517905-92-9 Usage
Uses
Used in Organic Chemistry:
FMOC-(R)-3-Amino-3-(4-cyano-phenyl)-propionic acid is used as a protected amino acid for [its role in peptide synthesis], allowing for the controlled formation of peptide bonds in complex chemical structures.
Used in Pharmaceutical Research:
In the pharmaceutical industry, FMOC-(R)-3-Amino-3-(4-cyano-phenyl)-propionic acid is used as a building block for [the development of new drugs], contributing to the synthesis of potential therapeutic agents with unique properties.
Used in Academic Research:
FMOC-(R)-3-Amino-3-(4-cyano-phenyl)-propionic acid is used as a research tool for [exploring the properties and potential applications of novel compounds], advancing the understanding of organic chemistry and its applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 517905-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,7,9,0 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 517905-92:
(8*5)+(7*1)+(6*7)+(5*9)+(4*0)+(3*5)+(2*9)+(1*2)=169
169 % 10 = 9
So 517905-92-9 is a valid CAS Registry Number.
517905-92-9Relevant articles and documents
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 (2004)
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.