62247-22-7 Usage
General Description
Ethyl 3-amino-3-(pyridin-3-yl)propanoate is a chemical compound with the molecular formula C11H14N2O2. It is a derivative of propanoic acid and contains a pyridine ring. ethyl 3-aMino-3-(pyridin-3-yl)propanoate is often used in pharmaceutical research and development as a building block for the synthesis of various drug molecules. It has potential applications in the development of new medications for the treatment of neurological disorders, cancer, and other diseases. Ethyl 3-amino-3-(pyridin-3-yl)propanoate may also be used in the field of organic chemistry as a reagent for the preparation of complex organic compounds. However, it is important to handle this chemical with care, as it may pose hazards to human health and the environment.
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 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%).
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
