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OVSINNBCLPSKAZ-UHFFFAOYSA-N

Compound with spectra: 5 NMR

OVSINNBCLPSKAZ-UHFFFAOYSA-N
SpectraBase Compound ID sD72sUXUAE
InChI InChI=1S/C20H12ClO2P/c21-24-22-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)23-24/h1-12H
InChIKey OVSINNBCLPSKAZ-UHFFFAOYSA-N
Mol Weight 350.74 g/mol
Molecular Formula C20H12ClO2P
Exact Mass 350.026344 g/mol

View Spectrum of OVSINNBCLPSKAZ-UHFFFAOYSA-N

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

View Spectrum of OVSINNBCLPSKAZ-UHFFFAOYSA-N

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

View Spectrum of OVSINNBCLPSKAZ-UHFFFAOYSA-N

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6

View Spectrum of OVSINNBCLPSKAZ-UHFFFAOYSA-N

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

View Spectrum of OVSINNBCLPSKAZ-UHFFFAOYSA-N

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • CYCLIC-(R)-[1,1'-BINAPHTHALENE]-2,2'-DIYL-PHOSPHOROCHLORIDITE
  • CYCLIC-(S)-[1,1'-BINAPHTHALENE]-2,2'-DIYL-PHOSPHOROCHLORIDITE
  • 4-CHLORO-3,5-DIOXA-4-PHOSPHACYCLOHEPTA-[2.1-ALPHA;3.4-ALPHA']-DINAPHTHALENE
  • NO NAME
XRCJOWMGXYFERD-UHFFFAOYSA-N
MUPVYVGOFQFGPL-UHFFFAOYSA-N
4-(3,5-DIOXA-4-PHOSPHACYCLOHEPTA-[2.1-ALPHA;3.4-ALPHA']-DINAPHTHALENE-4-YLOXY)-HEPTANE
SRUGRYZWXYRILX-UHFFFAOYSA-N
IRFGXKDBWFMVFW-UHFFFAOYSA-O
[1-[2-[di(phenyl)phosphanylmethoxy]naphthalen-1-yl]naphthalen-2-yl]oxymethyl-di(phenyl)phosphane
2-[1-[2-(2-ethoxy-2-keto-ethoxy)-1-naphthyl]-2-naphthoxy]acetic acid ethyl ester
Titaniun(IV), bis(1,1'-binaphthyl-2,2'-diolate)
1,1'-Dinaphthyl, 2,2'-bis(N,N-dimethylthiocarbamoyloxy)-
(aR/S)-(2'-allyloxy-1,1'-binaphth-2-oxy)butanoic acid
Title Journal or Book Year
Diastereoselective formation of 18-membered ring BINOL-hydrogen phosphonate dimers - Quasi-covalent hydrogen bonds? Canadian Journal of Chemistry 2007
Tunable Ligands for Asymmetric Catalysis:  Readily Available Carbohydrate-Derived Diarylphosphinites Induce High Selectivity in the Hydrovinylation of Styrene Derivatives Journal of the American Chemical Society 2001

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