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(3S,4S,5R)-5-benzyloxy-N-[(1S)-1-(tert-butoxycarbonyl)-3-methylbutyl]-3-(9-fluorenylmethoxycarbonylamino)-4-hydroxypiperidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

646057-70-7

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646057-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 646057-70-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,6,0,5 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 646057-70:
(8*6)+(7*4)+(6*6)+(5*0)+(4*5)+(3*7)+(2*7)+(1*0)=167
167 % 10 = 7
So 646057-70-7 is a valid CAS Registry Number.

646057-70-7Relevant academic research and scientific papers

Constrained Derivatives of Stylostatin 1. 1. Synthesis and Biological Evaluation as Potential Anticancer Agents

Forns, Pilar,Piró, Jordi,Cuevas, Carmen,García, Mònica,Rubiralta, Mario,Giralt, Ernest,Diez, Anna

, p. 5825 - 5833 (2003)

Hydroxyaminolactams have been used as constrained surrogates of the Ser-Leu dipeptide in the synthesis of analogues of the cycloheptapeptide stylostatin 1 (2). The rate of cyclization through formation of the Ile-Pro amide bond allowed us to prove that th

Asymmetric synthesis of β-pseudopeptides from chiral 3,4-aziridinolactams

Piro, Jordi,Forns, Pilar,Blanchet, Jerome,Bonin, Martine,Micouin, Laurent,Diez, Anna

, p. 995 - 1004 (2002)

The preparation of chiral 3,4-aziridinopiperidine-2-ones 1 and their reactivity with a range of nucleophiles has been studied. In all cases, nucleophilic attack on compounds 1 occurred exclusively at the C(3) centre, leading to the asymmetric synthesis of

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