One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, category: benzofuran, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 89424-83-9, Name is 1,3-Dihydroisobenzofuran-5-carbaldehyde, molecular formula is C9H8O2
(Chemical Equation Presented) Diastereoselective aldol reactions of chlorotitanium enolate derived from 20-hydroxypropiophenone are reported. The corresponding aldol products were prepared in moderate to excellent yields. In general, the expected syn diastereoisomers were obtained. Utilization of trans-cinnamaldehyde, 4-methoxybenzaldehyde, and 4-butoxybenzaldehyde in the aldol reaction afforded mainly unexpected anti aldol adducts. Three reasonable transition states for the reactions have been assigned to explain the diastereochemical outcome of the process depending on substitution pattern on aldehydes. This transition-state model using alkoxy at the 4-position of aromatic aldehydes considerably amplifies the synthetic utility of aldol reaction in diastereoselective synthesis. Copyright Taylor & Francis Group, LLC.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. category: benzofuran, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 89424-83-9, in my other articles.
Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H1266O – PubChem