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CAS 870777-20-1

:

[2-(benzyloxy)-3-bromo-5-methylphenyl]boronic acid

Description:
[2-(Benzyloxy)-3-bromo-5-methylphenyl]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 organic synthesis applications, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a benzyloxy group, a bromo atom, and a methyl group, contributing to its unique reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, which are essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the bromine substituent can serve as a leaving group in nucleophilic substitution reactions, enhancing its versatility in synthetic pathways. The compound's structural characteristics, including its molecular geometry and electronic properties, play a significant role in its reactivity and interactions with other chemical species. Overall, [2-(benzyloxy)-3-bromo-5-methylphenyl]boronic acid is a valuable intermediate in organic chemistry.
Formula:C14H14BBrO3
InChI:InChI=1/C14H14BBrO3/c1-10-7-12(15(17)18)14(13(16)8-10)19-9-11-5-3-2-4-6-11/h2-8,17-18H,9H2,1H3
SMILES:Cc1cc(c(c(c1)Br)OCc1ccccc1)B(O)O
Synonyms:
  • 2-Benzyloxy-3-bromo-5-methylphenylboronic acid(contains varying amounts of Anhydride)
  • Boronic acid, B-[3-bromo-5-methyl-2-(phenylmethoxy)phenyl]-
  • See more synonyms
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