(2-(N,N-Dimethylsulfamoyl)-4,5-difluorophenyl)boronic acid
98%
- Product Code: 89013
CAS:
1704065-67-7
| Molecular Weight: | 265.05 g./mol | Molecular Formula: | C₈H₁₀BF₂NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384293 | |
| Melting Point: | Boiling Point: | ||
| Density: | 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. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The difluoro and sulfamoyl groups enhance its reactivity and selectivity, allowing for precise modifications in target molecules. It is often employed in the development of active pharmaceutical ingredients (APIs) and in the synthesis of intermediates for drug discovery. Additionally, its unique structure can be leveraged in material science for creating advanced polymers or functionalized materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿40,630.00 |
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(2-(N,N-Dimethylsulfamoyl)-4,5-difluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The difluoro and sulfamoyl groups enhance its reactivity and selectivity, allowing for precise modifications in target molecules. It is often employed in the development of active pharmaceutical ingredients (APIs) and in the synthesis of intermediates for drug discovery. Additionally, its unique structure can be leveraged in material science for creating advanced polymers or functionalized materials.
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