5-Ethyl-4-methyl-6-(pyrrolidin-1-yl)pyrimidin-2-amine is a chemical compound characterized by its pyrimidine core, which is a six-membered heterocyclic ring containing two nitrogen atoms at positions 1 and 3. This compound features an ethyl group at the 5-position and a methyl group at the 4-position, contributing to its hydrophobic characteristics. The presence of a pyrrolidine ring at the 6-position introduces additional steric and electronic properties, enhancing its potential biological activity. The amino group at the 2-position is indicative of its basic nature, allowing for interactions with various biological targets. This compound may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can influence binding affinity and selectivity for specific receptors or enzymes. Its unique combination of functional groups and ring structures suggests potential applications in drug discovery and development, particularly in areas related to neurological or metabolic disorders.

5-ethyl-4-methyl-6-(pyrrolidin-1-yl)pyrimidin-2-amine

424803-29-2: 5-Ethyl-4-methyl-6-(pyrrolidin-1-yl)pyrimidin-2-amine is a chemical compound characterized by its pyrimidine core, which is a six-membered heterocyclic ring containing two nitrogen atoms at positions 1 and 3. This compound features an ethyl group at the 5-position and a methyl group at the 4-position, contributing to its hydrophobic characteristics. The presence of a pyrrolidine ring at the 6-position introduces additional steric and electronic properties, enhancing its potential biological activity. The amino group at the 2-position is indicative of its basic nature, allowing for interactions with various biological targets. This compound may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can influence binding affinity and selectivity for specific receptors or enzymes. Its unique combination of functional groups and ring structures suggests potential applications in drug discovery and development, particularly in areas related to neurological or metabolic disorders.

CAS 424803-29-2

5-ethyl-4-methyl-6-(pyrrolidin-1-yl)pyrimidin-2-amine

5-ethyl-4-methyl-6-(1-pyrrolidinyl)-2-pyrimidinamine

Ref: 10-F314760