838-32-4

Basic information

• Product Name: 2-(4-BROMO-PHENYL)-7-METHYL-IMIDAZO[1,2-A]PYRIDINE
• Synonyms: 2-(4-BROMO-PHENYL)-7-METHYL-IMIDAZO[1,2-A]PYRIDINE
• CAS NO: 838-32-4
• Molecular Formula: C₁₄H₁₁BrN₂
• Molecular Weight: 287.15454
• Mol File: 838-32-4.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-BROMO-PHENYL)-7-METHYL-IMIDAZO[1,2-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-BROMO-PHENYL)-7-METHYL-IMIDAZO[1,2-A]PYRIDINE(838-32-4)
• EPA Substance Registry System: 2-(4-BROMO-PHENYL)-7-METHYL-IMIDAZO[1,2-A]PYRIDINE(838-32-4)

Safety Data

• Hazardous Substances Data: 838-32-4(Hazardous Substances Data)

Usage

Class

Imidazo[1,2-a]pyridine compounds It belongs to a specific group of organic compounds characterized by a pyridine ring fused to an imidazole ring.

Molecular structure

Pyridine ring fused to an imidazole ring The compound's core structure features a five-membered nitrogen-containing pyridine ring connected to a five-membered imidazole ring.

Usage

Building block and intermediate in synthesis It is commonly used as a building block and intermediate in the synthesis of pharmaceuticals, agrochemicals, and other biologically active compounds.

Importance in research

Valuable tool in medicinal chemistry and drug development The unique structure and properties of 2-(4-bromo-phenyl)-7-methyl-imidazo[1,2-a]pyridine make it a valuable tool for researchers in medicinal chemistry and drug development.

Upstream product

• 108-89-4 picoline 
• 99-73-0 para-bromophenacyl bromide 
• 695-34-1 2-Amino-4-methylpyridine 
• 299456-72-7 1-(4-bromophenyl)ethanone O-acetyl oxime 
• 99-90-1 para-bromoacetophenone 
• 59862-55-4 p-bromoacetophenone oxime 
• 13466-41-6 4-methyl-1H-pyridin-2-one 
• 136106-08-6 4-methyl-1-[2-(4-bromophenyl)-2-oxoethyl]pyridinium bromide 

Downstream Products

• 727652-08-6 C₁₅H₁₁BrN₂O 
• 118000-55-8 4-(7-Methyl-imidazo[1,2-a]pyridin-2-yl)-benzaldehyde 
• 365565-90-8 methanesulfonic acid 4-[4-(7-methyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-but-3-ynyl ester 
• 365565-92-0 methanesulfonic acid 4-[4-(7-methyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-butyl ester 

Relevant articles and documents

Solvent and catalyst-free synthesis of imidazo[1,2-a]pyridines by grindstone chemistry

The present work describes the solvent and catalyst-free synthesis of imidazo[1,2-a]pyridines in excellent to nearly quantitative yields from 2-aminopyridines and a wide variety of ω-bromomethylketones using a grindstone procedure at 25°C to 30°C for 3 to

Rapid Construction of Fused Heteropolycyclic Aromatics via Palladium-Catalyzed Domino Arylations of Imidazopyridine Derivatives

By using diaryliodonium salts, a novel approach of a palladium-catalyzed cascade of diarylation/intramolecular dehydrogenative coupling reaction has been developed in the synthesis of phenanthro-imidazopyridine fused heteropolycycles. The method can toler

Synthesis and antimicrobial activity of novel imidazo[1,2-a]pyridinopyrimidine-2,4,6(1H,3H,5H)-triones and thioxopyrimidine-4,6(1H,5H)diones

A novel series of imidazo[1,2-a]pyridinopyrimidine-2,4,6(1H,3H,5H)-triones and thioxopyrimidine-4,6(1H,5H)diones were synthesized via multistep synthesis starting from 2-aminopyridine on cyclisation with phenacyl bromide followed by Vilsmeier-Haack and Kn