(3-fluoro-5-(4-Methylpiperazine-1-carbonyl)phenyl)boronic acid
98%
- Product Code: 89122
CAS:
1704082-15-4
| Molecular Weight: | 266.07 g./mol | Molecular Formula: | C₁₂H₁₆BFN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400450 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which is essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the 4-methylpiperazine moiety enhances its potential as a building block in drug discovery, particularly for targeting central nervous system disorders or as a component in the development of kinase inhibitors. Its fluorine substituent can improve metabolic stability and binding affinity, making it a useful intermediate in the design of bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿33,440.00 |
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(3-fluoro-5-(4-Methylpiperazine-1-carbonyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which is essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the 4-methylpiperazine moiety enhances its potential as a building block in drug discovery, particularly for targeting central nervous system disorders or as a component in the development of kinase inhibitors. Its fluorine substituent can improve metabolic stability and binding affinity, making it a useful intermediate in the design of bioactive compounds.
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