CAS 849052-17-1
:{3-bromo-2-[(2-chlorobenzyl)oxy]-5-methylphenyl}boronic acid
Description:
{3-bromo-2-[(2-chlorobenzyl)oxy]-5-methylphenyl}boronic acid, with the CAS number 849052-17-1, 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 bromine atom and a chlorobenzyl ether moiety, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of the methyl group on the phenyl ring enhances its lipophilicity, which may influence its biological activity and solubility. Boronic acids are often utilized in Suzuki coupling reactions, making this compound potentially valuable in the synthesis of complex organic molecules. Additionally, the halogen substituents can provide sites for further functionalization, allowing for the development of diverse derivatives. Overall, this compound's structural features suggest it may have applications in drug development, particularly in the design of inhibitors or other biologically active molecules.
Formula:C14H13BBrClO3
InChI:InChI=1/C14H13BBrClO3/c1-9-6-11(15(18)19)14(12(16)7-9)20-8-10-4-2-3-5-13(10)17/h2-7,18-19H,8H2,1H3
SMILES:Cc1cc(c(c(c1)Br)OCc1ccccc1Cl)B(O)O
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Found 3 products.
3-Bromo-2-(2'-chlorobenzyloxy)-5-methylphenylboronic acid
CAS:Formula:C14H13BBrClO3Purity:95%Color and Shape:SolidMolecular weight:355.41923-Bromo-2-(2'-chlorobenzyloxy)-5-methylphenylboronic acid
CAS:<p>3-Bromo-2-(2'-chlorobenzyloxy)-5-methylphenylboronic acid</p>Purity:≥95%Molecular weight:355.42g/mol(3-Bromo-2-((2-chlorobenzyl)oxy)-5-methylphenyl)boronic acid
CAS:Formula:C14H13BBrClO3Purity:95%Molecular weight:355.42


