2-Cyclopropylmethoxyphenylboronic acid pinacol ester is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group, which is further substituted with a methoxy group and a cyclopropyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The pinacol ester functionality enhances its stability and solubility, facilitating its use in reactions like Suzuki coupling, where it acts as a coupling partner for the formation of carbon-carbon bonds. The presence of the cyclopropyl group may impart unique steric and electronic properties, influencing reactivity and selectivity in chemical reactions. Additionally, the compound's structure suggests potential applications in drug development, particularly in targeting specific biological pathways due to its ability to interact with biomolecules. Overall, this compound represents a versatile building block in synthetic organic chemistry.

2-CyclopropylMethoxyphenylboronic acid pinacol ester

1185836-98-9: 2-Cyclopropylmethoxyphenylboronic acid pinacol ester is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group, which is further substituted with a methoxy group and a cyclopropyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The pinacol ester functionality enhances its stability and solubility, facilitating its use in reactions like Suzuki coupling, where it acts as a coupling partner for the formation of carbon-carbon bonds. The presence of the cyclopropyl group may impart unique steric and electronic properties, influencing reactivity and selectivity in chemical reactions. Additionally, the compound's structure suggests potential applications in drug development, particularly in targeting specific biological pathways due to its ability to interact with biomolecules. Overall, this compound represents a versatile building block in synthetic organic chemistry.

2-Cyclopropylmethoxyphenylboronic acid pinacol ester

2-(2-(Cyclopropylmethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS 1185836-98-9

2-CyclopropylMethoxyphenylboronic acid pinacol ester

2-Cyclopropylmethoxyphenylboronic acid pinacol ester

Ref: IN-DA008UC5

2-(2-(Cyclopropylmethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Ref: 54-OR1054573

2-(2-(Cyclopropylmethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Ref: 10-F691702