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CAS 1256358-70-9

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B-[3-[(4-Chlorophenoxy)methyl]phenyl]boronic acid

Description:
B-[3-[(4-Chlorophenoxy)methyl]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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a chlorophenoxy group, enhancing its lipophilicity and potentially influencing its biological activity. The boronic acid moiety contributes to its reactivity, particularly in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic synthesis. This compound may exhibit properties such as moderate solubility in organic solvents and stability under standard laboratory conditions. Its structural characteristics suggest potential applications in drug development, particularly in targeting specific biological pathways or as a building block in the synthesis of more complex molecules. As with many boronic acids, it may also have implications in materials science, particularly in the development of sensors or catalysts.
Formula:C13H12BClO3
InChI:InChI=1S/C13H12BClO3/c15-12-4-6-13(7-5-12)18-9-10-2-1-3-11(8-10)14(16)17/h1-8,16-17H,9H2
InChI key:InChIKey=PCSYEFAEONRRRW-UHFFFAOYSA-N
SMILES:C(OC1=CC=C(Cl)C=C1)C2=CC(B(O)O)=CC=C2
Synonyms:
  • Boronic acid, B-[3-[(4-chlorophenoxy)methyl]phenyl]-
  • B-[3-[(4-Chlorophenoxy)methyl]phenyl]boronic acid
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