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CAS 850568-49-9

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1-Ethyl (2E)-3-(4-boronophenyl)-2-propenoate

Description:
1-Ethyl (2E)-3-(4-boronophenyl)-2-propenoate, with the CAS number 850568-49-9, is an organic compound characterized by its unique structure that includes an ethyl group, a propenoate moiety, and a boron-containing phenyl group. This compound typically exhibits properties associated with both organic esters and boron-containing compounds, which may influence its reactivity and solubility. The presence of the boron atom can enhance its utility in various applications, particularly in organic synthesis and materials science, where boron compounds are often used as catalysts or in the formation of boron-containing polymers. Additionally, the propenoate structure suggests potential for polymerization reactions, making it a candidate for use in creating functionalized materials. Its reactivity may also be influenced by the electron-withdrawing nature of the boron group, which can affect the compound's stability and interaction with other chemical species. Overall, this compound's characteristics make it of interest in both academic research and industrial applications.
Formula:C11H13BO4
InChI:InChI=1S/C11H13BO4/c1-2-16-11(13)8-5-9-3-6-10(7-4-9)12(14)15/h3-8,14-15H,2H2,1H3/b8-5+
InChI key:InChIKey=OVNZUEJWYIMMSW-VMPITWQZSA-N
SMILES:C(=C/C(OCC)=O)\C1=CC=C(B(O)O)C=C1
Synonyms:
  • Ethyl (E)-3-(4-boronophenyl)-2-propenoate
  • 1-Ethyl (2E)-3-(4-boronophenyl)-2-propenoate
  • 2-Propenoic acid, 3-(4-boronophenyl)-, 1-ethyl ester, (2E)-
  • (E)-[4-(3-Ethoxy-3-oxoprop-1-en-1-yl)phenyl]boronic acid
  • [4-((E)-3-Ethoxy-3-oxo-1-propen-1-yl)phenyl]boronic acid
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