3-Fluoro-4-(4-methylpiperidine-1-carbonyl)phenylboronic acid
98%
- Product Code: 90149
CAS:
1449132-53-9
| Molecular Weight: | 265.09 g./mol | Molecular Formula: | C₁₃H₁₇BFNO₃ |
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| EC Number: | MDL Number: | MFCD20265245 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The fluorine and piperidine moieties enhance its reactivity and selectivity, allowing for the creation of specific target compounds. Additionally, it is employed in the development of advanced materials, where its structural properties contribute to the design of novel polymers and catalysts. Its applications also extend to biochemical research, where it is used as a building block for probes and inhibitors in studying biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | £422.71 |
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3-Fluoro-4-(4-methylpiperidine-1-carbonyl)phenylboronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The fluorine and piperidine moieties enhance its reactivity and selectivity, allowing for the creation of specific target compounds. Additionally, it is employed in the development of advanced materials, where its structural properties contribute to the design of novel polymers and catalysts. Its applications also extend to biochemical research, where it is used as a building block for probes and inhibitors in studying biological pathways.
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