(2-(Benzyloxy)-6-fluorophenyl)boronic acid
98%
- Product Code: 43750
CAS:
1217500-53-2
| Molecular Weight: | 246.0420 g./mol | Molecular Formula: | C₁₃H₁₂BFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11617256 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
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 intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its structure, featuring a benzyloxy and fluorine substituent, allows for selective reactivity and functionalization in targeted synthetic pathways. Additionally, it may be employed in the development of bioactive compounds or materials with specific electronic properties due to its aromatic and electron-withdrawing characteristics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿774.00 |
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(2-(Benzyloxy)-6-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its structure, featuring a benzyloxy and fluorine substituent, allows for selective reactivity and functionalization in targeted synthetic pathways. Additionally, it may be employed in the development of bioactive compounds or materials with specific electronic properties due to its aromatic and electron-withdrawing characteristics.
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