3-Methyl-1-(2-(piperidin-1-yl)phenyl)butan-1-one, identified by its CAS number 147770-03-4, is a synthetic organic compound that belongs to the class of ketones. This substance features a butanone backbone with a methyl group and a phenyl ring substituted with a piperidine moiety, contributing to its unique chemical properties. The presence of the piperidine ring suggests potential interactions with biological systems, making it of interest in medicinal chemistry and pharmacology. The compound is likely to exhibit moderate lipophilicity due to its hydrophobic aromatic and aliphatic components, which may influence its solubility and permeability in biological membranes. Additionally, the structural complexity may lead to diverse reactivity patterns, including potential for electrophilic substitution or nucleophilic attack at various sites. As with many organic compounds, safety and handling precautions should be observed, as the specific toxicity and environmental impact of this compound would require further investigation. Overall, 3-methyl-1-(2-(piperidin-1-yl)phenyl)butan-1-one represents a notable example of a functionalized ketone with potential applications in various fields.

3-methyl-1-(2-(piperidin-1-yl)phenyl)butan-1-one

147770-03-4: 3-Methyl-1-(2-(piperidin-1-yl)phenyl)butan-1-one, identified by its CAS number 147770-03-4, is a synthetic organic compound that belongs to the class of ketones. This substance features a butanone backbone with a methyl group and a phenyl ring substituted with a piperidine moiety, contributing to its unique chemical properties. The presence of the piperidine ring suggests potential interactions with biological systems, making it of interest in medicinal chemistry and pharmacology. The compound is likely to exhibit moderate lipophilicity due to its hydrophobic aromatic and aliphatic components, which may influence its solubility and permeability in biological membranes. Additionally, the structural complexity may lead to diverse reactivity patterns, including potential for electrophilic substitution or nucleophilic attack at various sites. As with many organic compounds, safety and handling precautions should be observed, as the specific toxicity and environmental impact of this compound would require further investigation. Overall, 3-methyl-1-(2-(piperidin-1-yl)phenyl)butan-1-one represents a notable example of a functionalized ketone with potential applications in various fields.

CAS 147770-03-4

3-methyl-1-(2-(piperidin-1-yl)phenyl)butan-1-one

Repaglinide Impurity 19

Ref: 4Z-R-1142