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Methyltriphenylphosphonium chloride

Compound with spectra: 2 NMR, 2 FTIR, and 1 Raman

Methyltriphenylphosphonium chloride
SpectraBase Compound ID IXVA20BaVuo
InChI InChI=1S/C19H18P.ClH/c1-20(17-11-5-2-6-12-17,18-13-7-3-8-14-18)19-15-9-4-10-16-19;/h2-16H,1H3;1H/q+1;/p-1
InChIKey QRPRIOOKPZSVFN-UHFFFAOYSA-M
Mol Weight 312.78 g/mol
Molecular Formula C19H18ClP
Exact Mass 312.083465 g/mol
Parent InChIKey AZFQCTBZOPUVOW-UHFFFAOYSA-M

View Spectrum of Methyltriphenylphosphonium chloride

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CH2Cl2

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31P NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent C3H7NO dimethylforma

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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 H56851

View Spectrum of Methyltriphenylphosphonium chloride

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 H56851
Technique KBr1

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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 H56851
  • methyl-triphenylphosphanium chloride
Methyltriphenylphosphonium iodide
Triphenylmethylphosphonium Bromide
TRIPHENYLMETHYLPHOSPHONIUM PERCHLORATE
METHYLTRIPHENYLPHOSPHONIUM TRIFLUOROMETHANESULPHONATE
TRIPHENYL-METHYL-PHOSPHONIUM-ION
Tetraphenylphosphonium chloride
Tetraphenylphosphoniumchloride (partially hydrolyzed)
TETRAPHENYL-PHOSPHONIUM-ION
Tetraphenylphosphonium iodide
Tetraphenylphosphonium bromide
TETRAPHENYLPHOSPHONIUM PENTAFLUOROTELLURIDE
TETRAPHENYLPHOSPHONIUM ACETATE
TETRAPHENYLPHOSPHONIUM DICYANOAMIDE
Title Journal or Book Year
Quasiphosphonium intermediates. Part 3. Preparation, structure, and reactivity of alkoxyphosphonium halides in the reactions of neopentyl diphenylphosphinite, dineopentyl phenylphosphonite, and trineopentyl phosphite with halogenomethanes and the effect of phenoxy-substituents on the mechanism of alkyl–oxygen fission in Michaelis–Arbuzov reactions J. Chem. Soc., Perkin Trans. 2 1983

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