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CAS 913835-51-5

:

[3-[(E)-3-ethoxy-3-oxo-prop-1-enyl]phenyl]boronic acid

Description:
[3-[(E)-3-ethoxy-3-oxo-prop-1-enyl]phenyl]boronic acid, with the CAS number 913835-51-5, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an ethoxy-substituted propenyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the ethoxy and keto groups contributes to its reactivity and solubility in organic solvents. Additionally, the compound may exhibit specific biological activities, potentially serving as a building block in drug development or as a tool in chemical biology. Its structural features suggest that it could participate in cross-coupling reactions, a common method in the formation of carbon-carbon bonds in organic synthesis. Overall, this compound represents a versatile structure with potential applications in both research and industry.
Formula:C11H13BO4
InChI:InChI=1/C11H13BO4/c1-2-16-11(13)7-6-9-4-3-5-10(8-9)12(14)15/h3-8,14-15H,2H2,1H3/b7-6+
Synonyms:
  • 3-((E)-3-ETHOXY-3-OXO-1-PROPEN-1-YL)BENZENEBORONIC ACID 98
  • 3-((E)-3-Ethoxy-3-oxo-1-propen-1-yl)benzeneboronic
  • 2-Propenoic acid, 3-(3-boronophenyl)-, 1-ethyl ester, (2E)- (9CI)
  • 3-((E)-3-ETHOXY-3-OXO-1-PROPEN-1-YL)BENZENEBORONIC ACID
  • (E)-(3-(3-Ethoxy-3-oxoprop-1-en-1-yl)phenyl)boronic acid
  • 3-(E-3-ETHOXY-3-OXO-1-PROPEN-1-YL)PHENYLBORONIC ACID
  • 3-((E)-3-Ethoxy-3-oxo-1-propen-1-yl)benzeneboronic acid 98%
  • ETHYL 3-BORONOCINNAMATE
  • 3-(trans-3-Ethoxy-3-oxo-1-propen-1-yl)benzeneboronic acid, 98%
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