(2,3,5,6-Tetrafluorophenyl)boronic acid
96%
- Product Code: 36287
CAS:
511295-01-5
| Molecular Weight: | 193.8914 g./mol | Molecular Formula: | C₆H₃BF₄O₂ |
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| EC Number: | MDL Number: | MFCD04039310 | |
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| Density: | Storage Condition: | -20°C |
Product Description:
(2,3,5,6-Tetrafluorophenyl)boronic acid 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 fluorinated aromatic ring enhances its reactivity and stability, making it suitable for creating complex organic molecules with high precision. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, enabling applications in biochemical research and diagnostics. Its unique structure also makes it a useful intermediate in the synthesis of fluorinated compounds, which are often sought after for their enhanced properties in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,746.00 |
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(2,3,5,6-Tetrafluorophenyl)boronic acid
(2,3,5,6-Tetrafluorophenyl)boronic acid 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 fluorinated aromatic ring enhances its reactivity and stability, making it suitable for creating complex organic molecules with high precision. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, enabling applications in biochemical research and diagnostics. Its unique structure also makes it a useful intermediate in the synthesis of fluorinated compounds, which are often sought after for their enhanced properties in medicinal chemistry.
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