(4,5-Difluoro-2-((4-hydroxypiperidin-1-yl)sulfonyl)phenyl)boronic acid
98%
- Product Code: 89166
CAS:
1704069-01-1
| Molecular Weight: | 321.11 g./mol | Molecular Formula: | C₁₁H₁₄BF₂NO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384288 | |
| 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 boronic acid reagent to form carbon-carbon bonds. Its difluoro and sulfonyl groups enhance its reactivity and selectivity, making it valuable in the synthesis of complex molecules, including pharmaceuticals and agrochemicals. Additionally, the presence of the hydroxypiperidine moiety can improve solubility and stability, facilitating its use in aqueous or polar solvent systems. It is also employed in the development of boron-based probes or sensors for detecting specific biological targets due to its ability to interact with diols and other functional groups.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿29,950.00 |
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(4,5-Difluoro-2-((4-hydroxypiperidin-1-yl)sulfonyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its difluoro and sulfonyl groups enhance its reactivity and selectivity, making it valuable in the synthesis of complex molecules, including pharmaceuticals and agrochemicals. Additionally, the presence of the hydroxypiperidine moiety can improve solubility and stability, facilitating its use in aqueous or polar solvent systems. It is also employed in the development of boron-based probes or sensors for detecting specific biological targets due to its ability to interact with diols and other functional groups.
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