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CAS 4433-79-8

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N-(4-Chloro-2,5-dimethoxyphenyl)-3-oxobutanamide

Description:
N-(4-Chloro-2,5-dimethoxyphenyl)-3-oxobutanamide, with the CAS number 4433-79-8, is an organic compound characterized by its amide functional group and a substituted aromatic ring. The presence of the 4-chloro and 2,5-dimethoxy groups on the phenyl ring contributes to its unique chemical properties, including potential biological activity. The compound features a ketone group adjacent to the amide, which can influence its reactivity and stability. Typically, such compounds may exhibit moderate solubility in organic solvents and limited solubility in water due to their hydrophobic aromatic structure. The presence of chlorine and methoxy groups can also affect the compound's electronic properties, potentially enhancing its reactivity in electrophilic substitution reactions. Additionally, the compound may be of interest in medicinal chemistry for its potential pharmacological applications, although specific biological activities would require further investigation. Overall, N-(4-Chloro-2,5-dimethoxyphenyl)-3-oxobutanamide represents a complex structure with diverse chemical characteristics.
Formula:C12H14ClNO4
InChI:InChI=1S/C12H14ClNO4/c1-7(15)4-12(16)14-9-6-10(17-2)8(13)5-11(9)18-3/h5-6H,4H2,1-3H3,(H,14,16)
InChI key:InChIKey=MOUVJGIRLPZEES-UHFFFAOYSA-N
SMILES:N(C(CC(C)=O)=O)C1=C(OC)C=C(Cl)C(OC)=C1
Synonyms:
  • 1-Acetoacetylamino-2,5-dimethoxy-4-chlorobenzene
  • 1-Acetoacetylamino-4-chloro-2,5-dimethoxy-benzene
  • 2',5'-Dimethoxy-4'-chloro-acetoacetanilide
  • 2,5-Dimethoxy-4-chloro-N-acetoacetyl aniline
  • 4-Chloro-2, 5-Dimethoxy-Acetoaceto Anilide
  • 4′-Chloro-2′,5′-dimethoxyacetoacetanilide
  • AcetoAcet-2,5-dimethoxy-4-chloroanilide
  • Acetoacetanilide, 4′-chloro-2′,5′-dimethoxy-
  • Acetoaceto-2,5-dimethoxy-4-chloroanilide
  • Acetoacetyl-2,5-dimethoxy-4-chloroanilide
  • See more synonyms
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