2,6-Difluorophenylboronic Acid Pinacol Ester
≥95%
- Product Code: 89589
CAS:
863868-37-5
| Molecular Weight: | 240.05 g./mol | Molecular Formula: | C₁₂H₁₅F₂O₂B |
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| EC Number: | MDL Number: | MFCD09801043 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
2,6-Difluorophenylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound’s stability and reactivity make it a preferred choice for introducing the 2,6-difluorophenyl group into complex molecules. It is also employed in the development of bioactive compounds and in research focused on creating new drug candidates. Its role in facilitating efficient and selective coupling reactions highlights its importance in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿684.00 |
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| 5.000 | 10-20 days | ฿1,989.00 |
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| 25.000 | 10-20 days | ฿8,550.00 |
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2,6-Difluorophenylboronic Acid Pinacol Ester
2,6-Difluorophenylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound’s stability and reactivity make it a preferred choice for introducing the 2,6-difluorophenyl group into complex molecules. It is also employed in the development of bioactive compounds and in research focused on creating new drug candidates. Its role in facilitating efficient and selective coupling reactions highlights its importance in modern synthetic chemistry.
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