572923-10-5 Usage
Description
(S)-4-(4-ETHYL-2-OXOOXAZOLIDIN-3-YL)BENZONITRILE is a chemical compound that belongs to the oxazolidinone class of compounds. It is a nitrile derivative with a benzene ring and a substituted oxazolidinyl group. This unique structure and functionalities make it an interesting and potentially valuable compound for further study in the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
(S)-4-(4-ETHYL-2-OXOOXAZOLIDIN-3-YL)BENZONITRILE is used as a chemical compound for the development of new drugs and medications. Its specific properties and potential uses would depend on further research and testing, but its unique structure and functionalities make it a promising candidate for creating innovative pharmaceutical solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 572923-10-5 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, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 572923-10:
(8*5)+(7*7)+(6*2)+(5*9)+(4*2)+(3*3)+(2*1)+(1*0)=165
165 % 10 = 5
So 572923-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2/c1-2-10-8-16-12(15)14(10)11-5-3-9(7-13)4-6-11/h3-6,10H,2,8H2,1H3/t10-/m0/s1
572923-10-5Relevant 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.
