Thieno[3,2-B]Thiophene-2,5-Diyldiboronic Acid
98%
- Product Code: 51677
CAS:
1281324-46-6
| Molecular Weight: | 227.9 g./mol | Molecular Formula: | C₆H₆B₂O₄S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 567.1±60.0℃(Predicted) | |
| Density: | 1.65±0.1g/ml(Predicted) | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Thieno[3,2-b]thiophene-2,5-diyldiboronic acid is primarily used in the synthesis of organic electronic materials, particularly in the development of conjugated polymers and small molecules for organic semiconductors. Its diboronic acid groups make it a valuable building block for cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for creating π-conjugated systems. These systems are integral to the fabrication of organic field-effect transistors (OFETs), organic light-emitting diodes (OLEDs), and organic photovoltaics (OPVs). The compound’s ability to form stable and efficient charge transport materials contributes to advancements in flexible and lightweight electronic devices. Additionally, it is explored in the design of sensors and optoelectronic devices due to its unique electronic properties and structural versatility.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿10,630.00 |
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| 1.000 | 10-20 days | ฿39,800.00 |
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Thieno[3,2-B]Thiophene-2,5-Diyldiboronic Acid
Thieno[3,2-b]thiophene-2,5-diyldiboronic acid is primarily used in the synthesis of organic electronic materials, particularly in the development of conjugated polymers and small molecules for organic semiconductors. Its diboronic acid groups make it a valuable building block for cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for creating π-conjugated systems. These systems are integral to the fabrication of organic field-effect transistors (OFETs), organic light-emitting diodes (OLEDs), and organic photovoltaics (OPVs). The compound’s ability to form stable and efficient charge transport materials contributes to advancements in flexible and lightweight electronic devices. Additionally, it is explored in the design of sensors and optoelectronic devices due to its unique electronic properties and structural versatility.
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