CymitQuimica logo

CAS 480438-54-8

:

[3-fluoro-4-(propan-2-yloxy)phenyl]boronic acid

Description:
[3-Fluoro-4-(propan-2-yloxy)phenyl]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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and an isopropoxy group, which can influence its reactivity and solubility. The fluorine atom typically enhances the compound's electronic properties, potentially increasing its lipophilicity and altering its interaction with biological targets. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, a vital method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the isopropoxy group may provide steric hindrance, affecting the compound's reactivity and selectivity in chemical reactions. Overall, this compound exemplifies the diverse functionalities of boronic acids in synthetic and pharmaceutical chemistry.
Formula:C9H12BFO3
InChI:InChI=1/C9H12BFO3/c1-6(2)14-9-4-3-7(10(12)13)5-8(9)11/h3-6,12-13H,1-2H3
SMILES:CC(C)Oc1ccc(cc1F)B(O)O
Synonyms:
  • (3-Fluoro-4-isopropoxyphenyl)boronic acid
  • boronic acid, B-[3-fluoro-4-(1-methylethoxy)phenyl]-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.