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

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Reagent Code: #146981
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CAS Number 1179993-72-6

science Other reagents with same CAS 1179993-72-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 794.85 g/mol
Formula C₃₈H₅₄Br₂N₂S₃
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic solar cells (OSCs). Its structure supports strong intermolecular interactions and efficient charge transport, making it valuable in donor-acceptor type semiconducting materials. It is also employed in organic field-effect transistors (OFETs) and sensors due to its responsive electronic properties when exposed to specific analytes. The presence of bromine allows for further functionalization via cross-coupling reactions, enabling tailored modifications for specific device requirements.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,690.00
inventory 250mg
10-20 days ฿4,560.00
inventory 1g
10-20 days ฿13,300.00
inventory 5g
10-20 days ฿43,000.00

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4,7-Bis(5-bromo-4-dodecyl-2-thienyl)-2,1,3-benzothiadiazole
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Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic solar cells (OSCs). Its structure supports strong intermolecular interactions and efficient charge transport, making it valuable in donor-acceptor type semiconducting materials. It is also employed in organic field-effect transistors (OFETs) and sensors due to its responsive electronic properties when exposed to specific analytes. The presence of bromine allows for further

Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic solar cells (OSCs). Its structure supports strong intermolecular interactions and efficient charge transport, making it valuable in donor-acceptor type semiconducting materials. It is also employed in organic field-effect transistors (OFETs) and sensors due to its responsive electronic properties when exposed to specific analytes. The presence of bromine allows for further functionalization via cross-coupling reactions, enabling tailored modifications for specific device requirements.

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