34569-15-8

Basic information

• Product Name: 1H-Benzimidazole,5-chloro-2-ethyl-(9CI)
• Synonyms: 1H-Benzimidazole,5-chloro-2-ethyl-(9CI);1H-BenziMidazole, 6-chloro-2-ethyl-;6-chloro-2-ethyl-1H-Benzimidazole
• CAS NO: 34569-15-8
• Molecular Formula: C₉H₉ClN₂
• Molecular Weight: 180.63416
• Product Categories: BENZIMIDAZOLE
• Mol File: 34569-15-8.mol
• Article Data: 1

Chemical Properties

• Melting Point: 168-170 °C
• Boiling Point: 376.0±15.0 °C(Predicted)
• Appearance: /
• Density: 1.291±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 10.59±0.10(Predicted)
• CAS DataBase Reference: 1H-Benzimidazole,5-chloro-2-ethyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazole,5-chloro-2-ethyl-(9CI)(34569-15-8)
• EPA Substance Registry System: 1H-Benzimidazole,5-chloro-2-ethyl-(9CI)(34569-15-8)

Safety Data

• Hazardous Substances Data: 34569-15-8(Hazardous Substances Data)

Usage

General Description

1H-Benzimidazole, 5-chloro-2-ethyl-(9CI) is a chemical compound with the molecular formula C9H9ClN2. It is an aromatic organic compound that consists of a benzene ring fused to an imidazole ring. This chemical is commonly used in the pharmaceutical industry as a starting material for the synthesis of various types of drugs. It is also known for its potential biological activities and has been studied for its antimicrobial, antiparasitic, and anticancer properties. Additionally, it has been used as a building block in the synthesis of various heterocyclic compounds, making it a versatile and valuable chemical in organic synthesis.

Upstream product

• 71-23-8 propan-1-ol 
• 95-83-0 4-Chloro-1,2-phenylenediamine 

Downstream Products

• 91709-06-7 N-<(2,4-dinitrophenyl)thio>-2-ethyl-5-chlorobenzimidazole 

Relevant articles and documents

Ag-TiO2/clay composite photocatalyst for the oxidation-cyclization of 1,2-diamine compounds with propylene glycol or alcohols

Silver-loaded TiO2 (Ag-TiO2) and acidic clay (K10 montmorillonite) composite photocatalyst has been successfully applied for the light-induced conversion of o-phenylenediamine (OPD) and its derivatives to substituted benzimidazoles with various alcohols in acetonitrile using UV-A and solar light. The influence of the various photocatalysts, solvents, and substituents on the yield and selectivity of the products has been investigated. The mechanism of photocatalysis is proposed. Loading silver on TiO2 enhances product yield and selectivity both in UV and solar light. In the presence of primary alcohols, 2-aminothiophenol forms only disulfide and hence Ag-TiO2/ clay can be used as a green catalyst for the synthesis of disulfides.