One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Safety of 3-Methylbenzofuran-2-carboxylic acid, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 24673-56-1, Name is 3-Methylbenzofuran-2-carboxylic acid, molecular formula is C10H8O3
A versatile catalyst for intermolecular direct arylation of Indoles with benzoic acids as arylating reagents
(Figure Presented) Coupled together: With a versatile catalyst system (Pd(TFA)2/Ag2CO3/propionic acid) both electron-rich and -deficient benzoic acids serve as arylating reagents for the direct functionalization of a wide rage of indoles by a combination of decarboxylation and C-H bond activation. Depending on the nature of the benzoic acids, the reaction occurs selectively at either the C2- or C3-position of indoles, which may arise from two different catalytic pathways (see scheme; TFA = trifluoroacetate).
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Safety of 3-Methylbenzofuran-2-carboxylic acid, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 24673-56-1, in my other articles.
Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H2795O – PubChem