3-(Morpholin-4-ylmethyl)-1H-indole, with the CAS number 5379-88-4, is a chemical compound characterized by its indole core, which is a bicyclic structure consisting of a benzene ring fused to a pyrrole ring. This compound features a morpholine group, a six-membered ring containing both oxygen and nitrogen atoms, attached to the indole at the 3-position via a methylene bridge. The presence of the morpholine moiety contributes to its potential as a pharmacophore in medicinal chemistry, often enhancing solubility and bioavailability. The compound may exhibit various biological activities, making it of interest in drug discovery and development. Its structural characteristics suggest potential interactions with biological targets, which could lead to therapeutic applications. Additionally, the compound's stability, solubility, and reactivity can be influenced by the functional groups present, making it a subject of study in organic synthesis and medicinal chemistry. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-rich nature of the indole nitrogen.

3-(morpholin-4-ylmethyl)-1H-indole

5379-88-4: 3-(Morpholin-4-ylmethyl)-1H-indole, with the CAS number 5379-88-4, is a chemical compound characterized by its indole core, which is a bicyclic structure consisting of a benzene ring fused to a pyrrole ring. This compound features a morpholine group, a six-membered ring containing both oxygen and nitrogen atoms, attached to the indole at the 3-position via a methylene bridge. The presence of the morpholine moiety contributes to its potential as a pharmacophore in medicinal chemistry, often enhancing solubility and bioavailability. The compound may exhibit various biological activities, making it of interest in drug discovery and development. Its structural characteristics suggest potential interactions with biological targets, which could lead to therapeutic applications. Additionally, the compound's stability, solubility, and reactivity can be influenced by the functional groups present, making it a subject of study in organic synthesis and medicinal chemistry. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-rich nature of the indole nitrogen.

CAS 5379-88-4

3-(morpholin-4-ylmethyl)-1H-indole

3-MORPHOLIN-4-YLMETHYL-1H-INDOLE

Ref: 10-F471234