2-Fluoro-6-(thiazol-2-yl)pyridine-3-boronic acid
95%
- Product Code: 91672
CAS:
2225181-42-8
| Molecular Weight: | 224.0198432 g./mol | Molecular Formula: | C₈H₆BFN₂O₂S |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | -20℃, sealed and 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 facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds. These compounds are often explored for their potential therapeutic properties, including antimicrobial, anticancer, and anti-inflammatory activities. Additionally, its thiazole and pyridine moieties make it valuable in designing heterocyclic compounds, which are frequently found in agrochemicals and materials science applications. Its fluorine substituent can enhance the stability and bioavailability of the resulting molecules, making it a versatile building block in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿10,520.00 |
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| 0.025 | 10-20 days | ฿45,060.00 |
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| 0.100 | 10-20 days | ฿135,200.00 |
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2-Fluoro-6-(thiazol-2-yl)pyridine-3-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 facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds. These compounds are often explored for their potential therapeutic properties, including antimicrobial, anticancer, and anti-inflammatory activities. Additionally, its thiazole and pyridine moieties make it valuable in designing heterocyclic compounds, which are frequently found in agrochemicals and materials science applications. Its fluorine substituent can enhance the stability and bioavailability of the resulting molecules, making it a versatile building block in medicinal chemistry.
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