N-(4-Chlorophenyl)-2-cyanoacetamide, with the CAS number 17722-17-7, is an organic compound characterized by its amide functional group and cyano group. It features a 4-chlorophenyl moiety, which contributes to its chemical properties and potential biological activity. The presence of the cyano group indicates that it may participate in various chemical reactions, such as nucleophilic additions or substitutions. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential applications in pharmaceuticals or agrochemicals, as compounds with similar frameworks often display interesting biological activities. Additionally, the chlorophenyl group may enhance lipophilicity, influencing the compound's interaction with biological systems. Safety and handling precautions should be observed, as with many organic compounds, due to potential toxicity or reactivity. Overall, N-(4-Chlorophenyl)-2-cyanoacetamide is a compound of interest in synthetic organic chemistry and medicinal chemistry research.

N-(4-Chlorophenyl)-2-cyanoacetamide

17722-17-7: 2-Cyano-N-(4-chlorophenyl)-acetamide, Acetamide, N-(4-chlorophenyl)-2-cyano-, Acetanilide, 4′-chloro-2-cyano-, Cyanoacetic acid p-chloroanilide, N-(4-Chlorophenyl)-α-cyanoacetamide, N-(4-Chlorophenyl)cyanoacetamide, N-(4-chlorophenyl)-2-cyanoacetamide, p-Chlorocyanoacetanilide, 4-Chloro-2-cyanoacetanilide, 4′-Chloro-2-cyanoacetanilide

N-(4-Chlorophenyl)-2-cyanoacetamide is a pyridine compound that can be synthesized from chloroacetonitrile and acetamide. It has been shown to react with an active methylene group in benzene or pyridine to produce a heterocycle. This reaction is reversible and can be used as a preparative method for the synthesis of heterocycles. The 1,3-dipolar cycloaddition of N-(4-chlorophenyl)-2-cyanoacetamide with nitro groups in nitrobenzene produces the corresponding 2-nitropyridines, which are important intermediates in the synthesis of other heterocycles. N-(4-Chlorophenyl)-2-cyanoacetamide has been used as an efficient method for the preparation of nitrogen nucleophiles that are useful for catalysis.

CAS 17722-17-7: N-(4-Chlorophenyl)-2-cyanoacetamide

N-(4-Chlorophenyl)-2-cyanoacetamide

Ref: 54-OR33321

N-(4-Chlorophenyl)-2-cyanoacetamide

Ref: 3D-FC132644

Acetamide, N-(4-chlorophenyl)-2-cyano-

Ref: IN-DA00257J

N-(4-chlorophenyl)-2-cyanoacetamide

Ref: 10-F374663