N'-((2-Chloro-7-methyl-3-quinoliny)methylene)-4-fluorobenzohydrazide is a chemical compound characterized by its complex structure, which includes a quinoline moiety and a hydrazide functional group. The presence of the chloro and fluoro substituents indicates that it may exhibit unique electronic and steric properties, potentially influencing its reactivity and biological activity. The quinoline ring is known for its role in various pharmacological applications, while the hydrazide group can participate in diverse chemical reactions, including hydrazone formation. This compound may be of interest in medicinal chemistry, particularly for its potential as an antitumor or antimicrobial agent, given the biological significance of both quinoline derivatives and hydrazides. Its solubility, stability, and reactivity would depend on the specific conditions and solvents used. As with many organic compounds, safety precautions should be taken when handling this substance, and its properties should be thoroughly investigated in a laboratory setting to understand its full potential and applications.

N'-((2-CHLORO-7-METHYL-3-QUINOLINYL)METHYLENE)-4-FLUOROBENZOHYDRAZIDE

388606-19-7: N'-((2-Chloro-7-methyl-3-quinoliny)methylene)-4-fluorobenzohydrazide is a chemical compound characterized by its complex structure, which includes a quinoline moiety and a hydrazide functional group. The presence of the chloro and fluoro substituents indicates that it may exhibit unique electronic and steric properties, potentially influencing its reactivity and biological activity. The quinoline ring is known for its role in various pharmacological applications, while the hydrazide group can participate in diverse chemical reactions, including hydrazone formation. This compound may be of interest in medicinal chemistry, particularly for its potential as an antitumor or antimicrobial agent, given the biological significance of both quinoline derivatives and hydrazides. Its solubility, stability, and reactivity would depend on the specific conditions and solvents used. As with many organic compounds, safety precautions should be taken when handling this substance, and its properties should be thoroughly investigated in a laboratory setting to understand its full potential and applications.

CAS 388606-19-7

N'-((2-CHLORO-7-METHYL-3-QUINOLINYL)METHYLENE)-4-FLUOROBENZOHYDRAZIDE

4-Fluorobenzoic acid 2-((2-chloro-7-methyl-3-quinolinyl)methylene) Hydrazide

Ref: 4Z-B-085221