115438-93-2

Basic information

• Product Name: 12-Benzenesulfonyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide
• CAS NO: 115438-93-2
• Molecular Weight: 457.348
• Mol File: 115438-93-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 12-Benzenesulfonyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 12-Benzenesulfonyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide(115438-93-2)
• EPA Substance Registry System: 12-Benzenesulfonyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide(115438-93-2)

Safety Data

• Hazardous Substances Data: 115438-93-2(Hazardous Substances Data)

Upstream product

• 13228-40-5 2-(2-pyridinyl)-1H-indole 
• 2524-52-9 ethyl-2-picolinate 
• 73282-12-9 1-phenylsulfonyl-2-(pyridin-2-yl)-1H-indole 
• 17157-48-1 bromoacetaldehyde 

Downstream Products

• 4802-79-3 1,2,3,4,6,7,12,12b-octahydroindolo(2,3-a)quinolizine 
• 239-15-6 indolo[2,3-a]quinolizine 

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