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Z-L-Pro-D-Val-OEt, also known as N-benzyloxycarbonyl-L-proline-D-valine-ethyl ester, is a tripeptide derivative featuring a unique combination of L-proline, D-valine, and an ethyl ester group. The "Z" prefix indicates the presence of a benzyloxycarbonyl (Z) protecting group, which is commonly used in peptide synthesis to prevent unwanted side reactions. This specific arrangement of amino acids and functional groups makes Z-L-Pro-D-Val-OEt a valuable compound in the field of organic chemistry, particularly for the synthesis of peptides and other biologically active molecules. Its chiral nature, with one L-amino acid and one D-amino acid, adds to its potential applications in the development of drugs and other therapeutic agents.

98807-10-4

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98807-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98807-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,8,0 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98807-10:
(7*9)+(6*8)+(5*8)+(4*0)+(3*7)+(2*1)+(1*0)=174
174 % 10 = 4
So 98807-10-4 is a valid CAS Registry Number.

98807-10-4Downstream Products

98807-10-4Relevant 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

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