[2,3-Difluoro-4-(hexyloxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with two fluorine atoms and a hexyloxy group. The fluorine substituents enhance the compound's electronic properties, potentially increasing its reactivity and solubility in various solvents. The hexyloxy group, a long alkyl chain, contributes to the compound's hydrophobic characteristics, which can influence its interactions in biological systems and materials science applications. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis and as building blocks in drug development. This compound may exhibit interesting properties in catalysis, sensor technology, and as a ligand in coordination chemistry. Its unique structure suggests potential applications in medicinal chemistry, particularly in the design of targeted therapies or as intermediates in the synthesis of more complex molecules.

[2,3-difluoro-4-(hexyloxy)phenyl]boronic acid

121219-20-3: [2,3-Difluoro-4-(hexyloxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with two fluorine atoms and a hexyloxy group. The fluorine substituents enhance the compound's electronic properties, potentially increasing its reactivity and solubility in various solvents. The hexyloxy group, a long alkyl chain, contributes to the compound's hydrophobic characteristics, which can influence its interactions in biological systems and materials science applications. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis and as building blocks in drug development. This compound may exhibit interesting properties in catalysis, sensor technology, and as a ligand in coordination chemistry. Its unique structure suggests potential applications in medicinal chemistry, particularly in the design of targeted therapies or as intermediates in the synthesis of more complex molecules.

CAS 121219-20-3

[2,3-difluoro-4-(hexyloxy)phenyl]boronic acid

2,3-Difluoro-4-(N-hexyloxy)phenylboronic acid

Ref: IN-DA009ATY

2,3-Difluoro-4-hexyloxybenzeneboronic acid

Ref: 54-PC8516

2,3-Difluoro-4-(n-hexyloxy)phenylboronic acid

Ref: 10-F016202