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CAS 35504-85-9

:

(2E)-4-(4-Fluorophenyl)-4-oxo-2-butenoic acid

Description:
(2E)-4-(4-Fluorophenyl)-4-oxo-2-butenoic acid, with the CAS number 35504-85-9, is an organic compound characterized by its unique structural features. It contains a butenoic acid backbone with a fluorophenyl substituent, which contributes to its chemical reactivity and potential biological activity. The presence of the fluorine atom enhances the lipophilicity and may influence the compound's interaction with biological targets. This compound typically exhibits properties such as being a solid at room temperature, with moderate solubility in organic solvents and limited solubility in water, which is common for many aromatic compounds. Its functional groups, including the keto and carboxylic acid groups, suggest potential for various chemical reactions, including esterification and condensation. The compound may also exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Overall, its unique structure and functional groups provide a basis for further exploration in both synthetic and applied chemistry contexts.
Formula:C10H7FO3
InChI:InChI=1S/C10H7FO3/c11-8-3-1-7(2-4-8)9(12)5-6-10(13)14/h1-6H,(H,13,14)/b6-5+
InChI key:InChIKey=CMSWGWOQRTZZAS-AATRIKPKSA-N
SMILES:C(/C=C/C(O)=O)(=O)C1=CC=C(F)C=C1
Synonyms:
  • (2E)-4-(4-Fluorophenyl)-4-oxo-2-butenoic acid
  • (E)-3-(p-Fluorobenzoyl)acrylic acid
  • 2-Butenoic acid, 4-(4-fluorophenyl)-4-oxo-, (2E)-
  • 2-Butenoic acid, 4-(4-fluorophenyl)-4-oxo-, (E)-
  • 4-(4-Fluoro-phenyl)-4-oxo-but-2-enoic acid
  • trans-3-(4-Fluorobenzoyl)acrylic acid
  • trans-β-(p-Fluorobenzoyl)acrylic acid
  • (2E)-4-(4-Fluorophenyl)-4-oxobut-2-enoic acid
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