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"N-(N-benzyloxycarbonyl-α-L-glutamyl)-glycine ethyl ester" is a complex organic compound with the molecular formula C18H22N2O6. It is a peptide derivative, specifically a dipeptide, which is formed by the condensation of two amino acids: N-benzyloxycarbonyl-α-L-glutamic acid and glycine. The N-benzyloxycarbonyl group is a protecting group used in peptide synthesis to prevent unwanted side reactions. The α-L-glutamyl part indicates that the glutamic acid is in its natural L-configuration and is linked to the next amino acid through an α-peptide bond. The glycine ethyl ester part suggests that the carboxylic acid group of glycine is esterified with ethanol, which can affect the compound's solubility and reactivity. N-(N-benzyloxycarbonyl-α-L-glutamyl)-glycine ethyl ester is often used in the synthesis of larger peptides and proteins, where the protecting group is later removed to allow further reactions or to cleave the peptide from a resin during solid-phase peptide synthesis.

4587-40-0

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4587-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4587-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,8 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4587-40:
(6*4)+(5*5)+(4*8)+(3*7)+(2*4)+(1*0)=110
110 % 10 = 0
So 4587-40-0 is a valid CAS Registry Number.

4587-40-0Relevant academic research and scientific papers

Phosphonium salt and its use

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, (2008/06/13)

The amidation and esterification of carboxylic acids with amines and hydroxyl group-containing compounds, respectively, are effected without incurring the drawbacks of reaction equilibrium by the reaction of the reactants, one of which has been activated in the reactive group by contact with a phosphonium salt obtained by reacting a phosphorous ester or phosphorous monoester salt with an organic base such as pyridine and an oxidizing agent such as halogens and mono or divalent meercury halide or acetate. The amidation can be applied to the preparation of peptides by the reaction of amino acids and/or peptides in which one of the reactive groups have been protected.

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