131829-49-7 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-3-Amino-3-(2-furyl)-propanoic acid is used as a building block in the synthesis of pharmaceuticals and other organic compounds. Its unique structure and properties allow it to be incorporated into the development of new drugs, potentially leading to innovative therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-3-Amino-3-(2-furyl)-propanoic acid is utilized for its potential biological activity and structural properties. Its furan ring and amino group can be exploited to design and develop novel drug candidates with specific therapeutic targets and mechanisms of action.
Further research and studies are required to fully explore the potential uses and applications of (S)-3-Amino-3-(2-furyl)-propanoic acid, as well as to understand its biological activity and therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 131829-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,8,2 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 131829-49:
(8*1)+(7*3)+(6*1)+(5*8)+(4*2)+(3*9)+(2*4)+(1*9)=127
127 % 10 = 7
So 131829-49-7 is a valid CAS Registry Number.
131829-49-7Relevant 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
Burkholderia cepacia lipase is an excellent enzyme for the enantioselective hydrolysis of β-heteroaryl-β-amino esters
Tasnadi, Gabor,Forro, Eniko,Fueloep, Ferenc
experimental part, p. 1771 - 1777 (2009/12/28)
The enantioselective (E >200) lipase PS-catalysed hydrolysis of β-heteroaryl-β-amino esters is described. The reactions were performed with H2O (0.5 equiv) in either diisopropyl ether or tert-butyl methyl ether at 25 °C. The resulting β-heteroaryl-substituted β-amino acid enantiomers were formed in high enantiomeric excess (ee ≥ 97%) and in good yield (≥40%).
