4-(3,5-Difluorophenyl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90374
CAS:
1402227-90-0
| Molecular Weight: | 340.1930664 g./mol | Molecular Formula: | C₁₆H₁₉BF₂O₃S |
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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 Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the production of biologically active compounds, including potential drug candidates. Additionally, it finds applications in material science, where it contributes to the synthesis of advanced organic materials, such as polymers or small molecules for electronic devices. Its fluorinated phenyl group can enhance the stability and reactivity of the final products, making it a versatile building block in various research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $248.42 |
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| 0.025 | 10-20 days | $729.07 |
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4-(3,5-Difluorophenyl)thiophene-2-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the production of biologically active compounds, including potential drug candidates. Additionally, it finds applications in material science, where it contributes to the synthesis of advanced organic materials, such as polymers or small molecules for electronic devices. Its fluorinated phenyl group can enhance the stability and reactivity of the final products, making it a versatile building block in various research and industrial applications.
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