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(2R,4R)-2-BENZYLOXY-4-[(1R)-1-PHENYLETHOXY]-6-TRIFLUOROMETHYL-3,4-DIHYDRO-PYRAN;MAJOR-ISOMER

Compound with spectra: 2 NMR, and 1 MS (GC)

(2R,4R)-2-BENZYLOXY-4-[(1R)-1-PHENYLETHOXY]-6-TRIFLUOROMETHYL-3,4-DIHYDRO-PYRAN;MAJOR-ISOMER
SpectraBase Compound ID 57mbi41EQlg
InChI InChI=1S/C21H21F3O3/c1-15(17-10-6-3-7-11-17)26-18-12-19(21(22,23)24)27-20(13-18)25-14-16-8-4-2-5-9-16/h2-12,15,18,20H,13-14H2,1H3
InChIKey JATJDWWGLRWTPR-UHFFFAOYSA-N
Mol Weight 378.39 g/mol
Molecular Formula C21H21F3O3
Exact Mass 378.144279 g/mol

View Spectrum of (2R,4R)-2-BENZYLOXY-4-[(1R)-1-PHENYLETHOXY]-6-TRIFLUOROMETHYL-3,4-DIHYDRO-PYRAN;MAJOR-ISOMER

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

View Spectrum of (2R,4R)-2-BENZYLOXY-4-[(1R)-1-PHENYLETHOXY]-6-TRIFLUOROMETHYL-3,4-DIHYDRO-PYRAN;MAJOR-ISOMER

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum B-52-925-8

View Spectrum of (2R,4R)-2-BENZYLOXY-4-[(1R)-1-PHENYLETHOXY]-6-TRIFLUOROMETHYL-3,4-DIHYDRO-PYRAN;MAJOR-ISOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
  • 2-Benzyloxy-4-(1'-phenylethoxy)-6-(trifluoromethyl)-3,4-dihydro-2H-pyran
(2S,4S)-2-BENZYLOXY-4-[(1R)-1-PHENYLETHOXY]-6-TRIFLUOROMETHYL-3,4-DIHYDRO-2H-PYRAN;MINOR-ISOMER
(2S,4R,6R)-2,4-Diphenyl-6-((E)-styryl)tetrahydro-2H-pyran
(2S,4S)-2,4-Diphenyl-6-((E)-styryl)tetrahydro-2H-pyran
4',5'-Diphenylspiro[cyclohexene-1,2'-1',3'-dioxacyclopentane]
(S)-1-PHENYLETHYL_BETA-D-GALACTOPYRANOSIDE
(R)-1-PHENYLETHYL_BETA-D-GALACTOPYRANOSIDE
.beta.-D-erythro-Hex-2-enopyranoside, phenyl 2,3-dideoxy-4,6-bis-O-(phenylmethyl)-
.alpha.-D-erythro-Hex-2-enopyranoside, phenyl 2,3-dideoxy-4,6-bis-O-(phenylmethyl)-
Methyl (2SR,5RS)-5-ethyl-2-phenyl-2,5-dihydro-3-furancarboxylate
1,5-ANHYDRO-2,3-DI-O-BENZOYL-4,6-DIDEOXY-L-THREOHEX-4-ENITOL
Title Journal or Book Year
A Stereoselective Synthesis of 2,6-Dideoxy-6,6,6-trifluoro-arabino-hexoses via an Asymmetric Diels - Alder Strategy Australian Journal of Chemistry 1999
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