4,7-Bis(5-bromo-2-thienyl)-2,1,3-benzothiadiazole

95%

Reagent Code: #141176
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CAS Number 288071-87-4

science Other reagents with same CAS 288071-87-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 458.20 g/mol
Formula C₁₄H₆Br₂N₂S₃
badge Registry Numbers
MDL Number MFCD16619295
thermostat Physical Properties
Melting Point 245.0 to 249.0 deg-C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

4,7-Bis(5-bromo-2-thienyl)-2,1,3-benzothiadiazole is a versatile building block and intermediate in organic synthesis, particularly for conjugated polymers used in optoelectronic devices. It serves as an electron-accepting unit in organic solar cells, contributing to broad light absorption and efficient charge transport, which improves power conversion efficiency. The bromo groups enable facile cross-coupling reactions (e.g., Suzuki or Stille coupling) for polymer chain extension. Additionally, it is employed in the fabrication of organic light-emitting diodes (OLEDs) as a component enhancing emission properties and device stability. Its conjugated structure also supports applications in chemical sensors, where changes in fluorescence or conductivity indicate analyte presence.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,200.00
inventory 1g
10-20 days ฿5,120.00
inventory 5g
10-20 days ฿19,380.00

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4,7-Bis(5-bromo-2-thienyl)-2,1,3-benzothiadiazole
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4,7-Bis(5-bromo-2-thienyl)-2,1,3-benzothiadiazole is a versatile building block and intermediate in organic synthesis, particularly for conjugated polymers used in optoelectronic devices. It serves as an electron-accepting unit in organic solar cells, contributing to broad light absorption and efficient charge transport, which improves power conversion efficiency. The bromo groups enable facile cross-coupling reactions (e.g., Suzuki or Stille coupling) for polymer chain extension. Additionally, it is emp

4,7-Bis(5-bromo-2-thienyl)-2,1,3-benzothiadiazole is a versatile building block and intermediate in organic synthesis, particularly for conjugated polymers used in optoelectronic devices. It serves as an electron-accepting unit in organic solar cells, contributing to broad light absorption and efficient charge transport, which improves power conversion efficiency. The bromo groups enable facile cross-coupling reactions (e.g., Suzuki or Stille coupling) for polymer chain extension. Additionally, it is employed in the fabrication of organic light-emitting diodes (OLEDs) as a component enhancing emission properties and device stability. Its conjugated structure also supports applications in chemical sensors, where changes in fluorescence or conductivity indicate analyte presence.

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