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D-Alanine, N-[N-[(phenylmethoxy)carbonyl]-L-alanyl]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64532-72-5

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64532-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64532-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,3 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64532-72:
(7*6)+(6*4)+(5*5)+(4*3)+(3*2)+(2*7)+(1*2)=125
125 % 10 = 5
So 64532-72-5 is a valid CAS Registry Number.

64532-72-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Z-L-Ala-D-Ala-OEt

1.2 Other means of identification

Product number -
Other names N-(N-benzyloxycarbonyl-L-alanyl)-D-alanine ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64532-72-5 SDS

64532-72-5Relevant academic research and scientific papers

ENANTIOSELECTIVE SYNTHESIS OF PEPTIDES USING (1R)-3-HYDROXY-1,8,8-TRIMETHYL-3-AZABICYCLOOCTANE-2,4-DIONE ((+)-N-HYDROXYCAMPHORIMIDE) AN ACTIVE ESTER GROUP

Takeda, Kazuyoshi,Tsuboyama, Kanoko,Suzuki, Akira,Ogura, Haruo

, p. 2545 - 2548 (2007/10/02)

The enantioselective coupling reaction of N-protected amino acid (+)-N-hydroxycamphorimide esters (-OCamp) with racemic amino acid esters is discussed.The coupling reaction of several amino acids showed high enantioselectivity.Keywords-enantioselective synthesis; (+)-N-hydroxycamphorimide; peptide, active ester; coupling reaction

Facile Synthesis of Cyclic Dipeptides and Detection of Racemization

Ueda, Toshihisa,Saito, Morinobu,Kato, Tetsuo,Izumiya, Nobuo

, p. 568 - 572 (2007/10/02)

Several cyclic dipeptides were synthesized by refluxing methanolic solution of dipeptide methyl esters in high yield and purity.Cyclic dipeptides prepared by the Fischer method, the Nitecki method, and the present methanol-reflux method were compared with

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