22460-53-3

Basic information

• Product Name: Cyclohexanone, 4-(1-methylethenyl)-
• CAS NO: 22460-53-3
• Molecular Formula: C9H14O
• Molecular Weight: 138.21
• Mol File: 22460-53-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 4-(1-methylethenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 4-(1-methylethenyl)-(22460-53-3)
• EPA Substance Registry System: Cyclohexanone, 4-(1-methylethenyl)-(22460-53-3)

Safety Data

• Hazardous Substances Data: 22460-53-3(Hazardous Substances Data)

Upstream product

• 31253-50-6 Acetic acid 4-isopropenyl-cyclohex-1-enyl ester 
• 70812-82-7 C₁₅H₂₀N₂O₄S 
• 19493-09-5 Methylenetriphenylphosphorane 
• 24903-95-5 nopinone 
• 917-64-6 methyl magnesium iodide 
• 17159-79-4 ethyl 4-oxocyclohexane-1-carboxylate 
• 18031-40-8 (S)-(-)-perillaldehyde 
• 145747-47-3 1-trimethylsilyloxy-4-isopropenyl-1-cyclohexene 
• 70850-38-3 8-isopropenyl-1,4-dioxa-spiro[4.5]decane 

Downstream Products

• 39725-32-1 4-(2-methyl-oxiranyl)-cyclohexanone 
• 1403244-52-9 C₉H₁₄O₃ 
• 177841-86-0 cis-4-isopropenylcyclohexanol 
• 910309-36-3 4-(1-methylcyclopropyl)cyclohexanone 
• 20549-17-1 2-Isobutyloxymethylen-4-isopropenyl-cyclohexan-1-on 
• 20549-18-2 2-Formyl-4-isopropenyl-cyclohexen-⁽¹⁾ 
• 20549-20-6 2-Hydroxymethyl-4-isopropenyl-cyclohexen-⁽¹⁾ 
• 13898-73-2 1-methyl-5-(1-methylethenyl)cyclohexene 
• 183613-97-0 cis-1-(hydroxymethyl)-4-isopropenylcyclohexane-1-ol 
• 855303-75-2 cis-(4-isopropenyl-1-trimethylsilyloxycyclohexyl)methanol 
• 855303-72-9 cis-4-isopropenyl-1-trimethylsilyloxycyclohexanecarbonitrile 
• 855303-74-1 cis-4-isopropenyl-1-trimethylsilyloxycyclohexanecarbaldehyde 
• 461685-59-6 cis-1-hydroxy-4-isopropenylcyclohexanecarbonitrile 
• 5034-21-9 4-(1-oxoethyl)-1-cyclohexanone 

Relevant articles and documents

Comprehensive kinetic and mechanistic considerations for the gas-phase behaviour of pinane-type compounds

The thermal behaviour of selected pinane-type compounds, α-pinene (1), β-pinene (2), pinane (3) and nopinone (4), has been investigated. The conversion of the bicyclic starting materials to their acyclic and monocyclic isomers as well as the consecutive reactions of the acyclic main isomerisation products are discussed. The conversion of 1-4 in a reaction network is presented and the experimental evidence for the formation of pyrolysis products by a biradical pathway is discussed. In addition to these results a kinetic model describing the isomerisation of the bicyclic compounds to their acyclic and monocyclic isomers is presented. A good correlation between kinetic simulations and experimental data is revealed. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

Synthetic Approach to the Amphilectane Diterpenes: The Use of Nitriles as Terminators of Carbocation-Olefin Cyclizations

A biomimetic approach to the synthesis of tricyclic terpenoid isonitriles from marine sponges is described which involves carbocation-olefin cyclization of polyolefinic precursors terminated by the stereoselective formation of a carbon-nitrogen bond.The k