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CAS 1221172-04-8

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2-Chloro-6-(trifluoromethoxy)-3-pyridinecarboxylic acid

Description:
2-Chloro-6-(trifluoromethoxy)-3-pyridinecarboxylic acid is a chemical compound characterized by its pyridine ring structure, which is substituted at the 2 and 6 positions with a chlorine atom and a trifluoromethoxy group, respectively. The presence of the carboxylic acid functional group at the 3-position contributes to its acidic properties. This compound is typically a solid at room temperature and is soluble in polar solvents due to the presence of the carboxylic acid group. Its trifluoromethoxy substituent enhances its lipophilicity and may influence its biological activity, making it of interest in pharmaceutical research. The chlorine atom can also affect the compound's reactivity and stability. Overall, 2-Chloro-6-(trifluoromethoxy)-3-pyridinecarboxylic acid is notable for its potential applications in medicinal chemistry and agrochemicals, where its unique structural features may contribute to specific interactions with biological targets.
Formula:C7H3ClF3NO3
InChI:InChI=1S/C7H3ClF3NO3/c8-5-3(6(13)14)1-2-4(12-5)15-7(9,10)11/h1-2H,(H,13,14)
InChI key:InChIKey=PKESEAIWVBVHEB-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=C(Cl)N=C(OC(F)(F)F)C=C1
Synonyms:
  • 2-Chloro-6-(trifluoromethoxy)-3-pyridinecarboxylic acid
  • 3-Pyridinecarboxylic acid, 2-chloro-6-(trifluoromethoxy)-
  • 2-Chloro-6-(trifluoromethoxy)nicotinic acid
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