COA of Formula: C6H5BrO2On May 25, 2019, Sattar, Omar D. Abdul; Shneshil, Mustafa K.; Mohammed, Mustafa K.; Dheyab, Hiba B.; Alwan, Osama K.; Hussein, Suaad A.; Mahmood, Maha A. published an article in Journal of Physics: Conference Series. The article was 《Synthesis and anti-bacterial activity of some azo compounds》. The article mentions the following:
Some azo compounds were prepared as I (R = 4-hydroxyphenyl, 3-chloro-4-hydroxyphenyl, 4-hydroxy-2-nitrophenyl, etc.) by the reaction of 4-amino benzamide with benzoyl chloride forming N-benzoyl-4-amino benzamide, the later was diazotized to give N-benzoyl-4-((substituted phenyl)diazenyl)benzamide I. The azo derivatives I were tested for their antibacterial activity against (S. aureus, S. epidermidis, E. coli and P. aeruginosa) by using disk diffusion method. The min. inhibitory concentrations (MICs) of the compounds also calculated by agar streak dilution method. In the experiment, the researchers used many compounds, for example, 2-Bromobenzene-1,4-diol(cas: 583-69-7COA of Formula: C6H5BrO2)
2-Bromobenzene-1,4-diol(cas: 583-69-7) belongs to organobromine compounds.The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.COA of Formula: C6H5BrO2
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary