[3-(3,5-Difluorobenzoyl)phenyl] acetate is an organic compound characterized by its structure, which includes a phenyl ring substituted with a 3,5-difluorobenzoyl group and an acetate moiety. This compound typically exhibits properties common to aromatic esters, such as moderate solubility in organic solvents and potential reactivity due to the presence of both the carbonyl and ester functional groups. The difluorobenzoyl substituent can influence the compound's electronic properties, potentially enhancing its reactivity or altering its interaction with biological targets. The presence of fluorine atoms often imparts unique characteristics, such as increased lipophilicity and stability against metabolic degradation. Additionally, the compound may exhibit specific spectral characteristics in techniques like NMR and IR spectroscopy, allowing for its identification and characterization. Its applications could span various fields, including pharmaceuticals, agrochemicals, or materials science, depending on its biological activity and chemical reactivity. Overall, [3-(3,5-difluorobenzoyl)phenyl] acetate represents a versatile compound with potential utility in diverse chemical contexts.

[3-(3,5-difluorobenzoyl)phenyl] acetate

890100-22-8: [3-(3,5-Difluorobenzoyl)phenyl] acetate is an organic compound characterized by its structure, which includes a phenyl ring substituted with a 3,5-difluorobenzoyl group and an acetate moiety. This compound typically exhibits properties common to aromatic esters, such as moderate solubility in organic solvents and potential reactivity due to the presence of both the carbonyl and ester functional groups. The difluorobenzoyl substituent can influence the compound's electronic properties, potentially enhancing its reactivity or altering its interaction with biological targets. The presence of fluorine atoms often imparts unique characteristics, such as increased lipophilicity and stability against metabolic degradation. Additionally, the compound may exhibit specific spectral characteristics in techniques like NMR and IR spectroscopy, allowing for its identification and characterization. Its applications could span various fields, including pharmaceuticals, agrochemicals, or materials science, depending on its biological activity and chemical reactivity. Overall, [3-(3,5-difluorobenzoyl)phenyl] acetate represents a versatile compound with potential utility in diverse chemical contexts.

CAS 890100-22-8

[3-(3,5-difluorobenzoyl)phenyl] acetate

3-Acetoxy-3',5'-difluorobenzophenone

Ref: IN-DA0042VE

3-Acetoxy-3′,5′-difluorobenzophenone

Ref: 10-F201811