9,10-[1,2]Benzenoanthracene-2,3,6,7,14,15(9H,10H)-hexaone

95%

Reagent Code: #153152
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CAS Number 2253629-27-3

science Other reagents with same CAS 2253629-27-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 344.27 g/mol
Formula C₂₀H₈O₆
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily in organic electronics and advanced materials research, this compound serves as a building block for high-performance semiconductor materials. Its rigid, planar structure and extended π-conjugation make it suitable for applications in organic field-effect transistors (OFETs) and photovoltaic devices. It is also explored in the development of n-type organic semiconductors due to its strong electron-accepting properties when functionalized. Additionally, it finds use in the synthesis of novel dyes and fluorescent probes for imaging applications, where stability and tunable optical properties are required. Its derivatization can enhance charge transport and solubility, making it valuable in solution-processable electronic materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿33,080.00
inventory 250mg
10-20 days ฿54,890.00

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9,10-[1,2]Benzenoanthracene-2,3,6,7,14,15(9H,10H)-hexaone
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Used primarily in organic electronics and advanced materials research, this compound serves as a building block for high-performance semiconductor materials. Its rigid, planar structure and extended π-conjugation make it suitable for applications in organic field-effect transistors (OFETs) and photovoltaic devices. It is also explored in the development of n-type organic semiconductors due to its strong electron-accepting properties when functionalized. Additionally, it finds use in the synthesis of nove

Used primarily in organic electronics and advanced materials research, this compound serves as a building block for high-performance semiconductor materials. Its rigid, planar structure and extended π-conjugation make it suitable for applications in organic field-effect transistors (OFETs) and photovoltaic devices. It is also explored in the development of n-type organic semiconductors due to its strong electron-accepting properties when functionalized. Additionally, it finds use in the synthesis of novel dyes and fluorescent probes for imaging applications, where stability and tunable optical properties are required. Its derivatization can enhance charge transport and solubility, making it valuable in solution-processable electronic materials.

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