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CAS 137756-89-9

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4-(2-Hydroxyethyl)phenylboronicacid

Description:
4-(2-Hydroxyethyl)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also features a hydroxyethyl substituent. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols due to the presence of the hydroxyl group. It exhibits properties typical of boronic acids, including the ability to form reversible complexes with diols, which makes it useful in various applications, including organic synthesis and as a reagent in the development of sensors and drug delivery systems. The compound's boronic acid functionality allows it to participate in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, its hydroxyethyl group can enhance its solubility and reactivity in biological systems, potentially leading to applications in medicinal chemistry. Overall, 4-(2-Hydroxyethyl)phenylboronic acid is a versatile compound with significant utility in both synthetic and biological chemistry.
Formula:C8H11BO3
InChI:InChI=1/C8H11BO3/c10-6-5-7-1-3-8(4-2-7)9(11)12/h1-4,10-12H,5-6H2
SMILES:c1cc(ccc1CCO)B(O)O
Synonyms:
  • [4-(2-Hydroxyethyl)phenyl]boronic acid
  • boronic acid, B-[4-(2-hydroxyethyl)phenyl]-
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