62247-22-7 Usage
Uses
Used in Pharmaceutical Research and Development:
Ethyl 3-amino-3-(pyridin-3-yl)propanoate is used as a building block for the synthesis of various drug molecules, particularly in the development of new medications for the treatment of neurological disorders, cancer, and other diseases. Its unique structure and functional groups make it a valuable component in the design and synthesis of pharmaceutical compounds.
Used in Organic Chemistry:
In the field of organic chemistry, ethyl 3-amino-3-(pyridin-3-yl)propanoate is used as a reagent for the preparation of complex organic compounds. Its versatile structure allows for various chemical reactions and transformations, contributing to the synthesis of a wide range of organic molecules.
Used in Drug Synthesis:
Ethyl 3-amino-3-(pyridin-3-yl)propanoate is used as a key intermediate in the synthesis of various drug molecules. Its presence in the molecular structure can impart specific biological activities and properties to the final drug product, making it an essential component in the development of novel therapeutic agents.
Used in Medicinal Chemistry:
In medicinal chemistry, ethyl 3-amino-3-(pyridin-3-yl)propanoate is used as a starting material for the design and synthesis of new drug candidates. Its unique structural features and functional groups can be exploited to create molecules with specific pharmacological properties, targeting various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 62247-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62247-22:
(7*6)+(6*2)+(5*2)+(4*4)+(3*7)+(2*2)+(1*2)=107
107 % 10 = 7
So 62247-22-7 is a valid CAS Registry Number.
62247-22-7Relevant academic research and scientific papers
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%).
Lithium perchlorate mediated three-component preparation of primaryaminoesters
Saidi, Mohammad R.,Azizi, Najmoddin
, p. 72 - 74 (2007/10/03)
A three-component reaction between an aldehyde, metallated hexamethyldisilazane and a functionalized organozinc compound proceeded smoothly in the presence of LiClO4 in diethyl ether to afford primary amino esters in good yields.
Azetidine compounds and process for production
-
, (2008/06/13)
Novel azetidine, and particularly 2-pyridyl-azetidine, compounds are disclosed. These compounds are produced from amino-esters by a sequence comprising conversion to the sulfonamide, reduction of the ester to the alcohol, sulfonation of the resultant alco
