| Weight | 247.301 g/mol |
|---|---|
| Formula | C16H13N3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 2 |
Solvent Yellow 5 (85-84-7)
1-phenylazo-2-naphthylamine
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- Azo-hydrazone tautomerism in azo dyes. I. A comparative study of 1-phenylazo-2-naphthol and 1-phenylazo-2-naphthylamine derivatives by electronic spectroscopy (Dyes and Pigments, 1981)
- Azohydrazone tautomerism in azo dyes. II. Raman, NMR and mass spectrometric investigations of 1-phenylazo-2-naphthylamine and 1-phenylazo-2-naphthol derivatives (Dyes and Pigments, 1982)
- Azo-hydrazone tautomerism in azo dyes. IV. Colour and tautomeric structure of adsorbed 1-phenylazo-2-naphthylamine and 1-phenylazo-2-naphthol dyes (Dyes and Pigments, 1984)
- Reversible ring opening and closure reactions of the triazine ligands derived from 1-phenylazo-2-naphthylamine and pyridine-2-aldehyde or quinoline-2-aldehyde structure and reactivity of the palladium (II) complexes (Inorganica Chimica Acta, 2005)
- Derivatives of 1-Phenylazo-2-Naphthylamine. The Effect of Substituent on Color (Journal of Organic Chemistry, 1966)
- Chronic toxicity of Yellow AB (1-phenylazo-2-naphthylamine) and Yellow OB (1-o-tolylazo-2-naphthylamine) (Toxicology and Applied Pharmacology, 1963)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-phenylazo-2-naphthylamine
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SMILESC1=CC=C(C=C1)N=NC2=C(C=CC3=CC=CC=C32)N
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InChIKeyKLCDQSGLLRINHY-UHFFFAOYSA-N
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