65311-23-1

Basic information

• Product Name: Ethanone, 2-(acetyloxy)-1-(1-cyclohexen-1-yl)-
• CAS NO: 65311-23-1
• Molecular Formula: C10H14O3
• Molecular Weight: 182.219
• Mol File: 65311-23-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-(acetyloxy)-1-(1-cyclohexen-1-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-(acetyloxy)-1-(1-cyclohexen-1-yl)-(65311-23-1)
• EPA Substance Registry System: Ethanone, 2-(acetyloxy)-1-(1-cyclohexen-1-yl)-(65311-23-1)

Safety Data

• Hazardous Substances Data: 65311-23-1(Hazardous Substances Data)

Upstream product

• 147894-98-2 acetic acid-(2-cyclohex-1-enyl-2-nitro-ethyl ester) 
• 931-49-7 1-ethenylcyclohexene 
• 75-75-2 methanesulfonic acid 
• 64-19-7 acetic acid 
• 27944-89-4 3-(cyclohex-1-en-1-yl)propiolic acid 
• 932-66-1 1-cyclohexenyl methyl ketone 
• 54781-35-0 ((1-(cyclohex-1-en-1-yl)vinyl)oxy)trimethylsilane 
• 108-24-7 acetic anhydride 
• 186581-53-3 diazomethane 
• 36278-22-5 1-cyclohexenoyl chloride 

Relevant articles and documents

Decarboxylative Oxyacyloxylation of Propiolic Acids: Construction of Alkynyl-Containing α-Acyloxy Ketones

Novel decarboxylative oxyacyloxylation of propiolic acids has been developed. This reaction provides an efficient access to alkynyl-containing α-acyloxy ketones from readily available starting materials and exhibits significant functional group tolerance. Furthermore, oxyacyloxylation of terminal alkynes and aliphatic propiolic acids was also developed. A possible reaction mechanism is proposed based on mechanistic studies.

Microwave-assisted transformation of α,β- and β,γ-unsaturated nitroalkenes into carbonyl compounds

Vinyl and allylic nitroalkenes have been converted into the corresponding carbonyl compounds in good yield using tin(II) chloride dihydrate under microwave irradiation.