Pentafluorophenylboronic acid
97%
- Product Code: 89534
Alias:
2,3,4,5,6-Pentafluorophenylboronic acid
CAS:
1582-24-7
| Molecular Weight: | 211.88 g./mol | Molecular Formula: | C₆H₂BF₅O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01074663 | |
| Melting Point: | 176-179°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Pentafluorophenylboronic acid is widely used in organic synthesis as a versatile reagent, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key intermediate for constructing complex molecules, including pharmaceuticals and agrochemicals, due to its ability to form stable boronate esters with diols and other functional groups. In materials science, it is employed to modify surfaces and create advanced polymers with specific properties. Additionally, it serves as a catalyst in certain chemical transformations, enhancing reaction efficiency and selectivity. Its electron-withdrawing pentafluorophenyl group makes it particularly effective in stabilizing reactive intermediates and improving reaction outcomes.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 97-100 |
| APPEARANCE | White powder |
| INFRARED SPECTRUM | Conforms to structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $43.65 |
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| 5.000 | 10-20 days | $141.57 |
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| 25.000 | 10-20 days | $703.15 |
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Pentafluorophenylboronic acid
Pentafluorophenylboronic acid is widely used in organic synthesis as a versatile reagent, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key intermediate for constructing complex molecules, including pharmaceuticals and agrochemicals, due to its ability to form stable boronate esters with diols and other functional groups. In materials science, it is employed to modify surfaces and create advanced polymers with specific properties. Additionally, it serves as a catalyst in certain chemical transformations, enhancing reaction efficiency and selectivity. Its electron-withdrawing pentafluorophenyl group makes it particularly effective in stabilizing reactive intermediates and improving reaction outcomes.
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