CymitQuimica logo

CAS 481725-36-4

:

[4-(bromoacetyl)-3-fluorophenyl]boronic acid

Description:
[4-(Bromoacetyl)-3-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 both a bromoacetyl group and a fluorine atom, contributing to its reactivity and potential applications in various chemical reactions, including Suzuki coupling. The bromoacetyl group enhances electrophilicity, making it a useful intermediate in the synthesis of more complex molecules. The presence of the fluorine atom can influence the compound's electronic properties and lipophilicity, which may affect its biological activity. Additionally, boronic acids are often utilized in drug development due to their ability to interact with biological targets. Overall, [4-(bromoacetyl)-3-fluorophenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry and pharmaceutical research.
Formula:C8H7BBrFO3
InChI:InChI=1/C8H7BBrFO3/c10-4-8(12)6-2-1-5(9(13)14)3-7(6)11/h1-3,13-14H,4H2
SMILES:c1cc(c(cc1B(O)O)F)C(=O)CBr
Synonyms:
  • 4-(Bromoacetyl)-3-fluorobenzeneboronic acid
  • B-[4-(2-Bromoacetyl)-3-fluorophenyl]boronic acid
  • boronic acid, B-[4-(2-bromoacetyl)-3-fluorophenyl]-
  • Qbqr Cf Dv1E
  • 4-Bromoacetyl-3-fluorophenylboronic acid
  • [4-(Bromoacetyl)-3-fluorophenyl]boronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.