2-Fluoro-6-(pyrrolidin-1-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
95%
- Product Code: 42463
CAS:
1309980-28-6
| Molecular Weight: | 292.16 g./mol | Molecular Formula: | C₁₅H₂₂BFN₂O₂ |
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| EC Number: | MDL Number: | MFCD15530269 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
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 the formation of carbon-carbon bonds, making it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. The presence of the pyrrolidinyl group enhances its reactivity and selectivity in these reactions. Additionally, it serves as a key intermediate in the development of bioactive compounds, especially in medicinal chemistry for drug discovery and optimization. Its fluorine atom can influence the pharmacokinetic properties of the resulting molecules, improving their stability and bioavailability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $107.13 |
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| 0.250 | 10-20 days | $167.70 |
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| 1.000 | 10-20 days | $452.03 |
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2-Fluoro-6-(pyrrolidin-1-yl)-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 the formation of carbon-carbon bonds, making it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. The presence of the pyrrolidinyl group enhances its reactivity and selectivity in these reactions. Additionally, it serves as a key intermediate in the development of bioactive compounds, especially in medicinal chemistry for drug discovery and optimization. Its fluorine atom can influence the pharmacokinetic properties of the resulting molecules, improving their stability and bioavailability.
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