1497405-14-7

Basic information

• Product Name: (3aS,8bS)-4-benzyl-8b-butyl-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole
• CAS NO: 1497405-14-7
• Molecular Weight: 305.463
• Mol File: 1497405-14-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3aS,8bS)-4-benzyl-8b-butyl-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole(CAS DataBase Reference)
• NIST Chemistry Reference: (3aS,8bS)-4-benzyl-8b-butyl-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole(1497405-14-7)
• EPA Substance Registry System: (3aS,8bS)-4-benzyl-8b-butyl-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole(1497405-14-7)

Safety Data

• Hazardous Substances Data: 1497405-14-7(Hazardous Substances Data)

Upstream product

• 934-42-9 2-butylcyclopentanone 
• 614-31-3 N-benzyl-N-phenylhydrazine 
• 1497405-24-9 C₂₂H₂₇NO 

Relevant articles and documents

Versatile access to chiral indolines by catalytic asymmetric fischer indolization

"Fisching" for complexity: The chiral Bronsted acid (R)-STRIP catalyzes the asymmetric Fischer indolization of a range of monosubstituted cyclopentanones and cyclohexanones to give chiral fused indolines bearing a quaternary stereogenic center at the 3-position. The method has been extended to include substrates bearing a tethered nucleophile, thus allowing for enantioselective indolization/ring-closing cascades to complex propellanes featuring two vicinal quaternary stereocenters. Copyright