57948-14-8

Basic information

• Product Name: 2,3-dimethyl-4-oxido-1-oxo-quinoxaline-6-carbaldehyde
• Synonyms: 2,3-dimethyl-4-oxido-1-oxo-quinoxaline-6-carbaldehyde
• CAS NO: 57948-14-8
• Molecular Formula: C11H10N2O3
• Molecular Weight: 218.2087
• Mol File: 57948-14-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: 2,3-dimethyl-4-oxido-1-oxo-quinoxaline-6-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-dimethyl-4-oxido-1-oxo-quinoxaline-6-carbaldehyde(57948-14-8)
• EPA Substance Registry System: 2,3-dimethyl-4-oxido-1-oxo-quinoxaline-6-carbaldehyde(57948-14-8)

Safety Data

• Hazardous Substances Data: 57948-14-8(Hazardous Substances Data)

Usage

Chemical compound

2,3-dimethyl-4-oxido-1-oxo-quinoxaline-6-carbaldehyde

Derivative of quinoxaline

Contains a benzene ring fused to a pyrazine ring

Contains aldehyde group

Potential reactant in organic synthesis reactions

Contains nitrogen and oxygen atom

Potentially reactive in biological systems
Properties and uses depend on specific application and reaction conditions

InChI:InChI=1/C11H10N2O3/c1-7-8(2)13(16)11-5-9(6-14)3-4-10(11)12(7)15/h3-6H,1-2H3

Upstream product

• 57948-17-1 6-(1,3-dioxolan-2-yl)benzo[c][1,2,5]oxadiazole 1-oxide 
• 57948-15-9 5-formylbenzo[1,2-c]1,2,5-oxadiazole N¹-oxide 
• 19155-93-2 4-azido-3-nitrobenzaldehyde 
• 57948-16-0 6-[1,3]dioxolan-2-yl-2,3-dimethyl-quinoxaline 1,4-dioxide 

Downstream Products

• 57948-19-3 2,3-Dimethyl-6-<(2-oxooxazolidin-3-yl)iminomethyl>chinoxalin-1,4-dioxid 

Relevant articles and documents

Synthesis and herbicidal activity of N-oxide derivatives

As part of an ongoing program on the chemistry and biological activity of N-oxide-containing molecules, a number of novel 1,2,5-oxadiazole N-oxide, benzo[1,2-c]1,2,5-oxadiazole N-oxide, and quinoxaline N,N'-dioxide derivatives were synthesized and evaluated for their herbicidal activity. Many of these compounds exhibited moderate to good herbicidal pre-emergence activity against Triticum aestivum. Dose - response studies were done on the more representative compounds (12, 20, and 26). The most active compound, butylcarbamoylbenzo[1,2-c]1,2,5-oxadiazole N-oxide, 26, displayed herbicidal activity at concentrations as low as 24 g/ha.