5-Bromo-3-(morpholin-4-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 bromine atom at the 5-position of the indole enhances its reactivity and can influence its biological activity. The morpholinylmethyl group at the 3-position introduces a morpholine ring, which is a six-membered heterocyclic structure containing oxygen and nitrogen, contributing to the compound's solubility and potential interactions with biological targets. This compound may exhibit pharmacological properties, making it of interest in medicinal chemistry and drug development. Its unique structure allows for various applications, particularly in the fields of biochemistry and pharmaceuticals, where it may serve as a lead compound for further modifications. As with many indole derivatives, it may also display interesting properties such as fluorescence or photostability, which can be advantageous in research and diagnostic applications. Safety and handling precautions should be observed due to the presence of bromine and the potential biological activity of the compound.

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

102043-55-0: 5-Bromo-3-(morpholin-4-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 bromine atom at the 5-position of the indole enhances its reactivity and can influence its biological activity. The morpholinylmethyl group at the 3-position introduces a morpholine ring, which is a six-membered heterocyclic structure containing oxygen and nitrogen, contributing to the compound's solubility and potential interactions with biological targets. This compound may exhibit pharmacological properties, making it of interest in medicinal chemistry and drug development. Its unique structure allows for various applications, particularly in the fields of biochemistry and pharmaceuticals, where it may serve as a lead compound for further modifications. As with many indole derivatives, it may also display interesting properties such as fluorescence or photostability, which can be advantageous in research and diagnostic applications. Safety and handling precautions should be observed due to the presence of bromine and the potential biological activity of the compound.

CAS 102043-55-0

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

4-((5-BROMO-1H-INDOL-3-YL)METHYL)MORPHOLINE

Ref: 10-F471259