Potassium 4-formylphenyltrifluoroborate is an organoboron compound characterized by the presence of a trifluoroborate group and a formylphenyl moiety. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. It is known for its utility in organic synthesis, particularly in cross-coupling reactions, where it serves as a versatile building block for the formation of carbon-carbon bonds. The trifluoroborate group enhances the reactivity of the compound, making it a valuable reagent in various chemical transformations. Additionally, the presence of the formyl group allows for further functionalization, enabling the synthesis of more complex molecules. Potassium 4-formylphenyltrifluoroborate is generally stable under standard laboratory conditions but should be handled with care due to the potential reactivity of boron compounds. As with many organoboron compounds, it is important to consider safety data and handling guidelines when working with this substance in a laboratory setting.

Potassium 4-formylphenyltrifluoroborate

374564-36-0: 4-Formylbenzenetrifluoroboric acid potassium salt~4-Formylphenyltrifluoroboric acid potassium salt, Potassium Trifluoro(4-Formylphenyl)Borate(1-)

Potassium;trifluoro-(4-formylphenyl)boranuide is an organic compound that has been shown to be a potent anti-proliferative agent. It is used in the synthesis of peptides and is a reagent for the preparation of ozonides. This compound has been shown to inhibit the growth of cancer cells, which may be due to its ability to inhibit the production of proteins necessary for cellular replication. The yield of this compound depends on the reaction conditions, such as pH and temperature.

CAS 374564-36-0: Potassium 4-formylphenyltrifluoroborate

Potassium;trifluoro-(4-formylphenyl)boranuide

Ref: 3D-FP105485

potassium trifluoro(4-formylphenyl)boranuide

Ref: IN-DA00I7DA

Potassium (4-formylphenyl)trifluoroborate

Ref: 54-PC11237

Potassium 4-formylphenyltrifluoroborate

Ref: 10-F034889