108335-04-2

Basic information

• Product Name: 1-(6-Bromo-9H-pyrido[3,4-b]indol-1-yl)-2-phenylethanone
• Synonyms: 1-(6-Bromo-9H-pyrido[3,4-b]indol-1-yl)-2-phenylethanone;Eudistomine S
• CAS NO: 108335-04-2
• Molecular Formula: C₁₉H₁₃BrN₂O
• Molecular Weight: 0
• Mol File: 108335-04-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(6-Bromo-9H-pyrido[3,4-b]indol-1-yl)-2-phenylethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(6-Bromo-9H-pyrido[3,4-b]indol-1-yl)-2-phenylethanone(108335-04-2)
• EPA Substance Registry System: 1-(6-Bromo-9H-pyrido[3,4-b]indol-1-yl)-2-phenylethanone(108335-04-2)

Safety Data

• Hazardous Substances Data: 108335-04-2(Hazardous Substances Data)

Upstream product

• 186495-31-8 C₃₃H₃₀BrN₂O₃P 
• 186495-29-4 6-Bromo-9-methoxymethyl-1-phenylacetyl-9H-β-carboline-3-carboxylic acid ethyl ester 
• 877-03-2 5-bromo-1H-indole-3-carboxaldehyde 

Relevant articles and documents

Iminophosphorane-mediated synthesis of 1-acyl-β-carbolines : A new access to the alkaloids eudistomin T, S and xestomanzamine A of marine origin

New syntheses of the alkaloids eudistomin T and S are described. The key step, formation of the 1-phenylacetyl β-carboline, involves a tandem aza Wittig/electrocyclic ring closure process. The first synthesis of the alkaloid xestomanzamine A is achieved by coupling of a N-protected harmane, now available via aza Wittig/electrocyclic ring closure process, with a 5-lithioimidazole derivative.