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CAS 16189-10-9

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(2E)-3-[2-(Acetyloxy)phenyl]-2-propenoic acid

Description:
(2E)-3-[2-(Acetyloxy)phenyl]-2-propenoic acid, commonly known as a derivative of cinnamic acid, is an organic compound characterized by its conjugated double bond system, which contributes to its reactivity and potential biological activity. This compound features an acetyloxy group attached to a phenyl ring, enhancing its lipophilicity and possibly influencing its interaction with biological systems. The presence of the propenoic acid moiety suggests that it may exhibit properties typical of unsaturated carboxylic acids, such as acidity and the ability to participate in various chemical reactions, including esterification and polymerization. Its structural configuration, particularly the E-configuration of the double bond, is significant for its stereochemical properties, which can affect its biological activity and interactions. This compound may be of interest in pharmaceutical and biochemical research due to its potential applications in drug development and as a biochemical probe. As with many organic compounds, its stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature.
Formula:C11H10O4
InChI:InChI=1S/C11H10O4/c1-8(12)15-10-5-3-2-4-9(10)6-7-11(13)14/h2-7H,1H3,(H,13,14)/b7-6+
InChI key:InChIKey=UXOWQQCLBQBRMQ-VOTSOKGWSA-N
SMILES:O(C(C)=O)C1=C(/C=C/C(O)=O)C=CC=C1
Synonyms:
  • (2E)-3-[2-(Acetyloxy)phenyl]-2-propenoic acid
  • (2E)-3-[2-(acetyloxy)phenyl]prop-2-enoic acid
  • (Z)-3-(2-acetoxyphenyl)prop-2-enoic acid
  • 2-Acetylcoumaric Acid
  • 2-Propenoic acid, 3-[2-(acetyloxy)phenyl]-, (2E)-
  • 2-Propenoic acid, 3-[2-(acetyloxy)phenyl]-, (E)-
  • Cinnamic acid, o-hydroxy-, acetate, (E)-
  • O-Acetylcoumaric Acid
  • trans-2-Acetoxycinnamic acid
  • 2-Acetoxycinnamic acid
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