3-(4-Methoxy-3,5-dimethylbenzyl)piperidine, identified by its CAS number 779323-34-1, is a chemical compound that features a piperidine ring substituted with a benzyl group. The benzyl moiety is further substituted with a methoxy group and two methyl groups, contributing to its unique structural characteristics. This compound is typically characterized by its moderate polarity due to the presence of both hydrophobic (the aromatic and aliphatic portions) and hydrophilic (the methoxy group) elements. It may exhibit basic properties due to the nitrogen atom in the piperidine ring, allowing it to participate in various chemical reactions, including nucleophilic substitutions. The presence of multiple methyl groups can influence its steric hindrance and overall reactivity. Additionally, this compound may have potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural similarity to biologically active molecules. Its solubility, stability, and reactivity can vary based on the solvent and environmental conditions, making it a subject of interest in both synthetic and applied chemistry.

3-(4-methoxy-3,5-dimethylbenzyl)piperidine

779323-34-1: 3-(4-Methoxy-3,5-dimethylbenzyl)piperidine, identified by its CAS number 779323-34-1, is a chemical compound that features a piperidine ring substituted with a benzyl group. The benzyl moiety is further substituted with a methoxy group and two methyl groups, contributing to its unique structural characteristics. This compound is typically characterized by its moderate polarity due to the presence of both hydrophobic (the aromatic and aliphatic portions) and hydrophilic (the methoxy group) elements. It may exhibit basic properties due to the nitrogen atom in the piperidine ring, allowing it to participate in various chemical reactions, including nucleophilic substitutions. The presence of multiple methyl groups can influence its steric hindrance and overall reactivity. Additionally, this compound may have potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural similarity to biologically active molecules. Its solubility, stability, and reactivity can vary based on the solvent and environmental conditions, making it a subject of interest in both synthetic and applied chemistry.

3-(4-Methoxy-3,5-dimethyl-benzyl)-piperidine

CAS 779323-34-1

3-(4-methoxy-3,5-dimethylbenzyl)piperidine

3-(4-Methoxy-3,5-dimethyl-benzyl)-piperidine

Ref: 54-OR307736