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CAS 957035-10-8

:

(3-benzyloxy-6-bromo-2-fluoro-phenyl)boronic acid

Description:
(3-Benzyloxy-6-bromo-2-fluoro-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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a benzyloxy group, a bromine atom, and a fluorine atom, contributing to its unique reactivity and potential applications in medicinal chemistry and material science. The presence of the bromine and fluorine substituents can influence the electronic properties and steric hindrance of the molecule, affecting its reactivity and interactions with other chemical species. Additionally, the boronic acid moiety allows for the formation of complexes with biomolecules, which can be exploited in drug design and development. Overall, this compound exemplifies the versatility of boronic acids in synthetic organic chemistry and their role in the development of novel therapeutic agents.
Formula:C13H11BBrFO3
InChI:InChI=1/C13H11BBrFO3/c15-10-6-7-11(13(16)12(10)14(17)18)19-8-9-4-2-1-3-5-9/h1-7,17-18H,8H2
SMILES:c1ccc(cc1)COc1ccc(c(c1F)B(O)O)Br
Synonyms:
  • [3-(Benzyloxy)-6-bromo-2-fluorophenyl]boronic acid
  • boronic acid, B-[6-bromo-2-fluoro-3-(phenylmethoxy)phenyl]-
  • 3-(Benzyloxy)-6-Bromo-2-Fluorophenylboronic Acid
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