Weight | 139.114 g/mol |
---|---|
Formula | C5H5N3O2 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
4-Amino-2-nitropyridine (14916-64-4)
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- Intramolecular catalysis. Part 7. The Smiles rearrangement of substituted 2-hydroxy-2-nitro- and -2,4-dinitro-diphenyl sulphones, as well as 2-amino-2,4-dinitrodiphenyl sulphide, 2-[(2-aminophenyl)thio]-3-nitropyridine and 2-hydroxy-2,4-dinitrodiphenyl ether (Journal of The Chemical Society-perkin Transactions 1, 1991)
- Structural and vibrational investigation of 2-amino-4-nitropyridine crystal (Journal of Molecular Structure, 1997)
- Na2S2O4: A Versatile Reagent for the One-Pot Synthesis of 2-Aryl-1H-imidazo[4,5-c]pyridines from 4-Amino-3-nitropyridine and Aldehydes via Reductive Cyclization (Synthetic Communications, 2010)
- 6-Amino-2-lower-alkyl-4-nitropyridine N-oxide compositions and coccidiostat process (1976)
- Investigation of structure, vibrational, electronic, NBO and NMR analyses of 2-chloro-4-nitropyridine (CNP), 2-chloro-4-methyl-5-nitropyridine (CMNP) and 3-amino-2-chloro-4-methylpyridine (ACMP) by experimental and theoretical approach (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2015)
- Microbial transformation of 2-amino-4-methyl-3-nitropyridine (Journal of Industrial Microbiology & Biotechnology, 2012)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=C(C=C1N)[N+](=O)[O-]
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InChIKeyZPFUWAVLEWIOEJ-UHFFFAOYSA-N
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