Jain, Kiran published the artcileReaction of 2-mercapto-4-chloro-6-bromobenzimidazole with chloroacetic acid, α-halogenoketones and alkyl bromides, Recommanded Product: 4-Bromo-2-chloro-6-nitroaniline, the main research area is bromochlorobenzimidazolethioacetophenone cyclization regiochem; thiazolobenzimidazolone preparation fungicide bactericide; thiazolobenzimidazole preparation fungicide bactericide; thiazinobenzimidazole preparation fungicide bactericide; fungicide bromochlorothiazolobenzimidazolone bromochlorothiazolobenzimidazole; bactericide bromochlorothiazolobenzimidazolone bromochlorothiazolobenzimidazole; cyclocondensation mercaptochlorobromobenzimidazole dibromoalkane regiochem; cyclization bromochlorobenzimidazolethioacetate regiochemistry.
6-Bromo-8-chlorothiazolo[3,2-a]benzimidazol-3(2H)-one (I), 3-aryl-6-bromo-8-chlorothiazolo[3,2-a]benzimidazoles (II, R = Ph, p-MeC6H4), 2,3-dihydro-6-bromo-8-chloro-thiazolo[3,2-a]benzimidazole (III, n = 2) and 4H-2,3-dihydro-7-bromo-9-chloro[1,3]thiazino[3,2-a]benzimidazole (III, n = 3) were prepared to study the directive influence of Br and Cl on the cyclization of chlorobromobenzimidazoles IV. Cyclization of IV (R1 = CH2CO2H, CH2COPh, CH2COC6H4Me) gave I and II, resp. Similarly, cyclocondensation of IV (R1 = H) with Br(CH2)2Br and Br(CH2)3Br gave III. I, II and III (n = 2) had fungicidal and bactericidal activities at 1:500 dilution
Journal of the Indian Chemical Society published new progress about Cyclization. 34033-41-5 belongs to class bromides-buliding-blocks, name is 4-Bromo-2-chloro-6-nitroaniline, and the molecular formula is C6H4BrClN2O2, Recommanded Product: 4-Bromo-2-chloro-6-nitroaniline.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary