6-Bromo-4-(piperazin-1-yl)quinoline is a chemical compound characterized by its quinoline core, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of a bromine atom at the 6-position enhances its reactivity and potential for further chemical modifications. The piperazine moiety at the 4-position introduces basic properties and can facilitate interactions with biological targets, making this compound of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Its structure suggests potential applications in areas such as antimicrobial or antitumor agents, given the biological activity often associated with quinoline derivatives. The compound's solubility, stability, and pharmacokinetic properties would be influenced by the functional groups present, particularly the piperazine ring, which can enhance solubility in biological systems. As with many synthetic compounds, safety and handling precautions are essential due to the presence of bromine, which can be hazardous. Overall, 6-bromo-4-(piperazin-1-yl)quinoline represents a versatile scaffold for further research and development in drug discovery.

6-bromo-4-(piperazin-1-yl)quinoline

474707-24-9: 6-Bromo-4-(piperazin-1-yl)quinoline is a chemical compound characterized by its quinoline core, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of a bromine atom at the 6-position enhances its reactivity and potential for further chemical modifications. The piperazine moiety at the 4-position introduces basic properties and can facilitate interactions with biological targets, making this compound of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Its structure suggests potential applications in areas such as antimicrobial or antitumor agents, given the biological activity often associated with quinoline derivatives. The compound's solubility, stability, and pharmacokinetic properties would be influenced by the functional groups present, particularly the piperazine ring, which can enhance solubility in biological systems. As with many synthetic compounds, safety and handling precautions are essential due to the presence of bromine, which can be hazardous. Overall, 6-bromo-4-(piperazin-1-yl)quinoline represents a versatile scaffold for further research and development in drug discovery.

CAS 474707-24-9

6-bromo-4-(piperazin-1-yl)quinoline

6-Bromo-4-(piperazin-1-yl)quinoline

Ref: IN-DA00DFSK

6-Bromo-4-(piperazin-1-yl)quinoline

Ref: 54-OR309249

6-Bromo-4-(piperazin-1-yl)quinoline

Ref: 10-F726816