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CAS 40392-27-6

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5-Nitro-2-phenyl-1H-isoindole-1,3(2H)-dione

Description:
5-Nitro-2-phenyl-1H-isoindole-1,3(2H)-dione, with the CAS number 40392-27-6, is a chemical compound characterized by its isoindole structure, which features a fused ring system comprising both aromatic and non-aromatic components. This compound typically exhibits a yellow to orange color due to the presence of the nitro group, which can influence its electronic properties and reactivity. The nitro group is known for its electron-withdrawing characteristics, which can affect the compound's acidity and reactivity in various chemical reactions. Additionally, the phenyl group contributes to the compound's stability and hydrophobicity. 5-Nitro-2-phenyl-1H-isoindole-1,3(2H)-dione may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its solubility can vary depending on the solvent, and it may undergo various chemical transformations, including reduction and substitution reactions. Overall, this compound represents a unique structure with potential applications in organic synthesis and pharmaceuticals.
Formula:C14H8N2O4
InChI:InChI=1S/C14H8N2O4/c17-13-11-7-6-10(16(19)20)8-12(11)14(18)15(13)9-4-2-1-3-5-9/h1-8H
InChI key:InChIKey=HNNCFMUZZXJQLR-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)N1C3=CC=CC=C3)=CC=C(N(=O)=O)C2
Synonyms:
  • 1H-Isoindole-1,3(2H)-dione, 5-nitro-2-phenyl-
  • 5-Nitro-2-phenyl-1H-isoindole-1,3(2H)-dione
  • N-Phenyl-4-nitrophthalimide
  • Phthalimide, 4-nitro-N-phenyl-
  • 4-Nitro-N-phenylphthalimide
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