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Diethyl (acetylamino)(3-aminobenzyl)propanedioate is a complex organic compound with the chemical formula C19H26N2O5. It is a derivative of propanedioic acid, featuring an acetylamino group and a 3-aminobenzyl group attached to the central carbon chain. This molecule is characterized by its ester linkages with two ethyl groups and an amide bond formed by the acetylamino group. It is a white crystalline solid and is soluble in organic solvents. diethyl (acetylamino)(3-aminobenzyl)propanedioate is of interest in the field of pharmaceuticals and chemical research due to its potential applications in the synthesis of various drugs and other organic compounds. Its specific properties and reactivity make it a valuable intermediate in the development of new chemical entities.

5454-72-8

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5454-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5454-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5454-72:
(6*5)+(5*4)+(4*5)+(3*4)+(2*7)+(1*2)=98
98 % 10 = 8
So 5454-72-8 is a valid CAS Registry Number.

5454-72-8Relevant academic research and scientific papers

Ribosomal Synthesis of Macrocyclic Peptides in Vitro and in Vivo Mediated by Genetically Encoded Aminothiol Unnatural Amino Acids

Frost, John R.,Jacob, Nicholas T.,Papa, Louis J.,Owens, Andrew E.,Fasan, Rudi

, p. 1805 - 1816 (2015/09/01)

A versatile method for orchestrating the formation of side chain-to-tail cyclic peptides from ribosomally derived polypeptide precursors is reported. Upon ribosomal incorporation into intein-containing precursor proteins, designer unnatural amino acids be

MACROCYCLIC PEPTIDOMIMETICS FOR ALPHA-HELIX MIMICRY

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Paragraph 00255, (2015/11/02)

Methods and compositions are provided for generating macrocyclic peptides constrained by side-chain-to-C-terminus non-peptidic tethers for use as functional and structural mimics of α-helical motifs, including in therapeutic applications. These methods can be used to produce libraries of conformationally constrained peptidomimetics to identify compounds with desired activity properties.

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