| Weight | 188.186 g/mol |
|---|---|
| Formula | C10H8N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
4-Nitro-1-naphthylamine (776-34-1)
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- Photoinitiated bulk polymerization of lauryl acrylate by N-acetyl-4-nitro-1-naphthylamine in the presence of N,N-dimethylaniline (Journal of Photochemistry and Photobiology A-chemistry, 1988)
- N-acetyl-4-nitro-1-naphthylamine as sensitizer of N, N-dimethylaniline for photoinitiated radical polymerization (Polymer, 2000)
- 4-Nitro-1-Naphthylamine (Organic Syntheses, 2003)
- 30. The monoreduction of 1 : 3-dinitronaphthalene and the separation of 3-nitro-1-naphthylamine and 4-nitro-2-naphthylamine (Journal of The Chemical Society (resumed), 1944)
- 11. Reactions of 3-nitro-1-naphthylamine, including anil formation, bromination, and the preparation of 1 : 2 : 3 : 4-tetrabromonaphthalene (Journal of The Chemical Society (resumed), 1944)
- 8. Decomposition of the diazonium salts of 4-nitro-1-naphthylamine by sodium sulphite and sodium acetate. Preparation of 4 : 4-dinitro-1 : 1-azonaphthalene (Journal of The Chemical Society (resumed), 1944)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C(=CC=C2[N+](=O)[O-])N
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InChIKeyBVPJPRYNQHAOPQ-UHFFFAOYSA-N
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