Discovery of isoxazolinone antibacterial agents. Nitrogen as a replacement for the stereogenic center found in oxazolidinone antibacterials was written by Snyder, Lawrence B.;Meng, Zhaoxing;Mate, Robert;D’Andrea, Stanley V.;Marinier, Anne;Quesnelle, Claude A.;Gill, Patrice;DenBleyker, Kenneth L.;Fung-Tomc, Joan C.;Frosco, MaryBeth;Martel, Alain;Barrett, John F.;Bronson, Joanne J.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2004.SDS of cas: 587-88-2 This article mentions the following:
A series of potential antimicrobial derivatives possessing bioisosteric replacements for the central oxazolidinone ring found in oxazolidinone antibacterials have been prepared The design concept involved replacement of the requisite sp3-hybridized stereogenic center found at the 5-position of the oxazolidinone with a nitrogen atom. The synthesis and antibacterial activity of three such ring systems, the benzisoxazolinones, e.g., I, pyrroles, e.g., II, and isoxazolinones, e.g., III, is described. In the experiment, the researchers used many compounds, for example, Ethyl 2-(4-fluorophenyl)acetate (cas: 587-88-2SDS of cas: 587-88-2).
Ethyl 2-(4-fluorophenyl)acetate (cas: 587-88-2) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.SDS of cas: 587-88-2
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics