Pinacol 3-fluoro-4-(2-fluorophenylsulfonamido) phenylboronic acid
95%
- Product Code: 44802
CAS:
1314069-48-1
| Molecular Weight: | 395.2285064 g./mol | Molecular Formula: | C₁₈H₂₀BF₂NO₄S |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily used in organic synthesis and medicinal chemistry as a key intermediate in the development of biologically active molecules. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, particularly in the synthesis of complex pharmaceutical compounds. The presence of fluorine atoms enhances its potential in drug design, as fluorinated compounds often exhibit improved metabolic stability and bioavailability. Additionally, its sulfonamide moiety contributes to its application in the creation of enzyme inhibitors, particularly targeting proteins involved in disease pathways. This chemical is also explored in the development of diagnostic agents and probes for studying biological systems due to its unique structural features.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,488.00 |
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| 0.250 | 10-20 days | ฿12,492.00 |
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| 1.000 | 10-20 days | ฿29,592.00 |
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Pinacol 3-fluoro-4-(2-fluorophenylsulfonamido) phenylboronic acid
This compound is primarily used in organic synthesis and medicinal chemistry as a key intermediate in the development of biologically active molecules. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, particularly in the synthesis of complex pharmaceutical compounds. The presence of fluorine atoms enhances its potential in drug design, as fluorinated compounds often exhibit improved metabolic stability and bioavailability. Additionally, its sulfonamide moiety contributes to its application in the creation of enzyme inhibitors, particularly targeting proteins involved in disease pathways. This chemical is also explored in the development of diagnostic agents and probes for studying biological systems due to its unique structural features.
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