5-(3-Fluorophenyl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90777
CAS:
1402174-30-4
| Molecular Weight: | 322.2026032 g./mol | Molecular Formula: | C₁₆H₂₀BFO₃S |
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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 like the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and materials science industries. The boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its fluorophenyl moiety can enhance the biological activity or modify the electronic properties of the resulting compounds, making it valuable in drug development and the design of functional materials. Additionally, its stability and reactivity make it a preferred choice for synthesizing intermediates in the production of agrochemicals and organic electronic materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿8,982.00 |
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| 0.025 | 10-20 days | ฿19,800.00 |
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5-(3-Fluorophenyl)thiophene-2-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and materials science industries. The boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its fluorophenyl moiety can enhance the biological activity or modify the electronic properties of the resulting compounds, making it valuable in drug development and the design of functional materials. Additionally, its stability and reactivity make it a preferred choice for synthesizing intermediates in the production of agrochemicals and organic electronic materials.
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