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methyl 3-(4-chlorophenyl)-3-butenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

218292-25-2

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218292-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 218292-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,2,9 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 218292-25:
(8*2)+(7*1)+(6*8)+(5*2)+(4*9)+(3*2)+(2*2)+(1*5)=132
132 % 10 = 2
So 218292-25-2 is a valid CAS Registry Number.

218292-25-2Relevant academic research and scientific papers

Highly Regioselective Palladium-Catalyzed Carboxylation of Allylic Alcohols with CO2

Mita, Tsuyoshi,Higuchi, Yuki,Sato, Yoshihiro

, p. 16391 - 16394 (2015)

Various allylic alcohols were carboxylated in the presence of a catalytic amount of PdCl2 and PPh3 using ZnEt2 as a stoichiometric transmetalation agent under a CO2 atmosphere (1atm). This carboxylation proceeded in a highly regioselective manner to afford branched carboxylic acids predominantly. The β,γ-unsaturated carboxylic acid thus obtained was successfully converted into an optically active γ-butyrolactone, a known intermediate of (R)-baclofen.

Highly regioselective palladium-catalysed oxidative allylic C-H carbonylation of alkenes

Chen, Huoji,Cai, Congbi,Liu, Xiaohang,Li, Xianwei,Jiang, Huanfeng

supporting information; experimental part, p. 12224 - 12226 (2011/12/14)

Pd-catalysed direct oxidative carbonylation of allylic C-H bonds with carbon monoxide was first described. This new procedure shows that the inherent requirement for a leaving group in the Tsuji-Trost palladium-catalysed allylic carbonylation can be lifted, which provides a new route for accessing more synthetically useful β-enoic acid esters with high regioselectivity. The Royal Society of Chemistry 2011.

An efficient synthesis of enantiomerically pure 2-[(2R)-arylmorpholin- 2-yl]ethanols, key intermediates of tachykinin receptor antagonist

Nishi, Takahide,Ishibashi, Koki,Nakajima, Katsuyoshi,Iio, Yukiko,Fukazawa, Tetsuya

, p. 3251 - 3262 (2007/10/03)

We report herein an efficient and practical synthetic method for the preparation of enantiomerically pure 2[(2R)-arylmorpholin-2-yl]ethanols 1a- d, key intermediates of tachykinin receptor antagonist. Sharpless catalytic asymmetric dihydroxylation of 4a-d was employed to introduce the required absolute stereochemistry, and cyclization of 7a-d was accomplished by the Mitsunobu reaction.

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