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CAS 1256358-67-4

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B-[3-[(2-Chlorophenoxy)methyl]phenyl]boronic acid

Description:
B-[3-[(2-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, which enhances its lipophilicity and may influence its biological activity. The boronic acid moiety allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the chlorine atom can affect the electronic properties of the molecule, potentially impacting its reactivity and interactions with biological targets. This compound may be of interest in the development of pharmaceuticals or agrochemicals, given the role of boron-containing compounds in drug design and their utility in various chemical transformations. Overall, B-[3-[(2-Chlorophenoxy)methyl]phenyl]boronic acid exemplifies the versatility of boronic acids in both synthetic and applied chemistry contexts.
Formula:C13H12BClO3
InChI:InChI=1S/C13H12BClO3/c15-12-6-1-2-7-13(12)18-9-10-4-3-5-11(8-10)14(16)17/h1-8,16-17H,9H2
InChI key:InChIKey=BQZSATLDHKVMHT-UHFFFAOYSA-N
SMILES:C(OC1=C(Cl)C=CC=C1)C2=CC(B(O)O)=CC=C2
Synonyms:
  • B-[3-[(2-Chlorophenoxy)methyl]phenyl]boronic acid
  • Boronic acid, B-[3-[(2-chlorophenoxy)methyl]phenyl]-
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