(2-Methoxy-5-(N-methylsulfamoyl)phenyl)boronic acid
98%
- Product Code: 89061
CAS:
1704081-32-2
| Molecular Weight: | 245.06 g./mol | Molecular Formula: | C₈H₁₂BNO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400429 | |
| Melting Point: | 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 serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and material science research. Additionally, it is employed in the development of bioactive compounds and advanced materials due to its ability to introduce specific functional groups into target molecules. Its sulfamoyl moiety also contributes to its potential use in designing molecules with enhanced biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,458.56 |
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(2-Methoxy-5-(N-methylsulfamoyl)phenyl)boronic 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. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and material science research. Additionally, it is employed in the development of bioactive compounds and advanced materials due to its ability to introduce specific functional groups into target molecules. Its sulfamoyl moiety also contributes to its potential use in designing molecules with enhanced biological activity.
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