Discovery of 2-Acetylquinoxaline

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Product Details of 25594-62-1, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 25594-62-1, in my other articles.

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Product Details of 25594-62-1, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 25594-62-1, Name is 2-Acetylquinoxaline, molecular formula is C10H8N2O

Iron-catalyzed Minisci acylation of N-heteroarenes with alpha-keto acids

An efficient and mild protocol has been developed for the Minisci acylation reactions of nitrogen-containing heteroarenes with alpha-keto acids. Distinct from the conventional Minisci acylation conditions, the chemistry was performed using non-noble metal Fe(II), instead of expensive Ag(I) salt, as catalyst. A wide range of substrates, including aliphatic or aromatic alpha-keto acids, as well as various N-heteroarenes, proved to be compatible with the protocol. Scale-up experiment also demonstrates the practicality of the approach.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Product Details of 25594-62-1, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 25594-62-1, in my other articles.

Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N762 | ChemSpider