2,3-Dichloroquinoxaline as a versatile building block for heteroaromatic nucleophilic substitution: A review of the last decade was written by Neri, Jannyely M.;Cavalcanti, Livia N.;Araujo, Renata M.;Menezes, Fabricio G.. And the article was included in Arabian Journal of Chemistry in 2020.Related Products of 2213-63-0 This article mentions the following:
An overview of the last decade on the remarkable versatility of DCQX as a substrate for SNAr reactions is described. Several examples in which DCQX reacts with N-, O-, S-, P- and C-nucleophiles, including controlled processes for the selective formation of mono- and disubstituted substrates are provided. Almost all polyfunctionalized quinoxalines synthesized using this approach have shown applications in different areas such as in biol. and technol. fields. In the experiment, the researchers used many compounds, for example, 2,3-Dichloroquinoxaline (cas: 2213-63-0Related Products of 2213-63-0).
2,3-Dichloroquinoxaline (cas: 2213-63-0) belongs to quinoxaline derivatives. Condensed heterocycles of quinoxalines have become attractive targets in synthetic and medicinal chemistry due to their significant biological activities. They are well-known for application in organic light emitting devices, polymers and pharmaceutical agents. The quinoxaline-containing polymers are applicable in optical devices due to their thermal stability and low band gap.Related Products of 2213-63-0
Referemce:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider