CymitQuimica logo

CAS 850589-54-7

:

(3-fluoro-5-isopropoxy-phenyl)boronic acid

Description:
(3-Fluoro-5-isopropoxy-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a fluorine atom and an isopropoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its reactivity, while the isopropoxy group may contribute to its solubility and steric properties. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The specific structural features of (3-fluoro-5-isopropoxy-phenyl)boronic acid may also impart unique biological activities, making it a subject of interest in drug development and material science.
Formula:C9H12BFO3
InChI:InChI=1/C9H12BFO3/c1-6(2)14-9-4-7(10(12)13)3-8(11)5-9/h3-6,12-13H,1-2H3
SMILES:CC(C)Oc1cc(cc(c1)F)B(O)O
Synonyms:
  • (3-Fluoro-5-isopropoxyphenyl)boronic acid
  • boronic acid, B-[3-fluoro-5-(1-methylethoxy)phenyl]-
  • 3-Fluoro-5-Isopropoxyphenylboronic Acid
  • 3-Fluoro-5-(Isopropoxy)Benzeneboronic Acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.