1245644-72-7 Usage
General Description
(S)-1-benzyl-3-hydroxypiperidin-2-one is a chemical compound that belongs to the class of piperidines. It is an organic compound with the molecular formula C13H15NO2 and a molecular weight of 217.26 g/mol. (S)-1-benzyl-3-hydroxypiperidin-2-one is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It has potential applications in the development of drug molecules and can be used as a building block for the production of various pharmaceuticals and biologically active compounds. The presence of a hydroxyl group and a benzyl group in its structure gives it unique chemical properties, making it useful in the synthesis of a wide range of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1245644-72-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,6,4 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1245644-72:
(9*1)+(8*2)+(7*4)+(6*5)+(5*6)+(4*4)+(3*4)+(2*7)+(1*2)=157
157 % 10 = 7
So 1245644-72-7 is a valid CAS Registry Number.
1245644-72-7Relevant articles and documents
Electrochemical deamination of alkoxyamine lactams
Romero-Iba?ez, Julio,Cruz-Gregorio, Enrique,Cruz-Gregorio, Silvano,Quintero, Leticia,Bernès, Sylvain,González-Perea, Mario,Sartillo-Piscil, Fernando
supporting information, (2020/08/11)
An anodic electrochemical deamination of 3-alkoxyamine lactams to 3-hydroxy lactams was developed. The electrochemical transformation was achieved by using reticulated vitreous carbon (RVC) and stainless-steel electrodes in aqueous ethanolic solution of NaOAc. This simple electrochemical procedure represents an ecofriendly alternative to the traditional chemical reductive deamination, which requires of a large excess of Zn (up to 40 equivalents) and acetic acid.
Chemoenzymatic enantioselective synthesis of 3-hydroxy-2-pyrrolidinones and 3-hydroxy-2-piperidinones
Kamal, Ahmed,Ramana, K. Venkata,Ramana, A. Venkata,Babu, A. Hari
, p. 2587 - 2594 (2007/10/03)
The enantioselective synthesis of 3-hydroxypyrrolidin-2-ones and 3-hydroxy piperidin-2-ones has been carried out in high enantiomeric excess employing immobilized lipase from Pseudomonas cepacia.
