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CAS 10553-13-6

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6-Nitro-1H-indole-3-carboxaldehyde

Description:
6-Nitro-1H-indole-3-carboxaldehyde is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a nitro group at the 6-position and an aldehyde functional group at the 3-position contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. This compound is typically a yellow to orange solid and is soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO). Its reactivity is influenced by the electron-withdrawing nature of the nitro group, which can enhance electrophilic substitution reactions. Additionally, the aldehyde group can participate in various chemical reactions, including condensation and reduction. 6-Nitro-1H-indole-3-carboxaldehyde may serve as an intermediate in the synthesis of more complex molecules and has potential applications in the development of pharmaceuticals, particularly in the study of biologically active compounds. As with many nitro-containing compounds, it should be handled with care due to potential toxicity and environmental concerns.
Formula:C9H6N2O3
InChI:InChI=1S/C9H6N2O3/c12-5-6-4-10-9-3-7(11(13)14)1-2-8(6)9/h1-5,10H
InChI key:InChIKey=KYFZSGBVGJNEPN-UHFFFAOYSA-N
SMILES:C(=O)C=1C=2C(=CC(N(=O)=O)=CC2)NC1
Synonyms:
  • 1H-indole-3-carboxaldehyde, 6-nitro-
  • 3-Formyl-6-nitroindole
  • 6-Nitro-1H-indole-3-carboxaldehyde
  • 6-Nitro-3-formylindole
  • 6-Nitro-3-indolecarboxaldehyde
  • Indole-3-carboxaldehyde, 6-nitro-
  • 6-Nitro-1H-indole-3-carbaldehyde
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