Vega, A. et al. published their research in Anales de Quimica (1968-1979) in 1977 | CAS: 6515-58-8

3-(Bromomethyl)benzoic acid (cas: 6515-58-8) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.Synthetic Route of C8H7BrO2

Synthesis, resolution, and characterization of the E and Z oximes of m-benzoylphenylacetic acid was written by Vega, A.;Prieto, J.;Moragues, J.. And the article was included in Anales de Quimica (1968-1979) in 1977.Synthetic Route of C8H7BrO2 This article mentions the following:

Oximation of m-PhCOC6H4CH2CO2H with H2NOH.HCl in pyridine and recrystallization from absolute EtOH gave (E)- and (Z)-m-PhC(:NOH)C6H4CH2CO2H. Beckmann rearrangement of the resp. oximes gave m-PhNHCOC6H4CH2CO2H and m-PhCONHC6N4CH2CO2H, which were also prepared from m-MeC6H4CO2H or m-O2NC6H4CO2H. In the experiment, the researchers used many compounds, for example, 3-(Bromomethyl)benzoic acid (cas: 6515-58-8Synthetic Route of C8H7BrO2).

3-(Bromomethyl)benzoic acid (cas: 6515-58-8) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. In the pharmaceutical industry organo bromine derivatives are used as sedatives, vasodilators, antiseptic agents, and anticancer agents.Synthetic Route of C8H7BrO2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary