7-(3,4-Dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-ol is a chemical compound characterized by its unique imidazo[1,2-c]pyrimidine core, which is fused with a phenyl group substituted with two methoxy groups at the 3 and 4 positions. This structure contributes to its potential biological activity, particularly in medicinal chemistry. The presence of the hydroxyl group at the 5-position of the pyrimidine ring enhances its solubility and may influence its interaction with biological targets. The compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, particularly as a lead compound in drug development due to its ability to interact with various biological pathways. Additionally, the methoxy groups can enhance lipophilicity, potentially improving the compound's bioavailability. As with many heterocyclic compounds, its reactivity and properties can be influenced by the presence of functional groups, making it a subject of interest in organic synthesis and medicinal research.

7-(3,4-dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-ol

371171-04-9: 7-(3,4-Dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-ol is a chemical compound characterized by its unique imidazo[1,2-c]pyrimidine core, which is fused with a phenyl group substituted with two methoxy groups at the 3 and 4 positions. This structure contributes to its potential biological activity, particularly in medicinal chemistry. The presence of the hydroxyl group at the 5-position of the pyrimidine ring enhances its solubility and may influence its interaction with biological targets. The compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, particularly as a lead compound in drug development due to its ability to interact with various biological pathways. Additionally, the methoxy groups can enhance lipophilicity, potentially improving the compound's bioavailability. As with many heterocyclic compounds, its reactivity and properties can be influenced by the presence of functional groups, making it a subject of interest in organic synthesis and medicinal research.

CAS 371171-04-9

7-(3,4-dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-ol

7-(3,4-dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-ol

Ref: IN-DA00C6E0

7-(3,4-dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-ol

Ref: 54-OR87278

7-(3,4-DIMETHOXYPHENYL)IMIDAZO[1,2-C]PYRIMIDIN-5-OL

Ref: 10-F390354