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(S)-2-[[[(9H-FLUOREN-9-YL)-METHOXY]-CARBONYL]-AMINO]-5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)-PENTANOIC-ACID

Compound with spectra: 2 NMR

(S)-2-[[[(9H-FLUOREN-9-YL)-METHOXY]-CARBONYL]-AMINO]-5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)-PENTANOIC-ACID
SpectraBase Compound ID 2qbWTQ8N18V
InChI InChI=1S/C21H17F6NO4/c22-20(23,24)17(21(25,26)27)9-16(18(29)30)28-19(31)32-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-17H,9-10H2,(H,28,31)(H,29,30)/t16-/m0/s1
InChIKey WVPUFIKXAKCIEY-INIZCTEOSA-N
Mol Weight 461.36 g/mol
Molecular Formula C21H17F6NO4
Exact Mass 461.106177 g/mol
Enantiomer InChIKey WVPUFIKXAKCIEY-MRXNPFEDSA-N
Racemate InChIKey WVPUFIKXAKCIEY-UHFFFAOYSA-N

View Spectrum of (S)-2-[[[(9H-FLUOREN-9-YL)-METHOXY]-CARBONYL]-AMINO]-5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)-PENTANOIC-ACID

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

View Spectrum of (S)-2-[[[(9H-FLUOREN-9-YL)-METHOXY]-CARBONYL]-AMINO]-5,5,5-TRIFLUORO-4-(TRIFLUOROMETHYL)-PENTANOIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Fmoc-Cha-OH
N-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-cyclohexyl-D-alanine
N-α-(9H-Fluoren-9-ylmethoxycarbonyl)-N-ε-(tert-butoxycarbonyl)-L-lysine
Nepsilon-(tert-Butoxycarbonyl)-Nalpha-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-lysine
N2,N6-DICARBOXY-L-LYSINE, N6-tert-BUTYL N2-[(FLUOREN-9-YL)METHYL]ESTER
N-α-(9H-Fluoren-9-ylmethoxycarbonylamino)-N-ε-trifluoracetyl-L-lysine
Nδ-tert-Butyloxycarbonyl-Nα-(9-fluorenylmethyloxycarbonyl)-L-ornithine
2-(9-H-Fluoren-9-ylmethoxycarbonlyamino)-pentanedioicacid 5-allyl ester
N-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTYL-BETA-(13)C-METHYLESTER
N-(9-Fmoc)-L-glutamic acid gamma-tert-butyl ester monohydrate
Title Journal or Book Year
Synthesis of enantiomerically pure (2S,3S)-5,5,5-trifluoroisoleucine and (2R,3S)-5,5,5-trifluoro-allo-isoleucine Beilstein Journal of Organic Chemistry 2013
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