6-Chloroimidazo[1,2-a]pyrimidine is a heterocyclic organic compound characterized by its fused imidazole and pyrimidine rings, with a chlorine substituent at the 6-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 the compound's lipophilicity and reactivity, making it a valuable candidate for further chemical modifications. Additionally, its structural features contribute to its ability to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The compound's solubility and stability can vary depending on the solvent and environmental conditions, which are important considerations in both laboratory and industrial applications. Overall, 6-chloroimidazo[1,2-a]pyrimidine represents a significant compound in the field of organic synthesis and drug discovery.

6-chloroimidazo[1,2-a]pyrimidine

944906-56-3: 6-Chloroimidazo[1,2-a]pyrimidine is a heterocyclic organic compound characterized by its fused imidazole and pyrimidine rings, with a chlorine substituent at the 6-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 the compound's lipophilicity and reactivity, making it a valuable candidate for further chemical modifications. Additionally, its structural features contribute to its ability to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The compound's solubility and stability can vary depending on the solvent and environmental conditions, which are important considerations in both laboratory and industrial applications. Overall, 6-chloroimidazo[1,2-a]pyrimidine represents a significant compound in the field of organic synthesis and drug discovery.

CAS 944906-56-3

6-chloroimidazo[1,2-a]pyrimidine

6-Chloroimidazo[1,2-a]pyrimidine

Ref: IN-DA00IIAF

6-Chloroimidazo[1,2-a]pyrimidine

Ref: 54-OR61303

6-Chloroimidazo[1,2-a]pyrimidine

Ref: 10-F377825