2,2':5',2''-Terthiophene-5,5''-dicarboxaldehyde

98%

Reagent Code: #241232
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CAS Number 13130-50-2

science Other reagents with same CAS 13130-50-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.4 g/mol
Formula C₁₄H₈O₂S₃
thermostat Physical Properties
Melting Point 220-224°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic photovoltaics (OPVs) and organic field-effect transistors (OFETs). Its aldehyde functional groups allow for easy extension of the π-conjugated system via cross-coupling or condensation reactions, enabling fine-tuning of electronic properties. It is also employed in the development of organic semiconductors due to its strong light absorption and charge transport characteristics. Additionally, it serves as a building block for push-pull type polymers when reacted with electron-rich or electron-deficient comonomers.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,790.00
inventory 250mg
10-20 days ฿13,280.00
inventory 1g
10-20 days ฿36,990.00
2,2':5',2''-Terthiophene-5,5''-dicarboxaldehyde
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Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic photovoltaics (OPVs) and organic field-effect transistors (OFETs). Its aldehyde functional groups allow for easy extension of the π-conjugated system via cross-coupling or condensation reactions, enabling fine-tuning of electronic properties. It is also employed in the development of organic semiconductors due to its strong light absorption and charge transport characteristics. Additionally

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic photovoltaics (OPVs) and organic field-effect transistors (OFETs). Its aldehyde functional groups allow for easy extension of the π-conjugated system via cross-coupling or condensation reactions, enabling fine-tuning of electronic properties. It is also employed in the development of organic semiconductors due to its strong light absorption and charge transport characteristics. Additionally, it serves as a building block for push-pull type polymers when reacted with electron-rich or electron-deficient comonomers.

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