Weight | 152.153 g/mol |
---|---|
Formula | C7H8N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
2,4-DIMETHYL-3-NITROPYRIDINE (1074-76-6)
1074-76-6
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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)
- Reactions in strongly basic media. Part 7. Correlation of the rates of alkaline hydrolysis of 2-substituted 3- and 5-nitropyridines, 4-nitropyridine N-oxide, and 2- and 4-substituted pyridine methiodides in aqueous dimethyl sulphoxide with an acidity function (Journal of The Chemical Society-perkin Transactions 1, 1987)
- Isomers of 1-azabicyclo(2.2.2)oct-3-yl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-5-nitropyridine-3-carboxylate (1990)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1074-76-6
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SMILESCC1=C(C(=NC=C1)C)[N+](=O)[O-]
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InChIKeyMOQKFCFVTVIJJS-UHFFFAOYSA-N
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Safety
Alternate Names
Estimated Properties
Boiling Point | 229.5 C | EPA T.E.S.T. |
---|---|---|
Boiling Point | 252.34 C | EPI Suite |
Density | 1.19 g/cm3 | EPA T.E.S.T. |
Flash Point | 112.06 C | EPA T.E.S.T. |
Melting Point | 65.78 C | EPI Suite |
Water Solubility | 2363.24 mg/L | EPA T.E.S.T. |
Water Solubility | 17037 mg/L | EPI Suite |
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Synthesis
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