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CAS 871329-71-4

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B-(5-Oxo-1-cyclopenten-1-yl)boronic acid

Description:
B-(5-Oxo-1-cyclopenten-1-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a cyclopentenone 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 cyclopentenone structure contributes to its reactivity, particularly in electrophilic addition reactions. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic synthesis. The compound may also exhibit unique solubility characteristics and stability profiles, influenced by the cyclopentenone ring and the boronic acid group. Its potential applications could extend to drug development, particularly in the design of inhibitors or other biologically active molecules. As with many boronic acids, care must be taken in handling due to their sensitivity to moisture and air, which can affect their stability and reactivity.
Formula:C5H7BO3
InChI:InChI=1/C5H7BO3/c7-5-3-1-2-4(5)6(8)9/h2,8-9H,1,3H2
InChI key:InChIKey=LEMUMNFZUFSWGV-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(=O)CCC1
Synonyms:
  • Boronic acid, (5-oxo-1-cyclopenten-1-yl)-
  • B-(5-Oxo-1-cyclopenten-1-yl)boronic acid
  • (5-Oxocyclopent-1-en-1-yl)boronic acid
  • Boronic acid, B-(5-oxo-1-cyclopenten-1-yl)-
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