5268-73-5

Upstream product

• 1220704-77-7 2-(decylthio)-4-methyl-3-(2-(3-p-tolylureido)phenyl)thiazol-3-ium iodide 
• 1220704-76-6 2-(decylthio)-4-methyl-3-(2-(3-phenylureido)phenyl)thiazol-3-ium iodide 
• 1220704-74-4 3-(2-(3-(3,5-bis(trifluoromethyl)benzyl)ureido)phenyl)-2-(ethylthio)-4-methylthiazol-3-ium iodide 
• 1220704-73-3 2-(ethylthio)-4-methyl-3-(2-(3-p-tolylureido)phenyl)thiazol-3-ium iodide 
• 1220704-72-2 2-(ethylthio)-4-methyl-3-(2-(3-phenylureido)phenyl)thiazol-3-ium iodide 
• 1220704-71-1 3-(2-(3-(3,5-bis(trifluoromethyl)benzyl)ureido)phenyl)-4-methyl-2-(methylthio)thiazol-3-ium iodide 
• 1220704-70-0 4-methyl-2-(methylthio)-3-(2-(3-(4-nitrophenyl)ureido)-phenyl)thiazol-3-ium iodide 
• 1220704-69-7 3-(2-(3-(3,5-bis(trifluoromethyl)phenyl)ureido)phenyl)-4-methyl-2-(methylthio)thiazol-3-ium iodide 
• 1220704-68-6 4-methyl-2-(methylthio)-3-(2-(3-p-tolylureido)phenyl)thiazol-3-ium iodide 
• 1220704-67-5 4-methyl-2-(methylthio)-3-(2-(3-phenylureido)phenyl)thiazol-3-iumiodide 

Downstream Products

• 170942-54-8 2-(1,2-propadienylthio)benzimidazole 
• 1226710-94-6 1-[3,5-bis(trifluoromethyl)benzyl]-3-[(1Z)-1-(methylsulfanyl)prop-1-en-2-yl]-1,3-dihydro-2H-benzimidazol-2-one 
• 1226710-89-9 1-[(1Z)-1-(benzylsulfanyl)prop-1-en-2-yl]-3-methyl-1,3-dihydro-2H-benzimidazol-2-one 
• 1226710-91-3 1-benzyl-3-[(1Z)-1-(benzylsulfanyl)prop-1-en-2-yl]-1,3-dihydro-2H-benzimidazol-2-one 
• 1226710-92-4 1-benzyl-3-[(1E)-1-(benzylsulfanyl)prop-1-en-2-yl]-1,3-dihydro-2H-benzimidazol-2-one 
• 1226710-96-8 1-[(1Z)-1-(methylsulfanyl)prop-1-en-2-yl]-3-(4-nitrobenzyl)-1,3-dihydro-2H-benzimidazol-2-one 
• 1226711-02-9 3-methyl-9-(4-nitrobenzyl)[1,3]thiazolo[3,2-a]benzimidazol-9-ium chloride 
• 134579-99-0 3,9-dimethylthiazolo<3,2-a>benzimidazolium iodide 
• 1226711-00-7 9-[3,5-bis(trifluoromethyl)benzyl]-3-methyl[1,3]thiazolo[3,2-a]benzimidazol-9-ium chloride 
• 55114-86-8 9-benzyl-3-methyl[1,3]thiazolo[3,2-a]benzimidazol-9-ium chloride 
• 782438-61-3 C₁₇H₁₈N₂OS 
• 5268-74-6 3-Methyl-thiazolo<3,2-a>benzimidazol-2-carbonsaeure 

Relevant academic research and scientific papers

Metathetic sulfur transfer mediated by N-(2-aminophenyl)-4-methyl-thiazolin-2-thione derivatives: a route to diversely substituted S-alkylcarbamothioates

A new route to S-alkylcarbamothioates is disclosed. In a first step, N-(2-aminophenyl)-4-methyl-thiazolin-2-thione is transformed into a mono- or disubstituted urea at nitrogen, and then in a second step, alkylated at sulfur. The resulting salts, after treatment with a base, gave S-alkylcarbamothioates in high isolated yields together with 3-methyl[1,3]thiazolo[3,2-a]benzimidazole under very mild conditions.

Reaction of 2-alkenylthiobenzimidazoles with iodine

The reaction of 2-allylthiobenzimidazole and 2-allylthio-1-methylbenzimidazole with iodine leads to the formation of dihydrothiazolo[3,2-a]benzimidazolium systems. 1998 Plenum Publishing Corporation.