Bio-Rad Laboratories, Inc. SpectraBase; SpectraBase Compound ID=BaqW1c8bpZL
http://spectrabase.com/compound/BaqW1c8bpZL (accessed Apr 01, 2020).

Methyldiphenylphosphine oxide
SpectraBase Compound ID BaqW1c8bpZL
InChI InChI=1S/C13H13OP/c1-15(14,12-8-4-2-5-9-12)13-10-6-3-7-11-13/h2-11H,1H3
InChIKey PEGCITODQASXKH-UHFFFAOYSA-N
Mol Weight 216.22 g/mol
Molecular Formula C13H13OP
Exact Mass 216.070404 g/mol
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2018 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number A11484
Copyright Copyright © 2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number A11484
Technique KBr0
Copyright Copyright © 2016-2018 Bio-Rad Laboratories, Inc. All Rights Reserved.
Source of Sample Alfa Aesar, Thermo Fisher Scientific
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number A11484
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Diphenylmethylphosphine oxide
  • PEGCITODQASXKH-UHFFFAOYSA-N
Title Journal or Book Year
Trimethylsilyl Halide-Promoted Michaelis-Arbuzov Rearrangement Organic Letters 2003
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
Nuclear magnetic resonance studies. IV. Carbon and phosphorus nuclear magnetic resonance of phosphine oxides and related compounds The Journal of Organic Chemistry 1975