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(2S,4R)-P-MENTHA-1(7),5-DIEN-2-YL-HYDROPEROXIDE;(1S,5R)-5-(1-METHYLETHYL)-2-METHYLIDEN-3-CYCLOHEXEN-1-YL-HYDROPEROXIDE

Compound with spectra: 2 NMR

(2S,4R)-P-MENTHA-1(7),5-DIEN-2-YL-HYDROPEROXIDE;(1S,5R)-5-(1-METHYLETHYL)-2-METHYLIDEN-3-CYCLOHEXEN-1-YL-HYDROPEROXIDE
SpectraBase Compound ID DxmgHHojMEo
InChI InChI=1S/C10H16O2/c1-7(2)9-5-4-8(3)10(6-9)12-11/h4-5,7,9-11H,3,6H2,1-2H3/t9-,10+/m0/s1
InChIKey ALLLDRGXVPEYEI-VHSXEESVSA-N
Mol Weight 168.24 g/mol
Molecular Formula C10H16O2
Exact Mass 168.11503 g/mol
Enantiomer InChIKey ALLLDRGXVPEYEI-ZJUUUORDSA-N

View Spectrum of (2S,4R)-P-MENTHA-1(7),5-DIEN-2-YL-HYDROPEROXIDE;(1S,5R)-5-(1-METHYLETHYL)-2-METHYLIDEN-3-CYCLOHEXEN-1-YL-HYDROPEROXIDE

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

View Spectrum of (2S,4R)-P-MENTHA-1(7),5-DIEN-2-YL-HYDROPEROXIDE;(1S,5R)-5-(1-METHYLETHYL)-2-METHYLIDEN-3-CYCLOHEXEN-1-YL-HYDROPEROXIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
  • 2-(S)-HYDROPEROXY-4-(R)-PARA-MENTHA-1(7),5-DIENE
(2R,4R)-P-MENTHA-1(7),5-DIEN-2-HYDROPEROXIDE;(1R,5R)-5-(1-METHYLETHYL)-2-METHYLIDEN-3-CYCLOHEXEN-1-YL-HYDROPEROXIDE
Hydroperoxide, 2-methylene-5-(1-methylethyl)-3-cyclohexen-1-yl, (1R-cis)-
5-Cyclodecen-1-ol, 7-methylene-4-(1-methylethyl)-, [1S-(1R*,5E,7R*)]-
METHANOL, [4-(1-METHYLETHYL)-2-CYCLOHEXEN-1-YLIDENE]- ACETATE
D-Germacrene
4-Isopropyl-6-methoxy-1-methyl-1-cyclohexene
(6S,7S)-.beta.-sesquiphellandrene
3-Methylene-6-[(2S)-6-methylhept-5-en-2-yl]cyclohexene
1-Oxo-5-methylene-8-isopropylcyclodeca-2,6-diene
2,6-Cyclodecadien-1-one, 5-methylene-8-(1-methylethyl)-, [S-(Z,E)]-
Title Journal or Book Year
Phytochemistry of Trattinnickia burserifolia, T. rhoifolia, and Dacryodes hopkinsii: chemosystematic implications Journal of the Brazilian Chemical Society 2004
Konkurrenz von Endoperoxid- und Hydroperoxid-Bildung bei der Umsetzung von Singulett-Sauerstoff mit cyclischen, konjugierten Dienen. Teil I Helvetica Chimica Acta 1989

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