2-Chloro-6-(difluoromethoxy)benzyl amine is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with a chlorine atom and a difluoromethoxy group. The presence of the amine functional group indicates that it can participate in hydrogen bonding, making it potentially soluble in polar solvents. The difluoromethoxy group introduces unique electronic properties due to the electronegativity of the fluorine atoms, which can influence the compound's reactivity and interaction with biological systems. This compound may exhibit specific pharmacological activities, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the chlorine and fluorine substituents can enhance lipophilicity, affecting the compound's absorption and distribution in biological systems. Safety and handling precautions should be observed due to the presence of halogenated groups, which may pose environmental and health risks. Overall, 2-Chloro-6-(difluoromethoxy)benzyl amine represents a complex molecule with potential utility in various chemical and pharmaceutical applications.

2-Chloro-6-(difluoromethoxy)benzyl amine

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(2-Chloro-6-(difluoromethoxy)phenyl)methanamine

CAS 1515925-06-0: 2-Chloro-6-(difluoromethoxy)benzyl amine

(2-Chloro-6-(difluoromethoxy)phenyl)methanamine

Ref: 54-PC101161

(2-Chloro-6-(difluoromethoxy)phenyl)methanamine

Ref: 10-F606023

(2-Chloro-6-(difluoromethoxy)phenyl)methanamine

Ref: 3D-QKC92506

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Ref: IN-DA01C0F5