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CAS 1221171-92-1

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2-(Trifluoromethoxy)-3-pyridinecarboxylic acid

Description:
2-(Trifluoromethoxy)-3-pyridinecarboxylic acid is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a trifluoromethoxy group (-O-CF3) significantly influences its chemical properties, imparting high electronegativity and lipophilicity. This compound typically exhibits acidic behavior due to the carboxylic acid functional group (-COOH), which can donate protons in solution. The trifluoromethoxy substituent enhances the compound's reactivity and can affect its solubility in various solvents. Additionally, the presence of fluorine atoms often contributes to increased stability and resistance to metabolic degradation, making it of interest in pharmaceutical applications. The compound's unique structure may also influence its interactions with biological targets, potentially leading to specific therapeutic effects. Overall, 2-(Trifluoromethoxy)-3-pyridinecarboxylic acid is notable for its distinctive functional groups and potential utility in medicinal chemistry and agrochemical formulations.
Formula:C7H4F3NO3
InChI:InChI=1S/C7H4F3NO3/c8-7(9,10)14-5-4(6(12)13)2-1-3-11-5/h1-3H,(H,12,13)
InChI key:InChIKey=XUHDHRKJBUCYSC-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=C(OC(F)(F)F)N=CC=C1
Synonyms:
  • 2-(Trifluoromethoxy)nicotinic acid
  • 2-(Trifluoromethoxy)-3-pyridinecarboxylic acid
  • 3-Pyridinecarboxylic acid, 2-(trifluoromethoxy)-
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