115465-65-1

Basic information

• Product Name: 12-Benzenesulfonyl-2-carboxy-3-ethyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide
• CAS NO: 115465-65-1
• Molecular Weight: 529.411
• Mol File: 115465-65-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 12-Benzenesulfonyl-2-carboxy-3-ethyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 12-Benzenesulfonyl-2-carboxy-3-ethyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide(115465-65-1)
• EPA Substance Registry System: 12-Benzenesulfonyl-2-carboxy-3-ethyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide(115465-65-1)

Safety Data

• Hazardous Substances Data: 115465-65-1(Hazardous Substances Data)

Upstream product

• 115438-95-4 2-(1-Benzenesulfonyl-1H-indol-2-yl)-5-ethyl-isonicotinic acid 
• 17157-48-1 bromoacetaldehyde 
• 115438-96-5 1-(benzenesulfonyl)-2-(5-ethyl-4-methyl-2-pyridyl)indole 
• 115438-97-6 2-(5-Ethyl-4-methyl-pyridin-2-yl)-1H-indole 
• 529-21-5 3-ethyl-4-methylpyridine 

Relevant articles and documents

A DIRECTED METALATION ROUTE TO THE ZWITTERIONIC INDOLE ALKALOIDS. SYNTHESES OF INDOLOQUINOLIZINE, FLAVOPEREIRINE, FLAVOCARPINE, AND DIHYDROFLAVOPEREIRINE

A protocol involving beta-lithiation of 2-(2-pyridinyl)indoles (4->5) and subsequent reaction with bromoacetaldehyde or oxirane has led to syntheses of the alkaloids indoloquinolizine (1), flavopereirine (2), flavocarpine (21), and dihydroflavopere