1160557-15-2

Basic information

• Product Name: 2-((4-nitrophenoxy)methyl)-5-bromo-1H-benzimidazole
• Synonyms: 2-((4-nitrophenoxy)methyl)-5-bromo-1H-benzimidazole
• CAS NO: 1160557-15-2
• Molecular Weight: 348.156
• Mol File: 1160557-15-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-((4-nitrophenoxy)methyl)-5-bromo-1H-benzimidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-((4-nitrophenoxy)methyl)-5-bromo-1H-benzimidazole(1160557-15-2)
• EPA Substance Registry System: 2-((4-nitrophenoxy)methyl)-5-bromo-1H-benzimidazole(1160557-15-2)

Safety Data

• Hazardous Substances Data: 1160557-15-2(Hazardous Substances Data)

Upstream product

• 1798-11-4 4-nitrophenoxyacetic acid 
• 1575-37-7 4-Bromo-benzene-1,2-diamine 
• 19076-89-2 ethyl 4-nitrophenoxyacetate 
• 100-02-7 4-nitro-phenol 

Downstream Products

• 1452579-70-2 C₂₀H₁₂BrCl₂N₃O₅S 
• 1452579-84-8 C₂₀H₁₂BrCl₂N₃O₅S 
• 1452579-72-4 C₂₀H₁₃BrN₄O₇S 
• 1452579-85-9 C₂₀H₁₃BrN₄O₇S 
• 1452579-74-6 C₂₁H₁₃BrN₄O₅S 
• 1452579-86-0 C₂₁H₁₃BrN₄O₅S 
• 1452579-76-8 C₂₁H₁₅BrFN₃O₅S 
• 1452579-87-1 C₂₁H₁₅BrFN₃O₅S 
• 1452579-78-0 C₂₀H₁₃BrClN₃O₅S 
• 1452579-88-2 C₂₀H₁₃BrClN₃O₅S 
• 1452579-79-1 C₂₂H₁₈BrN₃O₇S 
• 1452579-89-3 C₂₂H₁₈BrN₃O₇S 
• 1452579-80-4 C₂₁H₁₆BrN₃O₅S 
• 1452579-90-6 C₂₁H₁₆BrN₃O₅S 

Relevant articles and documents

Trimethylsilyl chloride catalyzed synthesis of substituted benzimidazoles using two phase system under microwave conditions, and their antimicrobial studies

A convenient method using TMSCl (20 mol%) and microwave-induced technique for the synthesis of various benzimidazole is described. This has reduced the reaction time drastically as well as improved the yield when compared to conventional heating. The synthesized compounds were evaluated for their in vitro antibacterial and antifungal activities against four strains each. Preliminary results indicated that, compounds 3e, 3f, 3g, 3k, 3m, 3n and 3o demonstrated very good antimicrobial activity, comparable to the first line standard drugs. The most effective compounds have exhibited activity at MIC of 6.25 μg/mL.

Tetra butyl ammonium chloride catalyzed synthesis of substituted benzimidazoles under microwave conditions

TBACl (10 mol %) was found to be a useful catalyst for the synthesis of substituted benzimidazoles. The method was proved to be simple, convenient and the product was isolated with good yield.