17392-20-0

Basic information

• Product Name: 2-(2-Quinoxalinyl)phenol
• Synonyms: 2-(2-Quinoxalinyl)phenol
• CAS NO: 17392-20-0
• Molecular Formula: C₁₄H₁₀N₂O
• Molecular Weight: 0
• Mol File: 17392-20-0.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-Quinoxalinyl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-Quinoxalinyl)phenol(17392-20-0)
• EPA Substance Registry System: 2-(2-Quinoxalinyl)phenol(17392-20-0)

Safety Data

• Hazardous Substances Data: 17392-20-0(Hazardous Substances Data)

Usage

Chemical structure

A phenolic compound containing a quinoxaline ring

Common uses

Antioxidant, food preservative

Properties

Anti-inflammatory, antimicrobial

Applications

Pharmaceutical, cosmetic, protective agent against oxidative stress, potential treatment for certain diseases

Research potential

Use in new material development, precursor in organic synthesis

Upstream product

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• 62-53-3 aniline 

Relevant articles and documents

Synthesis and luminescent properties of BF2 complexes with N,O-benzazine ligands

In this study we present a synthesis of six-membered BF2complexes with N–B–O type linkage based on 2-(2-hydroxyphenyl)-4-phenylquinazolines and 2-(2-hydroxyphenyl)quinoxaline. The photophysical properties of compounds were studied by absorption

Copper-Catalyzed Cascade Cycloamination of α-Csp3-H Bond of N-Aryl Ketimines with Azides: Access to Quinoxalines

A copper-catalyzed cycloamination of α-Csp3-H bond of N-aryl ketimines with sodium azide has been developed. This methodology provides an efficient access to quinoxalines and features mild reaction conditions and readily available ketimines with diverse functional group tolerance.

Synthesis of functionalized benzimidazoles and quinoxalines catalyzed by sodium hexafluorophosphate bound Amberlite resin in aqueous medium

A very simple, eco-friendly, and versatile method for the selective synthesis of 1,2-disubstituted benzimidazoles and quinoxalines in water-methanol (1:1) mixture with the aid of resin bound hexafluorophosphate ion as catalyst is reported. The method is also effective for the incorporation of quinoxaline nucleus at the A ring of pentacyclic triterpenoid, friedelin. A plausible mechanism for the formation of disubstituted benzimidazole has also been suggested.