
Triethoxyacetonitril
(EtO) 3 C.CN
C 3 H 16 3 N
159-161-5
Bauer
A., 229, 163
48, 1121
Ethylic diethyloxamate
CO(NEt 2 ).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
C 4 H 3 O(OEt) 2 .NH s
....
68-69
Demarcay
B. S. [2], 33, 575
40, 255
Suberamic acid
....
....
170
Z. C. [1865], 300
Base fr. crotonaldehyde
....
C S H 16 ON 2
200 (i. v.)
....
Combes
C. R., 96, 1862
44, 1079
150-160
AV"ertheim
A., 123 157; 130
"
269
Triethyloxamide
NHEt.CO.CO.NEt 2
C 9 H 16 S 2
257-259
Liquid
Wallach
B., 14, 741
40, 718
Dipropyloxamide
C 2 O 2 : N 2 H 2 Pr a
....
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.CHMe 2
....
86
Hofmann
B., 15, 756
42, 1053
mide
Propylbutyryl carbamide ....
NHPr.CO.NH.CO.CH 2 Et
n
....
99
B., 15, 757
Diethylic diamidosucciuate ....
COOEt.(CH.NH 2 ) 2 .COOEt
C 8 H 16 4 N 2
122 . c.
Glaus & Helpensteii
B., 14, 624
40, 578
i,
122
Glaus
B., 15, 1849
Ethylidene urethane
CH 3 .CH(NH.COOEt) 2
....
125 u. c.
Schmid
J. p. [2], 24, 124
j>
182 d.
126
Nencki
B., 7, 160
27, 458
C.H 16 .CO.NHj
C 8 H, ON
94
Hofmann
B., 15, 983
42 950
a. 200 d.
110
Felletar
Zf! F21 4 fifi 1 !
vi., 395
. vy. [_^J, ^, \J\JiJ
Capronimido-ether
C 5 H n .C(OEt) : NH
it
168
Liquid
Pinner
B., 17, 178
46, 723
Vinyldiacetonalkamine
CMe 2 .CH 2 .CH(OH).CH 2 Me.
....
123
Fischer
B., 17, 1794
46, 1291
NH
j
Piperpropylalkine
C 6 H 10 1 N.C 3 H 6 .OH
194
Liquid
Ladenburg
B., 14, 1880, 2406
....
194
....
Laun
B., 17, 680
46, 1054
Conhydrin
C 8 H 16 : 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 ....
NEt 2 .CH 2 .COOEt
C 8 H 17 2 N
177 c.
Liquid 10
Kraut
A., 182, 176
30, 625
Ethylic isoamylcarbamate ....
CjHu.NH.COOEt
218
Liquid
Custer
B., 12, 1329
Triethylglycocine .... (cf. J.
NEt 3 .CH a .CO.O
H
210-230 d.
A., 182, 175
Briihl
A., 177, 215
1 1
[1862], 333)
Octylic nitrite
CH 3 .(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 ** i i7- wv '>
D
j&uJ 1 _
JjiquiQ
1)
. j 1 j 1OOO
|)
Hydroxycaprylamide
C 6 H 13 .CH(OH).CO.NH 2
....
150
Erlenmeyer & Sigel
B., 7, 1108
28, 144
....
150
A., 177, 108
28, 1012
Diethamido-a-butyric acid
CH 2 Me.CH(NEt,,).COOH
....
135
Duvillier
C. R, 100, 860
48, 750
Piperpropylglycoline
HO.CH 2 .CH(OH).CH 2 .N :
223-227(195)
Cryst.
Roth
B., 15, 1150
42, 1195
Nitrosodibutylamine
N(C 4 H,) 2 .NO
C 8 H 19 ON 2
234-237 c.
Meyer and Forster
B., 10, 132
Nitrosodiisobutylamine
213-216
b.
Ladenburg
B., 12, 949
36, 704
a-ethylene diethyldicarba-
....
C 8 H 19 OjN 4
of.A.,119,356
124 p. d.
Volhard
P. R, 11, 268
ii., 5G5
mide
ft- !)
....
J)
201
H
Guanoline
....
C 8 H 18 4 N 6
....
114-115
Nencki
B., 7, 1590
28, 755
+H 2 O
....
*..i
100
!,
Hydroxypropylamylamine ....
C s H n .NH.C 3 H,.OH
C 9 H 19 ON
200
0+
Lieberraann & Paal
B., 16, 533
44, 910
Trinitro-umbelliferone
HO.C 6 (NO 2 ) 3 .CH : CH.CO.O
C 9 H 3 9 N,
....
216
Posen
B., 14, 2747
42, 839
i i
Quinoline quinone
N ; O,= l ; 1.4
C 9 H 6 2 N
....
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 l 6 U 3 iN
MM
ZOO ZOU
.Kaeyer oc xlomoiKa
, H>, JU^IiUi
*VJ, 1 ij
Nitrophenylpropiolic acid ...
NO 2 .(C:C.COOH)=1.2
C 9 H S 4 N
....
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
....
C 9 H 5 O 4 N
....
170
Bleibtreu
A., 59, 190
"., 94
/3-dinitroquinoline ....
....
C 9 H S 4 N 3
....
133-134 u. c
Glaus and Kramer
B., 18, 1248
48, 908
- ... ...
N ; (NCg^a, ; a,/3 s
>
....
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
C 9 H 6 8 N
....
227 d.
Fischer and Ta'uber
B., 17, 2927
48, 400
ii
.
+2H 3
187
> ?
1)
1884-
Michael
A., 225, 142;
48, 62
B., 17, 491
m-Toluylene isocyanate
C,H 3 Me(N:CO),
C 9 H 6 2 N 2
....
95
Lussy
B., 8, 291
28, 770
Nitroquinoline
N.N0 2 =a,/3 2 !
....
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) = a i ; 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
C 9 H 6 8 N 2
..
208
Stojentin
J. p., 32, 1
48, 1196
Phthalureiide
C 6 H 4 : (CO.NH) 2 ; CO=1.2
d. 185-190
Piutti
A., 214, 23
n
Hydroxycinuoline carboxylic
N : N.C 6 H 4 .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
C 6 H 4 .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
,, =5i ; ^i or a s
)
255 n. c.; p. d.
M. C., 3, 564
44, 94
(0 ....
....
)
....
m.a. 300
Weidel & Hazura
M. C., 3, 774
Nitropolyporic acid
....
C 9 H 6 4 N (?)
230
Stahlschmidt
A., 195, 365
36, 383
p-Nitrophenyl nitre-acrylic
....
C 9 H 6 6 N S
cf. B., 16, 850
196-197
Friedlander and
B., 14, 2577;
42, 402
acid
Mahly
A., 229, 210
Acetoxycyanobenzene
C 6 H 4 .CN.OAc=1.4
C 9 H 7 ON
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 ....
: ^ a i ; &
)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 a 2
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
+3H 2
>
J?
52
*
COMPOUNDS CONTAINING FOUR ELEMENTS.
489
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Benzylcyanide carboxylic
(COOH).(CH 2 .CN)=1.2
C 9 H 7 O 2 N
....
116
Wisliceiius
B., 18, 172
48, 532
acid
Amidophenylpropiolic acid....
NH 2 .(C;C.COOH)=1.2
i
cf.B.,16,679
128-130 d.
Baeyer and Bloem
B., 15, 2148
Methylphthalimide
C 6 H 4 .COO.C:NMe=1.2
I)
abt. 277
132
Grtebe and Pictet
B., 17, 1174
46, 1019
L 1
Phenylmetliylacetoxinie car-
C 6 H 4 .COO.N:CMe=1.2
....
157-159
Gabriel
B., 16, 1995
44, 1128
i i
boxyhc anhydride
C 6 H 4 .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
C 6 H 3 (NH n ).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
N0 2 .(CH:CH.COH)=1.3
C 9 H 7 O 3 N
....
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.C 6 H 4 .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
C 9 H 7 3 N 3
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).N0 2 =1.3
C 9 H 7 4 N
....
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
N0 2 . (CH.CH 2 .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
....
C 9 H 7 5 N
....
nod.
Baeyer
B., 13, 2262
40, 276
acid
Acetylic nitrobenzoate
COOAc.NO 2 =1.3
i)
....
130-132
Liebermann
B., 10, 863
32, 617
Nitrobenzoylacetic acid
NO 2 .(CO.CH 2 .COOH)=1.4
!
....
135 d.
Perkin & Bellenot
B., 17, 326
46, 1024
Carbostyrilic acid
CO 2 H.(NH.CO.CO 2 H)=1.2
11
+H 2
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
CO 2 H.(NH.CO.CO 2 H)=1.2
Q,H 7 6 N
....
200 d.
Hofmann & Konigs
B., 16, 734
Kynuric acid ,
....
55
+H 2
187
Kretschy
M. C., 4, 157
Nitrobenzalmalonic acid
NO,[.CH : C(COOH) 2 ] = 1.4
C 9 H 7 6 N
227
Stuart
....
43, 407
n-Nitro-uvitic acid .... ' .;
(COOH) 2 .Me.NO 2 =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,),
C 9 H 7 7 N 3
270 d.
Salkowski
B., 10, 1696
=1.4.3.5
Benzenylazoximethenyl
N I CPh.N : CMe.O
C 9 H 3 ON 2
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(NC 4 H 4 ) 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(C 4 H 3 .NH) 2
....
160
)
B., 18, 419
48, 809
)>
)5
1
160
i
B., 18, 1830
Hydroxytoluquinoxaliue
C 6 H 3 Me.N:CH.C(OH):N
)J
241-242; 247
Hinsberg
B., 18, 1232
48, 910
i i
Hydrazine cinnamic anhy-
C 6 H 4 .CH : CH.CO.N(NH 2 )
....
127
Fischer
B., 14, 480
40, 598
dride
i i
=1.2
Amidocarbostyril
N.OH.NH a -,=0^.0^ ;
....
nf. 320
Friedlander and
A., 229, 233
48, 1139
Lazarus
?
CHO.NH.NPh.C(NH).CN
C 9 H 8 ON 4
....
192-5-193-5
Bladin
B., 18, 1549
48, 980
Phenylhydantoin
CO.NH.CO.CH 2 .NMe
9 HAN 2
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).(CH 2 .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.C 6 H 4 C.CH 2 .C0 3 H
)
168-170 d.
Fischer and Tafel
A., 227, 303
48, 542
'- ] i
=1.2
Anhydroamidooxalyltoluidic
i
C 6 H 3 Me.NH.CO.C(OH) : N
)3
....
a. 300 s. d.
Hinsberg
B., 15, 2692
44, 323
acid
Dihydroxytoluquinoxaline ....
C 6 H 3 Me:[N:C(OH)] 2 :
nf. 295
Bladin
B , 18, 671
48, 785
o-nitrophenyl 0-alanine lac-
NO 2 .C 6 H 4 .CH.CH 2 .CO.NH.
C 9 H 8 3 N 3
impure
80
Einhorn
B., 16, 2649
46, 305
tam
1 1
Ni tro-cinnamide
NOj-CCH : CH.CO.NH 2 )=1.4
)J
155-156
Cahours
A. C. [3], 27, 452
i., 989
Ethoxynitrobenzonitril
CN.NO 2 .OEt=1.2.6
)
137
Bruyn
K. T., 2, 205
48, 656
Phenylhydrazinemesoxalic
N 2 HPh : C(COOH) 2
C 9 H 8 4 N 2
158-164
Elbers
A., 227, 340
48, 535
acid
>
))
163-164
Fischer
B., 17, 578
46, 1151
Nitrophenylnitropropylene
NO 2 .(CH I CMe.NO 2 )=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).N0 2 .NH 2
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.CH 2 .COjH)
C 9 H 8 5 N 2
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.C 3 H 5 )(N0 2 ) 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.NO 3 .(NH.CO.CO 2 H)
C 9 H 8 5 N 2
....
d. w. m. 150
Hinsberg
B., 15, 2691
=1.3.4
Ethylic dinitrobenzoate
COOEt.(NO 2 ) 2 =1.3.5
C 9 H 8 6 N,,
....
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
(NO 2 ) 3 .(CH : CH.CO 2 H)
JJ
cf.B.,13,1680
126-5
Gabriel and Zim-
B., 12, 600
36, 640
' =1.2.4
mermann
Methylic dinitromethylsali-
CO 2 Me.OMe.(NO 2 ) 2 =1.2.(?) 2
C 9 H 8 7 N 2
....
69
Salkowski
A., 173, 47
28,71
cylate
Ethylic dinitrosalicylate
C0 2 Et.OH.(N0 2 ) 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
(CH 2 .CH 2 .C0 2 H) 2 .OH.(N0 2 ) 2
JJ
....
137-5
Stehr
A., 225, 57
46, 1350
acid
=1.4.3.5
Dinitrohydrocoumaric acid
=1.2.(?) 2
C C H 5 .CH : CH.CO.NH 2
JJ
C 9 H 9 ON
155
141-5
Zwenger
Rossum
As., 5, 118
Z. C. fal 2, 362
vi., 716
vi., 471
Phenyllactimide
Ph.CH 2 .CH.NH.CO(?)
jj
146-147
Posen
L JJ y
A., 200, 97
38, 322
)j .... ....
Ph.CH.NH.CO.CH 2 (?)
jj
....
280
Schulze & Barbieri
J. p. [2], 27, 337
44, 1122
,,
))
j
290
Erlenmeyer & Lipp
A., 219, 179
44, 993
Phenyl a-hydroxypropioni-
Ph.CH 2 .CH(OH).CN
j)
....
57
jj
jj
44, 992
tril
Hydrocarbostyril
C 6 H,.N : C(OH).CH,.CH 2
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 .. ....
C 6 H 4 .CHMe.CO.NH=1.2
sb. 100
119
Weinberg
Trinius
A., 227, 262
48, 529
Xylylisocyanate
Me 2 .(N ; CO)=?
Jj
JJ
abt, 200
Liquid
Hofmann
P. E., 19, 108 ;
S4, 139 ; vii.,
B., 3, 657
407
E thenylamidocresol
C 6 H 3 Me.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)
C 7 H 6 .NH.C(NH).C(OH) ; N
C 9 H 9 ON 3
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.NO 2
C 9 H 9 2 N
....
64
Priebs
B., 16, 2591 ; A.,
46, 313; 48,
225, 319
161
a-Amidocinnamic acid
Ph.CH : C(NH 2 ).COOH
jj
d. 240-250
Plochl
B., 17, 1621
46, 1349
Benzimidoacetate
C 6 H 5 .C( :NH).OAc
jj
....
116
Pinner and Klein
B., 11, 9
34, 492
Anilido-pyruvic acid
C 6 H 5 .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
(C 2 H 2 .COOH).NH 2 =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
C 6 H 4 .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
C 9 H 9 O 2 N
....
63
Tieraann and
B., 14, 1976
Kohler
Hydroxydihydro-carbosty ril
C 6 H 4 .CH(OH).CH 2 .C(OH).N
1 1
)-
....
149
Einhorn
B., 17, 2011, 2013
46, 1338
=1.2
ii
+ 2H 2 Q
95-97
11
n
C 6 H 4 .CH 2 .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
C 9 H- 9 O3N
138-139
Miiller
B., 16, 2987
46, 584
acetate
_
Benzylic oxamate
NH 2 .CO.COO.CH 2 Ph
)I
....
134-135
Wallach and
B., 13, 507
38, 557
Liebmann
Hippurie acid
NHBz.CH 2 .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.CH a .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 ....
C 6 H 4 (,NO 2 >.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
C 6 H 4 .NH 2 .(CH 3 .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
NO 2 .(N 2 .CH 2 .COMe)=1.2
C 9 H 9 J N 3
123-124
Bamberger
B., 17, 2418
48, 157
Nitro-nitrosotetrahydro-
C 9 H 9 N(NO)(N0 2 )
n
....
137-138
Hoffmann and
B., 16, 730
44, 1143
quinoline
Koniga
Methylic nitrophenyl acetate
NO 2 .(CH 2 .COOMe)=1.4
C 9 H 9 4 N
....
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 ....
(CH 2 .CH 2 .CO 2 H).NO 2 =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.CO 2 H).N0 2 = 1 .4
....
87
Triuius
A., 227, 262
48, 529
>i
=1.2
5
....
110
11
ii
)J
Ethylic nitrobenzoate
COOEt.N0 2 =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.N0 2 =13
C 9 H 9 4 N
....
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-
C 6 H 4 (NO).(O.C0 2 Et)= ? .
....
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-
CH 2 :0 2 :C 6 H 3 .CH(NH S ).
....
210
Lorenz
B., 14, 794
40, 729
acetic acid
C0 2 H
Nitroethylbenzoic acid
CGOH.Et.NO 2 =1.4.?
ji
cf. A., 216, 220
155-156
Aschenbrandt
B., 12, 1304
36, 920
Nitroxylylic acid
(CH 2 .C0 2 H).Me.N0 2 =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.Me 2 .NO 2 =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
C 2 H 6
ft- ,1
)
ppd. fr. Ba.
175
Schmitz
A., 193, 168
36, 156
salt
ft- ,, I)
n )
)
cryst. fr.
214-220;rs.
11
)
>
C 2 H 6 O
162 ; and
remeltsl68
a-Amido-uvitic acid
Me.(C0 2 H) 2 .NH 2 =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 ...
C 5 HNMe 2 (COOH)j
n
....
245
Michael
A., 225, 121.
48, 62
Nitrophenyl /3-lactic acid ..
N0 2 .[CH(OH).CH 2 .C0 2 H]
C 9 H 9 6 N
....
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
CO 2 Me.OMe. NO 2 = 1.-4.6
abt. 100
Cahours-
A., 56, 315
i., 302
Ethylic nitrohydroxyben-
CO 2 Et.OH.NO 2 =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 ....
CO 2 H.OEt.NO 2 =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
(CH 2 .CH 2 .CO 2 H).OH.N0 2
)V
....
90-5
Stohr
A., 225, 57
46, 1350
Methoxynitrotoluic acid
C0 2 H.OMe.Me^r0 2 =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
C 5 H 3 NO(OAc) 2
tl
....
153-155
Oat
J.p., 27, 259
44, 791
Dinitro-acetoluide
Me.NHAc.(NO 2 ) 2 =1.4.3.5
C 9 H 9 6 N 3
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
C 9 H 9 6 N
....
94
Morgan
B., 17, 220
46, 747
Nitroveratric acid
COOH.(OMe) 2 .N0 2 =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
CO 2 Et.(NO.,) 2 =1.3.5
C 9 H 9 6 N 2
....
90
Staedel
A., 217, 182
44, 865
Diiiitrophenylurethane
(NH.COOEt).(NO 2 ) 2 =1.2.4
C 9 H 9 6 N 3
....
110-111
Hager
B., 17, 2029
48, 150
jj
=
J)
210
Losanitsch
B., 10, 691
Trinitroisopropylbenzene ...
Prf.(N0 2 ) 3 =?
J)
....
109
Fittig and others
A., 149, 329
Dinitroacetaniside
OMe.NHAc.(N0 2 ) 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,.(NO 2 ) 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
(CH 2 .CH 2 .CO 2 H).NH 2 .(NO. j ). !
1)
....
190
Stohr
A., 225, 57
46, 1350
acid
=1.4.3.5
Trinitroethyltoluene
Me.Et.(N0 2 ) 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
Me 3 .(NO 2 ) 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.(N0 2 ) 3 =1.3.2.4.6
C 9 H 9 7 N 3
....
72
Nolting and Salis
B., 15, 1864
44,59
Dinitrotyrosine
C 9 H 9 (N0 2 ) 2 N 3
)
115
Stadeler
J. [1860], 576
v., 934
Dimethyltrinitro-orcinol ....
Me.(OMe) 2 .(N0 2 ),=1.3.5.
C 9 H 9 S N 3
....
69-5
.fitenhouse
P. K., 19, 410
vii., 880
.. 2.4.6
Benzene azoaeetone
Ph.Nj.CH2.CO.Me
C 9 H I0 ON 2
....
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....
C 6 H 4 .CH 2 .CHM ei N.NO=1.2
jj
54-55
Jackson
B., 14, 884
40, 735
i i
Aniidohydrocarbostyril
C 6 H 4 .CH 2 : CH 2 .CO.N.NH 2
j>
....
143
Fischer and Kuzel
A., 221, 261
46, 441
i i
jj ....
C 6 H 3 (NH 2 ).C 2 H 4 .CO.NH
>j
211
Gabriel and Zim-
B., 12, 602
36, 640
i i
mermann
=1.4.5
PLenylmethyl oxamide
NHMe.CO.CO.NHPh
C 9 H 10 O a N 2
171-173
Wallach and West
B., 9, 266
30, 185
jj jj
JJ
Jl
179-181
Wallach
A., 184, 70
32, 187
Phenylmalonamide
NH 2 .CO.CH 2 .CO.NHPh
JJ
....
163
Freund
B., 17, 135
46, 728
Hippuramide
Ph.CO.NH.CH 2 .CO.NH 2
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...
NH 2 .CPh : NOAc
JJ
...
96
Schulz
B., 18, 1083
48, 897
Phenylbydrazinepyroracemic
Ph.N 2 H : 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.COJMH 2 )=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.CO 2 H).(NH 2 ) 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 a 2
-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
NO 2 .(NH.CO.Et.)=1.2
C 9 H,AN 2
....
63
Smith
A. C. J., 6, 172
48, 524
Nitrophenyl dimethyl ace-
NO 2 .(CMe.NOMe)=1.3
..
63-64
Gabriel
B., 15, 3063
44, 582
toxime
Salycyloxyacetic diamide ....
(CO.NH 2 ).(O.CH 2 .CO.NH 2 )
)J
....
158
Rossing
B., 17, 2997
48, 388
=1.2
Uramidophenylacetic acid ....
(NH.CO.NH 2 )(CH 2 .CO 2 H)
174 d.
Traube
B., 15, 2122
44, 193
= 1.4
Amidohippuric acid .... ..
NH 2 .(CO.NH.CH 2 .CO 2 H)
A., 78, 112
192
Schwanert
A., 112, 70-
=13
,, ,,
)!
3>
....
194
Conrad
J. p. [2], 15, .257,
32, 485
Nitroacetoluide
Me.NHAc.NO 2 =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
6 H 4 Me.(N 2 C 2 H il N 2 O 3 )= 1.4
C 9 H 10 3 N 4
....
154
Kimich
B., 10, 143
32, 326
Nitrophenylurethane
N0 2 .(NH.COOEt)=1.2
C 9 H I0 4 N 2
....
58
Eudolph .
B., 12, 1295
36, 921
=1.4
))
....
129
Hager
B., 17, 2625
48, 149
Nitrohpenyl |3-anilidopro-
N0 2 .[CH(NH 2 ).CH 2 .C0 2 H]
I)
120-122
Easier
B., 17, 1501
46, 1173
pionic acid
=1.4
Nitrophenyl /3-alanine
NO 2 .[CH(OH).CH 2 .CO.NH 2 ]
)J
.....
166-167
B., 17, 1494
46, 1172
=1.4
:>
,) !!
NO 2 .CH.CH 2 .CO.O.NH 3
5)
)
....
197.
220
Einhom
Erlenmeyer and
B., 16, 2646
A., 219, 179
46, 304
44, 993
J =1.4
NO 2 .[OH 2 .CH(NH 2 ).CO 2 H]
=1.4
Lipp
Nitroacetaniside
OMe.NHAc.NO 2 =1.2.?
>J
143
Mulhauser
A., 207, 242
42, 302
Ethylic nitroamidobenzoate
CO 2 Et.NH 2 .NO 2 =1.2.3
))
....
104
Hubner
A., 195, 40
36, 382
Methylic nitroamido-a-tol-
(CH 2 .CO 2 Me).NO 2 .NH 2
))
....
94
Gabriel and Meyer
B., 14, 825
40, 730
uate
=1.2.4
Nitro-amidohydrocinnamic
(CH 2 .CH 2 .C0 2 H).NO S .NH 2
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 ....
CO 2 H.NHEt.NO 2 =1.3.5
)
....
208
Roll wage
B., 10, 1704
34, 148
Dinitroethyltoluene ...
Me.Et.(N0 2 ) 2 =1.4.(?) 2
)>
....
Liquid
Jannasch and
B., 7, 1514
Dieckmann
.... ....
)>
....
52
))
Dinitropseudocumene
Me 3 .(N0 2 ) 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,(NO 2 ),.=1.2.3.5
C 9 H I0 5 N 2
....
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
Me 2 .NO 2 .NO 3 =1.3.4.2.6
Me 3 .OH.(NO 2 ) 2 =1.3.4.6.2.5
Me.NEt(NO),(NO 2 ) 2 =1.4.3.5
Me.NHEt.(NO 2 ) 3 =1.4.2.3.5
[O.C 3 H 5 (OH) 2 ].(N0 2 ) 2 =1.2.4
NMe 2 .NMe(NO).(NO 2 ) 3
= 1.3.(?) 3
C 6 H 5 .NH.CO.CH 2 .CH 3
U 9 H 10 5 N 2
c 9 n" o 6 N 4
i?
C 9 H 10 7 N 2
C<,H I0 7 N 6
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 ....
C 6 H 5 .NMeAc
C 6 H 6 .CH 2 .NHAc
CeHj-CHj-NHjAc
C 6 H 5 .CO.NMe 2
C 6 H 5 .CH : N.OEt
C fi H 4 (NH 2 ).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.NMe 2 = ?
Me.(CH 2 .CO.NH 8 )=1.3
=1.2
= 1.4
Me 2 .(NH.CHO)=1.3.4
Me 2 .(CO.NH 2 )=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
C 9 H",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.CH 2 .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.CH 2 .CH(NH 2 ).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(NH 2 ).CH 2 .COOH
cf.B.,15,1006
120-121
Poseii
A., 195, 143
36, 378
a-Amidohydratropic acid ....
CH 3 .CPh(NH 2 ).COOH
w.m. 260
Tiemann
B., 14, 1981
42, 57
a-
CH 2 (NH 2 ).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
CH 3 .CH(OPli).CO.NH 2
....
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.NH 2 )=1.2
110
Limpricht
A., 98, 264
v., 151
Melilotamide . ....
OH.(CH 2 .CH n .CO.NH )=1.2
70
Zwei er
As., 5, 120
vi., 716
n
OH.(CHMe.CO.NH 2 )
110-111
Hlasiwetz
A., 102, 162
iv., 489
Ethylic amidobenzoate
NH 2 .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 ...
NM e!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
NH 2 .(CH 2 .CH 2 .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
NH 2 .(CHMe.COOH)=1.4
11
128
Trinius
A., 227, 262
48, 529
Tolylglycociue
Me.(NH.CH 2 .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.CH 2 .OH)
11
+ lH 2 O
70-130
Tommasi
27, 628
Tolylamidoacetic acid
Me.[CH(NH 2 ).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
Me 3 .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
Me i .COOH.NH 2 =1.3.5.6
C s H n O.,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
C 5 NHMe :i .COOH
>
....
155
Michael
A., 225, 121
48,62
11
)1
-f2H 2
no
B
1J
Nitrosoethylphenyl carb-
....
C 9 H M 2 N :l
59-5
Fischer
A., 199, 286
amide
Glycolphenylguanidine
NHPh.C(: NH).NH.CH a .
ft
....
260 d.
Berger
B., 13, 993
38, 802
COjH
Nitropropylazobenzene
CH 3 .CH 2 .CH(NO 2 ).N : NPh
))
...
98-99
Meyer
B., 9, 386
30, 93
Nitroethylazotoluene
C 6 H 4 Me.N 2 .C 2 H 4 .N0 2 =1.2
))
87-88
Barbieri
B., 9, 388
30, 94
*>
=1.4
H
133
?
B., 9, 387
j>
Phenylamidolactic acid
Ph.C 2 H.,(OH)(NH 2 ).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 : .[CH 2 .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.[CH 2 .CH(NH.,).CO 2 H]
cf. B., 16, 854
167-168-
Blendernianii
Z. P. C., 6, 234
44, 878
11
=1.4
Methoxymandelatnide
OMe.[CH(OH).CO.NH 2 ]
)J
159
Tiemann
B., 14, 1977
48,57
=1.4
Methoxyphenylamidoacetic
OMe.[CH(NH 2 ).CO. 2 H]=1.4
5)
....
w. m. 225
M
B., 14, 1979
acid
Methoxyphenylglycocine ....
OMe.(NH.CH 2 .CO 2 H)=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
Me 2 .OMe.NO 2 =1.3(?) 2
i)
....
56-57
Pfaff
B., 16, 1136
44, 918
Nitromesitol
Me J .OH.NO 2 =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.
^H n 3 N,
127
Gross
B., 18, 2478
48, 1218
amidoxime
CO.NH,
Ethylnitrobenzenylamid-
NO 2 .[C(NH 2 ) : NOEt]=1.3
55
b. 15(?)
Schopf
B., 18, 1065
48, 896
oxirae
Nitro /3-phenylpropylene
N0 2 .[CH(OH).CH 2 .CH 2 .OH ;
C,H n O,N
108-101)
Baeyer & Drewseii
B., 15, 2861
44, 341
glycol
=1.2
Aruidophenylglyceric acid ....
NH 2 .[CH(OH).CH(OH).
U
218
Morgan
J. [1877], 788 ;
C0 2 H]=1.2
0. N. 36, 269
n-ethylnitro-orcinol
Me.OEt.OH.NO 2 =1.3.5.?
H
54
Weselsky and Bene-
M. C., 2, 371
40, 1140
dikt
-
>i
T
103
?>
)!
D
Triraethylpyrroline dicarb-
NMe.Me s .(OO t H) J =1.8JM.4
11
d. 240-245
Knorr
B., 18, 307
48, 555
oxylic acid
Ethylic amidonitrophenyl-
NH.CO 2 Et).NH 2 .NO 2 =1.2.4
C 9 H U 4 N 3
162
Hager
B., 17, 2631
48, 150
carbamate
Dinitroethyltoluidine
Me.KHEt.(NO 2 ),=1.4.3.5
126-126-5
Gattermann
B., 18, 1485
48, 975
Dinitrodimethyltoluidine ....
Me.NMe 2 .(N0 2 ) 2 =1.3(?) 2
11
107
Wurster and Riedel
B., 12, 1800
38, 109
,, ....
" !>
;>
....
168
n
11
11
Dinitrocumidine
Me.,.NH 2 .(N0 2 ) 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
Me 3 .NH.,.(NO 2 ),,=.1.3.5.2.4.6
C 9 H U 4 N 3
193-195
Fittig
A., 141, 138
vi., 300
Nitrobeiizylidenediure'ide ....
NO 2 C 6 H 4 .CH(NH.CO.NH 2 ) 2
C 9 H,,0 4 N 5
200 d.
Schiff
A., 151, 194
Menispermine
C 9 H 12 ON(?)
120
Pelletier & Uouerbe
A. C. [2], 54, 178
iii., 880
Ethylphenylcarbamide
NH 2 .CO.NEtPh
C 9 H 1 .,ON 3
62
Gebhardt
B., 17, 2095
46, 1321
,*
....
I)
99
B. 8., 4, 203
Phenylethylcarbaraide
NH 2 .CO.NH.CH 2 .CH 2 Ph
Ji
112
Spica
G. I., 9, 555
38, 242
n-phenamidopropionamide ....
NHPh.CHMe.CO.NH 2
)7
....
140-141
Tiemann aud Ste-
B., 15, 2035
44, 199
phan
Phenylraethamidoacetamide
Ph.CH(NHMe).CO.NH 2
155
Tiemann and Piest
B., 14, 1983
Methylphenamidoacetamide
NPhMe.CH 2 .CO.NH 2
))
163
Silberstein
B., 17. 2662
48, 160
Benzylic ethenylamidoxime
NH 2 .CMe : NO.CH 2 Ph
V
d. 200
Liquid
Nordmanu
B., 17, 2752
48, 239
Ethylic benzenylainidoxime
NH 2 .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
C 6 H 4 Et.NEt(NO)=1.4
1>
?
Gastiger
B. a, 42, 338
48, 381
Tolylaraidoacetamide
Me.(NH.CH 2 .CO.NH 2 )=1.4
M
....
162-163 d.
Meyer
B., 8, 1160
29, 402
Nitrosodimethyltoluidine ....
Me.NMe 2 .NO=1.3.?
>1
92
Wurster and Riedel
B., 12, 1797
38, 109
Acetdiamidotoluene
Me.NH 2 .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
C 9 H 12 2 N 2
152-153
Fischer and Jordan
B., 16, 2244
46, 53
acid
>i
NH 2 .NPli.CHMe.COOTI
?1
187
Reissert
B., 17, 1455
46, 1152
Ethylic amidophenylcarba-
NH 2 .(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.NH 2 ).(C 2 H 4 .C0 3 H)=?
)J
....
