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CAS 372193-68-5

:

{2-[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]phenyl}boronic acid

Description:
{2-[(1E)-3-methoxy-3-oxoprop-1-en-1-yl]phenyl}boronic acid, with the CAS number 372193-68-5, is an organic compound that features a boronic acid functional group, which is characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. This compound contains a phenyl ring substituted with a propenyl group that has a methoxy and a ketone functional group, contributing to its reactivity and potential applications in organic synthesis and medicinal chemistry. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in various chemical reactions, including Suzuki coupling reactions, which are widely used in the formation of carbon-carbon bonds. The presence of the methoxy group may enhance the compound's solubility and influence its electronic properties. Overall, this compound's unique structure and functional groups suggest potential utility in drug development and materials science, particularly in the design of biologically active molecules or as intermediates in synthetic pathways.
Formula:C10H11BO4
InChI:InChI=1/C10H11BO4/c1-15-10(12)7-6-8-4-2-3-5-9(8)11(13)14/h2-7,13-14H,1H3/b7-6+
Synonyms:
  • 2-propenoic acid, 3-(2-boronophenyl)-, methyl ester, (2E)-
  • {2-[(1E)-3-Methoxy-3-oxoprop-1-en-1-yl]phenyl}boronic acid
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