(4-((4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)methyl)-2-fluorophenyl)boronic acid
98%
- Product Code: 89187
CAS:
1704096-87-6
| Molecular Weight: | 491.48 g./mol | Molecular Formula: | C₂₈H₃₅BFNO₃Si |
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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, which is essential in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) group serves as a protecting group for the hydroxyl functionality on the piperidine ring, ensuring selective reactivity during multi-step synthetic processes. This compound is often employed in the development of drug candidates, where its structural features allow for precise modifications to enhance biological activity or improve pharmacokinetic properties. Additionally, its fluorine atom can influence the electronic properties of the molecule, making it useful in the design of compounds with specific binding affinities or metabolic stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿50,210.00 |
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(4-((4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)methyl)-2-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, which is essential in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) group serves as a protecting group for the hydroxyl functionality on the piperidine ring, ensuring selective reactivity during multi-step synthetic processes. This compound is often employed in the development of drug candidates, where its structural features allow for precise modifications to enhance biological activity or improve pharmacokinetic properties. Additionally, its fluorine atom can influence the electronic properties of the molecule, making it useful in the design of compounds with specific binding affinities or metabolic stability.
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