213833-72-8

Basic information

• Product Name: (2R,3R,5R)-2-(1,3-dioxolan-2-yl)-5-isopropenyl-2,3-dimethylcyclohexanone
• Synonyms: (2R,3R,5R)-2-(1,3-dioxolan-2-yl)-5-isopropenyl-2,3-dimethylcyclohexanone
• CAS NO: 213833-72-8
• Molecular Weight: 238.327
• Mol File: 213833-72-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3R,5R)-2-(1,3-dioxolan-2-yl)-5-isopropenyl-2,3-dimethylcyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,5R)-2-(1,3-dioxolan-2-yl)-5-isopropenyl-2,3-dimethylcyclohexanone(213833-72-8)
• EPA Substance Registry System: (2R,3R,5R)-2-(1,3-dioxolan-2-yl)-5-isopropenyl-2,3-dimethylcyclohexanone(213833-72-8)

Safety Data

• Hazardous Substances Data: 213833-72-8(Hazardous Substances Data)

Upstream product

• 6485-40-1 (R)-Carvone 
• 19693-75-5 2-methoxy-1,3-dioxolane 
• 213833-70-6 (3R,5R)-(5-isopropenyl-2,3-dimethylcyclohex-1-enyloxy)trimethylsilane 

Downstream Products

• 272767-22-3 (2R,3R)-2-(1,3-dioxolan-2-yl)-2,3-dimethyl-5-cyclohexenone 
• 272767-17-6 (2R,3R,5S)-2-(1,3-dioxolan-2-yl)-6-hydroxymethylene-5-isopropenyl-2,3-dimethylcyclohexanone 
• 272766-52-6 (2R,3R)-2-(1,3-dioxolan-2-yl)-2,3-dimethylcyclohexanone 
• 272767-23-4 (2R,3R)-2-(1,3-dioxolan-2-yl)-6-hydroxymethylene-2,3-dimethylcyclohexanone 
• 361521-89-3 (3R,4R)-3-(1,3-dioxolan-2-yl)-3,4-dimethyl-2-oxo-cyclohexanecarbonitrile 
• 272766-80-0 (1S,3R,4R)-3-(1,3-dioxolan-2-yl)-3,4-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile 
• 272766-76-4 (1R,3R,4R)-3-(1,3-dioxolan-2-yl)-3,4-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile 
• 272766-69-5 (1S,3R,4R,6S)-3-(1,3-dioxolan-2-yl)-6-isopropenyl-3,4-dimethyl-2-oxo-1-(3-oxo-butyl)-cyclohexanecarbonitrile 

Relevant articles and documents

Enantioselective synthesis of highly functionalised cyclohexanones starting from R-(-)-carvone

Copper (1) catalysed conjugate addition of methylmagnesium iodide to R- (-)-carvone and trapping the enolate as its trimethylsilyl enol ether, followed by a trityl perchlorate (TrClO4) catalysed Mukaiyama-aldol reaction, is an efficient method