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QUASIPHOSPHONIUM-IODIDE-#6

Compound with spectra: 1 NMR

QUASIPHOSPHONIUM-IODIDE-#6
SpectraBase Compound ID 5EOfU0z3K9d
InChI InChI=1S/C17H30O2P.HI/c1-16(2,3)13-18-20(7,19-14-17(4,5)6)15-11-9-8-10-12-15;/h8-12H,13-14H2,1-7H3;1H/q+1;/p-1
InChIKey FAJPYQIZMJTZNQ-UHFFFAOYSA-M
Mol Weight 424.3 g/mol
Molecular Formula C17H30IO2P
Exact Mass 424.102812 g/mol
Parent InChIKey OMUPNPYBEKERFW-UHFFFAOYSA-M

View Spectrum of QUASIPHOSPHONIUM-IODIDE-#6

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
QUASIPHOSPHONIUM-BROMIDE-#7
GCLOMYHCSRSBTP-UHFFFAOYSA-M
PHENYL(DIETHOXY)CHLOROSELENOPHOSPHONIUM CHLORIDE
Di-(1,2-dimethyl-1-propyl) phenylphosphonite
2,2-Dimethyl-1-propylhydrogenphenylphosphonate
GZUAKUUYYDMUMI-UHFFFAOYSA-N
DIPROPYL PHENYLPHOSPHONATE
C-PR-CH2-O-P-PH2
di(prop-2-enoxy)phosphorylbenzene
hexoxy(phenyl)phosphinic acid
DIETHYL PARA-METHYLPHENYLPHOSPHONATE
2-phenyl-1,3-dioxa-2$l^{5}-phosphacyclohept-5-ene 2-oxide
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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