Potassium Trifluoro[3-(methoxycarbonyl)bicyclo[1.1.1]pentan-1-yl]borate
≥95.0%(qNMR)
- Product Code: 223268
CAS:
2410559-74-7
| Molecular Weight: | 232.05 g./mol | Molecular Formula: | C₇H₉BF₃KO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31729418 | |
| Melting Point: | 265 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a reagent in organic synthesis, particularly in cross-coupling reactions to introduce the bicyclo[1.1.1]pentane (BCP) group into molecules. The BCP moiety is valued in medicinal chemistry as a bioisostere for phenyl or tert-butyl groups, improving pharmacokinetic properties such as metabolic stability and solubility. This potassium borate salt enables the formation of C–C bonds via transition metal-catalyzed reactions, allowing efficient incorporation of the BCP unit into drug candidates. Its application is especially prominent in the development of bioactive molecules and pharmaceuticals where structural rigidity and reduced lipophilicity are desired.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | ฿12,570.00 |
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Potassium Trifluoro[3-(methoxycarbonyl)bicyclo[1.1.1]pentan-1-yl]borate
Used as a reagent in organic synthesis, particularly in cross-coupling reactions to introduce the bicyclo[1.1.1]pentane (BCP) group into molecules. The BCP moiety is valued in medicinal chemistry as a bioisostere for phenyl or tert-butyl groups, improving pharmacokinetic properties such as metabolic stability and solubility. This potassium borate salt enables the formation of C–C bonds via transition metal-catalyzed reactions, allowing efficient incorporation of the BCP unit into drug candidates. Its application is especially prominent in the development of bioactive molecules and pharmaceuticals where structural rigidity and reduced lipophilicity are desired.
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