3,4-Thiophenedicarboxaldehyde

>98%(GC)

Reagent Code: #242286
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CAS Number 1073-31-0

science Other reagents with same CAS 1073-31-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 140.16 g/mol
Formula C₆H₄O₂S
badge Registry Numbers
MDL Number MFCD09033442
thermostat Physical Properties
Melting Point 81 °C
Boiling Point 293.888 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.371 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the development of donor-acceptor type materials for organic photovoltaics (OPVs) and organic field-effect transistors (OFETs). Its aldehyde functional groups allow for easy incorporation into π-conjugated systems via condensation reactions, such as in the preparation of thiophene-based Schiff bases or vinylene-bridged structures. Also employed in the fabrication of fluorescent sensors and dyes due to its electron-rich aromatic core and ability to coordinate with metal ions. Its rigid planar structure enhances charge carrier mobility in electronic devices.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,560.00
inventory 250mg
10-20 days ฿26,420.00
inventory 1g
10-20 days ฿71,340.00

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3,4-Thiophenedicarboxaldehyde
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Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the development of donor-acceptor type materials for organic photovoltaics (OPVs) and organic field-effect transistors (OFETs). Its aldehyde functional groups allow for easy incorporation into π-conjugated systems via condensation reactions, such as in the preparation of thiophene-based Schiff bases or vinylene-bridged structures. Also employed in the fabrication of fluorescent sensors and dyes

Used as a key intermediate in the synthesis of conjugated polymers and organic semiconductors, particularly in the development of donor-acceptor type materials for organic photovoltaics (OPVs) and organic field-effect transistors (OFETs). Its aldehyde functional groups allow for easy incorporation into π-conjugated systems via condensation reactions, such as in the preparation of thiophene-based Schiff bases or vinylene-bridged structures. Also employed in the fabrication of fluorescent sensors and dyes due to its electron-rich aromatic core and ability to coordinate with metal ions. Its rigid planar structure enhances charge carrier mobility in electronic devices.

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