146
Fischer and Kuzel
A., 221, 261
46, 441
acid
Acethydrazine anisoil
MeO.(N 2 H 2 Ac)=1.2
1)
125
Reisenegger
A., 221, 314
46, 440
Ethoxyphenylcarbamide
EtO.(NH.CO.NH 2 )=].4
....
160
Berlinerblau
J. p., 30, 97
48, 148
Nitrocumidine
Pr.NH 2 .NO 2 =?
>1
b. 100
Cahours
C. R., 26, 316
ii., 176
Mtroethyltoluidine
Me.NHEt.NO s = 1.4.5
1?
58-59
Gattermann
B., 18, 1483
48, 975
Nitrodimethyltoluidine
Me.NMe 2 .NO 2 =1.3.?
)>
84
Wurster and Riedei
B., 12, 1800
38, 109
Diamidociunamic acid
(CH 2 .OH 2 .CO 2 H).(NH 2 ) 2
)'
....
142-144
Gabriel
B., 15, 2291
44, 195
=1.3.4
Nitromesidine
Me 3 .NH 2 .NO 2 =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.NH 2 ) 2
C 9 H 12 2 N 4
....
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 H 2 ) 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.(NH 2 ) 2 =1.4.3.5
C 9 H )2 3 N 2
Liquid
Kayser
B., 15, 1136
42, 1203
Nitro-nitrosotrimethdiami-
NMe 2 .NMe(NO).NO 2 =1.4. ?
C 9 H 12 3 N 4
....
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.C 2 H 4 .OH
(; 9 H 13 ON
218-219(110
Liquid
Laun
B., 17, 676
46, 1011
Dimethamidomethoxy ben-
OMe.NMe 2 =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.C 2 H 4 .OH)=1.4
C,H 13 ON
286-288
37
Demi ile
B., 7, 636 ; A.,
27, 903
173, 129
Ethoxytoluidine .... , ...
Me.OEt.NH 2 =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
Me 3 .OH.NH 2 =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
C 9 H 13 ON,
....
108
Eenouf
B., 13, 2172
40, 152
mide
o-phenylhydrazinepropion-
NH 2 .NPh.CHMe.CO.NH 2
)
124
Reissert
B., 17, 1454
46, 1152
amide
Ethylphenylsemicarbazide ....
Ph.NH.CO.NjHjEt
)I
111-112
Fischer
A., 199, 295
11
Ph.N 2 H. 2 .CO.NHEt
JJ
....
151
Fischer
A., 190, 109
34,307
Nitrosotrimethdiamidoben-
NMe s .NMe(NO)=1.4
98-99
Wurster & Schobig
B., 12, 1809
38, 111
zene
Dimethainidophenylcarba-
NMe 2 .(NH.CO.NH 2 )=1.4
....
179
Binder
B., 12, 536
36, 628
mide
Ethylic dimethylpyi-roline-
C 4 NH 2 Me 2 .COOEt
C 9 H 13 2 N
290 (731)
117-118
Knorr
B., 18, 1564
48, 995
carboxylate
Nitrodiamidomesitylene
Me 3 .NO 2 .(NH 2 ) 2 =1.3.5.2.4.6
C 9 H 13 2 N S
....
184
Fittig
A., 141, 139
vi., 300
Ethylic ethylacetocyanace-
CEtAc(CN).COOEt
C 9 H I3 3 N
105-110
Liquid
Held
C. R., 98, 522
46, 727
tate
(2-15)
Camphoronamic acid
.
C 9 H 13 4 N
....
212
Hjelt
B., 13, 798
38, 670
Diamidoethoxy toluene
Me. OEt.(NHj) 3 = 1.4.3.5
C 9 H 14 ON 2
75
Staedel
A., 217, 221
44, 866
? -amidiue
C 4 H 3 O.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
C 9 H 12 N 2 (OH; 2
C 9 H 14 O 2 N.,
151
Riess
J. p. [2]. 30, 145
48, 235
Caffeine methhydroxide
C 8 H 10 O 2 N 4 .MeOH
Q,H u O a N 4
....
137-138
Schmidt
B., 16, 2588
46, 339
Ethylic cyanurate
EtO.C:N.C(OEt):N
C 9 H 15 ON
29
Mulder
R. T., 1, 191
44, 304
j
.C(OEt) : N
\
Phoronoxime
C 9 H 14 :N.OH
^
218 c.
48
Nageli
B., 16, 496
44, 728
Pseudopelletierine +2H 2 O ...
cf. C. R., 88, 716
11
246
46
Tanret
B. S., 36, 256
36, 658
Ecgonin
....
C 9 H I5 3 N
+H 2
198
Lossen
A., 133, 365
Triethylic cyauurate
....
C 9 H 15 3 N 3
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,H 15 5 N
....
212
Hjelt
B., 13, 799
38, 670
Ammonium anhydrocam-
C 9 H 18 5 N 2 (?)
,, (?)
125
Kachler & Spitzer
M. C., 6, 173
48, 807
phoronate
Triglycollamic triuramide ...
(NH.CONH.CO.CH 2 ) 3 N
C 9 H 16 6 N 7
cf.B.,5,1013
nf. 230
Mulder
B., 6, 1016
27, 48
Nitrosotriacetonamine
....
C 9 H 16 2 N 2
....
72-73
Heintz
A., 185, 6; 187,
233
Amidocamptioronamide
....
C 9 H 16 4 N 2
....
160
Hjelt
B., 13, 797
38, 670
Triacetonamiue
CO : (CH2.CMe 2 ) 2 : NH
c 9 n, 7 oN
....
34-6
Heintz
A., 178, 305
29, 382
11 ....
))
....
39-6
A., 174, 144
28, 351
>i
))
J)
+H 2
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 .... ..
C 9 H,.ON
240-245
....
Merling
B., 14, 1830
42, 216
s-
C 7 H 10 .OH.NMe 2
)I
198-205 d.
Ladeuburg
B., 14, 2404
)>
Isonitrosoisobutylketone
C 9 H 17 2 N
....
42
Lang
B., 18, 1364
Ethylic hydroxypentamate ....
....
C 9 H 17 O 3 N
77-77-5
Demarcay
A. C. [5], 20, 488
Ammonium hydroxycam-
C 9 H 13 (NH 4 )0,
C 9 H ir 6 N
....
178,
Kachler
A., 191, 143
34, 513
phorate
Isononylamide
CMe 2 .(CH 2 ) 3 .CHMe.CO.NH 2
C 9 H 19 ON
80-81
Kuhlhem
A., 173, 319
28, 354, 884
,, .... ....
1J
)
81
)
A., 176, 308
vii., 898
Pelargonamide
CH 3 .(CH 2 ) 7 .CO.NH 2
7
92-93
Schalfejeff
B., 6, 1252
27, 255
.,
J?
?r
99
Hofmann
B., 15, 984
42, 950
,,
C 8 H 17 CO.NH 2
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
CMe 3 .NH.CO.NH.CMe 3
242
)j
ij
(Enanthodiure'ide
C 6 H 13 .CH(NH.CO.NH 2 ) 2
C 9 H 20 2 N 4
166 d.
Schiff
A., 151, 186
Oxalyldiethylhydrazine
CO(NH.NEt 2 ) 2
C 9 H 22 ON 4
204
Fischer
A., 199, 297.
From ethylcarbaiuiue
cf. B. S., 11, 221
C 9 H 22 2 N 4
112
Gautier
C. R., 67, 8041
vi., 529
/3-Tetranitronaphthalene
C 10 H 4 (N0 2 ) 4
C 10 H=0 S N 4
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
C 10 H 3 .OH.(N0 2 )J
C 10 H 4 9 N 4
c H C O N
180
77
Merz.adj Weith
Gr6X 1 lj3J'd
B., 15, 2715
P. J. [3], 14,717
44, 344
48, 396
Nitro-j9-naphthoquinone
O.O.NO^W, ; (9
^lO-'-^-s^'a 1 - 1
C 10 H 6 4 N
158
Stenhouse & Groves
A., 194, 203
33, 417
=,".;()
)J
....
158
Liebermanu
B., 14, 1313
Nitrohydroxynaphthaqui-
C 10 H 4 (N0 2 )(OH):0 2
C 10 H 6 5 N
157 d.
Diehl and Merz
B., 11, 1318
34, 888
none
?-Trinitronaphthalene
C ln H 5 (N0 2 ) s
C 10 H 5 6 N 3
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
Beilsteinand 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
C 10 H 4 .OH.(N0 2 ) 3
C 10 H 5 7 N 3
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....
C 10 H 3 (N0 3 ) 4 .NH 3
C 10 H 6 9 N 5
....
194
Merz and Weith
B., 15, 2718
44,344
P-
))
?)
202
B., 15, 720
Pyridine pentacarboxylic acid
C 5 N(COOH) 5
C ln H 6 10 N
d.w.m. 220
Hantzsch
A., 215, 62
44, 85
n-isonitroso-/3-napthhone
C 6 H 4 .CH:CH.C:C.N.O.N
C 10 H 6 ON 2
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
.... .... ....
C 4 H 3 N.CO.C 4 H 3 N.CO
C 10 H 6 2 N 2
....
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
(N0 2 ) 2 =afl ;
C IO H,0 4 N t
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=a 1 fli 1 ;
)1
219-220
Dobner and Miller
B., 15, 3076
acid
Dinitro-a-naphtliol (Martius
OH^NOj^a.ajB, ;
C 10 H 6 6 N 2
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
.. - - 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.NO s ;NO a =A?;3 1
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 ....
C 10 H,(NH 2 XN0. 2 ) 3
C 10 H 6 6 N 4
....
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
(N0 2 ) 2 .(HO).C 6 H.CMe : CH.
10 H 6 7 N 2
....
220
Pechmann and
Cohen
B., 17, 2137
46, 1332
C00=(?) 2 .1.4.5
Cinnanyl cyanide
C 6 H 5 .CH:CH.CO.CN
C 10 H 7 ON.
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
C 10 H 7 .NO
C 10 H.ON
d. 134
84
Baeyer
B., 7, 1640
28, 452
....
89
B., 8, 616
Hydroxycomazone ....
....
C 10 H 7 ON 3
340-360
Krippendorff
J. p. [2], 32, 153
48, 1243
Phenylmalemimide
CO.CH : CPh.CO.NH
i i
C 10 H.0 2 N
210-211
Perkin
B., 14, 2547
n-Nitronaphthalene ....
C 10 H 7 .N0 2
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.N0 2 =fta i;
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,n 2 ;
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>,3 1 ;
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 fl l/-*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 ~~ a j 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
C 6 H 4 : (CO) 2 : CH.CO.NH 2
11
200 d.
Gabriel & Michael
B., 10, 1556
34, 230
= 1.2
Nitronaphthol
OH.N0 2 =/3 ini ;
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
= n A ;
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,;
C 10 H ; O a N
...<
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.C 10 H 5 O : NOH
187-187-5
Bernthsen and
B., 18, 208
48, 547
si
Semper
Phthalylglycocine
C 6 H 4 : (CO), : N.CH 2 .CO 2 H
C 10 H 7 4 N
....
191-192
Drechsel
J. p., 27, 418
44, 1126
=1.2
Dinitronaphthylamine
N l^.\^i^\.)^)^~^\ a ^pl j
C 10 H 7 4 N 3
....
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 ....
NO 2 .(CH : CH.CO.CO 2 H)
C 10 H 7 5 N
135-136
Baeyer & Drewsen
B., 15, 2862
44, 341
=1.2
Nitrobenzalmalonic acid
NO 2 .[CH:C(CO 2 H) 2 ]=1.2
C ie H 7 0N
....
161 d.
Stuart
....
47, 156
,, ,,
= 1.3
D
205 d.
....
47, 157
,i
=1.4
....
227 d.
47, 158
Nitrocarboxylcinnamic acid
(CH : CH.CO 2 H).NO 2 .CO 2 H
....
287 d.
Low
B., 18, 949
48. 799
=1.2.4
Pieoline tetiacarboxylic acid
5 NMe(CO 2 H) 4
C 10 H 7 8 N
....
199 d.
Hantzsch
A., 215, 57
44, 85
Nitroso-fl-amidonaphthalene
C JO H 6 .NO.NH 2
C 10 H 8 ON 2
150-152
Ilinski
B., 17, 392
46, 1035
Nitronaphthylamine
NH 2 .NO,=a,; a.
C 10 H 8 2 N 2
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
=fti ;
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-
C 10 H 6 (NOH) 2 =a 1 1 ;
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 ; NO 2 =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.N 2 .0 ( .,H 3 .COOH
1 J
230 p.d.
Widmann
B., 17,724
46, 1022
acid
Nitro-amido-a-naphthol
OH.NH 2 .NO 2 =ra(!).,
C 10 H 8 3 N 2
130
Ebell
B., 8, 564
28, 900
Nitromethylcarboatyril
tJ
181
Feer and Konigs
B., 18, 2397
48, 1235
Nitrophenylsuccinimide
NO J .C 6 H 4 .N.CO.(CH 2 ) 2 .CO
C 10 H 8 4 N 2
....
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
N0 2 .C 6 H 4 .N.CO.(CH,,) 2 CO
C 10 H 8 4 N 2
....
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. C e H 2 (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 ....
NO 2 .[CH I C(NO 2 ).CO 2 Me]
C 10 H 8 6 N 8
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.C0 2 H).OMe.(N0 2 )..
C IO H 8 7 N 2
192-193
Perkin
....
39, 417
Dinitrodiacetylhydroquinone
(OAc) 2 .(N0 2 ) 2 =1.4.(?) 2
C, H 8 8 N 2
...
94
Hesse
A., 200, 246
38, 317
JJ JJ
Jl
cf.A.,215,143
96
Nietzki
B., 11, 470
Ethylic dinitrophthalate
CO 2 Et.CO 2 H.(NO 2 ) !! =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
C 10 H 9 ON
75
Peine
B., 17, 2113
46, 1344
nitril
11 51
JJ
11
80^81
Pinner
B., 17, 2010
46, 1292
Acetamidophenylacetylene ....
C 6 H 4 (NHAc).C!CH=1.2
C 6 H 4 .CH 2 .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,/3 1 ;
246-247 u.c.
Friedlander and
B., 15, 336
42, 733
carbostyril)
Ostermeier
I =i; a i
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 a 2
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 !
=a 1 1 ; /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 = a i 5 ft a i
....
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 ^ a l J a i a 2
....
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.NH a
C 10 H 9 O a N
...
129-130
Claisen & Antweiler
B., 13, 2124
40, 169
Phenyl suceinimide (cf. A.,
Ph.N.CO.(CH 2 ) 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
C 6 H 4 .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
C 6 H 4 .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 .... ....
C 6 H 4 .CO.CO.NEt=1.2
i i
C 6 H 4 .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
C 9 H 8 N.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.CO 2 H
JJ
C lt) 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
C 6 H 4 .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.CH 2 .CH(OH).CO
C 10 H 9 3 N
....
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
N0 2 .(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
C 6 H 4 .CO.N(OEt).CO=1.2
270 p.d.
103-104 u.c.
Cohn
A., 205, 295
40, 586
I i
Acetyldioxindole
fr. C 6 H,.CH(OH).CO.NH
MM
127.
Suida
B., 12, 1327
36, 937
1 1 1
Aniido--methylumbelli-
i,Z
C 6 H 2 (NH 2 )(OH).CMe : CH.
247
Pechmann & Cohen
B., 17, 2138
46, 1332
i
ferone
COO=?.1.4.5
i
1
Nitroacetamido-a-toluic nitril
NHAc.NO 2 .(CH 2 .CN)=1.2.4
C 10 H 9 3 N 3
....
112-113
Gabriel
B., 15, 836
42, 1070
Isomtrosomethyldioxyquini-
C 6 H 4 .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
C 10 H 9 4 N
230 d.
Arppe
A., 93, 354
i i
Nitrobenzoylacetone
NO 2 .(CO.CH 2 .COMe)=1.2
..
55
Gevekoht
A., 221, 323
46, 445
Methylic nitrocinnamate ....
NO^CH : CH.CO 2 Me)=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.CO 2 H)=1.2
II
160
Suida
B., 11, 586
34, 586
Nitropropenylbenzoic acid ....
CO 2 H.NO 2 .(CMe : CH 2 )
....
154-155
Widmaun
B., 15, 2552
44, 330
=1.3.4
Nitrosobenzylmalonic acid ....
Ph.CH 2 .ON : C(COjH),
C 10 H 9 5 N
cf. B., 16, 609
120 d.
Conrad and Bischoff
A., 209, 217
42,39
Nitromethoxycinnamic acid
(CH : CH.C0 2 H).OMe.N0 2
n
....
238
SchnelL
B., 17, 1383
48, 1165
=1.2.5
Acetamidoisophthalic acid ....
(CO 2 H).NHAc. = 1.3.?
m
....
270-280 d.
Hofmann
B., 9, 1301
31, 90
Nitrophenylazo-acetoacetic
NCv(N 2 .CHAc.CO 2 H)=1.2
C IO H y 5 N 3
black 183
185
Bamberger
B., 17, 2417
48, 557
acid
Nitroacetamidonitrocinna-
(CH : CH.N0 2 ).NHAc.NO a
250-252
Friedlander and
A., 229, 233
48, 1139
mene
=1.4.?
Lazarus
Dinitroacetamidocinnamene
(CH:CH 2 ).NHAc.(N0 2 ) 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
(C0 2 Me) 2 .NO 2 =1.3.5
C 10 H 9 6 N
....
121-5
Beyer
J. p. [2], 25, 490
42, 1294
Ethylic nitrophthalate
(CO 2 Et).(CO 2 H).NO 2
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....
C 7 H 6 N.(CO 2 H) 3
....
212 d.
Hantzsch
A., 215, 52
44,85
Nitromeconin....
159-160
Anderson
A., 98, 47
iii., 863
Methoxycinnamic acid diazo-
(CH:CH.C0 2 H).OMe.
C 10 H 9 6 N 3
d. 151-152
Schnell
B., 17, 1385
46, 1165
nitrate
(N:N.N0 3 )=1.2.5
Nitroacetoisovanillic acid ....
CO 2 H.OAc.OMe.NO 2
C 10 H 9 7 N
....
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
C0 2 H.(OMe) 2 .COH.N0 2 =2
ii
....
166
Prinz
J. p. [2], 24, 357
42,402
.... ...
=2
248-249
Wegscheider
M. C., 4, 262
44, 998
Nitrohemipinic acid
(C0 2 H) 2 .(OMe) 2 .NO ;j
C 10 H 9 8 N
155
Prinz
J. p. [2], 24, 359
42, 402
=1.2.3.4.?
Benzenylazoximpropenyl ...
Ph.c : N.o.CEt : N
L 1
C 10 H I0 ON 2
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
C 10 H I0 ON 2
262
Liquid
Knudsen
B., 18, 1071
48, 898
i >
ethenyl
Acetamido-a-toluic nitril ...
NHAc.(CH 2 .CN)=1.4
)J
....
95-97
Gfebriel
B., 15, 835
42, 1070
Acetamido-a- (or /S-) phenyl-
NHAc.C 6 H 4 .C 2 H 2 N=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-
C 6 H 3 Me.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
C 10 H 10 3 N 2
65
Gross
B., 18, 1076
48, 898
I i
methenyl
Tolylhydantom
Me.(N.CO.NH.CO.CH 2 )=1.2
))
176
Ehrlich
B., 16, 743
44, 1106
i i
it " *"
=1.4
)1
210
Schwebel
B., 11, 1128
34, 798
Ethylindoxylnitrosamiiie ...
C 6 H 4 .C(OEt) : CH.N.NO
i i
)
84-85
Baeyer
B., 15, 781
48, 1102
=1.2
Ethylnitrosoindoxyl
C 6 H 4 .C(OEt) : C(NO).NH
5)
....
135
j)
B., 15, 784
=1.2
Ethylisatoxime
C 6 H 4 .C(NOEt).C(OH) : N
))
138
Baeyer and Com-
B., 16, 1707
44, 1131
I I
= 1.2
Sl/ULK
Ethylpseudoisatin-/3-oxime ....
C 6 H 4 .C(NOH).CO.NEt=1.2
I 1
160-162
Baeyer
B., 16, 2196
46,75
Ethoxycyanamidobenzoyl ....
C 7 H 5 (CN)NO.OEt
>J
*...
173
Griess
B., 2, 416
m-nitrocuminonitril
CN.Pr.NO 2 =?
....
71
Czumpelik
B., 2, 183
Azobenzene acetacetic acid ..,.
Ph.N 2 .CHAc.CO 3 H
C 10 H 10 3 N 2
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 .CH 3 (?)
))
....
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
N0 2 .(NH.CO.C0 2 Et)=1.2
C 10 H 10 6 N 2
....
112
Hubner
A., 209, 368
42, 180
Ethylic nitrophenylisonitro-
N0 2 .[C(NOH).CO 2 Et]=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
(CH 2 .CO 2 Et).(N0 2 ) 3 =1.2.4
C^H^OeN,
35
Gabriel and Meyer
B., 14, 824
Dinitrocuminic acid
C0 2 H.Pr.(N0 2 ) 3
))
cf. A., 69, 244
220
Lippmann and
B., 12, 79
Strecker
Dinitrodurylic acid
Me b .NO 2 .CO 2 H=1.2.4.3.6.5
II
205
Gissmann
A., 216, 207
44,334
Diacetdiamidodinitrobenzene
N 2 H 2 Ac 2 .(NO 2 ) 2 =?
C 10 H 10 6 N 4
....
245-246
Norton and Elliot
B., 11, 328
34,417
5)
(NHAc 2 ).(N0 2 ) 2 =1.4.(?) 3 '
))
258
Biedermanu and
B., 7, 1532
Ledoux
Ethylic dinitromethoxy-
CO 2 Et.OMe.(NO 2 ) 2 =1.2.(?)2
C 10 H 10 7 N 2
47
Salkowski
A., 173, 50
28,72
benzoate
j jj
=1.4.(?) 3
79
jj
A, 163, 59
Methylic dinitroethoxyben-
CO.,Me.OEt.(NO 2 ) 2 =1.2.(?) 2
)
80
jj
A., 173, 43 ; B.,
vii., 336
zoate
4,872
28,71
Methylic dinitrohydroxy-
OH.(NO 2 ) 2 .(CH 2 .CH 2 .
....
87
Stohr
A., 225, 57
46, 1350
phenylpropionate
CO 2 Me)=1.2.6.4
Dinitromethoxyphenylpro-
OMe. (NO 2 ) 2 . (CH 2 .CH 2 .COjH)
124
jj
J!
jj
pionic acid
=1.2.6.4
Benzoyltrimethyleneoxime ...
Ph.C(NOH).CH.CH 2 .CH 2
C 10 H n ON
86-87
Perkin
B., 17, 1442
44, 1155 ; 47,
! 1
845
Benzoylacetonamine
....
)
....
143
Fischer and Billow
B., 18, 2134
48, 1237
Mesitylcarbiruide
Me 3 .(N : CO)=1.3.5.6
218-220
Liquid
Eisenberg
B., 15, 1016
42, 956
Carbomesyl ,
C 6 H 2 Me.CH 2 .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.NAc 3
C 10 H U 2 N
....
Ill
Hofmann
B., 3, 771
24, 140 ; vii.,
946
Benzoylacetoxime
Ph.CO.ON : CMe 2
M
....
41-42
Janny
B., 16, 172
44, 581
Benzylic iso-nitrosoacetone
CH 3 .CO.CH : N.O.CH 2 Ph
j>
45-46
Meyer and Ceresole
B., 15, 3072
44, 572
>
244 u. c.
Ceresole
B., 16, 835
PhenylisonitroetLylmethyl
CH 3 .CO.CH,,C(NOH).Ph (?)
jj
....
65-5-66
)>
B., 17, 813
46, 1167
ketone
Benzylisonitrosoacetone
Ph.CH 2 .0(NOH).CO.CH 3
>
....
80-81
B., 15, 1876
44, 41
is ,,
I)
))
81
Meyer and Ceresole
B., 15, 3072
44, 572
Anilacetoacetic acid
Ph.N : CMe.CH,.CO 3 H
....
81
Knorr
B., 16, 2595
46, 334
Phenylacetimido-acetate
Ph.CH 2 .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.NH 2 )=1.4
)
186
Perkiii
J. [1877], 792
31, 411
n
=1.2
....
191-192
jj
J. [1877], 793
31, 415, 421
Amidopropenylbenzoic acid
COOH.C 3 H 5 .NH 2 =1.4.5
Tl
93-94
Widmann
B., 16, 2573
46, 317
Tetrahydroquinoline car-
N.COOH= ai ; j3, or a s
)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).CO s Me
C 10 H U 3 N
55-56
Mtiller
B., 16, 2987
46, 584
acetate
.
Ethylic phenylisonitroso-
Ph.C(NOH).CO 2 Et
J
112-113
Gabriel
B., 16, 519
44, 920
acetate
Ethylic phenyloxamate
NHPh.CO.CO 2 Et
)
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.CH 2 .CO 2 Me
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.CO 2 H
I)
....
110
Lossner
J. p. [2], 10, 254
28, 641
Benzoyllactamide
CH 3 .CH(OBz).CO.NH 2
....
124
Wisliceuus
A., 133, 281
vi., 772
Phenaceturic acid
Ph.CH 2 .CO.NH.CH 2 .CO 2 H
5
143
Salkowski
B., 12, 654
36, 662
Acetylphenamido-acetic acid
Ph.NAc.CH 2 .CO 2 H
185-186
Giacosa
Z. P. C., 8, 95
46, 1061
Phenylsuccinanaraic acid ....
NHPh.CO. (CH 2 ) 2 .OO 2 H
)
....
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.(CH 2 .CO 2 H)=1.2
))
....
142 d.
Suida
B., 12, 1328
), ) )T
=1.4
V
168-170
Gabriel
B., 15, 841
Malontoluidic acid
Me.(NH.CO.CH 2 .C0 2 R)=1.4
51
....
156 d.
Eugheimer and
B., 17, 740
46, 1023
Hoffmann
Dimethamidobenzoylformic
NMe 2 .(CO.CO 3 H)=1.4
)
....
187
Michler and Han-
B., 10, 2081
34, 421
acid
hardt
p-toluric acid ....
(C 2 H 2 O).NH.C 7 H 7 .CO 2 H
Ifift 1f{>i
Kraut
A., 98, 360
v., 869
Nitro-cuminic aldehyde
COH.Pr3.NO 2 =1.4.6 "
5J
AUVJ 1 U*J
Liquid
Einhorn and Hess
B., 17, 2019
46, 1352
COH.Pr.N0 2 =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.NH 2
))
189
Schnell
B., 17, 1384
46, 1165
=1.2.5
Hippuryl carbamide
NHBz.CH 2 .CO.NH.CO.NH.,
C 10 H 11 3 N 3
216 d.
Curtius
B., 16, 757
44, 1088
A midopheny lazoace tacetic
NH 2 .(N 2 .CHAc.C0 2 H)=1.2"
)>
157 d.
Bainberger
B., 17, 2420
48, 157
acid
Nitrotolylazoacetone
Me.NO 2 .(N 2 .CH 2 .CO.Me)
134-134-5
B., 17, 2421
48, 158
= 1.3.4
Pheuylmalamic acid
NHPh.CO.CH(OH).CH 2
C.OH.AN
145
Arppe
A., 96, 106
iii., 798
C0 2 H
Nitro-/9-phenyl lactylmethyl
N0 2 .[CH(OH).CH 2 .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
N0 2 .(CH 2 .CO 2 Et)=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
CO 2 H.(NH.CO 2 Et)=1.3
C 10 H n 4 N
cf. B.,11, 701
189
Griess
B., 9, 796
30, 413
Dimethylic amidoisophtha-
(CO 2 Me).,.NH 2 =].3.5
176
Beyer
J. p. [2], 25, 504
42, 1296
late
Ethylic p-nitrotoluate
(CO 2 Et).Me.NO 2 =?
55
Beilstein & Kreuslei
A., 144, 174
Nitrotolylpropionic acid
Me.NO 2 .[(CH 2 ) .CO..H]
130-136
Effront
B., 17, 2328
48, 152-
=1,2.5
Propylnitrobenzoic
CO 2 H.Pra.NO 2 =1.4.?
....
113
Korner
A., 216, 230
Isopropylnitrobeuzoic acid ....
CO 2 H.Pr/3.NO 2 =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
C 3 H 5 .OMe.OH.N0 2 = 1.3.4.5
43-44
Weselsky & Benedikt
M. C., 3, 388
42, 1201
Nitroxylylacetic acid
Me 2 .NO 2 .(CH 2 .CO 2 H)
"
....
139
Wispek
B., 16, 1579
44, 1096
Niti odiacetdiamidobenzene ...
(NHAc) 2 .NO 2 =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
C 9 H 8 NMe(NO 2 ) 2
D
148
Feer and Konigs.
B., 18, 2390
48, 1245
Phenyltartaramic acid _
NHPh.CO.(CH.OH) 2 .C0 2 H
C 10 H U 5 N
180 d.
Arppe
A., 93, 355
Ethylic nitromandelate
NO 2 .[CH(OH).CO 2 Et]=1.3
63
Beyer
J. p. [2], 31, 382
48, 983
Methylic nitrophenyl /3-lac-
NO 2 .[CH(OH).CH 2 .CO 2 Me)
.,
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
N0 2 .OMe.C0 2 Et=?.1.4
,,
....
98-100
Cahours
A. C. [3], 14, 492
i., 302
Methylic nitrohydro-p-cou-
NO 2 .OH.(CH 2 .CH 2 .CO 2 Me)
64
Stohr
A., 225, 57
46, 1350
marate
=U.4
Nitrohydroxyisopropylben-
NO 2 .(CMe 2 OH).CO 2 H=5.4. 1
n
....
190-191
Widmann.
B;, 15, 2549
44, 330
zoic acid
Ethoxynitrotoluic acid
CO 2 Et.Me.OEt.NO 2 =1.4.2.?
....
161-162^
Paterno & Canzoner
G. I., 9, 455
38, 247
Ethylic acetylcomenamate ....
C s H 2 N.OH.OAc.CO !! Et
fr. pyridine
152
Ost
J. p. [2], 29, 57
48, 49
?
NO 2 .[C(NH 2 ) : N.O.CO 2 Et]
C 10 H U 6 N 3
.... .
152-153
Schopff
B., 18, 1066
48, 896
=1.3
Methylic nitro-dimethylpro-
C0 2 Me.(OMe) 2 .N0 2 =1.3.4.?
C 10 H u OiN
127-128
Matsmoto .
B., 11, 134
34,502
tocatechuate
Methyh'c nitroveratrate
,,
-
143-144
11-
B., 11, 132
34, 501
dinitro-amidohydro-
NH 2 .(NO 2 ) 2 .(CH 2 .CH 2 .
C 10 H U O 6 N 3
102
Stohr
A., 225, 57
46, 1350
cinnamate
CO 2 Me)=1.2.6.4
Trinitroisocymene
Pr0.Me.(NO 2 ) 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
Me 2 .Et.(NO 2 ) 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.(NO 2 ) 3 =1.4
C 10 H n 7 N 3
..
111
Lallemand
A. C. [3], 49, 153
v., 795
Trinitrodiethoxybenzene
(OEt) 2 .(N0 2 ) 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.N 2 H 2 Ph(C 3 H 5 )
C 10 H 12 ON 2
....
96-97
Maly
Z. C. [2], 5, 263
vi., 1089
a-phenylhydrazidoisobutyric
Ph.N.CMe 2 .CO.NH
175
Eeissert
B., 17, 1459
46, 1153
anhydride
1 1
Toluene azoacetone
Me.(N s .CH 2 .COMe)=1.4
n-
114-115
Eichter & Miinzer
B., 17, 1928
46, 1342
Tetrahydroquinoline carba-
C,H 10 N.CO.NH,
....
146-5
Hoffmann and
B., 16, 733
44, 1144
mide
Konigs
Methylphenylhydrazinepyro-
Ph.NMe.N : CMe.CO 2 H
C 10 H 12 O 2 N 2
78 ; sf. 70
Fisher and Jourdan
B., 16, 2245
46, 53
racemic acid
Propionylbenzenylainidoxime
NH 2 .CPh : NO.CO.Et
IT
....
93
Schulz
B., 18, 1084
48, 897
Ethylphenylhydrazinegly-
N 2 EtPh : CH.CO 2 H
....
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.CH 2 .C(NH 2 ) : NOAc
C 10 H 12 O 2 N 2
....
124
Kuudsen
B., 18, 1070
48, 897
oxime
Phenylpropionylcarbamide ....
NHPh.CO.NH.C 3 H 5 O
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 ....
NH 2 .CO.(CH 2 ) 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
C 6 H 4 [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
(CH 2 .CO.NH 2 ) 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
C 9 H 9 NMe.NO 2
...
93-94
Feer and Konigs
B., 18, 2390
48, 1245
Ethylic phenylallophanate ....
