One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Application In Synthesis of 4-Benzyl-1,3-dihydroquinoxalin-2-one, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 106595-91-9, Name is 4-Benzyl-1,3-dihydroquinoxalin-2-one, molecular formula is C15H14N2O
Formal Deoxygenative Hydrogenation of Lactams Using PNHP-Pincer Ruthenium Complexes under Nonacidic Conditions
A formal deoxygenative hydrogenation of amides to amines with RuCl2(NHC)(PNHP) (NHC = 1,3-dimethylimizadol-2-ylidene, PNHP = bis(2-diphenylphosphinoethyl)amine) is described. Various secondary amides, especially NH-lactams, are reduced with H2 (3.0-5.0 MPa) to amines at a temperature range of 120-150 C with 1.0-2.0 mol % of PNHP-Ru catalysts in the presence of Cs2CO3. This process consists of (1) deaminative hydrogenation of secondary amides to generate primary amines and alcohols, (2) dehydrogenative coupling of the transient amines with alcohols to generate imines, and (3) hydrogenation of imines to give the formally deoxygenated secondary amine products.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Application In Synthesis of 4-Benzyl-1,3-dihydroquinoxalin-2-one, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 106595-91-9
Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1915 | ChemSpider