CAS 243140-14-9
:2-(2-Methyl-1,3-dioxolan-2-yl)benzeneboronic acid
Description:
2-(2-Methyl-1,3-dioxolan-2-yl)benzeneboronic acid, with the CAS number 243140-14-9, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzene ring. This compound features a dioxolane ring, which contributes to its unique structural properties. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the dioxolane ring may enhance its solubility and stability in certain solvents. Additionally, compounds like this one are often explored for their potential in drug development, particularly in the context of targeting specific biological pathways or as intermediates in the synthesis of more complex molecules. Its reactivity and functional versatility make it a valuable compound in both academic research and industrial applications. Safety data and handling precautions should be considered, as with all chemical substances, to ensure proper usage and minimize risks.
Formula:C10H13BO4
InChI:InChI=1/C10H13BO4/c1-10(14-6-7-15-10)8-4-2-3-5-9(8)11(12)13/h2-5,12-13H,6-7H2,1H3
SMILES:CC1(c2ccccc2B(O)O)OCCO1
Synonyms:- [2-(2-Methyl-1,3-Dioxolan-2-Yl)Phenyl]Boronic Acid
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Found 3 products.
2-(2-Methyl-1,3-dioxolan-2-yl)phenylboronic acid
CAS:Formula:C10H13BO4Color and Shape:SolidMolecular weight:208.01882-(2-Methyl-1,3-dioxolan-2-yl)benzeneboronic acid
CAS:<p>2-(2-Methyl-1,3-dioxolan-2-yl)benzeneboronic acid</p>Formula:C10H13BO4Purity:97%Color and Shape: white crystalline powderMolecular weight:208.02g/mol(2-(2-Methyl-1,3-dioxolan-2-yl)phenyl)boronic acid
CAS:Formula:C10H13BO4Purity:95.0%Molecular weight:208.02


