562817-53-2 Usage
General Description
2,6-Piperidinedione, 3-hydroxy-1-[(4-methoxyphenyl)methyl]-, (3S)- is a chemical compound with the molecular formula C13H15NO4. It is also known as (3S)-3-hydroxy-1-[(4-methoxyphenyl)methyl]piperidin-2,6-dione and belongs to the class of organic compounds known as piperidinediones. 2,6-Piperidinedione, 3-hydroxy-1-[(4-methoxyphenyl)methyl]-, (3S)- has been found to have potential antifungal and antimicrobial properties. Its 3S enantiomer is reported to have inhibitory effects on the bacterial enzyme enoyl-acyl carrier protein reductase, which makes it a potential candidate for the development of new antibacterial agents. Additionally, it has been studied for its potential use as an intermediate in the synthesis of pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 562817-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,2,8,1 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 562817-53:
(8*5)+(7*6)+(6*2)+(5*8)+(4*1)+(3*7)+(2*5)+(1*3)=172
172 % 10 = 2
So 562817-53-2 is a valid CAS Registry Number.
562817-53-2Relevant academic research and scientific papers
A general approach to (5S,6R)-6-alkyl-5-benzyloxy-2-piperidinones: Application to the asymmetric syntheses of neurokinin substance P receptor antagonist (-)-L-733,061 and (-)-deoxocassine
Liu, Liang-Xian,Ruan, Yuan-Ping,Guo, Zheng-Qing,Huang, Pei-Qiang
, p. 6001 - 6009 (2007/10/03)
A general approach to (5S,6R)-6-alkyl-5-benzyloxy-2-piperidinones based on the regio- and diastereoselective reductive alkylation of (S)-3- benzyloxyglutarimide 7 is described. This method opens an entrance to chiral nonracemic substituted 3-piperidinols.
Asymmetric synthesis of (+)-L-733, 060 and (+)-CP-99, 994 based on a new chiral 3-piperidinol synthon.
Huang, Pei-Qiang,Liu, Liang-Xian,Wei, Bang-Guo,Ruan, Yuan-Ping
, p. 1927 - 1929 (2007/10/03)
[reaction: see text] Selective and potent neurokinin substance P receptor antagonists (+)-L-733, 060 (1) and (+)-CP-99, 994 (2) have been synthesized starting from a new (3S)-piperidinol synthon derived from l-glutamic acid. The methods featured a C-2 reg
