718596-77-1 Usage
Uses
Used in Academic Research:
(S)-3-Amino-3-(4-cyano-phenyl)-propionic acid is used as a subject of study in academic research for its unique structural features and potential applications in synthetic chemistry. Researchers are interested in exploring its properties, reactivity, and possible interactions with other compounds.
Used in Synthetic Chemistry:
In the field of synthetic chemistry, (S)-3-Amino-3-(4-cyano-phenyl)-propionic acid is used as a building block or intermediate in the synthesis of more complex molecules. Its amino acid backbone and functional groups make it a valuable component in the development of novel chemical entities.
Used in Peptide Synthesis:
(S)-3-Amino-3-(4-cyano-phenyl)-propionic acid is used as a component in peptide synthesis, where its amino acid structure can be incorporated into larger peptide chains. This may have potential applications in the development of new pharmaceuticals or bioactive molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 718596-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,8,5,9 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 718596-77:
(8*7)+(7*1)+(6*8)+(5*5)+(4*9)+(3*6)+(2*7)+(1*7)=211
211 % 10 = 1
So 718596-77-1 is a valid CAS Registry Number.
718596-77-1Relevant academic research and scientific papers
Development of a commercial process for (S)-β-phenylalanine (1)
Grayson, J. Ian,Roos, Juergen,Osswald, Steffen
scheme or table, p. 1201 - 1206 (2011/12/16)
The development of a commercial manufacturing route for (S)-β-phenylalanine 8, a key pharmaceutical building block, is described. The different approaches which were investigated, based on catalytic asymmetric hydrogenation of enamide intermediates and on biocatalysis using acylase and lipase hydrolyses, are compared. The lipase resolution route was chosen for scale-up, and the final two-step process, based on readily available raw materials, is shown to be robust at full manufacturing scale
Synthesis of the enantiomers and N-protected derivatives of 3-amino-3-(4-cyanophenyl)propanoic acid
Solymar, Magdolna,Kanerva, Liisa T.,Fueloep, Ferenc
, p. 1893 - 1897 (2007/10/03)
Racemic ethyl 3-amino-3-(4-cyanophenyl)propanoate was synthesized and the enantiomers separated through enantioselective N-acylation by Candida antarctica lipase A (CAL-A) in neat butyl butanoate. The free amino acid enantiomers were transformed to the Boc and Fmoc-protected derivatives.
