Weight | 152.153 g/mol |
---|---|
Formula | C7H8N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3-Methyl-2-nitroaniline (601-87-6)
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- Electrostatic modeling of the linear optical susceptibilities of 2-methyl-4-nitroaniline, m-nitroaniline, 3-methyl-4-nitropyridine N-oxide and 2-carboxylic acid-4-nitropyridine-1-oxide crystals (Chemical Physics Letters, 2010)
- Calculating the second-order nonlinear optical susceptibilities of 3-methyl-4-nitropyridine N-oxide, 2-carboxylic acid-4-nitropyridine-1-oxide, 2-methyl-4-nitroaniline, and m-nitroaniline crystals (International Journal of Quantum Chemistry, 2011)
- Reactions of 3-phenylglycidic esters. V: Reaction of methyl 3-(4-methoxyphenyl)glycidate with 2-nitroaniline and synthesis of 1,5-benzodiazepine derivatives (Chemical & Pharmaceutical Bulletin, 1985)
- Reporter molecules as probes of DNA conformation: Structure of a crystalline complex containing 2-Methyl-4-nitroaniline ethylene dimethylammonium hydrobromide 5-iodocytidylyl(35)guanosine (Biochemical and Biophysical Research Communications, 1984)
- Elongation method and supermolecule approach for the calculation of nonlinear susceptibilities. Application to the 3-Methyl-4-Nitropyridine 1-Oxide and 2-Methyl-4-Nitroaniline crystals (Journal of Computational Methods in Sciences and Engineering archive, 2006)
- Voltammetric determination of Ioxynil and 2-methyl-3-nitroaniline using C18 modified carbon paste electrodes (Analytical and Bioanalytical Chemistry, 1996)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=C(C(=CC=C1)N)[N+](=O)[O-]
-
InChIKeyVDCZKCIEXGXCDJ-UHFFFAOYSA-N
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