203394-24-5

Basic information

• Product Name: 3H-Pyrido[3,4-b]indole, 4,9-dihydro-4-phenyl-
• CAS NO: 203394-24-5
• Molecular Formula: C17H14N2
• Molecular Weight: 246.312
• Mol File: 203394-24-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3H-Pyrido[3,4-b]indole, 4,9-dihydro-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-Pyrido[3,4-b]indole, 4,9-dihydro-4-phenyl-(203394-24-5)
• EPA Substance Registry System: 3H-Pyrido[3,4-b]indole, 4,9-dihydro-4-phenyl-(203394-24-5)

Safety Data

• Hazardous Substances Data: 203394-24-5(Hazardous Substances Data)

Upstream product

• 102-96-5 (2-nitroethenyl)benzene 
• 120-72-9 indole 
• 87-13-8 diethyl 2-ethoxymethylenemalonate 
• 203393-79-7 4-(p-trifluoromethylphenyl)-β-carboline 
• 75-09-2 dichloromethane 
• 497-19-8 sodium carbonate 
• 5027-78-1 2-phenyl-2-(3-indolyl)-1-aminoethane 
• 51626-47-2 3-(2-nitro-1-phenylethyl)-1H-indole 

Relevant articles and documents

Synthesis of 4-phenyl-3,4-dihydro-β-carboline

4-Phenyl-3,4-dihydro-β-carboline was prepared using the Bischler-Napieralski reaction on β-phenyltryptamine. 2004 Springer Science + Business Media, Inc.

The base-free van Leusen reaction of cyclic imines on water: Synthesis of N-fused imidazo 6,11-dihydro β-carboline derivatives

Construction of imidazoles has been demonstrated on water under base-free conditions. The reaction of dihydro β-carboline imines and p-toluenesulfonylmethyl isocyanides furnished the corresponding substituted N-fused imidazo 6,11-dihydro β-carboline derivatives in very good yields under ambient conditions. The use of deuterium oxide (D2O) as a solvent enabled the incorporation of deuterium isotopes in the imidazole ring.

4-substituted beta-carbolines and analogs thereof

This invention relates to 4-substituted beta -carbolines and beta -carboline analogs that inhibit Ca+2 influx and interleukin-2 (IL-2) production. The 4-substituted beta -carbolines and beta -carboline analogs of this invention are represented by formula