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CAS 1217500-57-6

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B-[3-Chloro-2-(phenylmethoxy)phenyl]boronic acid

Description:
B-[3-Chloro-2-(phenylmethoxy)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, particularly in organic synthesis and medicinal chemistry. The compound features a chloro substituent and a phenylmethoxy group, contributing to its unique reactivity and solubility properties. Typically, boronic acids exhibit moderate to high solubility in polar organic solvents, and their reactivity can be influenced by the electronic and steric effects of substituents on the aromatic rings. This specific compound may be utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the presence of the chloro group may enhance its electrophilic character, making it a valuable intermediate in the development of pharmaceuticals or agrochemicals. Overall, B-[3-Chloro-2-(phenylmethoxy)phenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C13H12BClO3
InChI:InChI=1S/C13H12BClO3/c15-12-8-4-7-11(14(16)17)13(12)18-9-10-5-2-1-3-6-10/h1-8,16-17H,9H2
InChI key:InChIKey=WRDFNKULHBAPKO-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(B(O)O)C=CC=C2Cl
Synonyms:
  • B-[3-Chloro-2-(phenylmethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-chloro-2-(phenylmethoxy)phenyl]-
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