2-(4-nitrophenyl)-3,4,3',4'-bis(ethylenedioxy)-5,2'-bithiophene

Reagent Code: #216071
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CAS Number 1350699-14-7

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 403.436 g/mol
Formula C₁₈H₁₃NO₆S₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its extended π-conjugated system enhances charge carrier mobility, making it valuable for high-performance semiconductor materials. The electron-withdrawing nitro group improves electron affinity, which aids in n-type semiconductor behavior. It is also employed in the development of donor-acceptor type copolymers to tune bandgap and improve light absorption in solar cells. Due to its solubility and stability, it supports solution-processing techniques like spin coating and inkjet printing for flexible electronics.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿25,650.00
2-(4-nitrophenyl)-3,4,3',4'-bis(ethylenedioxy)-5,2'-bithiophene
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Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its extended π-conjugated system enhances charge carrier mobility, making it valuable for high-performance semiconductor materials. The electron-withdrawing nitro group improves electron affinity, which aids in n-type semiconductor behavior. It is also employed in the development of donor-acceptor type copo

Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its extended π-conjugated system enhances charge carrier mobility, making it valuable for high-performance semiconductor materials. The electron-withdrawing nitro group improves electron affinity, which aids in n-type semiconductor behavior. It is also employed in the development of donor-acceptor type copolymers to tune bandgap and improve light absorption in solar cells. Due to its solubility and stability, it supports solution-processing techniques like spin coating and inkjet printing for flexible electronics.

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