CAS 444094-88-6

2-(4-Chlorophenyl)ethylboronic acid pinacol ester

Description:

2-(4-Chlorophenyl)ethylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid moiety and a pinacol ester functional group. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and ethanol, but may have limited solubility in water due to the hydrophobic nature of the chlorophenyl group. The presence of the boronic acid functionality allows for participation in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The chlorophenyl substituent can influence the electronic properties and reactivity of the compound, potentially enhancing its utility in drug development and material science. Additionally, the pinacol ester group provides stability and can facilitate the handling and storage of the boronic acid derivative. Overall, this compound is significant in the field of synthetic organic chemistry due to its versatile reactivity and functional group compatibility.

2-(4-Chlorophenyl)ethylboronic acid pinacol ester

CAS: 444094-88-6

Formula: C₁₄H₂₀BClO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 266.5714

Ref: IN-DA00DIQR

2-(4-Chlorophenethyl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane

CAS: 444094-88-6

2-(4-Chlorophenethyl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane

Purity: 98%

Molecular weight: 266.57g/mol

Ref: 54-OR1030931

2-(4-Chlorophenethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 444094-88-6

Purity: 98%

Molecular weight: 266.5700073

Ref: 10-F696500