(4-(2-(4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)ethoxy)-3-fluorophenyl)boronic acid
98%
- Product Code: 89230
CAS:
1704082-87-0
| Molecular Weight: | 521.5 g./mol | Molecular Formula: | C₂₉H₃₇BFNO₄Si |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates by facilitating the synthesis of biologically active compounds. Additionally, the fluorine atom in its structure can enhance the metabolic stability and binding affinity of the resulting molecules, making it useful in designing more effective therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $290.24 |
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(4-(2-(4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)ethoxy)-3-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates by facilitating the synthesis of biologically active compounds. Additionally, the fluorine atom in its structure can enhance the metabolic stability and binding affinity of the resulting molecules, making it useful in designing more effective therapeutic agents.
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