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CAS 214360-76-6

:

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

Description:
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, with the CAS number 214360-76-6, is an organic compound that features a phenolic structure substituted with a dioxaborolane moiety. This compound is characterized by its boron-containing dioxaborolane ring, which contributes to its unique reactivity and potential applications in organic synthesis, particularly in cross-coupling reactions. The presence of the tetramethyl groups enhances its stability and solubility in organic solvents. As a phenol derivative, it exhibits typical phenolic properties, such as the ability to act as a weak acid and participate in hydrogen bonding. The compound may also exhibit interesting optical properties due to its aromatic system. Its applications may extend to materials science, pharmaceuticals, and as a reagent in various chemical transformations. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.
Formula:C12H17BO3
InChI:InChI=1S/C12H17BO3/c1-11(2)12(3,4)16-13(15-11)9-6-5-7-10(14)8-9/h5-8,14H,1-4H3
InChI key:InChIKey=MUKIFYQKIZOYKT-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(O)=CC=C2
Synonyms:
  • 2-(3-Hydroxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
  • 3-Hydroxyphenylboronic acid pinacol ester
  • 3-Hydroxyphenylboronic acid,Pinacol cyclic ester
  • Phenol, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)phenol
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
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