4-Fluoro-5-hydroxyindole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a fluorine atom at the 4-position and a hydroxyl group at the 5-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding. The fluorine substituent can influence the compound's reactivity and biological activity, potentially enhancing its lipophilicity and altering its interaction with biological targets. 4-Fluoro-5-hydroxyindole may be of interest in medicinal chemistry and research, particularly in studies related to neurotransmitter systems, as indole derivatives are often associated with serotonin and related pathways. Its synthesis and characterization involve standard organic chemistry techniques, and it may serve as a precursor or intermediate in the development of pharmaceuticals or agrochemicals. Safety and handling precautions should be observed due to the potential reactivity of halogenated compounds.

4-fluoro-5-hydroxyindole

288386-04-9: 4-Fluoro-5-hydroxyindole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a fluorine atom at the 4-position and a hydroxyl group at the 5-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding. The fluorine substituent can influence the compound's reactivity and biological activity, potentially enhancing its lipophilicity and altering its interaction with biological targets. 4-Fluoro-5-hydroxyindole may be of interest in medicinal chemistry and research, particularly in studies related to neurotransmitter systems, as indole derivatives are often associated with serotonin and related pathways. Its synthesis and characterization involve standard organic chemistry techniques, and it may serve as a precursor or intermediate in the development of pharmaceuticals or agrochemicals. Safety and handling precautions should be observed due to the potential reactivity of halogenated compounds.

CAS 288386-04-9

4-fluoro-5-hydroxyindole

1H-Indol-5-ol, 4-fluoro-

Ref: IN-DA002WR3

4-Fluoro-5-hydroxy-1H-indole

Ref: 54-PC3466

4-Fluoro-1H-indol-5-ol

Ref: 10-F209060