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trans-ß-Styrylboronic acid pinacol ester

Compound with spectra: 2 NMR, 2 FTIR, 1 Raman, and 6 MS (GC)

trans-ß-Styrylboronic acid pinacol ester
SpectraBase Compound ID 5E0hzP0Cets
InChI InChI=1S/C14H19BO2/c1-13(2)14(3,4)17-15(16-13)11-10-12-8-6-5-7-9-12/h5-11H,1-4H3/b11-10+
InChIKey ARAINKADEARZLZ-ZHACJKMWSA-N
Mol Weight 230.1 g/mol
Molecular Formula C14H19BO2
Exact Mass 230.14781 g/mol

View Spectrum of trans-ß-Styrylboronic acid pinacol ester

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

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Raman Spectrum
Copyright Copyright © 2017-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number L19529

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FTIR Spectrum
Copyright Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number L19529
Technique Neat

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ATR-IR Spectrum
Copyright Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number L19529

View Spectrum of trans-ß-Styrylboronic acid pinacol ester

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum C5-2004-1819-3

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum ASC-360-SM26-3a

View Spectrum of trans-ß-Styrylboronic acid pinacol ester

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum CCC-10-SM8-3a

View Spectrum of trans-ß-Styrylboronic acid pinacol ester

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-57-3484-2

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum A1-18-432/SM9-3d

View Spectrum of trans-ß-Styrylboronic acid pinacol ester

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum ACI-58-SM4-2a

View Spectrum of trans-ß-Styrylboronic acid pinacol ester

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (E)-PINACOL-(2-PHENYLETHENYL)-BORONATE
  • (E)-4,4,5,5-tetramethyl-2-styryl-1,3,2-dioxaborolane
  • (E)-2-Phenylethenyboronic acid pinacol ester
4,4,5,5-tetramethyl-2-[(Z)-2-phenylethenyl]-1,3,2-dioxaborolane
4,4,5,5-tetramethyl-2-[(Z)-3-methylpent-1-enyl]-1,3,2-dioxaborolane
2-((Z)-2-Cyclopentyl-vinyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
(E)-2-(2-cyclopentylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-PENT-1-EN-3-OL
METHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-PENTA-2E,4E-DIENOATE
METHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-PENTA-2Z,4E-DIENOATE
(E)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)acrylic acid methyl ester
ETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-PENTA-2,4-DIENOATE
2-{(E)-3-[4,4-(Dimethoxy)butoxy]propen-1-yl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Title Journal or Book Year
Mild and stereoselective hydroborations of functionalized alkynes and alkenes using pinacolborane The Journal of Organic Chemistry 1992
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