7-Chloroimidazo[1,2-a]pyrimidine is a heterocyclic organic compound characterized by its fused imidazole and pyrimidine rings, with a chlorine substituent at the 7-position of the imidazole ring. This compound typically exhibits a pale yellow to off-white crystalline appearance. It is known for its potential biological activity, particularly in medicinal chemistry, where it may serve as a scaffold for the development of pharmaceuticals, especially in the context of targeting specific enzymes or receptors. The presence of the chlorine atom can influence its reactivity and solubility, making it a valuable compound in drug design. Additionally, its structural features contribute to its ability to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The compound's properties, such as melting point, boiling point, and solubility, can vary based on the specific conditions and solvents used. Overall, 7-chloroimidazo[1,2-a]pyrimidine represents a significant interest in both synthetic and medicinal chemistry due to its unique structure and potential applications.

7-ChloroiMidazo[1,2-a]pyriMidine

944896-70-2: 7-Chloroimidazo[1,2-a]pyrimidine is a heterocyclic organic compound characterized by its fused imidazole and pyrimidine rings, with a chlorine substituent at the 7-position of the imidazole ring. This compound typically exhibits a pale yellow to off-white crystalline appearance. It is known for its potential biological activity, particularly in medicinal chemistry, where it may serve as a scaffold for the development of pharmaceuticals, especially in the context of targeting specific enzymes or receptors. The presence of the chlorine atom can influence its reactivity and solubility, making it a valuable compound in drug design. Additionally, its structural features contribute to its ability to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The compound's properties, such as melting point, boiling point, and solubility, can vary based on the specific conditions and solvents used. Overall, 7-chloroimidazo[1,2-a]pyrimidine represents a significant interest in both synthetic and medicinal chemistry due to its unique structure and potential applications.

CAS 944896-70-2

7-ChloroiMidazo[1,2-a]pyriMidine

7-Chloroimidazo[1,2-A]pyrimidine

Ref: IN-DA01BCSH

7-chloroimidazo[1,2-a]pyrimidine

Ref: 3D-UMB89670