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SJPNPKITLLEYLT-UHFFFAOYSA-M

Compound with spectra: 2 NMR

SJPNPKITLLEYLT-UHFFFAOYSA-M
SpectraBase Compound ID F86ACuY8kC2
InChI InChI=1S/C18H24OP.ClH/c1-18(2,3)15-19-20(4,16-11-7-5-8-12-16)17-13-9-6-10-14-17;/h5-14H,15H2,1-4H3;1H/q+1;/p-1
InChIKey SJPNPKITLLEYLT-UHFFFAOYSA-M
Mol Weight 322.82 g/mol
Molecular Formula C18H24ClOP
Exact Mass 322.12533 g/mol
Parent InChIKey KKJHZHTZDAVMPP-UHFFFAOYSA-M

View Spectrum of SJPNPKITLLEYLT-UHFFFAOYSA-M

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of SJPNPKITLLEYLT-UHFFFAOYSA-M

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • QUASIPHOSPHONIUM-CHLORIDE-#3
QUASIPHOSPHONIUM-IODIDE-#1
QUASIPHOSPHONIUM-BROMIDE-#2
WJVDDBWYUVZNML-UHFFFAOYSA-M
BORON TRIFLUORIDE-TRIPHENYLPHOSPHINOXIDE COMPLEX
methyltriphenylphosphonium tetraphenylborate(1-)
[p-(dimethylamino)phenyl]diphenylmethylphosphonium iodide
1,1-Dimethy-1-ethyl diphenylphosphinithioate
ETHYL DIPHENYLSELENOPHOSPHINATE
Diphenylphosphinic acid, ethyl ester
Acetic acid, trifluoro-, anhydride with diphenylphosphinous acid
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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