Ethyl 4-(2,6-difluorophenyl)-4-oxo-butanoate, identified by its CAS number 493004-53-8, is an organic compound characterized by its ester functional group and a distinctive aromatic ring. This compound features a butanoate backbone, which includes a ketone (oxo) group at the 4-position and an ethyl ester group. The presence of the 2,6-difluorophenyl substituent introduces significant electronic and steric effects, influencing its reactivity and potential applications. Typically, compounds of this nature may exhibit biological activity, making them of interest in pharmaceutical research. The fluorine atoms can enhance lipophilicity and metabolic stability, potentially affecting the compound's pharmacokinetics. Ethyl 4-(2,6-difluorophenyl)-4-oxo-butanoate may be synthesized through various organic reactions, including esterification and acylation processes. Its physical properties, such as solubility and boiling point, would depend on the molecular structure and the presence of functional groups. Overall, this compound represents a class of molecules that could be valuable in medicinal chemistry and material science.

ethyl 4-(2,6-difluorophenyl)-4-oxo-butanoate

493004-53-8: Ethyl 4-(2,6-difluorophenyl)-4-oxo-butanoate, identified by its CAS number 493004-53-8, is an organic compound characterized by its ester functional group and a distinctive aromatic ring. This compound features a butanoate backbone, which includes a ketone (oxo) group at the 4-position and an ethyl ester group. The presence of the 2,6-difluorophenyl substituent introduces significant electronic and steric effects, influencing its reactivity and potential applications. Typically, compounds of this nature may exhibit biological activity, making them of interest in pharmaceutical research. The fluorine atoms can enhance lipophilicity and metabolic stability, potentially affecting the compound's pharmacokinetics. Ethyl 4-(2,6-difluorophenyl)-4-oxo-butanoate may be synthesized through various organic reactions, including esterification and acylation processes. Its physical properties, such as solubility and boiling point, would depend on the molecular structure and the presence of functional groups. Overall, this compound represents a class of molecules that could be valuable in medicinal chemistry and material science.

CAS 493004-53-8

ethyl 4-(2,6-difluorophenyl)-4-oxo-butanoate

Ethyl 4-(2,6-difluorophenyl)-4-oxobutyrate

Ref: 10-F207798