(2-(N-Methylsulfamoyl)phenyl)boronic acid
97%
- Product Code: 89032
CAS:
956283-09-3
| Molecular Weight: | 215.03 g./mol | Molecular Formula: | C₇H₁₀BNO₄S |
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| EC Number: | MDL Number: | MFCD09038342 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This chemical 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 essential for coupling with aryl or vinyl halides, making it valuable in pharmaceutical and material science research. Additionally, it finds application in the development of sensors and probes due to its ability to interact with specific biological or chemical targets. Its sulfamoyl group further enhances its utility in designing compounds with potential biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft19,878.23 |
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| 0.250 | 10-20 days | Ft36,362.61 |
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(2-(N-Methylsulfamoyl)phenyl)boronic acid
This chemical 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 essential for coupling with aryl or vinyl halides, making it valuable in pharmaceutical and material science research. Additionally, it finds application in the development of sensors and probes due to its ability to interact with specific biological or chemical targets. Its sulfamoyl group further enhances its utility in designing compounds with potential biological activity.
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