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CAS 51867-83-5

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N-(3-Amino-4-chlorophenyl)acetamide

Description:
N-(3-Amino-4-chlorophenyl)acetamide, with the CAS number 51867-83-5, is an organic compound characterized by its amide functional group and an aromatic ring. This substance features a chlorinated phenyl group, which contributes to its chemical reactivity and potential biological activity. The presence of the amino group (-NH2) enhances its solubility in polar solvents and may influence its interaction with biological systems. Typically, compounds like this can exhibit properties such as moderate to high melting points and may be stable under standard laboratory conditions. Its structure suggests potential applications in pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. Additionally, the chlorophenyl moiety may impart unique electronic properties, making it a candidate for further research in medicinal chemistry. Safety and handling precautions should be observed, as with many amides and chlorinated compounds, due to potential toxicity or reactivity. Overall, N-(3-Amino-4-chlorophenyl)acetamide represents a compound of interest in both synthetic and applied chemistry contexts.
Formula:C8H9ClN2O
InChI:InChI=1S/C8H9ClN2O/c1-5(12)11-6-2-3-7(9)8(10)4-6/h2-4H,10H2,1H3,(H,11,12)
InChI key:InChIKey=MIIPQGGYCFVDAI-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=CC(N)=C(Cl)C=C1
Synonyms:
  • 1-Amino-3-acetylamino-6-chloro-benzene
  • 4-Chloro-3-amino acetanilide
  • 5-Acetamido-2-chloroaniline
  • 5-Acetylamido-2-Chloroaniline
  • Acetamide, N-(3-amino-4-chlorophenyl)-
  • N-(3-Amino-4-chlorophenyl)acetamide
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