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DL-15-Deoxy-16-hydroxy-16-(trifluoromethyl)-prostaglandin-E2,epimer-1

Compound with spectra: 4 NMR

DL-15-Deoxy-16-hydroxy-16-(trifluoromethyl)-prostaglandin-E2,epimer-1
SpectraBase Compound ID KqeXuqN6rYH
InChI InChI=1S/C21H31F3O5/c1-2-3-12-20(29,21(22,23)24)13-8-10-16-15(17(25)14-18(16)26)9-6-4-5-7-11-19(27)28/h4,6,8,10,15-16,18,26,29H,2-3,5,7,9,11-14H2,1H3,(H,27,28)/b6-4+,10-8+
InChIKey WCQZTKXGUDCWSV-ONNLMXTPSA-N
Mol Weight 420.47 g/mol
Molecular Formula C21H31F3O5
Exact Mass 420.212359 g/mol

View Spectrum of DL-15-Deoxy-16-hydroxy-16-(trifluoromethyl)-prostaglandin-E2,epimer-1

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3

View Spectrum of DL-15-Deoxy-16-hydroxy-16-(trifluoromethyl)-prostaglandin-E2,epimer-1

13C NMR Spectrum
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3

View Spectrum of DL-15-Deoxy-16-hydroxy-16-(trifluoromethyl)-prostaglandin-E2,epimer-1

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of DL-15-Deoxy-16-hydroxy-16-(trifluoromethyl)-prostaglandin-E2,epimer-1

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • DL-15-Deoxy-16-hydroxy-16-(trifluoromethyl)-prostaglandin-E2,epimer-2
DL-15-Deoxy-16-hydroxy-16-(difluoromethyl)-prostaglandin-E2,epimer-1
METHYL-(4,5,6S)-7-[(1S,2S,3S)-3-HYDROXY-2-[(E)-(3S)-3-HYDROXY-4-PHENOXY-1-BUTENYL]-5-OXOCYClOPENTYL]-4,5-HEPTADIENOATE
METHYL-(4,5,6S)-7-[(1R,2R,3R)-3-HYDROXY-2[(E)-(3R)-3-HYDROXY-4-PHENOXY-1-BUTENYL]-5-OXOCYClOPENTYL]-4,5-HEPTADIENOATE
Prost-13-en-1-oic acid, 11,15-dihydroxy-7,9-dioxo-, (11.alpha.,13E,15S)-
7-([1R,2R,3R,5S]-2-[4-(3-Chloro-phenoxy)-3-hydroxy-trans-1-butenyl]-3,5-dihydroxy-cyclopentyl)-cis-5-heptenoate
16-(META-CHLOROPHENOXY)-PROSTAGLANDIN PGF2 ALPHA
15-EPI-16-(META-CHLOROPHENOXY)-PROSTAGLANDIN PGF2 ALPHA
CLOPROSTENOL
1-(Trifluoromethyl)-2,3,5,6,7,7a-hexahydroinden-1-ol
8-Hydroxy-6-methylbicyclo[5.4.0]undec-5-en-2-one
Title Journal or Book Year
Prostaglandins and congeners. 27. Synthesis of biologically active 16-halomethyl derivatives of 15-deoxy-16-hydroxyprostaglandin E2 The Journal of Organic Chemistry 1980

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