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CAS 957062-67-8

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B-[2-Chloro-6-fluoro-3-(phenylmethoxy)phenyl]boronic acid

Description:
B-[2-Chloro-6-fluoro-3-(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, including organic synthesis and medicinal chemistry. The compound features a phenylmethoxy group, which enhances its lipophilicity and may influence its biological activity. The presence of chlorine and fluorine substituents on the aromatic ring can significantly affect the compound's electronic properties and reactivity. Boronic acids are often utilized in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules. Additionally, the specific structural features of this compound may contribute to its potential as a pharmaceutical agent, particularly in targeting specific biological pathways. Overall, B-[2-Chloro-6-fluoro-3-(phenylmethoxy)phenyl]boronic acid exemplifies the versatility of boron-containing compounds in both synthetic and medicinal chemistry.
Formula:C13H11BClFO3
InChI:InChI=1S/C13H11BClFO3/c15-13-11(7-6-10(16)12(13)14(17)18)19-8-9-4-2-1-3-5-9/h1-7,17-18H,8H2
InChI key:InChIKey=LXIZYHYNGUDZKO-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(Cl)C(B(O)O)=C(F)C=C2
Synonyms:
  • 3-(Benzyloxy)-2-Chloro-6-Fluorophenylboronic Acid
  • B-[2-Chloro-6-fluoro-3-(phenylmethoxy)phenyl]boronic acid
  • [3-(Benzyloxy)-2-chloro-6-fluorophenyl]boronic acid
  • boronic acid, B-[2-chloro-6-fluoro-3-(phenylmethoxy)phenyl]-
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