One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, name: 2,3-Dichloroquinoxaline, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 2213-63-0, Name is 2,3-Dichloroquinoxaline, molecular formula is C8H4Cl2N2
Heterocyclic Systems Containing Bridgehead Nitrogen Atom: Synthesis of 2,3-Dihydrothiazolo<3',2':2,3><1,2,4>triazino<5,6-b>indole, 4H-2,3-Dihydro<1,3>thiazino<3',2':2,3><1,2,4>triazino<5,6-b>indole and Related Heterocycles
8-Bromo-5H-2,3-dihydro-1,2,4-triazino<5,6-b>indole-3-thione (II) on condensation with 1,2-dibromoethane and 1,3-dibromopropane gives the cyclized products 7-bromo-2,3-dihydrothiazolo<3',2':2,3><1,2,4>triazino<5,6-b>indole (III) and 4H-8-bromo-2,3-dihydro<1,3>thiazino<3',2':2,3><1,2,4>triazino<5,6-b>indole (IV) respectively, and not the angular isomers VI and VII.The unequivocal synthesis of the latter (VI and VII) has been accomplished by the reaction of 5-bromoisatin-3-thiosemicarbazone (I) with 1,2-dibromoethane and 1,3-dibromopropane respectively.Condensation of II with 2,3-dichloroquinoxaline on the other hand, yields the angular isomer 3-bromoquinoxalino<2',3':4,5>thiazolo<2,3-c>indolo<2,3-e><1,2,4>triazine (V), identical with a sample obtained unambigously by the reaction of I with 2,3-dichloroquinoxaline.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, name: 2,3-Dichloroquinoxaline, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 2213-63-0
Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1462 | ChemSpider