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GCLOMYHCSRSBTP-UHFFFAOYSA-M

Compound with spectra: 1 NMR

GCLOMYHCSRSBTP-UHFFFAOYSA-M
SpectraBase Compound ID JJGkd1vr5Tq
InChI InChI=1S/C17H30O2P.ClH/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 GCLOMYHCSRSBTP-UHFFFAOYSA-M
Mol Weight 332.85 g/mol
Molecular Formula C17H30ClO2P
Exact Mass 332.167195 g/mol
Parent InChIKey OMUPNPYBEKERFW-UHFFFAOYSA-M

View Spectrum of GCLOMYHCSRSBTP-UHFFFAOYSA-M

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
QUASIPHOSPHONIUM-BROMIDE-#7
QUASIPHOSPHONIUM-IODIDE-#6
PHENYL(DIETHOXY)CHLOROSELENOPHOSPHONIUM CHLORIDE
Di-(1,2-dimethyl-1-propyl) phenylphosphonite
2,2-Dimethyl-1-propylhydrogenphenylphosphonate
GZUAKUUYYDMUMI-UHFFFAOYSA-N
DIPROPYL PHENYLPHOSPHONATE
di(prop-2-enoxy)phosphorylbenzene
hexoxy(phenyl)phosphinic acid
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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