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CAS 1218790-92-1

:

B-[2-[(3,5-Difluorophenoxy)methyl]phenyl]boronic acid

Description:
B-[2-[(3,5-Difluorophenoxy)methyl]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 structure features a phenyl ring substituted with a 3,5-difluorophenoxy group, enhancing its lipophilicity and potentially influencing its biological activity. This compound is typically a white to off-white solid and is soluble in organic solvents, which facilitates its use in chemical reactions. Its boronic acid moiety allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the presence of fluorine atoms can impart unique electronic properties, potentially affecting the compound's reactivity and interaction with biological targets. Overall, B-[2-[(3,5-Difluorophenoxy)methyl]phenyl]boronic acid is a versatile compound with significant implications in both synthetic and pharmaceutical chemistry.
Formula:C13H11BF2O3
InChI:InChI=1S/C13H11BF2O3/c15-10-5-11(16)7-12(6-10)19-8-9-3-1-2-4-13(9)14(17)18/h1-7,17-18H,8H2
InChI key:InChIKey=HHJHWQLXFNFSHA-UHFFFAOYSA-N
SMILES:C(OC1=CC(F)=CC(F)=C1)C2=C(B(O)O)C=CC=C2
Synonyms:
  • Boronic acid, B-[2-[(3,5-difluorophenoxy)methyl]phenyl]-
  • (2-((3,5-Difluorophenoxy)methyl)phenyl)boronic acid
  • B-[2-[(3,5-Difluorophenoxy)methyl]phenyl]boronic acid
  • [2-(3,5-Difluorophenoxymethyl)phenyl]boronic acid
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