(6-(thiazol-4-yl)pyridin-3-yl)boronic acid
95%
- Product Code: 89373
CAS:
1264511-59-2
| Molecular Weight: | 206.02938 g./mol | Molecular Formula: | C₈H₇BN₂O₂S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds, such as drug candidates targeting specific enzymes or receptors. Its thiazole and pyridine moieties contribute to its potential in designing molecules with enhanced binding affinity and selectivity, often explored in medicinal chemistry for treating diseases like cancer or infections. Additionally, it may be utilized in material science for developing functionalized polymers or advanced materials with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿86,000.00 |
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| 0.100 | 10-20 days | ฿258,000.00 |
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(6-(thiazol-4-yl)pyridin-3-yl)boronic acid
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds, such as drug candidates targeting specific enzymes or receptors. Its thiazole and pyridine moieties contribute to its potential in designing molecules with enhanced binding affinity and selectivity, often explored in medicinal chemistry for treating diseases like cancer or infections. Additionally, it may be utilized in material science for developing functionalized polymers or advanced materials with tailored properties.
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