3-Bromo-2-phenyl-imidazo[1,2-a]pyrimidine is a heterocyclic compound characterized by its fused imidazole and pyrimidine rings, which contribute to its biological activity and chemical properties. The presence of a bromine atom at the 3-position and a phenyl group at the 2-position enhances its reactivity and solubility in organic solvents. This compound typically exhibits a planar structure, which is favorable for interactions with biological targets, making it of interest in medicinal chemistry. It may possess various pharmacological properties, including potential anti-cancer or anti-inflammatory activities, due to its ability to interact with specific enzymes or receptors. The compound's stability is influenced by the electronic effects of the bromine and phenyl substituents, which can affect its reactivity and binding affinity. Additionally, its synthesis often involves multi-step organic reactions, highlighting its complexity and the need for careful handling in laboratory settings. Overall, 3-bromo-2-phenyl-imidazo[1,2-a]pyrimidine represents a significant class of compounds in drug discovery and development.

3-bromo-2-phenyl-imidazo[1,2-a]pyrimidine

904814-72-8: 3-Bromo-2-phenyl-imidazo[1,2-a]pyrimidine is a heterocyclic compound characterized by its fused imidazole and pyrimidine rings, which contribute to its biological activity and chemical properties. The presence of a bromine atom at the 3-position and a phenyl group at the 2-position enhances its reactivity and solubility in organic solvents. This compound typically exhibits a planar structure, which is favorable for interactions with biological targets, making it of interest in medicinal chemistry. It may possess various pharmacological properties, including potential anti-cancer or anti-inflammatory activities, due to its ability to interact with specific enzymes or receptors. The compound's stability is influenced by the electronic effects of the bromine and phenyl substituents, which can affect its reactivity and binding affinity. Additionally, its synthesis often involves multi-step organic reactions, highlighting its complexity and the need for careful handling in laboratory settings. Overall, 3-bromo-2-phenyl-imidazo[1,2-a]pyrimidine represents a significant class of compounds in drug discovery and development.

CAS 904814-72-8

3-bromo-2-phenyl-imidazo[1,2-a]pyrimidine

3-BROMO-2-PHENYL-IMIDAZO[1,2-A]PYRIMIDINE

Ref: IN-DA00GVBR

3-Bromo-2-phenylimidazo[1,2-a]pyrimidine

Ref: 54-OR1050743

3-Bromo-2-phenylimidazo[1,2-a]pyrimidine

Ref: 10-F217443