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CAS 182344-25-8

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4-Fluoronaphthalene-1-boronic acid

Description:
4-Fluoronaphthalene-1-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a fluorinated naphthalene ring. 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 boronic acid group imparts unique reactivity, allowing it to participate in Suzuki coupling reactions, which are valuable in organic synthesis for forming carbon-carbon bonds. The fluorine atom enhances the compound's electronic properties, potentially influencing its reactivity and interactions with other molecules. Additionally, 4-fluoronaphthalene-1-boronic acid may exhibit interesting photophysical properties, making it useful in various applications, including materials science and medicinal chemistry. Safety data should be consulted, as boronic acids can be sensitive to moisture and may require careful handling. Overall, this compound serves as a versatile building block in synthetic organic chemistry.
Formula:C10H8BFO2
InChI:InChI=1/C10H8BFO2/c12-10-6-5-9(11(13)14)7-3-1-2-4-8(7)10/h1-6,13-14H
InChI key:InChIKey=IDCGAEJGZLYEAZ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C2=C(C(F)=CC1)C=CC=C2
Synonyms:
  • (4-Fluoro-1-Naphthyl)Boronicacid
  • (4-Fluoro-1-naphthyl)boronic acid
  • (4-Fluoronaphthalen-1-Yl)Boronic Acid
  • 4-Fluoro-1-Naphthaleneboronic Acid
  • 4-Fluoronaphtalene-1-Boronic Acid
  • 4-Fluoronaphthalene-1-boronic acid ,98%
  • Akos Brn-0210
  • B-(4-Fluoro-1-naphthalenyl)boronic acid
  • Boronic acid, (4-fluoro-1-naphthalenyl)-
  • Boronic acid, B-(4-fluoro-1-naphthalenyl)-
  • 4-FLUORONAPHTHALENE-1-BORONIC ACID
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