[2-Fluoro-5-(1-methylethoxy)phenyl]boronic acid is an organoboron 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 phenyl ring substituted with a fluorine atom and an isopropoxy group, which can influence its reactivity and solubility. The fluorine atom can enhance the compound's electronic properties, potentially affecting its interaction with biological targets. Boronic acids are typically polar and can exhibit moderate solubility in polar solvents, while the presence of the isopropoxy group may increase lipophilicity. This compound may be utilized in cross-coupling reactions, particularly in the synthesis of complex organic molecules. Additionally, its unique structure may confer specific biological activities, making it a candidate for further research in drug development. As with many boronic acids, care should be taken in handling due to potential reactivity with moisture and other nucleophiles.

[2-fluoro-5-(1-methylethoxy)phenyl]boronic acid

849062-30-2: [2-Fluoro-5-(1-methylethoxy)phenyl]boronic acid is an organoboron 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 phenyl ring substituted with a fluorine atom and an isopropoxy group, which can influence its reactivity and solubility. The fluorine atom can enhance the compound's electronic properties, potentially affecting its interaction with biological targets. Boronic acids are typically polar and can exhibit moderate solubility in polar solvents, while the presence of the isopropoxy group may increase lipophilicity. This compound may be utilized in cross-coupling reactions, particularly in the synthesis of complex organic molecules. Additionally, its unique structure may confer specific biological activities, making it a candidate for further research in drug development. As with many boronic acids, care should be taken in handling due to potential reactivity with moisture and other nucleophiles.

(2-Fluoro-5-isopropoxyphenyl)boronic acid

<p>[2-Fluoro-5-(1-methylethoxy)phenyl]boronic acid</p>

CAS 849062-30-2

[2-fluoro-5-(1-methylethoxy)phenyl]boronic acid

(2-Fluoro-5-isopropoxyphenyl)boronic acid

Ref: IN-DA004VM7

[2-Fluoro-5-(1-methylethoxy)phenyl]boronic acid

Ref: 54-PC412085

(2-Fluoro-5-isopropoxyphenyl)boronic acid

Ref: 10-F228714