New Advances in Chemical Research, May 2021. The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry.Product Details of 59564-59-9, In a article, mentioned the application of 59564-59-9, Name is 3,4-Dihydroquinoxalin-2(1H)-one, molecular formula is C8H8N2O
The electrochemical reduction of quinoxalino<2,3-b>quinoxaline gives fluoflavine (2) the structure of which is discussed.The electrochemical reduction of fluoflavine in acidic medium leads to a hexahydroquinolino<2,3-b>quinoxaline.A reduction mechanism is proposed based on cyclic voltammetry results and preparative electrolysis.The results obtained in the case of quinoxalino<2,3-b>quinoxaline are used to rationalize the results obtained in the case of pyrazino<2,3-b>pyrazines and pyrazino<2,3-b>quinoxalines.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Product Details of 59564-59-9, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 59564-59-9, in my other articles.
Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N153 | ChemSpider