CAS 198211-79-9
:Boronic acid, (2-methoxy-4-methylphenyl)-
Description:
Boronic acid, specifically (2-methoxy-4-methylphenyl)-, is an organic compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a substituted aromatic ring. This compound features a methoxy group (-OCH3) and a methyl group (-CH3) on the aromatic ring, which contribute to its unique chemical properties. The presence of the boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The methoxy and methyl substituents can influence the compound's reactivity, solubility, and overall stability. Typically, boronic acids exhibit moderate solubility in polar solvents and can form stable complexes with diols, which is a key aspect of their utility in biological applications. Additionally, the compound's structure may allow for specific interactions with biological targets, enhancing its potential in drug development. Overall, (2-methoxy-4-methylphenyl)boronic acid is a versatile compound with significant applications in synthetic and medicinal chemistry.
Formula:C8H11BO3
Synonyms:- 2-Methoxy-4-methylphenylboronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
Boronic acid, B-(2-methoxy-4-methylphenyl)-
CAS:Formula:C8H11BO3Purity:95%Color and Shape:SolidMolecular weight:165.9821(2-Methoxy-4-methylphenyl)boronic acid
CAS:(2-Methoxy-4-methylphenyl)boronic acidPurity:95%Molecular weight:165.98g/mol(2-Methoxy-4-methylphenyl)boronic acid
CAS:<p>(2-Methoxy-4-methylphenyl)boronic acid is a macrocyclic compound that has been found to have biological activity. It has been shown to be able to inhibit the production of lipid droplets, which may be due to its ability to inhibit the synthesis of lipids in the liver. This natural product can also act as a lead compound for drug discovery.</p>Formula:C8H11BO3Purity:Min. 95%Molecular weight:165.98 g/mol