NHPh.CO.NH.CO 2 Et
IO H 12 S N S
....
120
Stojentin
J. p., 32, 1
48, 1196
benzenylamidoxime
NH 2 .CPh : N.O.CO 2 Et
>j
127
Falck
B., 18, 2467
48, 1217
carbonate
Acetylphenylhydroxyethen-
HO.CHPh.C(NH 2 ) : 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
NO 2 .NEtAc=1.4
))
117-5
Weller
B., 16, 31
44, 579
>!
))
MM
118
Nolting and Collin
B., 17, 267
46, 1013
Ethylic benzenylamidoxime-
C0 2 Et.[C(NH 2 ) : N.OH]=1.4
))
135
Miiller
B., 18, 2486
48, 1227
carboxylate
Urethane benzaniide
(CO:mi 2 ).(NH.CO 2 Et)=1.3
....
157-158
Wachendorff
B., 11, 704
34, 675
Ethylic uramidobeuzoate ...
CO s Et.(NH.CO.NH ! )=1.3
ij
....
176
Griess
J. p. [2], 4, 293
25,81; vii., 166
Dimethamidophenyloxamic
NMe- 2 .(NH.CO.C0 2 H)=1.4
))
....
192 d.
Sendtner
B., 12, 531
36, 627
acid
Tolylhydautoic acid
Me.[N(CO.NH s )(CH 8 .CO 2 H);
:j
....
d. w. m. 200
Schwebel
B., 11, 1129
34, 798
=1.4
Acetamidonitroethylbenzene
Et.NHAc.NO 2 =1.4.?
-....
45-47
Paucksch
B., 17, 770
46, 1143
Nitroacetoxylidiue
Me 2 .NHAc.NO 2 = 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-
NO 2 .[CH(OH).C(OEt) : NH;
C 10 H 12 4 N 2
84
Beyer
J. p. [2], 31, 382
48, 983
imidoether
=1.3
Ethylic uitramido-a-toluate...
(CH2.CO 2 Et).NO 2 .NH 2 =1.2.4
J)
....
100
Gabriel and Meyer
B., 14, 825
40, 730
Dinitrocymene
Pr.Me.(NO 2 ) 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
Me 4 .(N0 2 ) 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.(N0 2 ) 2 =?
Q 10 H 12 S N 3
....
93
Studer
B., 14, 1474
40, 898
,, ..
i)
>
cf. A., 21 1,244
93
Liebmann
B., 14, 1843
Nitroacetamidodimethyl-
(OMe) .NHAc.N0 2 =1.4(?) 2
)J
....
164
Baessler
B., 17, 2121
46, 1329
quinol
Dinitrothymol
PrMe.QH,(NO 2 ) 2 =1.4.6.(?)
JJ
cf.B., 10,611
55
Lallemand
A. C. [3], 49, 152
v., 795
a-dinitrodiethoxybenzene ...
(OEt) s .(NO s ) s =lA2.?
C 10 H I2 6 N 2
....
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) ;! .(NO 2 ) 2 =1.4.2.?
(OEt) 2 .OH.(N0 2 ) 2 =1.4.2.(?) 2
CMe 2 1 NO.CHjPh
Ph.CH : NOPr
Ph.NEt.Ac
))
Ph.NMe.C 3 H 5 O
Ph.NH.OC.(CH ) 2 .CH 3
C 10 H 12 8 N 2
C 10 H 12 0-N 2
C 10 H I3 ON
)
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)=?
Me 2 .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
Me 3 .(NH.CHO)=2
N.OMe=a, ; ft
(NMe).OH=a, ; a,
N.Me.OH=a,/3 1 ; a,
NHAc.NHC 2 H 3 .NH 2 =?
Ph.CH(OH).C(OEt):NH
NH 2 .CHPh.(CH 2 ) 2 .C0 2 H(?)
NHPh.CO 2 Pr
NHPh.CO 2 Pr0
NMePh.C0 2 Et
NHPh.CH 2 .CO 2 Et
CH 3 .CH(NHPh).CH 2 .CO 2 H
NHPh.CMe2.COjH
?)
))
C 10 H 13 ON 3
C 10 H 13 2 N
j)
j)
)?
)
j)
'
282-283
...4
278-282
+2H 2
+5H 3 O
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
C 10 H 13 3 N
.
96-7 u. c.
Wagner
J. p. [2], 32, 70
48, 1212
Methylic dimethamidoben-
NMe s .CO a Me=1.3
M
270 u.c.
Liquid
Griess
B., 6, 587
26, 1146; vli.,
zoate
187
Ethylic tolylcarbamate
Me.(NH.CO s Et)=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.NO 2 =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.CO 2 H.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
Me 2 .(NH.CH 2 .CO 2 H) = 1.3. ?
.,
....
132-134
Ehrlich
B., 16, 206
44, 594
Nitrosopropylcresol
Pr.Me.OH.NO 2 =?. 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 ....
Me 4 .NO 2 =l. 2.3.5.6
11
MM
165
Ador and Killiet
B., 12, 332
36, 527
Ethylic lutidinecarboxylate
N.Me 2 .CO 2 Et=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-
C 5 HMe 3 NMe.COO
abt. 340
102-103
Hantzsch
B., 17, 1025
46, 1045
i i
nyunde
Dimethamidophenyl oxamide
NMe 2 .(NH.CO.CO.NH 2 )=1.4
C 10 H 13 2 N,
....
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.NO 2 =1.2
C 10 H 13 3 N
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.CH 2 .CO 2 H)=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
CO 2 H.NH 2 .(CMe. ! .OH)
J
nf. 270
Widmaun
B., 16, 2571
46, 317
acid
=1.3.4
Nitrocarvacrol
Pr.Me.OH.NO 3 =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 / 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]
. 1J 11, 1 - i
^*v oyo
1 OQ 1 *>(!
GT in OIQ
00 QQQ
n
11 11
J J
.....
13O 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.Me 2 .OH.CO 2 Et=?
)1
140
Collie
A., 226, 294
48, 374
boxylate
Nitrodiethoxy benzene
(OEt) 2 .N0 2 =1.4.5
C 10 H 13 4 N
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.NO 2 =11.2.1
C 10 H 13 4 N
....
124
Pastronich
M. G, 4, 191
44, 1006
Ethylic ethylcomenamate ....
C 5 H 3 EtNO 2 .CO 2 Et
114-115
Mennel
J. p. [2], 32, 176
48, 1204
Ethylic dimethylpyrroline
N.Me 2 .CO 2 H.CO 2 Et
....
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
NEt 2 .(NO 2 ) 2 =1.2.4
C 10 H 13 4 N 3
....
180
Lippmann and
M. C., 4, 788
46, 179
Fleissner
Diethylnitropyrogallol
(OEt) 2 .OH.N0 2 =?
C 10 H 13 5 N
....
123
Weselsky and Bene-
M. G, 2, 217
42,54
dikt
Ethylic phenylethenylamid-
Ph.CH 2 .C(NH 2 ) : NOEt
C 10 H 14 ON 2
....
58
Knudsen
B., 18, 1072
48, 897
oxime
a-Phenamidoisobutyramide....
NHPh.CMe 2 CO.NH 2
J*
....
137
Tiemann
B., 15, 2042
44, 199
Nitrosodiethylaniline
C 6 H 4 .NO.NEt 2 =1.4
M
....
84
Kopp
B., 8, 622
,, ....
....
84
Lippmann and
B., 16, 1422
Fleissner
Acetyldimethdiamidobenzene
NMe 2 .NHAc=L4
335 d.
130
Wurster
B., 12, 525
36, 627
jj
....
131
Witt
....
36,360
Propylphenyl carbamide ....
NH 2 .CO.NH.C 6 H 4 Pr=1.4
l)
143
Francksen
B., 17, 1225
46, 1008
Toluidopropionamide
Me.(NH.CHMe.CO.NH 2 )
125
Tiemann & S tephan
B., 15, 2038
44, 199
=1.2
=1.4
i)
....
145
n
B., 15, 2037
Pseudocumylcarbamide
Me 3 .(NH.CO.NH 2 )=?
t)
..
d.w.m. 227
Engel
B., 18, 2233
48, 1216
Diazocamphor
C 8 H 14 .c7c.N : N.6
....
73-74
Schiff
B., 14, 1375
42,527
Diisobutyryl dicyanide
....
C 10 H 14 2 N 3
226-228
L. 15
Moritz
....
39, 14
Dibutyryl dicyanide
....
j
232-235
....
....
39, 17
Ethylic phenyhydroxy-
HO.CHPh.C(NH 2 ) : NOEt
....
89
Gross
B., 18, 1079
48, 898
ethenylamidoxime
Nitrodiethylaniline
N0 2 .NEt 2 =1.4
....
76
Lippmann and
B., 16, 1422 ;
44, 868, 1100
Fleissner
M. G, 4, 284
Diamidocuminic acid
CO 2 H.Pr0.(NH 2 ) 2 =?
....
192
Lippmann
B., 15, 2144
44, 194
Phenylacediamine acetate ....
Ph.CH 2 .C(: NH).NH 2 +HAc
....
192-193
Bernthsen
B., 8, 1320
29, 607
Fr. juglone
C 6 H 2 2 (NMe 2 ) 2
....
173-174
Mylius
B., 18, 467
48, 804
Ethoxycaffeme
C 8 H 9 N 4 2 .OEt
C 10 H 14 3 N 4
....
140
Fischer
B., 14, 640; A.,
40, 614 ; 44,
215, 253
355
Methylphenylpropylalkine ....
NPhMe.C 3 H 6 .OH
C 10 H 15 ON
262
*.
Laun
B., 17, 678
46, 1011
Ethylphenylethylalkine
NPhEt.C 2 H 4 .OH
267-268-5
....
B., 17, 677
Diethamidophenol
OH.NEt 2 =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.NMe 2 =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.C 3 H 6 .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.C 2 H 4 .OH)= 1 .4
290-300
Liquid
Demole
B., 7, 637; A.,
27, 903
dine
173, 133
C, n H,, : N.OH
v. C 10 H 17 ON
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.NH 2 =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.NH 2 =1.3.4 or
C 10 H 15 ON
....
153
Wiirster&Sendtnei
B., 12, 1807
38, 110
zene
1.4.3
,,
+H 2
82
Camplierimide
C IO H 15 2 N
A., 60, 329
180 s. t.
Ballo
A., 197, 332
Hydrazineaniso'il carbamide
MeO.(N s Hj.CO.NHt)=1.2
G 10 H 15 2 N 3
110
Reisenegger
A., 221, 314
46, 440
Nitrocamphor
. C 10 H 14 .OH.N0 2
C 10 H 15 3 N
83
Schiff
B., 13, 1403
38, 891
Amidocamphoric anhydride
C 8 H 13 (NH 2 ):(CO) 2 .0
sb. 150
208
Wreden
A., 163, 339
26, 896; vii.,
237
Diethylic y-amidoisophtha-
(C0 2 Et) 2 .NH,=1.3.?
C l( ,H 15 4 N
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
?
C 4 H 3 O.C(NH 3 .C 2 H 3 2 ).
305-310
153
Tonnies and Staub
B., 17, 856
46, 1130
CMe 2 .O
i
Ethylic diethylcyanurcar-
C 3 Et 2 O 3 N 3 .COjEt
C.oHjjO.N,
....
107
Wurtz and Henn-
C. R., 100, 1419
48, 969
boxylate
inger
Methoxycyanconiine
C 9 H 1S N( : NH).OMe
C 10 H 16 ON 2
225
.....
Meyer
J. p. [2], 126, 353
44, 353
Methylhydroxycyanconiine
C 9 H 13 N( : NMe).OH
275-276
76-5
J. p. [2], 126, 348
Dimethoxyhydroxycaffeine ...
C 8 H 9 O 2 N 4 .OH.(OMe) 2
C 10 H 16 5 N 4
....
178-179
Fischer
B., 14, 642
40, 614
Amidocamphor
C M H 14 .OH.NH 2
C 10 H 17 ON
246-4
solid
Schiff
B., 13, 1404
38, 892
Carvoxime
C 10 H 16 : NOH
v. C 10 H 15 ON
70-71
Goldschmidt and
B., 18, 2220
48, 1210
Ziirrer
Camphoroxime
it
249-254
115
Nageli
B., 16, 498
44, 728
Isocamphoroxime
HO.C 9 H )5 :C1NH(?)
125
B., 17, 806
46, 1190
Acetyl y-coniceme ....
C 8 H 14 AcN
252-255
Liquid
Hofmann
B., 18, 116
48, 563
Methoxycyanethine ....
C 9 H 14 N 3 .OMe
C 1U H 17 ON 3
130
Riess
J. p. [2], 30, 145
48, 235
Ethylic mesitylate
C r H 12 O.CO 2 Et
C 1U H 17 3 N
290
85
Pinner
B., 15, 578
42, 941
,,
)5
J)
....
tO
B., 14, 1074
40, 796
Amidocamphoric acid
C 3 H I3 .NH 2 .(C0 2 H) 2
C 10 H 17 4 N
....
160
Wreden
A., 163, 340
25, 896
Ethylimidodiethyldioxamide
NEt(CO.CO.NHEt) 2
C 10 H 17 4 N 3
135-138 d.
Schiff
B., 17, 403
46, 907
Campholenic nitril+hy-
C 9 H u ,.CN+NH. i .OH
C 10 H 18 ON 2
....
101
Goldschmidt and
B., 17, 2070
46, 1364
droxylamine
Ziirrer
Acetyl copellidine
C 8 H l6 AcN
C 10 H 19 ON
254
*..
Diirkopf
B., 18, 924
48, 817
Ethylic diethamidocrotonic
NEt 2 .CMe I CH.C0 2 Et
C U H 19 2 N
160-163(20)
-liquid
Kuckert
B., 18, 619
48, 750
acid
Ethylic oxyhexinamate
C 6 H r O(OEt) 2 .NH 2
C 10 H 18 3 N
....
78-7
Demarjay
A. C. [5], 20, 490
isooxyhexinamate ....
94-95
A. C. [5], 20, 492
ethyldiglycollamidate
....
C 10 H 19 4 N
200-220
.liquid
Heintz
A., 145, 230
Isobutylvaleryl carbamide ...
NHBu/s.CO.NH.C.H^O
C 10 H 2l) O,N s
....
02
Hofmann
B., 15, 758
42, 1053
Ethylidenepropylurethane ....
CH 3 .CH(NH.CO 2 Pr) 2
C 10 H 20 4 N 2
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
C 9 H 18 NOMe
I
U. i\J\J
4
Fischer
B., 16, 1606
44, 1153
Dinaethyloxyconine ....
C s H 15 Me 2 ON
I*
25-226
.liquid
Hofmann
B., 18, 119
48, 563
Ethyloxyconine
C 8 H 16 EtON
?J
40-242
....
Ladeuburg
B., 14, 2409
42, 166
Alkaloid fr. Lupinus lutens
C 10 H 21 2 N
69-270
2'5
Schulz
B. S. [1879], 874
38, 416
Tripropoxyacetonitril (?) ....
(PrO) 3 .CN (2)
C 10 H 21 3 N(?)
16-219
....
Bauer
A., 229, 163
48, 1121
Diisobutylglyoxylamide
(BuSO) 2 .CH.CO.NH a
....
2-45
Pinner and Klein
B., 11, 1479
36, 47
Dipiperal ly lal kam ine
....
C 10 IL 3 ON 2 (?)
80-290 p. d.
Liquid
Ladeuburg
C. R., 93, 338
40, 1158
Dioxyisoamylamine
(C 6 H n O) 2 NH
49-251
L. 20
Radziszewski and
B., 17, 839
46, 1190
Schramm
Allyl cyanide +ethylalcohol
C 4 H 6 N.3C 3 H 6
C 10 H SS 3 N
73-174
.liquid
Rintie
B., 6, 389
26, 880; vii., 49
Nitro-a-naphthonitril
C 10 H 6 .N0 3 .CN
C n H 6 2 N 2
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
C 10 H 6 .NO 2 .CN
C U H 6 2 N 2
....
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
C 10 H 5 (N0 2 ) 2 .C0 2 H
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
C 10 H 7 .N : CO
C U H 7 ON
269-270
Hofraann
P. K., 19, 108 ;
24, 139 ; vii.,
B., 3, 658
407, 844
CjsH^OjNst?)
C 11 H 7 O 3 N(?)
cf. A., 21 0,89
191
Hesse
A., 226, 241
48, 276
Nitro-[>-naplitlioic acid
COjlLNO^a!.?
C n H 7 4 N
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 = fl l-?
)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-
C 10 H 2 Me(NO 2 )(OH) 2 : 2
C U H 7 6 N
....
255-260
Thorner
B., 12, 1633
38,47
thaquiuone
Dinitrocitraconanil
....
C,,H 7 6 N 3
cf. A., 85, 21
120
Kudnew
Z. C. [2], 7, 203
24, 712
Trinitro-a-methoxynaphtha-
C le H 4 .OMe.(NO 2 ) 3
C U H ; 7 N 3
128
Staedel
B., 14, 900 ; A.,
40, 724; ,.44,
lene
217, 172
863
-s-
J)
J>
213
11
)>
n
Dipyridilcarboxylic acid
C 10 H 7 ON 2 .CO 2 H
C n H 3 2 N 2
....
179 .
Skraup
B., 15, 896
42, 1112
11 i>
....
182-5-184
Skraup & Vortmam
M. C., 3, 370, 597
44, 88
Tolnquinoxalinedicarboxylic
C c H 3 Me I (.N : C.C0 2 H)., :
C U H 8 4 N 3
....
d. 145
Hinsberg
B., 18, 1233
48, 910
acid
Dinitro-8-methylnaphthalene
C 10 H 5 Me(N0 2 ) 2
))
....
206
Schulze
B., 17, 844
46, 1184
a-naphthylformamide
C 10 H 7 .NH(CHO)
C U H 9 ON
....
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
C 10 H 7 .CO.NH 2
....
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.C 4 H 3 :NH
J)
77-78
Ciamician & Denn-
B., 17, 433, 2956
46, 1044; 48,
stedt
379
Phenylcitraconirnide
Ph.N : C 6 H 4 O 2
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
C 6 H 4 :(CO) 2 :NC 3 H 5 =1.2
n
....
70-71
Wallach & Kamensk
B., 14, 171
Hydroxfurfuraniline
C 6 H 4 (OH).NC 6 H 4 O=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.NO 2 =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
C 10 H 6 .OMe.NO=fta 1 ;(?)
C 10 H 9 2 N
....
75
Ilinski
B., 17, 2588
48, 168
11 11
=a l a 2 ;(?)
98-100
11
B., 17, 2591
11
Methyl /3-nitroso-a-naphthol
O : C 10 H, : 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
?
C 10 H 6 :0 2 :NMe
225
Zincke
B., 12, 1646
38, 49
Methamido-a-naphthaqui-
C 10 H 6 (NHMe):0 2
....
232 u.c.
Plimpton
....
37, 640
none
Amido-a-naphthoic acid
C 10 H,(NH 2 ).C0 2 H
,,
fr. C 2 H 6 O
Sll-812 u.c.
Ekstrand
B., 18, 78
48, 548
n ~ a ~ 11 11
11
f r. H 2 O
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 ; 3
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=a 1 ,/3 2 ;
....
232
Friedlander and
B., 16, 1838
44, 1149
ketone
Gohring
Methylquinoline carboxylic
N.Me.CO 8 H=a 1 AA ;
....
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,/3 1 /3 2 ;
....
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, ; |3 2
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 ....
NO 2 .(CH:CH.CH:'CH.
C U H 9 3 N
....
153
Einhorn
B., 17, 2027
46, 1345
CHO)=1.2
Acetyl-p-methylpseudisatin
...
....
172
Duisberg
B., 18, 197
48, 544
Phthalylpropionamide
C 6 H 4 : (C0) 2 : C 2 H 3 .CO.NH 2
....
193-195
Gabriel and Michael
B., 11, 1014
34, 735
=1.2
Indogenide of pyroracemic
NH.C 6 H 4 .CO.C : CMe.CO 2 H
,,
....
197
Baeyer
B., 16, 2199
46, 76
acid
=1.2
Phthalomethimidylacetic acid
NMe.CO.C 6 H 4 .C : CH.CO.H
n
....
212 d.
Gabriel
B., 18, 2453
48, 1228
I I
=1.2
Quininic acid
C 9 H 6 N(OMe).CO 2 H
....
280 d.
Skraup
M. C., 2, 592
42, 221
.... ....
11
....
280
Forst & Bohringer
B., 15, 521
42, 982
Ethylic nitrophenylpropiolate
NO 2 .(CiC.CO 2 Et)=1.2
C U H 9 4 N
....
60-61
Baeyer
B., 13, 2259
40, 275
=1.4
a
....
126
Drewsen
A., 212, 156
42, 847
Ethylic isatogenate
3O.C 6 H 4 .N.O.C.CO 2 Et
,,
cf.B.,15,V80
115
Baeyer
B., 14, 1741
42, 198
Nitrocinnamylacrylic acid ....
N0 2 .(CH : CH.CH I CH.
....
217-5
Diehl and Einhorn
B., 18, 2331
48, 1223
C0 2 H)=1.2
Succinylamidobenzoic acid ....
C 2 H 4 : (00), : N.C 6 H 4 .CO 2 H
....
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
C n H 9 4 N,
....
226
Conrad & Guthzeit
B., 15, 2849
44, 315
Nitrobenzoyltrimethylene-
CH 2 .CH 2 .C(C0 2 H).CO.C 6 H 4 .
C U H 9 S N
....
176
Perkin & Bellenot
B., 18, 960
48, 795
carboxylic acid
NO,=1.4
Nitrophenylparaconic acid ....
NO 2 .(CH : CH.CH 2 .CO 2 H)'
C U H 9 6 N
....
171
Bolomonson
B., 18, 2155
48, 1224
=1.3
>i 11
=1.4
M
163
11
11
11
Phenylfurfurazide
Ph.N 2 H : C 5 H 4 O
C U H 1() ON 2
....
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
C 10 H 7 .NH.CO.NH 3
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 .C0 2 H
CnHjoOjNj
....
120
Schulz
B., 18, 2459
48, 1219
carboxylic acid
1 1
Benzenyl barbituric acid ....
Ph.CH 2 .CH : (CO.NH) 2 : CO
....
206
Conrad & Guthzeit
B., 15, 2846
44, 314
Diacetylhydrazine benzoic
C 6 H 4 .CO.NAc.NAc=1.2
....
112
Fischer and Eenouf
A., 212, 336
42, 1069
anhydride
1 1
Hydroxycarboxytoluquin-
HO.C : N.C 7 H 6 .N : C.CO.NH
C U H 10 3 N 4
brown 250
258
Hinsberg.
B., 18, 1231
48, 909
oxaline ure'ide
1 1
CO.NH 2
Nitraniline furfurol
N0 2 .(NH.C 5 H 5 2 )=1.3
C U H 10 4 N 2
....
100-120 d.
Schiff
A., 201, 357
Pyrotartaronitranil ....
NO 2 .(N : C S H 6 O 2 )=1:4
....
155
Arppe
A., 87, 228; 90, 144
iv., 775
Nitrophenyl /3-acetylalanine
NO 2 .(CH.CH 2 .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 ....
C 6 H 3 Me.N:CH.CH:N
..
....
135-136
Hinsberg
B., 17, 321
46, 1053
=1.3.4+C 2 H 2 O 4
Nitrotolylsuccinimide
Me.NO 2 .(N:C 2 2 :C 2 H 4 )
....
140
Taylor
B., 8, 1225 ; A.,
29, 602; 42, 181
=1.7.4
209, 379
Ethylic nitrosoindoxanthi-
NH.C 6 H 4 .CO.C(OH).C0 2 Et
C U H 10 O 5 N 2
113d.
Baeyer, 'i
B., 15, 777
42, 1101
nate
I 1
Ethylic dinitrocinnamate ...
N0 2 .j;.CH : C(NO 2 ).C0 2 Et]
C u H 10 p 6 N 2
...*
?
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-
N0 2 .[CO.CH(NO).CO.jEt]
....
220
Perkin & Bellenot
B., 17, 328
46, 1024
acetate
=1.4
Acetylmethylketole
C 6 H 4 .CH:CMe.NAc=1.2
C u H n ON
*..
195-196
Jackson
B., 14,. 880
40, 734
Ethylcarbostyril ,.
C 6 H 4 .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
C 6 H 4 .NH.CO.CEt t CH=1.2
....
168
Baeyer & Jackson
B., 13, 121
38,407
Dimethylpseudoquinoxyl ....
OH 4 .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.CH 2 .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.CO 2 H
....
183
Fischer and Hess
B., 17, 566
46, 1181
Tolylsuccinimide
Me.(N.CO.C 2 H 4 .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-
NH 2 .(C;C.C0 2 Et)=1.2
j
....
55
Baeyer and Bloem
B., 15, 2148
44, 196
late
Amidocinnamylacrylic acid....
NH 2 .(CH:CH.CH:CH.
ji
176-5
Diehl and Einhorn
B., 18, 2333
48, 1223
CO S H)=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.(CH 2 ) 2 .co.
C n H n 2 N 3
....
168
Schulz
B., 18, 2463
48, 1219
carboxylaruide
i i
NH a
Isonitrosoantipyrine
C 6 H ( .N.NMe.CMe.OH
11
explodesSOO
cryst.
Knorr
B., 17, 2039
46, 1378
i
(NO).CO=1.2
|
Ethylic nitrosobenzoylace-
HO.N : CBz.CO 2 Et
C 11 H 11 3 N
120-121
Perkin
....
47, 244
tate
Itaconanilic acid
11
....
189 d.
Gottlieb
A., 77, 284
Acetamidocinnamic acid
NHAc.(CH:CH.C0 2 H)=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
KC 6 H 4 .C(OH).CH.C0 2 Et
)>
120-121
Baeyer
B., 14, 1742
42, 198
=1.2
Ethylindoxylic acid
N.C 6 H 4 .C(OEt).CH.CO 2 H
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.CH 2
J
T - 1
Nitroantipyrine
C 6 H 4 .N.NMe.CMe.CH
))
270-280
Knorr
B., 17, 2040
46, 1378
L
(NO,).CO=1.2
1
Ethylic nitrosobenzoylacetate
HO.N : CBz.CO 2 Et
C U H U 4 N
....
121-122
Baeyer and Perkin
B., 16, 2133
46, 64
Ethylic nitrocinnamate
N0 3 .(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
NA Cs .C0 2 H=1.2
11
....
220
Bedson and King
....
37, 757
?
NHMe.CO.C 6 H 4 .CO.CH 3 .
11
145 p.d.
Gabriel
B., 18, 2452
48, 1228
CO 2 H
Ethylic indoxanthinate
NH.C f H 4 .CO.C(.OH).CO 2 Et
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
NO 2 .(CO.CH 2 .CO 2 Et)=1.4
CnH.AN
....
49-50
Perkin & Bellenot
B., 17, 327
46, 1024
Ethylic benzanioxalate
CO 2 H.(NH.CO.CO 2 Et)=l .2
11
180-181
Baeyer
B., 15, 777
42, 1101
i)
=1-3
11
225
Schiff
B., 17, 402
46, 906
Benzamsuccinic acid
C0 2 H.(NH.CO.C 2 H 4 .CO ;1 H)
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.N0 2 .(N 2 .CHAc.CO J H)
CuH.ANs
....
176
Bamberger
B., 17, 2421
48, 157
=1.3.4
-nitro-orcyldiglycollic acid....
.*
C U H H 8 N
140
Saarbach
J. p. [2], 21, 170
Benzenylazoximebutenyl ....
Ph,C:N.O.CPr:N
1 1
C U H 12 ON S
265
Liquid
Schulz
B., 18, 1085
48,897
Dimethyloxyquinizine
)
....
113
Knorr
B., 17, 549
46, 1153
1 1
11 ....
C 6 H 4 .N.NH.CMe.CHMe.CO
))
....
127-132
Knorr and Blank
B., 17, 2050
46, 1380
' i
=1.2
Tolumethyloxyquinizine
C 6 H 3 Me.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.CF 2 .CMe.NHP
C 11 H 12 2 N 2
150
Wechsler
B., 18, 1040
48, 900
I 1
Ethylquinazol carboxylic aek
C S H 6 N( : NEt).CO 2 H
....
126
Fischer and Kuze
A., 221, 261
46, 442
?'
v. B., 16, 653
))
....
181
)
B., 16, 654
44, 812
Nitrosomethyldiacetamido-
NAc 2 .(CH 2 .NO)=1.2
C n H 12 3 N 2
....
127-5-128-5
Gabriel and Meyer
B., 14, 2340
42, 189
benzeue
Nitrosoethylamidocinnamic
NEt(NO).(CH : CH.C0 2 H)
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. (N 2 .CHAc.CO 2 H)= 1 .4
ji
....
180-190 d.
Zublin
B., 11, 1419
34, 880
Quinoline ethylic nitrate ...
C 9 H-N+Et.O.NO 2
)>
....
89 u. c.
Claus and Tosse
B., 16, 1278
44, 1009
Ethylic beuzoylallophanate ..
NHBz.CO.NH.CO 2 Et
C U H 12 4 N 2
163
Kretschmar
B., 8, 104 ; C. C
28,563; 31,615
[1876], 233
Hippuramidoacetic acid
NHBz.CH 2 .CO.NH.CH 2
J>
206-5
Curtius
J. p. [2], 24, 239 ,
40, 1144; 44,
CO 2 H
26, 175
338
Ethylic amidobenzamoxalate
(CO.NH 2 ).(NH.CO.C0 2 Et)
J)
191-5
Schiff
B., ir, 402
46, 906
=1.3
Benzamsuccinamide
C0 2 H.(NH.CO.C 2 H 4 .CO.
228-229
Pellizzari
B., 18, 214
48, 533
NH 2 )=1.3
Ethylic a-nitramidocinna-
N0 2 .NH 2 .(CH : CH.CO. 2 Et)
J)
....
158-160
Friedlander and
A., 229, 233
48, 1139
mate
=?.2.1
Lazarus
Nitrophenyl--acetylalanine
NO 2 .(CH.OH .CO.O.NH 2 Ac
i " i
C n H,AN 2
141-142
Einhorn
B., 16, 2647
46, 305
= 1.4
146-150
Easier
B., 17, 1496
46, 1173
Pyrotartaronitranilic acid ...
NO.,(NH.C 5 H 6 2 .OH)=1.4
1)
....
150.+
Arppe
A., 87, 228; 90,
iv., 775
145
Ethylic nitrotolyloxamate ...
Me.NO 2 .(NH.CO.CO 2 Et)
..
127-128
Hinsberg
B., 15, 2691
44, 323
=1.3.4
Nitroacetamidohydrocinnamic
NHAc.NO 2 .(CH 2 .CH 2 .CO 2 H
)
174
Gabriel and Steu-
B., 15, 844
42, 1073
acid
=1.2.4
deroann.
Ethylic dinitrohydrociimamic
(N0 2 ) 2 .(CH : CH.C0 2 Et)
C n H 12 6 N 2
,~.
32
Gabriel and Zirn-
B., 12, 601
36, 640
acid
=1.2.4.(?)
raermann
Methylic nitrophenylmeth-
N0 2 .[CH(OMe).CH(JSI0 2 ).
C n H 12 O.N 2
....
117 118
Friedlandaif and
A., 229, 210 ; B.,
48, 1138
oxynitropropionate
CO 2 Me]=1.4
Mahly -
16, 852
Ethylic dinitroethoxyben-
CO 2 Et.OEt.(NO 2 ) 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
CO 2 Me)=1.2.6.4
Ethoxydinitrohydrocinnamic
OEt.(NO 2 ) 2 . (CH 2 .CH 2 .CO 2 H)
M
126
acid
=1.2.6.4
Trinitroethoxyphenylure-
OEt.(NO 2 ) 3 .(NH.CO 2 Et)
C U H 12 9 N 4
....
211-212 d.
Kohler
J. p. [2], 29, 257
46, 1161
thane
= 1.(?) 3 .4
Phenylangelamide ....
Ph.C 4 H 6 .CO.NH 2
C,,H 13 ON
....
128
Perkin
J. [1877], 790
Acetylhydromethylketole ....
C 6 H 4 .CH 2 .CHMe.NAc=1.2
i i
))
....
55-56
Jackson
B., 14, 883
40, 735
Ethoxytetrahydroquinoline ...
NH.H 3 .OH=a 1 ft/3 i 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
C 6 H 4 CH 2 .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.(CH 2 ) 2 .CMe : NOH or
C U H 13 2 N
....
22-123
Paal
B., 16, 2868
46, 599
tone
Me.CO.(CH 2 ) 2 .CPh: NOH
Ethylic amidocinnamate
NH 2 .(CH : CH.CO,Et)=1.2
))
....
