3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(2,2,2-trifluoroethoxy)pyridine
98%
- Product Code: 117430
CAS:
1073354-46-7
| Molecular Weight: | 303.09 g./mol | Molecular Formula: | C₁₃H₁₇BF₃NO₃ |
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| EC Number: | MDL Number: | MFCD07781172 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a boronic ester precursor. Its structure allows for the introduction of the pyridine moiety into complex molecules, making it valuable in the development of pharmaceuticals and agrochemicals. The trifluoroethoxy group enhances the compound's stability and reactivity, making it suitable for constructing biologically active molecules, including potential drug candidates. Additionally, it can be employed in materials science for the synthesis of advanced organic materials with specific electronic or optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £44.58 |
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| 0.250 | 10-20 days | £75.52 |
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| 1.000 | 10-20 days | £203.55 |
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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(2,2,2-trifluoroethoxy)pyridine
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a boronic ester precursor. Its structure allows for the introduction of the pyridine moiety into complex molecules, making it valuable in the development of pharmaceuticals and agrochemicals. The trifluoroethoxy group enhances the compound's stability and reactivity, making it suitable for constructing biologically active molecules, including potential drug candidates. Additionally, it can be employed in materials science for the synthesis of advanced organic materials with specific electronic or optical properties.
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