5-(1H-Pyrrol-1-yl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90758
CAS:
2223043-20-5
| Molecular Weight: | 293.1895 g./mol | Molecular Formula: | C₁₄H₂₀BNO₃S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for creating complex organic molecules, including pharmaceuticals, agrochemicals, and materials for organic electronics. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, polymers, and advanced materials like organic light-emitting diodes (OLEDs) or conductive polymers. Additionally, its pyrrole and thiophene moieties contribute to its utility in designing compounds with specific electronic or optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿15,552.00 |
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| 0.100 | 10-20 days | ฿46,602.00 |
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5-(1H-Pyrrol-1-yl)thiophene-2-boronic acid pinacol ester
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for creating complex organic molecules, including pharmaceuticals, agrochemicals, and materials for organic electronics. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, polymers, and advanced materials like organic light-emitting diodes (OLEDs) or conductive polymers. Additionally, its pyrrole and thiophene moieties contribute to its utility in designing compounds with specific electronic or optical properties.
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