2,3-Di(furan-2-yl)quinoxaline-6-carboxylic acid

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Reagent Code: #179278
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CAS Number 90846-59-6

science Other reagents with same CAS 90846-59-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.27 g/mol
Formula C₁₇H₁₀N₂O₄
badge Registry Numbers
MDL Number MFCD00999683
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of organic semiconductors and fluorescent materials. Its extended π-conjugated structure makes it suitable for applications in optoelectronic devices such as organic light-emitting diodes (OLEDs) and sensors. The compound exhibits strong fluorescence, which is exploited in the development of chemosensors for detecting metal ions or biological molecules. Additionally, its ability to form stable charge-transfer complexes supports its use in photovoltaic cells and dye-sensitized solar cells. The carboxylic acid group allows for easy functionalization and attachment to surfaces or polymers, enhancing its utility in material science and biosensor platforms.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,760.00
inventory 250mg
10-20 days ฿8,090.00
inventory 1g
10-20 days ฿23,620.00

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2,3-Di(furan-2-yl)quinoxaline-6-carboxylic acid
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Used as a key intermediate in the synthesis of organic semiconductors and fluorescent materials. Its extended π-conjugated structure makes it suitable for applications in optoelectronic devices such as organic light-emitting diodes (OLEDs) and sensors. The compound exhibits strong fluorescence, which is exploited in the development of chemosensors for detecting metal ions or biological molecules. Additionally, its ability to form stable charge-transfer complexes supports its use in photovoltaic cells and

Used as a key intermediate in the synthesis of organic semiconductors and fluorescent materials. Its extended π-conjugated structure makes it suitable for applications in optoelectronic devices such as organic light-emitting diodes (OLEDs) and sensors. The compound exhibits strong fluorescence, which is exploited in the development of chemosensors for detecting metal ions or biological molecules. Additionally, its ability to form stable charge-transfer complexes supports its use in photovoltaic cells and dye-sensitized solar cells. The carboxylic acid group allows for easy functionalization and attachment to surfaces or polymers, enhancing its utility in material science and biosensor platforms.

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