One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Recommanded Product: 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
Condensed bridgehead nitrogen heterocyclic systems: Synthesis and bioactivity of 2,3-dihydrothiazolo[3?,2?: 2,3]-as-triazino[5,6-b] indole, 2,3-dihydro-4H-[1,3]thiazino[3?,2?: 2,3]-as-triazino[5,6-b]indole and quinoxalino[2?,3?: 4,5]thiazolo[3,2-b]indolo[2,3-e]-as-triazine and their isomeric systems
2,3-Dihydro-8-isopropyl-5H-as-triazino[5,6-b]indole-3-thione 2 on condensation with 1,2-dibromoethane, 1-3-dibromopropane and 2,3-dichloroquinoxaline gives the cyclized products, 7-isopropyl-2,3-dihydrothiazolo[3?,2?:2,3]-as-triazino[5,6-b] indole 3, 2,3-dihydro-8-isopropyl-4H-[1,3]thiazino[3?,2?:2,3]-as-triazino [5,6-b]indole 4 and 9-isopropylquinoxalino[2?,3?: 4,5]thiazolo[3,2-b]indolo[2,3-e]-as-triazine 5, respectively and not the angular isomers, 7-isopropyl-2;3-dihydro[2?,3?:3,4]-as-triazino[5,6-b]indole 6, 8-isopropyl-1H-2,3-dihydro[1,3]thiazino[2?,3?:3,4]-as-triazino [5,6-b]indole 7 and 3-isopropyl-quinoxalino [2?,3?:4,5]thiazolo[2,3-c]indolo[2,3-e]-as-triazine 8. The unequivocal synthesis of the latter 6, 7 and 8 has been accomplished by reaction of 5-isopropylisatin-3-thiosemicarbazone 1 with 1,2-dibromoethane, 1,3-dibromopropane and 2,3-dichloroquinoxaline, respectively. The bioactivity of the synthesized compounds have also been evaluated.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Recommanded Product: 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 | C8H6N1458 | ChemSpider