1450725-08-2

Basic information

• Product Name: 3-bromo-2-(2-bromophenyl)imidazo[1,2-a]pyridine
• Synonyms: 3-bromo-2-(2-bromophenyl)imidazo[1,2-a]pyridine
• CAS NO: 1450725-08-2
• Molecular Weight: 352.028
• Mol File: 1450725-08-2.mol

Chemical Properties

• CAS DataBase Reference: 3-bromo-2-(2-bromophenyl)imidazo[1,2-a]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-2-(2-bromophenyl)imidazo[1,2-a]pyridine(1450725-08-2)
• EPA Substance Registry System: 3-bromo-2-(2-bromophenyl)imidazo[1,2-a]pyridine(1450725-08-2)

Safety Data

• Hazardous Substances Data: 1450725-08-2(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 49851-55-0 2,2'-dibromoacetophenone 
• 115769-03-4 2-(2-bromophenyl)imidazo[1,2-α]pyridine 
• 2142-69-0 2-bromophenyl methyl ketone 

Downstream Products

• 1450725-06-0 1-(m-tolyl)pyrido[2′,1′:2,3]imidazo[4,5-c][1,2,3]triazolo[1,5-a]-quinoline 
• 1450724-98-7 1-(4-fluorophenyl)pyrido[2′,1′:2,3]imidazo[4,5-c][1,2,3]triazolo-[1,5-a]quinoline 
• 1450724-97-6 C₂₅H₂₁N₅ 
• 1450724-96-5 C₂₆H₂₃N₅ 
• 1450724-95-4 C₂₅H₂₁N₅ 
• 1450724-93-2 1-(4-methoxyphenyl)pyrido[2′,1′:2,3]imidazo[4,5-c][1,2,3]-triazolo[1,5-a]quinoline 
• 1450724-92-1 phenylpyrido[2′,1′:2,3]imidazo[4,5-c][1,2,3]triazolo[1,5-a]quinoline 
• 1450725-15-1 3-bromo-2-(2-(4-phenyl-1H-1,2,3-triazol-1-yl)phenyl)imidazo[1,2-a]-pyridine 

Relevant articles and documents

Chemodivergent synthesis of: N -(pyridin-2-yl)amides and 3-bromoimidazo[1,2- a] pyridines from α-bromoketones and 2-aminopyridines

N-(Pyridin-2-yl)amides and 3-bromoimidazo[1,2-a]pyridines were synthesized respectively from α-bromoketones and 2-aminopyridine under different reaction conditions. N-(Pyridin-2-yl)amides were formed in toluene via C-C bond cleavage promoted by I2/s

Synthesis of 5-Aryl-5H-pyrido[2',1':2,3]imidazo[4,5-b]indoles by Domino Pd- and Cu-Catalyzed C-N Coupling Reactions

A series of 5-aryl-5H-pyrido[2',1':2,3]imidazo[4,5- b ]indoles was successfully prepared in good yields by a practical four-step strategy. In this procedure, the key step was demonstrated to be the domino Pd-and Cu-catalyzed C-N coupling reactions of 3-br

Copper-catalyzed tandem azide-alkyne cycloaddition, Ullmann type C-N coupling, and intramolecular direct arylation

A ligand-free copper-catalyzed tandem azide-alkyne cycloaddition (CuAAC), Ullmann-type C-N coupling, and intramolecular direct arylation has been described. The designed strategy resulted in the synthesis of a novel trazole-fused azaheterocycle framework.