7-78
Tried lander and
B., 15, 1422
42, 1209
Weinberg
Ethamidocinnamic acid
NHEt.(CH: CH.C0 2 H)=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
....
C n H 13 2 N
d. 190
145-150
Schiff
A., 210, 118
42,304
acid
Isopropylnitrostyrene
(CH I CH 3 ).N0 2 .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.OO 3 H=a 1 ;/3, or a 3
...
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.CH 2 .CO 2 Et
C U H 13 3 N
....
38-30
Eugheimer and
B., 17, 740
46, 1023
Hoffmann
Ethylic hippurate
NHBz.CH 2 .CO 2 Et
)
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.C0 2 Et)=1.4
))
66-67
Klinger
A., 184, 285
31,712
Tolylsuccinamic acid
Me.[NH.CO,(CH 2 ) 2 .C0 2 H]
)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.CH 2 .CO.NH.CHj.CO.
CU^AN,
....
202
Curtius
J. p. [2], 26, 194
44, 339
NH 2
Diazoimidoethoxyphenylure-
N:N.C 6 H 3 (OEt).N.C0 2 Et
)
....
b. 100
Kohler
J. p. [2], 29, 257
46, 1160
thane
i i
Amidotolylazo-acetacetic acid
Me.<NH 2 .(N 2 .CHA c.CO 2 H)
162
Bamberger
B., 17, 2421
48, 158
=1.3.4
Diacetdiamidobenzamide ....
(NHAc) 2 .(CO.NH 2 )=1.3.5
a. 265
Muretow
Z. C. [2], 6, 642
vii., 130
Anilidopyrotartaric acid
C0 2 H.CMe(NHPh).CHj.
C n H 13 Q 4 N
101-102
Wechsler
B., 18, 1048
48, 900
C0 3 H
Ethylic nitrohydrociunamate
NQ s .(CH 2 .CH 2 .CO 2 Et)=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.N0 2 .(CH 2 .CHMe.C0 2 H)
n
....
139
Effront
B., 17, 2326
48, 152
=1.2.5
Ethylic nitromesitylenate ....
CO 2 Et.Me 2 .NO 2 =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.N0 2 .(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(co 2 Et).CH.: c :
C U H 13 5 N
+H 2
80-81
Lerch
M. C., 5, 367
48,46
CH.COjEt
Ethylic nitrophenyl-|3-lactate
N0 2 .[CH(OH).CH 2 .C0 2 Et]
....
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
C 6 H 4 (N0 2 )[C 2 H 3 (OH).CHO]
)>
125 p. d.
Baeyer & Drewsen
B., 16, 2205
46, 58
+acetic aldehyde
+CH 3 .CHO
Ethylic ethoxynitrobenzoic
CO 2 Et.OEt.NO 2 =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.N0 2 [(CH 2 ) 2 .C0 2 Et]
....
30
Stohr
A., 225, 57
46, 1350
=1.2.4
Nitrodiethoxybenzaldehyde
(OEt) 2 .N0 2 .CHO=1.4.?.5
H
129-130
Hantzsch
J. p. [2], 22, 472
40, 167
Methoxyisopropylnitroben-
Prf.OMe.N0 2 .C0 2 H=?
jl
145-146
Paterno & Canzoneri
G. I., 10, 233
38, 884
zoic acid
Dmitroacetpseudocumidide ....
Me 3 .NHAc.(NO s ),=1.3.4.(?) s
C U H 13 6 N 3
....
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
Me 3 .NHAc.(N0 2 ) 2
C U H I3 6 N 3
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
CO 2 Et.(OMe) 2 .NO 2 =1.3.4.?
C n H 13 6 N
99-100
Tiemann and Mats-
B., 9, 941 ; 1],
30, 524
moto
132
Trinitrolaurol (?)
....
C n H I3 6 N 3
..
84
Fittig and others
A., 145, 150
Ethylic dinitroamidohydro-
NH 2 . (N0 2 ) 2 .(CH 2 .CH 2 .CO 2
95
Stohr
A., 225, 57
46, 1350
cinnamate
Et)=1.2.6.4
Dimtroethoxyphenylure-
OEt.(N0 2 ) 2 .(NH.C0 2 Et)
C^H^N,
....
141
Kohler
J. p. [2], 29, 257
46, 1161
thane
=1.(?) 2 .4
Methyltrinitrothymol
Me.Pr.OMe.(NO 2 ) 3
)>
....
92
....
Z. C. [1871], 415
1.4.5.2.3.6
Diethyltrinitro-orcinol
Me.(OEt) 2 .(NO 2 ) 3 =1.3.5.2.4.6
C U H 13 8 N 3
....
61-5
Stenhouse
P. R, 19, 410 ;
24, 358; vii.,
Z.G [1871], 229
880
Ethylamidohydrocarbostyril
C 6 H 4 .N(NHEt).CO.(CH 2 ) 2
C n H 14 ON s
.to
74
Fischer and Kuzel
A., 221, 261
46, 442
i i
=1.2
Ethylhydrocarbazostyril
C 6 H 4 .(CH 2 ) 2 .CO.NH.NEt
l_ 1
)
165-5
u
B., 16, 1452
44, 1132
=1.2
Butyrylbenzenylamidoxime
NH 2 .CPh : NO.CO.Pr*
C^H^N,
MM
94
Schulz
B., 18, 1084
48, 897
Ethylic phenylhydraziuepyro-
Ph.N 2 H : CMe.CO.,Et
JJ
114-115
Fischer & Jourdan
B., 16, 2243
46,53
racemate
Tolylsuccinamide
Me.(NH.CO.C 2 H 4 .CO.NH 2 )
....
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).(CH 2 .CH 2 .C0 2 H)
C 11 H 14 3 N 2
....
78
Fischer and Kuzel
A., 221, 261 ; B.,
44, 1132 ; 46,
namic acid
=1.2
16, 1451
440
Ethylic amidotolyloxamate....
Me.NH 2 .(NH.CO.CO 2 Et)
....
168
Tiemann
B., 3, 222
=1.2.4
Nitracetopseudocumidide ....
Me 3 .NHAc.NO 2 =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(NH 2 ):N.O.
C U H 14 4 N 2
....
106-107
Gross
B., 18, 2480
48, 1218
nylamidoxime carbonate
CO 2 Et
Nitroethoxyphenylure thane
OEt.N0 2 .(NH.CO 2 Et)=l.?.4
C U H 14 6 N 2
....
71
Kohler
J. p. [2], 29, 257
46, 1159
Diethylbenzamide
C 6 H 5 .CO.NEt 2
C U H 16 ON
280-282 c.
Liquid
Hallmann
B., 9, 846
30, 418
Acetylpropylanilide
C 6 H 5 .NPr"Ac
)
254 u. c.
56 u. c.
Glaus and Eoques
B., 16, 913
Isovaleranilde
C 6 H 6 .NH.(CH 2 ) 2 .CHMe 2
)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
C 6 H 6 .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.NH 2 )=1.4
)>
cf. B., 8, 442
138-139
Paterno and Spica
G. I., 9, 400
38, 163
Cyanocamphor
C 10 H 14 .CN.OH
)
250 p.d.
127-128
Haller
C. R, 87, 843
36, 329
Acetopseudocumidide
Me 3 .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
Me 3 .NHAc=1.3.5.6
C U H 15 ON
....
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 a 2
....
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; a i
270
Liquid
Dobner and Miller
B., 17, 1707
46, 1374
dine
Benzenyleth oximidoethy 1
EtO.CPh : N.OEt
C u H 15 O a N
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.C0 2 Bu?
216
80
Mylius
B., 5, 973
26, 266 ; vii.,
946
a-phenamidovaleric acid
CHMe s .CH(NHPh).C0 2 H
....
a. 110
Duvillier
A. C. (5), 21, 433
40, 713
Cumylic carbamate ....
NH 2 .CO 2 .CH 2 .C 6 H 4 Pr
v. a. 200
88-89
Spica
G. I., 5, 394
29, 582
Ethylic tolylamidoacetate ....
Me.(NH.CH 3 .CO s Et)=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
NEt 2 .C0 2 H=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
C 6 H 4 Pr.CH(NH 2 ).C0 2 H(?)
....
197 d.
Ploschl
B., 14, 1317
42, 515
Ethylic xylylcarbamate
NH(C s H 9 ).C0 2 Et
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:O 2 =1.4.(?) 3
....
74
Zincke
B., 14, 97
40, 596
Ethylic collidine carboxylate
C 5 HNMe 3 .CO 2 Et
256
Liquid
Michael
A., 225, 121
48, 61
Toluidine diacetamide
C 6 H 4 Me.N(CH 2 .CO.NH 2 ) 2
C U H 14 2 N 3
....
250
Meyer
B., 8, 1163
29, 402
=1.4
Ethylic ethoxyphenylcarba-
OEt.(NH.C0 2 Et)=1.4
C n H 15 3 N
250-270 p.d.
94
Kohler
J. p. [2], 29, 257
46, 1159
mate
Methylic dimethamidoanis-
CO 3 Me.OMe.NMe,=1.4.?
288
Liquid
Griess
B., 6, 588
26, 1146; vii.,
sate
188
Ethylanhydracetdiamido-
C 6 H 3 Me.N:CMe.NHEt.N0 3
C U H, 5 3 N 8
....
93
Hiibner
A., 210, 328
42, 505
toluene nitrate
i i
Ethylic amidoveratrate
CO 2 Et.(OMe). 2 =1.3.4.
C 1I H I5 4 N
i>.
88-89
Matsmoto
B., 11, 135
34, 502
Diethylic ethylcyanurdicar-
C 3 EtO 3 N 3 (CO 2 Et) 2
CuHujC^Nj
....
123
Wurtz and Hennin-
C. B., 100, 1419
48, 969
boxylate
ger
Diethylphenylcarbamide
NHPh.CO.NEt 2
C n H 16 ON 2
.in
85
Gebhardt
B., 17, 3039
48, 383
Cuminylcarbamide
C 6 H 4 Pr.(CH 2 .NH.CO.NH 2 )
....
133
Eaab
B., 8, 1151
29, 398
=?
Acetyltrimethdiamidoben-
NMe 2 .NMeAc=1.4
95
Wurster & Schobig
B., 12, 1811
38, 111
zene
ji
+xH 2 O
78
n
Acetyldimethdiamidotoluene
Me.NMe 2 .NHAc=1.3.4
)
....
158
Wurster and Eiedel
B., 12, 1801
38, 109
Isocymyl carbamide ^
Me.Pr3.(NH.CO.NH 2 )=1.3.?
...
176
Kelbe and Warth
A., 221, 157
46,47
Ethylanhydracetdiamido-
C 6 H 3 Me.N :CMe.NHEt(OH)
B
93
Hiibner
A., 210, 328
42, 505
toluene hydrate
1 |
..
+2H 2
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
C n H 16 2 N 2
....
116
Eeissert
B., 17, 1456
46, 1152
propionate
Pilocarpin
J>
159
Blyth
....
33, 317
Ethylic amidoethoxyphenyl
OEt.NH 2 .(NH.C0 2 Et)=l.?.4
C 11 H 16 3 N
....
88
Kohler
J. p. [2], 29, 257
46, 1160
carbarn ate
i>
=1.?.4
))
121
j
46, 1161
Diethoxy-oxydimethylpurin
C 5 N 4 Me 2 O(OEt) 3
C n H 16 3 N 4
....
126-127
Fischer
B., 17, 337
46, 997
Ethoxyethyltheobromin
C.H 6 EtN 2 O 4 .OEt
C n H J6 6 N 2
....
155
)>
A., 215, 306
44, 357
Furfurol diurethane
C 4 H 3 O.CH(NH.CO 2 Et),
....
169
Bischoff
B., 7, 1081
Ethylphenylpropylalkine ....
NPhEt.C 3 H 6 .OH
C U H 17 ON
261-263
....
Laun
B., 17, 678
46, 1011
Acetylcyanethine
C 9 H 13 N 2 .NHAc
C U H 17 ON 3
59
Meyer
J. p. [2], 30, 115
48, 140
Dioxyethene toluidine
C 6 H 4 Me.N(0 2 H 4 .OH) 2 =1.4
C,,H 17 3 N
338-340
Liquid
Demole
A, 173, 137; B.,
27, 904
7,638
Phoronimide
O.CMeBuP.CH,, .CMe.CO.
C U H 17 3 N
....
205
Pinner
B., 14, 1080
40, 797
NH.CO
Ethoxycyanconiine
C 9 H I2 N(NH).OEt
C U H 19 ON 3
229-231
Liquid
Meyer
J. p. [2], 22, 277
40, 55
Ethylhydroxycyanconiine ....
C 9 H 17 N(NEt).OH
267-268
43
J. p. [2], 26, 350
44, 353
Ethoxyhydroxycyanconiine....
C 9 H 12 (OEt)N 2 .OH
C 11 H 19 3 N 2
....
51
Eiess
J. p. [2], 30, 145
48, 235
?
....
))
...
a. 320
Pinner
B., 14, 1077
40, 797
Ethoxycyanethine
C 9 H 14 N 3 .OEt
C U H 19 ON 3
300
115
Riess
J. p. [2], 30, 145
48, 235
Borneol urethane
cf. C. R., 94, 869
C 11 H J9 2 N
....
115
Haller
C. R., 93, 1511
42, 625
C 24 H J8 4 N 2 (?)
( ),(!)
....
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
C 13 H 14 2 N(f)
....
45 ; af. 38
Gerrard
B., 16, 798
Phoronamide ...
NH 2 .CO.CMe.CHj.CMe(.O).
C 11 H 20 3 N 2
....
a. 300
Pinner
B., 14, 1079
40, 797
CH 2 .CMe 2 .CO.NH s
Valerodiacetonamine
Bu/3.CH.CH 2 .CO.CH 2 .
C U H 31 ON
....
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
C 8 H 16 N.CO 2 Et
245
MM
Schotten
B., 15, 1947
44, 220
Ethylic oxyheptinamate
C 7 H 9 0(OEt) 2 .NH 2
C n F 21 3 N
87
Demarcay
A. C. [5], 20, 494
Isovaleral diurethane
C 5 H 10 (NH.C0 2 Et) 3
C 11 H 22 4 N 2
...
126
Bischoff
B., 7, 633, 634
27, 891
Amidocamphoronamide
....
C U H 33 6 N 3
MM
144-145
Hjelt
B., 13, 797
38, 670
+C 2 H 6
.
Methylnonylacetoxime
C 9 H 19 .CMe:NOH
CnH.sON
cf.B., 17,1575
42
Spiegler
M. C., 5, 241
46, 1115
Diisoamylcarbamide
CO(NH.CH.CH 2 .CHMe 2 ) 2
C n H 24 ON 3
270
37-39
Ouster
B., 12, 1331
36, 913
Tetraethylallylalkine
(NEt 2 ) 2 .C 3 H 5 .OH
C n H 26 ON 3
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)
....
C 12 H 4 8 N 2
+2H 2
a. 280 d.
Wohler
A., 37, 273; 66, 49
ii., 602
Hexanitrodiresorcinol
C 12 (N0 2 ) 6 (OH) 4
C 1S H 4 16 N 6
d. w. m. 230
Benedikt & Julius
M. C., 5, 177
46, 1140
a-Tetranitrocarbazole
C 13 H 6 (N0 3 ) 4 N
C 13 H 6 O 8 N 6
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[C 6 H 2 (N0 2 ) 3 ] 3
0, 3 H 6 12 N 7
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
C 12 H 6 4 N 4
d.a. 131
131
Glaus
B., 8, 40
28, 647
Dinitrodiphenylene oxide ....
....
C I2 H,0 6 N 2
....
200
Hoffmeister
A., 159, 214
Tetranitrodiphenyl
fr.(.C 6 H 4 .N0 2 )=(1.4) 3
C 12 H e 8 N 4
140
Losanitsch
B.,4, 405
24, 509; vii., 938
Tetranitrophenyl oxide
0[C 6 H 3 (N0 2 ) 2 ] 2 =(1.2.4) 3
C I2 H 6 9 N 4
....
195
Willgerodt
B., 13, 887
38, 643
C 6 H 4 (N0 2 ).O.C,H 2 (N0 2 ) 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
6 H 4 (NO) 2 .O.C 6 H 3 (N0 2 )3
C 12 H 6 9 N 4
153
Willgerodt and
B., 17, 1766
46, 1328
=1.4; 1.2.4.6
Huetlin
Tetranitro-diresorcinol
[.C 6 H(OH) 3 (N0 2 ) 2 ] 2
C 13 H 6 13 N 4
....
268
Benedikt and Hiibl
M. C., 2, 330
40, 1134
a-naphthoyl cyanide
C 10 H 7 (CO.CN)=a
C 12 H 7 ON
....
101
Boessneck
B., 15, 3065
44, 595
a-phenylpyridine ketone
C 6 H 4 .CO.C b NH 3 =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
C 10 H 6 .CO.NH.CO
C 13 H 7 2 N
....
a. 280
Behr and Dorp
A., 172, 270
27, 1168
i i
Pyrroline phthalimide ..
C 4 H 3 N:C.C 6 H 4 .CO.O
240-241
Ciamician and
B., 17, 2958
48, 379
1 1
Dennstedt
Nitroazophenylene
C 12 H 7 2 N 3
209-210
Glaus
B., 8, 40
28, 647
Trinitroazobenzene
....
C 12 H 7 6 N S
....
112
Petrieff
Z. C. [2], 6, 564
vii., 1183
Ph.N 2 .C 6 H 2 (N0 2 ) 3
....
142
Fischer
A., 190, 133
34, 309
C 6 H 4 (N0 2 ).N 2 .C 6 H 3 (N0 2 ) 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.C 6 H 2 (N0 2 ) 3 =1.2.4.6
C 13 H 7 7 N 3
....
1
Willgerodt
B., 12, 1278
C 6 H 4 (N0 2 ).O.C 6 H 3 (N0 2 ) 2
n
....
114
Willgerodt and
B., 17, 1765
46, 1328
=1.4; 1.2.4-
Huetlin
=1.2; 1.2.4
....
119
Trinitroazoxybenzene
....
C 12 H 7 0-N 6
cf. B., 6, 557
152
Schmidt
Z. C. [2], 5, 421
vi., 272
Trinitrodioxyazobeuzene
....
C 12 H 7 8 N 6
MM
102
Petrieff
B., 6, 558
26, 1028
Tetranitrodiphenylamine ....
NH[C 6 H 3 (N0 2 ) 2 ] 2 =(1.2.4) 3
j)
180
Hager
B., 17, 2630
48, 150
....
192
Gnehm and Wyss
B., 10, 1320
34, 52
C 6 H 4 (N0 2 ).NH.C 6 H 2 (N0 2 ) 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 ....
....
C 12 H 7 9 N 5
....
52
Petrieff
B., 6, 558
26, 1028
Nitrosocarbazole
C 6 H 4 .C 6 H 4 .N.NO
C 13 H 8 ON,
....
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
....
C 12 H 8 3 N 3
154
Grsebe and Caro
A., 158, 275
vii., 26
a- ,,
....
,,
....
214
vii., 25
Dinitrodiphenyl
(.C 6 H 4 .N0 2 ) 2 =1.2 ; 1.4
C 12 H 8 4 N 2
....
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
(.C 5 NH 3 .COOH) 2 =(1.2.6) 2
214-215
Skraup
M. C., 3, 590
,> ,.
i>
+ 2H 2
217 d.
B., 15, 896
42, 1112
), )! !>
)>
....
217 d.
Skraup & Vortmann
M. C., 3, 370
44,88
Dinitroazobenzene
(:N.C 6 H 4 .N0 2 ) 2 =(1.3) 2
c 12 H 8 o 4 isr 4
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.C 6 H 3 (N0 2 ) 2 =?
C 12 H 8 5 N 2
....
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. C 6 H 4 Ph.OH=1.4
....
154
Latschinoff and
B., 6, 195 ; J. R,
26, 750 ; vii.,
Engelhardt
5, 52
938
Dinitrodihydroxydiphenyl ....
[.C 6 H 3 (OH).N0 2 ] 3 =(?.1.2) 2
C 12 H 8 6 N S
....
w. m. 150
Goldstein
B., 7, 735
27, 1093
....
....
184
J. E., 6, 193
Trinitrodiphenylamine
....
C 12 H 3 6 N 4
135
Norton and Allen
B., 18, 1997
48, 1214
Ph.NH.C 6 H 3 (N0 2 ) 3 =?
....
175
Austen
A.J.S.[3],13,279
32, 760
175
Clemm
B., 3, 126
....
C 6 H 4 (N0 2 ).C 6 H 3 (N0 2 ) 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,H 4 (NO a ).C 6 H 3 (N0 2 ) 2
C 12 H 8 6 N 4
....
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
C 12 H 4 (N0 2 ) 2 (OH) 4
C 12 H 8 8 N 2
d.w.m. 170
Hazura
M. C., 4, 610
44, 1114
Ethenyl ainidonaphthol
C 10 H 6 .N : CMe.O
C 12 H 9 ON
Liquid
Bottcher
C. C. [1884], 898
48, 659
Azoazoxybenzene
C 12 H 9 ON 3
....
85
Ziniu
A., 114, 225
i., 480
Nitrodiphenyl
Ph.C 6 H 4 .N0 2 =1.2
C 12 H 9 O 2 N
....
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 ....
C 10 H 7 .CO.CO.NH 2
>1
151
Boessneck
B., 15, 3066
44, 595
Nitroazobenzene
Ph.N 2 .C 6 H 4 .N0 2 =1.4
C 12 H 9 2 N 3
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.?
C 12 H 9 3 N
....
d.w.m. 200
Zincke
B., 18, 789
48, 787
Nitrohydroxydiphenyl
fr.Ph.C 6 H 4 .OH=1.4
))
....
67
Latschinoff
R, 6,195; J.R.,5,52
26,750;vii.,938
C 6 H 4 (OH).C 6 H 4 .N0 2
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
C 10 H 7 .NH.CO.COOH
I
180 d.
Ballo
B., 6, 247
26, 913; vii., 848
Pyrroline methylbenzoic acid
C 4 H 3 N: CH.C 6 H 4 .CO 2 H=1.2
JJ
....
174-184
Ciamicianand Denn
B., 17, 2958
48, 379
stedt
Phenoxynicotinic acid
C 5 H 3 N(OPh).CO 2 .H=U.4
....
275-280
Pechmann & Welsh
B., 17, 2394
47, 153; 48, 175
o-Nitroazoxybenzene
....
C 12 H 9 S N 3
....
49
Zinin
A., 114, 220
i., 480
P- ,,
....
....
153
A., 114, 221
Nitrobenzeneazophenol
C 6 H 4 (OH).N 2 .C 6 H 4 .N0 2
)J
....
183-184
Meldola
47, 659
=(1.4) 2
Nitroso-nitrodiphenylamiue
Ph.N(NO).C 6 H 4 .N0 2 = ?
))
....
133-5
Witt
B., 11, 757
33, 205
Nitro-acetonaphthol
C 10 H 6 .NO 2 .OAc=a/3
C 12 H 9 4 N
....
61
Bottcher
B., 16, 1938
44, 1113
Methylic nitro-a-naphthoate.
Ci H 6 .NO 2 .CO 2 Me=?a
J)
109-110
Graeff
B., 16, 2252
46, 81
1> )> "P" >!
= ?/3
)>
112
D
B., 16, 2254
)
Dinitro-diphenylamine
Ph.NH.0 6 H 3 (NO 2 ) 2 =1.2.4
C I2 H 9 4 N 3
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(C 6 H 4 .N0 2 ) 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 ....
C 6 H 4 (N0 2 ).N 2 .C,H 3 (OH) 2
powder
Meldola
47, 660
=1.4 ; 4.3.1
Dinitroamidoazobenzene (m-)
C 6 H 4 (N0 2 ).N S .C 6 H 3 (N0 2 ).
C 12 H 9 4 N 6
MM
175-176
Hallmann
B., 9, 390
30, 93
NH 2
(m-)
))
A., 121, 272
195-5
Griess
P. T., 3, 678
lv., 461
(P-)
II
A., 121, 271
224-5
)
Dinitroacetonaphthalide
NHAc.(NO 3 ) 2
C 12 H 9 S N 3
cf. B., 4, 850
247
Liebermann and
B., 9, 333
30,81
=aA" 2 ; or a i! "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^
C 12 H 9 6 N 3
....
251
Ebell
B., 8, 564
28,900
aJJ^a.t ; or a, ; a,/:
Phthalylaspartic acid
C 6 H 4 : (00)j : N.CH(CO 2 H).
C 12 H 9 0,N
233
Piutti
G. I., 14, 473
48, 796
Trinitrohydrazobenzene
Ph.NH.NH.C 6 H 2 (NO 2 ) 3
C 13 H 9 6 N 6
....
181 d.'
Fischer
A., 190, 132
34, 309
Picric acid + benzene
C 6 H 6 +C 6 H 2 (OH)(N0 2 ) 3
C 12 H 9 ? N 3
A., 109, 247
85-90
Fritzsche
J. p., 73, 212
iv., 405
B. S., 7, 30
Trinitro-a-ethoxynaphthalen
C 10 H 4 .OEt.(N0 2 ) 3
148
Staedel
B., 14, 900; A
40, 724; 44, 863
217, 170
,, -ft-
jj
....
186
u
Diphenylnitrosamine
Ph 3 N.NO
C 12 H 10 ON 3
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.N 2 .C 6 H 4 .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.N 2 .OPh(?)
....
154
Scichilone
G. I. [1882], 108
42, 726
Phenylazonitrolic acid
Ph.N 2 .C 6 H 4 .NOH
C 13 H 10 ON 3
....
134
Janovsky
M. C., 6, 157
48,789
Hydroxydipheuylnitrosamine
C,H 4 .OH.(NPh.NO)=1.4
C 12 H 10 2 N 2
....
95
Philip and Calm
B., 17, 2433
48, 155
Nitrodiphenylamine
Ph.NH.C 6 H 4 .N0 2 =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.C 6 H 4 .OH
JJ
cf. B., 3, 235
145
Wallach and Kie-
B., 14, 2618
42,394
penheuer
a-Eesorcinolazobenzene
Ph.N 3 .C 6 H 3 (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.H 4 .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,H 4 .C 6 H 4 .NH 3
....
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
C 10 H 7 .CO.NH.CO.NH 2
B
....
15
Vieth
A., 180, 322
0, 87
Nitroamidoazobenzene
....
C 13 H 10 2 N 4
....
95
Griess
;2], 5, 857
i., 921
n
N0 2 .C 6 H 4 .N 2 .C 6 H 4 .NH 2
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.C 3 H,,
Ci 2 H 10 O 3 N 2
....
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.N0 3 =aA; (?)
C 12 H 10 3 N :
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 (I I ( '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
C 6 H 4 : 2 +C 6 H 4 .NO 2 .NH 2
C 13 H 10 4 N 2
....
94-97
Hebebrand
B., 15, 1976
+P- 11
H
....
115-120
ii
11
Diuitrohydrazobenzene
N0 2 .C 6 H 4 .NH.NH.C 6 H 4 .NO 2
C 12 H 10 4 N 4
....
220
Lermontoff
B., 5, 234
Dinitroamidodiphenylamine
NH 2 .C 6 H 4 .NH.C 6 H S (N0 2 ) 2
'
....
172
Leymann
B., 15, 1237
42, 1057
Dinitro-a-ethoxynaphthalene
OEt.(N0 2 ) 2 =a 1
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 ....
C 6 H 6 +C 6 H 2 .NH 2 .(N0 3 ) 3
C 12 H 10 OjN 4
....
108-5
Mertens
B., 11, 843
=1.2.4.6
Trinitrobenzene+ aniline ....
C 6 H 3 (N0 2 ) 3 +NH 2 Ph
....
123-124
Hepp
A., 215, 356;
36, 51; 44, 316
B. S. [2], 30, 4
Pyridine methopicrate
C 5 NH 5 +C 6 H 2 .OMe.(N0 2 ) 3
C 12 H 10 7 N 4
+pi 2 o
34
Ostermayer
B., 18, 592, 599
48, 813
Hydroxydiphenylamine
Ph.NH.C 6 H 4 .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
C 10 N 7 .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
C 10 H 7 .CH 2 .CO.NH 2
....
180-181
Boessneck
B., 16, 641
44, 808
Acetonylquinoline
N.(CH 2 .CO.Me)=a 1 /3, ;
....
76
Fischer and Kuzel
B., 16, 164
44, 588
Amidobenzeneazophenol
NH 2 .C 6 H 4 .N 2 .C 6 H 4 .OH
C 13 H n ON 3
....
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
C 12 H U O2N
....
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-
C 10 H 6 (NMe 2 ):0 2 (?)
....
118
Plimpton
37, 642
none
Ethamido-a-naphthaquinone
C 10 H 6 (NHEt):0 3 (?)
....
139-140
37, 641
H 11 11
C 10 H 6 .O.NEt.O
,,
....
140
Zincke
B., 12, 1646
38,49
Amidobenzene azoresorcinol
NH 2 .C 6 H 4 .N 2 .C 6 H 3 (OH) 2
C 12 H n 3 N 3
...
too high to
Meldola
47, 661
=1.4; 4.3.1
determine
Nitrocinnatnenylvinylme-
NO 2 .C 6 H 4 .CH : CH.CH : CH.
CuHuOjN
...
73-5
Diehl and Einhorn
B., 18, 2327
48, 1222
thylketone
COMe=1.2
Nitroethoxynaphthalene
OEt.NO 2 =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
C 10 H 4 (OH)(NMe 2 ):0 2 =/3,;
C 12 H,,0 3 N
....
149-150
Mylius
B., 18, 465
48, 803
(3,0,0,
Ethoxyquinoline carboxylic
N.OEt.COOH=a,0,/3 2 ;
M
133
Friedlander and
B., 17, 460
46, 1020
acid
Gohring
,,
=a,/3,a 2 ;
....
145-146
Konigs and Korner
B., 16, 2154
46,84
Ethylic hydroxyquinoline
N.OH.COOEt=a,/3,a 2 ;
....
206-207
B., 16, 2155
carboxylate
? acid
....
H
....
148-149
Weltner
B., 18, 794
48, 794
Nitrocinnamylacetone
N0 2 .(CH : CH.CO.CH 2 Ac)
C 12 H n 4 N
....
112-113
Fischer and Kuzel
B., 16, 36
44,587
=1.2
Nitrobenzoyltetramethylene
(CH 2 ) 3 .C(C0 2 H).CO.C 6 H 4 .
C IS H U 5 N
....
172
Perkin and Bellinoi
B., 18, 957
48, 795
carboxylic acid
N0 2 =1.4
Nitropeucedanin (cf. A., 176,
....
....
100 d.
Bothe
J. p., 46, 371
iv., 386
78)
Anilinetrinitraniline
C 6 H 2 (N0 2 ) 3 .NH 2 +Ph.NH 2
C, 2 H U 6 N 5
123-125
Hepp
A., 215, 359
Diamidophenyloxide
C 12 H 12 ON 2
....
185
Hoffmeister
A., 159, 209
vii., 941
Ethylnaphthylnitrosamine ...
C, H 7 .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:N 2 (C 6 H 4 .NH 2 ) 2 =(1.4) 2
C 12 H 12 ON 4
....
182-184
Mixter
A. J. C., 5, 1
46, 301
Diacetamido-o-toluic nitril ....
NAc 2 .(CH 2 CN)=1.4
C 12 H 12 2 N 2
....
152-153
Gabriel
B., 15, 835
42, 1070
? amide
0,,H, ON.(CO.NH 2 )
....
264
Weltner
B., 18, 794
48, 794
Acetoxyphenylethenylazox-
AcO.CHPh.C : N.O.CMe : N
C 12 H 12 3 N 2
....
52
Gross
B., 18, 1077
48, 898
imethenyl
Phenylethenylazoximepro-
O.N : C(CH 2 Ph).N : C.(CH 2 ) 2 .
H
....
59 T 60
Knudsen
B., 18, 2484
48, 1218
1 1, 1 ' J
penylcarboxyhc acid
CO 2 H
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
?
....
C 12 H 12 3 N 3
brown 150
172 d.
Paal
B., 17, 2762
48, 250
Urocaniuic acid
(>*
C 12 H 12 4 N 4
+4H 2
212-213
Jaffe
B., 7, 1671
Trisuccinamide
(C 4 H 4 2 ) 3 N 2
C 12 H I2 6 N 2
....
83
Chiozza and Ger-
A., 90, 108
v., 462
hardt
/3-hydroxypyridine oxalate ....
(C 5 H 6 NO) 2 +H 2 C 2 4
(?)
....
175
Fischer and Eenouf
B., 17, 1896
46, 1370
Ethylic dinitrophenylacetace-
C 6 H 3 (N0 2 ) 2 .(CHAc.COOEt)
C 12 H 12 ; N 2
....
