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(1Z,3E)-1,4-diphenyl-2-(ethoxycarbonyl)-1,3-butadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

334024-11-2

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334024-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 334024-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,0,2 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 334024-11:
(8*3)+(7*3)+(6*4)+(5*0)+(4*2)+(3*4)+(2*1)+(1*1)=92
92 % 10 = 2
So 334024-11-2 is a valid CAS Registry Number.

334024-11-2Downstream Products

334024-11-2Relevant academic research and scientific papers

Cobalt-catalyzed regio- and stereoselective intermolecular enyne coupling: An efficient route to 1,3-diene derivatives

Mannathan, Subramaniyan,Cheng, Chien-Hong

supporting information; experimental part, p. 1923 - 1925 (2010/06/20)

The reaction of alkynes with vinyl arenes or vinyl trimethyl silane in the presence of a cobalt(II) complex, Zn and ZnI2 in CH 2Cl2 at rt to 50 °C provides 1,3-dienes in good to excellent yields. The Royal Society of Chemistry 2010.

A new manifold for the Morita reaction: Diene synthesis from simple aldehydes and acrylates/acrylonitrile mediated by phosphines

Palmelund, Anders,Myers, Eddie L.,Tai, Lik Ren,Tisserand, Steve,Butts, Craig P.,Aggarwal, Varinder K.

, p. 4128 - 4130 (2008/09/16)

Dienes have been formed with good stereoselectivity and in good yield from simple aldehydes and acrylates/acrylonitrile in the presence of a phosphine and a Lewis acid through a modification of the Morita reaction. The Royal Society of Chemistry.

A Convenient Horner-Emmons Approach to the Synthesis of Substituted Ethyl 1,3-Butadiene-2-carboxylates, and Related Compounds

Janecki, Tomasz,Bodalski, Ryszard

, p. 506 - 510 (2007/10/02)

The Horner-Emmons reaction of the allylphosphonates 3 with aldehydes gives substituted 1,3-butadiene-2-carboxylates 12 in satisfactory yields.By suitable modification of reactants a variety of 3-alkenyl-2(5H)-furanones 13 and 3-alkenylcoumarins 14 are pre

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