6-Bromo-4-(pyridazin-4-yl)quinoline is a chemical compound characterized by its unique structure, which combines a quinoline core with a bromine substituent and a pyridazine moiety. The presence of the bromine atom at the 6-position of the quinoline ring enhances its reactivity and may influence its biological activity. The pyridazine group, attached at the 4-position, contributes to the compound's potential pharmacological properties. This compound is typically studied for its applications in medicinal chemistry, particularly in the development of novel therapeutic agents. Its molecular structure suggests potential interactions with biological targets, making it of interest in drug discovery. Additionally, the compound's solubility, stability, and reactivity can vary based on the surrounding conditions, such as pH and solvent. As with many heterocyclic compounds, it may exhibit interesting optical and electronic properties, which can be explored for various applications in materials science and organic electronics. Overall, 6-bromo-4-(pyridazin-4-yl)quinoline represents a versatile scaffold for further chemical modifications and investigations.

6-broMo-4-(pyridazin-4-yl)quinoline

1086063-18-4: 6-Bromo-4-(pyridazin-4-yl)quinoline is a chemical compound characterized by its unique structure, which combines a quinoline core with a bromine substituent and a pyridazine moiety. The presence of the bromine atom at the 6-position of the quinoline ring enhances its reactivity and may influence its biological activity. The pyridazine group, attached at the 4-position, contributes to the compound's potential pharmacological properties. This compound is typically studied for its applications in medicinal chemistry, particularly in the development of novel therapeutic agents. Its molecular structure suggests potential interactions with biological targets, making it of interest in drug discovery. Additionally, the compound's solubility, stability, and reactivity can vary based on the surrounding conditions, such as pH and solvent. As with many heterocyclic compounds, it may exhibit interesting optical and electronic properties, which can be explored for various applications in materials science and organic electronics. Overall, 6-bromo-4-(pyridazin-4-yl)quinoline represents a versatile scaffold for further chemical modifications and investigations.

CAS 1086063-18-4

6-broMo-4-(pyridazin-4-yl)quinoline

6-broMo-4-(pyridazin-4-yl)quinoline

Ref: IN-DA008TD0

6-Bromo-4-(pyridazin-4-yl)quinoline

Ref: 10-F788498