6637-22-5

Basic information

• Product Name: 2,3-DIMETHYL-6-METHOXYQUINOXALINE
• Synonyms: 2,3-DIMETHYL-6-METHOXYQUINOXALINE;6-methoxy-2,3-dimethylquinoxaline;EINECS 229-636-9
• CAS NO: 6637-22-5
• Molecular Formula: C₁₁H₁₂N₂O
• Molecular Weight: 188.23
• EINECS: 229-636-9
• Mol File: 6637-22-5.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 300.8 °C at 760 mmHg
• Flash Point: 103.5 °C
• Appearance: /
• Density: 1.13 g/cm³
• Vapor Pressure: 0.00195mmHg at 25°C
• Refractive Index: 1.595
• CAS DataBase Reference: 2,3-DIMETHYL-6-METHOXYQUINOXALINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIMETHYL-6-METHOXYQUINOXALINE(6637-22-5)
• EPA Substance Registry System: 2,3-DIMETHYL-6-METHOXYQUINOXALINE(6637-22-5)

Safety Data

• Hazardous Substances Data: 6637-22-5(Hazardous Substances Data)

Usage

General Description

2,3-Dimethyl-6-methoxyquinoxaline is a chemical compound with the molecular formula C11H12N2O. It is a heterocyclic compound with a quinoxaline ring, two methyl groups, and a methoxy group. 2,3-DIMETHYL-6-METHOXYQUINOXALINE has potential applications in pharmaceuticals, as it has been studied for its potential anti-inflammatory and neuroprotective properties. It is also used as a building block in the synthesis of various organic compounds, making it a valuable tool in organic chemistry research. However, its specific properties and potential uses are still being investigated, and further research is needed to fully understand its applications.

InChI:InChI=1/C11H12N2O/c1-7-8(2)13-11-6-9(14-3)4-5-10(11)12-7/h4-6H,1-3H3

Upstream product

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Relevant articles and documents

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.

Hydrogen Auto-transfer Synthesis of Quinoxalines from o-Nitroanilines and Biomass-based Diols Catalyzed by MOF-derived N,P Co-doped Cobalt Catalysts

A Co-based heterogeneous catalyst supported on N,P co-doped porous carbon (Co@NCP) is prepared via a facile in-situ doping-carbonization method. The Co@NCP composite features a large surface area, high pore volume, high-density and strong basic sites. Furthermore, doping of P atoms can regulate the electronic density of Co. Therefore, Co@NCP exhibits good performance for the synthesis of quinoxalines from o-nitroanilines and biomass-derived diols under alkali-free conditions.

Nickel-Catalyzed Direct Synthesis of Quinoxalines from 2-Nitroanilines and Vicinal Diols: Identifying Nature of the Active Catalyst

The inexpensive and simple NiBr2/1,10-phenanthroline system-catalyzed synthesis of a series of quinoxalines from both 2-nitroanilines and 1,2-diamines is demonstrated. The reusability test for this system was performed up to the seventh cycle, which afforded good yields of the desired product without losing its reactivity significantly. Notably, during the catalytic reaction, the formation of the heterogeneous Ni-particle was observed, which was characterized by PXRD, XPS, and TEM techniques.