| Weight | 107.156 g/mol |
|---|---|
| Formula | C7H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,5-DIMETHYLPYRIDINE (589-93-5)
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- [Ru(HNO)(pybuS4)], the First HNO Complex Resulting from Hydride Addition to a NO Complex (pybuS42=2,6-Bis(2-mercapto- 3,5-di-tert-butylphenylthio)dimethylpyridine(2)) (Chemistry: A European Journal, 2001)
- 3,5Dibenzoyl4(3phenoxyphenyl)1,4dihydro2,6dimethylpyridine (DP7) as a new multidrug resistance reverting agent devoid of effects on vascular smooth muscle contractility (British Journal of Pharmacology, 2004)
- An Efficient and Eco-Friendly Procedure for the Synthesis of Hantzsch Ethyl 1,4-Dihydro-2,6-Dimethylpyridine-3,5-Dicarboxylates Under Mild and Green Conditions (Letters in Organic Chemistry, 2006)
- Structural and spectroscopic evidence of hydrogen bonding in 3-bromo-5-hydroxy-2,6-dimethylpyridine and 3-chloro-5-hydroxy-2,6-dimethylpyridine (Journal of Molecular Structure, 1997)
- Syntheses, crystal structures, spectral and thermal analysis and biological activities of copper(II)-pyridine-2,5-dicarboxylate complexes with 4-methylimidazole, imidazole, and 3,4-dimethylpyridine (Solid State Sciences, 2009)
- 3,5-Dibenzoyl-4-(3-phenoxyphenyl)-1,4-dihydro-2,6-dimethylpyridine (DP7): A new multidrug resistance inhibitor devoid of effects on Langendorff-perfused rat heart (European Journal of Pharmacology, 2007)
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SMILESCC1=CN=C(C=C1)C
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InChIKeyXWKFPIODWVPXLX-UHFFFAOYSA-N
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2,5-DIMETHYLPYRIDINE
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