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Silane, [1,2-cyclohexanediylbis(oxy)]bis[trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13871-93-7

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13871-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13871-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,7 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13871-93:
(7*1)+(6*3)+(5*8)+(4*7)+(3*1)+(2*9)+(1*3)=117
117 % 10 = 7
So 13871-93-7 is a valid CAS Registry Number.

13871-93-7Relevant academic research and scientific papers

Palladium-catalyzed silylation of alcohols with hexamethyldisilane

Shirakawa, Eiji,Hironaka, Koji,Otsuka, Hidehito,Hayashi, Tamio

, p. 3927 - 3929 (2006)

The combination of hexamethyldisilane and a catalytic amount of [PdCl(η3-C3H5)]2-PPh 3 was found to be effective for the trimethylsilylation of alcohols, where both of the two trimethylsilyl groups of hexamethyldisilane were transferred to alcohols without coproduction of any stoichiometric amount of byproduct but H2. The Royal Society of Chemistry 2006.

Why Are Silyl Ethers Conformationally Different from Alkyl Ethers? Chair-Chair Conformational Equilibria in Silyloxycyclohexanes and Their Dependence on the Substituents on Silicon. The Wider Roles of Eclipsing, of 1,3-Repulsive Steric Interactions, and o

Marzabadi, Cecilia H.,Anderson, J. Edgar,Gonzalez-Outeirino, Jorge,Gaffney, Piers R. J.,White, Christopher G. H.,Tocher, Derek A.,Todaro, Louis J.

, p. 15163 - 15173 (2007/10/03)

An NMR study of the diaxial/diequatorial chair equilibrium in a range of silylated derivatives of trans-1,4- and trans-1,2-dihydroxycyclohexane is reported and discussed with a view to explaining unusually large populations of chair conformations with axi

A FACILE SYNTHESIS OF 2,3,4,6-TETRA-O-BENZYL-D-GLUCOPYRANOSYLIDENE ACETALS USING TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE CATALYST

Yoshimura, Juji,Horito, Shigeomi,Hashimoto, Hironobu

, p. 375 - 376 (2007/10/02)

The application of acetalization of aldehydes and ketones by alkoxysilanes in the presence of trimethylsilyl trifluoromethanesulfonate catalyst to lactones and di-O-trimethylsilyl-α-diols gave readily the corresponding spiro ortho esters.

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