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CAS 845551-45-3

:

{3-[(2-chlorobenzyl)oxy]phenyl}boronic acid

Description:
{3-[(2-chlorobenzyl)oxy]phenyl}boronic acid 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, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. This compound features a phenyl ring substituted with a 2-chlorobenzyl ether, enhancing its reactivity and solubility in organic solvents. The presence of the chlorine atom introduces additional electronic effects, potentially influencing the compound's reactivity and interaction with biological systems. Boronic acids are typically polar, which can affect their solubility and interaction with other molecules. This compound may also exhibit interesting properties in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Its structural characteristics suggest potential applications in organic synthesis, materials science, and as a building block in the design of more complex molecules. As with many boronic acids, care should be taken in handling due to their sensitivity to moisture and air.
Formula:C13H12BClO3
InChI:InChI=1/C13H12BClO3/c15-13-7-2-1-4-10(13)9-18-12-6-3-5-11(8-12)14(16)17/h1-8,16-17H,9H2
SMILES:c1ccc(c(c1)COc1cccc(c1)B(O)O)Cl
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