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CAS 20767-04-8

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(2E)-3-(3,5-Dimethoxyphenyl)-2-propenoic acid

Description:
(2E)-3-(3,5-Dimethoxyphenyl)-2-propenoic acid, also known as a derivative of cinnamic acid, is an organic compound characterized by its conjugated double bond system and the presence of a phenyl ring substituted with two methoxy groups. This structure contributes to its potential biological activity and reactivity. The compound typically appears as a solid or crystalline substance and is soluble in organic solvents, while its solubility in water is limited due to its hydrophobic nature. The methoxy groups enhance the lipophilicity of the molecule, which may influence its interaction with biological systems. As a member of the phenylpropanoid family, it may exhibit antioxidant properties and has been studied for its potential therapeutic applications. The compound's reactivity can be attributed to the presence of the double bond, making it susceptible to various chemical reactions, including electrophilic addition and polymerization. Overall, (2E)-3-(3,5-Dimethoxyphenyl)-2-propenoic acid is of interest in both synthetic organic chemistry and medicinal chemistry due to its unique structural features and potential applications.
Formula:C11H12O4
InChI:InChI=1S/C11H12O4/c1-14-9-5-8(3-4-11(12)13)6-10(7-9)15-2/h3-7H,1-2H3,(H,12,13)/b4-3+
InChI key:InChIKey=VLSRUFWCGBMYDJ-ONEGZZNKSA-N
SMILES:C(=C/C(O)=O)\C1=CC(OC)=CC(OC)=C1
Synonyms:
  • Cinnamic acid, 3,5-dimethoxy-, (E)-
  • (2E)-3-(3,5-Dimethoxyphenyl)-2-propenoic acid
  • 3,5-Dimethoxy-trans-cinnamic acid
  • 2-Propenoic acid, 3-(3,5-dimethoxyphenyl)-, (E)-
  • 2-Propenoic acid, 3-(3,5-dimethoxyphenyl)-, (2E)-
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