Ethyl 4-oxo-4-[3-(trifluoromethyl)phenyl]butanoate, identified by its CAS number 166312-68-1, is an organic compound characterized by its ester functional group and a trifluoromethyl substituent on a phenyl ring. This compound features a butanoate backbone, which contributes to its reactivity and potential applications in organic synthesis. The presence of the trifluoromethyl group enhances its lipophilicity and may influence its biological activity, making it of interest in medicinal chemistry. The carbonyl group (4-oxo) indicates that it can participate in various chemical reactions, such as nucleophilic additions or condensation reactions. Ethyl esters like this one are often used in the synthesis of pharmaceuticals and agrochemicals due to their ability to undergo hydrolysis to yield corresponding acids. Additionally, the compound's structural features suggest potential applications in materials science and as intermediates in the synthesis of more complex molecules. Overall, ethyl 4-oxo-4-[3-(trifluoromethyl)phenyl]butanoate is a versatile compound with significant implications in various fields of chemistry.

ethyl 4-oxo-4-[3-(trifluoromethyl)phenyl]butanoate

166312-68-1: Ethyl 4-oxo-4-[3-(trifluoromethyl)phenyl]butanoate, identified by its CAS number 166312-68-1, is an organic compound characterized by its ester functional group and a trifluoromethyl substituent on a phenyl ring. This compound features a butanoate backbone, which contributes to its reactivity and potential applications in organic synthesis. The presence of the trifluoromethyl group enhances its lipophilicity and may influence its biological activity, making it of interest in medicinal chemistry. The carbonyl group (4-oxo) indicates that it can participate in various chemical reactions, such as nucleophilic additions or condensation reactions. Ethyl esters like this one are often used in the synthesis of pharmaceuticals and agrochemicals due to their ability to undergo hydrolysis to yield corresponding acids. Additionally, the compound's structural features suggest potential applications in materials science and as intermediates in the synthesis of more complex molecules. Overall, ethyl 4-oxo-4-[3-(trifluoromethyl)phenyl]butanoate is a versatile compound with significant implications in various fields of chemistry.

CAS 166312-68-1

ethyl 4-oxo-4-[3-(trifluoromethyl)phenyl]butanoate

Benzenebutanoic acid, γ-oxo-3-(trifluoromethyl)-, ethyl ester

Ref: IN-DA001WN3

Ethyl 4-oxo-4-(3-trifluoromethylphenyl)butyrate

Ref: 10-F207952