(6-(4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)pyridin-3-yl)boronic acid
98%
- Product Code: 89364
CAS:
1704073-93-7
| Molecular Weight: | 460.46 g./mol | Molecular Formula: | C₂₆H₃₃BN₂O₃Si |
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| EC Number: | MDL Number: | MFCD28400350 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) protecting group enhances stability during reactions, allowing selective transformations. It is often employed in the development of drug intermediates and bioactive compounds, where precise control over molecular structure is critical. Additionally, its piperidine moiety can contribute to the modulation of biological activity, making it useful in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,820.22 |
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(6-(4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)pyridin-3-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) protecting group enhances stability during reactions, allowing selective transformations. It is often employed in the development of drug intermediates and bioactive compounds, where precise control over molecular structure is critical. Additionally, its piperidine moiety can contribute to the modulation of biological activity, making it useful in medicinal chemistry research.
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