CAS 1451393-25-1
:5-Borono-6-fluoro-3-pyridinecarboxylic acid
Description:
5-Borono-6-fluoro-3-pyridinecarboxylic acid is an organic compound characterized by the presence of a boronic acid functional group and a fluorine atom attached to a pyridine ring. This compound features a pyridine backbone, which is a six-membered aromatic ring containing one nitrogen atom. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and organic synthesis. The fluorine substituent can influence the compound's reactivity and biological activity, often enhancing lipophilicity and metabolic stability. Additionally, the carboxylic acid group contributes to the compound's acidity and solubility in polar solvents. Overall, 5-Borono-6-fluoro-3-pyridinecarboxylic acid is significant in the development of pharmaceuticals and agrochemicals, particularly in the context of drug design and synthesis strategies that involve Suzuki coupling reactions. Its unique structural features make it a valuable building block in organic synthesis and medicinal chemistry.
Formula:C6H5BFNO4
InChI:InChI=1S/C6H5BFNO4/c8-5-4(7(12)13)1-3(2-9-5)6(10)11/h1-2,12-13H,(H,10,11)
InChI key:InChIKey=BCLGBTWNYVSWCI-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(C(O)=O)C=NC1F
Synonyms:- 5-Borono-6-fluoro-3-pyridinecarboxylic acid
- 3-Pyridinecarboxylic acid, 5-borono-6-fluoro-
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