| Weight | 148.121 g/mol |
|---|---|
| Formula | C7H4N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-Nitrobenzonitrile (612-24-8)
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- Au25 Clusters as Electron-Transfer Catalysts Induced the Intramolecular Cascade Reaction of 2-nitrobenzonitrile (Scientific Reports, 2013)
- The Dimerization of 2-Amino-5-nitrobenzonitrile (Journal of the American Chemical Society, 1960)
- Activity of 2-(3,4-dichlorophenoxy)-5-nitrobenzonitrile (MDL-860) against picornaviruses in vitro. (Antimicrobial Agents and Chemotherapy, 1982)
- Inhibition of coxsackie B3 virus induced myocarditis in mice by 2-(3,4-dichlorophenoxy)-5-nitrobenzonitrile (Journal of Medical Virology, 2004)
- Antiviral activity and mechanism of action of 2-(3,4-dichlorophenoxy)-5-nitrobenzonitrile (MDL-860). (Antimicrobial Agents and Chemotherapy, 1982)
- The preparation of 2-Fluoro-5-nitrobenzonitrile and the proton magnetic resonance spectra of some compounds containing the N-(2-Cyano-4-nitrophenyl) group (Australian Journal of Chemistry, 1967)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C(=C1)C#N)[N+](=O)[O-]
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InChIKeySWBDKCMOLSUXRH-UHFFFAOYSA-N
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