2H-Imidazol-2-one, with the specified structure and CAS number 2212022-56-3, is a complex organic compound characterized by its unique bicyclic structure that incorporates both imidazole and pyrazolo-pyridine moieties. This compound features multiple functional groups, including fluoro and methyl substituents, which can influence its chemical reactivity and biological activity. The presence of the imidazole ring suggests potential applications in medicinal chemistry, as imidazole derivatives are often associated with various pharmacological properties. The stereochemistry indicated by the (4S) configuration suggests that the compound may exhibit chiral properties, which can affect its interaction with biological targets. Additionally, the presence of multiple aromatic rings may contribute to its lipophilicity, potentially impacting its solubility and permeability in biological systems. Overall, this compound's intricate structure and substituent patterns suggest it may be of interest in drug development and research, particularly in the context of targeting specific biological pathways or receptors.

2H-Imidazol-2-one, 1-[(4S)-2-(4-fluoro-3,5-dimethylphenyl)-4,5,6,7-tetrahydro-4-methyl-2H-pyrazolo[4,3-c]pyridin-3-yl]-3-(4-fluoro-1-methyl-1H-indazol-5-yl)-1,3-dihydro-

2212022-56-3: 2H-Imidazol-2-one, with the specified structure and CAS number 2212022-56-3, is a complex organic compound characterized by its unique bicyclic structure that incorporates both imidazole and pyrazolo-pyridine moieties. This compound features multiple functional groups, including fluoro and methyl substituents, which can influence its chemical reactivity and biological activity. The presence of the imidazole ring suggests potential applications in medicinal chemistry, as imidazole derivatives are often associated with various pharmacological properties. The stereochemistry indicated by the (4S) configuration suggests that the compound may exhibit chiral properties, which can affect its interaction with biological targets. Additionally, the presence of multiple aromatic rings may contribute to its lipophilicity, potentially impacting its solubility and permeability in biological systems. Overall, this compound's intricate structure and substituent patterns suggest it may be of interest in drug development and research, particularly in the context of targeting specific biological pathways or receptors.

(S)-1-(4-Fluoro-1-methyl-1H-indazol-5-yl)-3-(2-(4-fluoro-3,5-dimethylphenyl)-4-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridin-3-yl)-1H-imidazol-2(3H)-one

CAS 2212022-56-3

2H-Imidazol-2-one, 1-[(4S)-2-(4-fluoro-3,5-dimethylphenyl)-4,5,6,7-tetrahydro-4-methyl-2H-pyrazolo[4,3-c]pyridin-3-yl]-3-(4-fluoro-1-methyl-1H-indazol-5-yl)-1,3-dihydro-

(S)-1-(4-Fluoro-1-methyl-1H-indazol-5-yl)-3-(2-(4-fluoro-3,5-dimethylphenyl)-4-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridin-3-yl)-1H-imidazol-2(3H)-one

Ref: 54-PC1008119