117894-26-5

Basic information

• Product Name: (S)-(+)-5-phenyl-2-cyclohexen-1-one
• Synonyms: (S)-(+)-5-phenyl-2-cyclohexen-1-one
• CAS NO: 117894-26-5
• Molecular Weight: 172.227
• Mol File: 117894-26-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: (S)-(+)-5-phenyl-2-cyclohexen-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-5-phenyl-2-cyclohexen-1-one(117894-26-5)
• EPA Substance Registry System: (S)-(+)-5-phenyl-2-cyclohexen-1-one(117894-26-5)

Safety Data

• Hazardous Substances Data: 117894-26-5(Hazardous Substances Data)

Upstream product

• 35376-41-1 5-phenylcyclohex-2-en-1-one 
• 557-20-0 diethylzinc 
• 542-05-2 acetonedicarboxylic acid 
• 104-55-2 3-phenyl-propenal 
• 115495-48-2 (1E,4E)-1-phenyldeca-1,4-dien-3-one 
• 5208-89-9 (E)-1-phenyl-1,4-pentadien-3-ol 
• 73291-51-7 (E)-1-phenylpenta-1,4-dien-3-one 
• 14371-10-9 (E)-3-phenylpropenal 
• 1019840-83-5 (S,E)-7-phenyldeca-3,9-dien-5-one 
• 1019840-82-4 (S,E)-6-phenylnona-2,8-dien-4-one 
• 1019840-71-1 (S,E)-4-phenyltrideca-1,7-dien-6-one 
• 930276-98-5 (1E,4E)-1-cyclohexyl-5-phenylpenta-1,4-dien-3-one 
• 72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 1694-31-1 tert-butyl acetoacetate 

Relevant articles and documents

Synergistic Cu-amine catalysis for the enantioselective synthesis of chiral cyclohexenones

An unprecedented utilization of 1,3-acetonedicarboxylic acid as a 1,3-bis-pro-nucleophile and a reactive acetone surrogate in enantioselective catalysis has been reported. By synergistically activating the ketodiacid by copper catalysis and an α,β-unsatur

Asymmetric Ni-catalyzed conjugate allylation of activated enones

The nickel-catalyzed enantioselective addition of allylboronic acid pinacol ester, allylB(pin), is described. This reaction is highly effective with dialkylidene ketones and favors the allylation of the benzylidene site in nonsymmetric substrates. The rea

A simple asymmetric organocatalytic approach to optically active cyclohexenones

Optically active 2,5-disubstituted-cyclohexen-2-one derivatives have been prepared in a one-pot process consisting of five reaction steps: an organocatalytic asymmetric conjugated addition of β-ketoesters to α,β-unsaturated aldehydes that proceeds in aque