2-(Piperidino)thiophene-4-boronic acid pinacol ester
95%
- Product Code: 89670
CAS:
2223033-58-5
| Molecular Weight: | 311.24784 g./mol | Molecular Formula: | C₁₅H₂₆BNO₃S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for introducing thiophene derivatives into complex molecules, which is valuable in the development of pharmaceuticals and organic materials. Its boronic ester group facilitates efficient coupling with aryl or vinyl halides, enabling the construction of carbon-carbon bonds. This makes it a useful tool in the synthesis of biologically active compounds, agrochemicals, and advanced materials like conjugated polymers for optoelectronic applications. Additionally, its piperidine moiety can contribute to the pharmacological properties of the final products, making it relevant in drug discovery and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿10,782.00 |
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| 0.025 | 10-20 days | ฿31,734.00 |
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2-(Piperidino)thiophene-4-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for introducing thiophene derivatives into complex molecules, which is valuable in the development of pharmaceuticals and organic materials. Its boronic ester group facilitates efficient coupling with aryl or vinyl halides, enabling the construction of carbon-carbon bonds. This makes it a useful tool in the synthesis of biologically active compounds, agrochemicals, and advanced materials like conjugated polymers for optoelectronic applications. Additionally, its piperidine moiety can contribute to the pharmacological properties of the final products, making it relevant in drug discovery and medicinal chemistry.
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