2,3-Di(furan-2-yl)quinoxaline

98%

Reagent Code: #131490
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CAS Number 57490-73-0

science Other reagents with same CAS 57490-73-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.26 g/mol
Formula C₁₆H₁₀N₂O₂
thermostat Physical Properties
Melting Point 131-132 °C
Boiling Point 360.5±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.272±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used in organic electronics as a fluorescent material due to its strong emission properties. Commonly applied in the development of OLEDs (organic light-emitting diodes) for display technologies and organic solar cells owing to its excellent electron transfer characteristics. Acts as a sensor component for detecting metal ions in solution, especially in environmental monitoring, and in chemical and biological sensors that respond to environmental changes via fluorescence shifts. Also investigated as a photosensitizer in photodynamic therapy for cancer treatment. Its planar structure and electron-deficient core make it suitable for use in supramolecular chemistry and molecular recognition systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,500.00
inventory 250mg
10-20 days ฿24,620.00

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2,3-Di(furan-2-yl)quinoxaline
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Used in organic electronics as a fluorescent material due to its strong emission properties. Commonly applied in the development of OLEDs (organic light-emitting diodes) for display technologies and organic solar cells owing to its excellent electron transfer characteristics. Acts as a sensor component for detecting metal ions in solution, especially in environmental monitoring, and in chemical and biological sensors that respond to environmental changes via fluorescence shifts. Also investigated as a ph

Used in organic electronics as a fluorescent material due to its strong emission properties. Commonly applied in the development of OLEDs (organic light-emitting diodes) for display technologies and organic solar cells owing to its excellent electron transfer characteristics. Acts as a sensor component for detecting metal ions in solution, especially in environmental monitoring, and in chemical and biological sensors that respond to environmental changes via fluorescence shifts. Also investigated as a photosensitizer in photodynamic therapy for cancer treatment. Its planar structure and electron-deficient core make it suitable for use in supramolecular chemistry and molecular recognition systems.

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