(5-Fluoro-2-(N-methylsulfamoyl)phenyl)boronic acid
98%
- Product Code: 186485
CAS:
1218790-75-0
| Molecular Weight: | 233.03 g./mol | Molecular Formula: | C₇H₉BFNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15143479 | |
| Melting Point: | Boiling Point: | 432.2±55.0 °C(Predicted) | |
| Density: | 1.49±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. It plays an important role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in drug discovery processes. Commonly utilized in the preparation of potential sulfonyl-containing therapeutic agents, including those investigated for anticancer and anti-inflammatory activities. Its boronic acid group facilitates palladium-catalyzed coupling, making it valuable in medicinal chemistry for constructing complex aromatic frameworks.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | $191.18 |
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| 1g | 10-20 days | $514.65 |
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| 5g | 10-20 days | $2,056.74 |
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(5-Fluoro-2-(N-methylsulfamoyl)phenyl)boronic acid
Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. It plays an important role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in drug discovery processes. Commonly utilized in the preparation of potential sulfonyl-containing therapeutic agents, including those investigated for anticancer and anti-inflammatory activities. Its boronic acid group facilitates palladium-catalyzed coupling, making it valuable in medicinal chemistry for constructing complex aromatic frameworks.
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