(3-(N,N-Dipropylsulfamoyl)phenyl)boronic acid
95%
- Product Code: 36633
CAS:
1449145-31-6
| Molecular Weight: | 285.17 g./mol | Molecular Formula: | C₁₂H₂₀BNO₄S |
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| EC Number: | MDL Number: | MFCD20265249 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its structure, featuring a boronic acid group and a dipropylsulfamoyl moiety, makes it valuable in the development of pharmaceuticals and agrochemicals, enabling the creation of complex molecules. Additionally, it is employed in the preparation of biologically active compounds, serving as an intermediate in drug discovery processes. Its unique properties also make it suitable for use in material science, particularly in the design of advanced polymers and sensors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,680.00 |
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| 0.250 | 10-20 days | ฿7,812.00 |
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| 1.000 | 10-20 days | ฿23,292.00 |
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(3-(N,N-Dipropylsulfamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its structure, featuring a boronic acid group and a dipropylsulfamoyl moiety, makes it valuable in the development of pharmaceuticals and agrochemicals, enabling the creation of complex molecules. Additionally, it is employed in the preparation of biologically active compounds, serving as an intermediate in drug discovery processes. Its unique properties also make it suitable for use in material science, particularly in the design of advanced polymers and sensors.
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