(2-(2-fluorophenyl)pyrimidin-5-yl)boronic acid
95%
- Product Code: 56303
CAS:
2225172-10-9
| Molecular Weight: | 217.9921232 g./mol | Molecular Formula: | C₁₀H₈BFN₂O₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
(2-(2-fluorophenyl)pyrimidin-5-yl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl halides, making it valuable in the development of biologically active compounds, such as potential drug candidates targeting specific diseases. Additionally, it is used in the preparation of functionalized pyrimidine derivatives, which are important in medicinal chemistry for their diverse pharmacological properties.
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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(2-(2-fluorophenyl)pyrimidin-5-yl)boronic acid
(2-(2-fluorophenyl)pyrimidin-5-yl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl halides, making it valuable in the development of biologically active compounds, such as potential drug candidates targeting specific diseases. Additionally, it is used in the preparation of functionalized pyrimidine derivatives, which are important in medicinal chemistry for their diverse pharmacological properties.
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