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CAS 57556-49-7

:

N-(4-Amino-2-chlorophenyl)acetamide

Description:
N-(4-Amino-2-chlorophenyl)acetamide, also known by its CAS number 57556-49-7, is an organic compound characterized by the presence of an acetamide functional group attached to a chlorinated aromatic ring. This compound features a 4-amino group and a 2-chloro substituent on the phenyl ring, which contributes to its chemical reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amine and amide functionalities. The compound's structure suggests potential applications in pharmaceuticals, particularly in the development of drugs targeting various biological pathways. Its properties, such as melting point, boiling point, and specific reactivity, can vary based on purity and environmental conditions. As with many amides, it may participate in hydrogen bonding, influencing its interactions in biological systems. Safety data should be consulted for handling and usage, as the presence of chlorine and amino groups can impart specific hazards.
Formula:C8H9ClN2O
InChI:InChI=1/C8H9ClN2O/c1-5(12)11-8-3-2-6(10)4-7(8)9/h2-4H,10H2,1H3,(H,11,12)
InChI key:InChIKey=LWAYASXDHDEGAO-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=C(Cl)C=C(N)C=C1
Synonyms:
  • 4-Acetylamino-3-chloroaniline
  • Acetanilide, 4-amino-2-chloro-
  • N-(4-Amino-2-chlorophenyl)acetamide
  • N-(4-Amino-2-chlorphenyl)acetamid
  • NSC 88986
  • acetamide, N-(4-amino-2-chlorophenyl)-
  • 4′-Amino-2′-chloroacetanilide
  • 4-AMINO-2-CHLORO ACETANILIDE
  • N1-(4-AMINO-2-CHLOROPHENYL)ACETAMIDE
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