3323-84-0

Upstream product

• 14779-17-0 2-amino-5-methylbenzothiazole 
• 79-04-9 chloroacetyl chloride 
• 621-40-9 (3-methylphenyl)thiourea 

Downstream Products

• 1190213-60-5 2-(4-(3,4-dichlorophenyl)-1,2,3-selenadiazol-5-ylthio)-N-(5-methylbenzo[d]thiazol-2-yl)acetamide 
• 1313371-69-5 4-amino-5-[2-(4-hydroxyphenyl)ethyl]-3-[N-(6-methylbenzothiazole-2-yl)acetamido]thio-4H-1,2,4-triazole 
• 1313371-64-0 4-amino-5-(2-cyclohexylethyl)-3-[N-(6-methylbenzothiazole-2-yl)acetamido]thio-4H-1,2,4-triazole 
• 1352229-00-5 C₂₀H₁₅ClN₄OS₂ 
• 1200398-04-4 2-{[4-(3,4-dichlorophenyl)-1,2,3-thiadiazol-5-yl]sulfanyl}-N-(5-methyl-1,3-benzothiazol-2-yl)acetamide 
• 1188890-74-5 2-(4-(2,4-dibromophenyl)-1,2,3-thiadiazol-5-ylthio)-N-(5-methylbenzo[d]thiazol-2-yl)acetamide 

Relevant academic research and scientific papers

Synthesis of some novel triazole derivatives and investigation of their antimicrobial activities

The aim of this study is to synthesize new triazole derivatives and investigate their antimicrobial activities. 4-Amino-5-(2-cyclohexylethyl)-3-[N- (benzothiazole-2-yl)aceta mido]thio-4H-1,2,4-triazole and 4-amino-5-[2-(4- hydroxyphenyl)ethyl]-3-[N-(benzo

Synthesis of new 2-(substituted benzothiazolylcarbamoyl)benzimidazoles as potential CNS depressants

The synthesis of a series of 2-(substituted benzothiazolylcarbamoyl/benzothiazolylamino-carbamoyl)benzimidazoles 41-60 is reported. Their synthesis has been achieved by chloroacetylating the substituted 2-aminobenzothiazoles and 2-hydrazinobenzothiazoles. The N- chloroacetyl derivatives thus formed have been reacted with o- phenylenediamine in the presence of sulphur to afford the final products. Extension of this sequence of reaction by incorporating certain sulphonamidohydrazines is also described.