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(2S,1'R)-N2-(1-Carboxyethyl)lysin is a synthetic derivative of the natural amino acid lysine, characterized by its specific stereochemistry, with the 2S and 1'R configurations. (2S,1'R)-N2-(1-Carboxyethyl)lysin features a carboxyethyl group attached to the nitrogen atom at the second position of the lysine molecule, which introduces a carboxylic acid functionality to the molecule. This modification can significantly alter the chemical properties and reactivity of the lysine, potentially affecting its solubility, stability, and ability to form complexes with other molecules. Such derivatives are often studied in biochemistry and medicinal chemistry for their potential applications in drug development, as they can serve as building blocks for new pharmaceuticals or as probes to understand protein structure and function.

4382-14-3

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4382-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4382-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4382-14:
(6*4)+(5*3)+(4*8)+(3*2)+(2*1)+(1*4)=83
83 % 10 = 3
So 4382-14-3 is a valid CAS Registry Number.

4382-14-3Downstream Products

4382-14-3Relevant academic research and scientific papers

Amino Acids, 5. - Stereoselective Synthesis of α,α'-Imino Dicarboxylic Acids

Effenberger, Franz,Burkard, Ulrike

, p. 334 - 358 (2007/10/02)

The trifluoromethanesulfonates 1, 11, and 26, resp., of enantiomerically pure lactates, β-phenyllactates, and dimethyl α-hydroxyglutarate (25) react with (S)- and (R)-α-amino acid esters 2, 5, 8, 14, 17, 20, and 23, resp., to yield diastereoselectively th

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