2,3-Dichloro-6-fluorobenzenamine is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with two chlorine atoms and one fluorine atom, along with an amino group (-NH2). This compound typically appears as a solid at room temperature and is soluble in organic solvents. The presence of halogen substituents (chlorine and fluorine) can significantly influence its chemical reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The amino group contributes to its basicity and can participate in hydrogen bonding, affecting its solubility and interaction with other molecules. Due to its structural features, 2,3-Dichloro-6-fluorobenzenamine may exhibit biological activity, making it of interest in pharmaceutical research and development. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, this compound's unique combination of functional groups and substituents makes it a subject of interest in both synthetic and applied chemistry.

2,3-Dichloro-6-fluorobenzenamine

1017777-51-3: 2,3-Dichloro-6-fluorobenzenamine, 2,3-Dichloro-6-fluoroaniline, Benzenamine, 2,3-dichloro-6-fluoro-

CAS 1017777-51-3: 2,3-Dichloro-6-fluorobenzenamine

2,3-Dichloro-6-fluoroaniline

Ref: 3D-SQB77751

2,3-Dichloro-6-fluoroaniline

Ref: 54-PC302656

2,3-Dichloro-6-fluoroaniline

Ref: 10-F342692