3-(4-Fluoropyridin-2-yl)phenylboronic acid
95%
- Product Code: 91820
CAS:
2225154-99-2
| Molecular Weight: | 217.0040632 g./mol | Molecular Formula: | C₁₁H₉BFNO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, such as drug candidates targeting various diseases. Additionally, it may be employed in material science for designing advanced polymers or organic electronic materials. Its fluoropyridine moiety adds unique electronic properties, enhancing its utility in specialized chemical applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿13,400.00 |
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| 0.025 | 10-20 days | ฿40,200.00 |
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| 0.100 | 10-20 days | ฿120,600.00 |
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3-(4-Fluoropyridin-2-yl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, such as drug candidates targeting various diseases. Additionally, it may be employed in material science for designing advanced polymers or organic electronic materials. Its fluoropyridine moiety adds unique electronic properties, enhancing its utility in specialized chemical applications.
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