(2-Methoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)boronic acid
98%
- Product Code: 89060
CAS:
1704080-61-4
| Molecular Weight: | 314.17 g./mol | Molecular Formula: | C₁₂H₁₉BN₂O₅S |
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| EC Number: | MDL Number: | MFCD28400411 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly as a key intermediate in the development of various biologically active molecules. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic compounds, including drugs and agrochemicals. The presence of the methoxy and sulfonyl groups enhances its reactivity and selectivity in these reactions. Additionally, it is explored in the design of potential therapeutic agents, especially in the field of oncology, where boronic acid derivatives are known to exhibit inhibitory effects on certain enzymes or proteins involved in cancer progression. Its structural features also make it a candidate for use in the development of sensors or probes for biochemical applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿39,447.00 |
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(2-Methoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly as a key intermediate in the development of various biologically active molecules. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic compounds, including drugs and agrochemicals. The presence of the methoxy and sulfonyl groups enhances its reactivity and selectivity in these reactions. Additionally, it is explored in the design of potential therapeutic agents, especially in the field of oncology, where boronic acid derivatives are known to exhibit inhibitory effects on certain enzymes or proteins involved in cancer progression. Its structural features also make it a candidate for use in the development of sensors or probes for biochemical applications.
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