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CAS 890092-41-8

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5-Chloro-4-methyl-3-pyridinecarboxylic acid

Description:
5-Chloro-4-methyl-3-pyridinecarboxylic acid is a heterocyclic organic compound characterized by its pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a carboxylic acid functional group (-COOH) at the 3-position contributes to its acidity and reactivity, while the chloro substituent at the 5-position and the methyl group at the 4-position influence its chemical properties and potential applications. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its structure allows for various chemical reactions, including nucleophilic substitutions and coupling reactions, making it of interest in pharmaceutical and agrochemical research. Additionally, the presence of the chlorine atom can enhance biological activity or alter the compound's interaction with biological targets. As with many pyridine derivatives, it may also exhibit specific biological activities, which can be explored for potential therapeutic applications.
Formula:C7H6ClNO2
InChI:InChI=1S/C7H6ClNO2/c1-4-5(7(10)11)2-9-3-6(4)8/h2-3H,1H3,(H,10,11)
InChI key:InChIKey=DNYPAJVKUAHQHN-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C(C)=C(Cl)C=NC1
Synonyms:
  • 3-Pyridinecarboxylic acid, 5-chloro-4-methyl-
  • 5-Chloro-4-methyl-3-pyridinecarboxylic acid
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