(4-Methoxy-3-(N-((4-methoxycyclohexyl) methyl)sulfamoyl)phenyl)boronic acid
98%
- Product Code: 89321
CAS:
1704082-65-4
| Molecular Weight: | 357.23 g./mol | Molecular Formula: | C₁₅H₂₄BNO₆S |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly as a key intermediate in the development of biologically active molecules. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic compounds, including potential drug candidates. Additionally, the presence of sulfamoyl and methoxy groups enhances its utility in designing molecules with specific binding properties, often targeting enzymes or receptors in medicinal chemistry. Its application extends to the preparation of advanced materials and ligands for catalysis, where its structural features contribute to tailored reactivity and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $2,070.64 |
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(4-Methoxy-3-(N-((4-methoxycyclohexyl) methyl)sulfamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly as a key intermediate in the development of biologically active molecules. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic compounds, including potential drug candidates. Additionally, the presence of sulfamoyl and methoxy groups enhances its utility in designing molecules with specific binding properties, often targeting enzymes or receptors in medicinal chemistry. Its application extends to the preparation of advanced materials and ligands for catalysis, where its structural features contribute to tailored reactivity and selectivity.
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