3-Thiopheneboronic 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 white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and ethanol. The boronic ester functionality allows for participation in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis and materials science. The thiophene moiety contributes to its electronic properties, potentially enhancing its reactivity and interaction with other molecules. Additionally, this compound may exhibit moderate stability under standard laboratory conditions but should be handled with care due to the potential reactivity of the boron center. Its applications can extend to pharmaceuticals, agrochemicals, and the development of organic electronic materials. As with many organoboron compounds, it is essential to consider safety and environmental regulations when handling and disposing of this substance.

3-Thiopheneboronic acid pinacol ester

214360-70-0: Thiophene-3-boronic acid pinacol ester, 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(3-thienyl)-, 4,4,5,5-Tetramethyl-2-(3-thienyl)-1,3,2-dioxaborolane, 4,4,5,5-Tetramethyl-2-Thiophen-3-Yl-1,3,2-Dioxaborolane, 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-Thiophene

Thiophene-3-boronic acid, pinacol ester

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CAS 214360-70-0: 3-Thiopheneboronic acid pinacol ester

Thiophene-3-boronic acid, pinacol ester

Ref: 54-OR30612

3-ThiopheneboRonic acid pinacol esteR

Ref: 3D-FT40756

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-thiophene

Ref: 10-F021636

1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(3-thienyl)-

Ref: IN-DA00I457