CAS 957034-74-1
:(3-benzyloxy-4-fluoro-phenyl)boronic acid
Description:
(3-Benzyloxy-4-fluoro-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. This compound features a phenyl ring substituted with a benzyloxy group and a fluorine atom, which can influence its reactivity and solubility. The presence of the fluorine atom may enhance the compound's electronic properties, potentially affecting its interactions in biological systems or catalysis. The boronic acid moiety contributes to its acidity and reactivity, allowing it to participate in cross-coupling reactions, which are valuable in the synthesis of complex organic molecules. Additionally, the compound's structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the aromatic system and functional groups that can facilitate further modifications. Overall, (3-benzyloxy-4-fluoro-phenyl)boronic acid is a versatile compound with significant implications in organic synthesis and drug development.
Formula:C13H12BFO3
InChI:InChI=1/C13H12BFO3/c15-12-7-6-11(14(16)17)8-13(12)18-9-10-4-2-1-3-5-10/h1-8,16-17H,9H2
SMILES:c1ccc(cc1)COc1cc(ccc1F)B(O)O
Synonyms:- [3-(Benzyloxy)-4-fluorophenyl]boronic acid
- boronic acid, B-[4-fluoro-3-(phenylmethoxy)phenyl]-
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Found 3 products.
3-Benzyloxy-4-Fluorophenylboronic Acid
CAS:Formula:C13H12BFO3Purity:97%Color and Shape:SolidMolecular weight:246.04203-(Benzyloxy)-4-fluorobenzeneboronic acid
CAS:<p>3-(Benzyloxy)-4-fluorobenzeneboronic acid</p>Formula:C13H12BFO3Purity:98%Color and Shape: white solidMolecular weight:246.04g/mol3-Benzyloxy-4-fluorophenylboronic acid
CAS:Formula:C13H12BFO3Purity:97%Color and Shape:SolidMolecular weight:246.04


