4-Fluoro-2-((4-methylpiperazin-1-yl)methyl)phenylboronic acid
98%
- Product Code: 90587
CAS:
1704063-83-1
| Molecular Weight: | 252.1 g./mol | Molecular Formula: | C₁₂H₁₈BFN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400163 | |
| 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, where it acts as a key intermediate for constructing complex molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of the fluorine atom and the piperazine moiety enhances its reactivity and selectivity in these reactions, allowing for the creation of diverse and biologically active compounds. Additionally, its structural features make it suitable for use in medicinal chemistry research, where it can be incorporated into drug candidates targeting specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿19,380.00 |
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4-Fluoro-2-((4-methylpiperazin-1-yl)methyl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of the fluorine atom and the piperazine moiety enhances its reactivity and selectivity in these reactions, allowing for the creation of diverse and biologically active compounds. Additionally, its structural features make it suitable for use in medicinal chemistry research, where it can be incorporated into drug candidates targeting specific biological pathways.
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