218897-95-1

Basic information

• Product Name: 1,2,3,6-Tetrahydro-azepino[4,5-b]indole-5-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
• Synonyms: 1,2,3,6-Tetrahydro-azepino[4,5-b]indole-5-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
• CAS NO: 218897-95-1
• Molecular Weight: 366.503
• Mol File: 218897-95-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,2,3,6-Tetrahydro-azepino[4,5-b]indole-5-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,6-Tetrahydro-azepino[4,5-b]indole-5-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(218897-95-1)
• EPA Substance Registry System: 1,2,3,6-Tetrahydro-azepino[4,5-b]indole-5-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(218897-95-1)

Safety Data

• Hazardous Substances Data: 218897-95-1(Hazardous Substances Data)

Upstream product

• 951-98-4 2-Oxo-propionic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 218897-93-9 3-Bromo-2-oxo-propionic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 218897-94-0 1-Bromomethyl-2,3,4,9-tetrahydro-1H-β-carboline-1-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 

Downstream Products

• 218897-96-2 1,2,3,4,5,6-Hexahydro-azepino[4,5-b]indole-5-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 

Relevant articles and documents

Synthesis of vinca alkaloids and related compounds, LXXXVII. Reversed enantioselectivity in different approaches

Using the same chiral auxiliaries during the enantioselective synthesis of vincamine the absolute configuration depends on the selected approach.Starting from Wenkert enamine the natural (+)-vincamine, while using the reaction sequence through vincadiffor