Brief introduction of 2-Chloro-3-methoxyquinoxaline

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.SDS of cas: 32998-25-7, you can also check out more blogs about32998-25-7

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.SDS of cas: 32998-25-7, In a article, mentioned the application of 32998-25-7, Name is 2-Chloro-3-methoxyquinoxaline, molecular formula is C9H7ClN2O

Reactions of 2,3-dichloroquinoxaline 1 with various acid hydrazides 2 in acetonitrile under PTC conditions give the corresponding oxadiazinoquinoxalines 3, which on reaction with sodium alkoxides in alcohol yielded the respective ring opened products i.e. 2-acylhydrazino-3-alkoxyquioxalines 4. The compound 4 has been also synthesised from 2-acylhydrazino-3-chloroquinoxaline 5, which is obtained by the reaction of 1 with 2 in DMF at room temperature.

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.SDS of cas: 32998-25-7, you can also check out more blogs about32998-25-7

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1122 | ChemSpider