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CAS 1221171-98-7

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2-(Trifluoromethoxy)-4-pyridinecarboxylic acid

Description:
2-(Trifluoromethoxy)-4-pyridinecarboxylic acid is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a trifluoromethoxy group (-O-CF3) at the 2-position and a carboxylic acid group (-COOH) at the 4-position contributes to its unique chemical properties. This compound is likely to exhibit strong acidity due to the carboxylic acid functional group, while the trifluoromethoxy group can enhance its lipophilicity and influence its reactivity and solubility in various solvents. The trifluoromethyl group is known for its electron-withdrawing effects, which can stabilize negative charges in reaction intermediates, making this compound potentially useful in various chemical syntheses and applications in pharmaceuticals or agrochemicals. Additionally, the presence of fluorine atoms can impart unique biological activity and enhance the compound's metabolic stability. Overall, 2-(Trifluoromethoxy)-4-pyridinecarboxylic acid is a compound of interest in medicinal chemistry and materials science due to its distinctive structural features and potential applications.
Formula:C7H4F3NO3
InChI:InChI=1S/C7H4F3NO3/c8-7(9,10)14-5-3-4(6(12)13)1-2-11-5/h1-3H,(H,12,13)
InChI key:InChIKey=PGAJZMZZYBMULE-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(C(O)=O)=CC=N1
Synonyms:
  • 2-(Trifluoromethoxy)isonicotinic acid
  • 4-Pyridinecarboxylic acid, 2-(trifluoromethoxy)-
  • 2-(Trifluoromethoxy)-4-pyridinecarboxylic acid
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