419557-33-8

Basic information

• Product Name: 2-(3-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE
• Synonyms: 2-(3-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE;2-(3-Bromo-phenyl)-imidazo[1,2-a]pyridine >98%;2-(3-broMophenyl)IMidazo[1,2-ɑ]Pyridine;2-(3-bromophenyl)Imidazo91,2-ɑ)Pyridine
• CAS NO: 419557-33-8
• Molecular Formula: C13H9BrN2
• Molecular Weight: 273.13
• Mol File: 419557-33-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-(3-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE(419557-33-8)
• EPA Substance Registry System: 2-(3-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE(419557-33-8)

Safety Data

• Hazardous Substances Data: 419557-33-8(Hazardous Substances Data)

Usage

General Description

2-(3-Bromo-phenyl)-imidazo[1,2-a]pyridine is a chemical compound with the molecular formula C11H7BrN2. It is a heterocyclic aromatic compound that contains both imidazole and pyridine rings. Its structure consists of a bromine-substituted phenyl group attached to an imidazo-pyridine core. 2-(3-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE has been studied for its potential use in pharmaceutical applications, particularly in the development of new drugs. Its unique structure and properties make it a promising candidate for further research in medicinal chemistry and drug discovery.

Upstream product

• 24280-05-5 N-[1-(3-bromophenyl)ethylidene]hydroxyl amine 
• 274-76-0 imidazo[1,2-a]pyridine 

Downstream Products

• 881040-26-2 2-(3-bromophenyl)imidazo[1,2-a]pyridine-3-carbaldehyde 
• 1450625-63-4 ethyl 2-(3-bromophenyl)imidazo[1,2-a]pyridine-3-carboxylate 

Relevant articles and documents

CuCl2-catalyzed N[sbnd]O bond cleavage of oxime esters: Approach to imidazoheterocycles and furo[3,2-c]chromenyl fused imidazoles

An articulate approach to a diverse set of imidazoheterocycles in good to high yields via a copper-catalyzed aza-annulation of several oxime esters with a group of 2-amino-azaarenes was developed. The above cyclization reaction probably proceeds via a single electron transfer process which embodies a new technique for creating two new C[sbnd]N bonds for imidazole ring synthesis. Gratifyingly, the implementation of this chemistry could be further stretched to the synthesis of a novel class of fused imidazoles bearing a furo[3,2-c]chromene moiety via a sequential C[sbnd]N bond formation, followed by C(sp2)-H functionalization/5-endo-dig-oxacyclization (C[sbnd]C and C[sbnd]O bonds) of in situ produced fused imidazoles with cyclic enynones in the presence of copper(II) as a π-electrophilic Lewis acid catalyst.

IMIDAZOPYRIDINE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT ELEMENTS CONTAINING SAME

An imidazopyridine derivative shown by the following formula (1).