Trifluoro(2,5-dimethyl-thiophen-3-yl)-borate potassium salt is a chemical compound characterized by its unique structure, which includes a borate group and a thiophene ring substituted with methyl groups. The presence of trifluoromethyl groups enhances its reactivity and solubility in various organic solvents. This compound is typically used in organic synthesis and as a reagent in various chemical reactions due to its ability to act as a Lewis acid. The potassium salt form indicates that it is likely soluble in polar solvents, making it useful in applications involving ionic interactions. Additionally, the thiophene moiety contributes to its electronic properties, potentially allowing for applications in organic electronics or as a precursor in the synthesis of more complex organic materials. Safety data should be consulted for handling, as the trifluoromethyl group can impart toxicity and environmental concerns. Overall, this compound exemplifies the intersection of organoboron chemistry and heterocyclic compounds, showcasing its potential utility in both academic and industrial settings.

trifluoro(2,5-diMethyl-thiophen-3-yl)-Borate potassiuM salt

1294455-24-5: Trifluoro(2,5-dimethyl-thiophen-3-yl)-borate potassium salt is a chemical compound characterized by its unique structure, which includes a borate group and a thiophene ring substituted with methyl groups. The presence of trifluoromethyl groups enhances its reactivity and solubility in various organic solvents. This compound is typically used in organic synthesis and as a reagent in various chemical reactions due to its ability to act as a Lewis acid. The potassium salt form indicates that it is likely soluble in polar solvents, making it useful in applications involving ionic interactions. Additionally, the thiophene moiety contributes to its electronic properties, potentially allowing for applications in organic electronics or as a precursor in the synthesis of more complex organic materials. Safety data should be consulted for handling, as the trifluoromethyl group can impart toxicity and environmental concerns. Overall, this compound exemplifies the intersection of organoboron chemistry and heterocyclic compounds, showcasing its potential utility in both academic and industrial settings.

<p>Potassium 2,5-Dimethylthiophene-3-Trifluoroborate</p>

CAS 1294455-24-5

trifluoro(2,5-diMethyl-thiophen-3-yl)-Borate potassiuM salt

Potassium 2,5-Dimethylthiophene-3-Trifluoroborate

Ref: 54-PC108918