CAS 488713-34-4
:Boronic acid, [5-fluoro-2-(methoxymethoxy)phenyl]-
Description:
Boronic acid, specifically 5-fluoro-2-(methoxymethoxy)phenyl boronic acid, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is substituted with a fluorine atom and a methoxymethoxy group. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid group, which can engage in hydrogen bonding. The fluorine substitution can influence the electronic properties of the molecule, potentially enhancing its reactivity in various chemical reactions, including Suzuki coupling reactions, which are significant in organic synthesis. The methoxymethoxy group may also provide additional steric and electronic effects, impacting the compound's behavior in chemical reactions. Overall, boronic acids are known for their utility in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and polymers.
Formula:C8H10BFO4
Synonyms:- (5-Fluoro-2-(methoxymethoxy)phenyl)boronicacid
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Found 4 products.
5-Fluoro-2-(methoxymethoxy)phenylboronic acid
CAS:Formula:C8H10BFO4Purity:97%Color and Shape:SolidMolecular weight:199.97205-Fluoro-2-(methoxymethoxy)phenylboronic acid
CAS:5-Fluoro-2-(methoxymethoxy)phenylboronic acidPurity:≥95%Molecular weight:199.97g/mol(5-FLUORO-2-(METHOXYMETHOXY)PHENYL)BORONIC ACID PINACOL ESTER
CAS:Formula:C14H20BFO4Purity:95+%Molecular weight:282.12(5-Fluoro-2-(methoxymethoxy)phenyl)boronic acid
CAS:Formula:C8H10BFO4Purity:97%Molecular weight:199.97


