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CAS 21168-42-3

:

ethyl 4-chloro-7-(trifluoromethyl)quinoline-3-carboxylate

Description:
Ethyl 4-chloro-7-(trifluoromethyl)quinoline-3-carboxylate is a chemical compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. This compound features a chloro substituent at the 4-position and a trifluoromethyl group at the 7-position, contributing to its unique chemical properties. The ethyl ester functional group at the 3-position enhances its reactivity and solubility in organic solvents. The presence of the trifluoromethyl group often imparts increased lipophilicity and can influence biological activity, making this compound of interest in medicinal chemistry and drug development. Additionally, the chloro group can participate in various chemical reactions, such as nucleophilic substitutions. Ethyl 4-chloro-7-(trifluoromethyl)quinoline-3-carboxylate may exhibit specific pharmacological properties, although detailed biological activity would require further investigation. Overall, this compound is notable for its structural complexity and potential applications in various fields, including pharmaceuticals and agrochemicals.
Formula:C13H9ClF3NO2
InChI:InChI=1/C13H9ClF3NO2/c1-2-20-12(19)9-6-18-10-5-7(13(15,16)17)3-4-8(10)11(9)14/h3-6H,2H2,1H3
SMILES:CCOC(=O)c1cnc2cc(ccc2c1Cl)C(F)(F)F
Synonyms:
  • Ethyl 4-chloro-7-(trifluoromethyl)quinoline-3-carboxylate
  • 4-chloro-7-(trifluoromethyl)quinoline-3-carboxylic acid
  • 3-Quinolinecarboxylic acid, 4-chloro-7-(trifluoromethyl)-, ethyl ester
  • ETHYL 4-CHLORO-7-TRIFLUOROMETHYL-3-CARBOXYLATE
  • 4-CHLORO-7-TRIFLUOROMETHYLQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
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