4-Isopropylsulfonylbenzeneboronic acid
97%
- Product Code: 90570
CAS:
850567-98-5
| Molecular Weight: | 228.07 g./mol | Molecular Formula: | C₉H₁₃BO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06659866 | |
| Melting Point: | 126-128 | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other biomolecules, making it valuable in biochemical research and medical applications.
Product Specification:
| Test | Specification |
|---|---|
| CARBON BY ELEMENTAL ANALYSIS | 45.4 47.9% |
| Melting point | 126 128? |
| OXYGEN BY ELEMENTAL ANALYSIS | 26.7 28.5% |
| PURITYHPLC | 97 100% |
| SULFUR BY ELEMENTAL ANALYSIS | 13.2-14.5 |
| PROTON NMR SPECTRUM | Conforms to Structure |
| APPEARANCE | White to off-white Solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €15.30 |
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| 1.000 | 10-20 days | €43.79 |
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| 5.000 | 10-20 days | €211.06 |
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4-Isopropylsulfonylbenzeneboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other biomolecules, making it valuable in biochemical research and medical applications.
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