Ethyl 3,5-bis(trifluoromethyl)benzoate is an organic compound characterized by its ester functional group and the presence of two trifluoromethyl groups attached to a benzene ring. The molecular structure features a benzoate moiety, where the ethyl group is esterified with a benzoic acid derivative. The trifluoromethyl groups significantly influence the compound's physical and chemical properties, enhancing its lipophilicity and potentially affecting its reactivity and stability. This compound is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. It is known for its applications in organic synthesis and as an intermediate in the production of various fluorinated compounds. Additionally, the presence of fluorine atoms can impart unique characteristics, such as increased thermal stability and altered solubility in organic solvents. Safety data should be consulted, as compounds with trifluoromethyl groups can exhibit toxicity and environmental persistence. Overall, Ethyl 3,5-bis(trifluoromethyl)benzoate is a notable compound in the field of fluorinated organic chemistry.

Ethyl 3,5-bis(trifluoromethyl)benzoate

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ETHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE

3,5-Bis-trifluoromethyl-benzoic acid ethyl ester

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CAS 96617-71-9: Ethyl 3,5-bis(trifluoromethyl)benzoate

ETHYL 3,5-BIS(TRIFLUOROMETHYL)BENZOATE

Ref: IN-DA003Q6L

Ethyl 3,5-bis(trifluoromethyl)benzoate

Ref: 54-PC3553

3,5-Bis-trifluoromethyl-benzoic acid ethyl ester

Ref: 10-F317498

Ethyl 3,5-Bis(Trifluoromethyl)Benzoate

Ref: 3D-FE84306