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Z-glycyl-4,6-O-benzylideneglucosaminylalanine methyl ester is a complex organic compound that belongs to the class of glycosyl amino acids. It is characterized by a glycosidic bond between a glucosamine moiety and an alanine residue, with the latter being modified by a benzylidene group at the 4,6-positions. The compound is further protected by a Z-group (benzyloxycarbonyl), which is a common protecting group in peptide synthesis to prevent unwanted side reactions. The methyl ester group indicates that the carboxylic acid function of the alanine is esterified, which can be important for solubility and reactivity in certain chemical reactions. Z-glycyl-4,6-O-benzylideneglucosaminylalanine methyl ester is typically used in the synthesis of complex carbohydrates, glycopeptides, and other biomolecules, where the controlled addition of sugar moieties is required. Its structure provides a stable intermediate that can be further modified or incorporated into larger molecules in a controlled manner.

79943-47-8

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79943-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79943-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,4 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79943-47:
(7*7)+(6*9)+(5*9)+(4*4)+(3*3)+(2*4)+(1*7)=188
188 % 10 = 8
So 79943-47-8 is a valid CAS Registry Number.

79943-47-8Relevant academic research and scientific papers

SYNTHESIS OF PEPTIDES CONTAINING D-GLUCOSAMINIC ACID, II. SYNTHESIS OF SOME TRI- AND HEXAPEPTIDES

Gall-Istok, K.,Zara-Kaczian, E.,Kisfaludy, L.,Deak, Gy.

, p. 221 - 230 (2007/10/02)

Using the azide method of fragment condensation, the acetates of the tripeptides glycylalanyl-4,6-O-benzylideneglucosaminic amide, glycyl-4,6-O-benzylideneglucosaminylalanine amide, 4,6-O-benzylideneglucosaminylglycylalanine amide and that of the hexapept

SYNTHESIS OF PEPTIDES CONTAINING D-GLUCOSAMINIC ACID, I. SYNTHETIC METHODS

Deak, Gy.,Gall-Istok, K.,Zara-Kaczian, E.,Kisfaludy, L.

, p. 375 - 384 (2007/10/02)

The azide method has been found suitable for the preparation of peptides containing D-glucosaminic acid as the N-terminal amino acid, protected from lactonization in the form of the 4,6-O-benzylidene derivative.When acted upon by dicyclohexylcarbodiimide,

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