(4-(2-(4-(2-((tert-Butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)ethoxy)-3-fluorophenyl)boronic acid
98%
- Product Code: 89233
CAS:
1704081-82-2
| Molecular Weight: | 550.5599999999999 g./mol | Molecular Formula: | C₃₀H₄₀BFN₂O₄Si |
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| EC Number: | MDL Number: | MFCD28805758 | |
| 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. 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 stability and selectivity during synthesis, ensuring the compound remains intact under various reaction conditions. Additionally, its piperazine moiety contributes to its potential application in drug development, as piperazine derivatives are often explored for their biological activity. The fluorine atom further modifies its reactivity and interaction with biological targets, making it a versatile intermediate in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,464.45 |
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(4-(2-(4-(2-((tert-Butyldiphenylsilyl)oxy)ethyl)piperazin-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 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 stability and selectivity during synthesis, ensuring the compound remains intact under various reaction conditions. Additionally, its piperazine moiety contributes to its potential application in drug development, as piperazine derivatives are often explored for their biological activity. The fluorine atom further modifies its reactivity and interaction with biological targets, making it a versatile intermediate in medicinal chemistry.
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