2-Chloro-N-(2-ethoxyphenyl)acetamide is an organic compound characterized by its amide functional group, which is derived from acetic acid. The presence of a chloro substituent on the second carbon of the acetamide structure contributes to its reactivity and potential biological activity. The ethoxyphenyl group enhances its lipophilicity, which may influence its solubility and interaction with biological membranes. This compound typically appears as a solid or crystalline substance and may exhibit moderate stability under standard conditions. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of both the chloro and ethoxy groups that can modulate biological activity. Additionally, the compound may be subject to various chemical reactions, including nucleophilic substitutions and hydrolysis, depending on the reaction conditions. Safety data should be consulted for handling and storage, as the presence of chlorine may pose certain hazards. Overall, 2-chloro-N-(2-ethoxyphenyl)acetamide is a compound of interest in chemical research and development.

2-chloro-N-(2-ethoxyphenyl)acetamide

21118-77-4: 2-Chloro-N-(2-ethoxyphenyl)acetamide is an organic compound characterized by its amide functional group, which is derived from acetic acid. The presence of a chloro substituent on the second carbon of the acetamide structure contributes to its reactivity and potential biological activity. The ethoxyphenyl group enhances its lipophilicity, which may influence its solubility and interaction with biological membranes. This compound typically appears as a solid or crystalline substance and may exhibit moderate stability under standard conditions. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of both the chloro and ethoxy groups that can modulate biological activity. Additionally, the compound may be subject to various chemical reactions, including nucleophilic substitutions and hydrolysis, depending on the reaction conditions. Safety data should be consulted for handling and storage, as the presence of chlorine may pose certain hazards. Overall, 2-chloro-N-(2-ethoxyphenyl)acetamide is a compound of interest in chemical research and development.

CAS 21118-77-4

2-chloro-N-(2-ethoxyphenyl)acetamide

2-Chloro-N-(2-ethoxyphenyl)acetamide

Ref: IN-DA002L74

2-Chloro-N-(2-ethoxy-phenyl)-acetamide

Ref: 10-F058143