3'-Octyl-[2,2'-bithiophene]-5-carbaldehyde

98%

Reagent Code: #222287
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CAS Number 2582829-55-6

science Other reagents with same CAS 2582829-55-6

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inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in organic electronics as a key intermediate for synthesizing conjugated polymers and small molecules in organic semiconductors. Its structure supports charge transport, making it suitable for applications in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The aldehyde group allows for further functionalization via cross-coupling or condensation reactions, enabling fine-tuning of electronic properties. Also explored in dye-sensitized solar cells and as a building block for push-pull chromophores due to its electron-rich bithiophene core and side-chain solubilizing group.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,280.00
inventory 250mg
10-20 days ฿6,420.00
inventory 1g
10-20 days ฿20,720.00
3'-Octyl-[2,2'-bithiophene]-5-carbaldehyde
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Used in organic electronics as a key intermediate for synthesizing conjugated polymers and small molecules in organic semiconductors. Its structure supports charge transport, making it suitable for applications in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The aldehyde group allows for further functionalization via cross-coupling or condensation reactions, enabling fine-tuning of electronic properties. Also explored in dye-sensitized solar cells and as a building block for

Used in organic electronics as a key intermediate for synthesizing conjugated polymers and small molecules in organic semiconductors. Its structure supports charge transport, making it suitable for applications in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The aldehyde group allows for further functionalization via cross-coupling or condensation reactions, enabling fine-tuning of electronic properties. Also explored in dye-sensitized solar cells and as a building block for push-pull chromophores due to its electron-rich bithiophene core and side-chain solubilizing group.

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