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CAS 2121511-65-5

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B-(5-Chloro-4-ethoxy-2-fluorophenyl)boronic acid

Description:
B-(5-Chloro-4-ethoxy-2-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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a chlorine atom, an ethoxy group, and a fluorine atom, contributing to its unique reactivity and potential applications in cross-coupling reactions, such as Suzuki-Miyaura coupling. The presence of the boronic acid moiety allows for the formation of stable complexes with various substrates, making it valuable in the development of pharmaceuticals and agrochemicals. Additionally, the specific substitutions on the phenyl ring can influence the compound's solubility, stability, and biological activity. Overall, B-(5-Chloro-4-ethoxy-2-fluorophenyl)boronic acid exemplifies the versatility of boronic acids in synthetic chemistry and their role in facilitating complex molecular transformations.
Formula:C8H9BClFO3
InChI:InChI=1S/C8H9BClFO3/c1-2-14-8-4-7(11)5(9(12)13)3-6(8)10/h3-4,12-13H,2H2,1H3
InChI key:InChIKey=NYWZHXXGUJPFIR-UHFFFAOYSA-N
SMILES:O(CC)C1=C(Cl)C=C(B(O)O)C(F)=C1
Synonyms:
  • Boronic acid, B-(5-chloro-4-ethoxy-2-fluorophenyl)-
  • B-(5-Chloro-4-ethoxy-2-fluorophenyl)boronic acid
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