CAS 1644466-71-6: 9,9-diphenyl-fluoren-3-boronic acid pinacol ester

Description: 9,9-Diphenyl-fluoren-3-boronic acid pinacol ester is an organoboron compound characterized by its boronic acid functionality, which is typically used in Suzuki coupling reactions, a vital method in organic synthesis for forming carbon-carbon bonds. This compound features a fluorenyl backbone, which contributes to its stability and potential applications in materials science, particularly in organic electronics and photonics. The pinacol ester moiety enhances its solubility and reactivity, making it suitable for various synthetic applications. It is generally a white to off-white solid, and its molecular structure includes two phenyl groups attached to the fluorenyl core, which can influence its electronic properties. The compound is sensitive to moisture and should be handled under an inert atmosphere to prevent hydrolysis of the boronic acid group. Its applications extend to medicinal chemistry and the development of fluorescent materials, owing to the unique optical properties imparted by the fluorenyl structure. Safety data should be consulted for handling and storage, as with all chemical substances.

2-(9,9-diphenyl-9H-fluoren-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 1644466-71-6

• Formula: C₃₁H₂₉BO₂
• Purity: 95%
• Color and Shape: Solid
• Molecular weight: 444.37175999999994

2-(9,9-Diphenyl-9H-Fluoren-3-Yl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane

CAS: 1644466-71-6

• Purity: 98%+
• Molecular weight: 444.37g/mol

2-(9,9-Diphenyl-9H-fluoren-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 1644466-71-6

• Formula: C₃₁H₂₉BO₂
• Purity: >98.0%(T)(HPLC)
• Color and Shape: White to Orange to Green powder to crystal
• Molecular weight: 444.38

2-(9,9-Diphenyl-9H-fluoren-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 1644466-71-6

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• Formula: C₃₁H₂₉BO₂
• Purity: Min. 95%
• Molecular weight: 444.4 g/mol