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CAS 141550-13-2

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3,3-Dimethylallylboronic acid pinacol ester, 2-(3-Methyl-but-2-enyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
3,3-Dimethylallylboronic acid pinacol ester, also known by its systematic name 2-(3-Methyl-but-2-enyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, is a boronic acid derivative characterized by its unique structure that includes a boron atom bonded to a dioxaborolane ring. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols and other nucleophiles, making it useful in organic synthesis and medicinal chemistry. The presence of the dimethylallyl group enhances its reactivity and selectivity in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Additionally, the pinacol ester functionality contributes to its stability and solubility in organic solvents. This compound is often utilized in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, due to its versatile reactivity. Its specific applications may vary, but it is generally valued for its role in facilitating various chemical transformations in synthetic organic chemistry.
Formula:C11H21BO2
Synonyms:
  • 3-Methyl-2-butenylboronic acid pinacol ester
  • 4,4,5,5-Tetramethyl-2-(3-Methylbut-2-Enyl)-1,3,2-Dioxaborolane
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