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(2Z,4E)-2-styrylbut-2-enedioic acid dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106352-52-7

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106352-52-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106352-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106352-52:
(8*1)+(7*0)+(6*6)+(5*3)+(4*5)+(3*2)+(2*5)+(1*2)=97
97 % 10 = 7
So 106352-52-7 is a valid CAS Registry Number.

106352-52-7Downstream Products

106352-52-7Relevant academic research and scientific papers

Decarboxylative olefination of potassium benzoates via bimetallic catalysis strategy

Khalaj, Mehdi,Ghazanfarpour-Darjani, Majid,Taheri, Saeed,Sedaghat, Sajjad,Hoseyni, Seyed Jalal

, p. 2013 - 2019 (2018/09/25)

Abstract: A novel synthesis of styrene derivatives through decaroxylative olefination of potassium benzoates with alkynes using Pd2dba3/CuBr as catalyst system has been developed. The protocol proceeded smoothly and in most cases Z-alkene was the main product. Electron-rich potassium benzoates reacted more efficiently than those of electron-deficient substrates. Heteroaromatic and electron-deficient aryl alkynes were not consistent with this transformation. Graphical abstract: [Figure not available: see fulltext.].

A homogeneous, recyclable polymer support for rh(I)-catalyzed c-c bond formation

Jana, Ranjan,Tunge, Jon A.

experimental part, p. 8376 - 8385 (2011/12/04)

A robust and practical polymer-supported, homogeneous, recyclable biphephos rhodium(I) catalyst has been developed for C-C bond formation reactions. Control of polymer molecular weight allowed tuning of the polymer solubility such that the polymer-supported catalyst is soluble in nonpolar solvents and insoluble in polar solvents. Using the supported rhodium catalysts, addition of aryl and vinylboronic acids to the electrophiles such as enones, aldehydes, N-sulfonyl aldimines, and alkynes occurs smoothly to provide products in high yields. Additions of terminal alkynes to enones and industrially relevant hydroformylation reactions have also been successfully carried out. Studies show that the leaching of Rh from the polymer support is low and catalyst recycle can be achieved by simple precipitation and filtration.

Rhodium-catalyzed regio- and stereoselective codimerization of alkenes and electron-deficient internal alkynes leading to 1,3-dienes

Shibata, Yu,Hirano, Masao,Tanaka, Ken

supporting information; experimental part, p. 2829 - 2831 (2009/05/27)

(Chemical Equation Presented) A cationic rhodium(I)/H8-BINAP complex catalyzes codimerization of alkenes bearing no r-hydrogen and electron-deficient internal alkynes, leading to 1,3-dienes in good yields with moderate to excellent regio- and stereoselectivity. The same complex also catalyzes codimerization of an acrylate and phenyl-substituted electron-rich internal alkynes, leading to 1,3-dienes.

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