6-Bromo-2-(3,4,5-trimethoxy-phenyl)-quinoline-4-carboxylic acid is a chemical compound characterized by its complex structure, which includes a quinoline core substituted with a bromine atom and a carboxylic acid functional group. The presence of the trimethoxyphenyl group enhances its potential for biological activity, as methoxy groups can influence solubility and reactivity. This compound is typically studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its unique structural features that may interact with biological targets. The bromine substitution can also affect the compound's electronic properties and reactivity, making it a subject of interest in synthetic organic chemistry. Additionally, the carboxylic acid group can participate in various chemical reactions, such as esterification or amidation, further expanding its utility in chemical synthesis. Overall, this compound exemplifies the intricate relationship between molecular structure and chemical behavior, making it a valuable subject for research in both organic and medicinal chemistry.

6-BROMO-2-(3,4,5-TRIMETHOXY-PHENYL)-QUINOLINE-4-CARBOXYLIC ACID

351329-63-0: 6-Bromo-2-(3,4,5-trimethoxy-phenyl)-quinoline-4-carboxylic acid is a chemical compound characterized by its complex structure, which includes a quinoline core substituted with a bromine atom and a carboxylic acid functional group. The presence of the trimethoxyphenyl group enhances its potential for biological activity, as methoxy groups can influence solubility and reactivity. This compound is typically studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its unique structural features that may interact with biological targets. The bromine substitution can also affect the compound's electronic properties and reactivity, making it a subject of interest in synthetic organic chemistry. Additionally, the carboxylic acid group can participate in various chemical reactions, such as esterification or amidation, further expanding its utility in chemical synthesis. Overall, this compound exemplifies the intricate relationship between molecular structure and chemical behavior, making it a valuable subject for research in both organic and medicinal chemistry.

CAS 351329-63-0

6-BROMO-2-(3,4,5-TRIMETHOXY-PHENYL)-QUINOLINE-4-CARBOXYLIC ACID

6-Bromo-2-(3,4,5-trimethoxy-phenyl)-quinoline-4-carboxylic acid

Ref: 10-F014462