3-Fluoro-4-iodophenol is an organic compound characterized by the presence of both fluorine and iodine substituents on a phenolic ring. The molecular structure features a hydroxyl group (-OH) attached to a benzene ring, which is further substituted at the 3-position with a fluorine atom and at the 4-position with an iodine atom. This compound is typically a solid at room temperature and may exhibit a range of physical properties such as solubility in organic solvents and varying degrees of polarity due to the electronegative halogen atoms. The presence of both halogens can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the compound may have applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Its unique combination of functional groups can also impart specific biological activities, which may be of interest in medicinal chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

3-Fluoro-4-iodophenol

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3-Fluoro-4-iodophenol is a planar molecule with linear chains and intermolecular hydrogen bonds. It has a crystal structure that is stabilized by the hydrogen bonds. 3-Fluoro-4-iodophenol has a planar shape with three rings and four lone pairs of electrons. The lone pairs are located on the carbon atoms that are in the 4th position on each of the two benzene rings, which means they are located on opposite sides of the molecule, forming a "C" shape. The lone pairs form an intermolecular hydrogen bond, stabilizing the molecule's shape.

CAS 122927-84-8: 3-Fluoro-4-iodophenol

3-Fluoro-4-iodophenol

Ref: 3D-FF77464

Phenol, 3-fluoro-4-iodo-

Ref: IN-DA000JSO

3-Fluoro-4-iodophenol

Ref: 10-F226296

3-Fluoro-4-iodophenol

Ref: 54-PC103580