Potassium Trifluoro(trifluoromethyl)borate
≥98%
- Product Code: 91078
CAS:
42298-15-7
| Molecular Weight: | 175.91 g./mol | Molecular Formula: | CBF₆K |
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| Density: | Storage Condition: | room temperature |
Product Description:
Potassium trifluoro(trifluoromethyl)borate is primarily used in organic synthesis as a versatile reagent. It is particularly valuable in the formation of carbon-carbon and carbon-heteroatom bonds, making it a key component in the development of pharmaceuticals and fine chemicals. Its strong electrophilic properties enable it to participate in various catalytic processes, including cross-coupling reactions, which are essential for constructing complex molecular structures. Additionally, it is employed in the synthesis of boron-containing compounds, which have applications in materials science and as intermediates in organic transformations. Its stability and reactivity under mild conditions make it a preferred choice in advanced synthetic methodologies.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystaline |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿2,290.00 |
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| 1.000 | 10-20 days | ฿7,190.00 |
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| 5.000 | 10-20 days | ฿29,200.00 |
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Potassium Trifluoro(trifluoromethyl)borate
Potassium trifluoro(trifluoromethyl)borate is primarily used in organic synthesis as a versatile reagent. It is particularly valuable in the formation of carbon-carbon and carbon-heteroatom bonds, making it a key component in the development of pharmaceuticals and fine chemicals. Its strong electrophilic properties enable it to participate in various catalytic processes, including cross-coupling reactions, which are essential for constructing complex molecular structures. Additionally, it is employed in the synthesis of boron-containing compounds, which have applications in materials science and as intermediates in organic transformations. Its stability and reactivity under mild conditions make it a preferred choice in advanced synthetic methodologies.
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