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(5S)-5-[2-(9-FLUORENYLMETHOXYCARBONYLAMINO)-ETHYL]-2,2-BIS-(TRIFLUOROMETHYL)-1,3-DIOXOLAN-4-ONE

Compound with spectra: 1 NMR, and 1 MS (GC)

(5S)-5-[2-(9-FLUORENYLMETHOXYCARBONYLAMINO)-ETHYL]-2,2-BIS-(TRIFLUOROMETHYL)-1,3-DIOXOLAN-4-ONE
SpectraBase Compound ID HhomIZuj9mV
InChI InChI=1S/C22H17F6NO5/c23-21(24,25)20(22(26,27)28)33-17(18(30)34-20)9-10-29-19(31)32-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16/h1-8,16-17H,9-11H2,(H,29,31)/t17-/m0/s1
InChIKey IZUDKZMXICLSRF-KRWDZBQOSA-N
Mol Weight 489.37 g/mol
Molecular Formula C22H17F6NO5
Exact Mass 489.101092 g/mol
Enantiomer InChIKey IZUDKZMXICLSRF-QGZVFWFLSA-N
Racemate InChIKey IZUDKZMXICLSRF-UHFFFAOYSA-N

View Spectrum of (5S)-5-[2-(9-FLUORENYLMETHOXYCARBONYLAMINO)-ETHYL]-2,2-BIS-(TRIFLUOROMETHYL)-1,3-DIOXOLAN-4-ONE

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)-5-[2-(9-FLUORENYLMETHOXYCARBONYLAMINO)-ETHYL]-2,2-BIS-(TRIFLUOROMETHYL)-1,3-DIOXOLAN-4-ONE

MS (GC) Spectrum
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Source of Spectrum SB-136-770-15
  • (S)-5-{2'-[(9"-Fluorenyl)methoxycarbonylamino]ethyl}-2,2-bis(trifluoromethyl)-1,3-dioxolan-4-one
5-(4-FMOC-AMINOMETHYL-3,5-DIMETHOXYPHENOXY)-VALERIC-ACID
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-keto-glutaric acid O1-tert-butyl ester O5-ethyl ester
HGWWUSCXTSPYKV-UHFFFAOYSA-N
3-[[1-(9-H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-3-METHYLBUTYL]-HYDROXY-PHOSPHINOYL]-PROPIONIC-ACID
Nα-(9-Fluorenylmethyloxycarbonyl)-Nε-(4-methyltrityl)-L-lysine
3-[(R/S)-1-ALLYLOXYCARBONYL-2-(ALLYLOXYCARBONYLAMINO)-ETHYLSULFANYL]-(R)-2-(FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PROPIONIC-ACID
(2S)-3-(3,5-dimethoxyphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propionic acid tert-butyl ester
Fmoc-Gln(Trt)-OH
1-[N-(9-Fluorenylmethyloxycarbonyl)-(1S,2S)-1-amino-2-hydroxy-4-pentenyl]-4-methyl-2,6,7-trioxabicyclo[2.2.2]octane
1-[N-(9-Fluorenylmethyloxycarbonyl)-(1S,2S)-1-aminobut-3-en-2-ol]-4-methyl-2,6,7-trioxabicyclo[2.2.2]octane
Title Journal or Book Year
Orthogonally Protected, Carboxy-Activated L-Homoisoserine, 2-Methyl-L-homoisoserine, and Homoisocysteine Derivatives. New Building Blocks for Peptide and Depsipeptide Modification Monatshefte für Chemie - Chemical Monthly 2005
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