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CAS 149105-19-1

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2-Carboxyphenylboronic acid

Description:
2-Carboxyphenylboronic acid is an organic compound characterized by the presence of both a carboxylic acid group and a boronic acid group attached to a phenyl ring. Its molecular structure features a phenyl ring with a carboxylic acid (-COOH) group and a boronic acid (-B(OH)2) group positioned at the ortho position relative to each other. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to its ability to form hydrogen bonds. 2-Carboxyphenylboronic acid is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron source. Additionally, it can form reversible complexes with diols, making it useful in various applications, including drug delivery and sensor technology. Its reactivity and functional groups allow for diverse applications in medicinal chemistry and materials science, highlighting its significance in both academic and industrial research.
Formula:C7H7BO4
InChI:InChI=1/C7H7BO4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4,11-12H,(H,9,10)
SMILES:c1ccc(c(c1)C(=O)O)B(O)O
Synonyms:
  • 2-Boronobenzoic acid
  • 2-Carboxybenzeneboronic acid
  • (2-Dihydroxyboronyl)Benzoic Acid
  • 2-(Dihydroxyboryl)Benzoic Acid
  • Rarechem Ah Pb 0146
  • O-Carboxyphenylboronic Acid
  • 2-CarboxyphenylboronicAcid
  • 2-(Dihydroxyboranyl)Benzoic Acid
  • 2-Carboxyphenylboronic acid ,98%
  • 2-CARBOXYPHENYLBORONIC ACID
  • 2-CarboxyphenylboronicAcid97+%
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