14225-75-3

Basic information

• Product Name: 5-CHLORO-2-(2-CHLORO-PHENYL)-1H-BENZOIMIDAZOLE
• Synonyms: 5-CHLORO-2-(2-CHLORO-PHENYL)-1H-BENZOIMIDAZOLE;5-Chloro-2-(2-chlorophenyl)benziMidazole, 95%;5-chloro-2-(2-chlorophenyl)-1H-1,3-benzodiazole
• CAS NO: 14225-75-3
• Molecular Formula: C₁₃H₈Cl₂N₂
• Molecular Weight: 263.12
• Mol File: 14225-75-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 457.3°Cat760mmHg
• Flash Point: 262.8°C
• Appearance: /
• Density: 1.427g/cm³
• Vapor Pressure: 1.5E-08mmHg at 25°C
• Refractive Index: 1.697
• CAS DataBase Reference: 5-CHLORO-2-(2-CHLORO-PHENYL)-1H-BENZOIMIDAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-CHLORO-2-(2-CHLORO-PHENYL)-1H-BENZOIMIDAZOLE(14225-75-3)
• EPA Substance Registry System: 5-CHLORO-2-(2-CHLORO-PHENYL)-1H-BENZOIMIDAZOLE(14225-75-3)

Safety Data

• Hazardous Substances Data: 14225-75-3(Hazardous Substances Data)

Usage

General Description

5-CHLORO-2-(2-CHLORO-PHENYL)-1H-BENZOIMIDAZOLE is a chemical compound with the molecular formula C13H8Cl2N2. It is a benzimidazole derivative with two chlorine atoms and a phenyl group attached to the benzene ring. 5-CHLORO-2-(2-CHLORO-PHENYL)-1H-BENZOIMIDAZOLE has potential applications in the pharmaceutical industry, particularly in the development of drugs for treating various medical conditions. It may also have uses in academic research and chemical synthesis due to its unique structure and properties. Further study and experimentation may reveal additional potential uses for this chemical.

InChI:InChI=1/C13H8Cl2N2/c14-8-5-6-11-12(7-8)17-13(16-11)9-3-1-2-4-10(9)15/h1-7H,(H,16,17)

Upstream product

• 89-98-5 2-chloro-benzaldehyde 
• 95-83-0 4-Chloro-1,2-phenylenediamine 
• 45743-05-3 2-chlorobenzimidamide 
• 1679-18-1 4-Chlorophenylboronic acid 

Relevant articles and documents

Sulfonic acid functionalized covalent organic frameworks as efficient catalyst for the one-pot tandem reactions

A covalent organic framework containing hydroxyl groups (HO-COF) has been predesigned and synthesized by the cyclotrimerization reaction of acetyls, which was used as a pre-established network to introduce propyl sulfonic acid through post-synthetic modification strategy, for the fabrication of SO3H-COF with graphene-like multilayer structure. SO3H-COF was employed as an effective heterogeneous catalyst for the synthesis of benzimidazoles, the synthesis of benzodiazepines and one-pot reductive amination of carbonyl compounds. The results indicated that the developed protocol has several advantages, such as high activity, broad substrate scope, short reaction time and excellent yields. The distinctive structures of SO3H-COF endowed the fantastic catalytic properties, good stability and circulation performance.