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Z-L-Val-D-Phe-OEt is a synthetic tripeptide compound, consisting of three amino acids: Z-L-Valine, D-Phenylalanine, and Ethyl Ester (OEt). The "Z" group is a protecting group used in peptide synthesis to prevent unwanted side reactions. L-Valine and D-Phenylalanine are amino acids, with L-Valine being one of the 20 standard amino acids used in protein synthesis, and D-Phenylalanine being a non-natural, D-enantiomeric form of the naturally occurring L-Phenylalanine. The Ethyl Ester (OEt) group is a functional group that can be used to improve the solubility and stability of the peptide. Z-L-Val-D-Phe-OEt is often used in pharmaceutical research and development, particularly in the synthesis of peptide-based drugs and as a building block for more complex peptide structures.

98807-13-7

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98807-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98807-13-7 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 98807-13:
(7*9)+(6*8)+(5*8)+(4*0)+(3*7)+(2*1)+(1*3)=177
177 % 10 = 7
So 98807-13-7 is a valid CAS Registry Number.

98807-13-7Downstream Products

98807-13-7Relevant 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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