2-(3-(Difluoromethoxy)-4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 41456
CAS:
1641580-18-8
| Molecular Weight: | 288.0706 g./mol | Molecular Formula: | C₁₃H₁₆BF₃O₃ |
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| EC Number: | MDL Number: | MFCD24039812 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in the pharmaceutical industry. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. This reaction is essential in the development of various drugs, agrochemicals, and advanced materials. Additionally, its specific fluorinated aromatic structure can contribute to the enhancement of metabolic stability and bioavailability in drug candidates, making it a crucial component in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $753.99 |
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2-(3-(Difluoromethoxy)-4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in the pharmaceutical industry. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. This reaction is essential in the development of various drugs, agrochemicals, and advanced materials. Additionally, its specific fluorinated aromatic structure can contribute to the enhancement of metabolic stability and bioavailability in drug candidates, making it a crucial component in medicinal chemistry research.
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