1228040-46-7

Basic information

• Product Name: 3-benzyl-7-methyl-2-phenylimidazo[1,2-a]pyridine
• Synonyms: 3-benzyl-7-methyl-2-phenylimidazo[1,2-a]pyridine
• CAS NO: 1228040-46-7
• Molecular Weight: 298.387
• Mol File: 1228040-46-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3-benzyl-7-methyl-2-phenylimidazo[1,2-a]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-benzyl-7-methyl-2-phenylimidazo[1,2-a]pyridine(1228040-46-7)
• EPA Substance Registry System: 3-benzyl-7-methyl-2-phenylimidazo[1,2-a]pyridine(1228040-46-7)

Safety Data

• Hazardous Substances Data: 1228040-46-7(Hazardous Substances Data)

Upstream product

• 5350-40-3 N-benzylidene-N-(4-methylpyridin-2-yl)amine 
• 536-74-3 phenylacetylene 
• 329-89-5 6-aminonicotinic amide 
• 100-52-7 benzaldehyde 
• 695-34-1 2-Amino-4-methylpyridine 

Relevant articles and documents

Magnetic nanostructure-anchored mixed-donor ligand system based on carboxamide and N-heterocyclic thiones: An efficient support of CuI catalyst for synthesis of imidazo[1,2-a]pyridines in eutectic medium

A Cu-incorporated nanocatalyst has been developed by immobilizing copper iodide on a magnetically retrievable mixed-donor ligand system, containing carboxamide, imidazolidine-2-thione and imidazole-2-thione donor groups and characterized by various analys

Exploration of imidazole and imidazopyridine dimers as anticancer agents: Design, synthesis, and structure–activity relationship study

Dimerization of proteins/receptors plays a critical role in various cellular processes, including cell proliferation and differentiation. Therefore, targeting such dimeric proteins/receptors by dimeric small molecules could be a potential therapeutic appr

CuSO4-glucose for in situ generation of controlled Cu(I)-Cu(II) bicatalysts: Multicomponent reaction of heterocyclic azine and aldehyde with alkyne, and cycloisomerization toward synthesis of N-fused imidazoles

The catalytic efficiency of mixed Cu(I)-Cu(II) system in situ generated by partial reduction of CuSO4 with glucose in ethanol (nonanhydrous) under open air has been explored. With this catalysis, the multicomponent cascade reaction of A3-coupling of heterocyclic amidine with aldehyde and alkyne, 5-exo-dig cycloisomerization, and prototropic shift has afforded an efficient and eco-friendly synthesis of therapeutically important versatile N-fused imidazoles. Diverse heterocyclic amidines, several of which are known to be poorly reactive, and aldehydes are compatible in this catalytic process.