CAS 885692-91-1
:3-Methylthiophene-2-boronic acid pinacol ester
Description:
3-Methylthiophene-2-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a thiophene ring. This compound typically exhibits a molecular structure that includes a methyl group attached to the thiophene, enhancing its reactivity and solubility in organic solvents. The pinacol ester moiety contributes to its stability and makes it useful in various synthetic applications, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is vital in the formation of carbon-carbon bonds. The presence of the boronic acid group allows for the selective functionalization of the thiophene ring, making it a valuable intermediate in organic synthesis and materials science. Additionally, this compound may exhibit properties such as moderate polarity and potential for coordination with metal catalysts, which can influence its reactivity in chemical transformations. Overall, 3-Methylthiophene-2-boronic acid pinacol ester serves as an important building block in the development of pharmaceuticals and advanced materials.
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Found 4 products.
4,4,5,5-Tetramethyl-2-(3-methylthiophen-2-yl)-1,3,2-dioxaborolane
CAS:Formula:C11H17BO2SPurity:95%Color and Shape:SolidMolecular weight:224.12753-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene
CAS:Formula:C11H17BO2SPurity:>98.0%(GC)(T)Color and Shape:White to Almost white powder to crystalMolecular weight:224.133-Methylthiophene-2-boronic acid, pinacol ester
CAS:3-Methylthiophene-2-boronic acid, pinacol esterFormula:C11H17BO2SPurity:97%Color and Shape: white solidMolecular weight:224.13g/mol4,4,5,5-Tetramethyl-2-(3-methylthiophen-2-yl)-1,3,2-dioxaborolane
CAS:Formula:C11H17BO2SPurity:95%Color and Shape:Liquid, No data available.Molecular weight:224.13



