1303503-69-6

Basic information

• Product Name: 5-phenyl-5H-pyrido[4,3-b]indole
• Synonyms: 5-phenyl-5H-pyrido[4,3-b]indole
• CAS NO: 1303503-69-6
• Molecular Weight: 244.296
• Mol File: 1303503-69-6.mol

Chemical Properties

• CAS DataBase Reference: 5-phenyl-5H-pyrido[4,3-b]indole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-phenyl-5H-pyrido[4,3-b]indole(1303503-69-6)
• EPA Substance Registry System: 5-phenyl-5H-pyrido[4,3-b]indole(1303503-69-6)

Safety Data

• Hazardous Substances Data: 1303503-69-6(Hazardous Substances Data)

Upstream product

• 13534-90-2 dibromo-3,4 pyridine 
• 62-53-3 aniline 
• 239137-42-9 3-bromo-N-phenylpyridin-4-amine 
• 244205-40-1 (2-bromophenyl)boronic acid 
• 244-69-9 γ-carboline 
• 591-50-4 iodobenzene 

Downstream Products

• 1303503-70-9 8-bromo-5-phenyl-5H-pyrido[4,3-b]indole 
• 1303503-83-4 8-[9,10-di(naphthalen-2-yl)-anthracen-2-yl)-1,5-diphenyl-5H-pyrido[4,3-b]indole 
• 1303503-73-2 8-[9,10-di(naphthalen-2-yl)-anthracen-2-yl]-5-phenyl-5H-pyrido[4,3-b]indole 
• 1303503-72-1 8-(9,10-diphenylanthracen-2-yl)-5-phenyl-5H-pyrido[4,3-b]indole 

Relevant articles and documents

Efficient access to β- and γ-carbolines from a common starting material by sequential site-selective Pd-catalyzed C–C, C–N coupling reactions

Two efficient and practical approaches are reported for the synthesis of β- and γ-carboline derivatives from 3,4-dibromopyridine as a common starting material. The β-carbolines were prepared by site-selective Pd-catalyzed C–C coupling with o-bromophenylboronic acid and subsequent cyclization by double C–N coupling with amines. γ-Carbolines were prepared from the same starting material by C–N coupling with anilines and subsequent annulation by domino C–C/C–N coupling with o-bromophenylboronic acid.

COMPOUND HAVING A SUBSTITUTED ANTHRACENE RING STRUCTURE AND PYRIDOINDOLE RING STRUCTURE, AND ORGANIC ELECTROLUMINESCENT ELEMENT

The present invention relates to a compound having a substituted anthracene ring structure and a pyridoindole ring structure, which is represented by the following general formula (1) or the following general formula (2); and an organic electroluminescent device having a pair of electrodes and at least one organic layer interposed therebetween, in which the compound having a substituted anthracene ring structure and a pyridoindole ring structure, which is represented by the following general formula (1) or the following general formula (2), is used as a constituent material of the aforementioned at least one organic layer.