(3-BROMOPHENYL)ACETIC ACID METHYL ESTER CAS:150529-73-0

(3-Bromophenyl)acetic acid methyl ester (C10H11BrO2) is a notable compound in the realm of organic chemistry, characterized by a brominated benzene ring connected to an acetic acid moiety via an ester functional group. This structural arrangement allows for a variety of chemical reactions that can be exploited for both synthetic applications and biological investigations. One of the primary uses of (3-bromophenyl)acetic acid methyl ester lies in its role as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals. The bromine atom on the aromatic ring significantly influences the reactivity of the compound, allowing it to participate in electrophilic substitution reactions. This characteristic makes it possible to introduce additional functional groups that can enhance the biological activity or improve the pharmacokinetic profiles of the resulting compounds. Moreover, the ester functionality of (3-bromophenyl)acetic acid methyl ester facilitates hydrolysis reactions, leading to the formation of the corresponding carboxylic acid or alcohol, which can further be utilized in diverse synthetic pathways. This versatility enables chemists to design tailored compounds for specific applications, thereby expanding its utility in the development of new drugs or agrochemicals. In addition to its synthetic applications, there is growing interest in the biological activities of (3-bromophenyl)acetic acid methyl ester and its derivatives. Compounds containing brominated phenyl rings have been shown to exhibit antimicrobial, anti-inflammatory, and antitumor properties. Such findings underscore the compound's potential as a starting point for drug discovery efforts aimed at identifying novel therapeutics. Furthermore, the methyl ester form enhances solubility in organic solvents, which is advantageous for conducting chemical reactions and biological assays. Ongoing research into (3-bromophenyl)acetic acid methyl ester may reveal additional insights into its pharmacological effects and broaden its applications across various fields, including medicinal chemistry and materials science. In summary, (3-bromophenyl)acetic acid methyl ester serves as an important building block in synthetic chemistry, with promising applications in drug development and agrochemical synthesis. Its distinctive structure, along with the potential for further modifications, positions it as a valuable compound for continued exploration and innovation in chemical research.