(1R)-1-(2-Fluoro-3-methylphenyl)ethylamine is an organic compound characterized by its amine functional group and a substituted ethyl structure. The presence of a fluorine atom at the 2-position of the aromatic ring, along with a methyl group at the 3-position, contributes to its unique chemical properties and potential biological activity. This compound is likely to exhibit chirality due to the presence of a stereocenter at the carbon atom bonded to the amine group, which can influence its interaction with biological systems, particularly in pharmacology. The fluorine substitution can enhance lipophilicity and metabolic stability, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in areas targeting neurotransmitter systems. As with many amines, it may exhibit basic properties, forming salts with acids and participating in various chemical reactions typical of amines, such as alkylation and acylation. Safety and handling considerations should be observed due to the potential reactivity and biological effects of amines.

(1R)-1-(2-FLUORO-3-METHYLPHENYL)ETHYLAMINE

1213036-11-3: (1R)-1-(2-Fluoro-3-methylphenyl)ethylamine is an organic compound characterized by its amine functional group and a substituted ethyl structure. The presence of a fluorine atom at the 2-position of the aromatic ring, along with a methyl group at the 3-position, contributes to its unique chemical properties and potential biological activity. This compound is likely to exhibit chirality due to the presence of a stereocenter at the carbon atom bonded to the amine group, which can influence its interaction with biological systems, particularly in pharmacology. The fluorine substitution can enhance lipophilicity and metabolic stability, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in areas targeting neurotransmitter systems. As with many amines, it may exhibit basic properties, forming salts with acids and participating in various chemical reactions typical of amines, such as alkylation and acylation. Safety and handling considerations should be observed due to the potential reactivity and biological effects of amines.

(R)-1-(2-fluoro-3-methylphenyl)ethan-1-amine

CAS 1213036-11-3

(1R)-1-(2-FLUORO-3-METHYLPHENYL)ETHYLAMINE

(R)-1-(2-fluoro-3-methylphenyl)ethan-1-amine

Ref: 54-PC1001798

(R)-1-(2-fluoro-3-methylphenyl)ethan-1-amine

Ref: 10-F553007