5,6-Difluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole

99%

Reagent Code: #94035
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CAS Number 1421762-30-2

science Other reagents with same CAS 1421762-30-2

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scatter_plot Molecular Information
Weight 662.023 g/mol
Formula C₂₀H₂₂F₂N₂S₃Sn₂
badge Registry Numbers
MDL Number MFCD32856173
inventory_2 Storage & Handling
Storage Room temperature, dark, sealed, dry

description Product Description

This compound, 5,6-difluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole, is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for optoelectronic devices. Its structure, featuring a difluoro-substituted benzothiadiazole core and thiophene units with trimethylstannyl groups, makes it highly suitable for applications in organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). The presence of trimethylstannyl groups facilitates efficient cross-coupling reactions, such as Stille coupling, enabling precise tuning of the material's electronic properties. This chemical is often employed as a key building block in the synthesis of low-bandgap polymers, which are essential for enhancing the efficiency of solar cells by broadening the absorption spectrum. Additionally, its electron-deficient difluoro-benzothiadiazole core contributes to improved charge transport characteristics, making it valuable in the design of high-performance organic semiconductors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,627.00
inventory 1g
10-20 days ฿16,362.00
inventory 250mg
10-20 days ฿6,237.00

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5,6-Difluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole
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This compound, 5,6-difluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole, is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for optoelectronic devices. Its structure, featuring a difluoro-substituted benzothiadiazole core and thiophene units with trimethylstannyl groups, makes it highly suitable for applications in organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). The presence of trimethylstannyl

This compound, 5,6-difluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole, is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for optoelectronic devices. Its structure, featuring a difluoro-substituted benzothiadiazole core and thiophene units with trimethylstannyl groups, makes it highly suitable for applications in organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). The presence of trimethylstannyl groups facilitates efficient cross-coupling reactions, such as Stille coupling, enabling precise tuning of the material's electronic properties. This chemical is often employed as a key building block in the synthesis of low-bandgap polymers, which are essential for enhancing the efficiency of solar cells by broadening the absorption spectrum. Additionally, its electron-deficient difluoro-benzothiadiazole core contributes to improved charge transport characteristics, making it valuable in the design of high-performance organic semiconductors.

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