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N,N'-DIMETHYL-N,N'-BIS-[(3A'R,4'AR)-7'-OXOOCTAHYDRO-6'A,7'A-DIAZA-7'-PHOSPHACYCLOPENTA-[A]-PENTALENE-7'-YL]-HEXANE-1,6-DIAMINE

Compound with spectra: 2 NMR

N,N'-DIMETHYL-N,N'-BIS-[(3A'R,4'AR)-7'-OXOOCTAHYDRO-6'A,7'A-DIAZA-7'-PHOSPHACYCLOPENTA-[A]-PENTALENE-7'-YL]-HEXANE-1,6-DIAMINE
SpectraBase Compound ID GErmfUUBCmw
InChI InChI=1S/C24H46N6O2P2/c1-25(33(31)27-17-7-11-21(27)22-12-8-18-28(22)33)15-5-3-4-6-16-26(2)34(32)29-19-9-13-23(29)24-14-10-20-30(24)34/h21-24H,3-20H2,1-2H3/t21-,22-,23-,24-/m1/s1
InChIKey QFZACEVXYXLMIY-MOUTVQLLSA-N
Mol Weight 512.6 g/mol
Molecular Formula C24H46N6O2P2
Exact Mass 512.315749 g/mol
Enantiomer InChIKey QFZACEVXYXLMIY-ZJZGAYNASA-N

View Spectrum of N,N'-DIMETHYL-N,N'-BIS-[(3A'R,4'AR)-7'-OXOOCTAHYDRO-6'A,7'A-DIAZA-7'-PHOSPHACYCLOPENTA-[A]-PENTALENE-7'-YL]-HEXANE-1,6-DIAMINE

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

View Spectrum of N,N'-DIMETHYL-N,N'-BIS-[(3A'R,4'AR)-7'-OXOOCTAHYDRO-6'A,7'A-DIAZA-7'-PHOSPHACYCLOPENTA-[A]-PENTALENE-7'-YL]-HEXANE-1,6-DIAMINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
N,N'-DIMETHYL-N,N'-BIS-[(3A'R,4'AR)-7'-OXOOCTAHYDRO-6'A,7'A-DIAZA-7'-PHOSPHACYCLOPENTA-[A]-PENTALENE-7'-YL]-BUTANE-1,4-DIAMINE
(3A-R,7A-R)-2-AMINO-1,3-BIS-(2',2'-DIMETHYLPROPYL)-N,N'-DIMETHYLOCTAHYDRO-2H-1,3,2-BENZODIAZAPHOSPHOLE-2-OXIDE
(3A-R,7A-R,1'-S)-1,3-DIMETHYLOCTAHYDRO-2-(N-METHYL-1'-BENZENETHANAMINO)-2H-1,3,2-BENZODIAZAPHOSPHOLE-2-OXIDE
RYJRMMFSYFDIIW-SMIHKQSGSA-N
GTUSGNPTJVLJAY-OMKBGSMGSA-N
3-Amino-N-(4-cyanophenyl)thieno[2,3-b]pyridine-2-carboxamide
3-quinazolineacetamide, N-(3-ethoxypropyl)-1,2,3,4-tetrahydro-4-oxo-2-thioxo-
[1S-(1.alpha.,6.beta.,10.alpha.)]-10-Bromo-3,3,5,5,9-pentamethyl-2,4-dioxabicyclo[4.4.0]dec-8-ene
4-(p-chlorophenyl)-2,5-dioxo-4-methyl-1-imidazolidineacetamide
5-[(5-nitro-2-pyridyl)thio]-4-(p-tolylsulfonyl)thiazole
Title Journal or Book Year
Catalytic, Enantioselective Addition of Substituted Allylic Trichlorosilanes Using a Rationally-Designed 2,2‘-Bispyrrolidine-Based Bisphosphoramide Journal of the American Chemical Society 2001
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