2-[(3-Chloro-4-fluorophenyl)amino]acetohydrazide, with the CAS number 2370-44-7, is a chemical compound characterized by its hydrazide functional group, which is linked to an aromatic ring containing both chlorine and fluorine substituents. This compound typically exhibits properties associated with both hydrazides and aromatic amines, including potential reactivity due to the presence of the hydrazide moiety, which can participate in various chemical reactions such as condensation and acylation. The chlorine and fluorine atoms on the phenyl ring can influence the compound's electronic properties, potentially enhancing its reactivity and solubility in organic solvents. Additionally, the presence of these halogens may impart biological activity, making such compounds of interest in medicinal chemistry and drug development. The compound's structure suggests it may be involved in hydrogen bonding and other intermolecular interactions, which can affect its physical properties, such as melting point and solubility. Overall, 2-[(3-chloro-4-fluorophenyl)amino]acetohydrazide is a versatile compound with potential applications in various fields, including pharmaceuticals and agrochemicals.

2-[(3-chloro-4-fluorophenyl)amino]acetohydrazide (non-preferred name)

2370-44-7: 2-[(3-Chloro-4-fluorophenyl)amino]acetohydrazide, with the CAS number 2370-44-7, is a chemical compound characterized by its hydrazide functional group, which is linked to an aromatic ring containing both chlorine and fluorine substituents. This compound typically exhibits properties associated with both hydrazides and aromatic amines, including potential reactivity due to the presence of the hydrazide moiety, which can participate in various chemical reactions such as condensation and acylation. The chlorine and fluorine atoms on the phenyl ring can influence the compound's electronic properties, potentially enhancing its reactivity and solubility in organic solvents. Additionally, the presence of these halogens may impart biological activity, making such compounds of interest in medicinal chemistry and drug development. The compound's structure suggests it may be involved in hydrogen bonding and other intermolecular interactions, which can affect its physical properties, such as melting point and solubility. Overall, 2-[(3-chloro-4-fluorophenyl)amino]acetohydrazide is a versatile compound with potential applications in various fields, including pharmaceuticals and agrochemicals.

2-(3-Chloro-4-fluoroanilino)acetohydrazide

N-(3-Chloro-4-fluorophenyl)glycinehydrazide

CAS 2370-44-7

2-[(3-chloro-4-fluorophenyl)amino]acetohydrazide (non-preferred name)

2-(3-Chloro-4-fluoroanilino)acetohydrazide

Ref: IN-DA002O7N

N-(3-Chloro-4-fluorophenyl)glycinehydrazide

Ref: 54-PC5673