CAS 915402-04-9

2,3-Dimethyl-4-methoxyphenylboronic acid, pinacol ester

Description:

2,3-Dimethyl-4-methoxyphenylboronic acid, pinacol ester, is an organoboron compound characterized by the presence of a boronic acid functional group and a pinacol ester moiety. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and ethanol, while being less soluble in water. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The methoxy group enhances the electron density on the aromatic ring, influencing its reactivity and stability. Additionally, the dimethyl substituents provide steric hindrance, which can affect the compound's reactivity and selectivity in various chemical reactions. Overall, this compound is significant in the field of medicinal chemistry and materials science, where it can be utilized in the development of pharmaceuticals and advanced materials.

4,4,5,5-TETRAMETHYL-2-(2,3-DIMETHYL-4-METHOXYPHENYL)-[1,3,2]DIOXABOROLANE

CAS: 915402-04-9

Formula: C₁₅H₂₃BO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 262.1523

Ref: IN-DA006L6F

2,3-Dimethyl-4-methoxyphenylboronic acid, pinacol ester

CAS: 915402-04-9

2,3-Dimethyl-4-methoxyphenylboronic acid, pinacol ester

Purity: 98%

Molecular weight: 262.15g/mol

Ref: 54-OR361160

2-(4-Methoxy-2,3-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 915402-04-9

Purity: 98%

Molecular weight: 262.1600037

Ref: 10-F623455