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CAS 423753-00-8

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(2E)-3-(2-bromo-4-ethoxy-5-methoxyphenyl)prop-2-enoic acid

Description:
(2E)-3-(2-bromo-4-ethoxy-5-methoxyphenyl)prop-2-enoic acid is an organic compound characterized by its unique structural features, including a prop-2-enoic acid backbone and a substituted phenyl group. The presence of a bromo substituent, along with ethoxy and methoxy groups on the aromatic ring, contributes to its chemical reactivity and potential biological activity. The double bond in the prop-2-enoic acid portion indicates that it can participate in various addition reactions, making it a versatile intermediate in organic synthesis. The compound's functional groups suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Its solubility and stability can be influenced by the substituents on the phenyl ring, which may also affect its interaction with biological targets. Overall, this compound exemplifies the complexity of organic molecules and their potential utility in various chemical and biological contexts.
Formula:C12H13BrO4
InChI:InChI=1/C12H13BrO4/c1-3-17-11-7-9(13)8(4-5-12(14)15)6-10(11)16-2/h4-7H,3H2,1-2H3,(H,14,15)/b5-4+
Synonyms:
  • (2E)-3-(2-Bromo-4-ethoxy-5-methoxyphenyl)acrylic acid
  • 2-propenoic acid, 3-(2-bromo-4-ethoxy-5-methoxyphenyl)-, (2E)-
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