(4-((4-(2-((tert-Butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)methyl)-2-fluorophenyl)boronic acid
98%
- Product Code: 89191
CAS:
1704096-94-5
| Molecular Weight: | 520.52 g./mol | Molecular Formula: | C₂₉H₃₈BFN₂O₃Si |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is crucial in creating complex molecules, including drug candidates and biologically active compounds. The tert-butyldiphenylsilyl (TBDPS) protecting group in the structure helps stabilize the molecule during synthetic processes, allowing selective reactions to occur without interference. Its application is significant in the synthesis of targeted therapies, especially in cancer research, where boronic acid derivatives are explored for their potential as protease inhibitors. Additionally, the fluorophenyl moiety enhances the compound's ability to interact with biological targets, making it a promising intermediate in drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿50,210.00 |
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(4-((4-(2-((tert-Butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)methyl)-2-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is crucial in creating complex molecules, including drug candidates and biologically active compounds. The tert-butyldiphenylsilyl (TBDPS) protecting group in the structure helps stabilize the molecule during synthetic processes, allowing selective reactions to occur without interference. Its application is significant in the synthesis of targeted therapies, especially in cancer research, where boronic acid derivatives are explored for their potential as protease inhibitors. Additionally, the fluorophenyl moiety enhances the compound's ability to interact with biological targets, making it a promising intermediate in drug discovery.
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