4,7-Bis(5-bromo-4-dodecylthiophen-2-yl)-5-fluorobenzo[c][1,2,5]thiadiazole

98%

Reagent Code: #157488
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CAS Number 1373834-93-5

science Other reagents with same CAS 1373834-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 812.84 g/mol
Formula C₃₈H₅₃Br₂FN₂S₃
thermostat Physical Properties
Boiling Point 732.0±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.267±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily in organic electronics, this compound serves as a key building block in the synthesis of conjugated polymers for high-performance organic solar cells (OSCs) and organic field-effect transistors (OFETs). Its structure supports strong intermolecular interactions and efficient charge transport due to extended π-conjugation and the presence of electron-withdrawing groups. The bromine functionalities allow for further cross-coupling reactions, enabling polymerization with donor units to form low-bandgap materials. These materials exhibit broad light absorption into the near-infrared region, enhancing photovoltaic efficiency. Additionally, the dodecyl side chains improve solubility in organic solvents, facilitating solution processing for thin-film device fabrication. Its fluorinated benzothiadiazole core enhances electron affinity, contributing to improved open-circuit voltage in solar cell applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,560.00

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4,7-Bis(5-bromo-4-dodecylthiophen-2-yl)-5-fluorobenzo[c][1,2,5]thiadiazole
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Used primarily in organic electronics, this compound serves as a key building block in the synthesis of conjugated polymers for high-performance organic solar cells (OSCs) and organic field-effect transistors (OFETs). Its structure supports strong intermolecular interactions and efficient charge transport due to extended π-conjugation and the presence of electron-withdrawing groups. The bromine functionalities allow for further cross-coupling reactions, enabling polymerization with donor units to form lo

Used primarily in organic electronics, this compound serves as a key building block in the synthesis of conjugated polymers for high-performance organic solar cells (OSCs) and organic field-effect transistors (OFETs). Its structure supports strong intermolecular interactions and efficient charge transport due to extended π-conjugation and the presence of electron-withdrawing groups. The bromine functionalities allow for further cross-coupling reactions, enabling polymerization with donor units to form low-bandgap materials. These materials exhibit broad light absorption into the near-infrared region, enhancing photovoltaic efficiency. Additionally, the dodecyl side chains improve solubility in organic solvents, facilitating solution processing for thin-film device fabrication. Its fluorinated benzothiadiazole core enhances electron affinity, contributing to improved open-circuit voltage in solar cell applications.

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