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Z-L-Pro-L-Val-OEt, also known as N-benzyloxycarbonyl-L-prolyl-L-valine ethyl ester, is a peptide derivative that consists of three amino acids: L-proline, L-valine, and a protecting group, N-benzyloxycarbonyl (Z). The ethyl ester (OEt) group is attached to the carboxylic acid end, making it a useful compound in peptide synthesis. This specific sequence of amino acids is not found in any known natural proteins, but it can be used as a building block for the creation of novel peptides with potential applications in drug development, research, and other biotechnological fields. The Z group serves as a temporary protecting group that shields the amino group during peptide synthesis, preventing unwanted side reactions, and is later removed to reveal the free amino group.

98807-03-5

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98807-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98807-03-5 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, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 98807-03:
(7*9)+(6*8)+(5*8)+(4*0)+(3*7)+(2*0)+(1*3)=175
175 % 10 = 5
So 98807-03-5 is a valid CAS Registry Number.

98807-03-5Downstream Products

98807-03-5Relevant 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

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