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Details

Stereochemistry ACHIRAL
Molecular Formula C7H8N2O
Molecular Weight 136.1512
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-METHYL-N-NITROSOANILINE

SMILES

CN(N=O)C1=CC=CC=C1

InChI

InChIKey=MAXCWSIJKVASQC-UHFFFAOYSA-N
InChI=1S/C7H8N2O/c1-9(8-10)7-5-3-2-4-6-7/h2-6H,1H3

HIDE SMILES / InChI

Molecular Formula C7H8N2O
Molecular Weight 136.1512
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The binding affinity of carcinogenic N-nitrosodimethylamine and N-nitrosomethylaniline to cytochromes P450 2B4, 2E1 and 3A6 does not dictate the rate of their enzymatic N-demethylation.
2010-06
Characterization of CYP2A13*2, a variant cytochrome P450 allele previously found to be associated with decreased incidences of lung adenocarcinoma in smokers.
2008-11
Rabbit liver microsomal system: study of interaction with two model N-nitrosamines and their metabolism.
2004-12
The effect of substituents in the aromatic ring on carcinogenicity of N-nitrosomethylaniline in F344 rats.
1983
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:44:34 GMT 2025
Edited
by admin
on Mon Mar 31 18:44:34 GMT 2025
Record UNII
9SM68I29WQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-METHYL-N-NITROSOBENZENAMINE
HSDB  
Preferred Name English
N-METHYL-N-NITROSOANILINE
Systematic Name English
NSC-137
Code English
PHENYLMETHYLNITROSAMINE
Common Name English
ANILINE, N-METHYL-N-NITROSO-
Systematic Name English
NITROSOMETHYLANILINE
Systematic Name English
METHYLNITROSO PHENYLAMINE
Systematic Name English
N-METHYL-N-NITROSOBENZENAMINE [HSDB]
Common Name English
METHYLPHENYLNITROSAMINE
Common Name English
BENZENAMINE, N-METHYL-N-NITROSO-
Systematic Name English
METHYLNITROSOANILINE
Systematic Name English
N-NITROSO-N-METHYLANILINE
Systematic Name English
N-METHYL-N-PHENYLNITROSAMINE
Common Name English
Code System Code Type Description
HSDB
5072
Created by admin on Mon Mar 31 18:44:34 GMT 2025 , Edited by admin on Mon Mar 31 18:44:34 GMT 2025
PRIMARY
CAS
614-00-6
Created by admin on Mon Mar 31 18:44:34 GMT 2025 , Edited by admin on Mon Mar 31 18:44:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID9021053
Created by admin on Mon Mar 31 18:44:34 GMT 2025 , Edited by admin on Mon Mar 31 18:44:34 GMT 2025
PRIMARY
RS_ITEM_NUM
1466607
Created by admin on Mon Mar 31 18:44:34 GMT 2025 , Edited by admin on Mon Mar 31 18:44:34 GMT 2025
PRIMARY
FDA UNII
9SM68I29WQ
Created by admin on Mon Mar 31 18:44:34 GMT 2025 , Edited by admin on Mon Mar 31 18:44:34 GMT 2025
PRIMARY
PUBCHEM
11957
Created by admin on Mon Mar 31 18:44:34 GMT 2025 , Edited by admin on Mon Mar 31 18:44:34 GMT 2025
PRIMARY
NSC
137
Created by admin on Mon Mar 31 18:44:34 GMT 2025 , Edited by admin on Mon Mar 31 18:44:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-366-5
Created by admin on Mon Mar 31 18:44:34 GMT 2025 , Edited by admin on Mon Mar 31 18:44:34 GMT 2025
PRIMARY