882187-78-2

Basic information

• Product Name: 7-methyl-3-phenylimidazo[1,2-α]pyridine
• Synonyms: 7-methyl-3-phenylimidazo[1,2-α]pyridine
• CAS NO: 882187-78-2
• Molecular Weight: 208.263
• Mol File: 882187-78-2.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 7-methyl-3-phenylimidazo[1,2-α]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 7-methyl-3-phenylimidazo[1,2-α]pyridine(882187-78-2)
• EPA Substance Registry System: 7-methyl-3-phenylimidazo[1,2-α]pyridine(882187-78-2)

Safety Data

• Hazardous Substances Data: 882187-78-2(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 874-39-5 7-Methyl-imidazo[1,2-a]pyridine 
• 6635-33-2 7-methyltetrazolo[1,5-a]pyridine 
• 536-74-3 phenylacetylene 
• 4926-28-7 2-Bromo-4-picoline 
• 695-34-1 2-Amino-4-methylpyridine 
• 5153-67-3 nitrostyrene 
• 108-90-7 chlorobenzene 
• 122-78-1 phenylacetaldehyde 
• 98-80-6 phenylboronic acid 
• 71-43-2 benzene 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 7436-90-0 2,2-dibromostyrene 

Downstream Products

• 65964-65-0 7-methyl-2,3-dibenzimidazo[1,2-α]pyridine 

Relevant articles and documents

Cobalt-Catalyzed Direct Arylation of Imidazo[1,2-a]pyridine with Aryl Iodides

The Co(II)Cl2·6H2O catalyzed C–H activation/direct arylation of imidazo[1,2-a]pyridine with aryl/heteroaryl iodide is reported. The cost effective, ligand and additive free protocol using KOAc successfully afforded 3-arylimidazo[1,2-

Metal-free, base catalyzed oxidative amination and denitration reaction: Regioselective synthesis of 3-arylimidazo[1,2-a]pyridines

A metal-free, regioselective strategy for the synthesis of 3-arylimidazo[1,2-a]pyridines from β-nitrostyrenes and 2-aminopyridines using triethylamine as the catalyst and H2O2 (30% aq.) as the oxidant is reported. The use of an inexp

Switching of Regioselectivity in a Perfluorohexyl Iodide Mediated Synthesis of Phenylimidazo[1,2-a]pyridines

3-Phenylimidazo[1,2-a]pyridines were synthesized through the perfluorohexyl iodide mediated coupling of 2-aminopyridines and phenylacetylenes. In situ iodination of the terminal alkyne by perfluorohexyl iodide reverses the polarity by generating a transient electrophilic iodoalkyne, and this alters the regioselectivity of the phenyl group. The reaction then proceeds by tandem electrophilic alkynylation and cyclization to form the fused-ring product. The protocol affords the 3-phenyl isomer with full regioselectivity and is complementary to reported methodologies for the synthesis of the 2-phenyl isomer starting from the same substrates.