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CAS 131838-19-2

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B-(5-Bromo-1-naphthalenyl)boronic acid

Description:
B-(5-Bromo-1-naphthalenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a brominated naphthalene moiety. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar organic solvents such as methanol and ethanol, while being less soluble in non-polar solvents. The presence of the bromine atom enhances its reactivity, making it useful in various organic synthesis applications, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds. The boronic acid functionality allows for the formation of stable complexes with diols, making it valuable in the development of sensors and in medicinal chemistry for drug design. Additionally, this compound may exhibit interesting electronic properties due to the conjugated naphthalene system, which can influence its behavior in photonic applications. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential toxicity and reactivity.
Formula:C10H8BBrO2
InChI:InChI=1S/C10H8BBrO2/c12-10-6-2-3-7-8(10)4-1-5-9(7)11(13)14/h1-6,13-14H
InChI key:InChIKey=FLHLQGCANXDHSN-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C2=C(C(Br)=CC=C2)C=CC1
Synonyms:
  • Boronic acid, B-(5-bromo-1-naphthalenyl)-
  • (5-Bromonaphthalen-1-yl)boronic acid
  • B-(5-Bromo-1-naphthalenyl)boronic acid
  • Boronic acid, (5-bromo-1-naphthalenyl)-
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