572923-07-0 Usage
Description
(S)-4-ETHYL-3-(4-METHOXYPHENYL)OXAZOLIDIN-2-ONE is a chemical compound with the molecular formula C13H17NO3, belonging to the class of oxazolidinones. As an enantiomer, it possesses a chiral center and exists in two mirror-image forms. (S)-4-ETHYL-3-(4-METHOXYPHENYL)OXAZOLIDIN-2-ONE is recognized for its biological and pharmaceutical activities, with its ethyl and methoxyphenyl groups offering unique properties for applications in medicine and agriculture.
Uses
Used in Pharmaceutical Industry:
(S)-4-ETHYL-3-(4-METHOXYPHENYL)OXAZOLIDIN-2-ONE is used as an intermediate in the synthesis of pharmaceuticals due to its antimicrobial and antibacterial properties. Its unique structure allows for the development of new drugs targeting various medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-4-ETHYL-3-(4-METHOXYPHENYL)OXAZOLIDIN-2-ONE is used as a component in the development of new agrochemicals, leveraging its antimicrobial properties to protect crops from harmful bacteria and other pathogens, thereby enhancing agricultural productivity and crop quality.
Check Digit Verification of cas no
The CAS Registry Mumber 572923-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,2,9,2 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 572923-07:
(8*5)+(7*7)+(6*2)+(5*9)+(4*2)+(3*3)+(2*0)+(1*7)=170
170 % 10 = 0
So 572923-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO3/c1-3-9-8-16-12(14)13(9)10-4-6-11(15-2)7-5-10/h4-7,9H,3,8H2,1-2H3/t9-/m0/s1
572923-07-0Relevant articles and documents
Palladium-catalyzed synthesis of N-aryloxazolidinones from aryl chlorides
Ghosh, Arun,Sieser, Janice E.,Riou, Maxime,Cai, Weiling,Rivera-Ruiz, Luis
, p. 2207 - 2210 (2007/10/03)
(Matrix presented) An efficient method for intermolecular N-arylation of oxazolidinones using Pd2dba3 and various phosphine ligands in the presence of a weak base is reported. The conditions allow the use of cheaper aryl chlorides containing functionalities such as enolizable ketones, amides, etc., which would be incompatible with other coupling methods. The coupling reaction can be used to prepare enantiopure N-aryl β-amino alcohols. Depending on the stereoelectronic nature of the aryl chloride, careful choice of ligand was necessary for the success of these reactions.
