1417819-12-5

Basic information

• Product Name: 2-chloro-6-phenylbenzo[4,5]imidazo[2,1-a]isoquinoline
• Synonyms: 2-chloro-6-phenylbenzo[4,5]imidazo[2,1-a]isoquinoline
• CAS NO: 1417819-12-5
• Molecular Weight: 328.801
• Mol File: 1417819-12-5.mol

Chemical Properties

• CAS DataBase Reference: 2-chloro-6-phenylbenzo[4,5]imidazo[2,1-a]isoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-6-phenylbenzo[4,5]imidazo[2,1-a]isoquinoline(1417819-12-5)
• EPA Substance Registry System: 2-chloro-6-phenylbenzo[4,5]imidazo[2,1-a]isoquinoline(1417819-12-5)

Safety Data

• Hazardous Substances Data: 1417819-12-5(Hazardous Substances Data)

Upstream product

• 615-43-0 2-iodophenylamine 
• 57381-37-0 2-bromo-5-chloro-benzonitrile 
• 174265-12-4 2-bromo-5-chlorobenzaldehyde 
• 120-46-7 1,3-diphenylpropanedione 
• 14225-85-5 2-(2-bromo-5-chloro-phenyl)-1H-benzoimidazole 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 22868-35-5 2-(3-chloro-phenyl)-1H-benzoimidazole 

Relevant articles and documents

An efficient synthesis of 6-arylbenzo[4,5]imidazo[2,1-a] isoquinolines via sequential α-arylation of carbonyl and deacylation catalyzed by CuI

Dibenzoyl methane was found to undergo α-arylation of carbonyl and deacylation reaction with 2-(2-bromophenyl)-1H-benzo[d]imidazoles catalyzed by CuI in the presence of Cs2CO3, and provided an efficient synthesis of 6-arylbenzo[4,5]i

Selective synthesis of benzo[4,5]imidazo[2,1-a]isoquinolines via copper-catalyzed tandem annulation of alkynylbenzonitriles with 2-Iodoanilines

An efficient copper-catalyzed cascade cyclization reaction for selectively synthesizing a variety of benzo[4,5]imidazo[2,1-a]isoquinoline derivatives has been developed. The reaction features the formation of three different C–N bonds in sequence. In the

Nucleophilic addition of benzimidazoles to alkynyl bromides/palladium- catalyzed intramolecular C-H vinylation: Synthesis of benzo[4,5]imidazo[2,1-a] isoquinolines

An efficient "one-pot" route for the synthesis of benzo[4,5]imidazo[2,1-a] isoquinolines has been developed via nucleophilic addition of 2-aryl benzimidazoles to alkynyl bromides and subsequent palladium-catalyzed intramolecular C-H vinylation.