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(E)-3,4-diphenylbut-3-en-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70338-42-0

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70338-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70338-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,3 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70338-42:
(7*7)+(6*0)+(5*3)+(4*3)+(3*8)+(2*4)+(1*2)=110
110 % 10 = 0
So 70338-42-0 is a valid CAS Registry Number.

70338-42-0Relevant academic research and scientific papers

Chemoselective Luche-Type Reduction of α,β-Unsaturated Ketones by Magnesium Catalysis

Jang, Yoon Kyung,Magre, Marc,Rueping, Magnus

supporting information, p. 8349 - 8352 (2019/10/16)

The chemoselective reduction of α,β-unsaturated ketones by use of an economic and readily available Mg catalyst has been developed. Excellent yields for a wide range of ketones have been achieved under mild reaction conditions, short times, and low catalyst loadings (0.2-0.5 mol %).

Copper-catalyzed regio- and stereoselective intermolecular three-component oxyarylation of allenes

Itoh, Taisuke,Shimizu, Yohei,Kanai, Motomu

supporting information, p. 2736 - 2739 (2014/06/09)

A copper(II)-catalyzed intermolecular three-component oxyarylation of allenes using arylboronic acids as a carbon source and TEMPO as an oxygen source is described. The reaction proceeded under mild conditions with high regio- and stereoselectivity and functional group tolerance. A plausible reaction mechanism is proposed, involving carbocupration of allenes, homolysis of the intervening allylcopper(II), and a radical TEMPO trap.

Free-radical-initiated coupling reaction of alcohols and alkynes: Not co but C-C bond formation

Liu, Zhong-Quan,Sun, Liang,Wang, Jian-Guo,Han, Jie,Zhao, Yan-Kai,Zhou, Bo

supporting information; scheme or table, p. 1437 - 1439 (2009/09/07)

This work demonstrates an efficient method to prepare allylic alcohols via direct C-C bond formation using electron-rich alkynes and aliphatic alcohols initiated by tert-butyl hydroperoxide.

Chemoenzymatic dynamic kinetic resolution of allylic alcohols: A highly enantioselective route to acyloin acetates

Bogar, Krisztian,Vidal, Pilar Hoyos,Alcantara Leon, Andres R.,Baeckvall, Jan-E.

, p. 3401 - 3404 (2008/02/12)

Dynamic kinetic resolution (DKR) of a series of sterically hindered allylic alcohols has been conducted with Candida antarctica lipase B (CALB) and ruthenium catalyst 1. The optically pure allylic acetates obtained were subjected to oxidative cleavage to

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