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(1R,4R,5R,9S,11R)-4,5-EPOXYCARYOPHYLL-8(14)-EN-12-OIC_ACID

Compound with spectra: 2 NMR

(1R,4R,5R,9S,11R)-4,5-EPOXYCARYOPHYLL-8(14)-EN-12-OIC_ACID
SpectraBase Compound ID 6wnHeJI6RJF
InChI InChI=1S/C15H22O3/c1-9-4-5-12-15(3,18-12)7-6-11-10(9)8-14(11,2)13(16)17/h10-12H,1,4-8H2,2-3H3,(H,16,17)/t10-,11-,12-,14-,15-/m1/s1
InChIKey FQFXKSTXOZAVQJ-URFZWBKFSA-N
Mol Weight 250.34 g/mol
Molecular Formula C15H22O3
Exact Mass 250.156895 g/mol
Enantiomer InChIKey FQFXKSTXOZAVQJ-YLXLXVFQSA-N

View Spectrum of (1R,4R,5R,9S,11R)-4,5-EPOXYCARYOPHYLL-8(14)-EN-12-OIC_ACID

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

View Spectrum of (1R,4R,5R,9S,11R)-4,5-EPOXYCARYOPHYLL-8(14)-EN-12-OIC_ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
1,5,5-TRIMETHYL-8-METHYLENE-13-(E)-1-PROPENYL-4-BETA,7-ALPHA-12,14-DIOXATRICYClO-[9.3.0.0(4.7)]-TETRADECANE
13-VINYL-1,5,5-TRIMETHYL-8-METHYLENE-4-BETA,7-ALPHA-12,14-DIOXATRICYClO-[9.3.0.0(4.7)]-TETRADECANE
(1-R,4-R,5-R,6-R,9-S,11-R)-4,5-EPOXY-8-(14)-CARYOPHYLLENE-6,12-DIOL
ACALYCIXENIOLIDE-F
GIBBEROSIN-Q;(1S,4S,9R,11S)-15-ACETOXY-XENIAPHYLLA-8(9)-EN-5,12-DIONE
GIBBEROSIN-O;(1S,4S,9R,11S)-15-ACETOXY-16-NOR-XENIAPHYLLA-8(19)-EN-5,12-DIONE
MANAARENOLIDE_A;(1-R,3-R,4-S,7-R,11-S,12-S,15-S)-4-HYDROXY-7-HYDROPEROXY-11,12-EPOXYCEMBR-8-(19)-EN-16,3-OLIDE
MANAARENOLIDE_C;(1-R,3-R,4-S,7-R,11-S,12-S,15-S)-4,7-DIHYDROXY-11,12-EPOXYCEMBR-8-(19)-EN-16,3-OLIDE
MANAARENOLIDE_D;(1-R,3-R,4-S,7-S,11-S,12-S,15-S)-4,7-DIHYDROXY-11,12-EPOXYCEMBR-8-(19)-EN-16,3-OLIDE
(3S,4S,5R)-5-Acetoxy-3-bromo-4-hydroxycaryophyll-8(13)-ene
Title Journal or Book Year
New β-Caryophyllene-Derived Terpenoids from the Soft Coral Sinularia nanolobata Journal of Natural Products 2004
Biotransformation of caryophyllene by Diplodia gossypina Phytochemistry 1990

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