| Weight | 152.153 g/mol |
|---|---|
| Formula | C7H8N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,6-Dimethyl-3-nitropyridine (15513-52-7)
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- Observation of attractive intermolecular CHO interaction in the crystal packing of 3-chloro- and 3-bromo-2,6-dimethyl-4-nitropyridine N-oxide (Vibrational Spectroscopy, 1997)
- Syntheses, calcium channel modulation effects, and nitric oxide release studies of O2-alkyl-1-(pyrrolidin-1-yl) diazen-1-ium-1,2-diolate 4-aryl(heteroaryl)-1,4-dihydro-2,6-dimethyl-3-nitropyridine-5-carboxylates (Drug Development Research, 2003)
- Vibrational properties and X-ray crystal structure of 3-iodo-2,6-dimethyl-4-nitropyridine N-oxide (Vibrational Spectroscopy, 2001)
- Synthesis of dialkyl 1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylates and alkyl 1,4-dihydro-2,6-dimethyl-3-nitropyridine-5-carboxylates possessing a c-4 2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl (uracil) substituent to determine calcium channel modulation structure-activity relationships (Journal of Heterocyclic Chemistry, 2004)
- Isomers of 1-azabicyclo(2.2.2)oct-3-yl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-5-nitropyridine-3-carboxylate (1990)
- Racemic isopropyl 1,4-dihydro-2,6-dimethyl-4-(6-methyl-2-pyridyl)-3-nitropyridine-5-carboxylate hemi-benzene solvate (Acta Crystallographica Section C-crystal Structure Communications, 2000)
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SMILESCC1=NC(=C(C=C1)[N+](=O)[O-])C
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InChIKeyAETHUDGJSSKZKT-UHFFFAOYSA-N
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