| Weight | 198.225 g/mol |
|---|---|
| Formula | C12H10N2O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
4-NITROSODIPHENYLAMINE (86-30-6, 156-10-5)
p-nitroso-N-phenylaniline · 4-nitroso-N-phenylaniline, monohydrochloride · para-nitroso-N-phenylaniline
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- Formation of 4-ethoxy-4'-nitrosodiphenylamine in the reaction of the phenacetin metabolite 4-nitrosophenetol with glutathione. (Biological chemistry Hoppe-Seyler, 1987)
- PRODUCTION OF 4-NITROSODIPHENYLAMINE (1973)
- Method for producing 4-nitrosodiphenylamine (1977)
- Method for preparing 4-nitrodiphenylamine and 4-nitrosodiphenylamine from carbanilide (2000)
- Structure of 4-nitrosodiphenylamine (Acta Crystallographica Section C-crystal Structure Communications, 1991)
- Structure of 4-Nitrosodiphenylamine. (ChemInform, 1991)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - p-nitroso-N-phenylaniline
- 4-nitroso-N-phenylaniline, monohydrochloride
- para-nitroso-N-phenylaniline
- 4-nitroso-N-phenylaniline
-
SMILESC1=CC=C(C=C1)NC2=CC=C(C=C2)N=O
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InChIKeyOIJHFHYPXWSVPF-UHFFFAOYSA-N
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