![{3-chloro-4-[(2-chlorobenzyl)oxy]phenyl}boronic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F195540-3-chloro-4-2-chlorobenzyl-oxy-phenyl-boronic-acid.webp&w=3840&q=75)
CAS 870777-26-7
:{3-chloro-4-[(2-chlorobenzyl)oxy]phenyl}boronic acid
Description:
{3-chloro-4-[(2-chlorobenzyl)oxy]phenyl}boronic acid, with the CAS number 870777-26-7, 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 chlorinated phenyl ring, enhancing its reactivity and potential applications in medicinal chemistry and organic synthesis. The presence of the 2-chlorobenzyl ether moiety contributes to its lipophilicity, which can influence its biological activity and solubility in organic solvents. Boronic acids are often utilized in Suzuki coupling reactions, making this compound valuable in the synthesis of complex organic molecules. Additionally, the chlorinated substituents may impart specific electronic properties, affecting the compound's reactivity and interaction with biological targets. Overall, this compound's unique structure and functional groups position it as a significant candidate for research in drug development and materials science.
Formula:C13H11BCl2O3
InChI:InChI=1/C13H11BCl2O3/c15-11-4-2-1-3-9(11)8-19-13-6-5-10(14(17)18)7-12(13)16/h1-7,17-18H,8H2
SMILES:c1ccc(c(c1)COc1ccc(cc1Cl)B(O)O)Cl
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Found 3 products.
(3-Chloro-4-((2-chlorobenzyl)oxy)phenyl)boronic acid
CAS:Formula:C13H11BCl2O3Purity:95%Color and Shape:SolidMolecular weight:296.94163-Chloro-4-(2'-chlorobenzyloxy)phenylboronic acid
CAS:3-Chloro-4-(2'-chlorobenzyloxy)phenylboronic acidPurity:95%Molecular weight:296.94g/mol
