52612-58-5

Basic information

• Product Name: (3E,5Ξ)-6,9,10-trimethyl-undeca-3,5,9-trien-2-one
• CAS NO: 52612-58-5
• Molecular Weight: 206.328
• Mol File: 52612-58-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (3E,5Ξ)-6,9,10-trimethyl-undeca-3,5,9-trien-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3E,5Ξ)-6,9,10-trimethyl-undeca-3,5,9-trien-2-one(52612-58-5)
• EPA Substance Registry System: (3E,5Ξ)-6,9,10-trimethyl-undeca-3,5,9-trien-2-one(52612-58-5)

Safety Data

• Hazardous Substances Data: 52612-58-5(Hazardous Substances Data)

Upstream product

• 52612-57-4 6,9,10-trimethyl-undeca-3t,5c,9-trien-2-one 
• 64708-55-0 3-Hydroxy-4-isopropenyl-3,6,7-trimethyl-6-octen-1-yne 

Downstream Products

• 72074-84-1 beta-irone 
• 72074-86-3 (+-)-4t-(2,5t,6,6-Tetramethyl-cyclohex-2-en-r-yl)-but-3-en-2-on 
• 72074-85-2 (+-)-4t-(2,5c,6,6-tetramethyl-cyclohex-2-en-r-yl)-but-3-en-2-one 
• 162282-94-2 1-(1,3,4-trimethyl-3-cyclohexenyl)-1-penten-4-one 
• 79-68-5 gamma-irone 
• 81456-93-1 (1'RS,5'RS)-4-(2',5',6',6'-tetramethylcyclohex-2'-enyl)butan-2-one 

Relevant articles and documents

Photochemical transformations of terpenoids in the presence of cyclodextrins

The effect of complexation of terpene compounds with cyclodextrins on photolysis depends on the type of cyclodextrin and on the structure of the initial substrates. In some cases, only a change in the reaction rate is observed; in other cases, the complexation results in allylic rearrangements, hydride and acyl shifts, and cyclization with the formation of four-, five-, and six-membered cycles, whereas only cis-trans isomerization reactions are observed in the absence of complexation.

Novel synthesis of dienones and enones from propargyl alcohols and allyl alcohols with 2,2 dimethoxypropane: synthesis of ionone and irone

-