(2-(4-(Methoxycarbonyl)piperidin-1-yl)pyrimidin-5-yl)boronic acid
95%
- Product Code: 89010
CAS:
1536398-19-2
| Molecular Weight: | 265.07 g./mol | Molecular Formula: | C₁₁H₁₆BN₃O₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic molecules, especially in pharmaceutical research. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biaryl structures, which are common in drug molecules. Its piperidine and pyrimidine moieties contribute to its potential use in developing bioactive compounds, such as kinase inhibitors or other therapeutic agents. Additionally, its methoxycarbonyl group enhances its reactivity and versatility in various chemical transformations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿14,500.00 |
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(2-(4-(Methoxycarbonyl)piperidin-1-yl)pyrimidin-5-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic molecules, especially in pharmaceutical research. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biaryl structures, which are common in drug molecules. Its piperidine and pyrimidine moieties contribute to its potential use in developing bioactive compounds, such as kinase inhibitors or other therapeutic agents. Additionally, its methoxycarbonyl group enhances its reactivity and versatility in various chemical transformations.
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