1-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)pyrrolidine
95%
- Product Code: 39184
CAS:
1256360-38-9
| Molecular Weight: | 305.2000 g./mol | Molecular Formula: | C₁₇H₂₅BFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17214292 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester functional group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. The presence of the fluorine atom enhances its reactivity and selectivity in these transformations, making it valuable for constructing complex molecular architectures. Additionally, the pyrrolidine moiety can contribute to the compound's solubility and stability, facilitating its use in various synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $244.44 |
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1-(2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)pyrrolidine
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester functional group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. The presence of the fluorine atom enhances its reactivity and selectivity in these transformations, making it valuable for constructing complex molecular architectures. Additionally, the pyrrolidine moiety can contribute to the compound's solubility and stability, facilitating its use in various synthetic pathways.
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