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CAS 170981-26-7

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2-Fluoro-4-methylphenylboronic acid

Description:
2-Fluoro-4-methylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both a fluorine atom and a methyl group. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. Its molecular structure features a boron atom bonded to a hydroxyl group and an aryl group, which enhances its reactivity in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the fluorine atom can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with biological targets. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in drug delivery and sensor applications. Overall, 2-Fluoro-4-methylphenylboronic acid is a versatile compound with significant utility in synthetic organic chemistry.
Formula:C7H8BFO2
InChI:InChI=1/C7H8BFO2/c1-5-2-3-6(8(10)11)7(9)4-5/h2-4,10-11H,1H3
SMILES:Cc1ccc(c(c1)F)B(O)O
Synonyms:
  • 2-Fluoro-4-Methylbenzeneboronic Acid
  • Boronic acid, (2-fluoro-4-methylphenyl)- (9CI)
  • 2-Fluoro-4-Methylphenylboronic
  • 2-Fluoro-4-methylphenylboronic acid ,97%
  • (2-Fluoro-4-Methylphenyl)Boronic Acid
  • 2-Fluoro-4-methylphenylboronic Acid (contains varying amounts of Anhydride)
  • 2-FLUORO-4-METHYLPHENYLBORONIC ACID
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