(3-((4-(2-((tert-butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid
98%
- Product Code: 89104
CAS:
1704081-26-4
| Molecular Weight: | 582.6 g./mol | Molecular Formula: | C₂₉H₃₉BN₂O₆SSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28805767 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry as a versatile intermediate. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The piperazine moiety enhances its potential as a building block for designing drug candidates, particularly in the development of CNS (central nervous system) drugs, due to its ability to interact with biological targets. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective group for alcohols, allowing selective reactions in multi-step synthetic processes. Its sulfonyl group further contributes to its reactivity, enabling modifications for drug discovery and development. Overall, this compound is a key reagent in the synthesis of biologically active molecules and advanced materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿41,210.00 |
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(3-((4-(2-((tert-butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)sulfonyl)-4-Methoxyphenyl)boronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry as a versatile intermediate. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The piperazine moiety enhances its potential as a building block for designing drug candidates, particularly in the development of CNS (central nervous system) drugs, due to its ability to interact with biological targets. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective group for alcohols, allowing selective reactions in multi-step synthetic processes. Its sulfonyl group further contributes to its reactivity, enabling modifications for drug discovery and development. Overall, this compound is a key reagent in the synthesis of biologically active molecules and advanced materials.
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