60068-02-2

Basic information

• Product Name: 2-Cyclohexen-1-one, 2,6,6-trimethyl-3-(2-methylpropoxy)-
• CAS NO: 60068-02-2
• Molecular Formula: C13H22O2
• Molecular Weight: 210.316
• Mol File: 60068-02-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexen-1-one, 2,6,6-trimethyl-3-(2-methylpropoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one, 2,6,6-trimethyl-3-(2-methylpropoxy)-(60068-02-2)
• EPA Substance Registry System: 2-Cyclohexen-1-one, 2,6,6-trimethyl-3-(2-methylpropoxy)-(60068-02-2)

Safety Data

• Hazardous Substances Data: 60068-02-2(Hazardous Substances Data)

Upstream product

• 565-69-5 ethyl isopropyl ketone 
• 1629-58-9 4-penten-3-one 
• 64095-45-0 2,2-dimethyl-5-oxo-heptanoic acid methyl ester 
• 909530-07-0 1,5,5-trimethyl-6-(3-phenylpropyl)-7-oxabicyclo[4.1.0]heptan-2-ol 
• 909530-06-9 2,4,4-trimethyl-3-(3-phenylpropyl)cyclohexen-2-ol 
• 60067-97-2 3-isobutyloxy-6,6-dimethylcyclohex-2-en-1-one 
• 74-88-4 methyl iodide 

Downstream Products

• 63184-87-2 5-(2,6,6-trimethyl-3-oxocyclohexen-1-yl)-3-methyl-2-trans-penten-4-yn-1-ol 
• 825614-90-2 3-allyl-2,4,4-trimethyl-2-cyclohexen-1-one 
• 825614-92-4 3-(2,3-dihydroxypropyl)-2,4,4-trimethyl-2-cyclohexen-1-one 
• 825614-94-6 3-[2-(tert-butyldimethylsilyloxy)ethyl]-2,4,4-trimethyl-2-cyclohexen-1-one 
• 825614-95-7 3-[2-(tert-butyldimethylsilyloxy)ethyl]-6-hydroxy-2,4,4-trimethyl-2-cyclohexen-1-one 
• 83646-52-0 3-(2-hydroxyethyl)-2,4,4-trimethyl-2-cyclohexen-1-ol 
• 75203-87-1 3-(2-hydroxyethyl)-2,4,4-trimethyl-2-cyclohexen-1-one 
• 186451-82-1 2,4,4-trimethyl-3-(2-oxoethyl)-2-cyclohexen-1-one 
• 909530-03-6 2,4,4-trimethyl-3-(3-phenylpropyl)cyclohex-2-enone 
• 909530-06-9 2,4,4-trimethyl-3-(3-phenylpropyl)cyclohexen-2-ol 
• 909530-07-0 1,5,5-trimethyl-6-(3-phenylpropyl)-7-oxabicyclo[4.1.0]heptan-2-ol 
• 63184-86-1 2,6,6-trimethylcyclohexane-1,3-dione 
• 514-78-3 canthaxanthin 
• 72008-26-5 (2E,4Z)-5-(2,6,6-trimethyl-3-oxo-1-cyclohexen-1-yl)-1-hydroxy-2,4-pentadiene 

Relevant articles and documents

A brief and stereoselective synthesis of limonoid models, with antifeedant activity against Locusts migratoria

A short stereoselective preparation of havanensin-type limonoid models is reported. The synthesis is based on a radical domino reaction of an epoxyketone to a bicyclic hydroxyketone, and is achieved in six and nine steps from simple cyclohexenones. The epoxyhavanensin derivatives show significant antifeedant activity against Spodoptera littoralis and Spodoptera frugiperda, and the epoxyketone 21 shows potent antifeedant activity against Locusts migratoria.

Hydroxy-acetylene-substituted cyclohexenone

A total synthesis of canthaxanthin or dinor-canthaxanthin, known food coloring agents, from pentols.