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(4R,5S)-5-HYDROXY-2-HEXEN-4-OLIDE

Compound with spectra: 2 NMR

(4R,5S)-5-HYDROXY-2-HEXEN-4-OLIDE
SpectraBase Compound ID BDYt4n1RAyQ
InChI InChI=1S/C6H8O3/c1-4(7)5-2-3-6(8)9-5/h2-5,7H,1H3/t4-,5-/m1/s1
InChIKey BGMOXLYBBTWIMD-RFZPGFLSSA-N
Mol Weight 128.13 g/mol
Molecular Formula C6H8O3
Exact Mass 128.047344 g/mol
Enantiomer InChIKey BGMOXLYBBTWIMD-WHFBIAKZSA-N

View Spectrum of (4R,5S)-5-HYDROXY-2-HEXEN-4-OLIDE

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

View Spectrum of (4R,5S)-5-HYDROXY-2-HEXEN-4-OLIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
  • (5R,6R)-5-(1-HYDROXYETHYL)-2(5H)-FURANONE
(5R,1'S)-5-(1'-Hydroxyethyl)-2(5H)-furanone
No Name
(5S,6R)-5-(1-HYDROXYETHYL)-2(5H)-FURANONE
2(5H)-Furanone, 5-(1-methylethyl)-
Methyl 4,5-dihydroxy-2-hexenoate
2-Propyl-2H-furan-5-one
2(5H)-Furanone, 5-(methoxymethyl)-, (S)-
(2R)-2-(2-hydroxyethyl)-2H-furan-5-one
Ethyl (4r*,5r*)-(e)-4,5-dihydroxy-2-hexenoate
Methyl (E)-4,5-Epoxyhex-2-enoate
Title Journal or Book Year
The glycosidic precursor of (Z)-5-ethylidene-2(5H)-furanone in Halocarpus biformis juvenile foliage Phytochemistry 1996
(+)-Osmundalactone, γ-lactones and spiromentins from the fungus Paxillus atrotomentosus Phytochemistry 1995

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