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Home  > Potassium 3-trifluoroboratopropionate tert-butyl ester

AA09138

1023357-66-5 | Potassium 3-trifluoroboratopropionate tert-butyl ester

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 -   +

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*All prices are in USD.

Description
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+]

 

Upstream Synthesis Route
  • 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.
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