| Weight | 118.139 g/mol |
|---|---|
| Formula | C7H6N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Aminobenzonitrile (1885-29-6)
o-aminobenzonitrile
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- Intramolecular Charge Transfer with the Planarized 4-Aminobenzonitrile 1-tert-Butyl-6-cyano-1,2,3,4-tetrahydroquinoline (NTC6) (Journal of the American Chemical Society, 2004)
- Electrochemical copolymerization of aniline with o-aminobenzonitrile (Electrochimica Acta, 1994)
- Synthesis of 4-Arylaminoquinazolines and 2-Aryl-4-arylaminoquinazolines from 2-Aminobenzonitrile, Anilines and Formic Acid or Benzaldehydes (Tetrahedron, 2000)
- Laser-induced fluorescence spectroscopy and structure of microsolvated molecular clusters. Part 2.Laser-induced fluorescence spectroscopy of jet-cooled ethyl 4-aminobenzoate, methyl 4-aminobenzoate, 4-aminobenzonitrile and their dimethylamino and pyrrolidino derivatives (Journal of the Chemical Society, Faraday Transactions, 1992)
- Synthesis of quinazoline-2,4(1H,3H)-dione from carbon dioxide and 2-aminobenzonitrile using mesoporous smectites incorporating alkali hydroxide (Catalysis Science & Technology, 2014)
- An efficient synthesis of quinazoline-2,4(1H,3H)-dione from CO2 and 2-aminobenzonitrile using [Hmim]OH/SiO2 as a base functionalized Supported Ionic Liquid Phase Catalyst (Journal of CO 2 Utilization, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - o-aminobenzonitrile
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SMILESC1=CC=C(C(=C1)C#N)N
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InChIKeyHLCPWBZNUKCSBN-UHFFFAOYSA-N
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Similar Compounds
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2-Aminobenzonitrile
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