(4-(N,N-Diethylsulfamoyl)-3,5-dimethylphenyl)boronic acid
98%
- Product Code: 89253
CAS:
1704067-22-0
| Molecular Weight: | 285.17 g./mol | Molecular Formula: | C₁₂H₂₀BNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384284 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its diethylsulfamoyl and dimethylphenyl groups contribute to its stability and reactivity, enhancing its effectiveness in various catalytic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | $1,468.11 |
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(4-(N,N-Diethylsulfamoyl)-3,5-dimethylphenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its diethylsulfamoyl and dimethylphenyl groups contribute to its stability and reactivity, enhancing its effectiveness in various catalytic processes.
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