(4-Methoxy-3-(N-methylsulfamoyl)phenyl)boronic acid
98%
- Product Code: 89322
CAS:
874459-71-9
| Molecular Weight: | 245.06 g./mol | Molecular Formula: | C₈H₁₂BNO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27931062 | |
| 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 boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its methoxy and sulfamoyl groups enhance its reactivity and selectivity in complex molecular constructions. Additionally, it is employed in the development of bioactive molecules and drug intermediates, contributing to the synthesis of compounds with potential therapeutic applications. Its stability and compatibility with various reaction conditions make it a versatile tool in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $936.06 |
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(4-Methoxy-3-(N-methylsulfamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its methoxy and sulfamoyl groups enhance its reactivity and selectivity in complex molecular constructions. Additionally, it is employed in the development of bioactive molecules and drug intermediates, contributing to the synthesis of compounds with potential therapeutic applications. Its stability and compatibility with various reaction conditions make it a versatile tool in modern synthetic chemistry.
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