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CAS 50651-39-3

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N-(4-Methoxy-3-nitrophenyl)acetamide

Description:
N-(4-Methoxy-3-nitrophenyl)acetamide, with the CAS number 50651-39-3, is an organic compound characterized by its acetamide functional group attached to a substituted aromatic ring. The presence of a methoxy group (-OCH3) and a nitro group (-NO2) on the phenyl ring contributes to its chemical reactivity and polarity. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to the hydrophobic nature of the aromatic system. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity in electrophilic aromatic substitution reactions. Additionally, the methoxy group can provide some electron-donating characteristics, affecting the overall electronic distribution within the molecule. N-(4-Methoxy-3-nitrophenyl)acetamide may be of interest in various fields, including medicinal chemistry and materials science, due to its potential biological activity and utility as a synthetic intermediate. Safety and handling precautions should be observed, as with many nitro-substituted compounds, due to potential toxicity and environmental concerns.
Formula:C9H10N2O4
InChI:InChI=1S/C9H10N2O4/c1-6(12)10-7-3-4-9(15-2)8(5-7)11(13)14/h3-5H,1-2H3,(H,10,12)
InChI key:InChIKey=MYIUWCZXTNZSMN-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(OC)C=CC(NC(C)=O)=C1
Synonyms:
  • 2-Nitro-4-acetamidoanisole
  • 2-Nitro-4-acetylamino-anisole
  • 3'-Nitro-p-acetanisidide
  • 4'-Methoxy-3'-nitroacetanilide
  • 4-Acetamido-2-nitroanisole
  • 4-Acetylamino-2-nitroanisole
  • Acetamide, N-(4-methoxy-3-nitrophenyl)-
  • N-(4-Methoxy-3-nitrophenyl)acetamide
  • Nsc 14685
  • p-Acetanisidide, 3′-nitro-
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