CAS 194470-10-5
:9-FLUORENONE-1-BORONIC ACID
Description:
9-Fluorenone-1-boronic acid is an organic compound characterized by the presence of a fluorenone moiety and a boronic acid functional group. It typically appears as a solid at room temperature and is soluble in polar organic solvents. The compound features a boron atom bonded to a hydroxyl group and an aryl group, which contributes to its reactivity, particularly in forming covalent bonds with diols and other nucleophiles. This property makes it valuable in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. The presence of the fluorenone structure imparts unique photophysical properties, making it useful in various applications, including fluorescence studies and as a building block in materials science. Additionally, 9-fluorenone-1-boronic acid can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for constructing carbon-carbon bonds in organic synthesis. Overall, its distinctive structural features and reactivity profile make it a significant compound in both academic research and industrial applications.
Formula:C13H9BO3
InChI:InChI=1/C13H9BO3/c15-13-10-5-2-1-4-8(10)9-6-3-7-11(12(9)13)14(16)17/h1-7,16-17H
SMILES:c1ccc2c(c1)c1cccc(c1C2=O)B(O)O
Synonyms:- Akos Brn-0099
- (9-oxo-9H-fluoren-1-yl)boronic acid
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Found 3 products.
9-Fluorenone-1-boronic acid
CAS:Formula:C13H9BO3Purity:97%Color and Shape:SolidMolecular weight:224.01989-Fluorenone-1-boronic acid
CAS:<p>9-Fluorenone-1-boronic acid</p>Purity:98%Molecular weight:224.02g/mol



