N-(6-Chloro-2-(trifluoromethyl)phenyl)((4-pyridylcarbonylamino)amino)formamide is a complex organic compound characterized by its unique structural features. It contains a chloro-substituted phenyl group, which contributes to its potential biological activity, particularly in medicinal chemistry. The trifluoromethyl group enhances lipophilicity and may influence the compound's interaction with biological targets. The presence of the pyridylcarbonylamino moiety suggests potential for hydrogen bonding and interactions with various biological receptors. This compound is likely to exhibit specific solubility characteristics, influenced by its polar and non-polar functional groups. Its formamide functional group indicates potential for reactivity, particularly in amide bond formation or hydrolysis. Overall, this compound may be of interest in pharmaceutical research, particularly for its potential applications in drug development, given its structural complexity and the presence of functional groups that can participate in various chemical interactions. However, detailed studies would be necessary to fully understand its properties, reactivity, and biological activity.

N-(6-CHLORO-2-(TRIFLUOROMETHYL)PHENYL)((4-PYRIDYLCARBONYLAMINO)AMINO)FORMAMIDE

1022565-22-5: N-(6-Chloro-2-(trifluoromethyl)phenyl)((4-pyridylcarbonylamino)amino)formamide is a complex organic compound characterized by its unique structural features. It contains a chloro-substituted phenyl group, which contributes to its potential biological activity, particularly in medicinal chemistry. The trifluoromethyl group enhances lipophilicity and may influence the compound's interaction with biological targets. The presence of the pyridylcarbonylamino moiety suggests potential for hydrogen bonding and interactions with various biological receptors. This compound is likely to exhibit specific solubility characteristics, influenced by its polar and non-polar functional groups. Its formamide functional group indicates potential for reactivity, particularly in amide bond formation or hydrolysis. Overall, this compound may be of interest in pharmaceutical research, particularly for its potential applications in drug development, given its structural complexity and the presence of functional groups that can participate in various chemical interactions. However, detailed studies would be necessary to fully understand its properties, reactivity, and biological activity.

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CAS 1022565-22-5

N-(6-CHLORO-2-(TRIFLUOROMETHYL)PHENYL)((4-PYRIDYLCARBONYLAMINO)AMINO)FORMAMIDE

N-(6-chloro-2-(trifluoromethyl)phenyl)((4-pyridylcarbonylamino)amino)formamide

Ref: 3D-XQB56522