4-(3-Thienyl)furan-2-boronic acid pinacol ester
95%
- Product Code: 90395
CAS:
2223011-21-8
| Molecular Weight: | 294.17426 g./mol | Molecular Formula: | C₁₄H₁₉BO₄S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thienyl and furan moieties contribute to its use in the development of conjugated polymers and organic electronic materials, which are essential in applications like organic light-emitting diodes (OLEDs) and organic photovoltaics. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿10,080.00 |
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| 0.025 | 10-20 days | ฿29,304.00 |
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4-(3-Thienyl)furan-2-boronic acid pinacol ester
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thienyl and furan moieties contribute to its use in the development of conjugated polymers and organic electronic materials, which are essential in applications like organic light-emitting diodes (OLEDs) and organic photovoltaics. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.
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