CAS 1021306-45-5

Fluoren-9-one-2-boronic acid pinacol ester

Description:

Fluoren-9-one-2-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid moiety and a fluorenone structure. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents such as dichloromethane and tetrahydrofuran. It is known for its utility in organic synthesis, particularly in cross-coupling reactions, where it serves as a versatile building block for the formation of carbon-carbon bonds. The boronic acid functionality allows for the formation of stable complexes with diols, making it useful in various applications, including drug development and materials science. Additionally, the pinacol ester group enhances the stability of the boronic acid, making it easier to handle and store. The compound's reactivity can be influenced by the presence of functional groups on the fluorenone structure, allowing for further derivatization and modification. Overall, Fluoren-9-one-2-boronic acid pinacol ester is a valuable compound in synthetic organic chemistry due to its unique properties and reactivity.

Formula: C₁₉H₁₉O₃B

Synonyms:

• 2-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-fluoren-9-one
• fluoren-9-one-2-boronic acid, pinacol ester

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)fluoren-9-one

CAS: 1021306-45-5

Formula: C₁₉H₁₉BO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 306.1634

Ref: IN-DA009480

2-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-fluoren-9-one

CAS: 1021306-45-5

2-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-fluoren-9-one

Purity: 95%

Molecular weight: 306.16g/mol

Ref: 54-OR303499

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-fluoren-9-one

CAS: 1021306-45-5

Purity: 95%

Molecular weight: 306.1700134

Ref: 10-F696247