482620-69-9

Basic information

• Product Name: (R)-N-[(R)-1-(4-Benzoyl-phenyl)-ethyl]-2-hydroxy-2-phenyl-acetamide
• Synonyms: (R)-N-[(R)-1-(4-Benzoyl-phenyl)-ethyl]-2-hydroxy-2-phenyl-acetamide
• CAS NO: 482620-69-9
• Molecular Weight: 359.425
• Mol File: 482620-69-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-N-[(R)-1-(4-Benzoyl-phenyl)-ethyl]-2-hydroxy-2-phenyl-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-N-[(R)-1-(4-Benzoyl-phenyl)-ethyl]-2-hydroxy-2-phenyl-acetamide(482620-69-9)
• EPA Substance Registry System: (R)-N-[(R)-1-(4-Benzoyl-phenyl)-ethyl]-2-hydroxy-2-phenyl-acetamide(482620-69-9)

Safety Data

• Hazardous Substances Data: 482620-69-9(Hazardous Substances Data)

Upstream product

• 79316-80-6 [4-(1-bromoethyl)phenyl](phenyl)methanone 
• 482620-66-6 4-(1-azidoethyl)benzophenone 
• 18220-90-1 4-ethylbenzophenone 
• 611-71-2 (R)-Mandelic Acid 
• 482620-67-7 4-(1-aminoethyl)benzophenone 

Downstream Products

• 482620-70-2 4-[(1R)-aminoethyl]benzophenone 

Relevant articles and documents

Studies on the enantioselective catalysis of photochemically promoted transformations: "Sensitizing receptors" as chiral catalysts

A strategy for the enantioselective catalysis of photomediated reactions in solution is described, involving the use of chiral molecular receptors possessing appendant triplet-sensitizing moieties. Energy transfer is selectively directed to bound substrate as a consequence of the distance dependence of triplet-triplet energy transfer. This effect, which is equivalent to a binding-induced rate enhancement, enables substoichiometric chirality transfer from the receptor template to the substrate, as observed in the intramolecular enone-olefin photo [2 + 2]cycloaddition of a quinolone substrate.