1346545-68-3

Basic information

• Product Name: 5-benzyl-5H-pyrido[3,2-b]indole
• Synonyms: 5-benzyl-5H-pyrido[3,2-b]indole
• CAS NO: 1346545-68-3
• Molecular Weight: 258.323
• Mol File: 1346545-68-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-benzyl-5H-pyrido[3,2-b]indole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-benzyl-5H-pyrido[3,2-b]indole(1346545-68-3)
• EPA Substance Registry System: 5-benzyl-5H-pyrido[3,2-b]indole(1346545-68-3)

Safety Data

• Hazardous Substances Data: 1346545-68-3(Hazardous Substances Data)

Upstream product

• 13534-89-9 2,3-dibromopyridine 
• 244205-40-1 (2-bromophenyl)boronic acid 
• 1312012-32-0 3-bromo-2-(2-bromophenyl)pyridine 
• 100-46-9 benzylamine 
• 98-80-6 phenylboronic acid 
• 101601-80-3 3-amino-2-phenylpyridine 
• 134896-35-8 2-phenyl-3-nitropyridine 
• 1360168-61-1 benzo[4,5]pyrido[3,2-b]iodol-5-ium trifluoromethanesulfonate 

Relevant articles and documents

Copper-Catalyzed Synthesis of β- And δ-Carbolines by Double N-Arylation of Primary Amines

Two efficient and practical approaches are reported for the synthesis of β- and δ-carbolines from 3,4-dibromopyridine. The synthesis is based on site-selective Cu-catalyzed double C-N coupling reactions and subsequent annulations by twofold Pd-catalyzed C-N coupling with amines.

First synthesis of benzopyridoiodolium salts and twofold Buchwald-Hartwig amination for the total synthesis of quindoline

The first synthesis of cyclic benzopyridoiodolium salts is described. These hypervalent iodine intermediates are used in an efficient strategy for the construction of the -carboline core. This novel approach involves a twofold palladium-catalyzed Buchwald