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CAS 116378-40-6

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(3-Amino-5-carboxylphenyl)boronic acid

Description:
(3-Amino-5-carboxylphenyl)boronic acid, with the CAS number 116378-40-6, is an organic compound that features a boronic acid functional group attached to a phenyl ring substituted with both an amino group and a carboxylic acid group. This compound is characterized by its ability to form reversible covalent bonds with diols, making it useful in various applications, including drug development and materials science. The presence of the amino and carboxyl groups contributes to its solubility in polar solvents and enhances its reactivity. Additionally, the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, which are pivotal in organic synthesis. The compound's structure enables it to act as a potential ligand in coordination chemistry and as a building block in the synthesis of more complex molecules. Overall, (3-Amino-5-carboxylphenyl)boronic acid is a versatile compound with significant implications in both research and industrial applications.
Formula:C7H8BNO4
InChI:InChI=1/C7H8BNO4/c9-6-2-4(7(10)11)1-5(3-6)8(12)13/h1-3,12-13H,9H2,(H,10,11)
SMILES:c1c(cc(cc1B(O)O)N)C(=O)O
Synonyms:
  • 3-Amino-5-(Dihydroxyboranyl)Benzoic Acid
  • 3-Amino-5-Carboxyphenylboronic Acid
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