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PHENYLMETHYL-DIMETHOXY-PHOSPHONIUM-TETRAFLUOROBORATE

Compound with spectra: 1 NMR

PHENYLMETHYL-DIMETHOXY-PHOSPHONIUM-TETRAFLUOROBORATE
SpectraBase Compound ID BPwzCFO3w3v
InChI InChI=1S/C9H14O2P.BF4/c1-10-12(3,11-2)9-7-5-4-6-8-9;2-1(3,4)5/h4-8H,1-3H3;/q+1;-1
InChIKey NSWJEKCLYWHHDX-UHFFFAOYSA-N
Mol Weight 272.0 g/mol
Molecular Formula C9H14BF4O2P
Exact Mass 272.07606 g/mol
Parent InChIKey RBQHPSQVWZEUDO-UHFFFAOYSA-N

View Spectrum of PHENYLMETHYL-DIMETHOXY-PHOSPHONIUM-TETRAFLUOROBORATE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
DIFLUORO-METHOXY-PHENYLPHOSPHORANE
phenylphosphonous acid, diethyl ester
Phenyl-ethylene-phosphite
O-METHYLETHYLPHENYLPHOSPHINITE
diisopropoxy(phenyl)phosphane
Dimethoxy(p-tolyl)phosphane
METHYL-PHENYL-PROPYL-PHOSPHINE-METHYLIODIDE
diethylmethylphenylphosphonium iodide
BIS(HYDROXYMETHYL)METHYL(PHENYL)PHOSPHONIUM IODIDE
(R)-HYDROXYMETHYL-(METHYL)-PHENYLPHOSPHINE-BORANE
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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