94
Heckmann
A., 220, 128
46, 178
tate
=4.2.1
Diethylic dinitrophthalate ....
(C0 2 Et) 2 .(N0 2 ) 2 =1.2.(?) 2
C 12 H 12 8 N 2
....
91
Beilstein and Kur-
B. S. [2], 34, 327
40, 436
batow
Aniline phenate
Ph.NH 2 +C 6 H 5 .OH
C 13 H I3 ON
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
C 9 H 6 PrPON
Ifi7 Ifift
,,,. ,
B-I H OOQQ
UJ 4 1OO
W K final i H
.j 17, $iZot>
Acetamidopropenylbenzoic
NHAc.C 3 H 6 .C0 2 H=1.2.5
C 12 H 13 3 N
..
210-212
n
B., 16, 2575
46, 318
acid
Acetyltetrahydrocinchoninic
. j
fr. C C H 5 (C0 2 H).CH 2 .CH :
H
....
164-5
Weidel
M. C., 3, 64
42, 531
acid
CH.NH=1.2
Methylcumazonic acid
C 6 H 3 (CO 2 H).CMe 2 .O.CMe : N
218
Widmann
B., 16, 2576
46, 303
=1.2
Cotarnine
....
M
+H 2
100
nf\4- V\ i on
....
ii., 89
Nitrosomethylanilidopyrotar-
CO.NMe.CO.CH 2 .CMe.NPh.
i j
C 12 H, 3 3 N 3
not D. IzO
147
Beckett & Wright
Wechsler
28, 576
B., 18, 1044
48, 900
tarimide
NO
Ethylic aeetylphenyloxamate
NAcPh.CO.CO 2 Et
C 12 H 13 4 N
....
64-65
Klinger
A., 184, 268
31, 711
n
,,
....
66-67
B., 8, 311
28, 1025
Ethylic nitropropenylbenzo-
ate
N0 2 .C 3 H 6 .C0 2 Et=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.NO 2 .(.CH.CH 2 .CO.O)
C 12 H 13 4 N
....
73
Einhorn and Hess
B., 17, 2022
46, 1352.
phenyllactic acid
L _1
=1.3.4
Nitrocumenylacrylic acid ....
Pr/3.NO,,(CH:CH.C0 2 H)
"
....
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
C0 2 H.(NH.CO.CH 2 .C0 2 Et)
172-173
Sehiff
B., 17, 403
46,906
= 1.3
Nitro-aceteugenol
C 3 H 5 .OMe.OAc.NO 2 =1.4.3.?
....
61
Weselsky and Bene-
M. C., 3, 391
42, 1201
dikt
Ethylic nitrophenylazoacet-
NO 2 .(.N 2 .CHAc.CO 2 Et)=1.2
C 12 H 13 5 N 3
....
92-93
Bamberger
B., 17, 2416
48, 157
acetate
Nitroquinol dipropionate ....
(O.C 3 H 5 O) 2 .NO 2 =1.4.5
C 13 H I3 6 N
....
86
Hesse
A., 200, 247
38, 317
Diethylic nitrophthalate
(COOEt) 2 .NO 2 =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
CO 2 H.(CMe 2 .OAc).NO 2
131-133
Widmann
B., 16, 2569
46, 317
acid
=1.4.5
Ethylic diacetylcomenamate
C 5 H 2 N(OAc) 2 .CO 2 Et
fr. pyridine
38
Ost
J. p. [2], 29, 57
48,49
nitro-opianate
COH.NO 2 .(OMe) 2 .C0 2 Et
C 13 H 13 7 N
....
96
Prinz
J. p. [2], 24, 358
42, 402
=6.13.2.1
Methylethyloxyquinizine ....
C 6 H 4 .N.NH.CMe.CHEt. CO
C 18 H 14 ON 2
108
Knorr and Blank
B., 17, 2051
46, 1380
i i
=1.2
Toludimethyloxyquinizine ....
C 6 H 3 Me.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.CH 2 .C(NHAc):NAc
C 13 H 14 2 N 2
172-173
Luckenbach
B., 17, 1425
46, 1134
Methylanilidopyrotartar-
CO.NMe.CO.CH 2 .CMe.NH
103
Wechsler
B., 18, 1043
48, 900
imide
Ph
Toluidopyrotartarimide
CO.NH.OO.CH 2 .CMe.NH.
181
B., 18, 1051
48, 901
i i
C 6 H 4 Me=1.2
Ethylpseudoisatin-a-ethyl-
C 6 H 4 .CO.C(NOEt).NEt=1.2
n
....
99
Baeyer
B., 16, 2193
46,74
oxime
Ethylic azobenzene acetace-
Ph.N 2 .CHAc.CO 2 Et
C 12 H 14 3 N 3
ii
59-5
ZUblin
B., 11, 1418
34, 880
tate
Diacetylphenyloxethenyl
AcO.CHPh.C(NH 3 ) : NOAc
C I3 H 14 4 N 2
....
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.(N0 2 ) 2 .CO 3 Et=?
C 12 H 14 6 N 3
77-5
J. [1858], 271
Deoxyamalic acid
C 12 H 14 6 N 4
260
Fischer and Eeese
A., 221, 336
46, 467
Ethylic nitrophenylnitro-
NO 2 .[CH(OMe).CH(NO.,).
C 12 H 14 O.N 2
77
Friedlander and
B., 16, 852 ; A.,
48, 1138
methoxypropionate
CO,Et]=1.4
Mahly
229, 210
Methylic nitrophenylnitro-
NO 2 .[CH(OEt).CH(NO 2 ).
n
110
ethoxypropionate
CO 2 Me]=1.4
"
Methylic ethyldinitrohydro-
OEt.(N0 2 ) 2 .(CH 2 .CH 2 .CO i!
^
....
36
Stohr
A., 225, 57
46, 1350
p-coumarate
Me)=1.2.6.4
Ethylic methyldinitrohydro-
OMe.(NO 2 ) 2 .(CH 2 .CH !! .C0 2
71
p-coumarate
Et)=1.2.6.4
)J
Diethylic dinitrosuccinosuc-
C 12 H 14 8 N 2
brown 100
113-114 d.
Ebert
A., 229, 45
48, 1122
cinate
Cumenylacrylamide
a-ethoxy hydromethyl quino-
line
Pr3.(C 2 H 2 .CO.NH 2 )=?
NMe.H 3 .OEt=a 1 /3 1 /3 s a ;j ; a,
C 12 H 16 ON
269-270(716)
185-186
Liquid
Perkin
Fischer
J. [1877], 790
B., 16, 718
3t, 399
44, 1147
Hydroeumostyril
C 9 H s Pr/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.
?
....
C 13 H I5 2 N
a. 300
78-80
Canzoneri & Spica
G. I., 14, 448
48, 751
Cumenylamidoacrylic acid ...
C 9 H n .0 2 H(NH 2 ).CO 2 H
J)
....
154-155
W id maun
B., 17, 2283
48,56
o-amidocumenylacrylic acid
cjBv > <sm&cja f co&
165
D
jj
D
m -
>
165
j)
Isoamylidene-m-amidoben-
....
)J
130 ; sf. 100
Schiif
A., 210, 119
42, 304
zoic acid
Ethylic dimethamidobenzoyl
NMe 2 .(CO.CO 2 Et)=1.4
C 12 H 15 3 N
...
95
Michler and Hau-
B., 10, 2082
34, 421
formate
hardt
Anliydro-amidophenolethyl
O.C 6 H 4 .NH.CMe.CH 2 .CO 2 Et
107-108
Hantzsch
B., 16, 1950
44, 1111
acetacetate
=1.2
Acetamidocumic acid
Pr/3.NHAc.C0 2 H=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.C 6 H 10 O 2 N
1
....
94
Schotten
B., 17, 2545
48, 176
Cuminuric acid
....
1)
A., 109, 31
168
Jacobsen
B., 12, 1514
38, 38
Hy drocotarn iue
....
)>
+iH 2
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 ...
C0 2 Et.(NH.C0 2 Et)=1.3
C 12 H 16 4 N
100-101
Wachendorff
B., 11, 702
34, 674
Diethylic amidophthalate ...
(CO 2 Et) 2 .NH 2 =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-
C0 2 H. (NH 2 + H Ac).C 3 H 5
})
....
160
Widmann
B., 16, 2574
46, 318
benzoic acid
=1.3.4
Acetamidohydroxypropyl-
CO s H.(NHAc).(CMe 2 .OH)
n
nf. 280
51
B., 16, 2572
46, 317
benzoic acid
=1.3.4
Dimethylic collidine dicar-
N.Me 3 .(C0 2 Me) 2 =1.2.4.6.3.5
)
285-287
82
Hantzsch
B., 16, 1947
44, 1082
boxylate
Monethylic collidine dicar-
N.Me 3 .CO 2 H.OO 2 Et
)>
....
157
Michael
A., 225, 121
48,61
boxylate
=1.2.46.3.5
Triacetamidophenol
OII.(NHAc) 3 =1.2.4.6
C 12 H 16 4 N 3
263 d.
Bamberger
B., 16, 2401
46, 309
Ethylic hydroxyisopropyl
CO 2 Et.(CMe. 2 OH).NO 2
C 12 H 16 6 N
96
Widmann
B., 15, 2550
44,330
nitrobenzoate
=1.4.5
Isopropylnitrophenyllactic
[OH(OH).CH 5 .C0. 2 H].NO S
)>
119-120
Einhorn and Hess
B., 17, 2024
46, 1353
acid
Pr0=1.2.4
Ethylic nitrodimethamido-
(NH.CO.CO 2 Et).NMe 2 .NO 2
C 12 H 15 5 N 3
152
Wurster and
B., 12, 1805
38, 110
phenyloxamate
=1.4.6
Sendtner
/3-butyranilbetame oxalate ....
NH 2 Ph.CHMe,CH 2 .COO
C 12 H 16 6 N
....
137-139
Balbiano
B.,13,313;G. I.,
38, 462, 542
+C 2 H 2 4
10, 137
Aniline citrate
C 6 H 5 .NH.O.C 6 H 6 4 (OH) 2
C 12 H 1S 7 N
b. 100
Pebal
A., 82, 91
iv., 427
Ethylic cyanuro-carboxylate
(NCO.C0 2 Et),
C 12 H 15 9 N 3
118-119
Wurtz & Henninger
('. R, 100, 1419
48, 969
Triethoxytrinitrobenzene ....
(OEt) 3 .(N0 2 ) 3 =1.2.3.4.5.6
)
93
Weselskyand Bene-
M. G, 2, 218
42,54
dikt
Piperidylphenylcarbamide ....
PhHN.CO.N:C 5 H 10
C 12 H 16 OK 2
168
Gebhardt
B., 17, 3041
48, 384
Benzoylpiperylhydrazine ...
C 5 H 10 N.NHBz
n
195
Knorr
A., 221, 297
46, 467
Picramide+aniline
C 6 H.,.OH.(NH 2 ) 3 +NH, 1 Ph
C 12 H 16 ON 4
123-125
Hepp
A., 215, 344
44,316
Diethyl terephthalaldoxime
Ispphthalimidethyl ether ....
C 6 H 4 (CH:NOEt) 2 =1.4
C 6 H 4 [C(OEt):NH] 2 =1.3
C 12 H 16 2 N 2
))
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.C0 2 Et).NMe 2 =1.4
C 1S H 16 3 N 2
117
Sendtner
B., 12, 531
36, 627
oxamate
Acetamide+auisaldehyde ....
Nitroisovaleryl toluide
v. C 12 H 16 2 N 2
Me.N0 2 .NH(C 6 H 9 0)=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
C 6 H 8 2 .NH 2 .NH.C 7 H 6
(.CMe.N:C.C0 2 Et) 2
C 12 Hi' 6 4 N 2
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).CH 2 .CO.NH 2 ].
i)
150
Einhorn and Hess
B., 17, 2023
46, 1353
mide
N0 2 .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 .(N0 2 ) 2 =1.4.(?) 2
C 12 H I6 4 N 2
....
65
Korner
B., 11, 1865; A.,
36, 142 ; 44,
216, 226
322
Ethyl dinitrothymol
Pr 2 .Me.OEt=1.4.6
C 12 H 16 5 N 2
52-53
Ladenburg and
B., 10, 1219
34,60
Engelbrecht
Triethoxydinitrobenzene ....
(OEt) 3 .NO 2 =1.2.3.4.?
C 12 H 16 ; N 2
73
Weselskyand Bene-
M. C., 2, 217
42, 54
dikt
Pipecoline picrate
C 6 H 13 N+C 6 H 2 .OH.(N0 2 ) 3
C^H^N,
136-138
Hesekiel
B., 18, 913
48,812
Tetramethylic azinsuccinate
[.N: C(CO 2 Me).CH 2 .CO 2 Me] 2
C 12 H 16 8 N 2
149-150
Curtius and Koch
B., 18, 1301
48, 886
Capronanilide
C 6 H 3 .NH(C 6 H n O)
C 12 H 17 ON
....
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-
Me 4 .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=a 1 /3 1 ; 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 ....
C 6 H 4 Me.(NH.CO 2 Bu0)=1.2
C 12 H 17 2 N
275-280 p. d.
L. 10
Hofmaun & Mylius
B., 5, 974 ; P. E.,
vii., 1180; 26,
19, 108
266
Ethylic a-xylylglycocine
Me 2 .(NH.CH 2 .CO 2 Et)= 1.3.?
))
Liquid
Ehrlich,
B., 16, 206
44, 594
Carvacrol glycollamide
Me.Pr.(O.CH 2 .C0 2 H)=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.NH 2 .(C 2 H 4 .C0 2 H)=1.3.?
j
103-105
Widmann
B., 17, 2283
48, 56
Mesitylurethane
Me 3 .(NH.CO 2 Et)=1.3.5.6
u
....
61-62
Eisenberg
B., 15, 1016
42, 956
Isobutylethoxynitrobenzene
Bu0.OEt.NO 2 =?
C 12 H 17 3 N
300 d.
Liquid
Liebmann
B., 15, 1991
44,59
Diethylic dimethylpyrroline
N.Me 2 .(CO 2 Et) 3 =1.2,5.3.4
C 12 H 17 4 N
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.Me 3 .(CO 2 Me) 2 .H 2
5
....
156
Hantzsch
B., 16, 1947
44, 1082
dicarboxylate
1.2 4 6.3.5.5.6
Oxypropyltoluidine oxalate....
NH(C 3 H 7 0)(C 7 H 7 )+C 2 H 2 4
C 12 H 17 5 N
KM
151
Morley
41, 388
Helicinaldoxime
C 6 H n O 5 .O.C 6 H 4 .CH : NOH
C 12 H 17 7 N
190
Tiemaiin and Kees
B., 18, 1663
48, 1072
s=LS
Pentanitrolactose
C 12 H 17 (N0 2 ) 5 U
C.jH.AiN,
139'2 p.d.
Ge
J. E. [1882], 253
42, 1043
Diruethaniidothymoquinone
Me.Pr.(NHMe) 2 :O.,=2
C 12 H 18 0,N 2
203
Zincke
B., 14, 95
40, 596
1
....
C 12 H 18 5 N 2
....
81
Ehrenberg
J. p., 32, 97
48, 1192
Diethyldime thylarnmouium
(O.NMe 2 Et 2 ).(NO 2 ) 3 =1.2.4.6
C 12 H 18 7 N 4
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
C 12 H 18 (N0 2 ) 4 U
C 12 H 1S 0, 9 N 4
80-81
Ge
J. E. [1882], 253
42, 1043
Diethamidoethoxybenzene ....
OEt.NEt 2 =1.2
C 12 H 19 ON
227-228
Liquid
Foster
J. p. [2], 21, 364
38, 465
(754-3)
Camphorethylimide
c 8 H 14 :(co) 2 :NEt
C 12 H 19 2 N
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
C 6 H 3 Me.Pr.NH 2 +HAc
)
....
112
Widmann
B., 15, 169
42, 728
Ethylcyanethine carboxylate
C,,H 13 N 2 .NH.C0 2 t
C 12 H 19 2 N 3
247
easily
Meyer
J. p., 30, 115
48, 140
Triethyldicarbopyrrolamide
C 4 H 3 EtN(CO.NHEt) 2
>
229-230
Bell
B., 10, 1864
36, 525
Oxytetrolamide
C 12 H 9 6 (NH 2 ) S
C 12 H 19 5 N 6
B. S., 33, 575
177-177-5
Demanjay
A. C. [5], 20, 479
40, 255
Triuitrolactose
C 12 H 19 (N0 2 ) 3 U
C 12 H 19 17 N 3
....
36-86
Ge
J. E. [1882], 253
42, 1043
Oxalylpiperidine
(C 5 H 10 N.CO) 2
C 12 H 20 2 N 2
a. 350
88-89
Wallach
A., 214, 278
11
)
J
a. 360
90
Schotten
B., 15, 426
42, 983
Acrole'in-ammonia
C 12 H 20 3 N 2
....
d. 100
Eedtenbacher
A., 47, 114
i., 57
Diethoxyhydroxycaffei'ne ....
C 8 H 9 N 4 2 (OEt) 2 .OH
C 12 H 20 5 N 4
A., 215,274
195-205 d.
Fischer
B., 14, 641
40, 614
Diethylic oxaldiamidopro-
(.CO.NH.CHMe.CO 2 Et) 2
C 12 H 20 6 N 2
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 ..
C 9 H 15 .NH.CO 2 Et
C 13 H 21 2 N(?
115
Haller
C. E., 98, 578
46, 755
Lsevo-
))
)>
....
126-127
11
11
11
Triethylic amidotriglycollatt
N(CH2.C0 2 Et) 3
C 12 H 21 6 N
280-290 p. d
....
Heintz
A., 140, 264
vi., 647
Diacetonamiue anhydride ..
C 12 H 24 ON 2
....
83
Antrick
A., 227, 365
48, 503
Amylisocaproylcarbamide ..
Me.(CH 2 ) 4 .NH.CO.NH.CO.
C 12 H 24 2 N 2
....
94
Hofmann
B., 15, 758
42, 1053
(CH 2 ).,Pr0
Amylcaproylcarbamide
Me.(CH 2 ) 4 .NH.CO.NH.CO.
)
97
)*
11
(CH 2 ) 4 Me
Diisoamyloxamide
....
^J
B., 13, 516
128-129
Wallach
A., 214, 316
44, 49
Diamyloxamide
(.eO.NH.C 6 H n ) 2
>J
139
Wurtz
A. C. [3], 30, 490
iv., 285
Lauramide
C n H 23 .CO.NH 2
C,-H.ON
102
Krafft and StaufFei
B., 15, 1729
42, 1273
Pinitrodiphenylene ketone...
fr.(C 6 H 4 ) 2 :CO=(1.2) 2
^12 .5^ -*
C 13 H 6 5 N 2
...
290
Schultz
A., 203, 104
38, 814
a-Dinitrodiphenylene ketone
fr.co:(G 6 H 4 ) 2 :o
C 13 H 6 0,N 2
....
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:C 12 H 6 (N0 2 ) 4
C 13 H 6 9 N 4
MM
225
Staedel
A., 218, 339
44, 991
Tetranitrodiphenylic car-
[C 6 H 3 (N0 2 ) 2 ] 2 C0 3
C 13 H 6 O n N 4
125-5
Kempf
J. p. [2], 1, 407
24, 342
bonate
Quinone
Fr.o-naphthoquinoline
C l3 HjO.F
....
205-207 d.
Skraup and Cobenzl
M. C., 4, 436
44, 1014
Nitrodiphenylene ketone ....
C 6 H 4 .OO.C 6 H 3 .N0 2
C 13 H 7 8 N
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-
C 6 H.,(NO,) .O.CPh:N
1- - " " p
CuHjO^f.
....
218
Hiibner
A., 210, 394
42, 507
phenol
=(?) r l.a
Diuitrophenylic m-nitroben-
C 6 H 4 (N0 2 ).C0 2 .C 6 H 3 (N0 2 ) 2
C I3 H 7 8 N 3
....
150
List and Limpricht
A., 90, 201
i., 556
zoate
Phenanthroline carboxylic
O,NH 3 .CH : C(CO,H).C^NH 3
C 13 H 8 2 N 2
....
277
Skraup and Fischer
M.-G, 5, 253
48, 393
acid
=1.2.3.4.5.6 ; 5.6.1.2.3.4
Dinitrofluorene
C 12 H 6 (N0 2 ) 2 :CH 2
C 13 H 8 4 N 2
....
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:C 12 H 8 (N0 2 ) 2
C 13 H 8 5 N 2
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
C 6 H 4 (N0 2 ).C 6 H 3 (N0 2 ).C0 2 H
C 13 H 8 6 N 2
....
252
Strasser & Schultz
A., 210, 192
42, 521
acid
=1.4; 1.2.4
Trinitrobenzanilide
C 6 H,(N0 2 ) 2 .NH.CO.C 6 H 4
C 13 H 8 7 N 4
165
Hiibner
B., 10, 1708
34, 142
NO 2 =1.3.4; 1.3
11 .... ....
,, =1.13; 1.2
))
178
11
11
)1
11 .... ....
,, =1.13; 1.?
))
202
11
11
Tetranitrodiphenylmethane
CH 2 :c" 2 H 6 (N0 2 ) 4
C 13 H 8 8 N 4
212
172
11
Doer
11
B., 5, 795
Ti
26,170;vii.,948
11
Nitrobenzyl picrate
J
N0 2 .C 6 H 4 .CH 2 .O.C 6 H,,(NO,,) 3
C 13 H S 0,N 4
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.C 6 H 3 (N0 2 )J 2
C 13 H 8 9 N 6
....
a. 200
Losauitch
B., 10, 690, 1296
j,
204
B., 11, 1541
Benzenylamidophenol
C 6 H 4 .O.CPh:N=1.2
C 13 H 9 ON
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
6 H 4 .C 6 H 4 .C:NOH
M
B., 17, 807
192
Spiegler
M. C., 5, 195
46, 1182
i i
3-hydroxynaphthoquinoline
HO.C 10 H 5 : C 3 NH 3
....
w.m. 250 p.d
Gentil
B., 18, 202
48, 561
Nitrofluorene (A. C. [5], 7, 497)
C 6 H 4 .OH,,.C 6 H 3 .NO 2 =1.2 ;
C 13 H 9 2 N
....
154
Strasburger
B., 17, 108
46, 754
1.2.4
Carbazolic acid
C 12 H S N.CO 2 H
....
271-272
Ciamician & Silber
G. I. [1882], 272
42, 1103
Nitroanhydrobenzoyldiami-
C H 3 (NO 2 ).NH.CPh : N
C 13 H 9 0,N 3
196
Stover
B., 7, 1317
28, 271
dobenzene
?1 2
D
....
196
Hiibner
A., 208, 308
40, 1131
Nitrobenzophenone
C 6 H 4 (NO 2 ).COPh =1.3
C 13 H 9 O 3 N
....
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 (1 H 4 (NO).OBz=1.4
168-175 d.
Walker
B., 17, 400
46, 1003
Benzoxynitrobenzene
C 6 H 4 (N0 2 ).OBz=1.2
C 13 H 9 4 N
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
C 12 H 8 (NO 3 ).C0 2 H
....
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....
C 10 H 6 .NO 2 .CO 2 Et
....
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
....
+H 2
206
Skraup
B., 15, 896
a-phenylpyridinedicarboxylic
N.CO 2 H.(C 6 H 4 .CO 2 H)=1.3.2
,,
....
230-235 d.
Skraup & Cobenzl
M. C., 4, 436
44, 1014
acid
m-nitrobenzylidenenitrani-
....
C 13 H 9 4 N 3
114
....
J. [1870], 760
line
Dinitrobenzanilide
C 6 H 4 (NO 2 ).NH.CO.C 6 H 4 .
C 13 HAN 3
187
McHugh
B., 7, 1268 ; 8, 36
28, 271
N0 2 =(1.3) 2
Nitrobenzeneazosalicylic acid
C 6 H 4 (N0 2 ).N 2 .C 6 H 3 (OH).
3)
...
225 d. (?)
Meldola
47, 666
CO 2 H=1.4 ; 4.1.2
Dinitrobenzamidophenol
fr. C 6 H 4 (OH).NHBz=1.2
C 13 H 9 6 N 3
173
Morse
B., 7, 1320
28,272;vii.,903
Benzamidodiuitrophenol
OH.NHBz.(NO 2 ) 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.N0 2 .NH(CO.C 6 H 4 .N0 2 )
jj
....
225
Hiibner
A., 210, 380
42, 506
=1.?.4 ; (1.3)
Benzoxydinitroamidobenzene
OBz.NH 2 .(N0 2 ) 2 =1.2.(?) 2
j.
....
218-219
A., 205, 74 ; 210,
42, 507
395
Dinitrophenamidobenzoic
C 6 H 3 (N0 2 ) 2 .NH.C 6 H 4 .C0 2 H
j-
262-264
Jourdan
B., 18, 1449
48, 988
acid
=4.2.1 ; 1.2
Benzyl picrate
(O.CH 2 Ph).(NO 2 ) 3 =1.2.4.6
C 13 H 9 7 N 3
....
149
Kumpf
B., 17, 1076
46, 1005
Trinitrobenzylphenol
C 6 H 4 (NO,).CH 2 .C 6 H 2 (OH)
148
Eennie
41,36
(NO 2 ) 2 =1.4 ; 1.4.3.5
0-Dinitrophenylnitrobenzyl
C 6 H 4 (N0 2 ).CH 2 .O.C 6 H 3
.
....
137
Kumpf
B., 17, 1077
46, 1005
oxide
(NO 2 ) 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,H 4 (N0 2 ).CH 2 .O.C 6 H a
C 13 H 9 0,N.
198
Finkentscher
A., 217, 177-182
oxide
(NO 2 ),=1.4; 1.2.4
Anilidocarbamidophenol
O.C 6 H 4 .N : C.NHPh=1.2
i i
13 H 10 ON 2
173
Kalckhoff
B., 16, 1826
44, 1110
Hydroxybenzenylphenylene-
NH.C 6 H 4 .N : C.C 6 H 4 .OH
222-5
Hiibner and Men-
B., 13, 463 ; A.,
38, 556
amidiue
=(1.2) 2
sching
210, 345
Diamidodiphenylene ketone
fr. (C 6 H 4 ) 2 :CO=(1.2) 2
3)
....
286
Schultz
A., 203, 95
38, 814
Benzylidenenitranil ine
Ph.CH:N.C 6 H 4 .N0 2 =U
C 13 H 10 2 N 2
66
Lazorenco
J. [1870], 760
Nitrobenzylideneaniline
C 6 H 4 (NO 2 ).CH : NPh=1.3
61
B
=1.4
jj
93
Fischer
B., 14, 2526
42,393
Nitrobenzanilide
C 6 H 4 (N0 2 ).CO.NHPh=1.3
C 13 H 10 3 N 2
144
Engler and Volk-
B., 8, 35
28, 643
hausen
....
144
Mears
B., 9, 774
30, 309
Benzamidonitrobenzene
C 6 H 4 (N0 2 ).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
C 6 H 4 (OH).N 2 .C 6 H 4 .C0 2 H
....
220
Griess
B., 14, 2033
42, 48
= 1.?; 1.3
Benzoylnitroatnidophenol ....
OH.NHBz.NO 2 =1.2.4orl.4.2
C 13 H 10 4 N- 2
200 d.
Post
A., 205, 73
Nitrosalicylanilide
OH.NO 2 .(CO.NHPh)=1.3.4
....
224
Mensching&HUbnp]
B., 13, 462 ; A.,
38, 556
210, 343
Nitrobenzamidophenol
HO.C 6 H 4 .NH.CO.C 6 H 4 .N0 2
....
139 d.
Morse
B., 7, 1320
28, 272
Salicylnitranilide
HO.C 6 H 4 .CO.NH.C 6 H 4 .
..
154
Hiibner
A., 210, 345
NO 2 =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.C 6 H 4 .CO.C 6 H 3 (NH,).NO ; ,
115
Haarmann
B., 6, 339
26, 907
=1.2 ; ?.1.4
Dinitrodiphenylmethane
fr. Ph.CH 2 .C 6 H 4 .N0 2 =1.3
94
Becker
B., 15, 2092
44, 203
CH.:C 12 H 8 (N0 2 ) 2
118
Pratorius
A., 194. 366
36. 319
a
....
118
Staedel
B., 11, 745
34,671
fr. Ph.CH 2 .C,H 4 .N0 2 =1.4
172
Doer
B., 5, 795
vii.,948;26,170
>!
"
....
175
Easier
B., 16, 2719
46, 310
"
CH 2 :0 12 H S (N0 2 ) 2
183
Doer
B., 5, 795
26, 170
....
I)
31
183
Pratorius
A., 194, 369
36, 319
Eesorcinolazobenzoic acid ....
C 6 H 3 (OH) 2 .N 2 .C t H 4 .C0 2 H
13
....
d.
Griess
B., 14, 2034
42, 49
=1.3.?; 1.3
Dinitrotolylphenyl
(3-dinitrophenylbenzyloxide....
fr. Ph.C 6 H 4 .Me=1.4
Ph.CH,.O.C 8 H 3 (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
C 6 H 4 (N0 2 ).CH 2 .O.C 6 H 4 (N0 2 )
129
"
B., 17, 1077
"
=1.4; 1.2
=(1.4),
183
Benzyldinitrophenol....
Dinitrodiphenylcarbamide ....
Ph.CH 2 .C 6 H 2 (OH)(N0 2 ) 2
CO(NH.C 6 H 4 .N0 2 ) 2 =(1.3) 2
31
87-88
233
Rennie
Losanitsch
13
41, 222
B., 16, 50
D
44, 583
Benzyldinitroquinol
=2
(O.CH 2 Ph).OH.(N0 2 ) 2
31
a. 100
137
Bruckner
Pellezzari
B., 7, 1235
G. I., 13, 501
46, 437
Ethylic dinitro-a-naphthoate
-0- ,,
C IO H 6 (N0 2 ) 2 .C0 2 Et
33
143 u.c.
Ek strand
B., 17, 1601
46, 1361
"
31
141 u.c.
B., 17, 1603
,i
Formodiphenylamine
H.CO.NPh,
C 13 H n ON
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.NPh 2
C^H^ON
....
1
Tobias
B., 15, 2866
Diphenylacetoxime
Ph 2 : NOH
5>
B., 16, 823
139-5-140
Jaimy
B., 15, 2782
44,580
Beuzanilide ....
C 6 H-.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.C 6 H 4 .NH 2 =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.C 6 H 4 .NH.COH = 1.4
n
172
Zimmermann
B., 13, 1967
40, 176
Hydroxybenzaldehydeanilide
HO.C 6 H 4 .CH:NPh=1.4
ji
190-191
Herzfeld
B., 10, 1272
34,66
Pseudocinnamylpyrroline ....
C 4 H 4 N.CO.CH : CHPh
H
141-142
Ciamician & Denu-
B., 17, 2947
48, 378
stedt
Diamidohydracridine ketone
CO.C 8 H 4 .NH.C li H 2 (NH 2 ),,
C 13 H,,ON 3
....
222-223
Jourdan
B., 18, 1452
48, 988
i- . L
=2.1 ; U.2.4
Phenylic phenylcarbamate ....
NHPh.CO 2 Ph
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.CH 2 .C 6 H 4 .NO 2 =1.3
i)
....
Liquid
Becker
B., 15, 2091
=1.4
31
Easier
B., 16, 2717
46, 310
Benzoxyamidobenzene
C 6 H 4 (OBz).NH 2 =1.2
jj
unstable
Bottcher
B., 16, 630
= 1.4
51
....
153-154
Hiibner
A., 210, 379
42, 505
Formylhydroxydiphenyl-
C 6 H 4 .OH.(NPkCOH=1.4
J
178
Philip and C.'alm
B., 17, 2436
48, 156
amine
Hydroxybenzanilide
HO.C 6 H 4 .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 (?)
C c H 4 .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.C 6 H 4 .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
C 10 H 7 .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.CH 2 .C 6 H 4 .N0 2 =1.4
C U H 1I Q,N
91
Kumpf
B., 17, 1077
46, 1005
Nitrophenylbenzyl oxide ....
Ph.CH 2 .O.C 6 H 4 .NO 2 =1.2
Jl
29
i
B., 17, 1076
)
j
=1.4
))
....
106
)
B., 17, 1075
)
Beuzylnitrophenol ....
OH.N0 2 .CH 2 Ph=1.2.4
Jl
71 ; 74-75
Eennie
41, 221
Methylic pyrrolinemethyl-
C 4 H 3 N : CH.C 6 H 4 .CO. i Me
)>
....
104-105
Ciamician & Denn-
B., 17, 2959
48, 37!)
benzoate
stedt
Nitrocarbanilide
NHPh.CO.NH.C 6 H 4 .NO 2
C 13 H U 3 N 3
187
Bruckner
B., 7, 1236
28, 166
Amidobenzeneazosalicylic
NH 2 .C 6 H 4 .N,,C 6 H S (OH).
