[4-(cyclohexylsulfamoyl)phenyl]boronic acid
98%
- Product Code: 89267
CAS:
871329-66-7
| Molecular Weight: | 283.15 g./mol | Molecular Formula: | C₁₂H₁₈BNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07363754 | |
| Melting Point: | 270-276 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical research and drug development. Additionally, it is employed in the preparation of advanced materials, such as polymers and liquid crystals, due to its ability to introduce specific functional groups into molecular structures. Its stability and reactivity also make it suitable for use in catalysis and as a building block in the synthesis of bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿6,930.00 |
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[4-(cyclohexylsulfamoyl)phenyl]boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical research and drug development. Additionally, it is employed in the preparation of advanced materials, such as polymers and liquid crystals, due to its ability to introduce specific functional groups into molecular structures. Its stability and reactivity also make it suitable for use in catalysis and as a building block in the synthesis of bioactive compounds.
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