(3-(4-(tert-Butoxycarbonyl)piperazine-1 -carbonyl)-4-fluorophenyl)boronic acid
98%
- Product Code: 65476
CAS:
1704082-92-7
| Molecular Weight: | 352.16 g./mol | Molecular Formula: | C₁₆H₂₂BFN₂O₅ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its boronic acid functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic compounds. The tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety allows for selective deprotection, enabling controlled modification of the molecule during multi-step synthetic processes. Additionally, the fluorine substituent enhances the compound’s reactivity and stability, making it suitable for use in the preparation of fluorinated drug candidates, which are often sought after for their improved metabolic stability and bioavailability. This chemical is also explored in the design of enzyme inhibitors and receptor ligands, particularly in targeting diseases where boron-containing compounds show therapeutic potential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿32,710.00 |
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(3-(4-(tert-Butoxycarbonyl)piperazine-1 -carbonyl)-4-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its boronic acid functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic compounds. The tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety allows for selective deprotection, enabling controlled modification of the molecule during multi-step synthetic processes. Additionally, the fluorine substituent enhances the compound’s reactivity and stability, making it suitable for use in the preparation of fluorinated drug candidates, which are often sought after for their improved metabolic stability and bioavailability. This chemical is also explored in the design of enzyme inhibitors and receptor ligands, particularly in targeting diseases where boron-containing compounds show therapeutic potential.
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