CymitQuimica logo

CAS 166744-78-1

:

4-Benzyloxy-2-fluorobenzeneboronic acid

Description:
4-Benzyloxy-2-fluorobenzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in forming covalent bonds with various nucleophiles. This compound features a fluorine atom and a benzyloxy group attached to a benzene ring, contributing to its unique chemical properties. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The fluorine substituent can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in chemical reactions. Additionally, the benzyloxy group can serve as a protecting group or a leaving group in various synthetic pathways. Overall, 4-Benzyloxy-2-fluorobenzeneboronic acid is a versatile compound with applications in medicinal chemistry, materials science, and organic synthesis, owing to its functional groups and structural characteristics.
Formula:C13H12BFO3
InChI:InChI=1/C13H12BFO3/c15-13-8-11(6-7-12(13)14(16)17)18-9-10-4-2-1-3-5-10/h1-8,16-17H,9H2
SMILES:c1ccc(cc1)COc1ccc(c(c1)F)B(O)O
Synonyms:
  • 4-Benzyloxy-2-fluorophenylboronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.