(1S)-1-(2-Fluoro-4-methoxyphenyl)ethylamine is an organic compound characterized by its amine functional group and a substituted aromatic ring. The presence of a fluorine atom and a methoxy group on the phenyl ring contributes to its unique chemical properties, including potential variations in polarity and reactivity. The compound's stereochemistry, indicated by the (1S) designation, suggests a specific three-dimensional arrangement of atoms that can influence its biological activity and interactions with other molecules. Typically, compounds like this may exhibit properties such as solubility in organic solvents, potential for hydrogen bonding due to the amine group, and varying degrees of lipophilicity depending on the substituents on the aromatic ring. Such characteristics make it of interest in medicinal chemistry, particularly in the development of pharmaceuticals where modifications to the aromatic system can enhance efficacy or selectivity for biological targets. Additionally, the fluorine atom can enhance metabolic stability and influence the compound's pharmacokinetic properties.

(1S)-1-(2-FLUORO-4-METHOXYPHENYL)ETHYLAMINE

1149804-63-6: (1S)-1-(2-Fluoro-4-methoxyphenyl)ethylamine is an organic compound characterized by its amine functional group and a substituted aromatic ring. The presence of a fluorine atom and a methoxy group on the phenyl ring contributes to its unique chemical properties, including potential variations in polarity and reactivity. The compound's stereochemistry, indicated by the (1S) designation, suggests a specific three-dimensional arrangement of atoms that can influence its biological activity and interactions with other molecules. Typically, compounds like this may exhibit properties such as solubility in organic solvents, potential for hydrogen bonding due to the amine group, and varying degrees of lipophilicity depending on the substituents on the aromatic ring. Such characteristics make it of interest in medicinal chemistry, particularly in the development of pharmaceuticals where modifications to the aromatic system can enhance efficacy or selectivity for biological targets. Additionally, the fluorine atom can enhance metabolic stability and influence the compound's pharmacokinetic properties.

CAS 1149804-63-6

(1S)-1-(2-FLUORO-4-METHOXYPHENYL)ETHYLAMINE

(S)-1-(2-Fluoro-4-methoxyphenyl)ethan-1-amine

Ref: IN-DA01KLBQ

(S)-1-(2-Fluoro-4-methoxyphenyl)ethan-1-amine

Ref: 54-PC1005417

(1S)-1-(2-FLUORO-4-METHOXYPHENYL)ETHYLAMINE

Ref: 10-F847702