1264995-14-3

Basic information

• Product Name: (-)-ethyl (R)-5-methyl-2-(1-benzyl-2,5-dimethyl-1H-indol-3-yl)hexanoate
• Synonyms: (-)-ethyl (R)-5-methyl-2-(1-benzyl-2,5-dimethyl-1H-indol-3-yl)hexanoate
• CAS NO: 1264995-14-3
• Molecular Weight: 391.554
• Mol File: 1264995-14-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (-)-ethyl (R)-5-methyl-2-(1-benzyl-2,5-dimethyl-1H-indol-3-yl)hexanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-ethyl (R)-5-methyl-2-(1-benzyl-2,5-dimethyl-1H-indol-3-yl)hexanoate(1264995-14-3)
• EPA Substance Registry System: (-)-ethyl (R)-5-methyl-2-(1-benzyl-2,5-dimethyl-1H-indol-3-yl)hexanoate(1264995-14-3)

Safety Data

• Hazardous Substances Data: 1264995-14-3(Hazardous Substances Data)

Upstream product

• 702702-73-6 1-benzyl-2,5-dimethylindole 
• 1196-79-8 2,5-Dimethyl-1H-indole 
• 100-39-0 benzyl bromide 

Relevant articles and documents

Rhodium(II)-catalyzed enantioselective C-H functionalization of indoles

A catalytic, enantioselective method for the C-H functionalization of indoles by diazo compounds has been achieved. With catalytic amounts of Rh 2(S-NTTL)4, the putative Rh-carbene intermediates from α-alkyl-α-diazoesters react with indoles at C(3) to provide α-alkyl-α-indolylacetates in high yield and enantioselectivity. From DFT calculations, a mechanism is proposed that involves a Rh-ylide intermediate with oxocarbenium character.