CymitQuimica logo

CAS 871329-84-9

:

3-borono-5-fluoro-benzoic acid

Description:
3-Borono-5-fluoro-benzoic acid is an organic compound characterized by the presence of a boron functional group and a fluorine atom attached to a benzoic acid structure. This compound features a boronic acid moiety, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The fluorine atom, located at the 5-position of the benzene ring, can influence the compound's electronic properties and reactivity. The carboxylic acid group (-COOH) contributes to its acidity and solubility in polar solvents. This compound is often utilized in the development of pharmaceuticals and agrochemicals, as well as in cross-coupling reactions in organic synthesis, such as Suzuki-Miyaura coupling. Its unique combination of functional groups allows for diverse reactivity and potential applications in material science and drug development. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any risks associated with its use.
Formula:C7H6BFO4
InChI:InChI=1/C7H6BFO4/c9-6-2-4(7(10)11)1-5(3-6)8(12)13/h1-3,12-13H,(H,10,11)
SMILES:c1c(cc(cc1B(O)O)F)C(=O)O
Synonyms:
  • (3-Carboxy-5-Fluoro)Benzeneboronic Acid
  • 3-Carboxy-5-fluorobenzeneboronic acid(contains varying amounts of Anhydride)
  • 3-CARBOXY-5-FLUOROPHENYLBORONIC ACID
  • 3-Fluoro-5-Carboxyphenylboronic acid
  • 3-Carboxy-5-fluorophenylboronic acid >=95%
  • 3-Borono-5-fluoro-benzoic acid
  • 3-Carboxy-5-fluorobenzeneboronic
  • Benzoic acid, 3-borono-5-fluoro-
  • (3-Carboxy-5-fluoro)benzeneboronicacid98%
  • 3-Carboxy-5-fluorophenylboronic Acid (contains varying amounts of Anhydride)
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.