1225230-86-3

Basic information

• Product Name: (2S,12bS)-isopropyl 4-methyl-2-phenyl-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine-3-carboxylate
• Synonyms: (2S,12bS)-isopropyl 4-methyl-2-phenyl-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine-3-carboxylate
• CAS NO: 1225230-86-3
• Molecular Weight: 400.521
• Mol File: 1225230-86-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,12bS)-isopropyl 4-methyl-2-phenyl-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,12bS)-isopropyl 4-methyl-2-phenyl-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine-3-carboxylate(1225230-86-3)
• EPA Substance Registry System: (2S,12bS)-isopropyl 4-methyl-2-phenyl-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine-3-carboxylate(1225230-86-3)

Safety Data

• Hazardous Substances Data: 1225230-86-3(Hazardous Substances Data)

Upstream product

• 61-54-1 tryptamine 
• 542-08-5 isopropyl acetoacetate 
• 104-55-2 3-phenyl-propenal 

Relevant articles and documents

Organocatalyzed enantioselective one-pot three-component access to indoloquinolizidines by a Michael addition-Pictet-Spengler sequence

The enantioselective three-component Michael addition-Pictet-Spengler sequence of β-ketoesters 1, α,β-unsaturated aldehydes 2 and tryptamines 4 represents a facile and rapid one-pot access to highly substituted indoloquinolizidines in moderate to excellent yields and good to excellent enantioselectivities.