(4-((4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)methyl)phenyl)boronic acid
98%
- Product Code: 89188
CAS:
1704082-69-8
| Molecular Weight: | 473.49 g./mol | Molecular Formula: | C₂₈H₃₆BNO₃Si |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. Its application extends to the development of bioactive compounds and materials science, where precise molecular construction is essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿29,230.00 |
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(4-((4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)methyl)phenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. Its application extends to the development of bioactive compounds and materials science, where precise molecular construction is essential.
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