On June 30, 2011, Hatano, Akihiko; Okada, Munehiro; Shimazaki, Kei; Uehara, Sanae; Ishikawa, Yuta; Matsumoto, Arata; Fujita, Yudai; Nishimura, Makoto published an article.COA of Formula: C13H11BrS The title of the article was Inhibitory effects on microbial growth using the derivatives of benzyl phenyl sulfide. And the article contained the following:
We investigated the antimicrobial activities of twelve derivatives of benzyl Ph sulfide by using Min. Inhibitory Concentration (MIC) and Min. Bactericidal Concentration (MBC) values against 10 microbial strains. These derivatives of benzyl Ph sulfides were synthesized by means of the nucleophilic coupling reaction at our laboratory MIC testing revealed that all synthetic derivatives of benzyl and 4-methoxybenzyl Ph sulfides had no effect against the tested microbial strains. However, the compounds of 4-nitrobenzyl Ph sulfide showed antimicrobial activity against many of the tested strains. Above all, 4-nitrobenzyl 4-chlorophenyl sulfide 11 exhibited the strongest and widest ranging inhibitory effects among the twelve synthetic compounds We researched the antimicrobial activities of the coupling materials of sulfide. As a result, it was considered important for the expression of antimicrobial activities that the sulfide had a 4-nitrobenzyl group and 4-chlorophenyl group in the same mol. as in the case of benzyl Ph sulfide. The experimental process involved the reaction of Benzyl(4-bromophenyl)sulfane(cas: 53136-21-3).COA of Formula: C13H11BrS
The Article related to benzyl phenyl sulfide growth inhibition, Microbial, Algal, and Fungal Biochemistry: Antimicrobial Sensitivity and other aspects.COA of Formula: C13H11BrS
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