CymitQuimica logo

CAS 352534-82-8

:

B-(3-Bromo-2-ethoxy-5-fluorophenyl)boronic acid

Description:
B-(3-Bromo-2-ethoxy-5-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. 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 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 halogen and alkoxy substituents can influence the compound's solubility, stability, and overall reactivity. As with many boronic acids, it is important to handle this compound with care, as it may exhibit sensitivity to moisture and air, which can affect its stability and reactivity in synthetic applications.
Formula:C8H9BBrFO3
InChI:InChI=1S/C8H9BBrFO3/c1-2-14-8-6(9(12)13)3-5(11)4-7(8)10/h3-4,12-13H,2H2,1H3
InChI key:InChIKey=VCQYFCFOYYCYJA-UHFFFAOYSA-N
SMILES:O(CC)C1=C(B(O)O)C=C(F)C=C1Br
Synonyms:
  • Boronic acid, (3-bromo-2-ethoxy-5-fluorophenyl)-
  • (3-Bromo-2-ethoxy-5-fluorophenyl)boronic acid
  • Boronic acid, B-(3-bromo-2-ethoxy-5-fluorophenyl)-
  • 3-Bromo-2-ethoxy-5-fluorophenylboronic acid
  • B-(3-Bromo-2-ethoxy-5-fluorophenyl)boronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.