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CAS 1451393-14-8

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B-[4-Bromo-2,6-difluoro-3-(phenylmethoxy)phenyl]boronic acid

Description:
B-[4-Bromo-2,6-difluoro-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 solubility and reactivity, and the presence of bromine and fluorine substituents on the aromatic ring contributes to its electronic properties and potential reactivity. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the specific arrangement of substituents can influence the compound's biological activity, making it a candidate for further investigation in drug development. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their role in the development of complex organic molecules.
Formula:C13H10BBrF2O3
InChI:InChI=1S/C13H10BBrF2O3/c15-9-6-10(16)11(14(18)19)12(17)13(9)20-7-8-4-2-1-3-5-8/h1-6,18-19H,7H2
InChI key:InChIKey=ZROLYOUHNLANTP-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(OCC2=CC=CC=C2)=C(Br)C=C1F
Synonyms:
  • Boronic acid, B-[4-bromo-2,6-difluoro-3-(phenylmethoxy)phenyl]-
  • B-[4-Bromo-2,6-difluoro-3-(phenylmethoxy)phenyl]boronic acid
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