2-Chloro-6-pyrrolidin-1-yl-pyrazine is a chemical compound characterized by its unique structure, which includes a pyrazine ring substituted with a chlorine atom and a pyrrolidine moiety. The presence of the chlorine atom at the 2-position of the pyrazine ring contributes to its reactivity and potential biological activity. The pyrrolidine group, a five-membered nitrogen-containing ring, enhances the compound's solubility and may influence its pharmacological properties. This compound is often studied in medicinal chemistry for its potential applications in drug development, particularly in the context of neuropharmacology and as a scaffold for designing new therapeutic agents. Its molecular interactions, stability, and reactivity can be influenced by the electronic effects of the chlorine substituent and the steric effects of the pyrrolidine ring. As with many heterocyclic compounds, understanding its properties requires consideration of its synthesis, reactivity, and potential applications in various fields, including pharmaceuticals and agrochemicals.

2-Chloro-6-pyrrolidin-1-yl-pyrazine

642459-09-4: 2-Chloro-6-pyrrolidin pyrazine, 2-chloro-6-(1H-pyrazol-1-yl)pyrazine,  2-chloro-6-(pyrrolidin-1-yl)pyrazine

CAS 642459-09-4: 2-Chloro-6-pyrrolidin-1-yl-pyrazine

2-Chloro-6-(pyrazol-1-yl)pyrazine

Ref: IN-DA00EBMZ

2-Chloro-6-(pyrazol-1-yl)pyrazine

Ref: 3D-SAB45909

2-Chloro-6-(1H-pyrazol-1-yl)pyrazine

Ref: 54-OR11510

2-Chloro-6-(1H-pyrazol-1-yl)pyrazine

Ref: 10-F209851