2-Fluorophenethylamine is an organic compound characterized by the presence of a fluorine atom attached to a phenethylamine structure. It features a phenyl ring (a six-membered aromatic ring) bonded to an ethylamine chain, where the amino group (-NH2) is connected to the ethyl group. The fluorine substitution at the second position of the phenyl ring influences the compound's electronic properties, potentially affecting its reactivity and interaction with biological systems. This compound is typically colorless to pale yellow in appearance and is soluble in polar organic solvents. It may exhibit basic properties due to the amino group, allowing it to participate in various chemical reactions, including alkylation and acylation. 2-Fluorophenethylamine is of interest in medicinal chemistry and pharmacology, as modifications to the phenethylamine structure can lead to compounds with varying biological activities, including potential applications in neuropharmacology. As with many amines, it may also be sensitive to oxidation and can form salts with acids. Proper handling and safety precautions are essential due to its potential biological effects.

2-Fluorophenethylamine

52721-69-4: 2-(2-Fluorophenyl)-ethylamine, 2-(2-Fluorophenyl)Ethanamine, 2-(2-Fluorophenyl)Ethanaminium, 2-Fluoro-benzeneethanamine, o-Fluorophenethylamine, Benzeneethanamine, 2-fluoro-, 2-Fluorophenethylamine, o-Fluorophenylethylamine, 2-Fluorobenzeneethanamine

2-Fluorophenethylamine is a molecule that can switch between two forms, one hydrophobic and one hydrophilic. When it is in the hydrophobic form, 2-fluorophenethylamine can bind to water molecules to form potential use products. When 2-fluorophenethylamine is in the hydrophilic form, it can desorb from the surface of water. 2-Fluorophenethylamine has been shown to be a neurotransmitter and may have potential use as an anti-depressant or anti-anxiety medication. It has also been suggested that 2-fluorophenethylamine may be used for the treatment of Parkinson's disease, because of its ability to inhibit dopamine degradation. An experiment conducted with spectra found that 2-fluorophenethylamine reacts with hydrogen bonds and other weak interactions to form dimers and monomers. The vibrational spectrum of this molecule shows that there are no strong

CAS 52721-69-4: 2-Fluorophenethylamine

2-Fluorophenethylamine

Ref: 3D-FF64400

2-(2-Fluorophenyl)ethylamine

Ref: 3B-F0933