(4-(piperidin-3-yl)-3-(trifluoromethyl)phenyl)boronic acid
95%
- Product Code: 91315
CAS:
2256708-80-0
| Molecular Weight: | 273.0592096 g./mol | Molecular Formula: | C₁₂H₁₅BF₃NO₂ |
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| Density: | Storage Condition: | -20℃ |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the construction of complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates. Additionally, its trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting molecules, which is advantageous in medicinal chemistry. The compound is also explored in materials science for designing advanced organic materials with specific electronic or optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿41,220.00 |
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(4-(piperidin-3-yl)-3-(trifluoromethyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the construction of complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates. Additionally, its trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting molecules, which is advantageous in medicinal chemistry. The compound is also explored in materials science for designing advanced organic materials with specific electronic or optical properties.
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