20420-56-8

Basic information

• Product Name: di[1,2,4]triazolo[4,3-a:3,4-c]quinoxaline
• Synonyms: di[1,2,4]triazolo[4,3-a:3,4-c]quinoxaline
• CAS NO: 20420-56-8
• Molecular Formula: C10H6N6
• Molecular Weight: 210.2
• Mol File: 20420-56-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: di[1,2,4]triazolo[4,3-a:3,4-c]quinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: di[1,2,4]triazolo[4,3-a:3,4-c]quinoxaline(20420-56-8)
• EPA Substance Registry System: di[1,2,4]triazolo[4,3-a:3,4-c]quinoxaline(20420-56-8)

Safety Data

• Hazardous Substances Data: 20420-56-8(Hazardous Substances Data)

Upstream product

• 73029-86-4 2,3-bis(hydrazino)quinoxaline 
• 122-51-0 orthoformic acid triethyl ester 
• 2213-63-0 2,3-dichloroquinoxaline 

Relevant articles and documents

Synthesis and antimicrobial activity of some novel quinoxalines

2-Hydrazino-3-chloroquinoxaline 2 was prepared and reacted with active methylene compounds, potassium thiocyanate, carbon disulfide, phenylisothiocyanate, acetic acid, ethyl chloroformate, triethyl orthoformate, and Lawessen's reagent (LR) to give a new class of fused quinoxalines 4-16, respectively. Also, 2,3-dihydrazinoquinoxaline 3 was prepared and reacted with carbon disulfide, phenyl isothiocyanate, and triethyl orthoformate to give the corresponding di[1,2,4] triazolo-[4,3-a:3′,4′-c]-quinoxalines 17-19, respectively. Reaction of 3 with LR gave the corresponding di[1,2,4,3] triazophospholo[4,5-a:5′,4′-c]quinoxaline-1,6-dithione (20). It was found that all synthesized compounds exhibit antimicrobial activity and that compound 20 had a broad spectrum of activity. Copyright Taylor & Francis Group, LLC.