
CAS 1187591-17-8
:2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
Description:
2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is an organoboron compound characterized by the presence of a boron-containing dioxaborolane moiety and a benzoic acid functional group. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents, which is common for many organoboron compounds. The dioxaborolane structure contributes to its reactivity, particularly in cross-coupling reactions, making it valuable in organic synthesis and materials science. The presence of the carboxylic acid group enhances its potential for hydrogen bonding and solubility in polar solvents. Additionally, this compound may exhibit unique optical properties due to its aromatic system, which can be exploited in various applications, including fluorescence and sensor technology. Its stability and reactivity can be influenced by environmental factors such as temperature and pH. Overall, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is a versatile compound with significant implications in synthetic chemistry and material development.
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Found 4 products.
2-Carboxyphenylboronic acid, pinacol ester
CAS:Formula:C13H17BO4Purity:95%Color and Shape:SolidMolecular weight:248.08272-Carboxyphenylboronic acid, pinacol ester
CAS:2-Carboxyphenylboronic acid, pinacol esterFormula:C13H17BO4Purity:97%Color and Shape: white powderMolecular weight:248.08g/mol2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
CAS:Formula:C13H17BO4Purity:95%Color and Shape:SolidMolecular weight:248.092-Carboxyphenylboronic Acid Pinacol Ester
CAS:Controlled Product<p>Applications 2-Carboxyphenylboronic Acid Pinacol Ester is a reagent used for the synthesis of Biaryl amides as M1 muscarinic acetylcholine receptor agonists.<br>References Budzik, B., et al.: Bioorg. Med. Chem. Lett., 20, 3540-3544 (2010);<br></p>Formula:C13H17BO4Color and Shape:NeatMolecular weight:248.08



