1201528-28-0

Basic information

• Product Name: (R)-3-(4,7-dihydro-1H-indol-2-yl)-1,3-diphenylpropan-1-one
• CAS NO: 1201528-28-0
• Molecular Weight: 327.426
• Mol File: 1201528-28-0.mol

Chemical Properties

• CAS DataBase Reference: (R)-3-(4,7-dihydro-1H-indol-2-yl)-1,3-diphenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-(4,7-dihydro-1H-indol-2-yl)-1,3-diphenylpropan-1-one(1201528-28-0)
• EPA Substance Registry System: (R)-3-(4,7-dihydro-1H-indol-2-yl)-1,3-diphenylpropan-1-one(1201528-28-0)

Safety Data

• Hazardous Substances Data: 1201528-28-0(Hazardous Substances Data)

Upstream product

• 26686-10-2 4,7-dihydro-1H-indole 
• 94-41-7 benzalacetophenone 

Relevant articles and documents

Chiral Bronsted acid catalyzed asymmetric Friedel-Crafts alkylation reaction of indoles with α,β-unsaturated ketones: Short access to optically active 2- and 3-substituted indole derivatives

The asymmetric Friedel-Crafts alkylation reaction of indoles with α,β-unsaturated ketones catalyzed by chiral phosphoric acid is reported. A wide range of indoles and 4,7-dihydroindoles were allowed to react with α,β-unsaturated ketones to give the corres

Enantioselective Friedel-Crafts alkylation of 4,7-dihydroindoles with enones catalyzed by primary-secondary diamines

A study was conducted to demonstrate the development of a new chiral primary-secondary diamine catalyst derived from amino acid and its application in the asymmetric Friedel-Crafts alkylation of 4,7-dihydroindoles with α-βunsaturated enones. A array of pr