(2-Fluoro-4-((4-methylpiperidin-1-yl)methyl)phenyl)boronic acid
98%
- Product Code: 67376
CAS:
1704064-21-0
| Molecular Weight: | 251.11 g./mol | Molecular Formula: | C₁₃H₁₉BFNO₂ |
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| EC Number: | MDL Number: | MFCD28400181 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which makes it a valuable building block in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the development of pharmaceuticals, agrochemicals, and advanced materials. Its specific structure, incorporating a fluorine atom and a piperidine moiety, enhances its potential in designing biologically active molecules, particularly in the creation of enzyme inhibitors or receptor modulators. The compound’s ability to form stable complexes with diols also makes it useful in sensor technologies for detecting carbohydrates or other diol-containing molecules. Additionally, its unique properties may contribute to its application in the synthesis of novel drug candidates targeting neurological disorders or cancer therapies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿77,300.00 |
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(2-Fluoro-4-((4-methylpiperidin-1-yl)methyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which makes it a valuable building block in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the development of pharmaceuticals, agrochemicals, and advanced materials. Its specific structure, incorporating a fluorine atom and a piperidine moiety, enhances its potential in designing biologically active molecules, particularly in the creation of enzyme inhibitors or receptor modulators. The compound’s ability to form stable complexes with diols also makes it useful in sensor technologies for detecting carbohydrates or other diol-containing molecules. Additionally, its unique properties may contribute to its application in the synthesis of novel drug candidates targeting neurological disorders or cancer therapies.
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