CymitQuimica logo

CAS 845551-44-2

:

[4-(benzyloxy)-3-chlorophenyl]boronic acid

Description:
[4-(Benzyloxy)-3-chlorophenyl]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, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. This compound features a chlorophenyl group substituted with a benzyloxy moiety, contributing to its unique reactivity and solubility properties. The presence of the chlorine atom enhances its electrophilic character, while the benzyloxy group can influence its steric and electronic properties. Typically, boronic acids like this one are utilized in organic synthesis, medicinal chemistry, and materials science due to their versatility in forming carbon-carbon bonds. Additionally, the compound's solubility in organic solvents and its stability under various conditions make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. As with many boronic acids, care must be taken in handling due to potential reactivity with moisture and air.
Formula:C13H12BClO3
InChI:InChI=1/C13H12BClO3/c15-12-8-11(14(16)17)6-7-13(12)18-9-10-4-2-1-3-5-10/h1-8,16-17H,9H2
SMILES:c1ccc(cc1)COc1ccc(cc1Cl)B(O)O
Synonyms:
  • boronic acid, B-[3-chloro-4-(phenylmethoxy)phenyl]-
  • 4-Benzyloxy-3-chlorophenylboronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.