Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde

93%

Reagent Code: #241226
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CAS Number 37882-75-0

science Other reagents with same CAS 37882-75-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.24 g/mol
Formula C₈H₄O₂S₂
badge Registry Numbers
MDL Number MFCD03931117
thermostat Physical Properties
Melting Point 274°C(dec.)(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in organic semiconductor synthesis, particularly in the production of high-performance conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances π-conjugation and promotes strong intermolecular stacking, improving charge carrier mobility. Also employed in the development of donor-acceptor type copolymers due to its electron-deficient character when combined with electron-rich units. Additionally, serves as a building block in synthesizing functional dyes and fluorescent probes for sensing applications.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,580.00
inventory 1g
10-20 days ฿4,560.00
inventory 5g
10-20 days ฿20,090.00
Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
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Used as a key intermediate in organic semiconductor synthesis, particularly in the production of high-performance conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances π-conjugation and promotes strong intermolecular stacking, improving charge carrier mobility. Also employed in the development of donor-acceptor type copolymers due to its electron-deficient character when combined with electron-rich units. Additionally, serv

Used as a key intermediate in organic semiconductor synthesis, particularly in the production of high-performance conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances π-conjugation and promotes strong intermolecular stacking, improving charge carrier mobility. Also employed in the development of donor-acceptor type copolymers due to its electron-deficient character when combined with electron-rich units. Additionally, serves as a building block in synthesizing functional dyes and fluorescent probes for sensing applications.

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