CymitQuimica logo

CAS 910553-12-7

:

2-Methylthiophene-3-boronic acid pinacol ester

Description:
2-Methylthiophene-3-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 suitable for various synthetic applications, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is widely used in organic synthesis for forming carbon-carbon bonds. The presence of the boron atom allows for the formation of complexes with Lewis bases, making it useful in coordination chemistry. Additionally, this compound may exhibit moderate to high polarity due to the functional groups present, influencing its solubility and interaction with other chemical species. Overall, 2-Methylthiophene-3-boronic acid pinacol ester is a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in materials science.
Formula:C11H17BO2S
Synonyms:
  • 2-Methylthiophene-3-boronic acid pinacol ester
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-methyl-3-thienyl)-
  • 4,4,5,5-tetramethyl-2-(2-methylthiophen-3-yl)-1,3,2-dioxaborolane
  • 4,4,5,5-tetramethyl-2-(2-methyl-3-thiophenyl)-1,3,2-dioxaborolane
  • 4,4,5,5-TetraMethyl-2-(2-Methyl-3-thienyl)-1,3,2-dioxaborolane
  • 4,4,5,5-Tetramethyl-2-(2-methylthiophen-3-yl)
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.