CymitQuimica logo

CAS 180516-87-4

:

4-Carboxylphenylboronic acid pinacol ester

Description:
4-Carboxylphenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a carboxylic acid moiety attached to a phenyl ring. This compound typically exhibits a pinacol ester structure, which enhances its stability and solubility in organic solvents. The boronic acid functionality allows for reversible covalent bonding with diols, making it useful in various applications, including organic synthesis and materials science. The carboxyl group contributes to its acidity and potential reactivity in coupling reactions. Additionally, this compound may exhibit properties such as moderate polarity and the ability to participate in hydrogen bonding due to the presence of both the carboxylic acid and boronic acid functionalities. Its applications can extend to medicinal chemistry, particularly in the development of boron-containing drugs and as a building block in the synthesis of complex organic molecules. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C13H17BO4
InChI:InChI=1/C13H17BO4/c1-12(2)13(3,4)18-14(17-12)10-7-5-9(6-8-10)11(15)16/h5-8H,1-4H3,(H,15,16)
SMILES:CC1(C)C(C)(C)OB(c2ccc(cc2)C(=O)O)O1
Synonyms:
  • 4-Carboxybenzeneboronic Acid Pinacol Cyclic Ester
  • 4-Carboxyphenylboronic Acid Pinacolate
  • 4-Carboxyphenylboronic Acid, Pinacol Cyclic Ester
  • 4-Carboxyphenylboronic Acid, Pinacol Ester
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-YL)benzoic acid
  • [4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborinan-2-YL) benzoic acid]
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoicacid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 8 products.