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Glycine, N-[N-[N-[(phenylmethoxy)carbonyl]glycyl]phenylalanyl]-, ethyl ester is a complex organic compound with the chemical formula C23H25NO5. It is a derivative of glycine, an amino acid, and features a phenylmethoxycarbonyl group attached to the glycine molecule. The compound is further modified with a phenylalanyl group, which is another amino acid, and an ethyl ester group. This specific arrangement of functional groups gives the compound unique properties and potential applications in various fields, such as pharmaceuticals or chemical research. The ethyl ester group suggests that it may be used in prodrug forms or as a protecting group in peptide synthesis.

4526-85-6

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4526-85-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4526-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,2 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4526-85:
(6*4)+(5*5)+(4*2)+(3*6)+(2*8)+(1*5)=96
96 % 10 = 6
So 4526-85-6 is a valid CAS Registry Number.

4526-85-6Downstream Products

4526-85-6Relevant academic research and scientific papers

Additives Based on Liquid Crystal Forming Structure Elements for Suppressing Racemization in Peptide Synthesis by the DCC- and Mixed Anhydrides Methods

Jeschkeit, H.,Strube, M.,Przybylski, J.,Miecznikowska, H.,Kupryszewski, G.

, p. 638 - 646 (2007/10/02)

A new type of additives suppressing racemization during peptide synthesis by the DCC- and mixed anhydrides methods are liquid crystal forming organic molecules or similar compounds with a specific long chain structure.The suppressing effect of the new additives was followed by the Anderson test, the modifid Young and n.m.r. tests.There was no racemization in a new Leu-enkephalin synthesis by the mixed anhydrides method with azoxybenzene as additive.

REACTION OF CARBOXYLATE SALTS WITH CYCLIC PHOSPHORAMIDATES : AMIDE BOND FORMATION BY PRIOR AMINE CAPTURE

Wakselman, M.,Acher, F.

, p. 2705 - 2708 (2007/10/02)

Tri- or tetraalkyl-ammonium carboxylates react with 2-alkylamino-2-oxo-1,3,2-benzodioxaphospholes at 25 deg C to give amides or peptides, probably by a nucleophilic attack on phosphorous followed by a cascade of intramolecular acyl transfer reaction.

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