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2-Propenoic acid, 3-[2-[(1E)-2-(trimethylsilyl)ethenyl]-1-cyclohexen-1-yl]-, 1,1-dimethylethyl ester, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

395642-79-2

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395642-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 395642-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,5,6,4 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 395642-79:
(8*3)+(7*9)+(6*5)+(5*6)+(4*4)+(3*2)+(2*7)+(1*9)=192
192 % 10 = 2
So 395642-79-2 is a valid CAS Registry Number.

395642-79-2Downstream Products

395642-79-2Relevant academic research and scientific papers

Synthesis and use of new substituted 1,3,5-hexatrienes in studying thermally induced 6π-electrocyclizations

Suennemann, Hans Wolf,Banwell, Martin G.,De Meijere, Armin

, p. 3879 - 3893 (2008/02/13)

An acyclic, two heterocyclic, and two bicyclic alkenylstannanes, 3, 4a, 4b, 8 and 11, respectively, were synthesized in yields ranging from 43 to 97 %, and each was subjected to a sequence of Stille and Heck couplings with 2-bromocyclohexenyl triflate (13

A one-pot sequence of Stille and Heck couplings: Synthesis of various 1,3,5-hexatrienes and their subsequent 6π-electrocyclizations

Von Zezschwitz, Paultheo,Petry, Frauke,De Meijere, Armin

, p. 4035 - 4046 (2007/10/03)

Palladium-catalyzed crosscoupling reactions of 2-bromocyclohex1-enyl triflates 7 and 11 with a variety of alkenylstannanes occurred chemoselectively at the site of the triflate leaving group to give bromobutadienes which readily underwent Heck reactions w

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