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CAS 1309980-91-3

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B-(3-Bromo-2-fluoro-6-methoxyphenyl)boronic acid

Description:
B-(3-Bromo-2-fluoro-6-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The phenyl ring features a bromine atom at the 3-position, a fluorine atom at the 2-position, and a methoxy group at the 6-position, contributing to its unique reactivity and properties. This compound is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is valuable for forming carbon-carbon bonds. The presence of the boronic acid group allows for the formation of stable complexes with diols, making it useful in various applications, including drug discovery and material science. Additionally, the halogen substituents can influence the electronic properties and reactivity of the compound, making it a versatile building block in the synthesis of more complex organic molecules. As with many boronic acids, it is important to handle this compound with care, as it may exhibit sensitivity to moisture and air.
Formula:C7H7BBrFO3
InChI:InChI=1S/C7H7BBrFO3/c1-13-5-3-2-4(9)7(10)6(5)8(11)12/h2-3,11-12H,1H3
InChI key:InChIKey=BBNKVONBBPZCIF-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OC)C=CC(Br)=C1F
Synonyms:
  • B-(3-Bromo-2-fluoro-6-methoxyphenyl)boronic acid
  • Boronic acid, B-(3-bromo-2-fluoro-6-methoxyphenyl)-
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