One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Application In Synthesis of (R)-4-Benzyl-2-oxazolidinone, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 102029-44-7, Name is (R)-4-Benzyl-2-oxazolidinone, molecular formula is C10H11NO2
Chiral Auxiliary-Bearing Isocyanides as Synthons: Synthesis of Strongly Fluorescent (+)-5-(3,4-Dimethoxyphenyl)-4-[[N-[(4S) -2-oxo-4- (phenylmethyl) -2-oxazolidinyl] ] carbonyl] oxazole and Its Enantiomer
Both (4S-(+)-3-(isocyanoacetyl)-4-(phenylmethyl)-2-oxazolidinone (R)-1 and its enantiomer (S)-1 have been synthesized as potentially useful synthons in asymmetric synthesis. Optically active (+)-5-(3,4-dimethoxyphenyl)-4-[[N-[(4S)-2-oxo-4-(phenylmethyl)-2-oxazolidinyl]] carbonyl]oxazole(S)-2and its enantiomer (R)-2 obtained by treating 3,4-dimethoxybenzoyl chloride with (S)-1 and (R)-1, respectively, in the presence of the nonionic Superbase P(MeNCH2CH2)3N, have high fluorescence quantum yields. The molecular structure of (S)-2 obtained by X-ray means is also presented.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application In Synthesis of (R)-4-Benzyl-2-oxazolidinone, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 102029-44-7, in my other articles.
Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H2047NO – PubChem