(E)-2-(2,4-Difluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 185007
CAS:
736987-78-3
| Molecular Weight: | 266.09 g./mol | Molecular Formula: | C₁₄H₁₇BF₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08276857 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.099 g/cm3 | Storage Condition: | -20°C, Inert Gas |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated organic molecules. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems with fluorine substitution. The presence of fluorine atoms enhances the compound’s utility in developing bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for lead optimization and in materials science for designing fluorinated π-conjugated systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿1,310.00 |
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| 1.000 G | 10-20 days | ฿3,950.00 |
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| 5.000 G | 10-20 days | ฿18,840.00 |
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| 25.000 G | 10-20 days | ฿94,200.00 |
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(E)-2-(2,4-Difluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated organic molecules. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems with fluorine substitution. The presence of fluorine atoms enhances the compound’s utility in developing bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for lead optimization and in materials science for designing fluorinated π-conjugated systems.
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