5-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
97%
- Product Code: 119875
CAS:
1038828-32-8
| Molecular Weight: | 238.06 g./mol | Molecular Formula: | C₁₂H₁₆BFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16994248 | |
| Melting Point: | Boiling Point: | 320.4±32.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the preparation of complex molecules, including pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the construction of carbon-carbon bonds. Additionally, it is employed in the development of advanced materials, including polymers and organic electronic components. The fluorine substituent enhances its reactivity and selectivity in various chemical transformations, making it valuable in medicinal chemistry for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft34,477.15 |
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| 0.250 | 10-20 days | Ft84,469.01 |
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| 1.000 | 10-20 days | Ft159,887.76 |
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5-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the preparation of complex molecules, including pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the construction of carbon-carbon bonds. Additionally, it is employed in the development of advanced materials, including polymers and organic electronic components. The fluorine substituent enhances its reactivity and selectivity in various chemical transformations, making it valuable in medicinal chemistry for drug discovery and development.
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