30065-40-8

Basic information

• Product Name: (1H-benzimidazol-2-ylsulfanyl)acetic acid (4-methoxybenzylidene)hydrazide
• Synonyms: (1H-benzimidazol-2-ylsulfanyl)acetic acid (4-methoxybenzylidene)hydrazide
• CAS NO: 30065-40-8
• Molecular Weight: 340.406
• Mol File: 30065-40-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1H-benzimidazol-2-ylsulfanyl)acetic acid (4-methoxybenzylidene)hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: (1H-benzimidazol-2-ylsulfanyl)acetic acid (4-methoxybenzylidene)hydrazide(30065-40-8)
• EPA Substance Registry System: (1H-benzimidazol-2-ylsulfanyl)acetic acid (4-methoxybenzylidene)hydrazide(30065-40-8)

Safety Data

• Hazardous Substances Data: 30065-40-8(Hazardous Substances Data)

Upstream product

• 30065-27-1 2-((1H-benzo[d]imidazole-2-yl)thio)acetohydrazide 
• 123-11-5 4-methoxy-benzaldehyde 
• 5429-62-9 ethyl 2-(1H-benzo[d]imidazol-2-ylthio)acetate 
• 134469-07-1 Benzimidazol-2-thiol 
• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 915159-39-6 C₁₉H₁₈N₄O₃S₂ 

Relevant articles and documents

Synthesis of 2-mercaptobenzimidazole derivatives as potential anti-microbial and cytotoxic agents

A series of novel 2-(1H-benzimidazol-2-ylsulfanyl)-N-(4-oxo-2-phenyl- thiazolidin-3yl)-acetamide 5a-j have been synthesized from various aldehydes and 2-(5-phenyl-[1,3,4]-oxadiazol-2-ylmethylsulfanyl)-1H-benzimidazole 6a-j from various benzoic acids. Thes

Green route for the heterocyclization of 2-mercaptobenzimidazole into β-lactum segment derivatives containing -CONH- bridge with benzimidazole: Screening in vitro antimicrobial activity with various microorganisms

The efficient and rapid synthesis of novel azetidin-2-ones 4a-j has been established. Thus, both microwave and conventional condensation 2-{(1H-benzimidazol)-ylthio}-N′-2-(substituted phenyl) hydrazide with chloroacetylchloride were carried out in DMF-ben