CymitQuimica logo

CAS 149507-36-8

:

3-TRIFLUOROMETHYL-4-METHOXY-PHENYLBORONIC ACID

Description:
3-Trifluoromethyl-4-methoxy-phenylboronic 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. This compound features a trifluoromethyl group, which enhances its lipophilicity and can influence its reactivity and biological activity. The methoxy group contributes to the compound's electronic properties, potentially affecting its reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely used in organic synthesis for forming carbon-carbon bonds. The presence of the boronic acid moiety makes it useful in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the trifluoromethyl group can impart unique properties, such as increased metabolic stability and altered pharmacokinetics. Overall, this compound is of interest in various fields, including organic synthesis, medicinal chemistry, and materials science, due to its versatile reactivity and functionalization potential.
Formula:C8H8BF3O3
InChI:InChI=1/C8H8BF3O3/c1-15-7-3-2-5(9(13)14)4-6(7)8(10,11)12/h2-4,13-14H,1H3
SMILES:COc1ccc(cc1C(F)(F)F)B(O)O
Synonyms:
  • 4-Methoxy-3-Trifluoromethylphenylboronic Acid
  • 4-Methoxy-3-(Trifluoromethyl)Benzeneboronic Acid
  • 4-Methoxy-3-(trifluoromethyl)benzeneboronic acid 98%
  • 4-Methoxy-3-(trifluoromethyl)benzeneboronicacid98%
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.