CymitQuimica logo

CAS 98546-51-1

:

4-(Methylthio)phenylboronic acid

Description:
4-(Methylthio)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has a methylthio substituent. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. It 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 methylthio group enhances its reactivity and solubility properties. Additionally, boronic acids like this one are often employed in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in the synthesis of complex organic molecules. The compound's reactivity can be influenced by factors such as pH and the presence of other functional groups. Safety precautions should be taken when handling this substance, as with many organoboron compounds, due to potential toxicity and environmental concerns.
Formula:C7H9BO2S
InChI:InChI=1S/C7H9BO2S/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3
InChI key:InChIKey=IVUHTLFKBDDICS-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC=C(SC)C=C1
Synonyms:
  • 4-(Methylsulfanyl)benzeneboronic acid
  • 4-(Methylsulfanyl)phenylboronic acid
  • 4-(Methylthio)benzeneboronic acid
  • B-[4-(Methylthio)phenyl]boronic acid
  • Benzeneboronic acid, p-(methylthio)-
  • Boronic acid, B-[4-(methylthio)phenyl]-
  • Boronic acid, [4-(methylthio)phenyl]-
  • [4-(Methylsulfanyl)phenyl]boronic acid
  • p-(Methylthio)phenylboronic acid
  • p-Methylthiobenzylboronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 7 products.