4-(Benzyloxy)-3-fluorophenol, with the CAS number 81228-25-3, is an organic compound characterized by the presence of a fluorine atom and a benzyloxy group attached to a phenolic structure. This compound typically exhibits properties associated with both aromatic compounds and alcohols, including moderate solubility in organic solvents and potential reactivity due to the hydroxyl group. The fluorine substitution can influence the compound's electronic properties, potentially enhancing its acidity and altering its reactivity in chemical reactions. The benzyloxy group contributes to the compound's hydrophobic character, which may affect its interactions in biological systems or its utility in synthetic applications. Additionally, the compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its synthesis and manipulation in laboratory settings require standard safety precautions due to the presence of reactive functional groups. Overall, 4-(Benzyloxy)-3-fluorophenol serves as a valuable building block in organic synthesis and may have applications in various fields, including pharmaceuticals and materials science.

4-(Benzyloxy)-3-fluorophenol

81228-25-3: 4-(Benzyloxy)-3-fluorophenol, with the CAS number 81228-25-3, is an organic compound characterized by the presence of a fluorine atom and a benzyloxy group attached to a phenolic structure. This compound typically exhibits properties associated with both aromatic compounds and alcohols, including moderate solubility in organic solvents and potential reactivity due to the hydroxyl group. The fluorine substitution can influence the compound's electronic properties, potentially enhancing its acidity and altering its reactivity in chemical reactions. The benzyloxy group contributes to the compound's hydrophobic character, which may affect its interactions in biological systems or its utility in synthetic applications. Additionally, the compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its synthesis and manipulation in laboratory settings require standard safety precautions due to the presence of reactive functional groups. Overall, 4-(Benzyloxy)-3-fluorophenol serves as a valuable building block in organic synthesis and may have applications in various fields, including pharmaceuticals and materials science.

CAS 81228-25-3

4-(Benzyloxy)-3-fluorophenol

4-BENZYLOXY-3-FLUORO-PHENOL

Ref: IN-DA00G48I

4-(Benzyloxy)-3-fluorophenol

Ref: 54-PC103193

4-(Benzyloxy)-3-fluorophenol

Ref: 10-F231105