2-Chloro-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 pyrrolidine group at the 4-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. The pyrrolidine moiety can enhance interactions with biological targets, while the chlorine substituent may influence its reactivity and lipophilicity. As with many heterocycles, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity. Overall, 2-chloro-4-(pyrrolidin-1-yl)pyrimidine represents a versatile scaffold for further chemical exploration and application in pharmaceuticals.

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

35691-20-4: 2-Chloro-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 pyrrolidine group at the 4-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. The pyrrolidine moiety can enhance interactions with biological targets, while the chlorine substituent may influence its reactivity and lipophilicity. As with many heterocycles, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity. Overall, 2-chloro-4-(pyrrolidin-1-yl)pyrimidine represents a versatile scaffold for further chemical exploration and application in pharmaceuticals.

CAS 35691-20-4

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

4-azetidin-1-yl-2-chloropyrimidine

Ref: IN-DA00BZHW

2-Chloro-4-(pyrrolidin-1-yl)pyrimidine

Ref: 54-OR11552

2-Chloro-4-pyrrolidin-1-ylpyrimidine

Ref: 10-F067419