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1,3-Dioxolane, 2,2'-(1,2-ethanediyl)bis[2-cyclohexyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85796-35-6

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85796-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85796-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85796-35:
(7*8)+(6*5)+(5*7)+(4*9)+(3*6)+(2*3)+(1*5)=186
186 % 10 = 6
So 85796-35-6 is a valid CAS Registry Number.

85796-35-6Downstream Products

85796-35-6Relevant academic research and scientific papers

Nouvelle synthese electrochimique de γ-bisdioxolannes symetriques et dissymetriques

Daubie, Christophe,Bacquet-Einhorn, Cathy,Lelandais, Daniel

, p. 1552 - 1554 (2007/10/02)

The electrochemical reduction of α-iodinated dioxolanes leads to the preparation of a series of symmetrical and nonsymmetrical γ-bisdioxolanes.

Preparation et oxydation anodique d'acides β-cetaliques. Application a la synthese de γ-bisdioxolannes symetriques et des γ-dicetones derivees.

Einhorn, Jacques,Soulier, Jean-Louis,Bacquet Cathy,Lelandais Daniel

, p. 584 - 587 (2007/10/02)

Anoxic oxidation of carboxylic acids with β-dioxolane substituents leads to good yields of symmetrical γ-bisdioxolanes.Hydrolysis of these compounds easily provides the corresponding γ-diketones.The synthesis of the starting acids is described.

A NEW ELECTROCHEMICAL ACCESS TO UNSYMMETRICAL γDIKETONES VIA THE CORRESPONDING γBISDIOXOLANES. APPLICATION TO THE SYNTHESIS OF DIHYDROJASMONE.

Bacquet-Einhorn, Cathy,Soulier, Jean-Louis,Lelandais, Daniel

, p. 305 - 306 (2007/10/02)

A series of unsymmetrical γ bisdioxolanes has been prepared by a mixed coupling of the Kolbe's radicals obtained by anodic oxidation of mixtures of two dioxolanes of γ ketoacids.

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