4-(3-Chloro-2-thienyl)-6-methyl-2-(1H-pyrrol-1-yl)pyrimidine is a synthetic organic compound characterized by its complex heterocyclic structure, which includes a pyrimidine core substituted with a thienyl group and a pyrrole moiety. The presence of the chlorine atom on the thienyl ring contributes to its reactivity and potential biological activity. This compound is typically studied for its pharmacological properties, particularly in the context of medicinal chemistry, where it may exhibit activity against specific biological targets. Its molecular structure suggests potential interactions with various enzymes or receptors, making it a candidate for drug development. The compound's solubility, stability, and reactivity can vary based on environmental conditions and the presence of other chemical species. As with many heterocyclic compounds, it may also display interesting electronic properties due to the conjugation within its aromatic systems. Safety and handling precautions should be observed, as with all chemical substances, particularly those with halogen substituents.

4-(3-CHLORO-2-THIENYL)-6-METHYL-2-(1H-PYRROL-1-YL)PYRIMIDINE

860788-69-8: 4-(3-Chloro-2-thienyl)-6-methyl-2-(1H-pyrrol-1-yl)pyrimidine is a synthetic organic compound characterized by its complex heterocyclic structure, which includes a pyrimidine core substituted with a thienyl group and a pyrrole moiety. The presence of the chlorine atom on the thienyl ring contributes to its reactivity and potential biological activity. This compound is typically studied for its pharmacological properties, particularly in the context of medicinal chemistry, where it may exhibit activity against specific biological targets. Its molecular structure suggests potential interactions with various enzymes or receptors, making it a candidate for drug development. The compound's solubility, stability, and reactivity can vary based on environmental conditions and the presence of other chemical species. As with many heterocyclic compounds, it may also display interesting electronic properties due to the conjugation within its aromatic systems. Safety and handling precautions should be observed, as with all chemical substances, particularly those with halogen substituents.

CAS 860788-69-8

4-(3-CHLORO-2-THIENYL)-6-METHYL-2-(1H-PYRROL-1-YL)PYRIMIDINE