1621431-71-7

Basic information

• Product Name: 6-phenylpyrido[2′,1′:2,3]imidazo[4,5-c]quinoline
• Synonyms: 6-phenylpyrido[2′,1′:2,3]imidazo[4,5-c]quinoline
• CAS NO: 1621431-71-7
• Molecular Weight: 295.343
• Mol File: 1621431-71-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 6-phenylpyrido[2′,1′:2,3]imidazo[4,5-c]quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenylpyrido[2′,1′:2,3]imidazo[4,5-c]quinoline(1621431-71-7)
• EPA Substance Registry System: 6-phenylpyrido[2′,1′:2,3]imidazo[4,5-c]quinoline(1621431-71-7)

Safety Data

• Hazardous Substances Data: 1621431-71-7(Hazardous Substances Data)

Upstream product

• 103-82-2 phenylacetic acid 
• 6851-99-6 2-bromo-1-(2-nitrophenyl)ethanone 
• 538-86-3 benzyl methyl ether 
• 98-86-2 acetophenone 
• 451-40-1 phenyl benzyl ketone 
• 93-55-0 1-phenyl-propan-1-one 
• 115769-03-4 2-(2-bromophenyl)imidazo[1,2-α]pyridine 
• 49851-55-0 2,2'-dibromoacetophenone 
• 552-89-6 2-nitro-benzaldehyde 
• 126267-63-8 2-(2-nitro-phenyl)-imidazo[1,2-a]pyridine 
• 253684-24-1 1-(2,2-dibromovinyl)-2-nitrobenzene 
• 504-29-0 2-aminopyridine 

Relevant articles and documents

An Approach to Quinoline-Fused Imidazopyridines via CDC of Ethers with Imidazopyridines under Metal-Free Conditions

An NH4I-catalyzed cross-dehydrogenative coupling (CDC) reaction of ethers with imidazopyridine cascade cyclization under transition-metal-free conditions has been developed. Cheap, commercially available ethers were used as both reagents and solvents, and green aqueous H2O2 was used as an oxidizing agent. A series of substituents on 2-(2-aminoaryl) imidazo[1,2-a]pyridines were tolerated, and the reaction gave quinoline-fused imidazopyridines in moderate to good yields.

An expeditious microwave assisted one-pot sequential route to pyrido fused imidazo[4,5-c] quinolines in green media

An expeditious microwave assisted one-pot sequential route to synthesize pyrido fused imidazo[4,5-c]quinolinesviathe Pictet-Spengler cyclization strategy has been developed. In this study, substituted 2-amino pyridines are condensed with 2-bromo-2′-nitroa

One-pot sequential reactions featuring a copper-catalyzed amination leading to pyrido[2′,1′:2,3]imidazo[4,5-c]quinolines and dihydropyrido[2′,1′:2,3]imidazo[4,5-c]quinolines

Tetracyclic skeletons combining an imidazo[1,2-a]pyridine moiety with a quinoline framework such as pyrido[2′,1′:2,3]imidazo[4,5-b]quinoline are stimulating increasing interests since they are close isosteres of a series of powerful antiproliferative comp