Benzenepropanoic acid, α-fluoro-4-methyl-β-oxo-, methyl ester, identified by CAS number 76435-48-8, is an organic compound characterized by its aromatic structure and functional groups. This compound features a benzene ring attached to a propanoic acid moiety, which is further substituted with a fluoro group and a methyl group, contributing to its unique chemical properties. The presence of the α-fluoro substituent can influence the compound's reactivity and biological activity, often enhancing its lipophilicity and altering its interaction with biological targets. The methyl ester functional group indicates that it can undergo hydrolysis to yield the corresponding acid, which may have implications in various chemical reactions and applications. This compound may be of interest in pharmaceutical research and development due to its potential biological activity, as well as in synthetic organic chemistry for the development of more complex molecules. As with many fluorinated compounds, it may exhibit distinct physical and chemical properties, such as increased stability and altered solubility compared to non-fluorinated analogs.

Benzenepropanoic acid, a-fluoro-4-methyl-b-oxo-, methyl ester

76435-48-8: Benzenepropanoic acid, α-fluoro-4-methyl-β-oxo-, methyl ester, identified by CAS number 76435-48-8, is an organic compound characterized by its aromatic structure and functional groups. This compound features a benzene ring attached to a propanoic acid moiety, which is further substituted with a fluoro group and a methyl group, contributing to its unique chemical properties. The presence of the α-fluoro substituent can influence the compound's reactivity and biological activity, often enhancing its lipophilicity and altering its interaction with biological targets. The methyl ester functional group indicates that it can undergo hydrolysis to yield the corresponding acid, which may have implications in various chemical reactions and applications. This compound may be of interest in pharmaceutical research and development due to its potential biological activity, as well as in synthetic organic chemistry for the development of more complex molecules. As with many fluorinated compounds, it may exhibit distinct physical and chemical properties, such as increased stability and altered solubility compared to non-fluorinated analogs.

CAS 76435-48-8

Benzenepropanoic acid, a-fluoro-4-methyl-b-oxo-, methyl ester