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CAS 16732-57-3

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Ethyl 5-nitroindole-2-carboxylate

Description:
Ethyl 5-nitroindole-2-carboxylate is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a nitro group (-NO2) at the 5-position and an ethyl ester functional group at the 2-position of the indole ring, contributing to its reactivity and solubility properties. Ethyl 5-nitroindole-2-carboxylate is typically a yellow to orange solid, and it is known for its potential applications in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the nitro group can enhance the compound's electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, the ethyl ester moiety can be hydrolyzed to yield the corresponding carboxylic acid, expanding its utility in synthetic pathways. As with many nitro compounds, it is important to handle this substance with care due to potential toxicity and environmental considerations.
Formula:C11H10N2O4
InChI:InChI=1/C11H10N2O4/c1-2-17-11(14)10-6-7-5-8(13(15)16)3-4-9(7)12-10/h3-6,12H,2H2,1H3
InChI key:DVFJMQCNICEPAI-UHFFFAOYSA-N
SMILES:CCOC(=O)c1cc2cc(ccc2[nH]1)N(=O)=O
Synonyms:
  • 5-Nitroindole-2-Carboxylic Acid Ethyl Ester
  • Labotest-Bb Lt00441291
  • Ethyl 5-Nitro-1H-Indole-2-Carboxylate
  • Ethyl 5-Nitro-2-Carboxylate
  • Oxalic Acid Mono-(N-Methyl)-Amide
  • Ethyl 5-Nitro Indole-2-Carbonate
  • 5-Nitroindole-2-Carboxylic
  • ethyl 5-amino-1H-indole-2-carboxylate
  • (Methylamino)(Oxo)Acetic Acid
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