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2-Butenoic acid, 2-methyl-3-[[(1S)-1-phenylethyl]amino]-, methyl ester, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

428454-82-4

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428454-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 428454-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,8,4,5 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 428454-82:
(8*4)+(7*2)+(6*8)+(5*4)+(4*5)+(3*4)+(2*8)+(1*2)=164
164 % 10 = 4
So 428454-82-4 is a valid CAS Registry Number.

428454-82-4Downstream Products

428454-82-4Relevant academic research and scientific papers

The asymmetric Michael-type alkylation of chiral β-enamino esters: Critical role of a benzyl ester group in the racemization of adducts

Pizzonero, Mathieu,Hendra, Frederic,Delarue-Cochin, Sandrine,Tran Huu-Dau, Marie-Elise,Dumas, Francoise,Cave, Christian,Nour, Mohammed,D'Angelo, Jean

, p. 3853 - 3857 (2005)

In contrast with keto diester (R)-10a bearing a methyl ester group at the quaternary carbon center, the benzyl ester analogue (R)-10a partially racemized during workup, thereby revealing that the nature of the ester group at the quaternary carbon center h

Asymmetric synthesis of glutamate derivatives

Seck, Rokhayatou,Gassama, Abdoulaye,Nour, Mohammed,Demange, Luc,Cavé, Christian

, p. 51 - 62 (2017/06/19)

Analogs of glutamic acid were synthesized through the asymmetric Michael reaction using chiral acyclic β-enaminoesters and various Michael acceptors. The influence of the alkoxy group of the enaminoesters and also the nature of the olefins in the presence

Michael reaction of acyclic β-enaminoesters derived from α-alkyl-β-ketoesters and chiral α-methylbenzylamine: Stereoselective generation of quaternary carbon centres

Maiti,Ghoshal,Mukhopadhyay,Achari,Banerjee

, p. 1072 - 1080 (2007/10/03)

Michael reaction of electrophilic olefins with acyclic β-enaminoester substrates derived from α-substituted β-ketoesters and (R)- or (S)-α-methylbenzylamine under neutral conditions resulted in the enantioselective formation of quaternary centres. The add

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