11-Cyano-N-(4-nitrophenyl)-9,10-dihydro-9,10-ethanoanthracene-11-carboxamide

95%

Reagent Code: #164984
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CAS Number 312505-69-4

science Other reagents with same CAS 312505-69-4

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inventory_2 Storage & Handling
Storage 2-8°C, dry

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Used in organic electronics as a semiconductor material due to its rigid, conjugated structure and electron-withdrawing cyano and nitro groups. It is incorporated into thin-film transistors and photovoltaic devices to enhance electron transport and improve device efficiency. Its fused ring system with bridging ethano group provides thermal stability and resistance to photo-degradation, making it suitable for long-lasting optoelectronic applications. Also explored in fluorescent sensors for detecting nitroaromatic explosives due to its selective quenching behavior in the presence of electron-deficient analytes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,200.00
inventory 250mg
10-20 days ฿14,250.00
inventory 1g
10-20 days ฿56,950.00

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11-Cyano-N-(4-nitrophenyl)-9,10-dihydro-9,10-ethanoanthracene-11-carboxamide
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Used in organic electronics as a semiconductor material due to its rigid, conjugated structure and electron-withdrawing cyano and nitro groups. It is incorporated into thin-film transistors and photovoltaic devices to enhance electron transport and improve device efficiency. Its fused ring system with bridging ethano group provides thermal stability and resistance to photo-degradation, making it suitable for long-lasting optoelectronic applications. Also explored in fluorescent sensors for detecting nitr

Used in organic electronics as a semiconductor material due to its rigid, conjugated structure and electron-withdrawing cyano and nitro groups. It is incorporated into thin-film transistors and photovoltaic devices to enhance electron transport and improve device efficiency. Its fused ring system with bridging ethano group provides thermal stability and resistance to photo-degradation, making it suitable for long-lasting optoelectronic applications. Also explored in fluorescent sensors for detecting nitroaromatic explosives due to its selective quenching behavior in the presence of electron-deficient analytes.

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