73029-86-4

Basic information

• Product Name: 2,3-Quinoxalinedione, 1,4-dihydro-, dihydrazone
• Synonyms: 2,3-dihydrazino quinoxaline;2,3-bis(hydrazino)quinoxaline;quinoxalinyl-2,3-dihydrazine;2,3-Dihydrazinochinoxalin;2,3-dihydrazinylquinoxaline
• CAS NO: 73029-86-4
• Molecular Formula: C8H10N6
• Molecular Weight: 190.21
• Mol File: 73029-86-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 419.9±28.0 °C(Predicted)
• Density: 1.62±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 2,3-Quinoxalinedione, 1,4-dihydro-, dihydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Quinoxalinedione, 1,4-dihydro-, dihydrazone(73029-86-4)
• EPA Substance Registry System: 2,3-Quinoxalinedione, 1,4-dihydro-, dihydrazone(73029-86-4)

Safety Data

• Hazardous Substances Data: 73029-86-4(Hazardous Substances Data)

Usage

General Description

2,3-Quinoxalinedione, 1,4-dihydro-, dihydrazone is a compound with chemical formula C8H10N4O2 that exists in the form of a dihydrazone. It is a derivative of quinoxalinedione and is used as a reagent in organic synthesis. Its dihydrazone form makes it useful in processes such as the derivatization and determination of carbonyl compounds, as well as in the synthesis of novel organic compounds. 2,3-Quinoxalinedione, 1,4-dihydro-, dihydrazone has potential applications in pharmaceuticals, agricultural products, and materials science due to its versatile reactivity and unique molecular structure. However, it is important to handle this chemical with care as it may pose health hazards if not properly handled and stored.

Upstream product

• 15804-19-0 2,3-dihydroxyquinoxaline 
• 95-54-5 1,2-diamino-benzene 
• 15804-19-0 quinoxaline-2,3-dione 
• 2213-63-0 2,3-dichloroquinoxaline 
• 1199-03-7 1,4-dihydro-quinoxaline-2,3-dithione 

Downstream Products

• 20420-56-8 Bis-symm-triazolo<4.3-a,3.4-c>chinoxalin 
• 1361954-68-8 N₃, N₁₀-diphenylbis[1,2,4]triazolo[4,3-a:3',4'-c]quinoxalin-3,10-diamine 
• 1361954-69-9 1,6-di(4-methoxyphenyl)-1,2,5,6-tetrahydrobis[1,2,4,5]triazaphospholo[4,5-a:4',5'-c]quinoxaline-1,6-disulfide 
• 1372797-36-8 2,3-bis-(benzylidenehydrazino)quinoxaline 
• 1372797-37-9 2,3-bis-(4'-chlorobenzylidenehydrazino)quinoxaline 
• 75380-48-2 2,3-bis(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-ylazo)quinoxaline 

Relevant articles and documents

Design, Synthesis, and Characterization of Quinoxaline Derivatives as a Potent Antimicrobial Agent

A series of quinoxalinone derivatives were synthesized by the reaction of o-phenylenediamine with oxalic acid to yield 1, 4-dihydro quinoxaline-2, 3-dione (1) and then treated with thionyl chloride to yield 2, 3 dichloro quinoxaline (2). This was further reacted with hydrazine hydrate to produce 2, 3-dihydrazinyl quinoxaline (3). This was finally reacted with substituted aromatic aldehydes to produce 2,3-bis[2-(sustituted benzylidine) hydrazinyl] quinoxalines (4). These quinoxalinone derivatives were characterized by infrared spectroscopy and nuclear magnetic resonance spectroscopy and MASS spectral data. All the synthesized compounds were evaluated for their antimicrobial activity. The results of the antimicrobial study revealed that compounds 4c, 4d, and 4i were active and exhibited better inhibitory activities as compared to standard drug ciprofloxacin. The results were further checked with protein legend interaction by using docking studies, and all the compounds exhibited good docking scores between ?8.72 and ?11.29?kcal/mol against dihydrofolate reductase protein fragment from Staphylococcus aureus (PDB ID-4XE6). Among all compound, 4c has shown maximum docking score and found in agreement to in vitro studies.

Organic electroluminescence material and organic electro-electronic device

The invention provides a compound with a structure as shown as formula I. The invention also provides an application of the compound in an organic electro-electronic device and the organic electro-electronic device. The compound provided by the invention