CAS 1451393-51-3
:5-Borono-2-fluoro-3-pyridinecarboxylic acid
Description:
5-Borono-2-fluoro-3-pyridinecarboxylic acid is a chemical compound characterized by its boron and fluorine substituents on a pyridine ring, which is a six-membered aromatic heterocycle containing nitrogen. This compound features a carboxylic acid functional group, contributing to its acidity and potential reactivity in various chemical reactions. The presence of the boron atom allows for potential applications in cross-coupling reactions, particularly in the synthesis of complex organic molecules, making it valuable in medicinal chemistry and materials science. The fluorine atom enhances the compound's lipophilicity and can influence its biological activity. Additionally, the pyridine ring provides a platform for further functionalization, enabling the development of derivatives with tailored properties. Overall, 5-Borono-2-fluoro-3-pyridinecarboxylic acid is a versatile building block in organic synthesis, with implications in drug discovery and the development of agrochemicals. Its unique structural features make it a subject of interest in both academic research and industrial applications.
Formula:C6H5BFNO4
InChI:InChI=1S/C6H5BFNO4/c8-5-4(6(10)11)1-3(2-9-5)7(12)13/h1-2,12-13H,(H,10,11)
InChI key:InChIKey=NINXDEFTKZXEEA-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C=C(B(O)O)C=NC1F
Synonyms:- 3-Pyridinecarboxylic acid, 5-borono-2-fluoro-
- 5-Borono-2-fluoro-3-pyridinecarboxylic acid
- 2-Fluoro-3-carboxypyridine-5-boronic acid
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