115465-64-0

Basic information

• Product Name: 12-Benzenesulfonyl-3-ethyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide
• CAS NO: 115465-64-0
• Molecular Weight: 485.401
• Mol File: 115465-64-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 12-Benzenesulfonyl-3-ethyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 12-Benzenesulfonyl-3-ethyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide(115465-64-0)
• EPA Substance Registry System: 12-Benzenesulfonyl-3-ethyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide(115465-64-0)

Safety Data

• Hazardous Substances Data: 115465-64-0(Hazardous Substances Data)

Upstream product

• 115438-98-7 1-Benzenesulfonyl-2-(5-ethyl-pyridin-2-yl)-1H-indole 
• 17157-48-1 bromoacetaldehyde 
• 21190-95-4 2-(5-ethyl-pyridin-2-yl)-indole 
• 13509-15-4 5-Ethylpyridin-2-carbonsaeureethylester 

Downstream Products

• 109721-87-1 flavopereirine 

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