CAS 1072952-23-8
:2-Borono-3-furancarboxylic acid
Description:
2-Borono-3-furancarboxylic acid is an organic compound characterized by the presence of a boron atom, a furan ring, and a carboxylic acid functional group. The furan ring contributes to its aromatic properties, while the boron atom enhances its reactivity, particularly in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. This compound typically exhibits moderate solubility in polar solvents due to the presence of the carboxylic acid group, which can also participate in hydrogen bonding. The boronic acid functionality allows for the formation of stable complexes with diols, which is useful in various applications, including drug development and materials science. Additionally, 2-Borono-3-furancarboxylic acid can serve as a building block in the synthesis of more complex molecules, particularly in the context of Suzuki-Miyaura coupling reactions. Its unique structural features and reactivity profile make it an important compound in the field of organic chemistry.
Formula:C5H5BO5
InChI:InChI=1S/C5H5BO5/c7-5(8)3-1-2-11-4(3)6(9)10/h1-2,9-10H,(H,7,8)
InChI key:InChIKey=ZFZHQLXZHYPTLQ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C(O)=O)C=CO1
Synonyms:- 3-Furancarboxylic acid, 2-borono-
- 2-(Dihydroxyboranyl)furan-3-carboxylic acid
- 2-Boronofuran-3-carboxylic acid
- 3-Carboxyfuran-2-boronic acid
- 2-Borono-3-furancarboxylic acid
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