One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, category: quinoxaline, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 80636-30-2, Name is 3,3-Dimethyl-3,4-dihydroquinoxalin-2(1H)-one, molecular formula is C10H12N2O
Palladium-catalyzed synthesis of quinoxaline derivatives
A palladium-catalyzed reductive N-heteroannulation of enamines derived from 2-nitrobenzenamines forming mixtures of 1,2-dihydroquinoxalines and 3,4-dihydroquinoxalin-2-ones is described. The reactions are performed using bis(dibenzylideneacetone)palladium(0), 1,3-bis(diphenylphosphino)propane, and 1,10-phenanthroline in DMF under 6 atm of carbon monoxide at 70 C.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. category: quinoxaline, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 80636-30-2, in my other articles.
Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N993 | ChemSpider