47059-11-0

Basic information

• Product Name: 3H-Pyrido[3,4-b]indole, 4,9-dihydro-9-(phenylmethyl)-
• CAS NO: 47059-11-0
• Molecular Formula: C18H16N2
• Molecular Weight: 260.338
• Mol File: 47059-11-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3H-Pyrido[3,4-b]indole, 4,9-dihydro-9-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-Pyrido[3,4-b]indole, 4,9-dihydro-9-(phenylmethyl)-(47059-11-0)
• EPA Substance Registry System: 3H-Pyrido[3,4-b]indole, 4,9-dihydro-9-(phenylmethyl)-(47059-11-0)

Safety Data

• Hazardous Substances Data: 47059-11-0(Hazardous Substances Data)

Upstream product

• 6502-82-5 N_b-formyltryptamine 
• 59414-85-6 2-(1-benzyl-1H-indol-3-yl)acetonitrile 
• 100-44-7 benzyl chloride 
• 4307-98-6 N-benzyltryptamine 
• 771-51-7 indole-3-acetonitrile 
• 116246-38-9 1-benzyl-N-formyltryptamine 
• 4894-26-2 3,4-dihydro-β-carboline 
• 100-39-0 benzyl bromide 

Downstream Products

• 79960-51-3 9-Benzyl-2-(4-chloro-butyryl)-2,3,4,9-tetrahydro-1H-β-carboline-1-carbonitrile 
• 1268809-80-8 C₂₇H₂₃N₃O₂ 
• 1268809-70-6 C₃₅H₂₇N₃O₂S 
• 1268809-69-3 C₃₇H₂₉N₃O₂ 
• 1268809-68-2 C₃₃H₂₆BrN₃O₂ 
• 1268809-67-1 C₃₃H₂₆BrN₃O₂ 
• 1268809-66-0 C₃₃H₂₆BrN₃O₂ 
• 1268809-65-9 C₃₃H₂₆FN₃O₂ 
• 1268809-64-8 C₃₄H₂₉N₃O₂ 
• 1268809-63-7 C₃₃H₂₇N₃O₂ 
• 1268809-62-6 C₂₆H₂₁N₃O₂ 
• 79960-32-0 α,α'-bis<1-(2-benzoyl-9-benzyl-1-cyano-1,2,3,4-tetrahydropyrido<3,4-b>indolyl)>-p-xylene 
• 79960-33-1 12-benzyl-12b-cyano-4-oxo-1,2,3,4,6,7,12,12b-octahydroindolo<2,3-a>quinolizine 
• 109355-96-6 13-benzyl-1-ethenyl-8,13,13b,14-tetrahydroindolo<2',3':3,4>pirido<2,1-b><2,7>naphthyridin-5<7H>-imine 

Relevant articles and documents

Cytotoxic activities of novel hexahydroindolizino[8,7-b]indole derivatives prepared by 1,3-dipolar cycloaddition reactions of 3,4-dihydro-β-carboline ylides

A series of 1-cyano and 2-cyanohexahydroindolizino[8,7-b]indole derivatives was prepared by 1,3-dipolar cycloaddition of acrylonitrile with ylides derived from 3,4-dihydro-β-carboline and its 6-methoxy, 6-benzyloxy, 9-methyl and 9-benzyl analogues. The pr

New approaches to the synthesis of eburnane alkaloids

The aldehyde which is a key precursor of the Eburnane alkaloid vincamine has been prepared in two ways. The first one involves a photochemical rearrangement of a spiro oxaziridine intermediate and the second is based on an imino Diels-Alder reaction follo