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CAS 849062-33-5

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

Description:
{3-[(3-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. This compound features a phenyl ring substituted with a 3-chlorobenzyl ether, enhancing its solubility and reactivity. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. It typically exhibits moderate to high stability under standard conditions but may be sensitive to moisture due to the presence of the boronic acid group. The compound's properties, such as solubility and reactivity, can be influenced by the presence of the chlorobenzyl group, which may also impart specific biological activities. Overall, {3-[(3-chlorobenzyl)oxy]phenyl}boronic acid is a versatile building block in the development of pharmaceuticals and agrochemicals, with applications in materials science and catalysis as well.
Formula:C13H12BClO3
InChI:InChI=1/C13H12BClO3/c15-12-5-1-3-10(7-12)9-18-13-6-2-4-11(8-13)14(16)17/h1-8,16-17H,9H2
SMILES:c1cc(cc(c1)Cl)COc1cccc(c1)B(O)O
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