(2,4,6-Trifluoro-3-propoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with trifluoromethyl and propoxy groups. The trifluoro substituents enhance the compound's electron-withdrawing properties, which can influence its reactivity and solubility in various solvents. The propoxy group contributes to the overall hydrophobic character of the molecule, potentially affecting its interactions in biological systems or during chemical reactions. This compound is likely to exhibit moderate stability under standard conditions but may be sensitive to moisture due to the boronic acid moiety, which can undergo hydrolysis. It is commonly utilized in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a key intermediate for the formation of carbon-carbon bonds. Additionally, its unique electronic properties may make it suitable for applications in materials science and medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals.

(2,4,6-trifluoro-3-propoxyphenyl)boronic acid

871125-73-4: (2,4,6-Trifluoro-3-propoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with trifluoromethyl and propoxy groups. The trifluoro substituents enhance the compound's electron-withdrawing properties, which can influence its reactivity and solubility in various solvents. The propoxy group contributes to the overall hydrophobic character of the molecule, potentially affecting its interactions in biological systems or during chemical reactions. This compound is likely to exhibit moderate stability under standard conditions but may be sensitive to moisture due to the boronic acid moiety, which can undergo hydrolysis. It is commonly utilized in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a key intermediate for the formation of carbon-carbon bonds. Additionally, its unique electronic properties may make it suitable for applications in materials science and medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals.

CAS 871125-73-4

(2,4,6-trifluoro-3-propoxyphenyl)boronic acid

(2,4,6-Trifluoro-3-isopropoxyphenyl)boronic acid

Ref: IN-DA0032BW

3-Isopropoxy-2,4,6-trifluorobenzeneboronic acid

Ref: 54-PC1923

(2,4,6-Trifluoro-3-isopropoxyphenyl)boronic acid

Ref: 10-F694067