CAS 121219-22-5

2,3-Difluoro-4-(octyloxy)-benzeneboronic acid

Description:

2,3-Difluoro-4-(octyloxy)-benzeneboronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a benzene ring substituted with two fluorine atoms at the 2 and 3 positions, enhancing its electronic properties and potentially influencing its reactivity. The presence of an octyloxy group at the 4-position contributes to its hydrophobic characteristics, which can affect solubility and interaction with biological membranes. This compound is likely to exhibit moderate to low solubility in water due to the hydrophobic octyloxy chain, while its boronic acid functionality allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling. Overall, 2,3-Difluoro-4-(octyloxy)-benzeneboronic acid is a versatile compound with potential applications in materials science and pharmaceuticals, particularly in the development of new organic materials and drug candidates.

Boronic acid,[2,3-difluoro-4-(octyloxy)phenyl]- (9CI)

CAS: 121219-22-5

Formula: C₁₄H₂₁BF₂O₃

Molecular weight: 286.1225

Ref: IN-DA007P48