Phenol, 3-fluoro-5-methoxy- is an organic compound characterized by the presence of a phenolic hydroxyl group (-OH) attached to a benzene ring, which also features a fluorine atom at the meta position (3-position) and a methoxy group (-OCH3) at the para position (5-position). This compound is part of the larger class of substituted phenols, which are known for their diverse chemical reactivity and biological activity. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its interaction with biological systems, potentially affecting its pharmacological properties. The methoxy group can also modify the electronic properties of the molecule, impacting its reactivity and solubility. Phenolic compounds often exhibit antioxidant properties and can be involved in various chemical reactions, including electrophilic substitution and oxidation. Due to its specific substitutions, 3-fluoro-5-methoxy-phenol may have applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. However, detailed studies would be necessary to fully understand its properties and potential uses.

Phenol, 3-fluoro-5-methoxy-

850793-25-8: Phenol, 3-fluoro-5-methoxy- is an organic compound characterized by the presence of a phenolic hydroxyl group (-OH) attached to a benzene ring, which also features a fluorine atom at the meta position (3-position) and a methoxy group (-OCH3) at the para position (5-position). This compound is part of the larger class of substituted phenols, which are known for their diverse chemical reactivity and biological activity. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its interaction with biological systems, potentially affecting its pharmacological properties. The methoxy group can also modify the electronic properties of the molecule, impacting its reactivity and solubility. Phenolic compounds often exhibit antioxidant properties and can be involved in various chemical reactions, including electrophilic substitution and oxidation. Due to its specific substitutions, 3-fluoro-5-methoxy-phenol may have applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. However, detailed studies would be necessary to fully understand its properties and potential uses.

CAS 850793-25-8

Phenol, 3-fluoro-5-methoxy-

3-Fluoro-5-methoxyphenol

Ref: IN-DA004OOK

3-Fluoro-5-methoxyphenol

Ref: 54-PC500163

3-Fluoro-5-methoxyphenol

Ref: 10-F079193