....
219-220 d.
Meldola
47, 667
acid
CO 2 H
Benzylnitroquinol
OH.(O.CH 2 Ph).N0 2 =1.4.5
C 13 H U 4 N
,,,,
137
Schiff
G. I., 13, 538
46, 433
,, .... ....
=1.4.6
3>
156-158 d.
>
thy lie nitro-a-imphthoate ....
C 10 H 6 .NO 2 .CO 2 Et=?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 ....
C 10 H 6 .NO i ,C0 2 Et=?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
C 6 H 3 .NMePh.(N0 2 ) 3
C 13 H n 4 N 3
167 u. c.
Leymann
B., 15, 1235
42, 1057
y-dinitrotolylphenylamine ....
C 6 H 2 Me.(NO 2 ) 2 .NHPh
JJ
142
Hepp
A., 215, 369
44, 317
Dinitrophenyltoluidine
C 6 H 4 Me.NH.C 6 H 3 (NO 2 ) 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.C 6 H 4 .NO.,), !
C 13 H U 4 N 5
190
Briickner
B., 7, 1235
28, 166
Benzylphenylnitrosamine ....
Ph.CH 2 .NPh.NO
C 13 H 12 ON 2
58
Antrick
A., 227, 360
48, 543
Benzoylphenylhydrazine
Ph.NH.NH.CO.Ph
....
168
Fischer
A., 190, 125
34, 308
Diphenylcarbamide ....
NH 2 .CO.NPh 2
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.C 6 H 4 .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
C 6 H 4 .NH 2 .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
C 6 H 4 (NH 2 ) 2 ?
140
Mixter
A. C. J., 6, 26
46, 1327
(?) ....
=1.3
(?)
....
260
Iliibner
A., 208, 298
Hydroxybenzylidenephenyl-
HO.C C H 4 .CH I N 2 HPh=1.2
jj
....
142-143
Kossing
B., 17, 3004
hydrazine
jj
>!
>j
142-143
Tiemann and Kees
B., 18, 1660
Methyloxyazobenzene
Ph.N 2 .O.C 6 H 4 Me
jj
53-5-54
Scichilone
G. I. [1882], 108
42, 726
Phenylazocresol (J., 1879,465)
Ph.N 2 .C 6 H 3 Me.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.C 6 H 4 .N5.C 6 H 4 Me "
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:C 12 H 8 (N0 2 ) 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:C 12 H 8 (N0 2 ) 2
C 13 H 12 ON 2
....
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.CH 2 .C 6 H 4 .NO 2
Cj.H.jOjN.
68
Strakosch
B., 6, 1062
27,80
Salicyl-a-amidoanilide
NH 2 .C 6 H 4 .NH.CO.C 6 H 4 .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
C 6 H 4 Me.N 2 .C 6 H 3 (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.N 2 .C,H 4 Me(OH)j=?.1.3.5
>?
....
183
Typke
B., 10, 1579
34, 219
Phenylmethylacetoxypyrimi-
C 4 N 2 HPh.Me.OAc
1J
B., 18, 760
40-41
Pinner
B., 18, 762
48, 752
dine
Nitrodiphenylguanidirie
NH : C(NHPh).NH.C 6 H 4 .
C 13 H, 2 2 N 4
....
131-132
Bruckner
B., 7, 1236
28, 166
NO,
Toluidineazonitrobenzene ....
N0 2 .C 6 H 4 .N 2 .C 6 H 3 Me.NH 2 "
....
198
Nolting and Binder
B. S., 42, 340
48, 385
=4.1 ; 5.1.2
Toluquinone + o-nitraniline
MM
C 13 H 12 4 N 2
37
Hebebrand
B., 15, 1976
Dinitrophendiamidotoluene
NH 2 .C 6 H 3 Me.NH.C 6 H 3
C 13 H 12 4 N 4
184
Leyniann
B., 15, 1237
42, 1057
(N0 2 ) 2 =4.1.2; (?) 3
a-Trinitrotolueneaniline
C 6 H 2 Me(NO 2 ) 3 .NH,Ph
C 13 H, 2 6 N 4
83-84
Hepp
A., 215, 365
44, 317
Lutidine picrate
(C 6 NH 3 Me 2 ).C 6 H 2 (N0 2 ) 8 .OH
C 13 H 12 ? N 4
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 ....
C 10 H 7 .NMeAc
C 13 H 13 ON
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
C 13 H 13 ON 3
170
Kiihn
B., 17, 2885
48, 261
Amidobenzdiamidobenzene....
NH 2 .C 6 H 4 .NH.CO.C S H 4 .
))
129
McHugh
B., 7, 1268
NH.,=(1.3) 2
p-Toluidineazophenol
NH 2 .C 6 H 3 Me.N 2 .C 6 H 4 .OH
?1
172
Wallach
B., 15, 2827
44, 584
j3-naphthylurethane
C 10 H 7 .NH.CO 2 Et
C 13 H,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.C 6 H 4 .CH : C.CO 2 Et
1)
71
Friedlander and
B., 16, 1837
44, 1149
boxylate
Goliring
Aniline salicylate
HO.C 6 H 4 .CO 2 H+NH 2 Ph
C 13 H 13 3 N
....
150
Guthrie
P. M. [5], 18, 27
=1.2
Acetamidocinnamenylacrylic
NHAc.C G H 4 .CH : CH.CH :
)
....
253 d.
Diehl and Einhorn
B., 18, 2333
48, 1223
acid
CH.CO 2 H=1.2
Nitroharmalin
C 13 H 13 (N0 2 )N 2
C 13 H 13 3 N 3
120
Fritzsche
A., 68, 355 ; 72,
iii., 9
306
Methylic coumalanilidic acid
C 4 N 3 (NHPh).C0 2 Me .C0 2 H
C 13 H 13 4 N
....
140 d.
Pechmann & Welsh
B., 17, 2393
47, 152 ; 48,
175
Ethylic acetindoxylate
N.C,H7c(OAc).CH.CO 2 Et
I>
....
138
Baeyer
B., 14, 1742
42, 198
i i
Etliylic nitrobenzoyltri-
CH 2 .CH 2 .C(CO s Et).CO.C.iH,.
l ', 3 IIiAN
84
Perkin & Bellenot
B., 18, 959
48, 795
methylene carboxylate
|_ 1
NO 2 =1.4
Aniline pyrogallate ....
C 6 H ; ,(OH) 3 .CO 2 H+C (i H 5 .NH 2
n
126-128
Guthrie
P. M. [5], 18, 109
Triacetylgallauiide
(OAc) 3 .CONH 2 =l. 2.3.5
C 13 H,,0 7 N
150
Schiff and Pous
B., 18, 489
48, 796
/3-diamidobenzhydrol
HO.CH : C 12 H 3 (NH 2 ) 2
C 13 H 14 ON 2
....
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.C 6 H 7 N 2
C 13 H 14 ON 4
*)
225
Keller
J. p. [2], 31, 363
48, 961
Ethylic benzenylazoxime-
O.N : CPh.N : C(CH 2 ) 2 .C0 2 Et
C 13 H 14 3 N 2
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
C 13 H 14 3 N a
....
235
Wechsler
B., 18, 1041
48, 900
CH 2
_j '
?
C 13 H U O 6 N 5
..
235
Stojentin
J. p., 32, 1
48, 1195
Toluidine phenate
C 6 H 4 Me.NH 2 +Ph.OH=1.4
C, 3 H 15 ON
31-1
Dyson
43,468
Diallylamidobenzoic acid _
N(C 3 H S ) 2 .C0 2 H=1.3
C 13 H 16 2 N
....
90
Griess
B., 5, 1041
26, 281 ; vii.,
168
Mesitylsuccinimide
C 6 H 2 Me 3 .N:(CO) 2 :C,H 4
137
Eisenberg
B., 15, 1018
42, 956
=1.3.5.6
Isonitrosotetramethyloxy-
fr.C 6 HMe 3 .N.NH.CMe.CH 2 .
C 13 H 15 2 N 3
....
156
Haller
B., 18, 708
48, 818
i
quinizine
CO=1.2.4.5.6
J
Ethylic ethylind'oxylate
N.C 6 H 4 .C(OEt).CH.CO 2 Et '
C 13 H 15 3 N
98
Baeyer
B., 14, 1742
48, 198
=1.2
Ethylic acetamidocinnamate
NHAc.(CH : CH.CO 2 Et)
J)
137
Friedliinder and
B., 15, 1423
42, 1209
=1.2
Weinberg
Ethylcumazonic acid
N : CEt.O.CMe 2 .C 6 H 3 .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-
....
C 13 H 16 4 N
....
78-79
Duisberg
B., 18, 198
48, 544
tate
ethylnitrobenzoyl-
NO 2 .C 6 H 4 .CO.CHEt.CO 2 Et
C 13 H 15 5 N
39-40
Perkin & Bellemot
B., 18, 953
48, 794
acetate
=1.4
benzamsucciuate ....
CO 2 H.C 6 H 4 .NH.CO.C 2 H 4 .
J)
174
Pellizzari
B., 18, 214
48, 533
OO 2 Et=1.3
Benzdiamidoacetamidoacetie
NHBz.CH 2 .CO.NH.CH 2 .CO
C 13 H 15 O 5 N 3
172
Curtius
B., 16, 756
44, 1087
acid
NH.CH 2 .CO 2 H
Tetramethyloxyquinizhie ....
C 6 HMe 3 .N.NH.CMe.CH n .CO
i i
C 13 H 16 ON 2
..
154-155
Haller
B., 18, 707
48, 818
=1.2.4.5.6
Ethylic azotolueneacetacetate
Me.(N 3 .CHAc.CO 2 Et)=1.4
C 13 H 16 3 N 2
.
74
ZUbliu
B., 11, 1420
Nitrobenzaldiacetonamine ....
N0 2 .C 6 H 4 .CH.CH 2 .CO.CH 2 .
.-
Liquid
Antrick
A., 227, 365
48, 503
L
CMe a .NH=1.2
j
11 =1-3
....
Liquid
,,
n
n 11
IT =1.4
ir
142'5
,,
yj
Ethylic /3-hippuramidacetic
NHBz.CH 2 .CO.NH.CH 2 .C(X
C 13 H 16 4 N 2
117
Curtius
J. p. [2], 26, 194
44, 339
acid
Et
nitrophenylethoxy-
NO 2 .C 6 H 4 .CH(OEt).CH(NO 2 ).
C 13 H 16 7 N 2
...
52
Friedliinder and
A., 229, 210 ; B.,
48, 1138
nitropropionate
CO s Et=1.4
Mahly
16, 852
.. ethyldinitrohydro-
OMe.(N0 2 ) 2 .(CH 2 .CH 2 .C0 2
Jl
49
Stohr
A., 225, 57
46, 1350
p-coumarate
Et)=1.2.6.4
Benzald iacetonamine
Pli.CH.NH.CMe 2 :(CH) 2 :CO
C 13 H 17 ON
230 d.
61-2
Heintz
A., 193, 62
36, 54
11 11
H
62-63
Fischer
B., 16, 2237
46, 54
Diethamidocinnamic acid ....
NEt 2 .(CH : CH.CO a H)=1.2
C 13 H, r 2 N
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.CH 2 .CO 2 Bu
NHBz.CH 2 .CO 2 Bu0
C 13 H 17 3 N
....
40-41
45-46
Campani & Bizzarri
G. L, 10, 257
38, 870
527)
"
Hydroxypropylcarboxyl-
phenylurethane
C 6 H 3 .C0 2 H.(CMe 2 .OH).
(NH.CO.,Et)
C 13 H 17 5 N
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-
C H,Me ; (NH), : CMe.CH^
CO 2 Et
82
91-93
jadenbnrg and
Eiigheimer
tnorr
B., 12, 953
B., 17, 550
36, 716
46, 1154
acetoacetate
Diacetamidomesitylene
Me a .(NHAc) 2 =1.3.5,2.4
,,
a. 300
jadenburg
A., 179, 177; B.,
38, 1036; 29,
Ethylic anilidopyrotartar-
aiuate
NH s .CO.CMe(NHPh).CH,.
C0 2 Et
C 13 H 19 3 N 2
125
Wechsler
8,677
B., 10, 1039
386
48, 900
Benzylidene urethane
Ph.CH(NH.C0 2 EtJ 2
C 13 H 18 4 N 2
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
C 6 H 3 Me(NH.CO 2 Et),
C 13 H 1S 4 N 2
137
Lussy
B., 7, 1264
28, 274
[sobutylacetarnidotoluene ...
Me.Bu.NHAc=1.5^
QuH M ON
162
Effront
B., 17, 2322
48, 152
Pentainethylacetanilide
C 6 Me 6 .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.OG 2 Et)=1.3.2
C 13 H 19 2 N
....
229
Kelbe and Warth
A., 221, 157
46,47
Diacetyltrimethtriamidoben -
NMej.NMeAc.NHAc 1.4.?
C I3 H 19 2 N 3
184
Wurster& Schobig
B., 12, 1813
38, 111
zene
Nitroisoamylethoxy benzene
OEt.C 5 H n .NO 2 =?
C 13 H 19 3 N
a. 300 d.
Liquid
Liebmann
B., 15, 1991
Dietkylic trimethylpyrroline
CO 2 Et.C:CMe.NMe.CMe:C.
C 13 H 19 4 N
....
72
Knorr
B., 18, 303
48, 555
dicarboxylate
CQ 2 Et
Diethyl-m -toluylenecarba-
C 6 H 3 Me(NH.CO.NHEt) 2
C^H^N,
175
Lussy
B., 8, 292
28, 770
mide
Diethoxyhydroxyethyltheo-
C 13 K, 7 N 2
152
Fischer
A., 215, 307
44, 357
bromine
Cyanallyl-allylalcoholate
C^H^ON
....
95-96
Z. C. [1870], 401
Allylalcohol+allylcyanide ...
3 H S .CN+3C 8 H 6 .OH
C 13 H 23 3 N
95-96
Rinne
B., 6, 389
vii., 49
Valerodiacetonamine oxalate
C U H,,ON+U 2 H 2 4
C^H^O^N
190 d.
Antrick
A., 227, 365
48, 502
CEnanthodiacetonamine
O 6 H 13 .CH.CH.,CO.CH,.
C^H^ON
....
29-5
j)
48, 503
i *
CMe 2 .NH
Fr. ethylcarbamine
MM
C 13 H S5 3 N 5
a. 200
Gautier
C. R., 67, 804
vi., 529
Oxalyldipiperidine ....
not C^HsjON,; as in orig.
C 13 H 26 ON 2
280-290 d.
Ladenburg
B., 14, 1879
Ethylio diisoamylcarbamate
N(C 5 H 11 ) 2 .CO 2 Et
C 13 H 27 2 N
246-247
L. 20
Ouster
B., 12, 1334
36, 914
Tetranitroanthraflavie acid
C 14 H 4 (N0 2 ) 4 4
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
C 14 H 6 (N0 2 ) 2 :0 2
C 14 H c O (i N 2
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- >*
NO i .C 6 H 3 :(CO) 2 :C 6 H 3 .N0 2
i)
a. 300
Bomer
B., 16, 364
44, 737
=3.2.1; 1.2.6
Dinitrohydroxyauthra-
C 6 H 4 ; (CO) 2 : C 6 H(NO 2 ) 2 .OH
C 14 H 6 7 N 2
268-270
Simoii
B., 14, 465; 15,
40, 608
quinone
=2.1; 1.2.4.6.5
692
Diuitroxantliopurpurin
C 14 H 4 O 2 (N0 2 ) 2 (OH) 2
C 14 H 6 8 N 2
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,
C 14 H 7 4 N
....
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. C C H 4 .CO.C' H 3 .C0 2 H
C 14 H 7 6 N
245-246
Fittig & Liepmann
A., 208, 8
38, 401
boxy lie acid
= 1.2; 1.2.3.
a-Nitroalizarin (A., 201, 353)
fr. C 6 H 4 :(CO) 2 :C 6 H 2 (OH) 2
C 14 H.O C N
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)
C 6 H 4 :(CO) 2 :0 6 H(OH) 2 .N0 2
))
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-
C 6 H 4 .C 6 H 4 .(^: N O N ' O
C U H 8 ON 2
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
(.C 6 H 3 .NH.CO) 2
C I4 H 8 2 N S
283 u.c.
Claus & Hemmaun
B., 16, 1762
44, 1127
anhydrimide
i i
Nitrophenylphthalimide .
C 6 H 4 :(CO) 2 :N.C 6 H 4 .N0 2
C 14 H 8 4 N 2
....
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
C 14 H 3 5 N 2
116d.
11
B., 14, 472
Nitroamidoxyanthraquinoue
....
240
Bourcart
B., 12, 1419
38, 263
Dinitrobeuzil . ... ...
C 14 H 8 O 6 N 2
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
(N0 2 .C 6 H 4 .CO) 2 0=(1.2) 2
C 14 H 8 7 N 2
....
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
(.C 6 H 3 .N0 2 .C0 2 H) 2 =(1.4.2) 2
C 14 H 3 8 N 2
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. (.C 6 H 4 .CO S H) 2 =(1.2) 2 ....
297
A., 203, 105
38, 814
Tetrauitrobenzyltolueue
C 14 H 8 8 N 4
160-161
Zincke
B., 5, 685
vii., 183; 25,
1005
Benzoylphenylisonitril
C s H 4 Bz.NC=1.4
C 14 H 9 ON
118-119
Dobner and Weiss
B., 14, 1838
42, 177
11
118-119
Dobner
A., 210, 271
42, 508
Phenanthreneqninonimide ....
C H 4 .C 6 H 4 .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
C 6 H 4 (OBz).CN=1.2
C 14 H 9 2 N
A., 99, 250
148-149
Henry
Z. C. [2], 6, 53 ;
vi., 1012
B., 2, 491
Phenylphthalimide
c e H 4 :(co) 2 :NPh
....
305
Dobner
A., 210, 267
11
205
Laurent&Gerhardt
J., 1847, 605
Benzoylanthranil
C 6 H,.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
C 6 H 4 .CO.C 6 H 4 .CH(NO)
i i
146
Liebermann and
B., 13, 1586
40, 99
Lindemann
Amidophenanthraquinone ....
CO.C 6 H 4 .C 6 H 3 (NH 2 ).CO
....
200 d.
Anschiitz & Meyer
B., 18, 1943
48, 1068
=2.1 ; 1.4.2
Amidoanthraquinoue
C & H 4 :(CO) 2 :C 6 H 3 .NH 2
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
N 2 :(C,H 4 .CO),:NH=(1.2) 2
C I4 H 9 2 N 3
.
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
G 6 H 4 :(CO) 2 :N.C 6 H 4 .OH
C 14 H 9 3 N
....
220
Ladeuburg
B., i>, 1528
31, 305
=0.8),
/3-Amidohydroxyanthraquin-
C 6 Er 4 :(CO) 2 :C 6 H 2 (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
C 14 H 9 3 N 3
160
Schopf
B., 18, 1067
48, 897
zenyl
" 1 1
Nitrobenzil .... ....
C 6 H 4 (NO 2 ).COBz=l.?
C,,H O,,N
110
Xi n in
As., 3, 153
vi., 306
a-Amidoalizarin
VJ 14 J -*'9 % -'4
)>
?
Perkin
J. [1877], 586
J3-
....
j>
....
a. 300
Schunck & Romer
B., 12, 588
36, 655
Nitrodiphenic acid ....
CO,H.C 6 H 4 .C 6 H 3 (NO 2 ).CO 2 H
C 14 H 9 6 N
217
Strasburger
B., 16, 2347
46, 329
=2.1 ; 1.4.2
Dinitro-a-naph thylsuccini-
C lo H s (N0 2 ) 2 .N:(00) !! :C. i H 4
C 14 H 9 6 N 3
250
Hiibner
A., 209, 382
42, 181:
mide
)
)
250
Haneniann
B., 10, 1713
Fr. papaveric acid
....
C 14 H 9 O.N
....
245-246-
Goldschmidt
M. C., 6, 372
48, 1081
Trinitrotolylphenylketone ...
C 6 H 3 (N0 2 ) 2 .CO.C 6 H 3 Me.N0 2
C 14 H 9 7 N 3
165
Plascuda & Zincke
B., 7, 983
28, 69
Hexanitro-p-ditolylamine ...
NH : C 12 H 2 Me. 2 (NO 2 ) 6
C 14 H 9 12 N.
....
258
Lehne
B., 13, 1545
40, 41
Dibenzenylazoxime
N:CPh.N:CPh.O
C 14 H 10 ON 4
290
108
Tiemann & Kriiger
B., 17, 1695
46, 1326
i i
Anthroxanaldehyde anilide...
O.N.C 6 H 4 .C.CH : NPlx
i }
It
40
Schillinger and
B., 16, 2224
46, 60
Wleiigel
Diphenyldicyanate
PhjAOjNj
C 14 H 1D 0.,N 2
....
175
Hofraann
B., 3, 765 ; 4,
24, 136 ; vii.,
246 ; As., 1, 57
407
Hydroxybenzenylazoxime-
N : CPh.O.N : C.C 6 H 4 .OH
J)
163
Schoff
B., 18, 2475
48, 1217
benzenyl
=1.3
Phthalyldiamidobenzene
C 6 H 4 :(NH.CO) 2 :C 6 H 4
J)
....
178
Biedermann
B., 10, 1165
32, 784
= 1.3; 1.2
=1.4; 1.2
))
....
182
B., 10, 1164
?
Amidobenzoid
NH.C 6 H 4 .CO.NH.C 6 H 4 .CO
))
225
Piutti
B., 16, 1321
44, 999,
i ' i
Phenylenamidinetoluic acid
NH.C 6 H 4 .N : C.C 6 H 4 .CO 2 H
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
[.CH 3 (NH 2 ).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
NH 2 .NH 2 =1.2
?
a. 130 d.
Perger
J. P. [2], 18, 138
1-
NH S .C 6 H J :(CO) S :C 6 H 3 .NH 3
sb.
a. 300
Romer
B., 16, 366
44, 737
=3.2.1; 1.2.6
Ph enyldiazonitrobenzylcyan-
N0 2 .C 6 H 4 .[CH(N : NPh).CN]
C 14 H 10 2 N 4
201-202
Perkin
B., 16, 341
43, 111
ide
= 1.4
....
C 14 H 10 3 N 3
....
188
Fried] iiuder&Miihly
A., 229, 210 ;
48, 1137
B., 16, 850
Azobenzoic acid
(:N.C 6 H 4 .C0 2 H)=(1.2) 2
C 14 H 10 4 N 2
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.C 6 H 4 .N0 2 ) 2
....
a. 280
Strakosch
B., 6, 329
26, 890
Hydro-anthracene diuitrite
C 6 H 4 .CH n .C 6 H 4 .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)
C 14 H 10 -(-N 2 4
C 14 H 10 4 N 2
....
194
Liebermann and
B., 13, 1586
40, 99
Lindenj aim
u-diiiitrodeoxybenzoin
....
C I4 H 10 6 N 2
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 ...
N0 2 .C 6 H 4 .CO.C 6 H 3 Me.N0 2
....
126-127
Plascuda & Zincke
B., 7, 983
28, 69
=1.4; 1.4.3
11
fr. Ph.CO.C 6 H 4 Me=1.3
145
Senff
A., 220, 225
46, 427
Methylic diuitrodiphenyl-
N0 2 .C 6 H 4 .C 6 H 3 (NO 2 ).CO 2 Me
C 14 H 10 6 N 2
....
156
Strasser & Schultz
A., 210, 192
42, 521
carboxylate
=1.4 ; 1.2.4
Dinitro-oxanilide
(.CO.NH.C 6 H 4 .N0 2 ) 2 =(1.4) 2
C 14 H 10 6 N 4
A., 209, 366
260
Hiibner & Rudolph
B., 8, 473
42, 180
=(1.2),
a. 300
Hiibner
A., 209, 369
42, 181
Pyridinedicarboxylic acid ....
Polymer
C 14 H 10 3 N 2
96 u. c.
Claus
B., 14, 1942
Tetranitrobenzyltoluene
fr. Ph.CH 2 .C 6 H 4 Me=1.4
C 14 H 10 8 N 4
160-161
Zinck6
B., 5, 685
Acetylcarbazole
C f H 4 .NAc.C 6 H 4
C 14 H n ON
a. 360 d.
69
Grsebe and Glaser
A., 163, 352
1 1
Benzilimide ....
11
C 42 H 32 4 N 2
130
Laurent
J. p., 35, 461
Imabeuzil .... .... . .
C,H 5 .C( : NH).CO.C 6 H 5
11
140
11
J. p., 27, 312 ; 35,
iii., 245
461
Phthalidanil
Ph.N : CH.C 6 H 4 .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.C 6 H 4 .NH 2
C 14 H n ON 3
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
C 14 H U 0,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
(?) +2H 2
Benzimidobenzoate NH : CPh.O.CPh : O
' "
99
148-5
Schaffer
Pinner and Klein
A., 169, 111
B., 11, 766
27, 165
34, 864
Nitrodiphenylethylene
CH 2 : CPh.C 6 H 4 .NO 2
11
86
Anschiitz & Bomig
B., 18, 664
48, 768
Piperonalanilide
CH 3 :o 2 :c 6 H 3 .cH:NPh
65
Lorenz
B., 14, 792
40, 729
=4.3.1
Naphthylsuccinimide
c 2 H 4 :(co) 2 :N.o, H 7
J)
....
152
Hiibner and Hane-
B., 10, 1713 ; A.,
42, 181
maim
209, 382
? (B., 8, 1050)
Dibenzhydroxamic acid
NBz 2 .OH (?)
C 14 H U 3 N 3
C 14 H 11 3 N
....
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.C0 2 H=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
OO s H.(CO.NHPh)=1.2
C.H 4 .C(OH):CH.N.N 2 .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
C 6 H 4 Me.(JO.C 6 H 4 .N0 2
....
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.C 6 H 4 .CH I N.C 8 H 4 .C0 2 E
C 14 H U 3 N
....
190
Schiff
A., 210, 116
42, 303
benzoic acid
= 1.2; 1.3
Anthracene nitrate
C, 4 H 10 +HN0 3
}
....
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
C l4 H n 3 N 3
86
Fischer
B., 10, 960
32, 607
Acetophenone nitrophenyl-
Bz.CH 2 .O.C 6 H 4 .NO 2 =1.4
C 14 H n 4 N
144
Mohlau
B., 15, 2498
44, 332
oxide
Benzoylamidosalicylic acid ..
CO 2 H.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.C 6 H 4 .CO) 2 NH=(1.2). !
JJ
....
197-199 d.
Schulerud
J. p. [2], 22, 289
40, 42
Hydroxyphthalanilic acid ...
HO.C 6 H 4 .NH.CO.C 6 H 4 .CO 2 H
)
223
Ladenburg
B., 9, 1528
31, 305
=(1.2),
Hydroxybenzyleneamido-
HO.C 6 H 4 .CH : N.C 6 H 3 (OH)
....
245 d.
Schiff
A., 210, 117.
42, 303
salicylic acid
CO 2 H=1.2; 5.2.1
Nitrosoacetophenone nitr-
Bz.CH 2 .N(NO).C 6 H 4 .N0 3
CuH.AN,
....
135-145
Mohlau
B., 15, 247.4
anilide
=1.4
1
))
254
Salkowski
B., 17, 509.;
46, 117(i
Dinitrobenzoylmethylaniline
fr. NMePhBz
C 14 H n 5 N 3
....
136
Hess
B., 18, 687-
48, 783
Acetophenonediuitranilide ..
CH 2 Bz.NH.C 6 H 3 (N0 2 ) 2
))
171-172
Mohlau
B., 15, 2479
44, 333
=1.2.4
Dinitrobeiizaniidotoluene ..
Me.NHBz.(NO s ) 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
C c H 3 Me(N0 2 ).NH.CO.C 6 H 4
1)
188-5
Hiibner
B., 10, 1712 ;
34, 144
NO 2 =U.4; 1.3
A., 210, 336
Benzoic+nitrobenzoic acids...
Ph.C0 2 H +C 6 H 4 (NO 2 ).C0 2 H
C 14 H n 6 N
....
136-137
Fittica
B., 9, 795 ; J. p
30, 411 ; 36,
[81 13, 184
153
Trinitrobenzyltolyl oxide ...
C 6 H 2 Me(N0 2 ) s .O.CH 2 .C 6 H 4 .
C 14 H 11 7 N 8
....
145
Staedel
B., 14, 899 ; A.
40, 724
NO 2 =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
C H H U 7 N 5
....
201
Petrieff
Z. C. [2], 6, 264
vi., 286; 26,
B., 6, 557
1027
Dibenzimide oxide
NH : CPh.O.CPh : NH
14 H 12 ON 2
....
106
Pinner and Klein
B., 11, 765
34, 804
Methylanilidocarbamido-
phenol
O.C 6 H 4 .N I C.NMePh=1.2
i i
>
a. 360
Liquid
Kalckhoff
B., 16, 1827
44, 1110
Araidobenzylideneamido-
NH 2 .C 6 H 4 .CH : N.C 6 H 4 .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.CH 2 .N(NO)Ph(!)
C I4 H 12 2 N 2
73
Mohlau
B., 15, 2472
44, 333
Benzoylbenzenylamidoxime
NHrCPh : N.OBz
>
....
140
Tienmnn & Kriiger , B., 17, 1694
46, 1326
Phenylhydrazinephenylgly-
N 2 HPh : CPh.CO 2 H
)
....
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.N 2 .O.C 6 H 4 Ac(?)
ji
....
84-5
Scichilone
G. I. [1882], 108
42, 726
Acetoxyazobenzene ....
Ph.N 2 .C 6 H 4 .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.C 6 H 4 .CH:N.C 6 H 4 .CO.
n
186
Schiff
A., 218, 185
46, 455
benzamide
NH 2 =1.2; 1.3
Nitroamidostilbene
NHj.C 8 H 4 .CH : CH.C 6 H 4 .NO 2
T?
229-230
Strakosch
B., 6, 330
6, 890
Tolylazophenylcarboxylic
C e H 4 Me.N,C 6 H 4 .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
C 14 H 12 3 N 2
Ill
Hess
B., 18, 687
48, 783
Acetophenonenitranilide
CH 2 Bz.NH.C 6 H 4 .NO 2 = 1 .4
....
167
Mohlau
B., 15, 2475
44, 333
Phenyluramidobenzoic acid..
NHPh.CO.NH.C 6 H 4 .CO,,H
n
270 d.
Kiihtt
B., 17, 2883
48, 201
= 1.3
Benzamidonitrotoluene
Me.NHBz.NO 2 =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
NO 2 ,C 6 H 4 .NH.CO.C 6 H 4 Me
))
A., 205, 118
110
Hubner
A., 210, 328
42, 504
=1.2 ; 1.4
Nitrobenzamidotoluene
C 6 H 4 Me.NH.CO.C 6 H 4 .NO 11
162
A., 210, 335 ; B.,
34, 144
=1.4; 1.3
10, 1712
Acetamidonitrodiphenyl
NO 2 .C 6 H 4 .C 6 H 4 .NHAc
246 or 264
Schmidt & Schultz
A., 207, 351
40, 911
=(1.4),
Diphenyldinitroethane
C 2 H 2 Ph 2 (N0 2 ) 2
C 14 H 12 4 N 2
.... -
300 d.
Gabriel
B., 18, 2438
48, 1229
Dinitrodibenzyl
(.CH 2 .C 6 H 4 .NO 2 ) 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
CH 3 .CH(C 6 H 4 .N0 2 ),.
....
149
Anschiitz & Romig
B., 18, 664
48, 768
Dinitrobenzyltoluene
fr. Ph.CH 2 .C 6 H 4 Me=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.C 6 H 4 .C0 2 H) 2 =(1.2) 2
)
B., 7, 1612
205
Homolka
B., 17, 1904
46, 1342
Disuccinyldiamidobenzene ...
c c H 4 [N:(co) 2 :c 2 H 4 ] 2
JJ
....
a. 360
Biedermaim
B., 9, 1668
31, 474
Diamidodiphenic acid
(.C 6 H 3 .NH 2 .C0 2 H) 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
....
C 14 H 12 4 N 4
....
110
Petrieff
B., 6, 556
26, 1027
Dinitrocresylbenzyl oxide ....
(O.CH 2 Ph).Me.(NO 2 ) 2
C 14 H 12 6 N 2
109
Fritzsche
A., 224, 137
46, 1337
= 1.4.2.6
Nitrocresylnitrobenzyl oxide
NO 2 .C 6 H 4 Me.O.CH 2 .C 6 H 4 .
)
163
)>
*,
NO 2 =2.4.1 ; 1.4
Dinitro-p-azoxytoluene
....
