486-18-0

Basic information

• Product Name: 3-ethylindolo[2,3-a]quinolizine
• Synonyms: 12H-indolo[2,3-a]quinolizin-5-ium, 3-ethyl-, inner salt; 3-Ethyl-12H-indolo[2,3-a]quinolizin-5-ium Inner Salt; 3-Ethylindolo[2,3-a]quinolizin-5-ium-12-ide; 486-18-0
• CAS NO: 486-18-0
• Molecular Formula: C₁₇H₁₄N₂
• Molecular Weight: 246.3065
• Mol File: 486-18-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 508.226°C at 760 mmHg
• Flash Point: 261.166°C
• Density: 1.191g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.673
• CAS DataBase Reference: 3-ethylindolo[2,3-a]quinolizine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ethylindolo[2,3-a]quinolizine(486-18-0)
• EPA Substance Registry System: 3-ethylindolo[2,3-a]quinolizine(486-18-0)

Safety Data

• Hazardous Substances Data: 486-18-0(Hazardous Substances Data)

Upstream product

• 42281-83-4 6,7-dihydroflavopereirine 
• 61-54-1 tryptamine 
• 21190-95-4 2-(5-ethyl-pyridin-2-yl)-indole 
• 115438-98-7 1-Benzenesulfonyl-2-(5-ethyl-pyridin-2-yl)-1H-indole 
• 13509-15-4 5-Ethylpyridin-2-carbonsaeureethylester 
• 69303-10-2 3-ethyl-6,7-dihydro-4H-indolo<2,3-a>quinolizin-4(12H)-one 
• 89652-82-4 3-acetyl-4-oxo-6,7-dihydro-12H-indolo<2,3-a>quinolizine 
• 49836-24-0 (E)-2-(ethoxymethylene)-3-oxobutanoic acid ethyl ester 
• 525-41-7 1-methyl-4,9-dihydro-3H-β-carboline 
• 61755-65-5 1-(1,4,6,7,12,12b-hexahydro-indolo[2,3-a]chinolizin-3-yl)-ethanol 
• 115465-64-0 12-Benzenesulfonyl-3-ethyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide 
• 115465-66-2 2-[1-Benzenesulfonyl-2-(5-ethyl-pyridin-2-yl)-1H-indol-3-yl]-ethanol 
• 37627-46-6 octahydro-1,2,3,4,6,7,12,12 b ethyl-3 indolo(2,3-a) quinolizidine 
• 78867-75-1 ((1H-indolyl-3)-2 ethylene)-1 ethyl-5 piperidone-2 

Relevant articles and documents

Short synthetic route to 5,6-dihydroflavopereirine and flavopereirine

A short synthetic route to 5,6-dihydroflavopereirine (1) and flavopereirine (2) is described.

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