1192069-13-8 Usage
Uses
Used in Pharmaceutical Industry:
(S)-3-amino-3-(2-thienyl)propanoic acid hydrochloride is used as a building block for the development of drugs targeting central nervous system disorders. Its unique structure and properties allow for the creation of novel therapeutic agents that can potentially address various neurological conditions.
Used in Research and Development:
In the field of medicinal chemistry, (S)-3-amino-3-(2-thienyl)propanoic acid hydrochloride serves as a valuable compound for research and development. Its chiral nature and the presence of the thienyl group make it an attractive candidate for the synthesis of new drugs and the exploration of its potential therapeutic effects on the central nervous system.
Used in Drug Design and Synthesis:
(S)-3-amino-3-(2-thienyl)propanoic acid hydrochloride is utilized as a key component in drug design and synthesis. Its structural features can be exploited to create new molecules with improved pharmacological properties, potentially leading to the development of more effective treatments for central nervous system disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 1192069-13-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,0,6 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1192069-13:
(9*1)+(8*1)+(7*9)+(6*2)+(5*0)+(4*6)+(3*9)+(2*1)+(1*3)=148
148 % 10 = 8
So 1192069-13-8 is a valid CAS Registry Number.
1192069-13-8Relevant articles and documents
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%).
