5-(3-Trifluoromethylphenyl)thiazole-4-boronic acid pinacol ester
95%
- Product Code: 90789
CAS:
2223041-95-8
| Molecular Weight: | 373.1981696 g./mol | Molecular Formula: | C₁₆H₁₉BF₃NO₃S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates targeting specific diseases. Additionally, it finds use in material science for creating advanced polymers or organic electronic materials due to its ability to introduce specific functional groups into molecular frameworks.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿8,280.00 |
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| 0.025 | 10-20 days | ฿24,300.00 |
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5-(3-Trifluoromethylphenyl)thiazole-4-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates targeting specific diseases. Additionally, it finds use in material science for creating advanced polymers or organic electronic materials due to its ability to introduce specific functional groups into molecular frameworks.
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