Recommanded Product: 2,3-Dichloroquinoxaline, New research progress on 2213-63-0 in 2021. Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. 2213-63-0, Name is 2,3-Dichloroquinoxaline, molecular formula is C8H4Cl2N2. In a Article，once mentioned of 2213-63-0
The condensation of 3-n-butyl-4-amino-5-mercapto-s-triazole 1 with chloroacetic acid, alpha-haloketones, benzoin, 2,3-dichloro-quinoxaline, carbon disulphide, aromatic carboxylic acids and aromatic carboxaldehydes furnished in one step, the cyclic products, 3-n-butyl 7H-s-triazolo [3,4-b] [1,3,4] thiadiazin-6 (5H)-one 2,6-aryl-3-n-butyl-7H-s-triazolo [3,4-b] [1,3,4] thiadiazines 3,3-n-butyl-6,7-diphenyl-5H-s-triazolo [3,4-b] [1,3,4] thiadiazine 4, 3-n-butyl-5H-s-triazolo [3′,4′:2,3] [1,3,4] thiadiazino [5,6-b] quinoxaline 5,3-n-butyl-s-triazolo [3,4-b] [1,3,4] thiadiazole-6 (5H)-thione 6, 3-n-butyl-6-aryl-s-triazolo [3,4-b] [1,3,4]-thiadiazoles 7 and 6-aryl-5,6-dihydro-3-n-butyl-s-triazolo [3,4-b] [1,3,4] thiadiazoles 8 respectively. The compounds have been characterized on the basis of elemental analysis and spectral data. The antibacterial and antifungal activity of some of the compounds have also been evaluated.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Recommanded Product: 2,3-Dichloroquinoxaline, you can also check out more blogs about2213-63-0
Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1464 | ChemSpider