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CAS 93-27-6

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N-(2-Methoxy-4-nitrophenyl)acetamide

Description:
N-(2-Methoxy-4-nitrophenyl)acetamide, with the CAS number 93-27-6, is an organic compound characterized by its acetamide functional group attached to a substituted phenyl ring. The presence of a methoxy group (-OCH3) and a nitro group (-NO2) on the aromatic ring contributes to its chemical reactivity and polarity. This compound typically appears as a solid at room temperature and is soluble in organic solvents, reflecting its non-polar characteristics due to the aromatic structure. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity in electrophilic substitution reactions. Additionally, the methoxy group can provide some electron-donating effects, affecting the overall electronic distribution within the molecule. N-(2-Methoxy-4-nitrophenyl)acetamide may be utilized in various chemical syntheses and research applications, particularly in the fields of medicinal chemistry and materials science, due to its unique structural features and potential biological activity. Safety precautions should be observed when handling this compound, as it may pose health risks.
Formula:C9H10N2O4
InChI:InChI=1S/C9H10N2O4/c1-6(12)10-8-4-3-7(11(13)14)5-9(8)15-2/h3-5H,1-2H3,(H,10,12)
InChI key:InChIKey=DQWRNQKJPNUTPJ-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=C(OC)C=C(N(=O)=O)C=C1
Synonyms:
  • 2-Acetamido-1-methoxy-5-nitrobenzene
  • 2-Acetylamino-1-methoxy-5-nitrobenzene
  • 2-Acetylamino-5-nitroanisole
  • 4′-Nitro-o-acetanisidide
  • 5-Nitro-2-(acetylamino)anisole
  • Acetamide, N-(2-methoxy-4-nitrophenyl)-
  • Ccris 1979
  • o-Acetanisidide, 4′-nitro-
  • N-(2-methoxy-4-nitrophenyl)-acetamid
  • N-(2-Methoxy-4-nitrophenyl)acetamide
  • N-(2-Methoxy-4-nitrophenyl)acetamide
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