(4-Chloro-3-(4-hydroxypiperidine-1-carbonyl)phenyl)boronic acid
98%
- Product Code: 89304
CAS:
1704080-30-7
| Molecular Weight: | 283.52 g./mol | Molecular Formula: | C₁₂H₁₅BClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400400 | |
| 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 is essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the hydroxypiperidine moiety can enhance the compound’s solubility and bioavailability, making it a potential intermediate in the development of drug candidates. Its specific structure may also be explored for targeting enzymes or receptors in biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | £2,487.87 |
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(4-Chloro-3-(4-hydroxypiperidine-1-carbonyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry 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 synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the hydroxypiperidine moiety can enhance the compound’s solubility and bioavailability, making it a potential intermediate in the development of drug candidates. Its specific structure may also be explored for targeting enzymes or receptors in biochemical studies.
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