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CAS 16642-92-5

:

(2E)-3-[4-(Trifluoromethyl)phenyl]-2-propenoic acid

Description:
(2E)-3-[4-(Trifluoromethyl)phenyl]-2-propenoic acid, commonly referred to as a trifluoromethyl-substituted cinnamic acid derivative, exhibits several notable characteristics. This compound features a propenoic acid backbone with a trifluoromethyl group attached to a phenyl ring, which significantly influences its chemical properties. The presence of the trifluoromethyl group enhances lipophilicity and can affect the compound's reactivity and biological activity. Typically, such compounds are characterized by their ability to participate in various chemical reactions, including electrophilic aromatic substitution and Michael addition. The double bond in the propenoic acid structure contributes to its reactivity, making it a potential candidate for polymerization or as an intermediate in organic synthesis. Additionally, the compound may exhibit interesting biological properties, which can be explored for applications in pharmaceuticals or agrochemicals. Its stability, solubility, and interaction with biological systems are influenced by the unique electronic effects of the trifluoromethyl group, making it a subject of interest in both synthetic and medicinal chemistry.
Formula:C10H7F3O2
InChI:InChI=1S/C10H7F3O2/c11-10(12,13)8-4-1-7(2-5-8)3-6-9(14)15/h1-6H,(H,14,15)/b6-3+
InChI key:InChIKey=ANRMAUMHJREENI-ZZXKWVIFSA-N
SMILES:C(F)(F)(F)C1=CC=C(/C=C/C(O)=O)C=C1
Synonyms:
  • (2E)-3-[4-(Trifluoromethyl)phenyl]-2-propenoic acid
  • (2E)-3-[4-(trifluoromethyl)phenyl]prop-2-enoate
  • (2E)-3-[4-(trifluoromethyl)phenyl]prop-2-enoic acid
  • (E)-3-(4-(Trifluoromethyl)phenyl)acrylic acid
  • (E)-3-(4-Trifluoromethylphenyl)-2-propenoic acid
  • (E)-3-(4-Trifluoromethylphenyl)acrylic acid
  • (E)-4-Trifluoromethylcinnamic acid
  • (E)-p-(Trifluoromethyl)cinnamic acid
  • 2-Propenoic acid, 3-[4-(trifluoromethyl)phenyl]-, (2E)-
  • 2-Propenoic acid, 3-[4-(trifluoromethyl)phenyl]-, (E)-
  • See more synonyms
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