[4-(diethylsulfamoyl)phenyl]boronic acid
98%
- Product Code: 91001
CAS:
850568-76-2
| Molecular Weight: | 257.11 g./mol | Molecular Formula: | C₁₀H₁₆BNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06659846 | |
| Melting Point: | 120-124°C | Boiling Point: | 428.2°C |
| Density: | 1.29g/mL | 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 acts as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and material science research. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, aiding in the detection of specific biomolecules. Its diethylsulfamoyl group further enhances its solubility and reactivity in various organic solvents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿7,767.00 |
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[4-(diethylsulfamoyl)phenyl]boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It acts as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and material science research. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, aiding in the detection of specific biomolecules. Its diethylsulfamoyl group further enhances its solubility and reactivity in various organic solvents.
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