Some scientific research about (R)-4-Phenyloxazolidin-2-one

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One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 90319-52-1, Name is (R)-4-Phenyloxazolidin-2-one, formurla is C9H9NO2. In a document, author is Wardell, James L., introducing its new discovery. Recommanded Product: 90319-52-1.

Racemic mefloquinium chlorodifluoroacetate: crystal structure and Hirshfeld surface analysis

In the racemic title molecular salt, C17H17F6N2O+center dot C2ClF2O3-(systematic name: 2-{[2,8-bis(trifluoromethyl) quinolin-4-yl](hydroxy) methyl} piperidin-1-ium chlorodifluoroacetate), the cation, which is protonated at the piperidine N atom, has the shape of the letter, L, with the piperidin-1-ium group being approximately orthogonal to the quinolinyl residue [the C-q-C-m-C-m-N-a (q = quinolinyl; m = methine; a = ammonium) torsion angle is 177.79 (18)degrees]. An intramolecular, charge-assisted ammonium-N-H center dot center dot center dot O(hydroxyl) hydrogen bond ensures the hydroxy-O and ammonium-N atoms lie to the same side of the molecule [O-h-C-m-C-m-N-a (h = hydroxyl) = -59.7 (2)degrees]. In the crystal, charge-assisted hydroxyl-O-H center dot center dot center dot O- (carboxylate) and ammonium-N+-H center dot center dot center dot O-(carboxylate) hydrogen bonds generate a supramolecular chain along [010]; the chain is consolidated by C-H center dot center dot center dot O interactions. Links between chains to form supramolecular layers are of the type C-Cl center dot center dot center dot pi (quinolinyl-C-6) and the layers thus formed stack along the a-axis direction without directional interactions between them. The analysis of the calculated Hirshfeld surface points to the dominance of F center dot center dot center dot H contacts to the surface (40.8%) with significant contributions from F center dot center dot center dot F (10.5%) and C center dot center dot center dot F (7.0%) contacts.

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Reference:
Oxazolidine – Wikipedia,
,Oxazolidine | C3H7NO – PubChem