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CAS 1072952-04-5

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B-(3-Ethoxy-5-formylphenyl)boronic acid

Description:
B-(3-Ethoxy-5-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and other nucleophiles. This compound features a phenyl ring substituted with both an ethoxy group and a formyl group, contributing to its reactivity and potential applications in organic synthesis and medicinal chemistry. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, the presence of the formyl group suggests potential reactivity in further transformations, such as condensation reactions. The ethoxy substituent enhances the solubility of the compound in organic solvents, facilitating its use in various chemical reactions. Overall, B-(3-Ethoxy-5-formylphenyl)boronic acid is a versatile building block in synthetic organic chemistry, particularly in the development of complex molecular architectures.
Formula:C9H11BO4
InChI:InChI=1S/C9H11BO4/c1-2-14-9-4-7(6-11)3-8(5-9)10(12)13/h3-6,12-13H,2H2,1H3
InChI key:InChIKey=UGWAEFBQEMQRJD-UHFFFAOYSA-N
SMILES:O(CC)C1=CC(B(O)O)=CC(C=O)=C1
Synonyms:
  • Boronic acid, B-(3-ethoxy-5-formylphenyl)-
  • B-(3-Ethoxy-5-formylphenyl)boronic acid
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