4-Methyl-3-(3-(4-Methylpiperidin-1-yl)propoxy)phenylboronic acid
98%
- Product Code: 90675
CAS:
1704064-30-1
| Molecular Weight: | 291.2 g./mol | Molecular Formula: | C₁₆H₂₆BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384331 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, making it valuable in the development of complex organic molecules, including potential drug candidates. Its structure, featuring a piperidine moiety, also suggests potential applications in medicinal chemistry, where it may be used to design and synthesize compounds targeting neurological or receptor-based diseases. Additionally, its properties could be explored in materials science for the development of advanced polymers or sensors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿110,000.00 |
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4-Methyl-3-(3-(4-Methylpiperidin-1-yl)propoxy)phenylboronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, making it valuable in the development of complex organic molecules, including potential drug candidates. Its structure, featuring a piperidine moiety, also suggests potential applications in medicinal chemistry, where it may be used to design and synthesize compounds targeting neurological or receptor-based diseases. Additionally, its properties could be explored in materials science for the development of advanced polymers or sensors.
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