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CAS 1193104-83-4

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[9,9-Bis(4-methylphenyl)-9H-fluoren-2-yl]boronic acid

Description:
[9,9-Bis(4-methylphenyl)-9H-fluoren-2-yl]boronic acid is an organoboron compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and materials science. This compound features a fluorenyl backbone substituted with two 4-methylphenyl groups, enhancing its stability and solubility in organic solvents. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic chemistry. Additionally, the compound may exhibit interesting photophysical properties due to its aromatic structure, which can be leveraged in optoelectronic applications. Its molecular structure contributes to its potential utility in drug discovery and development, particularly in the design of boron-containing pharmaceuticals. Overall, [9,9-Bis(4-methylphenyl)-9H-fluoren-2-yl]boronic acid is a versatile compound with significant implications in both synthetic and applied chemistry.
Formula:C27H23BO2
InChI:InChI=1S/C27H23BO2/c1-18-7-11-20(12-8-18)27(21-13-9-19(2)10-14-21)25-6-4-3-5-23(25)24-16-15-22(28(29)30)17-26(24)27/h3-17,29-30H,1-2H3
SMILES:Cc1ccc(cc1)C1(c2ccc(C)cc2)c2ccccc2c2ccc(cc12)B(O)O
Synonyms:
  • B-[9,9-Bis(4-methylphenyl)-9H-fluoren-2-yl]boron
  • 2-BATolF
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