5-(3,5-Difluorophenyl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90775
CAS:
1402227-88-6
| 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 used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially those containing thiophene and difluorophenyl moieties. Its application is significant in the development of pharmaceuticals, agrochemicals, and advanced materials. The boronic ester group facilitates efficient coupling with aryl or vinyl halides, enabling the creation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, it is employed in the production of organic electronic materials, such as semiconductors and light-emitting diodes (LEDs), due to the unique electronic properties of thiophene derivatives.
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-(3,5-Difluorophenyl)thiophene-2-boronic acid pinacol ester
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially those containing thiophene and difluorophenyl moieties. Its application is significant in the development of pharmaceuticals, agrochemicals, and advanced materials. The boronic ester group facilitates efficient coupling with aryl or vinyl halides, enabling the creation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, it is employed in the production of organic electronic materials, such as semiconductors and light-emitting diodes (LEDs), due to the unique electronic properties of thiophene derivatives.
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