4-(1-(4-(2-((tert-butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)ethyl)phenyl)boronic acid
98%
- Product Code: 90317
CAS:
1704082-49-4
| Molecular Weight: | 516.5700000000001 g./mol | Molecular Formula: | C₃₀H₄₁BN₂O₃Si |
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| EC Number: | MDL Number: | MFCD28805777 | |
| 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 the Suzuki-Miyaura reaction, where it acts as a boronic acid coupling partner. Its structure, featuring a piperazine ring and a tert-butyldiphenylsilyl (TBDPS) protecting group, makes it valuable in the synthesis of complex molecules, including pharmaceuticals and bioactive compounds. The TBDPS group provides stability during reactions, allowing selective deprotection when needed. Additionally, its boronic acid moiety enables the formation of carbon-carbon bonds, making it essential in constructing diverse organic frameworks. This chemical is often employed in medicinal chemistry for the development of drug candidates, particularly in targeting specific biological pathways or receptors. Its versatility and functional groups make it a useful intermediate in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿39,330.00 |
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4-(1-(4-(2-((tert-butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)ethyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid coupling partner. Its structure, featuring a piperazine ring and a tert-butyldiphenylsilyl (TBDPS) protecting group, makes it valuable in the synthesis of complex molecules, including pharmaceuticals and bioactive compounds. The TBDPS group provides stability during reactions, allowing selective deprotection when needed. Additionally, its boronic acid moiety enables the formation of carbon-carbon bonds, making it essential in constructing diverse organic frameworks. This chemical is often employed in medicinal chemistry for the development of drug candidates, particularly in targeting specific biological pathways or receptors. Its versatility and functional groups make it a useful intermediate in multi-step synthetic processes.
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