2-(4-(2,2-Difluoroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
≥95%
- Product Code: 118509
CAS:
864754-48-3
| Molecular Weight: | 284.11 g./mol | Molecular Formula: | C₁₄H₁₉BF₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08706127 | |
| Melting Point: | Boiling Point: | 346.705°C at 760 mmHg | |
| Density: | 1.117g/cm3 | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester functional group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. The difluoroethoxy group enhances its stability and reactivity, making it suitable for applications in drug discovery and development. Additionally, it is employed in the synthesis of complex organic molecules, including bioactive compounds and polymers, due to its ability to facilitate precise and efficient chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $133.12 |
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| 0.250 | 10-20 days | $199.55 |
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| 1.000 | 10-20 days | $498.47 |
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2-(4-(2,2-Difluoroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester functional group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. The difluoroethoxy group enhances its stability and reactivity, making it suitable for applications in drug discovery and development. Additionally, it is employed in the synthesis of complex organic molecules, including bioactive compounds and polymers, due to its ability to facilitate precise and efficient chemical transformations.
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