96464-10-7

Basic information

• Product Name: 2-(4-BROMOPHENYL)-6-CHLOROIMIDAZO[1,2-A]PYRIDINE
• Synonyms: 2-(4-BROMOPHENYL)-6-CHLOROIMIDAZO[1,2-A]PYRIDINE;BUTTPARK 14\02-79
• CAS NO: 96464-10-7
• Molecular Formula: C₁₃H₈BrClN₂
• Molecular Weight: 307.57
• Mol File: 96464-10-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-BROMOPHENYL)-6-CHLOROIMIDAZO[1,2-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-BROMOPHENYL)-6-CHLOROIMIDAZO[1,2-A]PYRIDINE(96464-10-7)
• EPA Substance Registry System: 2-(4-BROMOPHENYL)-6-CHLOROIMIDAZO[1,2-A]PYRIDINE(96464-10-7)

Safety Data

• Hazardous Substances Data: 96464-10-7(Hazardous Substances Data)

Usage

General Description

2-(4-Bromophenyl)-6-chloroimidazo[1,2-a]pyridine is a chemical compound that belongs to the class of imidazo[1,2-a]pyridines, which are known for their diverse biological activities. It is a heterocyclic compound containing a bromophenyl and a chloro group, which are both substituted on the imidazo[1,2-a]pyridine ring. 2-(4-BROMOPHENYL)-6-CHLOROIMIDAZO[1,2-A]PYRIDINE has demonstrated potential pharmaceutical properties such as anti-inflammatory, antiviral, and antitumor activities. It has also been studied for its potential use in the development of new drugs for various therapeutic applications. Additionally, it could potentially serve as a valuable building block in the synthesis of new chemical entities for medicinal chemistry research.

Upstream product

• 1072-98-6 5-chloro-2-pyridylamine 
• 99-73-0 para-bromophenacyl bromide 

Downstream Products

• 118000-65-0 4-(6-Chloro-imidazo[1,2-a]pyridin-2-yl)-benzaldehyde 
• 118000-64-9 4-(6-Chloro-imidazo[1,2-a]pyridin-2-yl)-benzonitrile 

Relevant articles and documents

Reduced Phenalenyl in Catalytic Dehalogenative Deuteration and Hydrodehalogenation of Aryl Halides

Dehalogenative deuteration reactions are generally performed through metal-mediated processes. This report demonstrates a mild protocol for hydrodehalogenation and dehalogenative deuteration of aryl/heteroaryl halides (39 examples) using a reduced odd alternant hydrocarbon phenalenyl under transition metal-free conditions and has been employed successfully for the incorporation of deuterium in various biologically active compounds. The combined approach of experimental and theoretical studies revealed a single electron transfer-based mechanism.

Synthesis of bridgehead nitrogen heterocycles on a solid surface

Bridgehead nitrogen heterocycles were synthesized from heteroaromatic amidines and cyclic or acyclic α-bromoketones under solvent-free conditions at room temperature on a solid surface in excellent yields, which are higher than those obtained with hithert