C 14 H 12 5 N 4
-
145
Petrieff
B., 16, 557
26, 1027
Formyldinitropheuyltohiyl-
C 6 H 3 (N0 2 ) 2 .NH.C 7 H 6 .NH.
)
157
Leymann
B., 15, 1237
42, 1057
enediamine
COH
Ethylene nitrophenylether ....
C 2 H 4 (O.C 6 H 4 .N0 2 ) 2 =(1.3) 2
C 14 H 12 6 N 2
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
C 14 H 13 ON
59
Hepp
B., 10, 329
J>
)
....
63
Hess
B., 18, 686
48, 783
Metliylic diphenylacetoxime
CPh 2 : NOMe
>
92
Spiegler
M. C., 5, 203
46, 1156
Acetophenone anilide
Ph.CO.CH 2 .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
NAcPh 2
)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.CH 2 .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
C 14 H 13 ON
....
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.C 6 H 4 .NHAc=1.4
T)
167
Osteii
A., 209,344; B.
vii., 937; 27,
7, 173
581
Tolylsalicylamide
HO.C 6 H 4 .CH ; N.C 6 H 4 Me
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.N 2 .C 6 H 4 .NHAc=1.4
C 14 H 13 ON 3
....
141
Schultz
B., 17, 463
jj
I! JJ
....
143
Berju
B., 17, 1400;
46, 1148 ; 48,
C. C. [1884], 87
660
Phenoxyaeetanilide
PhO.CH 2 .CO.NHPh
C I4 H J3 2 N
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.CO 2 H
....
164-168
Stockenius
J. [1878], 779
JJ JJ
)
..
173-175
Tieruann and Piest
B., 15, 2030
44, 198
Nitrodipheuylethane
Ph.CHMe.C 6 H 4 .N0 2
J)
79-80
Anschiitz & Romig
B., 18, 664
48, 768
Benzaiuidomethoxybenzene....
C 6 H 4 .OMe.NHBz =1.2
))
....
59-5
Mulhauser
A., 207, 244
42, 302
M
=1.4
?!
....
153-154
Lessen
A., 175, 299
28, 636
Methoxybeuzauilide
C 6 H 4 .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.CH 2 Ph).C0 2 H=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.C 6 H 4 .CO.NH.C 6 H 4 Me
....
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
CH 3 .CH(NHC 10 H r ).CH J .
f)
....
92
Knorr
B., 17, 543
46, 1198
acid
CO 3 H
Phenyllutidine carboxylic
C 5 NHPliMe 2 .C0 2 H
I)
....
189-190
Hantzscli
B., 17, 2913
48, 397
acid
Benzenylphenyluramidoxime
NHPb.CO.NH.CPh: NOH
C J4 H 13 2 N 3
....
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
C0 2 H.(NH.CNH.NHPh)
J>
....
165 d.
Traube
B., 15, 2120
44, 193
= 1.3
Nitrazotoluene
C 6 H 4 Me.N 2 .C 6 H 3 Me.N0 2
C 14 H 13 2 N 3
._.
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.C 6 H 4 .N 2 .C 6 H 4 .NHAc
-..
208
Walkch & Schulze
B., 15, 3021
44, 583
=?; 1.3
Dehydracetanilide
C 8 H ; 3 .NHPh
C u H 13 O a N
115
Oppenheim & Precbt
B., 9, 1100
30, 506
Nitrodiphenylmethylcarbinol
H(XCMePh.C 6 H 4 .NO 2
)
....
106-107
Auschiitz & Komig
B., 18, 664
48, 768
Nitrobenzyltolyloxide
C 6 H < Me.O.CH 2 .C 6 H 4 .NO 2
91
SVitzsche
A., 224, 137
46, 1337
=(1.4) 2
jj
=1.4; 1.?
))
....
181
Staedel
A., 217, 153
44, 864
Nitrotolylbenzyloxide
Ph.CH 2 .O.C 6 H 3 Me.NO 2
....
54
Tritzsche
A., 224, 137
46, 1337
=1.4.2
Ethylic a-naphthyloxamate....
C JO H 7 .NH.CO.CO 2 Et
)>
....
106
Ballo
B., 6, 249
vii., 848; 26,
913
Benzylnitrobenzenylamid-
Ph.CH 2 .O.N : C(NH 2 ).C 6 H 4 .
C 14 H 13 3 N 3
58
Schopf
B., 18, 1065
48, 896
oxime
NO 2 =1.3
Nitroazoxytoluene
C 6 H 4 Me.N 2 O.C 6 H 3 Me.NO 2
JJ
....
84
Petrieff
B., 6, 557
26, 1027
=1.4; 1.4.2
BenzdiamidonitroLoIueue ....
Me.NHBz.NH 2 .NO 2 =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.C 2 H 4 .O.C 6 H 4 .NO 2 =1.2
C 14 H 13 4 N
....
86
Weddige
J. p. [2], 24, 245
40, 1137
ether
Isopropylic nitro-|3-naph-
C 10 H 6 (N0 2 ).C0 2 Pr/i
1>
....
75-76
Graeff
B., 16, 2254
46,81
thoate
Isopropylic nitro-o-naph-
....
101-5
B., 16, 2252
J)
thoate
Phenyldimethylpyrroline di-
CO 2 H.C : CMe.NPh.CMe : C.
i i
))
....
d. 224
Knorr
B., 18, 307
48, 555
carboxylic acid
CO 2 H
Dinitrodibenzylamine
NH(CH5.C 6 H 4 .NO 2 ) 2
C 14 H 13 4 N 3
93
Strakosch
B., 6, 1058
27, 78
JJ
))
....
a. 100
u
B., 6, 1059
Dinitroditolylamine
NH(C 6 H 3 Me.NO 2 ) 2 = (1.4. ?)
)
191
Lellmann
B., 15, 832
42, 1060
Ethenyldinitrodiamidodi-
C I4 H 12 (N0 2 ) 2 N 2 +HN0 3
C 14 H 13 0-N 5
....
d.w.m. 182
Biedermann
B., 7, 540
27, 08
phenyl nitrate
Nitrosodibenzylamiiie
(Ph.CH 2 ) 2 N.NO
C 14 H 14 ON 2
52
Rohde
A., 151, 369
Benzylbenzenylamidoxime ....
NH 2 .CPh : N.O.CH 2 Ph
....
90-5
Kriiger
B., 18, 1056
48, 896
Methyldiphenylcarbamide ....
NHPh.CO.NMePh
203-205
104
Gebhardt
B., 17 2093
46, 1321
Phenamidoacetanilide
NHPh.CH 2 .CO.NHPh
1)
....
110-111
Meyer
B., 8, 1156
29, 372
Phenylbenzylcarbamide
CO : N 2 H 2 Ph.CH 2 Ph
....
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.C 6 H 4 .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,H 1 Me),NO=(1.4) 2
3)
....
100-101
Lehne
B., 13, 1544
....
1
....
103
Cosack
B., 13, 1092
38, 714
Acetdiamidodiphenyl
NH 2 .C 6 H 4 .C 6 H 4 .NHAc
199
Schultz
A., 207, 332
=(l-4) 2
Benzdiamidotoluene
C 6 H 3 Me.NHBz.NH 2 =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
C 6 H 4 Me.N 2 .C 6 H 3 Me.OH
J
112-113
Nblting and Kohn
B., 17, 354
46, 901
=1.4; U.4
Diamidomethylbenzophenone
NH 2 .C 6 H 4 .CO.C 6 H. i Me.NH 2
|)
....
a. 220 d.
Liebermann
B., 16, 1929
44, 1097
Acetdiamidoazobenzene
NHAe.C 6 H 4 .N 2 .C 6 H 4 .NH 2
C 14 H I4 ON 4
212
Nietzki
B., 17, 345
46, 1016
= 1.4; 1.?
Benzylphenylhydroxy-
HO.CHPh.C(NH 2 ) ; N.O.
C 14 H 14 2 N 2
102-103
Gross
B., 18, 1080
48, 898
ethenylamidoxime
CH 2 Ph
Phenylhydrazidophenyl-
N 2 H 2 Ph.CHPh.C0 2 H
)J
158 d.
Elbers
A., 227, 340
48, 534
acetic acid
Phenylhydrazine vanillin ....
(CH : N 2 HPh).OMe.OH
)1
105
Tiemann and Kees
B., 18, 1662
48, 1072
=1.3.4
Nitroditolylamine
C 6 H 4 Me.NH.C 6 H 3 Me.N0 2
If
....
85
Lellmann
B., 15, 831
42, 1060
=1.4 ; 1.4.7
Orcinoldiazotoluene
C 6 H 4 Me.N 3 .C 6 H 2 Me(OH) 2
>3
203-206
Scichlone
G. I, 12, 223
42, 1285
Diacetdiamidonaplithalene ....
C 10 H 6 (NHAc) 2 =
)3
234
Lawson
B., 18, 801, 2423
48, 803
Oxalyldiphenylhydrazine ....
Ph.N 2 H 2 .CO.CO.N 2 H 2 Ph
C 14 H 14 OJST 4
277-278
Fischer
A., 190, 131
34, 309
Ethylenediphenyldinitros-
....
....
157
Morley
B., 12, 1794
38, 112
amine
Nitrobenzeneazodimethani-
N0 2 .C 6 H 4 .N 2 .C 6 H 4 .NMe 2
157-158
Meldola
45, 120
liue
=1.3 ; 4.1
=(1-4),
>J
....
229-230
jj
45, 107
Nitrobenzeneazoamidoxyleiie
N0 2 .C 6 H 4 .N 2 .C 6 H 2 Me 2 .NH 2
))
Mixture (?)
141
J3
43, 428
=1.4; 1.3.5.4 and 1.4; 1.2.6.4
Dehydracetoplienylhydrazine
C s H 8 O 3 N.NHPh
C 14 H 14 3 N 2
....
207d.;sf.200
Perkin& Bernhardt
B., 17, 1523
46, 1121
Phenyldimethylpyridazindi-
....
C 14 H 14 4 N 2
....
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
C 2 H 4 (NH.C 6 H 4 .NO,,) 2 =(1.3) 2
C 14 H 14 4 N 4
....
206 u. c.
Gattermann and
B., 17, 778
46, 1142
Hager
Diuitrodiethoxynaphthalene
OEt.OEt=? ; ?
C H H 14 8 N 2
....
228-229
Alen
B. S. [2], 36, 433
42, 410
Trinitrobenzene dimethyl-
C 8 H 3 (NO,) 3 +NMe 2 Ph
C 14 H 14 8 N 4
B. S., 30, 5
106-108
Hepp
A., 215, 344
36, 51 ; 44,
aniline
=1.3.5
316
Dibenzylhydroxylamine
(Ph.CH,) 2 N.OH
C 14 H 15 ON
....
123
Schramm
B., 16, 2185
46, 51
Methylmethoxydiphenyl-
C 6 H 4 .OMe.NPhMe=1.4
313
Liquid
Philip and Calm
B., 17, 2431
48, 155
amine
Benztriamidotoluene
Me.(NH,) 2 .NHBz=1.3.5.4
C 14 H 15 ON 3
....
182-183
Kelbe
B., 8, 877
29, 270
....
183-185
Hubner
A., 208, 318
40, 1132
Diazoorcen-o-toluidine
....
C 14 H 15 2 N 3
..<.
203-206
....
G. I. [1882], 223
Ethylic ethoxycinchonate ....
N.OH.CO 2 H=1.2.4 ;
C 14 H 15 3 N
86
Konigs & Korner
B., 16, 2156
46, 85
Diacetamidopropenylbeuzoic
NAc 2 C 3 H 6 .CO 2 H=1.2.5
C 14 H ]6 4 N
....
215-216
Widmann
B., 16, 2575
46, 318
acid
Ethylic allylnitrobenzoylace-
NO,.C 8 H 4 .CO.CH(C 3 H 5 ).CO 2
C 14 H 15 5 N
....
45-46
Perkin & Bellenot
B., 18, 958
48, 795
tate
Et=1.4
Ethylic nitrobenzoyltetra-
CH,.(CH ),C(CO.Et).CO.
62-63
n
B., 18, 954
methylenecarboxylate
1 _ _ |
C 6 H 4 .N0 2 =1.4
Diethylic nitrobenzalmalonic
N0 2 .C 6 H 4 .CH:C(C0 2 Et) 2
C 14 H 15 6 N
53
Stuart
....
47, 158
acid
= 1.2
n jj
=1.4
....
93
....
Trinitranilinedimethylaniline
C 8 H s .NH a .(NO,) 3 +Ph.NMe,
C 14 H 15 6 N 5
139-141
Hepp
A., 215, 359
Diethylic nitrobenzoylma-
N0 2 .C 6 H 4 .CO.CH(C0 2 Et) 2
C 14 H 16 7 N
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
....
C 14 H 16 ON 2
...*
194-195
Bottinger
B., 17, 997
46, 1006
Nitrosodiethylnaphthylamine
C lo H 6 .NO.NEt 2
....
165
Smith
....
41, 182
Azoxytoluidine
(NH 2 .C 8 H 3 Me) 2 :N 2
C 14 H 18 ON 4
....
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
NH 2 .C 6 H 2 Me(OH).N 2 .C 6 H 3 .
....
212 d.
48, 975
Me.NH 2
51
212 d.
Graeff
A., 229, 340
48, 1128
Ethylenediamidophenol
C 2 H 4 (O.C 6 H 4 .NH 2 ) 2 =(1.2) 2
C 14 H 16 2 N 2
....
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.C 6 H 4 .CH(NH 2 ).) 2
....
180-5
Japp and Hooker
....
45, 675
Dibenzylamine nitrate
(Ph.CH,),NH + HNO,
C 14 H 18 3 N 2
186
Limpricht
A., 144, 304
vi., 337
Ethylic methyloxyquinizin-
C 8 H 4 .N.NH.CMe.CH(CH a .
1 i
....
138
Knorr and Blank
B., 17, 2052
46, 1380
acetate
i
CO 2 Et).CO=1.2
1
Diphenylguanylguanidine
NPh : C(NHPh).NH.C(NH 2 ):
C 14 H 16 3 N 8
231
Bamberger
B., 13, 1584
40, 44
nitrate
NH+HNX) 3
Diacetylmethylbenzylgly-
Me.(C : NOAc) 2 .CH 2 Ph
C 14 H 11( 4 N 2
....
80
Schramrn
B., 16, 2188
46, 52
oxime
Aniline oxalate
(.COONH 3 Ph) 3
....
nf. 180
Piria
C., 2, 305
iv., 427
o-Phenylenediimidobutyric
a
176
Knorr
B., 17, 545
46, 1198
acid
Acetylcarbazolin
C 12 H 14 NAc
C 14 H 17 ON
....
98
Grsebe and Adlers-
A., 202, 25
38, 660
kron
o-acetamido-cumenylacrylic
C 9 H 10 (NHAc).C 2 H 2 .CO 2 H
C 14 H 17 3 N
....
220
Widmann
B., 17, 2283
48, 56
acid
m -
....
240
()
n
Ethylic o-nitrocumenylacryl-
C 9 H 10 (N0 2 ).C 2 H 2 .C0 2 Et
C 14 H I7 4 N
...
Liquid
n
ate
m -
B
58-59
n
H
M
Triethylic /3-pyridinetricarb-
N.(CO 2 Et) 3 =1.2.4.6
C 14 H 17 6 N
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 ...
C 6 HMe 3 .N.NMe.CMe.CH, .
C 14 H 18 ON 2
....
105-106
Haller
B., 18, 708
48, 818
1 L -i
1
CO=1.3.4.6.5
j
a-conicei'ne pierate
C 8 H 16 N.C 6 H 2 (N0 2 ) 3 .OH
C 14 H 18 7 N 4
225
Hofmann
B., 18, 8, 11
48, 401
Isoamylic hippurate
NHBz.CH 2 .CO 2 .(CH 2 ) 2 .Pr/i
C 14 H 19 3 N
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.C 3 H 12 2 .OH
A., 68, 31
128
Laurent & Gerhard
A. C. [3], 24, 185
v., 448
m -aceta.mido-cumeny Ipro-
C 9 H 10 (NHAc).C 2 H 4 .CO 2 H
Tt
168
Widmann
B., 17, 2283
48, 56
pionic acid
Diethylic collidine-dicarb-
N.Me 3 .(C0 2 Et) 2 =?
C 14 H 19 4 N
308-310
Liquid
Hantzsch
A., 215, 21
44, 83
oxyfate
..
310
Liquid
B., 14, 1638
40, 1029
Glucovanillin aldoxime
C 6 H 3 (CH:NOH).OMe.(0.
C 14 H 19 S N
....
152
Tiemann and Kees
B., 18, 1664
48, 1072
C 6 H n 5 )=1.3.4
Glucoseacetonitrose ....
C 6 H-0(OAc) 4 .N0 3
C 14 H 19 12 N
145
Colley
C. R., 76, 436
26, 612
Picramide+dimethylaniline
NMe 2 Ph+C 6 H 2 (OH)(NH 2 ) 3
C 14 H M ON 4
139-141
Hepp
A., 215, 344
44, 316
Curaiuyldiacetamide
C 6 H 4 Pr.CH(NHAc) 2
C 14 H 20 2 N 2
....
212
Raab
B., 8, 1150
29, 398
Diethylic phenylenediglyco-
C 6 H 4 (NH:CH 2 .CO 4 Et) 2 =1.3
C 14 H 20 4 N 2
73
Zimmermaim
B., 15, 518
42, 957
collate
=1.4
83
B., 16, 515
44,797
=1.2
,,
135
B
()
Dinitrotetraethylbenzene ....
Et 4 .(NO 2 ) 2 =1.2.3.5.4.6
,,
....
115
Galle
B., 1C, 1745
44, 1092
Anisaldehyde+urethane ...
MeO.C 6 H 4 .CH(NH.C0 2 Et) 2
C^H^N,
....
171-172
Bischoff
B., 7, 1080
28, 146
=1.4
Diethylic collidinedicarb-
C 5 NMe 3 (CO.,Et), ! + HNO 3
C 14 H M 7 N S
....
92
Hantzsch
A., 215, 21
44, 83
oxylate nitrate
hydrocollidinecarb-
C 5 NH 2 Me 3 (CO 2 Et) 2
C 14 H,uO 4 N
310 d ; 315
131
B., 14, 1637 ; A.,
40, 1028 ; 44,
oxylate
215,8
82
Camphorethylimidethylimi-
j .
C 8 H 14 .CO.NEt.C : NEt
L i
C 14 H 24 ON 2
284-286
Liquid
Wallach and Ka-
B., 13, 520; 14,
38, 548 ; 40,
dine
menski .
162; A.,214,245
285
Azoxybenzotoluide
0:N 2 :(C 6 H 4 .CO.NH.C 6 H 4
C 14 H 24 3 N 4
....
290
Mixter
A. C. J., 5, 282
46, 666
Me) 2
n-Hexyl-n-cenanthylcarb-
C 6 H 13 .NH.CO.NH.C 7 H 13
C 14 H 23 O 2 N 2
....
97
Hofmann
B., 15, 759
42, 1053
amide
Myristamide ....
C 13 H 27 .CO.NH 2
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
C 14 H 36 3 N 2 ?
185
Couerbe
A. C. [2], 52, 352
iv., 745
Trinitrofluoranthene
C I5 H 3 6 N 3
nf. 300
Fittig and Gebhard
....
36, 166
Nitrobenzylidene phthalide
O.CO.C 6 H 4 .C : CPh.N0 2 =1.2
L 1
C 15 H 9 4 N
....
195 ; sf. 180
Gabriel
B., 18, 1255
48, 903
Phthalamidobenzoie acid ....
C 6 H 4 :(CO) 2 :N.C 6 H 4 .C0 2 H
....
217
B., 11, 2261
36, 324
ji
=1.2; 1.3
,,
276
B., 11, 2262
>!
>!
))
282
Pellizzari
B., 18, 216
48, 534
Nitromethylauthraquinone ....
C 6 H 4 :(CO) 2 :C 6 H 2 Me.OH
JJ
269-270
Romer and Link
B., 16, 697
44, 1139
=2.1 ; 1.2.4.5
Phenylpyridinetetracar-
N.Ph.(C0 2 H) 4 =1.4.2.3.5.6
C 16 H 9 8 N
205-207
Hantzsch
B., 17, 1517
46, 1194
boxylic acid
Nitrophenylquinoline
C 9 H 6 N.C B H 4 .N0 2 =a 1 /3 1 ; 1.3
C 15 H 10 2 N 2
124
Miller & Kinkelin
B., 18, 1903
48, 1144
Quinidinequinoline anilide ....
fr. N ; O 2 =a, ; 0,0,,
190+
Fischer and Renouf
B., 17, 1644
46, 1371
Diphenylparabanic acid
CO.NPh.CO.NPh.CO
i i
C 15 H^0 3 N 2
204
Hofmann
B., 2, 688
Benzenylazoximebenzenyl-
O.N : CPh.N : C.C 6 H 4 .C0 2 H
"
204
151
Stojentin
Schulz
J. p., 32, 1
B., 18, 2464
48, 1196
48, 1219
carboxylic acid
=1.2
Phenylcyanate + isatin
Phthalimidylnitrobenzyl ....
PhCNO+C 8 H 5 2 N
C 6 H 4 .CO.N:C.CHPh.NO 2
180 d.
199
Gumpert
Gabriel
J. p. [2], 31, 119
B., 18, 1261
48, 656
48, 903
Isatamidobenzoic acid
CO.NH.C 6 H 4 .C : N.OBz
i j
.t
251-253
Schiff
A., 210, 121
42, 304
Nitrobenzaldehyde indogen-
ide
CO.C,.H 4 .NH.C : CH.C 6 H 4 .
....
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.C 6 H 4 .C(NO :i ).CHPh.
C 15 H 10 6 N 2
....
110-113
Gabriel
B., 18, 1251
48, 902
1 ' NO 2 =1.2
Quinoline picrate
....
C 15 H 10 7 N 4
....
203
Goldschmidt and
W. A., 83, 7
40, 824
Schidt
Hydroxyquinoline picrate ....
N.OH=a i; a.
C 16 H I0 8 N 4
....
203-204
Skraup
M. C., 3, 536
44, 92
=o,; 3 2
i)
235-235-5
n.
M. C., 4, 695
46,87
11
....
235-236
M.C.,2,575; 3,545
Benzaldehyde indogenide ....
CO.C 6 H 4 .NH.C:CHPh
n
175-176
Baeyen
B., 16, 2197
46, 75
L 1
Benzalphthimidine
NH.CO.C 6 H 4 .C : CHPh=1.2
182-183
Gabriel
B., 18, 2435
48, 1229
i i
Imidodeoxybenzoincarbox-
C f ,H 4 .CO.N : C.CH 2 Ph=1.2
182-183
Gabriel & Michael
B., 11, 1682
36, 246
ylic anhydride
i i
Isobenzalphthalimidine
C 6 H 4 .CO.NH.CPh rCH
....
197
Gabriel
B., 18, 2449
48, 1231
L I
Formanthramine
C 14 H 9 .NH.CHO
....
242
Bollert
B., 16, 1640
44, 1140
Anthracenecarboxylamide ...
C 14 H 9 .(CO.NH 2 )
n
....
293-295
Bernstein
B., 16, 2611
46, 330
Phenylcarbostyril
N.OPh=a, 3! ;
C 15 H n ON
....
68-69
Friedlander
B., 15, 336
42, 733
Hydroxyphenylquinoline ....
C 9 H 6 N.C 6 H 4 .OH=a^ 3, ; 1.3
.
....
156
Miller. & Kinkelin
B., 18, 1908
48, 1145
Lactone of a-benzylphenyl-
C 6 H 4 .C0 2 .N : CPh.CH 2 =1.2
C I6 H n 2 N
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
6 H 4 :(CO) 2 :N.C 6 H 4 Me
....
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
O 6 il 4 . (OU) 2 . U 6 l 2 JleJM Ji.,
....
202
Eomer and Link
B., 16, 698
44, 1139
=2a : 1.2.4.5
Benzenylazoximebenzenyl-
o.N:cph.N:c.c 6 H 4 .co.
C 15 H n 2 N 3
....
160
Schulz
B., 18, 2467
48, 1219
carboxylamide
1 ' TLTTT
NH 2
Isatamidobenzamide
C 6 H 4 .NH.CO.C : N.C,H 4 .
....
280 d.
Schiff
A., 218, 185
46, 455
i i
CO.NH 2 =1.2; 1.3
Nitrosofurfurin (B., 11, 1250)
....
C 16 H n 4 N 3
112
G. L, 8, 76
34, 657
Phthalylamidobenzoic acid ....
C0 2 H.0 6 H 4 .CO.NH.C 6 H 4
C 16 H 1V< 6 N
275-277
Michael
B., 10, 579
32, 616
CO 2 H=I.2; 1.4
Phenylethenylazoximeben-
Ph.CH 2 .C : N.O.CPh TN
C 16 H 12 ON 2
82
Knudsan
B., 18, 1071
48, 897
zenyl
i 1
Acetophenonecarboxylic
.....
ii.
102
Roser
B., 18, 804
44, 797
phenylhydrazide
p-Methylisatinphenylimide
C s H 4 MeNO : NPh
239-240
Meyer
B., 16, 2267
46, 48
3-naphtho-diniethyloxyquin-
....
11.
129
Knorr
B., 17, 551
46, 1154
izine
Hydroxyphenyltoluquinoxal-
C 7 H 6 .N : CPh.C(OH) : N
11
....
196-197
Hinsberg
B., 18, 1229
48, 909
ine
Benzylnitrosophthalidine ....
C 6 H 4 .CO.N(NO).CH.CH 2 Ph
C 15 H 12 O 2 N 2
92-93
Gabriel
B., 18, 1263
48, 903
1- -, _ j__ - 1
Phthalyldiamidotoluen e
C 6 H 4 :(CO.NH) 2 :C s H 3 Me
....
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) ....
....
C 16 H 12 3 N 2
....
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
N0 2 .CPh : C(NH 2 ).C 6 H 4 .
C 16 H 12 4 N 2
147-150
Gabriel
B., 18, 2440
48, 1230
acid
CO 2 H=1.2
550
ORGANIC COMPOUNDS.
Name.
Constitution.
Formula.
Boiling
Point.
Melting
Point.
Authority.
Reference.
Watts' Diet.
& J. Ch. Soc.
Isatamidobenzoic acid
C 6 H 4 .NH.CO.C : N.C 6 H 4 .
C 16 H 12 4 N 2
+H 2
251-253 d.
Schiff
A., 210, 121
i i
CO 2 H=1.2 ; 1.3
Diethylic carboxamidoben-
CO(NH.C 6 H 4 .CO 2 Et) 2 =( 1 .3
C 15 H la 6 N 2
160
Wachendorff
B., 11, 701
34, 674
zoate
Methylindole picrate
C 9 H 9 N.C 6 H 2 (N0 2 ) 3 .OH
C 15 H 12 7 N 3
....
150
Fischer and Hess
B., 17, 563
46, 1181
Benzylphthalidine
C 6 H 4 .CO.NH.CH.CH 2 Ph
C 16 H 13 ON
135-137
Gabriel
B., 18, 1262
48, 903
i i
Amidomethylanthranol
CH.C 6 H 4 .C(OH).C 6 H 2 Me.
11
183
Homer and Link
B., 16, 704
44, 1138
NH,
Acetamidofluorene
C 6 H 4 .C 6 H,(NHAc).CH 2
187-188
Strasburger
B., 17, 108
46, 754
i " i
=1.2; 1.4.2
Acetyldiphenylacetoxime ...
PhjC : N.OAc
C 15 H 13 2 N
....
55
Spiegler
M. C., 5, 203
46, 1156
Dibenzoylhydrocyanide
HN : CBz,,
....
195
Zinin
Z. C. [2], 4, 710
vi., 329
Acetamidobenzophenone ...
Ph.CO.C 6 H 4 .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 : N 2 HPh)
C 15 H 13 2 N 3
....
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
C0 2 H.N(COH)(CH 2 Ph)=1.2
C 15 H 13 3 N
196 u.c.
C'laus & Glyckherr
B., 16, 1285
44, 1009
acid
Acetylnitrobenzylidene-
NPhAc.N : CH-C^.NOj
C 15 H 13 3 N 3
170
Schroeder
B., 17, 2098
46, 1323
phenylhydrazine
=1.3
Benzanishydroxamic acid ....
NBz(CO.C 6 H 4 .OMe).OH
C 16 H 13 4 N
131-132
Lessen
A., 175, 288
28, 635, 636
=1.4
Anisbenzhydroxamic acid ....
N(CO.C 6 H 4 .OMe)Bz.OH
....
147-148
A., 175, 294
=1.4
Methylic salicylatephenyl-
NHPh.C0 2 .C 6 H 4 .C0 2 Me
....
238
Snape
47, 775
carbamate
=1.2
Nitrophenoxyethylene
N0 2 .C 6 H 4 .O.C 2 H 4 .O.Bz=1.2
C 16 H 13 6 N
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.C 6 H 4 .NMe 2
C 15 H 13 5 N 3
142
Fischer
A., 206, 90
40, 587
benzophenone
Salicylethylenenitrophenol
HO.C 6 H 4 .C0 2 .C 2 H 4 .O.C 6 H 4 .
C 13 H 13 6 N
106
Wagner
J. p. [2], 28, 215
46, 436
ether
N0 2 =(1.2) 2
11
=1.2 ; 1.4
n
131
J. p. [2], 28, 221
Ethylenenitrophenoloxy--
N0 2 .C 6 H 4 .O.C 2 H 4 .O.C 6 H 4 .
130
Weddige
J. p. [2], 24, 241
40, 1139
benzoic acid
CO 2 H=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
C 15 H 14 ON 2
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 C 15 H 1(! O 2 N 2
See orig. paper
164
Plochl
B., 14, 1141
40, 820
Ethylenediphenylcarbamide
CH 2 .NPh.CO.NPh.CH 2
B
209
Michler and Keller
B., 14, 2183
42, 182
i i
Methoxyphenylphenamido-
C 6 H 4 .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
C 16 H 14 O 2 N 2
115
McCreath
B., 8, 1182
29, 401
Methylphenylhydrazine
N 2 MePh : CPh.COoH
116 d.
Elbers
A., 227, 340
48, 535
phenylglyoxylic acid
Beuzoylphenylethenylamid-
CH 2 Ph.C(NH 2 ) : 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-
NPh 2 .N : CMe.CO 2 H
C 15 H 14 2 N 2
....
145
Fischer and Hess
B., 17, 567
48, 1181
mio acid
Methylene dibenzamide
CH 2 (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).C 6 H 4 .Ac
))
54-55
Baeyer
B., 17, 972
46, 1021
phenone
=1.2
Phenylazoacetocresol
Ph.N 2 .C 6 H 3 Me.OAc=?.1.4
J)
....
67-68
Nolting and Kohn
B., 17, 353
46, 901
=?.1.2
))
....
81-82
B., 17, 364
46, 902
Nitrophenylhydroquinoline....
C 9 H 10 N.C 6 H 4 .NO 2 =1.2.3;1.3
)
100-101
Miller & Kinkelin
B., 18, 1906
48, 1145
Benzoylphenylhydroxy-
HO.CHPh.C(NH 2 ) I NOBz
C )B H 14 3 N 2
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
?
N 2 HPh:CH.C 6 H 4 .O.CH 2 .
))
....
105 ; sf. 60
fiossing
B., 17, 2995
48, 388
CO 2 H=1.2
Toluylnitrotoluide
C,,H 3 Me.NO,,.NH(CO.
....
165-166
Hiibner
A., 210, 331
42,504
C 6 H 4 Me)=1.3.4 ; 1.4
j3-benzoylnitroxylidine
Me 2 .N0 2 .NHBz=?
)
A., 208, 323
178
)!
B., 10, 1711
34, 143
a-
=?
)j
A., 208, 320
184-5
D
!
!
Carbonyldibenzenylamid-
CX)(O.N :.CPh.NH 2 ) 2
C 15 H 14 3 N 4
....
128-129
Falck
B., 18, 2471
48, 1217
oxime
Benzamidoethylenenitro-
NHBz.C 2 H 4 .O.C 6 H 4 .NO 2
C^AN,
....
94-95
Weddige
J. p. [2], 24, 249
40, 1138
phenyl ether
=1.2
Nitrophenyl-/3-lactanilide ....
C 6 H 4 .N0 2 .[CH(OH).CH.,.
1
176-178
Easier
B., 17, 1502
46, 1173
CO.NHPh]=1.4
Dinitroditolylmethane
fr. CH 2 (C 6 H 4 Me) 2
....
164 u.c.
Weiler
B., 7, 1183
28, 151
Dinitrodibenzylmetliane
CH 2 (CH 2 .C 6 H 4 .N0 2 ) 2
)
186
Sesemann
I. D. Zurich
28, 74
Dinitrophenylacetdiamido-
C 6 H 3 (NO 2 ) 2 .NH.C 6 H,Me.
