Imidazo[1,2-b]pyridazine, 6-chloro-3-[3-(trifluoromethoxy)phenyl]- is a heterocyclic compound characterized by its fused imidazole and pyridazine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the 6-position and a trifluoromethoxy group at the 3-position of the phenyl ring enhances its reactivity and solubility in various organic solvents. This compound is often studied for its potential biological activities, including its role in medicinal chemistry as a scaffold for drug development. The trifluoromethoxy group is particularly notable for its electron-withdrawing properties, which can influence the compound's pharmacokinetics and interactions with biological targets. Additionally, the structural features of this compound may impart specific characteristics such as stability under certain conditions and the ability to participate in various chemical reactions, making it of interest in both research and industrial applications. Overall, its unique structure and functional groups make it a valuable compound in the field of organic and medicinal chemistry.

IMIDAZO[1,2-B]PYRIDAZINE, 6-CHLORO-3-[3-(TRIFLUOROMETHOXY)PHENYL]-

928337-00-2: Imidazo[1,2-b]pyridazine, 6-chloro-3-[3-(trifluoromethoxy)phenyl]- is a heterocyclic compound characterized by its fused imidazole and pyridazine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the 6-position and a trifluoromethoxy group at the 3-position of the phenyl ring enhances its reactivity and solubility in various organic solvents. This compound is often studied for its potential biological activities, including its role in medicinal chemistry as a scaffold for drug development. The trifluoromethoxy group is particularly notable for its electron-withdrawing properties, which can influence the compound's pharmacokinetics and interactions with biological targets. Additionally, the structural features of this compound may impart specific characteristics such as stability under certain conditions and the ability to participate in various chemical reactions, making it of interest in both research and industrial applications. Overall, its unique structure and functional groups make it a valuable compound in the field of organic and medicinal chemistry.

CAS 928337-00-2

IMIDAZO[1,2-B]PYRIDAZINE, 6-CHLORO-3-[3-(TRIFLUOROMETHOXY)PHENYL]-

6-Chloro-3-(3-(trifluoromethoxy)phenyl)imidazo[1,2-b]pyridazine

Ref: IN-DA01KKG9

6-Chloro-3-(3-(trifluoromethoxy)phenyl)imidazo[1,2-b]pyridazine

Ref: 54-PC1006395

6-Chloro-3-(3-(trifluoromethoxy)phenyl)imidazo[1,2-b]pyridazine

Ref: 10-F695581