Weight | 136.154 g/mol |
---|---|
Formula | C7H8N2O |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
N-Nitroso-N-methylaniline (614-00-6)
phenylmethylnitrosamine · N-methyl-N-nitrosobenzenamine · N-methyl-N-nitrosoaniline
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- Evidence for Several Demethylase Enzymes in the Oxidation of Dimethylnitrosamine and Phenylmethylnitrosamine by Rat Liver Fractions (Cancer Research, 1979)
- alpha-Hydroxylation pathway in the in vitro metabolism of carcinogenic nitrosamines: N-nitrosodimethylamine and N-nitroso-N-methylaniline (Proceedings of the National Academy of Sciences of the United States of America, 1981)
- Evidence for an unstable DNA adduct from N-nitroso-N-methylaniline (Chemical Research in Toxicology, 1990)
- An investigation of the metabolism of N-nitroso-N-methylaniline by phenobarbital- and pyrazole-induced SpragueDawley rat liver and esophagus derived S-9 (Chemico-Biological Interactions, 1987)
- Stabilizer reactions in cast double base rocket propellants. Part II: Formation and subsequent reactions of Nnitroso derivatives of paranitroNmethylaniline and 2nitrodiphenylamine in mixedstabilizer propellants aged at 80C and 90C (Propellants, Explosives, Pyrotechnics, 1991)
- Metabolism of 15N-labelled N-nitrosodimethylamine and N-nitroso-N-methylaniline by isolated rat hepatocytes (Biochemical Pharmacology, 1984)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phenylmethylnitrosamine
- N-methyl-N-nitrosobenzenamine
- N-methyl-N-nitrosoaniline
- N-nitrosomethylaniline
- methylphenylnitrosamine
- N-nitrosomethylphenylamine
-
SMILESCN(C1=CC=CC=C1)N=O
-
InChIKeyMAXCWSIJKVASQC-UHFFFAOYSA-N
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