2-Chloro-N-{4-[(E)-phenyldiazenyl]phenyl}acetamide, with the CAS number 19680-35-4, is an organic compound characterized by its unique structural features. It contains a chloro group, an acetamide functional group, and a phenyldiazenyl moiety, which contributes to its potential as a dye or pigment due to the presence of the azo linkage. The compound exhibits moderate solubility in organic solvents, and its chemical structure suggests it may participate in various chemical reactions, including electrophilic aromatic substitution due to the electron-rich nature of the aromatic rings. The presence of the chloro substituent can influence its reactivity and stability, while the azo group can impart color properties, making it of interest in dye chemistry. Additionally, the compound may exhibit biological activity, which warrants further investigation into its potential applications in pharmaceuticals or agrochemicals. Overall, its distinct functional groups and structural characteristics make it a compound of interest in both synthetic and applied chemistry.

2-chloro-N-{4-[(E)-phenyldiazenyl]phenyl}acetamide

19680-35-4: 2-Chloro-N-{4-[(E)-phenyldiazenyl]phenyl}acetamide, with the CAS number 19680-35-4, is an organic compound characterized by its unique structural features. It contains a chloro group, an acetamide functional group, and a phenyldiazenyl moiety, which contributes to its potential as a dye or pigment due to the presence of the azo linkage. The compound exhibits moderate solubility in organic solvents, and its chemical structure suggests it may participate in various chemical reactions, including electrophilic aromatic substitution due to the electron-rich nature of the aromatic rings. The presence of the chloro substituent can influence its reactivity and stability, while the azo group can impart color properties, making it of interest in dye chemistry. Additionally, the compound may exhibit biological activity, which warrants further investigation into its potential applications in pharmaceuticals or agrochemicals. Overall, its distinct functional groups and structural characteristics make it a compound of interest in both synthetic and applied chemistry.

CAS 19680-35-4

2-chloro-N-{4-[(E)-phenyldiazenyl]phenyl}acetamide

2-Chloro-N-[4-(2-phenyldiazen-1-yl)phenyl]acetamide

Ref: 3D-UAA68035