2,6-Difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
97%
- Product Code: 61573
CAS:
1072945-00-6
| Molecular Weight: | 241.04 g./mol | Molecular Formula: | C₁₁H₁₄BF₂NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09037475 | |
| Melting Point: | Boiling Point: | 307.8±42.0°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a valuable intermediate for constructing complex molecules, especially in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs). Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. Additionally, it is employed in material science for the synthesis of advanced organic materials, including polymers and liquid crystals, due to its stability and reactivity. Its fluorine substituents also contribute to its utility in designing compounds with specific electronic or steric properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | €17.81 |
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| 1.000 | 10-20 days | €45.59 |
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| 5.000 | 10-20 days | €120.38 |
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2,6-Difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a valuable intermediate for constructing complex molecules, especially in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs). Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. Additionally, it is employed in material science for the synthesis of advanced organic materials, including polymers and liquid crystals, due to its stability and reactivity. Its fluorine substituents also contribute to its utility in designing compounds with specific electronic or steric properties.
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