(3-Fluoro-4-(methoxymethyl)phenyl)boronic acid
95%
- Product Code: 89120
CAS:
1313738-12-3
| Molecular Weight: | 183.97 g./mol | Molecular Formula: | C₈H₁₀BFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14687259 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in drug molecules. Additionally, it may be employed in the synthesis of agrochemicals and advanced materials, where its specific functional groups contribute to the desired properties of the final product. Its fluoro and methoxymethyl substituents can enhance the reactivity and selectivity in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,705.00 |
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| 0.250 | 10-20 days | ฿16,731.00 |
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(3-Fluoro-4-(methoxymethyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in drug molecules. Additionally, it may be employed in the synthesis of agrochemicals and advanced materials, where its specific functional groups contribute to the desired properties of the final product. Its fluoro and methoxymethyl substituents can enhance the reactivity and selectivity in various chemical transformations.
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