CAS 850568-50-2
:[3-(2-methyl-1,3-dioxolan-2-yl)phenyl]boronic acid
Description:
[3-(2-methyl-1,3-dioxolan-2-yl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a dioxolane moiety. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications including organic synthesis and medicinal chemistry. The dioxolane ring contributes to its solubility and stability in aqueous environments, while the boronic acid group can participate in Suzuki coupling reactions, a key method for forming carbon-carbon bonds. Additionally, this compound may exhibit unique reactivity due to the steric and electronic effects of the dioxolane substituent, influencing its interactions in biological systems or catalytic processes. Overall, [3-(2-methyl-1,3-dioxolan-2-yl)phenyl]boronic acid is a versatile building block in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C10H13BO4
InChI:InChI=1/C10H13BO4/c1-10(14-5-6-15-10)8-3-2-4-9(7-8)11(12)13/h2-4,7,12-13H,5-6H2,1H3
SMILES:CC1(c2cccc(c2)B(O)O)OCCO1
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Found 3 products.
(3-(2-Methyl-1,3-dioxolan-2-yl)phenyl)boronic acid
CAS:Formula:C10H13BO4Purity:97%Color and Shape:SolidMolecular weight:208.01883-(2-Methyl-1,3-dioxolan-2-yl)benzeneboronic acid
CAS:<p>3-(2-Methyl-1,3-dioxolan-2-yl)benzeneboronic acid</p>Purity:97%Molecular weight:208.02g/mol


