![{3-chloro-4-[(4-fluorobenzyl)oxy]phenyl}boronic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F195563-3-chloro-4-4-fluorobenzyl-oxy-phenyl-boronic-acid.webp&w=3840&q=75)
CAS 849062-39-1
:{3-chloro-4-[(4-fluorobenzyl)oxy]phenyl}boronic acid
Description:
{3-chloro-4-[(4-fluorobenzyl)oxy]phenyl}boronic acid, with the CAS number 849062-39-1, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that features both a chlorine and a fluorobenzyl ether substituent. This compound typically exhibits properties associated with 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 presence of the chlorine and fluorine substituents can influence its reactivity, solubility, and biological activity. Generally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the specific functional groups in this compound may impart unique characteristics, such as enhanced lipophilicity or altered electronic properties, which can affect its interaction with biological targets. Overall, this compound is of interest in research areas focused on drug development and materials science.
Formula:C13H11BClFO3
InChI:InChI=1/C13H11BClFO3/c15-12-7-10(14(17)18)3-6-13(12)19-8-9-1-4-11(16)5-2-9/h1-7,17-18H,8H2
SMILES:c1cc(ccc1COc1ccc(cc1Cl)B(O)O)F
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Found 3 products.
(3-chloro-4-((4-fluorobenzyl)oxy)phenyl)boronic acid
CAS:Formula:C13H11BClFO3Purity:98%Color and Shape:SolidMolecular weight:280.48703-Chloro-4-(4'-fluorobenzyloxy)phenylboronic acid
CAS:<p>3-Chloro-4-(4'-fluorobenzyloxy)phenylboronic acid</p>Purity:98%Molecular weight:280.49g/mol
