5-Chloro-6-(3-chlorophenyl)pyridazin-3(2H)-one is a chemical compound characterized by its pyridazine core, which is a six-membered aromatic ring containing two nitrogen atoms. The presence of chlorine substituents at the 5 and 3 positions enhances its reactivity and potential biological activity. This compound typically exhibits properties such as moderate solubility in organic solvents and may have limited solubility in water, which is common for halogenated organic compounds. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the chlorophenyl group that can influence biological interactions. The compound may also exhibit specific spectral characteristics, such as distinct absorption peaks in UV-Vis spectroscopy and unique signals in NMR spectroscopy, aiding in its identification and characterization. Additionally, the presence of the pyridazinone moiety may contribute to its potential as a bioactive agent, making it of interest in various fields, including agrochemicals and drug discovery.

5-chloro-6-(3-chlorophenyl)pyridazin-3(2H)-one

886497-43-4: 5-Chloro-6-(3-chlorophenyl)pyridazin-3(2H)-one is a chemical compound characterized by its pyridazine core, which is a six-membered aromatic ring containing two nitrogen atoms. The presence of chlorine substituents at the 5 and 3 positions enhances its reactivity and potential biological activity. This compound typically exhibits properties such as moderate solubility in organic solvents and may have limited solubility in water, which is common for halogenated organic compounds. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the chlorophenyl group that can influence biological interactions. The compound may also exhibit specific spectral characteristics, such as distinct absorption peaks in UV-Vis spectroscopy and unique signals in NMR spectroscopy, aiding in its identification and characterization. Additionally, the presence of the pyridazinone moiety may contribute to its potential as a bioactive agent, making it of interest in various fields, including agrochemicals and drug discovery.

CAS 886497-43-4

5-chloro-6-(3-chlorophenyl)pyridazin-3(2H)-one

3(2H)-Pyridazinone,5-chloro-6-(3-chlorophenyl)-

Ref: IN-DA0048M8

5-Chloro-6-(3-chlorophenyl)pyridazin-3(2H)-one

Ref: 54-OR0196

4-Chloro-3-(3-chlorophenyl)-5,6H-pyradazin-6-one

Ref: 10-F023490