2-(Difluoromethoxy)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
95%
- Product Code: 41880
CAS:
1628116-87-9
| Molecular Weight: | 271.07 g./mol | Molecular Formula: | C₁₂H₁₆BF₂NO₃ |
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| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group enables it to act as a key intermediate in the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its pyridine moiety can serve as a directing group in metal-catalyzed reactions, further expanding its utility in constructing heterocyclic compounds. The difluoromethoxy group enhances its stability and reactivity, making it suitable for applications in drug discovery and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $187.94 |
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| 0.250 | 10-20 days | $376.23 |
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2-(Difluoromethoxy)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group enables it to act as a key intermediate in the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its pyridine moiety can serve as a directing group in metal-catalyzed reactions, further expanding its utility in constructing heterocyclic compounds. The difluoromethoxy group enhances its stability and reactivity, making it suitable for applications in drug discovery and material science.
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