3-(Morpholin-3-ylmethyl)-1H-indole is a chemical compound characterized by its indole core, which is a bicyclic structure consisting of a benzene ring fused to a pyrrole ring. The presence of a morpholine group, specifically a morpholin-3-ylmethyl substituent, introduces a nitrogen-containing heterocyclic moiety that can influence the compound's solubility, polarity, and biological activity. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure suggests potential interactions with biological targets, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The compound may possess various functional properties, including potential anti-cancer or anti-inflammatory activities, depending on its specific interactions within biological systems. As with many indole derivatives, it may also exhibit fluorescence properties, which can be useful in various analytical applications. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

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

913718-45-3: 3-(Morpholin-3-ylmethyl)-1H-indole is a chemical compound characterized by its indole core, which is a bicyclic structure consisting of a benzene ring fused to a pyrrole ring. The presence of a morpholine group, specifically a morpholin-3-ylmethyl substituent, introduces a nitrogen-containing heterocyclic moiety that can influence the compound's solubility, polarity, and biological activity. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure suggests potential interactions with biological targets, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The compound may possess various functional properties, including potential anti-cancer or anti-inflammatory activities, depending on its specific interactions within biological systems. As with many indole derivatives, it may also exhibit fluorescence properties, which can be useful in various analytical applications. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

CAS 913718-45-3

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

3-(Morpholin-3-ylmethyl)-1H-indole

Ref: 3D-NLB71845