1-Methyl-N-(pyridin-4-ylmethyl)piperidin-4-amine, with the CAS number 416868-54-7, is a chemical compound characterized by its piperidine core, which is a six-membered saturated nitrogen-containing ring. This compound features a methyl group attached to the nitrogen atom of the piperidine ring and a pyridin-4-ylmethyl substituent, indicating the presence of a pyridine ring linked through a methylene (-CH2-) group. The structure suggests potential for hydrogen bonding and interactions due to the presence of both nitrogen atoms and aromatic systems. It may exhibit properties typical of amines, such as basicity and nucleophilicity, and could participate in various chemical reactions, including alkylation and acylation. The compound's unique structure may confer specific biological activities, making it of interest in medicinal chemistry and drug development. Its solubility, stability, and reactivity would depend on the surrounding conditions, such as pH and solvent polarity. Overall, this compound represents a class of piperidine derivatives that may have applications in pharmacology and organic synthesis.

1-methyl-N-(pyridin-4-ylmethyl)piperidin-4-amine

416868-54-7: 1-Methyl-N-(pyridin-4-ylmethyl)piperidin-4-amine, with the CAS number 416868-54-7, is a chemical compound characterized by its piperidine core, which is a six-membered saturated nitrogen-containing ring. This compound features a methyl group attached to the nitrogen atom of the piperidine ring and a pyridin-4-ylmethyl substituent, indicating the presence of a pyridine ring linked through a methylene (-CH2-) group. The structure suggests potential for hydrogen bonding and interactions due to the presence of both nitrogen atoms and aromatic systems. It may exhibit properties typical of amines, such as basicity and nucleophilicity, and could participate in various chemical reactions, including alkylation and acylation. The compound's unique structure may confer specific biological activities, making it of interest in medicinal chemistry and drug development. Its solubility, stability, and reactivity would depend on the surrounding conditions, such as pH and solvent polarity. Overall, this compound represents a class of piperidine derivatives that may have applications in pharmacology and organic synthesis.

CAS 416868-54-7

1-methyl-N-(pyridin-4-ylmethyl)piperidin-4-amine

1-methyl-N-(4-pyridinylmethyl)-4-piperidinamine trihydrochloride hydrate

Ref: 10-F360893