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CAS 1072951-48-4

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B-[3-Bromo-5-(trifluoromethoxy)phenyl]boronic acid

Description:
B-[3-Bromo-5-(trifluoromethoxy)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 bromine atom and a trifluoromethoxy group attached to a phenyl ring, contributing to its unique reactivity and potential for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling. The trifluoromethoxy group enhances the compound's electronic properties, potentially increasing its lipophilicity and influencing its biological activity. Additionally, the presence of the boronic acid moiety allows for the formation of stable complexes with biomolecules, which can be exploited in drug design and development. Overall, this compound is of interest in both synthetic organic chemistry and pharmaceutical research due to its versatile reactivity and functionalization potential.
Formula:C7H5BBrF3O3
InChI:InChI=1S/C7H5BBrF3O3/c9-5-1-4(8(13)14)2-6(3-5)15-7(10,11)12/h1-3,13-14H
InChI key:InChIKey=MRIQPQPZRLURMR-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(B(O)O)=CC(Br)=C1
Synonyms:
  • Boronic acid, B-[3-bromo-5-(trifluoromethoxy)phenyl]-
  • [3-Bromo-5-(trifluoromethoxy)phenyl]boronic acid
  • B-[3-Bromo-5-(trifluoromethoxy)phenyl]boronic acid
  • 3-Bromo-5-(trifluoromethoxy)phenylboronic acid
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