| Weight | 153.137 g/mol |
|---|---|
| Formula | C7H7NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
2-Nitrobenzyl alcohol (612-25-9)
o-nitrobenzyl alcohol
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- o-Nitrobenzyl Alcohol Derivatives: Opportunities in Polymer and Materials Science (Macromolecules, 2012)
- Isotope effects in photochemistry. 1. o-nitrobenzyl alcohol derivatives. (Journal of the American Chemical Society, 2004)
- In vitro activation of 2-aminobenzyl alcohol and 2-amino-6-nitrobenzyl alcohol, metabolites of 2-nitrotoluene and 2,6-dinitrotoluene (Chemical Research in Toxicology, 1989)
- Binding of 2-hydroxy-5-nitrobenzyl alcohol to rat alpha class glutathione S-transferases; evidence for binding at tryptophan 21 (Biochimica et Biophysica Acta, 1996)
- Transition-metal-free synthesis of quinolines from 2-nitrobenzyl alcohol in water (Tetrahedron Letters, 2015)
- o-Nitrobenzyl alcohol, a simple and efficient reagent for the photoreversible protection of aldehydes and ketones (Journal of The Chemical Society, Chemical Communications, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - o-nitrobenzyl alcohol
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SMILESC1=CC=C(C(=C1)CO)[N+](=O)[O-]
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InChIKeyBWRBVBFLFQKBPT-UHFFFAOYSA-N
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