CAS 860626-80-8
:(4-fluoropyridin-3-yl)boronic acid
Description:
(4-Fluoropyridin-3-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has a fluorine substituent. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. The presence of the fluorine atom can influence the electronic properties of the pyridine ring, potentially enhancing its reactivity in various chemical reactions, including Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. The compound's unique structure and reactivity profile make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals.
Formula:C5H5BFNO2
InChI:InChI=1/C5H5BFNO2/c7-5-1-2-8-3-4(5)6(9)10/h1-3,9-10H
SMILES:c1cncc(c1F)B(O)O
Synonyms:- boronic acid, B-(4-fluoro-3-pyridinyl)-
- (4-Fluoropyridin-3-yl)boronic acid
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Found 2 products.
4-Fluoropyridine-3-boronic acid
CAS:<p>4-Fluoropyridine-3-boronic acid</p>Purity:≥95%Color and Shape:SolidMolecular weight:140.91g/mol

