Weight | 127.574 g/mol |
---|---|
Formula | C6H6ClN |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2-Chloro-6-methylpyridine (18368-63-3)
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- Synthesis of Methylpyridine Derivatives (XXI). Amination of Chloro-2, 6-lutidines and Their N-Oxides via a Hetaryne Mechanism (Chemical & Pharmaceutical Bulletin, 1965)
- A comparative study on vibrational, conformational and electronic structure of 2-chloro-4-methyl-3-nitropyridine and 2-chloro-6-methylpyridine (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- [Nicotinic acid derivatives. V. Synthesis and some chemical properties of 2-chloro-3-cyano-6-methylpyridine]. (Acta Poloniae Pharmaceutica, 1974)
- [Syntheses of methylpyridine derivatives. XXVI. Ring-closure reaction of 3-acylamido-4-chloro-2,6-lutidine with potassium amide in liquid ammonia]. (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1972)
- Chlorotropic rearrangement of 3,5-dichloro-3-cyano-4-methylpyridine-2,6-(1H)-dione in the medium of polar solvents. Synthesis of 5-chloro-3-cyano-6-hydroxy-4-methylpyridin-2-one (Chemistry of Heterocyclic Compounds, 1999)
- ChemInform Abstract: INVESTIGATIONS ON THE REACTION COURSE OF DIETHYL 2-CHLORO-6-METHYLPYRIDINE-3,5-DICARBOXYLATE WITH N-ARYL- AND N-ARYL-N-ALKYLTHIOUREAS (ChemInform, 1982)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=NC(=CC=C1)Cl
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InChIKeyGXZDYRYYNXYPMQ-UHFFFAOYSA-N
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