3-Furanboronic acid pinacol ester is an organoboron compound characterized by the presence of a furan ring and a boronic acid moiety. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. It is known for its utility in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for forming carbon-carbon bonds. The pinacol ester functionality enhances its stability and solubility in organic solvents, making it a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. Additionally, the furan ring contributes to its reactivity, allowing for further functionalization. The compound is generally handled with care due to the potential reactivity of boron-containing compounds, and it may exhibit moderate toxicity. Proper storage conditions, typically in a cool, dry place, are recommended to maintain its integrity. Overall, 3-Furanboronic acid pinacol ester is a versatile reagent in modern organic chemistry.

3-Furanboronic acid pinacol ester

248924-59-6: 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan, 2-Furan-3-Yl-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane

Furan-3-boronic acid, pinacol ester

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

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

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CAS 248924-59-6: 3-Furanboronic acid pinacol ester

Furan-3-boronic acid, pinacol ester

Ref: 54-OR11010

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

Ref: IN-DA002PS1

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

Ref: 10-F010833

3-Furanboronic acid pinacol ester

Ref: 3D-FF39769