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(1R,4S)-1-Bicyclo[2.2.1]hept-2-yl-propan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25121-32-8

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25121-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25121-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,2 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25121-32:
(7*2)+(6*5)+(5*1)+(4*2)+(3*1)+(2*3)+(1*2)=68
68 % 10 = 8
So 25121-32-8 is a valid CAS Registry Number.

25121-32-8Downstream Products

25121-32-8Relevant academic research and scientific papers

Highly efficient methyl ketone synthesis by water-assisted C-C coupling between olefins and photoactivated acetone

Shiraishi, Yasuhiro,Tsukamoto, Daijiro,Hirai, Takayuki

scheme or table, p. 3117 - 3120 (2009/05/07)

(Chemical Equation Presented) Photoirradiation of an acetone/water mixture containing olefins affords the corresponding methyl ketones highly efficiently via a water-assisted CsC coupling between acetonyl radical and olefins.

ROLE OF THE ACETYLACETONYL RADICAL IN THE SENSITIZED PHOTOPRODUCTION OF BIS(ACETONYLACTONATO)COPPER(II)

Cow, Yuan L.,Buono,-Core, Gonzalo E.

, p. 1234 - 1239 (2007/10/02)

Benzophenone-sensitized photoproduction of Cu(acac)2 generated the acetylacetonyl radical (acac.) which could be trapped as acetylacetone by hydrogen as well as by a H-atom-donating agent, or as the corresponding nitroxide with 2-nitroso-2-methylpropane,

DECOMPOSITION DU PERCARBONATE DE O,O-t-BUTYLE ET O-ISOPROPENYLE EN SOLUTION DANS DES CYCLANES

Jaouhari, R.,Filliatre, C.,Maillard, B.,Villenave, J.J.

, p. 3137 - 3142 (2007/10/02)

Thermolysis of O,O-t-butyl and O-isopropenyl percarbonate in cyclohexane involves free-radical acetonylation of solvent.Free radicals derived from solvent add to the percarbonate double bond and after a double β-scission reaction, cyclohexylacetone carbon dioxide and t-butoxy radicals are formed.Abstracting H atoms from the solvent, t-butoxy radicals regenerate free radicals from solvent, and the reaction becomes a chain process.Extending the study to other cycloalkanes it has been shown that the process is a general synthesis method for cycloalkylacetones.On the other hand, competitive reactions of pairs of solvents have shown that the reactivity of the substrates depends on H atom lability and on more complex phenomena like transfers between hydrocarbons and C-centred free-radicals.

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