5-Chloro-1-(4-fluoro-phenyl)-3-piperidin-4-yl-1H-indole is a chemical compound characterized by its complex structure, which includes an indole core, a piperidine ring, and halogenated phenyl substituents. The presence of a chlorine atom and a fluorine atom in its structure suggests potential biological activity, as halogenated compounds often exhibit unique pharmacological properties. This compound is likely to be a solid at room temperature, with moderate solubility in organic solvents, reflecting the presence of both polar and non-polar functional groups. Its molecular structure may contribute to interactions with biological targets, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The piperidine moiety can enhance the compound's ability to cross biological membranes, while the indole structure is known for its role in various biological processes. Overall, this compound's unique combination of functional groups and structural features positions it as a candidate for further research in drug discovery and development.

5-CHLORO-1-(4-FLUORO-PHENYL)-3-PIPERIDIN-4-YL-1H-INDOLE

138900-27-3: 5-Chloro-1-(4-fluoro-phenyl)-3-piperidin-4-yl-1H-indole is a chemical compound characterized by its complex structure, which includes an indole core, a piperidine ring, and halogenated phenyl substituents. The presence of a chlorine atom and a fluorine atom in its structure suggests potential biological activity, as halogenated compounds often exhibit unique pharmacological properties. This compound is likely to be a solid at room temperature, with moderate solubility in organic solvents, reflecting the presence of both polar and non-polar functional groups. Its molecular structure may contribute to interactions with biological targets, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The piperidine moiety can enhance the compound's ability to cross biological membranes, while the indole structure is known for its role in various biological processes. Overall, this compound's unique combination of functional groups and structural features positions it as a candidate for further research in drug discovery and development.

CAS 138900-27-3

5-CHLORO-1-(4-FLUORO-PHENYL)-3-PIPERIDIN-4-YL-1H-INDOLE

5-Chloro-1-(4-fluorophenyl)-3-(piperidin-4-yl)-1H-indole

Ref: IN-DA0019SV

Sertindole Impurity 2 Acetate

Ref: 4Z-S-150004