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Z-LEU-GLY-OH is a chemical compound composed of the amino acids leucine and glycine, with the carboxyl group of the leucine residue protected by a benzyl group, indicated by the "Z" in its name. This protection prevents unwanted reactions during peptide synthesis, making it a valuable reagent in the creation of peptide chains and a building block for peptide-based drugs.

2706-38-9

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2706-38-9 Usage

Uses

Used in Pharmaceutical Industry:
Z-LEU-GLY-OH is used as a reagent in peptide synthesis for the development of peptide-based drugs. Its specific properties allow for the creation of peptides with various biological and therapeutic activities, contributing to the advancement of pharmaceutical research and drug development.
Used in Biotechnology Industry:
Z-LEU-GLY-OH is used as a building block in the creation of peptide chains for research into protein structure and function. Its role in peptide synthesis aids in understanding the mechanisms of action and potential applications of peptides in various biotechnological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2706-38-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,0 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2706-38:
(6*2)+(5*7)+(4*0)+(3*6)+(2*3)+(1*8)=79
79 % 10 = 9
So 2706-38-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H22N2O5/c1-11(2)8-13(15(21)17-9-14(19)20)18-16(22)23-10-12-6-4-3-5-7-12/h3-7,11,13H,8-10H2,1-2H3,(H,17,21)(H,18,22)(H,19,20)/t13-/m0/s1

2706-38-9Relevant academic research and scientific papers

Amino alcohols as C-Terminal Protecting Groups in Peptide Synthesis

Kashima, Choji,Harada, Kazuo,Fujioka, Yoko,Maruyama, Tatsuya,Omote, Yoshimori

, p. 535 - 540 (2007/10/02)

The synthesis of peptides using amino alcohols as C-terminal protecting groups is described.C-Terminal protection of amino acid could be accomplished by reduction of the terminal carboxyl group to a hydroxymethyl group, and regeneration of the carboxyl group could be achieved by Jones' oxidation.This method was applied to the formation of di- and tripeptides.

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