Potassium (bromomethyl)trifluoroborate
98.0%
- Product Code: 89417
CAS:
888711-44-2
| Molecular Weight: | 200.84 g./mol | Molecular Formula: | CH₂BBrF₃K |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09265154 | |
| Melting Point: | 220 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Primarily used in organic synthesis, this compound serves as a versatile reagent for the introduction of bromomethyl groups into various molecules. It is particularly valuable in cross-coupling reactions, such as Suzuki-Miyaura couplings, where it facilitates the formation of carbon-carbon bonds. The trifluoroborate moiety enhances stability and solubility, making it easier to handle and store compared to other organoboron reagents. Additionally, it is employed in the preparation of pharmaceuticals and agrochemicals, where precise functional group transformations are crucial. Its compatibility with a wide range of reaction conditions further broadens its utility in complex synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| TITRATION | 88 112% |
| PURITYHNMR | 98-100 |
| APPEARANCE | White to tan powder,crystals and/or chunks |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
| MELTING POINT | 220 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿480.00 |
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| 5.000 | 10-20 days | ฿1,180.00 |
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Potassium (bromomethyl)trifluoroborate
Primarily used in organic synthesis, this compound serves as a versatile reagent for the introduction of bromomethyl groups into various molecules. It is particularly valuable in cross-coupling reactions, such as Suzuki-Miyaura couplings, where it facilitates the formation of carbon-carbon bonds. The trifluoroborate moiety enhances stability and solubility, making it easier to handle and store compared to other organoboron reagents. Additionally, it is employed in the preparation of pharmaceuticals and agrochemicals, where precise functional group transformations are crucial. Its compatibility with a wide range of reaction conditions further broadens its utility in complex synthetic pathways.
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