(2-Fluoro-6-phenoxyphenyl)boronic acid
96%
- Product Code: 36357
CAS:
1056372-58-7
| Molecular Weight: | 232.0154 g./mol | Molecular Formula: | C₁₂H₁₀BFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11856031 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(2-Fluoro-6-phenoxyphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical and materials science industries to form carbon-carbon bonds, enabling the synthesis of complex organic molecules. The compound serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable for creating diverse chemical structures. Additionally, it may find applications in the development of sensors or polymers due to its ability to interact with diols and other functional groups.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,690.00 |
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(2-Fluoro-6-phenoxyphenyl)boronic acid
(2-Fluoro-6-phenoxyphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical and materials science industries to form carbon-carbon bonds, enabling the synthesis of complex organic molecules. The compound serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable for creating diverse chemical structures. Additionally, it may find applications in the development of sensors or polymers due to its ability to interact with diols and other functional groups.
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