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4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

Compound with spectra: 3 NMR, and 5 MS (GC)

4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane
SpectraBase Compound ID Fc3YqBT5cRp
InChI InChI=1S/C12H17BO2/c1-11(2)12(3,4)15-13(14-11)10-8-6-5-7-9-10/h5-9H,1-4H3
InChIKey KKLCYBZPQDOFQK-UHFFFAOYSA-N
Mol Weight 204.1 g/mol
Molecular Formula C12H17BO2
Exact Mass 204.13216 g/mol

View Spectrum of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

MS (GC) Spectrum
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany

View Spectrum of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QE-26-SM7-4d

View Spectrum of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum HE-1986-1297-0

View Spectrum of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KD-16-2923-9

View Spectrum of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum ASC-354-2625/SM5-2m

View Spectrum of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

11B NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

11B NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

11B NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZENE
  • C6H5-B-(O2C2ME4)
  • 1,3,2-DIOXABOROLANE, 4,4,5,5-TETRAMETHYL-2-PHENYL-
1H-Pyrazole-4-boronic acid pinacol ester
4,4,5,5-tetramethyl-2-[(Z)-2-phenylethenyl]-1,3,2-dioxaborolane
trans-ß-Styrylboronic acid pinacol ester
(E)-4,4,5,5-tetramethyl-2-(3-phenylprop-1-enyl)-1,3,2-dioxaborolane
(E)-4,4,5,5-tetramethyl-2-(3-(phenylthio)prop-1-enyl)-1,3,2-dioxaborolane
4,4,5,5-tetramethyl-2-(2-phenylethynyl)-1,3,2-dioxaborolane
4,4,5,5-tetramethyl-2-[(Z)-4-phenylbut-1-enyl]-1,3,2-dioxaborolane
2-(6-(Benzyloxy)hex-1-yn-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-(trans-3-Pentenyl-2)-4,4,5,5-tetramethyl-1,3-dioxa-2-borolane
2-Benzyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Title Journal or Book Year
A Comparative Study of the Relative Stability of Representative Chiral and Achiral Boronic Esters Employing Transesterification Monatshefte für Chemie - Chemical Monthly 2007
Borylation of Aryldiazonium Ions with N-Heterocyclic Carbene−Palladium Catalysts Formed without Added Base Organic Letters 2003
Mild Iridium-Catalyzed Borylation of Arenes. High Turnover Numbers, Room Temperature Reactions, and Isolation of a Potential Intermediate Journal of the American Chemical Society 2001

Wiley Registry of Mass Spectral Data 12th Edition
Author: Wiley

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