| Weight | 107.156 g/mol |
|---|---|
| Formula | C7H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3,5-DIMETHYLPYRIDINE (591-22-0)
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- SYNTHESIS, CHARACTERIZATION, AND REACTIVITY OF GROUP 12 METAL THIOCARBOXYLATES, M(SOCR)2LUT2 M = CD, ZN; R = CH3, C(CH3)3; LUT = 3,5-DIMETHYLPYRIDINE (LUTIDINE) (Inorganic Chemistry, 1997)
- [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)
- Coordination Compounds of Nickel(II) Salts with Substituted Pyridines. Square-Planar, Tetrahedral, and Octahedral Compounds of 3,4- and 3,5-Dimethylpyridine (Inorganic Chemistry, 1964)
- 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)
- Dehydrogenative Ga-Ga Coupling and Hydrogallation in Gallium Hydride Complexes of 3,5-Dimethylpyridine (Organometallics, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC(=CN=C1)C
-
InChIKeyHWWYDZCSSYKIAD-UHFFFAOYSA-N
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3,5-DIMETHYLPYRIDINE
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