(2S,3R,4S,5S,6R)-4-[(1S,2S)-3-hydroxy-1-(4-hydroxy-3-methoxy-phenyl)-2-(2-methoxyphenoxy)propoxy]-2-methoxy-6-methylol-tetrahydropyran-3,5-diol
Compound with spectra: 1 NMR
![(2S,3R,4S,5S,6R)-4-[(1S,2S)-3-hydroxy-1-(4-hydroxy-3-methoxy-phenyl)-2-(2-methoxyphenoxy)propoxy]-2-methoxy-6-methylol-tetrahydropyran-3,5-diol](/api/compound/HJE1Qhpg72d.png?ph=true&h=300&w=458 "(2S,3R,4S,5S,6R)-4-[(1S,2S)-3-hydroxy-1-(4-hydroxy-3-methoxy-phenyl)-2-(2-methoxyphenoxy)propoxy]-2-methoxy-6-methylol-tetrahydropyran-3,5-diol")
| SpectraBase Compound ID | HJE1Qhpg72d |
|---|---|
| InChI | InChI=1S/C24H32O11/c1-30-15-6-4-5-7-16(15)33-19(12-26)22(13-8-9-14(27)17(10-13)31-2)35-23-20(28)18(11-25)34-24(32-3)21(23)29/h4-10,18-29H,11-12H2,1-3H3/t18-,19+,20+,21-,22+,23+,24+/m1/s1 |
| InChIKey | OFKQFCRGVZFVIF-AEGUFYCKSA-N |
| Mol Weight | 496.5 g/mol |
| Molecular Formula | C24H32O11 |
| Exact Mass | 496.194462 g/mol |
| Enantiomer InChIKey | OFKQFCRGVZFVIF-DHLGUUOTSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
JUNIPETRIOLOSIDE-A;3-METHOXY-4-HYDROXYPHENYLPROPANE-7,8-(2',1'-O-BETA-D-GLUCOPYRANOSYL)-7,8,9-TRIOL
ZHXOCQVYPCSBDX-CXJYHRMHSA-N
HOVETRICHOSIDE-B;(1S,2R)-1-(4-HYDROXY-3-METHOXYPHENYL)-2-(4-HYDROXY-3-METHOXYPHENYL)-1,3-PROPANEDIOL-1-O-BETA-D-GLUCOPYRANOSIDE
HOVETRICHOSIDE-A;(1R,2S)-1-(4-HYDROXY-3-METHOXYPHENYL)-2-(4-HYDROXY-3-METHOXYPHENYL)-1,3-PROPANEDIOL-1-O-BETA-D-GLUCOPYRANOSIDE
(-)-(7-S,8-R,7'-E)-4,7,9,3',9'-PENTAHYROXY-3-METHOXY-8-4'-OXYNEOLIGN-7'-ENE-3'-O-BETA-D-GLUCOPYRANOSIDE
SESQUMAROCANOL-B-HEXAACETATE;4,4'',7'',9,9',9''-HEXAHYDROXY-3,3',3''-TRIMETHOXY-4',8''-EPOXY-8,8'-SESQUINEOLIGNAN-HEXAACETATE
(-)-(7-R,8-S)-4,7,9,3',9'-PENTAHYROXY-3-METHOXY-8-4'-OXYNEOLIGNAN-3'-O-BETA-D-GLUCOPYRANOSIDE
(erythro)-1-O-(o-Chlorobenzoyl)-3-O-benzoyl-1-[4'-(benzyloxy)-3'-methoxyphenyl]-2-(4"-formyl-2"-methoxyphenoxy)propane-1,3-diol
(7R,8S,7'R,8'S)-NEO-OLIVIL-9'-O-BETA-D-GLUCOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Lignin–carbohydrate model compounds. Formation of lignin–methyl arabinoside and lignin–methyl galactoside benzyl ethers via quinone methide intermediates | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |