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CAS 175276-71-8

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Ethyl 2-methyl-5-(3-nitrophenyl)-3-furancarboxylate

Description:
Ethyl 2-methyl-5-(3-nitrophenyl)-3-furancarboxylate is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features an ethyl ester functional group, a methyl group, and a nitrophenyl substituent, contributing to its unique chemical properties. The presence of the nitro group typically enhances the compound's reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. The furan moiety can participate in various chemical transformations, including oxidation and polymerization. Ethyl 2-methyl-5-(3-nitrophenyl)-3-furancarboxylate may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its solubility and stability in different solvents can vary, influencing its applications in synthesis and research. As with many organic compounds, safety precautions should be taken when handling this substance, as it may pose health risks or environmental hazards.
Formula:C14H13NO5
InChI:InChI=1S/C14H13NO5/c1-3-19-14(16)12-8-13(20-9(12)2)10-5-4-6-11(7-10)15(17)18/h4-8H,3H2,1-2H3
InChI key:InChIKey=JAHZJSHMYFDWKD-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C=C(OC1C)C2=CC(N(=O)=O)=CC=C2
Synonyms:
  • 3-Furancarboxylic acid, 2-methyl-5-(3-nitrophenyl)-, ethyl ester
  • Ethyl 2-Methyl-5-(3-Nitrophenyl)Furan-3-Carboxylate
  • Ethyl 2-methyl-5-(3-nitrophenyl)-3-furancarboxylate
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