(4-Chloro-benzyl)-(3-morpholin-4-yl-propyl)-amine, with the CAS number 107921-37-9, is a chemical compound characterized by its specific functional groups and structural features. It contains a benzyl moiety substituted with a chlorine atom at the para position, which contributes to its lipophilicity and potential biological activity. The presence of a morpholine ring indicates that the compound may exhibit properties typical of amines, such as basicity and the ability to form hydrogen bonds. The propyl chain linked to the morpholine adds to the compound's hydrophobic character, which can influence its solubility and permeability in biological systems. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential interactions with biological targets. Its unique structure suggests that it could exhibit various pharmacological activities, although specific biological data would be necessary to confirm its efficacy and safety profiles. As with many amine-containing compounds, it may also be sensitive to oxidation and other chemical transformations.

(4-CHLORO-BENZYL)-(3-MORPHOLIN-4-YL-PROPYL)-AMINE

107921-37-9: (4-Chloro-benzyl)-(3-morpholin-4-yl-propyl)-amine, with the CAS number 107921-37-9, is a chemical compound characterized by its specific functional groups and structural features. It contains a benzyl moiety substituted with a chlorine atom at the para position, which contributes to its lipophilicity and potential biological activity. The presence of a morpholine ring indicates that the compound may exhibit properties typical of amines, such as basicity and the ability to form hydrogen bonds. The propyl chain linked to the morpholine adds to the compound's hydrophobic character, which can influence its solubility and permeability in biological systems. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential interactions with biological targets. Its unique structure suggests that it could exhibit various pharmacological activities, although specific biological data would be necessary to confirm its efficacy and safety profiles. As with many amine-containing compounds, it may also be sensitive to oxidation and other chemical transformations.

CAS 107921-37-9

(4-CHLORO-BENZYL)-(3-MORPHOLIN-4-YL-PROPYL)-AMINE