C 16 H 14 6 N 4
....
163-164
Leymann
B., 15, 1237
42, 1057
toluene
NHAc=(?) 3 ; 2.1.4 or 4.1.2
Piuitroditolylcarbamide
CO(NH.C 6 H 3 Me.N0 2 ) 2
)1
...
233 d.
Perkin
.<*
37, 699
=(1.4.1),
Tetrahydroquinoline picrate
C^Hn+C^^NO^.OH
C 15 H 14 7 N 4
...*
125
Ostertneyer
C. C., 1884, 970
48, 672
Ethyl diphenylacetoxime ....
CPh 2 1 NOEt
C 16 H 15 ON
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
C 6 H 4 Bz.NMe 2 =?
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.CH 2 .NH.C 6 H 4 Ac= 1 . 2
79-81
Baeyer
B., 17, 971
46, 1021
Acetamidodiphenylmethane
Ph.CH 2 .C 6 H 4 .NHAc=1.3
1)
91
Becker
B., 15, 2092
Acetophenonemethauilide ....
Bz.CH 2 .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
C 6 H 4 Et.NHBz=1.2
147
Paucksch
B., 17, 2802
48, 256
11
=1.4
>
151
11
))
11
Tolylphenylacetamide
C 6 H 4 Me.CHPh.CO.NH 2 =1.4
>
151
Tanisch
B., 10, 997
32, 618
Acetamidotolyphenyl
Ph.C 6 H 3 Me.NHAc(2)
51
>.
114-25
Jackson
A. J. S., 13, 449
32, 762
11
)J
114-2
!
B., 8, 970
29, 269
Xylic anilide
Me 2 .(CO.NHPh)=1.3.4
)
....
138-5
Ador and Meier
B., 12, 1971
38, 252
Benzamidoxylene
Me 2 .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 : .C 6 H 4 .NMeAc
C 15 H 16 ON 3
...
139
Berju
B., 17, 1402 ;
46, 1148; 48,
C. C., 1884,871
660
Diphenylurethane
NPhj.COjEt
C 15 H 15 2 N
B., 5, 284
72 ; af. 66
Merz and Weith
B., 6, 1512
27, 375
11
Ph.C 6 H 4 .NH.CO 2 Et
)
....
110
Zimmermann
B., 13, 1965
40, 176
Tolylphenamidoacetic acid ....
Me.[CH(NHPh).C0 2 H]=1.3
)J
137-139
Bornemann
B., 17, 1471
46, 1163
Phenyltoluidoacetic acid
C 6 H 4 Me.NH.CHPh.C0 2 H
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 ..
C 6 H 4 Me.NH.CHPh.CO ii H
C 15 H 16 2 N
167-170
Stockeuius
J., 1878, 780
=1.4
Ethoxybenzanilide
C 6 H 4 .OEt.(CO.NHPb)=1.4
J)
....
170
Leuckart and
B., 18, 2340
48, 1224
Schmidt
Methylcarbophenyllutidy-
C 6 (NMe)HPh.OMe.COMe
M
160-161
Hantzsch
B., 17, 2915
48, 398
liumdehydride
Phenylethenylphenylurami-
Ph.CH 2 .C(NH.CO.NHPh) :
C 15 H 15 2 N 3
123
Knudsen
B., 18, 1074
48, 898
doxime
NOH
p-acetamidotolylazophenol ..
NHAc.C 6 H 3 Me.N 2 .C 6 H 4 .OH
)J
252-253
Wallach
B., 15, 2827
44, 584
Amidophenoxyetbyleneben-
NH 2 .C 6 H 4 .O.C 2 H 4 .OBz=1.2
C 15 H 15 3 N
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
C0 2 Me
Phenylhydroxyethenylphen-
HO.CHPh.C(NOH).NH.CO
C 1S H 16 3 N 3
155
Gross
B., 18, 2478
48, 1218
yluramidoxime
NHPh
E thylenearaidophenyloxy-
NH 2 .C 6 H 4 .O.C 2 H 4 .O.C 6 H 4 .
C 15 H 15 4 N
110
Wagner
J. p. [2], 28, 218
46, 436
benzoic acid
C0 2 H=(1.2) 2
=1.2 ; 1.4
>
185
J. p. [2], 28, 223
)
p-Tolyldimethylpyrroline
C0 2 H.C : CMe.N(C 6 H 4 Me).
d. 250
Knorr
B., 18, 308
48, 555
dicarboxylic acid
i
CMe I C.CO 2 H
Dinitroditolylguanidiiie
CN 3 H 3 (C 6 H 3 Me.N0 2 ) 2
C B H 15 4 N 6
197 d.
Perkin
37, 698
=(1.4),
Ethylic nitroeinnamylaceto-
C 6 H 4 (N0 2 )(CH:CH.CO.
C 15 H 15 6 N
120-5
Fischer and Kuzel
B., 16, 35, 163
44, 587
acetate
CHAc.C0 2 Et)=1.2
Benzylphenylethenylaruid-
CH 2 Ph.C(NH 2 ) : NO.CH 2 Ph
C 16 H 16 ON 2
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
NH 2 .CO.N(CH 2 Ph) 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
C 6 H 4 Me.NH.CH 2 .CO.NHPh
J>
82-83
Meyer
B., 8, 1161
89,402
Tolylanilidoacetamide
Me.[CH(NHPh).CONH 2 ]
127-128
Borueniann
B., 17, 1471
46, 1163
=1.3
Benzenyldimethylphenylen-
C 6 H 4 .N : CPb.NMe 2 .OH
)
152
Hubner
A., 210, 357
42,505
amidine
Phenylglycocintoluide
NHPh.CH 2 .CO.NH.C 6 H 4 Me
J)
....
171-172
Meyer
B., 8, 1158
29, 372
=1.4
Hydroxybenzylideneamido-
HO.C 6 H 4 .CH : N.C 6 H 4 .NMe 2
;)
134
Nuth
B., 18, 573
48, 784
dimethanilide
=1.2; 1.4
Ditolylcarbamide
CO(NH.C 6 H 4 Me) 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,,C 8 HMe 3 .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):C 12 H 8 (NH 2 ) 2
C 15 H 16 2 N 2
220
Staedel
A., 218, 339
44, 991
Ethoxybenzeueazocresol
EtO.C 6 H 4 .N 2 .C 6 H 3 Me.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
C 6 H 2 Me 3 .N 2 .C 6 H 3 (OH) 2
C 15 H,AN 2
....
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.N 2 .NEt.C 6 H 4 Me ....
55
Nolting and Binder
B. S., 42, 340
48, 386
j,
....
104-105
Dianisyl carbamide
CO(NH.C 6 H 4 .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
C 9 H 13 N+C 6 H 2 (N0 2 ) 3 .OH
C 16 H,AN 4
149
Waage
M. C., 4, 708
46, 172
9-naphthimidoisobutyl ether
C 10 H-.C(OBu0) : NH
C U H I7 ON
38
Pinner and Klein
B., 11, 1486
36, 48
Ammonium nitrophenyl-jS-
C 6 H 4 .NO 2 .[CH(NHPh).CH 2 .
C U H 17 4 N,
....
150-156
Easier
B., 17, 1502
46, 1173
anilidopropionate
CO 2 .NH 4 ]=1.4
Paraxanthine
....
C 15 H,AN 9
a. 250
Solomon
B., 16, 197
44, 601
Diamidotolyl carbamide
CO(NH.C 6 H 3 Me.NH 2 ) 2
C 15 H 18 ON 4
....
d.w.m.
Perkin
....
37, 700
Benzylammonium benzylcar-
CHjPh.NH.COj.CNHj.CH,
C 15 H 18 2 N 2
.t
99
Tiemann and Frid-
B., 14, 1970
42, 56
bamate
Ph)
lander
Oinnamodiacetonamine
CHPh : CH.CH.CH 2 .CO.
i
C IS H 19 ON
+|H 2
49
Antriek
A., 227, 365
48, 503
CH 2 .CMe 2 .NH
Benzoyltrope'ine
....
C 16 H 19 2 N
+JH 20
37
Ladenburg
B., 13, 1083
38, 715
(A., 217, 96)
+2H 2 O
58
o-Hydroxylbenzoyltrope'ine
C 16 H 19 3 N
....
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.C 6 H 4 .CH.CH 2 .CO.CH 2 .
C 16 H,AN
....
193d.
Antriek
A., 227, 365
48, 503
L
mine oxalate
CMe 3 .NH+C 2 H 2 O 4
i
Gluco-coumaraldoxime
C 6 H 4 (O.C 6 H U 6 )(CH:CH.
C lb H 19 ? 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.CO 2 Et) 2
C 15 H 2 AN.,
....
135-143
Bischoff
B., 7, 1079
28, 146
Dinitrolaserpetin
C 15 H 20 (N0 2 )A
C 16 Hj OgN 2
+H 2
115
Kulz
A. P. [3], 21, 161
46, 183
Eserin (Physostigmiu)
....
C 15 H 21 2 N 3
....
45
Jobst and Hesse
A., 129, 115
>. >.
....
d. 150
69
Vee
J. [1865], 457
Benzoylhomoconiinic acid ....
Ph.CO.C 8 H,AN
C 15 H 21 3 N
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-
C 6 H 2 Me 3 .N.NH.CMe.CH...
C.sHjAN
....
77-78
Haller
B., 18, 707
48, 818
acetate
J
CO 2 Et=1.2.4.5
Beuzylidene dipropylurethane
Ph.CH(NH.C0 2 Pra) 2
C 16 H 22 4 N 2
143
Bischoff
B., 7, 1082
28, 146
Ethylic toluylene diglyeocine
C 6 H 3 Me(NH.CH 2 .C0 2 Et) 2
....
70
Zimmermann and
B., 16, 516
44, 798
Knyrin
Methylcopellidine picrate ....
C 8 H 16 MeN+C 6 N 2 (N0 2 ) 3 .OH
C 15 H 22 7 N 4
....
112
Diirkopf
B., 18, 926
n-Octylformanilide ....
C S H 17 .C 6 H 4 .NH(CHO)=1.4
C^HjAN
....
56
Beran
B., 18, 135
48, 523
Alantamide . ....
C 14 H 20 (OH).CO.NH 2
HO "NT
210 ( 1
TT n
RQ 1 f\A
23 S
jvaiien
j ity 1OO
***j yio
Hydrosantonamide ....
....
C I5 H 23 3 N
J. [1876],620
190 d.
Cannizzaro
G. I., 6, 341
31, 471
1
C 16 H 23 4 N
....
86
Kuckert
B., 18, 620
48, 750
Oxametharie cyanurate
C 3 O 3 N 3 H 3 (NH 2 .CO.CO 2 Et) 3
C 16 Hj 4 O 12 N 8
....
155-160
Grimaux
B. S. [2], 21, 154
28, 564
Oxypentinamide
C 15 H,A(NH 3 ) 5
C 16 H 2 AN S
203-204
Demaryay
A. C. [5], 20, 487
Diisoamylcarbopyrrolamide
C 4 H 3 (C 5 H n )N.CO.NH
CnHjjONj
77
Bell
B., 10, 1866
36, 525
(C 5 H n )
C 14 H 29 .CO.NH 2
CTT <~W
*D
P T? on QOQ
l IS ATA
lo '31
MM
IjOUlS
\j, 11., oy, .)_.)
in., 414
Tetranitropyrene
C 16 H 6 8 N 4
a. 300
Graebe
A., 158, 293
24, 691 ; vii.,
1028
Dinitrodiphenyldiacetylene ....
(.C = C.C 6 H 4 .N0 2 ) 2 =(1.2) 2
C 16 H 8 4 N 8
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. C 10 H .O.C 6 H 4
C 16 H 8 5 N 2
>
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
....
C 16 H 8 7 N 2
sf. 73
Reimer
B., 14, 1801
anhydride
?
....
(C 16 H 9 ON 2 ) n
....
217
Zincke
B., 15, 286
Nitrodiphenyldiacetylene ...
Ph ^C - C^ C H NO 12
C 16 H 9 2 N
154-155
Baeyer and Lands-
B., 15, 58
42, 622
berg
Cyanbenzylidenephthalide ...
O.CO.C 6 H 4 .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-
C 6 H 4 .NH.C 10 H 4 :0 2
1)
I
307
Grsebe and Knecht
A., 202, 13
38, 664
quinone
a-tetranitronaphthylphenyl-
C 10 H 3 (N0 2 ) 4 .NHPh
C 16 H 9 8 N 5
162-5
Merz and Weith
B., 15, 2717
44, 344
amine
/-*" 11
1J
....
253
B., 15, 2720
11
Nitrosophenylnaphthylcarb-
C 6 H 4 .C 10 H 6 .N.NO
| I
C 16 H 10 ON 2
240
Graebe and Knecht
A., 202, 8
azole
C 16 H 10 O r N,
275
Zincke
B., 15, 285
Nitroso-|3-naphthoqumone-
I
C 16 H 10 3 N 2
I
245
B
B., 15, 284
42, 735
anilide
Nitro-a-naphthoquinoneani-
N0 2 .C 6 H 4 .NH.C 10 H 6 : 2
C 16 H I0 4 N 2
....
a. 270
Baltzer
B., 14, 1905
42, 205
lide
=1.3
-a-
=1.4
....
nf. 270
B., 14, 1904
-0- 11
C 10 H 4 (OH)(N0 2 ).O.NPh
| t
246-248
Brauns
B., 17, 1134
46, 1038
-0-
u
253
Korn
B., 17, 908
46, 1186
Azophenylglyoxylic acid
N 2 (C 6 H 4 .COX:0 2 H). ! =(1.3) 2
C 16 H 10 6 N 2
....
abt. 151
Thompson
B., 16, 1309
44, 998
11
+2H 2 O
134-5-135
Dinitroethoxyanthraquinone
fr. C 6 H 4 :(CO) 2 :C 6 H 3 .OEt
C 16 H 10 7 N 2
158
Simon
B., 15, 694
42, 863
=2.1 ; 1.2.4
Azophthalic acid
N 2 [C 6 H 3 .(C0 2 H) 2 ] 2 =(?.2.1) 2
C 16 H 10 8 N 2
brown 220
230-250 d.
Glaus and May
B., 14, 1331
42, 516
Picrate of /3-benzoquinoline
N.CO 2 H=a,ft ;
C 16 H I0 9 N 4
216 d.
Riedel
B., 16, 1614
44, 1152
carboxylic acid
Fr. Phenaiithraquiiione
MM
C 16 H H ON
..
241
Japp and Miller
B., 16, 2418
46, 329
+HCN
Diphenylfumarimide
CPh : CPh.CO.NH.CO
i i
C 16 H n O N
....
213
Reimer
B., 13, 746
40,48
Fr. Benzylcyanide
C 14 H 10 (CN).C0 2 H
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
"-
c 10 H 6 :(o 2 ):NPh
MM
190-191
Zincke
B., 12, 1645
38, 49
- ,,
Ph.NH.C 10 H 5 :O s
A., 211, 82
191
Liebermann
B., 14, 1666
a-
C 10 H b (OH).O.NPh=a^ 1 o B ;
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 = a il ft
230-231
,,
M. C., 3, 556
J)
Benzoylhydroxyquinoline ....
N.OH.Bz=a,/3 1 ft;
a. 270
Friedlander and
B., 16, 1839
44, 1149
Gohiing
Deoxyimidoisatin
....
C 16 H n 2 N 3
A., 194, 86
209-210 d.
Sommaruga
A., 190, 379
34, 507
Benzoylimidocoumarin
C 6 H 4 .CH.NBz.CH.CO.O= 1.2
i- i
C.eH.AN
170-171
Plochl & Wolfrum
B., 18, 1185
48, 898
Hydroxy-a-naphthaquinone-
C 10 H 4 (OH)(NHPh):0 2
210
Plagemann
B., 16, 896
anilide
Anilidojuglone
=3, ; fta,a 2
230
Mylius
B., 18, 473
48, 8P4
Acetaniidoanthraquinone ...
C 6 H 4 :(CO) 2 :C 6 H 3 .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
- ))
HNO 3 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.C 10 H 6 .NH.N.C 6 H 4 .NO 2
A =A ; 1.3
Nitrobenzeneazoamido-a-
naphthalene
Constitution.
C 6 H 4 1 (CO).: C 6 H 3 .NHAc
=2.1 ; 1.2.4
NO,.C 6 H 4 .N 2 .C 10 H 6 .OH
=1.4; <m
=1.3; a/3
=1.4; a/3
see orig. paper
fr. C 10 H 7 .NHPh
C 6 H 4 : (CO), : C 6 H 2 .OEt.NO,
=2.1; 1.2.5.6
C 6 H 3 (N0 2 ) 3 +C 10 H 8
C 10 H 8 +C,H 2 .OH.(NO..) S
= 1.3.4.6
=1.2.3.6
=
=1.2.4.6
C 6 H(OH) 2 (N0 2 ) 3 +C 10 H 8
Ph.CO.C : N.CPLCH : NH
I 1
C 10 H 7 .N(NO).C 6 H 5
C, H 6 .O.NPh.NH=j3 1 a. ;
Ph.N 2 .C,,,H 6 .OH=?a
=?
C 6 H 4 (N:C 6 H 4 0) 2
C 10 H 5 (OH)O.N 2 HPh
i 1
NH 2 .C 6 H 4 .NH.C 10 H 6 2 =1.4
C 10 H 7 .N 2 .C 6 H 3 (OH) 2 =?;?.1.3
(.NH.C 6 H 4 .CO.CNH.) 2
C 10 H 6 :(NH) 2 :N.C 6 H 4 .N0 2
=a,/3, ; 1.3
=a t B t ; 1.4
N0 2 .C 6 H 4 .N 2 .C 10 H 6 .NH S
=1.4 ; e.,/3, ;
Formula.
C,H,,0 :< N
C 16 H U 3 N 3
C 16 H U 4 N
C 16 H n 4 N 3
C 16 H n 7 N 3
C 16 H n 7 N 5
C 16 H U 8 N 3
C 16 H 12 ON 2
C 16 H 12 2 N 2
C 16 H 12 2 N 4
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-
NO 2 .C 6 H 4 .N a .C 10 H 6 .NH 3
C 16 H 12 2 N 4
....
202-203
Meldola
....
45, 114
naphthalene
= 1.3 ; a,a 2 ;
-a-
=1.4 ; a.0, ;
....
252
....
43, 430
J
C 6 H 4 .CO.N 2 Ph I C.CH 2 .CO 2 . H
....
160 d.
Roser
B., 18, 803
48, 797
i i
=1.2
Dinitrobeuzene-naphthalene
C 10 H 8 +C 6 H 4 (N0 2 ) 2 =1.3
C 16 H 12 4 N 2
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
C 10 H 8 +C 6 H 2 .NH.(N0 2 ) 3
C,,H 12 6 N 4
168-169
Liebermann and
B., 8, 378
=1.2.4.6
Palm
/3-napthylamine picrate
C 10 H..NH 2 +C 6 H 2 .OH.(N0 2 )
C 16 H 12 7 N 4
....
195
Liebermann
A., 183, 264
31, 607
p~
195
Scheiding
B., 8, 1652
29, 713
Quinoline methopicrate
C 9 H 7 N+C li H 2 .OMe.(N0 2 ) 3
....
164
Ostermeyer
B., 18, 594, 599 ;
48, 672
C. C. [1884], 970
,, )>
....
164-165
Coste
B., 15, 193
|3-methylquinoline picrate ...
C 10 H 9 N+C 6 H 2 .OH.(N0 2 ) 3
....
187
Dobner and Miller
B., 18, 1642
m-toluquinoline picrate
....
206-207
Skraup
M. C., 8, 381
42, 1216
Methylic fl-dinitrodiphenate
fr. (.C 6 H 4 .CO 2 Me) 3 =(1.2). l
C 16 H 12 9 N 2
131-132
Schultz
A., 203, 111
38, 814
a-
see orig. paper
....
177-178
n
Dinitro-a-dibeuzyldicar-
fr. (.CH 2 .C 6 H 4 .C0 2 H) 2
226
Eeimer
B., 14, 1804
42, 200
boxylic acid
-ft- >i ii
)(
....
242
M
B
Nitropapaveric acid
...
C 16 H 12 9 N 2
....
215
Goldschmidt
M. C., 6, 372
48, 1031
C 16 H 13 ON
B., 16, 69
238
Fischer & Rudolph
B., 15, 1502
42 1067
Acetylanthrainine
C 6 H 4 :(CH) 2 :C 8 H 3 .NHAc
240
Liebermann
A., 212, 61
42,860
240
Liebermann and
B., 15, 228
Bollert
Azophenol-a-naphthylamine
HO.C 6 H 4 .N,,C 10 H 6 .NH 2
C 18 H 13 ON b
+3 H,0
170
Weselsky and
B., 12, 229
=1.4
Benedikt
a-naphtholazoamidobenzene
NH 2 .C 6 H 4 .N 2 .C 10 H 6 .OH
....
Solid
Meldola
....
47, 662
= 1.4; aa
0-
=1.4 ; 49
u
Powder
47, 663
Benzylindolecarboxylic acid
C I6 H 13 2 N
....
195
Antrick
A., 227, 360
48, 543
9
C 6 H 4 .C 6 H 4 .C(CO 2 H) : C.
183
Tann anrl IVTillAr
Blfi 941 S
Aft OOQ
., 1 u , ^'ij.o
*O> >-,.!
1 1
CH 2 .NH 2
Ethylnitrosoanthrone
C 6 H 4 .CO.C 6 H 4 .CEt.NO
n
*
135
Liebermann and
B., 14, 475
40, 607
i i
Landshoff
Nitrodiphenylpyrazene
NO,,C 6 H 4 .C 3 N 2 HMePh=1.4
C 16 H 13 2 N 3
....
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).CO 2 H
C 16 H 13 3 N
....
131
Plochl
B., 17, 1618
46, 1348
Benzimidoeinnamic acid
Ph.CH.NBz.CH.CXXH
1 {
....
225
B., 16, 2816
46, 605
Ethylnitroanthrone
C 6 H 4 .CO.C,H 4 .CEt:NO s
5)
....
102
Liebermann and
B., 14, 474
40, 607
Landshoff
Aniidoethoxyanthraquinone
C 6 H 4 : (CO) 2 : C 6 H 2 .OEt.NK
....
182
Liebermann and
B., 15, 1796
44, 73
=2.1 ; 1.2.5.6
Hagen,
Oxyamidohydroisatin
C(OH) : N.c 6 H 4 .C(NH 2 ) : c
C 16 H 13 3 N 3
....
d.w.m. 187-
Sommaruga
A., 194, 100
(OH).C 6 .H 4 N:C.OH
190
Dihydroisatinamide
M. C., 1, 562
5)
213
5)
A., 194, 88
36, 63
Ethylanthracenehydride
C 6 H 4 .C(O.NO) 2 .C 6 H 4 .CEt.
C 16 H 13 6 N 3
....
130 d.
Liebermann and
B., 14, 473; A.,
40, 607 ; 42,
nitrite
O.NO
Landshoff
212, 1
862
Papaveric acid
....
C 16 H 13 7 N
233
Goldschmidt
M. G, 6, 372
48, 1080
Trinitrobenzamidophenylu r-
N0 2 .C 6 H 4 .CO.NH.C 6 H 2
C 16 H 13 9 N 6
....
210
Hager
B., 17, 2628
48, 150
ethane
(N0 2 ) 2 .NH.C0 2 Et
=!? 1 l-(?) 2 .4
Hydroisoindileucine ....
Ph.CH(OH).C:N.CPh.
C 16 H 14 ON 2
....
160
Engler and Hassen-
B., 18, 2243
46, 48
CH : NH L ~
kamp
Methylisatintolylimide
C 8 H 4 MeNO : N.C G H 4 Me
....
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
C 8 H 4 MeNO : N.C 6 H 4 Me
C 16 H 14 ON 2
....
259
Meyer
B., 16, 2264
46,48
=1.4; 1.4
Lactimide of benzdiamido-
Ph.CH.CH(NHBz).CO.NH
C 16 H 14 N 2
....
187
Plochl
B., 17, 1617
46, 1348
hydrocinnamic acid
I |
Phenylaspartic phenylimide
NHPh.C 2 H 3 : (CO), : NPh(?)
....
263
Piutti
G. I., 14, 473
48, 796
Ethoxybenzenylazoximeben-
N : CPh.O.N : C.C 6 H 4 .OEt
....
71
Schoff
B., 18, 2476
48, 1217
zenyl
i i
=1.3
Oxindole
see C S H 7 ON
....
120
Bedson
....
37, 93
Ethylic phenylenamidine-
NH.C 6 H 4 .N : C.C 6 H 4 .CO 2 Et
)>
....
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
....
C 16 H 14 3 N 6
....
295-300
Sommaruga
A., 190, 367
34, 507
Benzoylform-'y-amide
O,:(CPh.CO.NH 2 ) 2
C 18 H 14 4 N 2
130
Claisen
B., 10, 1665
34, 151
D
....
134-135
B., 12, 634, 635
36, 649
A cetbenzamidonitro toluene
Me.NO 2 .NBzAc=1.2.4
....
160
Cunerth
A., L72, 221
28, 83
Azophenylacetic acid
N 2 (C 6 H 4 .CH 2 .CO 2 H) 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
N 2 (C 6 H.,Me.CO 2 H) 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
N 2 (C 6 H 4 .O.CH 2 .C0 2 H) 2 =?
C 16 H 14 6 N 2
....
151-152
Thate
J. p. [2], 25, 267
42, 849
=(1.2),
....
162
J. p. [2], 29, 145
46, 1171
Succindiuitranilide
(CH 2 .CO.NH.C 6 H 4 .N0 2 ) 2
C 16 H 14 6 N 4
260
Hiibner
A., 209, 377
=(1.4),
Dinitrodiacetbenzidine
(.C 6 H 3 .NHAc.NO 2 ) 2 =(1.4.2) 2
a. 300
Strakosch
B., 5, 237
Azoxyphenoxyacetic acid ....
ON 2 (C a H 4 .O.CH 2 .C0 2 H) 2
C 16 H l4 O r N 2
....
186-187
Thate
J. p. [2], 29, 145
46, 1170
=(1.2) 2
Trinitrobenzmesidine
fr. C 6 H 2 Me 3 .NHBz
C 16 H 14 7 N 4
....
300
Schack
B., 10, 1711
Me 3 .(NO 2 ) 2 .(NH.CO.C 6 H 4 .
....
307
34, 144
NO 2 )=1.3.5.2.4.6 ; 1.3
Dibenzylgly collie nitril
(Ph.CH 2 )C(OH).CN
C 16 H,,ON
....
113 ; sf. 110
Spiegel
B., 13, 2221
40, 174
a-naphthylamine phenate ...
C 10 H 7 .NH 2 +Ph.OH
....
30-1
Dyson
....
43, 468
Aniline-S-naphthate
Ph.NH 2 +C 10 H 7 .OH
....
82-4
Benzoyltetrahydroquinoline
....
B., 13, 2400
75
Hoffmann & Konigs
B., 16, 734
44, 1144
Acetophenoneacetanilide ....
Ph.CO.CH 2 .NAcPh
C 16 H 16 2 N
....
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-
....
C 16 H 16 2 N 3
t...
a. 220 d.
Duisberg
B., 18, 193
48, 544
methyloxindole
Benzethylbenzhydroxyl-
Ph.CO.O.CPh.NO.Et
C 16 H 16 O a N
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.CH 2 .CO 2 .CH 2 Ph
M
289-9
85-5-86
Zanna & Guareschi
B., 14, 2242
Diphenylsuccinamic acid
NPh,,CO.C 2 H 4 .CO 2 H
....
119
Piutti
G. I, 14, 351
48, 783
Acetylacetoxydiphenylamine
C 6 H 4 .OAc.NPhAc=1.4
120
Philip and Calm
B., 17, 2437
48, 156
Benzophenoneurethane
C 6 H 4 Bz.(NH.C0 2 Et)=1.4
189
Dobner and Weiss
B., 14, 1839
42, 177
)> J)
....
189
Dobner
A, 210, 273
42, 508
Methylic m-diazoamidoben-
C 6 H 4 (C0 2 Me).N 2 .C 6 H 3 (NH. ! ).
C 16 H 16 4 N 3
160
Griess
A., 117, 12
iv., 294
zoic acid
CO 2 Me
Dianishydroxamic acid
N(CO.C 6 H 4 .OMe) 2 .OH=(1.4) 2
C 16 H 1S 6 N
....
142-143
Lessen
A., 175, 287
28, 636
Nitrobenzonitromesidide ....
Me 3 .NO 2 .(NH.CO.C 6 H 4 .NO,)
C 16 H J6 5 N 3
....
207
Hiibner
B., 10, 1711
34, 144
= 1.3.5.2.4; 1.3
a-trinitroazoxypheneto'il
....
C 16 H 16 9 N 5
....
168
Andreae
J. p. [2], 21, 334
38, 467
p~ ,,
u
....
187
,,
Phenyl-a-anilidocrotonamide
Ph.CH : CH.CH(NHPh).
C 16 H 16 ON,
171
Peine
B., 17, 2116
46, 1345
CONH 2
p-tolylamido-p-methyloxin-
....
166-167
Duisberg
B., 18, 191
48, 544
dole
Diacetylhydrazobenzene
Ph.NAc.NAc.Ph
C 16 H le 2 N 2
....
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-
N 3 EtPh:CPh.C0 2 H
C 16 H 16 2 N 2
....
109 d.
Elbers
A., 227, 340
48, 534
phenylglyoxylic acid
Ethidine dibenzamide (Hip-
CH 3 .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
>
....
210
Maier
A., 127, 162
iii., 155
i
>
J)
....
215
Schwarz
W. A., 77, 62
36, 650
Dibeiizyloxamide
(.CO.NH.UH 2 Ph) 2
....
216
Strakosch
B., 5, 694
vii., 182; 25,
1026
Succinanilide .... ....
(.CH 2 .CO.NHPh) 2
A., 68, 27
226-5-227
Menschutkin
A., 162, 187
25 4Q7 vii
Jl
*"', ^t7 1 j VIA.,
1183
Diacetdiamidodiphenyl
(.C 6 H 4 .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.C 6 H 4 Me) 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
C 6 H 4 Me.N 2 .C 6 H 3 Me.OAc
....
91
Nolting and Kohn
B., 17, 354
46, 901
=1.4; ?.1.4
Piperonylidene amidodi-
CH 2 : o 2 : c 6 H 3 .CH : N.c 6 H 4 .
110
Nuth
B., 18, 575
48, 784
methaniline
NMe 2 =4.3.1 ; 1.4
Betistenequinoxime
HO.N : c.c 14 H 14 .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
C 16 H 10 N 2 (OH) 2 (NH 2 ) S
C 16 H 16 2 N 4
v. C 16 H 16 3 N 4
215-217
Somiuaruga
A., 194, 96
36,63
Ethylic diphenylallophanate
C 16 H 16 3 N 2
....
98
Hofmann
B., 4, 247
24, 393 ; vii.,
408
Diphenylmalamide
NHPh.CO.CH 2 .CH(OH).
175 p.d.
Arppe
A., 96, 107
iii., 797
CO.NHPh
Benzamidophenylurethane ....
NHBz.C 6 H 4 .NH.CO 2 Et=1.4
M
230
Hager
B., 17, 2628
48, 150
p-Toluylnitroxylide
N0 2 .C 6 H.,Me 2 .NH.CO.C 6 H 4
))
187
Hiibner
A., 210, 333
42, 504
Me
P- D ,,
"
187
Bruckner
A., 205, 125
40, 94
Benznitromeaidine
Me 3 .NHBz.NO 2 =1.3.5.2.4
jj
168-5
Hiibner & Schack
B., 10, 1711
34, 144
Nitrobenzmesidine
Me 3 .(NH.CO.C 6 H 4 .NCg
....
205
)
=1.3.5.6; 1.3
Diamidohydrindie acid
C 16 H 10 N 2 (OH) 2 (NH 2 ) 2
C 18 H 16 8 N 4
v.C 16 H 16 2 N 4
215-217 d.
Sommaruga
A., 194, 96
36,63
Azoxyacetanilide
: N 2 (C 6 H 4 .NHAc) 2 =(1.4) 2
M
275-278
Mixter
A. C. J., 5, 1
46, 301
Glycolphenylcarbamate
C 2 H 4 (O.CO.NHPh) 2
C 16 H 16 4 N 2
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.NH 2 ] 2
browu 150
230 sf. b. 230
Burton
B., 16, 2232
46,63
Ethylenedibeiizamic acid ....
C 2 H 4 (NH.C 6 H 4 .CO 2 H) 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
N 2 (C 6 H 3 .OEt.N0 2 ) 2 =(1.2.?) 2
C 16 H 16 6 N 4
....
190
Andreae
J. p. [2], 21 
