(3-(N-(2,4-Dimethoxybenzyl)sulfamoyl) phenyl)boronic acid
98%
- Product Code: 65488
CAS:
1704082-90-5
| Molecular Weight: | 351.18 g./mol | Molecular Formula: | C₁₅H₁₈BNO₆S |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is known for its role in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal in forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including potential drug candidates. The presence of the sulfamoyl group enhances its reactivity and selectivity, making it valuable in designing and developing new therapeutic agents. Additionally, its structure, particularly the dimethoxybenzyl moiety, may contribute to its use in targeting specific biological pathways or receptors in drug discovery efforts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿44,800.00 |
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(3-(N-(2,4-Dimethoxybenzyl)sulfamoyl) phenyl)boronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is known for its role in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal in forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including potential drug candidates. The presence of the sulfamoyl group enhances its reactivity and selectivity, making it valuable in designing and developing new therapeutic agents. Additionally, its structure, particularly the dimethoxybenzyl moiety, may contribute to its use in targeting specific biological pathways or receptors in drug discovery efforts.
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