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CAS 1370587-22-6

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Ethyl 5-chloro-4-(trifluoromethyl)-2-pyridinecarboxylate

Description:
Ethyl 5-chloro-4-(trifluoromethyl)-2-pyridinecarboxylate is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features a chloro substituent at the 5-position and a trifluoromethyl group at the 4-position of the pyridine ring, contributing to its unique reactivity and properties. The ethyl ester functional group at the 2-position enhances its solubility in organic solvents and may influence its biological activity. The presence of the trifluoromethyl group typically imparts increased lipophilicity and can enhance the compound's potency in various applications, particularly in pharmaceuticals and agrochemicals. Additionally, the chlorine atom can participate in nucleophilic substitution reactions, making this compound a valuable intermediate in synthetic chemistry. Overall, Ethyl 5-chloro-4-(trifluoromethyl)-2-pyridinecarboxylate exhibits characteristics that make it of interest in research and development within the fields of medicinal chemistry and material science.
Formula:C9H7ClF3NO2
InChI:InChI=1S/C9H7ClF3NO2/c1-2-16-8(15)7-3-5(9(11,12)13)6(10)4-14-7/h3-4H,2H2,1H3
InChI key:InChIKey=QGRRMWWTQIZVMW-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C=1C=C(C(OCC)=O)N=CC1Cl
Synonyms:
  • Ethyl 5-chloro-4-(trifluoromethyl)-2-pyridinecarboxylate
  • 2-Pyridinecarboxylic acid, 5-chloro-4-(trifluoromethyl)-, ethyl ester
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