2-2-[(4-fluorophenyl)methoxy]phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 58604
CAS:
2246638-38-8
| Molecular Weight: | 328.19 g./mol | Molecular Formula: | C₁₉H₂₂BFO₃ |
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| EC Number: | MDL Number: | MFCD32206480 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. Its boronate ester functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. The presence of the fluorophenyl moiety enhances its reactivity and selectivity in these reactions, making it particularly useful in the development of bioactive compounds. Additionally, it serves as a building block in the creation of advanced materials, such as organic electronic components, due to its ability to facilitate precise molecular engineering. Its stability and compatibility with diverse reaction conditions further broaden its applicability in both academic research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $620.44 |
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| 1.000 | 10-20 days | $1,794.05 |
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2-2-[(4-fluorophenyl)methoxy]phenyl-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 various pharmaceuticals and agrochemicals. Its boronate ester functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. The presence of the fluorophenyl moiety enhances its reactivity and selectivity in these reactions, making it particularly useful in the development of bioactive compounds. Additionally, it serves as a building block in the creation of advanced materials, such as organic electronic components, due to its ability to facilitate precise molecular engineering. Its stability and compatibility with diverse reaction conditions further broaden its applicability in both academic research and industrial processes.
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