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CAS 183158-33-0

:

B-(1,2-Dihydro-5-acenaphthylenyl)boronic acid

Description:
B-(1,2-Dihydro-5-acenaphthylenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a bicyclic hydrocarbon structure. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and materials science. The acenaphthylene moiety contributes to its unique electronic and steric properties, which can influence its reactivity and interactions in chemical reactions. Additionally, boronic acids are known for their role in Suzuki coupling reactions, a widely used method for forming carbon-carbon bonds in organic chemistry. The compound's solubility, stability, and reactivity can vary depending on the specific conditions and solvents used. Overall, B-(1,2-Dihydro-5-acenaphthylenyl)boronic acid is a valuable building block in synthetic organic chemistry, particularly in the development of complex molecular architectures.
Formula:C12H11BO2
InChI:InChI=1S/C12H11BO2/c14-13(15)11-7-6-9-5-4-8-2-1-3-10(11)12(8)9/h1-3,6-7,14-15H,4-5H2
InChI key:InChIKey=RBYUCFIZMNKDGX-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C2C3=C(C=C1)CCC3=CC=C2
Synonyms:
  • (1,2-Dihydroacenaphthylen-5-yl)boronic acid
  • (5-Acenaphthenyl)boronic acid
  • 1,2-Dihydroacenaphthylen-5-Ylboronic Acid
  • 5-Acenaphtheneboronic acid
  • Acenaphthelene-5-boronicacid
  • B-(1,2-Dihydro-5-acenaphthylenyl)boronic acid
  • Boronic acid, (1,2-dihydro-5-acenaphthylenyl)-
  • Boronic acid, B-(1,2-dihydro-5-acenaphthylenyl)-
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