2-Chloro-5-fluoro-4-(pyrrolidin-1-yl)pyrimidine is a heterocyclic organic compound characterized by its pyrimidine core, which is a six-membered ring containing two nitrogen atoms at positions 1 and 3. The presence of a chlorine atom at the 2-position and a fluorine atom at the 5-position contributes to its reactivity and potential biological activity. The substitution of a pyrrolidine group at the 4-position enhances its lipophilicity and may influence its interaction with biological targets. This compound is typically used in medicinal chemistry and drug development, particularly in the design of pharmaceuticals that target specific biological pathways. Its molecular structure suggests potential applications in areas such as oncology or neurology, where pyrimidine derivatives are often explored for therapeutic effects. The compound's properties, including solubility, stability, and reactivity, can be influenced by the halogen substituents and the pyrrolidine moiety, making it a subject of interest for further research and development in chemical and pharmaceutical sciences.

2-chloro-5-fluoro-4-(pyrrolidin-1-yl)pyrimidine

923119-59-9: 2-Chloro-5-fluoro-4-(pyrrolidin-1-yl)pyrimidine is a heterocyclic organic compound characterized by its pyrimidine core, which is a six-membered ring containing two nitrogen atoms at positions 1 and 3. The presence of a chlorine atom at the 2-position and a fluorine atom at the 5-position contributes to its reactivity and potential biological activity. The substitution of a pyrrolidine group at the 4-position enhances its lipophilicity and may influence its interaction with biological targets. This compound is typically used in medicinal chemistry and drug development, particularly in the design of pharmaceuticals that target specific biological pathways. Its molecular structure suggests potential applications in areas such as oncology or neurology, where pyrimidine derivatives are often explored for therapeutic effects. The compound's properties, including solubility, stability, and reactivity, can be influenced by the halogen substituents and the pyrrolidine moiety, making it a subject of interest for further research and development in chemical and pharmaceutical sciences.

CAS 923119-59-9

2-chloro-5-fluoro-4-(pyrrolidin-1-yl)pyrimidine

2-chloro-5-fluoro-4-(1-pyrrolidinyl)pyrimidine

Ref: 10-F311475