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QUASIPHOSPHONIUM-BROMIDE-#2

Compound with spectra: 1 NMR

QUASIPHOSPHONIUM-BROMIDE-#2
SpectraBase Compound ID 7t5GzSm9yo2
InChI InChI=1S/C18H24OP.BrH/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 CTCFUZMUEWTUGN-UHFFFAOYSA-M
Mol Weight 367.27 g/mol
Molecular Formula C18H24BrOP
Exact Mass 366.074815 g/mol
Parent InChIKey KKJHZHTZDAVMPP-UHFFFAOYSA-M

View Spectrum of QUASIPHOSPHONIUM-BROMIDE-#2

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
QUASIPHOSPHONIUM-IODIDE-#1
SJPNPKITLLEYLT-UHFFFAOYSA-M
WJVDDBWYUVZNML-UHFFFAOYSA-M
BORON TRIFLUORIDE-TRIPHENYLPHOSPHINOXIDE COMPLEX
methyltriphenylphosphonium tetraphenylborate(1-)
1,1-Dimethy-1-ethyl diphenylphosphinithioate
ETHYL DIPHENYLSELENOPHOSPHINATE
Diphenylphosphinic acid, ethyl ester
Acetic acid, trifluoro-, anhydride with diphenylphosphinous acid
DIPHENYL(TERT-BUTYL)DICHLOROPHOSPHORANE
[(E)-4-bromobut-2-enyl]-triphenylphosphanium bromide
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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