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CAS 710348-63-3

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(2-hydroxy-1,1,2-trimethyl-propoxy)-(3-methylsulfanylphenyl)borinic acid

Description:
(2-hydroxy-1,1,2-trimethyl-propoxy)-(3-methylsulfanylphenyl)borinic acid, with the CAS number 710348-63-3, is a boronic acid derivative characterized by the presence of a boron atom bonded to a hydroxyl group and an organic moiety. This compound features a propoxy group that is substituted with three methyl groups, enhancing its hydrophobic properties. The presence of a 3-methylsulfanylphenyl group introduces a sulfur atom, which can influence the compound's reactivity and solubility. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals and in the field of materials science. The specific structural features of this compound suggest potential applications in catalysis and as a building block in organic synthesis. Additionally, the presence of functional groups may impart unique chemical reactivity, making it a subject of interest for further research in various chemical applications.
Formula:C13H19BO2S
InChI:InChI=1/C13H21BO3S/c1-12(2,15)13(3,4)17-14(16)10-7-6-8-11(9-10)18-5/h6-9,15-16H,1-5H3
SMILES:CC(C)(C(C)(C)OB(c1cccc(c1)SC)O)O
Synonyms:
  • 3-3-(Methylthio)phenylboronic acid pinacolate
  • 3-(Methylthio)phenylboronic acid pinacol ester
  • (2-hydroxy-1,1,2-trimethyl-propoxy)-(3-methylsulfanylphenyl)...
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[3-(methylthio)phenyl]-
  • 4,4,5,5-tetramethyl-2-(3-(methylthio)phenyl)-1,3,2-dioxaborolane
  • REF DUPL: 3-(methylthio)phenylboronic acid pinacolate
  • 3-(METHYLTHIO)PHENYLBORONIC ACID PINACOLATE
  • 2-(3-Methylthiophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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