AA09138
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 95% | in stock | $23.00 | $16.00 | - + | |
1g | 95% | in stock | $49.00 | $35.00 | - + | |
10g | 95% | in stock | $448.00 | $314.00 | - + | |
25g | 95% | in stock | $914.00 | $640.00 | - + | |
100g | 95% | in stock | $2,344.00 | $1,641.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA09138 |
Chemical Name: | Potassium 3-trifluoroboratopropionate tert-butyl ester |
CAS Number: | 1023357-66-5 |
Molecular Formula: | C7H13BF3KO2 |
Molecular Weight: | 236.0814 |
MDL Number: | MFCD09993465 |
SMILES: | F[B-](CCC(=O)OC(C)(C)C)(F)F.[K+] |
Potassium (3-(tert-butoxy)-3-oxopropyl)trifluoroborate is a versatile reagent commonly used in organic synthesis for the formation of carbon-carbon bonds through various cross-coupling reactions. This compound serves as a valuable building block in the synthesis of complex organic molecules due to its unique structure and reactivity.One important application of Potassium (3-(tert-butoxy)-3-oxopropyl)trifluoroborate is in Suzuki-Miyaura cross-coupling reactions, where it can react with aryl halides or pseudohalides in the presence of a palladium catalyst to form biaryl compounds. This transformation is instrumental in the construction of pharmaceuticals, agrochemicals, and materials with specific functional groups.Additionally, this reagent can participate in Negishi cross-coupling reactions, enabling the synthesis of organic compounds with high regio- and stereo-selectivity. By selectively introducing alkyl groups onto aryl or vinyl halides, Potassium (3-(tert-butoxy)-3-oxopropyl)trifluoroborate broadens the scope of accessible chemical structures in organic synthesis.Overall, the versatility and efficiency of Potassium (3-(tert-butoxy)-3-oxopropyl)trifluoroborate make it a valuable tool for chemists seeking to streamline the synthesis of complex organic molecules with precise control over structure and functionality. Its applications in carbon-carbon bond formation highlight its importance in advancing the field of chemical synthesis.