(4-(1-(4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)ethyl)phenyl)boronic acid
98%
- Product Code: 89215
CAS:
1704096-82-1
| Molecular Weight: | 487.51 g./mol | Molecular Formula: | C₂₉H₃₈BNO₃Si |
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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 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 its stability during reactions, allowing selective deprotection when needed. This compound is often employed in the synthesis of biologically active compounds, where precise control over molecular structure is critical. Additionally, its piperidine moiety can contribute to the development of compounds with potential therapeutic applications, such as central nervous system agents or enzyme inhibitors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft529,547.41 |
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(4-(1-(4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)ethyl)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 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 its stability during reactions, allowing selective deprotection when needed. This compound is often employed in the synthesis of biologically active compounds, where precise control over molecular structure is critical. Additionally, its piperidine moiety can contribute to the development of compounds with potential therapeutic applications, such as central nervous system agents or enzyme inhibitors.
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