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CAS 52661-56-0

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trans-3-(5-Nitro-2-furyl)acrolein

Description:
Trans-3-(5-Nitro-2-furyl)acrolein is an organic compound characterized by its unique structure, which includes a furan ring substituted with a nitro group and an acrolein moiety. This compound typically appears as a yellow to brown liquid and is known for its reactivity due to the presence of both the α,β-unsaturated aldehyde and the nitro group. The furan ring contributes to its aromatic properties, while the nitro group can enhance its electrophilic character, making it a potential candidate for various chemical reactions, including nucleophilic additions. Trans-3-(5-Nitro-2-furyl)acrolein may exhibit biological activity, which has drawn interest in medicinal chemistry and agrochemical research. Its synthesis often involves the reaction of appropriate precursors under controlled conditions to ensure the desired trans configuration is achieved. As with many organic compounds, safety precautions should be taken when handling this substance, as it may pose health risks or environmental hazards.
Formula:C7H5NO4
InChI:InChI=1S/C7H5NO4/c9-5-1-2-6-3-4-7(12-6)8(10)11/h1-5H/b2-1+
InChI key:InChIKey=DXWCZMGIIFEEPU-OWOJBTEDSA-N
SMILES:N(=O)(=O)C=1OC(/C=C/C=O)=CC1
Synonyms:
  • (2E)-3-(5-Nitro-2-furanyl)-2-propenal
  • (E)-3-(5-Nitro-2-furyl)acrolein
  • 2-Propenal, 3-(5-nitro-2-furanyl)-, (E)-
  • trans-3-(5-Nitro-2-furyl)acrolein
  • (E)-3-(5-Nitro-2-furyl)acrylaldehyde
  • 2-Propenal, 3-(5-nitro-2-furanyl)-, (2E)-
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