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Ethanone, 1-(3-hydroxy-1-cyclohexen-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15040-95-6

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15040-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15040-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,4 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15040-95:
(7*1)+(6*5)+(5*0)+(4*4)+(3*0)+(2*9)+(1*5)=76
76 % 10 = 6
So 15040-95-6 is a valid CAS Registry Number.

15040-95-6Relevant academic research and scientific papers

DoE (Design of Experiments) assisted allylic hydroxylation of enones catalysed by a copper-aluminium mixed oxide

Garcia-Cabeza, Ana Leticia,Marin-Barrios, Ruben,Azarken, Redouan,Moreno-Dorado, F. Javier,Ortega, Maria J.,Vidal, Hilario,Gatica, Jose M.,Massanet, Guillermo M.,Guerra, Francisco M.

, p. 8307 - 8314 (2014/01/06)

The allylic hydroxylation of enones using dioxygen as the oxidant has been studied. The reaction was first examined in the absence of any catalyst, using β-ionone as a model substrate. Then a new copper-aluminium mixed oxide, Cu-Al Ox, was prepared and ch

A Novel Synthesis Including Asymmetric Synthesis of α,β-Unsaturated γ-Hydroxy Carbonyl Compounds from Enones with Carbon Homologation

Satoh, Tsuyoshi,Motohashi, Shigeyasu,Tokutake, Norio,Yamakawa, Koji

, p. 2966 - 2973 (2007/10/02)

Reaction of the carbanion derived from 1-chloroalkyl aryl sulfoxides with enones gave 1,2-adducts in good yields.Treatment of the adduct with potassium benzenethiolate afforded α-phenylthio β,γ-unsaturated carbonyl compound through an α,β-epoxy sulfoxide.

A NOVEL SYNTHESIS OF α,β-UNSATURATED γ-HYDROXY CARBONYL COMPOUNDS FROM ENONES WITH CARBON HOMOLOGATION

Satoh, Tsuyoshi,Motohashi, Shigeyasu,Yamakawa, Koji

, p. 2889 - 2892 (2007/10/02)

The alkylation of enone with 1-chloroalkyl phenyl sulfoxide followed by treatment with thiophenolate afforded α-phenylthio-β,γ-unsaturated carbonyl compound, which was oxidized and then hydrolyzed to give α,β-unsaturated γ-hydroxy carbonyl compound in good yield.

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