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CAS 6958-37-8

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5-Nitroindole-3-carboxylic acid

Description:
5-Nitroindole-3-carboxylic acid is an organic compound characterized by its indole structure, which features a nitro group and a carboxylic acid functional group. The presence of the nitro group at the 5-position of the indole ring contributes to its reactivity and potential applications in various chemical reactions. The carboxylic acid group at the 3-position enhances its solubility in polar solvents and allows for further derivatization. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. It is often used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in various chemical transformations. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling, as nitro compounds can be sensitive and potentially hazardous. Overall, 5-Nitroindole-3-carboxylic acid is a versatile compound with significant implications in both research and industrial applications.
Formula:C9H6N2O4
InChI:InChI=1S/C9H6N2O4/c12-9(13)7-4-10-8-2-1-5(11(14)15)3-6(7)8/h1-4,10H,(H,12,13)
SMILES:c1cc2c(cc1N(=O)=O)c(c[nH]2)C(=O)O
Synonyms:
  • 5-Nitro-1H-indole-3-carboxylic acid
  • 2-Amino-4-(6-Nitro-1,3-Benzodioxol-5-Yl)-6-(3-Nitrophenyl)Pyridine-3-Carbonitrile
  • 1H-Indole-3-carboxylicacid, 5-nitro-
  • Indole-3-carboxylicacid, 5-nitro-
  • 5-Nitroindole-3-carboxylic acid
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