Weight | 190.202 g/mol |
---|---|
Formula | C10H10N2O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 1 |
2,3-DIMETHYL-5-NITROINDOLE (21296-94-6)
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- Stereochemistry of rings. XVI. Indole derivatives. 1. 2,3-Dimethyl-5-nitroindole (Acta Crystallographica Section C-crystal Structure Communications, 1989)
- ChemInform Abstract: Stereochemistry of Rings. Part 16. Indole Derivatives. Part 1. 2,3-Dimethyl-5-nitroindole (ChemInform, 1989)
- Heating N-substituted 2-methyl-3-phenyl-5-nitroindoles in methanol with excess base yields the corresponding azoxindoles. Under the same conditions 2-methyl-5-nitroindole is converted to bis(2-methyl- 5-nitroindol-3-yl)methane. Reaction of 1,2-dimethyl-3-formyl-5-nitroindole with benzyl cyanide gives 1,2- dimethyl-3-(~-cyano-~-phenyl)vinyl-5-nitroindoleo (Chemistry of Heterocyclic Compounds, 1990)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=C(NC2=C1C=C(C=C2)[N+](=O)[O-])C
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InChIKeyLKIMRQIKTONPER-UHFFFAOYSA-N
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