Ethyl 5-(4-bromophenyl)-5-oxo-pentanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of an alcohol (ethanol) and a carboxylic acid. This compound features a pentanoate backbone with a ketone functional group at the 5-position and a para-bromophenyl substituent, contributing to its unique chemical properties. The presence of the bromine atom enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. Ethyl 5-(4-bromophenyl)-5-oxo-pentanoate is typically a solid or liquid at room temperature, depending on its specific structure and purity. Its molecular structure suggests potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. Additionally, the compound's reactivity can be attributed to the electrophilic nature of the carbonyl group and the electron-withdrawing effect of the bromine atom, which may facilitate further chemical transformations. Safety and handling precautions should be observed due to the presence of bromine, which can be hazardous.

ethyl 5-(4-bromophenyl)-5-oxo-pentanoate

898792-67-1: Ethyl 5-(4-bromophenyl)-5-oxo-pentanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of an alcohol (ethanol) and a carboxylic acid. This compound features a pentanoate backbone with a ketone functional group at the 5-position and a para-bromophenyl substituent, contributing to its unique chemical properties. The presence of the bromine atom enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. Ethyl 5-(4-bromophenyl)-5-oxo-pentanoate is typically a solid or liquid at room temperature, depending on its specific structure and purity. Its molecular structure suggests potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. Additionally, the compound's reactivity can be attributed to the electrophilic nature of the carbonyl group and the electron-withdrawing effect of the bromine atom, which may facilitate further chemical transformations. Safety and handling precautions should be observed due to the presence of bromine, which can be hazardous.

CAS 898792-67-1

ethyl 5-(4-bromophenyl)-5-oxo-pentanoate

Ethyl 5-(4-bromophenyl)-5-oxovalerate

Ref: 10-F207645