CymitQuimica logo

CAS 190788-58-0

:

4-(METHYLTHIO)PHENYLBORONIC ACID PINACOLATE

Description:
4-(Methylthio)phenylboronic acid pinacolate is an organoboron compound characterized by the presence of a boronic acid functional group and a pinacolate ester. This compound typically exhibits properties associated with boron-containing compounds, such as the ability to form reversible covalent bonds with diols and sugars, making it useful in various applications, including organic synthesis and medicinal chemistry. The methylthio group enhances its solubility and reactivity, while the phenylboronic acid moiety allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds. The pinacolate portion contributes to the stability of the compound and can influence its reactivity. In terms of physical properties, it is generally a solid at room temperature, with potential solubility in organic solvents. The compound's reactivity and functional groups make it valuable in the development of pharmaceuticals and agrochemicals, as well as in materials science for creating advanced polymers and nanomaterials. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C13H19BO2S
InChI:InChI=1/C13H19BO2S/c1-12(2)13(3,4)16-14(15-12)10-6-8-11(17-5)9-7-10/h6-9H,1-5H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(cc2)SC)O1
Synonyms:
  • 4-Thioanisoleboronic Acid, Pinacol Ester
  • 4,4,5,5-Tetramethyl-2-[4-(Methylsulfanyl)Phenyl]-1,3,2-Dioxaborolane
  • 4,4,5,5-TetraMethyl-2-(4-(Methylthio)phenyl)-1,3,2-dioxaborolane
  • 4-Methylthiophenylboronic acid,pinacol ester
  • 4-(METHYLTHIO)PHENYLBORONIC ACID PINACOLATE
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[4-(methylthio)phenyl]-
  • 2-[4-(Methylthio)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.