(3-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid
98%
- Product Code: 65440
CAS:
1449132-41-5
| Molecular Weight: | 283.16 g./mol | Molecular Formula: | C₁₂H₁₈BNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20265316 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group is highly reactive with aryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for synthesizing advanced polymers and organic electronic materials. Its sulfonyl and piperidine moieties contribute to its stability and reactivity, making it a versatile intermediate in various chemical processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $558.66 |
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(3-((4-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group is highly reactive with aryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for synthesizing advanced polymers and organic electronic materials. Its sulfonyl and piperidine moieties contribute to its stability and reactivity, making it a versatile intermediate in various chemical processes.
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