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CAS 2719-15-5

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

Description:
N-(2-Methyl-4-nitrophenyl)acetamide, with the CAS number 2719-15-5, is an organic compound characterized by its amide functional group. It features a phenyl ring substituted with a methyl group and a nitro group, which contribute to its chemical reactivity and physical properties. 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 presence of the nitro group imparts significant electron-withdrawing properties, influencing the compound's reactivity in electrophilic aromatic substitution reactions. Additionally, the acetamide moiety enhances its potential for hydrogen bonding, which can affect its solubility and interaction with other molecules. N-(2-Methyl-4-nitrophenyl)acetamide may be utilized in various chemical syntheses and research applications, particularly in the fields of pharmaceuticals and agrochemicals, where its unique structural features can be leveraged for developing new compounds or studying reaction mechanisms. Safety data should be consulted for handling and usage, as nitro compounds can pose health risks.
Formula:C9H10N2O3
InChI:InChI=1S/C9H10N2O3/c1-6-5-8(11(13)14)3-4-9(6)10-7(2)12/h3-5H,1-2H3,(H,10,12)
InChI key:InChIKey=JZEOVPGWIWSSAK-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=C(C)C=C(N(=O)=O)C=C1
Synonyms:
  • 5-Nitro-2-acetamidotoluene
  • Acetamide, N-(2-methyl-4-nitrophenyl)-
  • Acetyl-p-nitro-o-toluidine
  • N-(2-methyl-4-nitrophenyl)acetamide
  • N1-(2-Methyl-4-nitrophenyl)acetamide
  • NSC 29042
  • o-Acetotoluidide, 4′-nitro-
  • 2′-Methyl-4′-nitroacetanilide
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