(3-Fluoro-5-(4-methylpiperazin-1-yl)phenyl)boronic acid
98%
- Product Code: 89071
CAS:
1704073-49-3
| Molecular Weight: | 238.07 g./mol | Molecular Formula: | C₁₁H₁₆BFN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24448996 | |
| 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 for the construction of complex molecules, especially in pharmaceutical research. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biologically active compounds. Its structure, featuring a fluorine atom and a methylpiperazine moiety, makes it valuable in designing drug candidates targeting neurological disorders or cancer. Additionally, it is employed in material science for developing advanced polymers or organic electronic materials. Its unique properties also make it useful in chemical biology for probing enzyme mechanisms or protein interactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿39,440.00 |
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(3-Fluoro-5-(4-methylpiperazin-1-yl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex molecules, especially in pharmaceutical research. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biologically active compounds. Its structure, featuring a fluorine atom and a methylpiperazine moiety, makes it valuable in designing drug candidates targeting neurological disorders or cancer. Additionally, it is employed in material science for developing advanced polymers or organic electronic materials. Its unique properties also make it useful in chemical biology for probing enzyme mechanisms or protein interactions.
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