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Z-Gly-Ala-OEt, also known as Z-glycylalanine ethyl ester, is a peptide derivative that consists of a glycine (Gly) and an alanine (Ala) residue connected by a peptide bond, with an ethyl ester (OEt) group attached to the carboxylic acid terminus. Z-Gly-Ala-OEt is a protected amino acid, where the "Z" group (benzyloxycarbonyl) is a protecting group that shields the amino group, preventing unwanted side reactions during peptide synthesis. Z-Gly-Ala-OEt is commonly used in the field of organic chemistry and peptide chemistry, particularly in the synthesis of larger peptides and proteins, as the protecting groups can be selectively removed at appropriate stages of the synthesis process.

4066-23-3

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4066-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4066-23-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4066-23:
(6*4)+(5*0)+(4*6)+(3*6)+(2*2)+(1*3)=73
73 % 10 = 3
So 4066-23-3 is a valid CAS Registry Number.

4066-23-3Relevant academic research and scientific papers

A New Synthesis of Peptides from Azides and Unactivated Carboxylic Acids

Zaloom, Jeffrey,Calandra, Michael,Roberts, David C.

, p. 2601 - 2603 (2007/10/02)

The title reaction, in which an azido compound is treated first with a tertiary phosphine, followed by warming in an inert solvent with a carboxylic acid, has been used to synthesize a number of small peptides and appears from mechanistic studies to proceed via a pentacoordinate phosphorus intermediate.

OPTICALLY ACTIVE N-HYDROXYTARTRIMIDES FOR ENANTIOSELECTIVE PEPTIDE SYNTHESIS

Teramoto, Takero,Deguchi, Mikito,Kurosaki, Toshikazu,Okawara, Makoto

, p. 1109 - 1112 (2007/10/02)

Preparations of optically active N-hydroxytartrimides were achieved. 1,3,4-Trihydroxysuccinimide ester of Z-L-alanine and 1-hydroxy-3,4-diacetoxysuccinimide ester of Z-D-alanine were allowed to react with D,L-alaninate to produce L-L form and D-D form of

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