95110-79-5

Basic information

• Product Name: Ethanone, 2-(4-chlorophenyl)-1-cyclohexyl-
• CAS NO: 95110-79-5
• Molecular Formula: C14H17ClO
• Molecular Weight: 236.741
• Mol File: 95110-79-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-(4-chlorophenyl)-1-cyclohexyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-(4-chlorophenyl)-1-cyclohexyl-(95110-79-5)
• EPA Substance Registry System: Ethanone, 2-(4-chlorophenyl)-1-cyclohexyl-(95110-79-5)

Safety Data

• Hazardous Substances Data: 95110-79-5(Hazardous Substances Data)

Upstream product

• 95150-10-0 1,2-epoxy-2-(4-chlorophenyl)-1-cyclohexyl-1-phenylsulfinylethane 
• 13307-61-4 Isobutylthiobenzene 
• 104354-60-1 cyclohexylchloromethyl phenyl sulfoxide 
• 72653-48-6 α-chloroisobutyl phenyl sulfide 
• 108-98-5 thiophenol 
• 102104-36-9 2-Benzenesulfinyl-2-chloro-1-(4-chloro-phenyl)-2-cyclohexyl-ethanol 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 78358-09-5 40chlorobenzyl methanesulfonate 

Relevant articles and documents

Alternative approach toward the generation of benzylic zinc reagent: Direct oxidative addition of active zinc into the carbon-oxygen bond of benzyl mesylates

The use of highly active zinc, prepared by the Rieke method, for the direct preparation of benzylic zinc mesylate was investigated. The oxidative addition of highly active zinc to benzyl mesylate was easily completed under mild conditions. The resulting benzylic zinc mesylates were employed in subsequent cross-coupling reactions with a broad range of electrophiles, and the formation of the corresponding products was successful.

A NOVEL SYNTHESIS OF DIALKYL KETONES AND α-SULFENYLATED CARBONYL COMPOUNDS FROM α,β-EPOXY SULFOXIDES

Treatment of α,β-epoxy sulfoides with excess sodium phenylselenide and various kinds of alkylthiolates gave dialkyl ketones and α-sulfenylated carbonyl compounds, respectively, in good yields under mild conditions.