6-Nitro-3-(piperidin-1-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 nitro group at the 6-position of the indole ring introduces electron-withdrawing characteristics, which can influence the compound's reactivity and biological activity. The piperidinylmethyl substituent at the 3-position adds a flexible aliphatic amine component, potentially enhancing the compound's interaction with biological targets, such as receptors or enzymes. This compound may exhibit pharmacological properties, making it of interest in medicinal chemistry. Its structure suggests potential applications in drug development, particularly in areas related to neuropharmacology or as a scaffold for further modifications. Additionally, the presence of both the nitro and piperidine groups may contribute to its solubility and lipophilicity, affecting its bioavailability and distribution in biological systems. Overall, 6-nitro-3-(piperidin-1-ylmethyl)-1H-indole represents a versatile structure for further exploration in chemical and pharmaceutical research.

6-nitro-3-(piperidin-1-ylmethyl)-1H-indole

101832-09-1: 6-Nitro-3-(piperidin-1-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 nitro group at the 6-position of the indole ring introduces electron-withdrawing characteristics, which can influence the compound's reactivity and biological activity. The piperidinylmethyl substituent at the 3-position adds a flexible aliphatic amine component, potentially enhancing the compound's interaction with biological targets, such as receptors or enzymes. This compound may exhibit pharmacological properties, making it of interest in medicinal chemistry. Its structure suggests potential applications in drug development, particularly in areas related to neuropharmacology or as a scaffold for further modifications. Additionally, the presence of both the nitro and piperidine groups may contribute to its solubility and lipophilicity, affecting its bioavailability and distribution in biological systems. Overall, 6-nitro-3-(piperidin-1-ylmethyl)-1H-indole represents a versatile structure for further exploration in chemical and pharmaceutical research.

CAS 101832-09-1

6-nitro-3-(piperidin-1-ylmethyl)-1H-indole

6-NITRO-3-(PIPERIDIN-1-YLMETHYL)-1H-INDOLE

Ref: 10-F471320