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CAS 62774-90-7

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2,6-dichloro-4-methylpyridine-3-carboxylic acid

Description:
2,6-Dichloro-4-methylpyridine-3-carboxylic acid is a heterocyclic organic compound characterized by its pyridine ring structure, which is substituted at the 2 and 6 positions with chlorine atoms and at the 4 position with a methyl group, along with a carboxylic acid functional group at the 3 position. This compound typically appears as a solid and is soluble in polar solvents due to the presence of the carboxylic acid group. It exhibits acidic properties, which can influence its reactivity and interactions in various chemical environments. The presence of chlorine substituents can enhance its biological activity and lipophilicity, making it of interest in pharmaceutical and agrochemical applications. Additionally, the compound may participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions, due to the electrophilic nature of the pyridine ring. Its unique structure and functional groups contribute to its potential utility in synthetic organic chemistry and material science.
Formula:C7H5Cl2NO2
InChI:InChI=1/C7H5Cl2NO2/c1-3-2-4(8)10-6(9)5(3)7(11)12/h2H,1H3,(H,11,12)
SMILES:Cc1cc(Cl)nc(c1C(=O)O)Cl
Synonyms:
  • 2,6-Dichloro-4-methyl-3-pyridinecarboxylic Acid
  • 2,6-Dichloro-4-Methylnicotinic Acid
  • 3-Pyridinecarboxylic acid, 2,6-dichloro-4-methyl-
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