5-Fluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole
97%
- Product Code: 119894
CAS:
1611002-56-2
| Molecular Weight: | 644.02 g./mol | Molecular Formula: | C₂₀H₂₃FN₂S₃Sn₂ |
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| EC Number: | MDL Number: | MFCD30489168 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for optoelectronic devices. It serves as a key building block in the synthesis of conjugated polymers and small molecules, which are essential components in organic solar cells, light-emitting diodes (OLEDs), and field-effect transistors (OFETs). The presence of the thiophene and benzo[c][1,2,5]thiadiazole units, along with the fluoro substituent, enhances the electronic properties, such as charge carrier mobility and light absorption efficiency. Additionally, the trimethylstannyl groups facilitate cross-coupling reactions, enabling precise modifications to tailor the material's properties for specific applications. This makes it a valuable compound in designing high-performance, energy-efficient electronic devices.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $143.15 |
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| 0.250 | 10-20 days | $286.30 |
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5-Fluoro-4,7-bis(5-(trimethylstannyl)thiophen-2-yl)benzo[c][1,2,5]thiadiazole
This compound is primarily utilized in the field of organic electronics, particularly in the development of advanced materials for optoelectronic devices. It serves as a key building block in the synthesis of conjugated polymers and small molecules, which are essential components in organic solar cells, light-emitting diodes (OLEDs), and field-effect transistors (OFETs). The presence of the thiophene and benzo[c][1,2,5]thiadiazole units, along with the fluoro substituent, enhances the electronic properties, such as charge carrier mobility and light absorption efficiency. Additionally, the trimethylstannyl groups facilitate cross-coupling reactions, enabling precise modifications to tailor the material's properties for specific applications. This makes it a valuable compound in designing high-performance, energy-efficient electronic devices.
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