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CAS 870778-91-9

:

{4-[(4-chlorobenzyl)oxy]phenyl}boronic acid

Description:
{4-[(4-chlorobenzyl)oxy]phenyl}boronic acid, with the CAS number 870778-91-9, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a 4-chlorobenzyl ether. This compound typically exhibits properties such as moderate solubility in polar organic solvents and water, depending on pH conditions due to the acidic nature of the boronic acid group. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis, medicinal chemistry, and as a building block in the development of pharmaceuticals. The presence of the chlorobenzyl group can enhance its lipophilicity and influence its biological activity. Additionally, boronic acids are often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds in organic synthesis. Overall, this compound is significant in both research and industrial applications due to its versatile reactivity and functional properties.
Formula:C13H12BClO3
InChI:InChI=1/C13H12BClO3/c15-12-5-1-10(2-6-12)9-18-13-7-3-11(4-8-13)14(16)17/h1-8,16-17H,9H2
SMILES:c1cc(ccc1COc1ccc(cc1)B(O)O)Cl
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