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CAS 849052-22-8

:

B-[3-Bromo-2-[(4-fluorophenyl)methoxy]phenyl]boronic acid

Description:
B-[3-Bromo-2-[(4-fluorophenyl)methoxy]phenyl]boronic acid, with the CAS number 849052-22-8, 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. This compound features a bromine atom and a methoxy group attached to a phenyl ring, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. The fluorophenyl moiety enhances its electronic properties, making it useful in various chemical reactions, including Suzuki coupling, which is a common method for forming carbon-carbon bonds. The presence of the boronic acid group also allows for potential applications in drug development, particularly in the design of inhibitors for certain biological targets. Overall, this compound's structural features suggest it may play a significant role in advanced materials science and pharmaceutical research.
Formula:C13H11BBrFO3
InChI:InChI=1S/C13H11BBrFO3/c15-12-3-1-2-11(14(17)18)13(12)19-8-9-4-6-10(16)7-5-9/h1-7,17-18H,8H2
InChI key:InChIKey=FAGFWOJETYFVAS-UHFFFAOYSA-N
SMILES:O(CC1=CC=C(F)C=C1)C2=C(B(O)O)C=CC=C2Br
Synonyms:
  • B-[3-Bromo-2-[(4-fluorophenyl)methoxy]phenyl]boronic acid
  • 3-Bromo-2-(4′-fluorobenzyloxy)phenylboronic acid
  • (3-Bromo-2-((4-fluorobenzyl)oxy)phenyl)boronic acid
  • Boronic acid, [3-bromo-2-[(4-fluorophenyl)methoxy]phenyl]-
  • Boronic acid, B-[3-bromo-2-[(4-fluorophenyl)methoxy]phenyl]-
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