23828-13-9 Usage
Description
(S)-2-[(S)-2-(2-Benzyloxycarbonylamino-acetylamino)-3-phenyl-propionylamino]-3-hydroxy-propionic acid is a complex peptide derivative with a 3-hydroxy-propionic acid core, featuring amino acid residues and functional groups such as acetyl and benzoyl moieties. Its unique molecular structure and functional groups suggest potential applications in various fields, including medicine, drug development, and organic chemistry.
Uses
Used in Pharmaceutical Industry:
(S)-2-[(S)-2-(2-Benzyloxycarbonylamino-acetylamino)-3-phenyl-propionylamino]-3-hydroxy-propionic acid is used as a potential candidate for drug development due to its complex molecular structure and the presence of functional groups that can be manipulated for various therapeutic purposes.
Used in Organic Chemistry:
In the field of organic chemistry, (S)-2-[(S)-2-(2-Benzyloxycarbonylamino-acetylamino)-3-phenyl-propionylamino]-3-hydroxy-propionic acid can be utilized as a building block or intermediate for the synthesis of more complex molecules, taking advantage of its reactive functional groups.
Further research and experimentation are required to fully explore the potential uses and properties of this compound, as its applications may extend beyond the current understanding.
Check Digit Verification of cas no
The CAS Registry Mumber 23828-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,2 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23828-13:
(7*2)+(6*3)+(5*8)+(4*2)+(3*8)+(2*1)+(1*3)=109
109 % 10 = 9
So 23828-13-9 is a valid CAS Registry Number.
23828-13-9Relevant articles and documents
TRIMETHYLSILYL CYANIDE, A REAGENT AND (CO)SOLVENT "PAR EXCELLENCE" FOR HOMOGENOUS PEPTIDE SYNTHESIS. A STRATEGY CIRCUMVENTING CLASSICAL DRAWBACKS? PART I
Antenuis, M.J.O,Becu, Chr
, p. 119 - 130 (2007/10/02)
Attention is called for a superb strategy of peptide synthesis in solution, making use of (per)silylated amino acide fragments.This old methodology may thus present renewed interest if the classical silylation is substituted by silyl cyanides during coupling.Thus, trimethylsilyl cyanide, by its pronounced silylating power affording only gaseous following-(by)products and by its excellent solubilizing properties in organic solvents, overcomes the difficulties and drawbacks that were encountered in previously described strategies that made use of extempore prepared (per)silylated amino acid residues.
