(3-((Dimethylamino)methyl)-4-fluorophenyl)boronic acid
95%
- Product Code: 89955
CAS:
1704063-96-6
| Molecular Weight: | 197.01 g./mol | Molecular Formula: | C₉H₁₃BFNO₂ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the pharmaceutical and materials science industries to create carbon-carbon bonds, enabling the synthesis of complex organic molecules. Its boronic acid group acts as a key functional group, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable for constructing biologically active compounds, such as drug candidates, and for developing advanced materials like organic semiconductors or polymers. Additionally, its fluorine substituent can enhance the stability and reactivity of the resulting products, making it useful in designing molecules with specific electronic or structural properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿8,460.00 |
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(3-((Dimethylamino)methyl)-4-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the pharmaceutical and materials science industries to create carbon-carbon bonds, enabling the synthesis of complex organic molecules. Its boronic acid group acts as a key functional group, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable for constructing biologically active compounds, such as drug candidates, and for developing advanced materials like organic semiconductors or polymers. Additionally, its fluorine substituent can enhance the stability and reactivity of the resulting products, making it useful in designing molecules with specific electronic or structural properties.
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