144
3 Brief Demonstration of the General Nomenclature Rules
3.12
Other Polynitrogen Parent Systems
Trivial names of freely substitutable polynitrogen parent structures as
recommended for further use by IUPAC and the most important substituent groups derived therefrom are compiled in Table 13. Differing
names and numberings as employed by Chern. Abstr. are enclosed in
parentheses.
Table 13. Retained trivial names for poly nitrogen parent structures". (In parentheses:
differing Chern. Abstr. names and numberings.)
o
II
H2N-C-NH-C02H
4
3
2
1
Allophanic acid
(Aminocarbonylcarbamic acid)
(N"')4 NH
NH 2(N")
II
II
H 2 N-C-NH-C-NH 2
5(N') (3) 3(2) (1) 1 (N)
Biguanide
(Imidodicarbonimidic diamide)
o
II
HN=N-C-NH-NH2
5(1) 4(2) 3 2(4) 1 (5)
Carbazone
(Diazenecarboxylic acid, hydrazide)
o
II
HN=N-C-N=NH
5
4 3 2
Carbodiazone
o
II
H 2 N-NH-C-NH-NH 2
5(2') 4(1 ') 3 2(1)
1 (2)
Carbonohydrazide
(Carbonic dihydrazide)
~-N=N-CH=N-NH2
(1)
(5)
(1-Formazano)
o
0
II
II ~
H2N-C-NH-C-~
4
1
Allophan( 0 )yl
[ (Aminocarbonyl)aminocarbonyll
o
0
II
II
H2N-C-NH-C-NH2
5(N') 4
3
2 1(N)
Biuret b
(Imidodicarbonic diamide)
o
II
~
HN=N-C-NH-NH-~
5
1
Carbazono
(Diazenylcarbonylhydrazino)
HN=C=NH
Carbodiimide
(Methanediimine)
HN=N-CH=N-NH2
5(1) 4(2) 3
2(4) 1(5)
Formazan
HN=N-CH=N-NH-~
(1)
(5)
(S-Formazano)
3 Brief Demonstration of the General Nomenclature Rules
3.12
Other Polynitrogen Parent Systems
Trivial names of freely substitutable polynitrogen parent structures as
recommended for further use by IUPAC and the most important substituent groups derived therefrom are compiled in Table 13. Differing
names and numberings as employed by Chern. Abstr. are enclosed in
parentheses.
Table 13. Retained trivial names for poly nitrogen parent structures". (In parentheses:
differing Chern. Abstr. names and numberings.)
o
II
H2N-C-NH-C02H
4
3
2
1
Allophanic acid
(Aminocarbonylcarbamic acid)
(N"')4 NH
NH 2(N")
II
II
H 2 N-C-NH-C-NH 2
5(N') (3) 3(2) (1) 1 (N)
Biguanide
(Imidodicarbonimidic diamide)
o
II
HN=N-C-NH-NH2
5(1) 4(2) 3 2(4) 1 (5)
Carbazone
(Diazenecarboxylic acid, hydrazide)
o
II
HN=N-C-N=NH
5
4 3 2
Carbodiazone
o
II
H 2 N-NH-C-NH-NH 2
5(2') 4(1 ') 3 2(1)
1 (2)
Carbonohydrazide
(Carbonic dihydrazide)
~-N=N-CH=N-NH2
(1)
(5)
(1-Formazano)
o
0
II
II ~
H2N-C-NH-C-~
4
1
Allophan( 0 )yl
[ (Aminocarbonyl)aminocarbonyll
o
0
II
II
H2N-C-NH-C-NH2
5(N') 4
3
2 1(N)
Biuret b
(Imidodicarbonic diamide)
o
II
~
HN=N-C-NH-NH-~
5
1
Carbazono
(Diazenylcarbonylhydrazino)
HN=C=NH
Carbodiimide
(Methanediimine)
HN=N-CH=N-NH2
5(1) 4(2) 3
2(4) 1(5)
Formazan
HN=N-CH=N-NH-~
(1)
(5)
(S-Formazano)
