
CAS 1061223-45-7
:4-Fluoro-2-hydroxyMethyl)phenylboronic acid
Description:
4-Fluoro-2-hydroxymethylphenylboronic 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. This compound features a fluorine atom and a hydroxymethyl group attached to a phenyl ring, contributing to its unique reactivity and potential applications in medicinal chemistry and materials science. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the fluorine substituent can enhance the compound's lipophilicity and influence its biological activity. The hydroxymethyl group may also provide sites for further functionalization or interaction with biological targets. Overall, 4-Fluoro-2-hydroxymethylphenylboronic acid is a versatile compound with significant implications in drug development and organic synthesis, particularly in the context of creating new therapeutic agents or materials with tailored properties.
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Found 6 products.
(4-Fluoro-2-(hydroxymethyl)phenyl)boronic acid
CAS:Formula:C7H8BFO3Purity:98%Color and Shape:SolidMolecular weight:169.94604-Fluoro-2-(hydroxymethyl)phenylboronic acid
CAS:<p>4-Fluoro-2-(hydroxymethyl)phenylboronic acid</p>Purity:95%Color and Shape:SolidMolecular weight:169.95g/mol(4-Fluoro-2-(hydroxymethyl)phenyl)boronic acid
CAS:Formula:C7H8BFO3Purity:98%Color and Shape:SolidMolecular weight:169.954-Fluoro-2-(hydroxymethyl)phenylboronic Acid
CAS:Controlled Product<p>Applications 4-Fluoro-2-(hydroxymethyl)phenylboronic Acid is a compound used in the preparation of 4,5-dihydro-1H-pyrazole derivatives as cholesterol 24 hydroxylase inhibitors.<br>References Kaku, T., et al.: Preparation of 4,5-dihydro-1H-pyrazole derivatives as cholesterol 24 hydroxylase inhibitors, WO 2010110400 (2010);<br></p>Formula:C7H8BFO3Color and Shape:NeatMolecular weight:169.95





