CAS 171364-81-1
:4-ACETYLPHENYLBORONIC ACID, PINACOL ESTER
Description:
4-Acetylphenylboronic acid, pinacol ester, is an organoboron compound characterized by the presence of a boronic acid functional group and an acetyl group attached to a phenyl ring. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as dichloromethane and ethanol. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The pinacol ester formation enhances its stability and solubility compared to the free boronic acid. This compound can participate in cross-coupling reactions, particularly in the synthesis of complex organic molecules. Additionally, it may exhibit properties that are beneficial in the development of sensors or in drug delivery systems due to its boron content. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential reactivity and toxicity.
Formula:C14H19BO3
InChI:InChI=1/C14H19BO3/c1-10(16)11-6-8-12(9-7-11)15-17-13(2,3)14(4,5)18-15/h6-9H,1-5H3
SMILES:CC(=O)c1ccc(cc1)B1OC(C)(C)C(C)(C)O1
Synonyms:- 1-[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]Ethanone
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Found 3 products.
4-ACETYLPHENYLBORONIC ACID, PINACOL ESTER
CAS:Formula:C14H19BO3Purity:97%Color and Shape:SolidMolecular weight:246.10994-Acetylphenylboronic acid, pinacol ester
CAS:<p>4-Acetylphenylboronic acid, pinacol ester</p>Formula:C14H19BO3Purity:95%Color and Shape: off-white to faint yellow crystalline solidMolecular weight:246.11g/mol1-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethanone
CAS:Formula:C14H19BO3Purity:95%Color and Shape:SolidMolecular weight:246.11


