N-(2-Fluorophenyl)-2-mercaptoacetamide is an organic compound characterized by the presence of a mercapto group (-SH) and an acetamide functional group. The molecular structure features a fluorophenyl moiety, which contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar organic solvents due to the presence of the polar acetamide group. The fluorine atom in the 2-position of the phenyl ring can influence the compound's reactivity and biological activity, often enhancing lipophilicity and altering electronic properties. N-(2-Fluorophenyl)-2-mercaptoacetamide may exhibit potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Additionally, the thiol group can participate in various chemical reactions, including nucleophilic substitutions and redox reactions, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and storage, as compounds containing thiol groups can be sensitive to oxidation and may have specific toxicity profiles.

N-(2-FLUOROPHENYL)-2-MERCAPTOACETAMIDE

217317-00-5: N-(2-Fluorophenyl)-2-mercaptoacetamide is an organic compound characterized by the presence of a mercapto group (-SH) and an acetamide functional group. The molecular structure features a fluorophenyl moiety, which contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar organic solvents due to the presence of the polar acetamide group. The fluorine atom in the 2-position of the phenyl ring can influence the compound's reactivity and biological activity, often enhancing lipophilicity and altering electronic properties. N-(2-Fluorophenyl)-2-mercaptoacetamide may exhibit potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Additionally, the thiol group can participate in various chemical reactions, including nucleophilic substitutions and redox reactions, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and storage, as compounds containing thiol groups can be sensitive to oxidation and may have specific toxicity profiles.

CAS 217317-00-5

N-(2-FLUOROPHENYL)-2-MERCAPTOACETAMIDE

N1-(2-fluorophenyl)-2-mercaptoacetamide

Ref: 54-PC31165