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#12;[1-R-(1-ALPHA,3-ALPHA,4-BETA,4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA)]-1,3-EPOXYMETHANE-3,4,4A,5,6,7A-HEXAHYDRO-4,5-DIHYDROXY-7-BETA-(HYDROXYMETHYL)-6,7-OXIRENO-C

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

#12;[1-R-(1-ALPHA,3-ALPHA,4-BETA,4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA)]-1,3-EPOXYMETHANE-3,4,4A,5,6,7A-HEXAHYDRO-4,5-DIHYDROXY-7-BETA-(HYDROXYMETHYL)-6,7-OXIRENO-C
SpectraBase Compound ID 5JDn7kR7XbP
InChI InChI=1S/C10H14O6/c11-2-10-5-4(7(13)8(10)16-10)6(12)3-1-14-9(5)15-3/h3-9,11-13H,1-2H2/t3-,4+,5-,6-,7-,8+,9-,10-/m1/s1
InChIKey HHBQQDMJWHJTEU-POVGEQBLSA-N
Mol Weight 230.22 g/mol
Molecular Formula C10H14O6
Exact Mass 230.079038 g/mol
Enantiomer InChIKey HHBQQDMJWHJTEU-QOKORHTASA-N

View Spectrum of #12;[1-R-(1-ALPHA,3-ALPHA,4-BETA,4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA)]-1,3-EPOXYMETHANE-3,4,4A,5,6,7A-HEXAHYDRO-4,5-DIHYDROXY-7-BETA-(HYDROXYMETHYL)-6,7-OXIRENO-C

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-64-8309-12

View Spectrum of #12;[1-R-(1-ALPHA,3-ALPHA,4-BETA,4A-ALPHA,5-BETA,6-ALPHA,7A-ALPHA)]-1,3-EPOXYMETHANE-3,4,4A,5,6,7A-HEXAHYDRO-4,5-DIHYDROXY-7-BETA-(HYDROXYMETHYL)-6,7-OXIRENO-C

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
  • [1R-(1.alpha.,3.alpha.,4.beta.,4a.alpha.,5.beta.,6.alpha.,7a.alpha.,7b.alpha.)]-1,3-(Epoxymethane)-4,5-(dihydroxy)-7.beta.-[(hydroxy)methyl]-6,7-oxirenocyclopenta[c]pyran
JIOGLUTOSIDE_A;CATALPOGENIN-1-O-ALPHA-L-ARABINOFURANOSIDE
2,4-Diethoxy-7-hydroxy-8,9-epoxy-9-(dimethyl-t-butylsiloxymethyl)-3-oxa-bicyclo[4.3.0]-cyclononane
ASBLKZYJALKYNT-JHMKVRFYSA-N
5,6-BETA-EPOXY-7-BETA-HYDROXY-8-BETA-METHYL-1-BETA-D-RHAMNOSIDAL_IRIDOID
CAMINOSIDE_B
PNYGGTAQUVGFFF-BYMJKTJBSA-N
REHMAGLUTOSIDE_D
Propyl (5'R)-5',6-anhydro-(2',3',4',6'-tetramethoxy-.alpha.-D-lyxo-hexos-5'-ulopyranosyl)-(1-> 4)-2,3-dimethoxy-.beta.-L-gulopyranoside
RUPESIN-E
6-O-PARA-HYDROXYBENZOYLAJUGOL
Title Journal or Book Year
Iridoids from Carbohydrates via Pauson−Khand Reaction:  Synthesis of Advanced Highly Oxygenated Cyclopentane-Annulated Pyranosides from d-Glucal Derivatives The Journal of Organic Chemistry 1999
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