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CAS 1315340-54-5

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B-(3-Bromo-2-ethoxy-6-fluorophenyl)boronic acid

Description:
B-(3-Bromo-2-ethoxy-6-fluorophenyl)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. This compound features a phenyl ring substituted with a bromine atom, an ethoxy group, and a fluorine atom, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, making it valuable in the formation of carbon-carbon bonds. Additionally, the halogen and ether substituents can influence the compound's solubility, stability, and reactivity, which are critical factors in its application in various chemical reactions. Overall, B-(3-Bromo-2-ethoxy-6-fluorophenyl)boronic acid is a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C8H9BBrFO3
InChI:InChI=1S/C8H9BBrFO3/c1-2-14-8-5(10)3-4-6(11)7(8)9(12)13/h3-4,12-13H,2H2,1H3
InChI key:InChIKey=CQJCRITVZWAMKV-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCC)C(Br)=CC=C1F
Synonyms:
  • Boronic acid, B-(3-bromo-2-ethoxy-6-fluorophenyl)-
  • B-(3-Bromo-2-ethoxy-6-fluorophenyl)boronic acid
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