(4-((4-(2-((tert-Butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)methyl)-3-fluorophenyl)boronic acid
98%
- Product Code: 89192
CAS:
1704073-71-1
| Molecular Weight: | 520.53 g./mol | Molecular Formula: | C₂₉H₃₈BFN₂O₃Si |
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| EC Number: | MDL Number: | MFCD28805768 | |
| 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 reagent. Its structure, featuring a piperazine moiety and a tert-butyldiphenylsilyl-protected hydroxyl group, makes it valuable in the preparation of complex molecules, especially in pharmaceutical research. The fluorophenyl group enhances its reactivity and selectivity in forming carbon-carbon bonds, which is crucial in the development of drug candidates. Additionally, the tert-butyldiphenylsilyl group provides stability during synthetic processes, allowing for selective deprotection when needed. This compound is often employed in the synthesis of biologically active molecules, including potential therapeutics targeting various diseases. Its application extends to material science, where it can be used to modify surfaces or create functionalized polymers with specific properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿41,180.00 |
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(4-((4-(2-((tert-Butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)methyl)-3-fluorophenyl)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 reagent. Its structure, featuring a piperazine moiety and a tert-butyldiphenylsilyl-protected hydroxyl group, makes it valuable in the preparation of complex molecules, especially in pharmaceutical research. The fluorophenyl group enhances its reactivity and selectivity in forming carbon-carbon bonds, which is crucial in the development of drug candidates. Additionally, the tert-butyldiphenylsilyl group provides stability during synthetic processes, allowing for selective deprotection when needed. This compound is often employed in the synthesis of biologically active molecules, including potential therapeutics targeting various diseases. Its application extends to material science, where it can be used to modify surfaces or create functionalized polymers with specific properties.
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