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CAS 5469-94-3

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N1,N3-Bis(4-methylphenyl)propanediamide

Description:
N1,N3-Bis(4-methylphenyl)propanediamide, with the CAS number 5469-94-3, is an organic compound characterized by its amide functional groups and a propanediamide backbone. This substance features two 4-methylphenyl groups attached to the nitrogen atoms of the diamide structure, contributing to its hydrophobic characteristics and potential for various applications in organic synthesis and materials science. The presence of the methyl groups on the phenyl rings enhances its steric bulk and may influence its solubility and reactivity. Typically, compounds of this nature exhibit moderate to high melting points and may be solid at room temperature. They can participate in hydrogen bonding due to the amide groups, which can affect their physical properties and interactions with other molecules. Additionally, N1,N3-Bis(4-methylphenyl)propanediamide may be explored for its potential use in pharmaceuticals, agrochemicals, or as intermediates in organic reactions, although specific applications would depend on further research and development.
Formula:C17H18N2O2
InChI:InChI=1S/C17H18N2O2/c1-12-3-7-14(8-4-12)18-16(20)11-17(21)19-15-9-5-13(2)6-10-15/h3-10H,11H2,1-2H3,(H,18,20)(H,19,21)
InChI key:InChIKey=CIGKFIJIRVGTGE-UHFFFAOYSA-N
SMILES:N(C(CC(NC1=CC=C(C)C=C1)=O)=O)C2=CC=C(C)C=C2
Synonyms:
  • N,N'-Bis(4-methylphenyl)malonamide
  • N<sup>1</sup>,N<sup>3</sup>-Bis(4-methylphenyl)propanediamide
  • NSC 26925
  • Propanediamide, N,N′-bis(4-methylphenyl)-
  • Propanediamide, N<sup>1</sup>,N<sup>3</sup>-bis(4-methylphenyl)-
  • p-Malonotoluidide
  • propanediamide, N~1~,N~3~-bis(4-methylphenyl)-
  • Propanediamide, N1,N3-bis(4-methylphenyl)-
  • N1,N3-Bis(4-methylphenyl)propanediamide
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