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(+)-(5S)-(4-METHOXYBENZYL)-5-(4-METHOXYBENZYLOXYMETHYL)-3-[(Z)-2,2,2-TRIFLUORO-1-(4-METHOXYANILINO)-ETHILIDEN]-AZOLAN-2-ONA

Compound with spectra: 2 NMR

(+)-(5S)-(4-METHOXYBENZYL)-5-(4-METHOXYBENZYLOXYMETHYL)-3-[(Z)-2,2,2-TRIFLUORO-1-(4-METHOXYANILINO)-ETHILIDEN]-AZOLAN-2-ONA
SpectraBase Compound ID IJN7FhxLTCm
InChI InChI=1S/C30H31F3N2O5/c1-37-24-10-4-20(5-11-24)17-35-23(19-40-18-21-6-12-25(38-2)13-7-21)16-27(29(35)36)28(30(31,32)33)34-22-8-14-26(39-3)15-9-22/h4-15,23,34H,16-19H2,1-3H3/b28-27-/t23-/m0/s1
InChIKey BHOJDKSBCFNDOK-TXYDOONASA-N
Mol Weight 556.58 g/mol
Molecular Formula C30H31F3N2O5
Exact Mass 556.218507 g/mol
Enantiomer InChIKey BHOJDKSBCFNDOK-FPDKYURTSA-N
Racemate InChIKey BHOJDKSBCFNDOK-DQSJHHFOSA-N

View Spectrum of (+)-(5S)-(4-METHOXYBENZYL)-5-(4-METHOXYBENZYLOXYMETHYL)-3-[(Z)-2,2,2-TRIFLUORO-1-(4-METHOXYANILINO)-ETHILIDEN]-AZOLAN-2-ONA

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (+)-(5S)-(4-METHOXYBENZYL)-5-(4-METHOXYBENZYLOXYMETHYL)-3-[(Z)-2,2,2-TRIFLUORO-1-(4-METHOXYANILINO)-ETHILIDEN]-AZOLAN-2-ONA

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(5Z)-1-benzyl-5-[1-(2,4-dimethoxyanilino)ethylidene]-2,4,6(1H,3H,5H)-pyrimidinetrione
(E)-Ethyl 2-(1,3-dioxoisoindolin-2-yl)-5-phenyl-2-propylpent-4-enoate
Benzyl (1S,3S,4R)-2-[(1R)-1-phenylethyl]-2-azabicyclo[2.2.2]oct-5-ene-3-carboxylate
3a,4,5,6-tetrahydro-1-oxo-2-benzyl-4-methylisoindolin-5,6-epoxide
N-ACETYL-2,5-BIS-(4-METHOXYPHENYL)-3,3,4,4-TETRACYANOPYRROLIDINE
Pyrrol-2(5H)-one, 4-acetyl-3-hydroxy-5-(4-methoxyphenyl)-1-[2-(4-morpholyl)ethyl]-
2H-pyrrol-2-one, 4-acetyl-5-(4-ethoxyphenyl)-1,5-dihydro-3-hydroxy-1-[2-(4-morpholinyl)ethyl]-
Ethyl 2-(p-Nitrobenzoyl-2-azabicyclo[2.2.1]hept-5-ene-3-endo-caerboxylate isomer
3-[3-(4-bromo-2,6-dimethylphenoxy)propyl]-2-(4-methoxyphenyl)-4(3H)-quinazolinone
2-methoxy-3-(4-methoxyanilino)naphthoquinone
Title Journal or Book Year
New Strategy for the Stereoselective Synthesis of Fluorinated β-Amino Acids The Journal of Organic Chemistry 2002
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