52736-71-7

Usage

Uses

Used in Pharmaceutical Industry:
2,3-DIMETHYL-6,7-DICHLOROQUINOXALINE is used as a building block in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Organic Electronic Materials:
2,3-DIMETHYL-6,7-DICHLOROQUINOXALINE is used as a potential component in the field of organic electronic materials, owing to its unique molecular structure that may offer specific properties for electronic applications.
Used in Biomedical Research:
2,3-DIMETHYL-6,7-DICHLOROQUINOXALINE is used in research for its potential biological activities, such as anti-cancer and anti-inflammatory properties, which could lead to the discovery of new treatments and therapies.

InChI:InChI=1/C10H8Cl2N2/c1-5-6(2)14-10-4-8(12)7(11)3-9(10)13-5/h3-4H,1-2H3

Upstream product

• 3298-96-2 2,3-bis(bromomethyl)-6,7-dichloroquinoxaline 
• 5348-42-5 4,5-Dichloro-1,2-phenylenediamine 
• 513-86-0 3-hydroxy-2-butanon 
• 6641-64-1 4,5-dichloro-2-nitroaniline 
• 513-85-9 2.3-butanediol 

Relevant academic research and scientific papers

NaOH-Mediated Direct Synthesis of Quinoxalines from o-Nitroanilines and Alcohols via a Hydrogen-Transfer Strategy

A NaOH-mediated sustainable synthesis of functionalized quinoxalines is disclosed via redox condensation of o-nitroamines with diols and α-hydroxy ketones. Under optimized conditions, various o-nitroamines and alcohols are well tolerated to generate the desired products in 44-99% yields without transition metals and external redox additives.

Green and efficient synthesis of quinoxaline derivatives via ceric ammonium nitrate promoted and in situ aerobic oxidation of α-hydroxy ketones and α-keto oximes in aqueous media

The direct conversion of α-hydroxy ketones and α-keto oximes into quinoxaline derivatives in the presence of a catalytic amount of ceric ammonium nitrate via metal-catalyzed aerobic oxidation followed by in situ trapping with aromatic 1,2-diamines in water as a green and efficient reaction media, is reported.

Quinoxalino-fused sultines and their application in Diels-Alder reactions

The synthesis of 7,8-disubstituted quinoxalino[2,3-d]-[1,2λ4]oxathiine 2-oxides 7a-c, precursors for quinoxalino-o-quinodimethanes 3a-c, and their application in the Diels-Alder reactions are reported.