572923-19-4 Usage
Description
(S)-3-(4-ACETYLPHENYL)-4-ISOPROPYLOXAZOLIDIN-2-ONE is a chiral chemical compound belonging to the class of oxazolidinones. It is characterized by its unique structural features, including the acetylphenyl and isopropyl moieties, which contribute to its chemical and biological properties. (S)-3-(4-ACETYLPHENYL)-4-ISOPROPYLOXAZOLIDIN-2-ONE has a non-superimposable mirror image, and the (S)-enantiomer is the specific form being referred to here. It holds potential pharmacological activities and is of particular interest in the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
(S)-3-(4-ACETYLPHENYL)-4-ISOPROPYLOXAZOLIDIN-2-ONE is used as a potential candidate for the development of new antibiotics due to its antibacterial properties. It works by inhibiting bacterial protein synthesis by targeting the ribosome, making it a promising agent for combating antibiotic-resistant bacteria.
Used in Antibacterial Applications:
In the field of antibacterial research, (S)-3-(4-ACETYLPHENYL)-4-ISOPROPYLOXAZOLIDIN-2-ONE is used as an antibacterial agent for its ability to interfere with bacterial protein synthesis, thereby inhibiting bacterial growth and potentially leading to the development of novel antibiotics to address the growing issue of antibiotic resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 572923-19-4 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 572923-19:
(8*5)+(7*7)+(6*2)+(5*9)+(4*2)+(3*3)+(2*1)+(1*9)=174
174 % 10 = 4
So 572923-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO3/c1-9(2)13-8-18-14(17)15(13)12-6-4-11(5-7-12)10(3)16/h4-7,9,13H,8H2,1-3H3/t13-/m1/s1
572923-19-4Relevant articles and documents
Copper-Catalyzed One-Pot Synthesis of N -Aryl Oxazolidinones from Amino Alcohol Carbamates
Mahy, William,Plucinski, Pawel K.,Frost, Christopher G.
, p. 5020 - 5023 (2015/01/08)
An efficient sequential intramolecular cyclization of amino alcohol carbamates followed by Cu-catalyzed cross-coupling with aryl iodides under mild conditions has been developed. The reaction occurred in good yields and tolerated aryl iodides containing functionalities such as nitriles, ketones, ethers, and halogens. Heteroaryl iodides and substituted amino alcohol carbamates were also well tolerated.
Cu-catalyzed N-arylation of oxazolidinones: An efficient synthesis of the κ-opioid receptor agonist CJ-15161
Ghosh, Arun,Sieser, Janice E.,Caron, Stephane,Couturier, Michel,Dupont-Gaudet, Kristina,Girardin, Melina
, p. 1258 - 1261 (2007/10/03)
An efficient method for intermolecular N-arylation of oxazolidinones using catalytic copper in the presence of a bidentate ligand is reported. The conditions allow the use of copper and can be used to prepare enantiopure N-aryl β-amino alcohols. A short,