2-(2-Fluorophenyl)pyridine-4-boronic acid
95%
- Product Code: 91472
CAS:
1354759-05-9
| Molecular Weight: | 217.0040632 g./mol | Molecular Formula: | C₁₁H₉BFNO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
2-(2-Fluorophenyl)pyridine-4-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group in coupling with aryl or vinyl halides, facilitated by a palladium catalyst. Additionally, it serves as a building block in medicinal chemistry for designing drug candidates, especially in the development of compounds targeting neurological disorders or cancer. Its fluorophenyl moiety can enhance binding affinity and metabolic stability in drug molecules. The compound is also employed in material science for synthesizing organic electronic materials, such as OLEDs, due to its structural versatility.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿8,982.00 |
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| 0.025 | 10-20 days | ฿29,700.00 |
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| 0.100 | 10-20 days | ฿82,800.00 |
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2-(2-Fluorophenyl)pyridine-4-boronic acid
2-(2-Fluorophenyl)pyridine-4-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group in coupling with aryl or vinyl halides, facilitated by a palladium catalyst. Additionally, it serves as a building block in medicinal chemistry for designing drug candidates, especially in the development of compounds targeting neurological disorders or cancer. Its fluorophenyl moiety can enhance binding affinity and metabolic stability in drug molecules. The compound is also employed in material science for synthesizing organic electronic materials, such as OLEDs, due to its structural versatility.
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