| Weight | 107.156 g/mol |
|---|---|
| Formula | C7H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,6-Dimethylpyridine (108-48-5)
2,6-lutidine
Score:
#944 in Physics
,
#2692 in Chemistry
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- 2,2' -dithiobis (3 -cyano -4,6 -dimethylpyridine) : A new class of acid corrosion inhibitors for mild steel (Corrosion Science, 2006)
- High-resolution 13C NMR configurational analysis of polypropylene made with MgCl2-supported Ziegler-Natta catalysts. 1. The model system MgCl2/TiCl4-2,6-dimethylpyridine/Al(C2H5)3 (Macromolecules, 1999)
- Steric Effects in Displacement Reactions. III. The Base Strengths of Pyridine, 2,6-Lutidine and the Monoalkylpyridines (Journal of the American Chemical Society, 1955)
- Characterization of acid surfaces by adsorption of 2,6-dimethylpyridine (Journal of Catalysis, 1984)
- Phase separation and coalescence in critically quenched isobutyric-acidwater and 2,6-lutidinewater mixtures (Physical Review A, 1979)
- Spin-free and spin-paired transition metal perchlorate complexes of 2,6-lutidine N-oxide (Inorganica Chimica Acta, 1969)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H226: Flammable liquid and vapor
Warning Flammable liquids - Category 3 - 2,6-lutidine
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SMILESCC1=NC(=CC=C1)C
-
InChIKeyOISVCGZHLKNMSJ-UHFFFAOYSA-N
- Pubchem - 2,6-Dimethylpyridine
- Wikipedia - 2,6-lutidine
2,6-Lutidine is a natural heterocyclic aromatic organic compound with the formula (CH3)2C5H3N. It is one of several dimethyl-substituted derivative of pyridine. It is a colorless liquid with mildly basic properties and a pungent, noxious odor.
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