52329-96-1

Basic information

• Product Name: Ethanone, 2-(2-methyl-1-cyclohexen-1-yl)-1-phenyl-
• CAS NO: 52329-96-1
• Molecular Formula: C15H18O
• Molecular Weight: 214.307
• Mol File: 52329-96-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-(2-methyl-1-cyclohexen-1-yl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-(2-methyl-1-cyclohexen-1-yl)-1-phenyl-(52329-96-1)
• EPA Substance Registry System: Ethanone, 2-(2-methyl-1-cyclohexen-1-yl)-1-phenyl-(52329-96-1)

Safety Data

• Hazardous Substances Data: 52329-96-1(Hazardous Substances Data)

Upstream product

• 583-60-8 2-Methylcyclohexanone 
• 20913-05-7 (Benzoylmethylene)triphenylphosphorane 
• 100-52-7 benzaldehyde 
• 25438-37-3 phenyl(trimethylsiloxy)acetonitrile 
• 98559-25-2 1-(bromomethyl)-2-methyl-1-cyclohexene 
• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 
• 29474-11-1 (2-methylcyclohex-1-en-1yl)methanol 
• 104654-69-5 Ethyl 2-methyl-1-cyclohex-1-ene carboxylate 
• 122135-83-5 ethyl 2-trifluoromethanesulfonyloxycyclohex-1-enecarboxylate 
• 93-89-0 benzoic acid ethyl ester 
• 2819-48-9 1,2-bis(methylene)cyclohexane 
• 137958-31-7 1,2-bis(methylene)-cyclohexane-magnesium 

Relevant articles and documents

PhI(OAc)2-mediated alkoxyoxygenation of β,γ-unsaturated ketoximes: Preparation of isoxazolines bearing two contiguous tetrasubstituted carbons

A PhI(OAc)2-promoted dioxygenation of allyl oximes, including one alkoxylation, has been developed. This reaction can give isoxazoline products bearing two contiguous tetrasubstituted carbons. Various oximes substrates bearing different aryl groups and tetrasubstituted-olefin moieties were compatible with the mild reaction conditions. A two-electron oxidation pathway was proposed based on results of preliminary mechanistic studies.

Reactions of substituted (2-butene-1,4-diyl)magnesium complexes with carboxylic esters and lactones: Formation of a versatile intermediate capable of generating substituted cyclopentenols, fused-ring cyclopentenols, or β,γ-unsaturated ketones

Reaction of the magnesium complexes of substituted 1,3-dienes with either carboxylic esters or lactones at low temperature (-78 to -10°C) generates the magnesium salt of a cyclopropanol. This intermediate can either be trapped as an acetate of the cyclopr