2-Phenylpyrimidine-5-boronic acid
95%
- Product Code: 91774
CAS:
1264510-78-2
| Molecular Weight: | 200.00166 g./mol | Molecular Formula: | C₁₀H₉BN₂O₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
2-Phenylpyrimidine-5-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 and agrochemicals. 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. Additionally, it serves as a building block in the development of bioactive compounds, such as kinase inhibitors, which are crucial in cancer research and treatment. Its stability and reactivity make it a valuable reagent in medicinal chemistry and material science.
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-Phenylpyrimidine-5-boronic acid
2-Phenylpyrimidine-5-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 and agrochemicals. 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. Additionally, it serves as a building block in the development of bioactive compounds, such as kinase inhibitors, which are crucial in cancer research and treatment. Its stability and reactivity make it a valuable reagent in medicinal chemistry and material science.
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