4,4,5,5-Tetramethyl-2-(thieno[3,2-b]thiophen-2-yl)-1,3,2-dioxaborolane
98%
- Product Code: 241571
CAS:
1004784-50-2
| Molecular Weight: | 266.19 g./mol | Molecular Formula: | C₁₂H₁₅BO₂S₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 376.9±22.0℃ at 760 mmHg | |
| Density: | 1.21±0.1 g/cm3 | Storage Condition: | 2-8℃ |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Particularly valuable in the preparation of conjugated polymers and small molecule semiconductors for organic electronics, such as organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). The thienothiophene moiety contributes to enhanced electronic properties and stability in the resulting materials. Its boronate ester group allows for efficient and selective coupling under mild conditions, making it suitable for constructing complex π-conjugated systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.200 | 10-20 days | £34.04 |
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| 1.000 | 10-20 days | £72.45 |
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| 5.000 | 10-20 days | £306.14 |
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4,4,5,5-Tetramethyl-2-(thieno[3,2-b]thiophen-2-yl)-1,3,2-dioxaborolane
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Particularly valuable in the preparation of conjugated polymers and small molecule semiconductors for organic electronics, such as organic photovoltaics (OPVs) and organic light-emitting diodes (OLEDs). The thienothiophene moiety contributes to enhanced electronic properties and stability in the resulting materials. Its boronate ester group allows for efficient and selective coupling under mild conditions, making it suitable for constructing complex π-conjugated systems.
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