(TRANS)-(3R,4S,4AR)-7-BROMO-8-METHOXY-4-[(2-METHOXYETHOXY)-METHOXY]-3-METHYL-2,3,4,4A-TETRAHYDRO-1H-XANTHEN-1-ONE
Compound with spectra: 1 NMR
![(TRANS)-(3R,4S,4AR)-7-BROMO-8-METHOXY-4-[(2-METHOXYETHOXY)-METHOXY]-3-METHYL-2,3,4,4A-TETRAHYDRO-1H-XANTHEN-1-ONE](/api/compound/1UuLJr6jCaA.png?ph=true&h=300&w=458 "(TRANS)-(3R,4S,4AR)-7-BROMO-8-METHOXY-4-[(2-METHOXYETHOXY)-METHOXY]-3-METHYL-2,3,4,4A-TETRAHYDRO-1H-XANTHEN-1-ONE")
| SpectraBase Compound ID | 1UuLJr6jCaA |
|---|---|
| InChI | InChI=1S/C19H23BrO6/c1-11-8-15(21)12-9-13-16(5-4-14(20)18(13)23-3)26-19(12)17(11)25-10-24-7-6-22-2/h4-5,9,11,17,19H,6-8,10H2,1-3H3/t11-,17+,19-/m1/s1 |
| InChIKey | RZPBZXSXMYGHBC-XTDINYQCSA-N |
| Mol Weight | 427.29 g/mol |
| Molecular Formula | C19H23BrO6 |
| Exact Mass | 426.067801 g/mol |
| Enantiomer InChIKey | RZPBZXSXMYGHBC-JVMOKEISSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
6-DEOXY-1,2:3,4-DI-O-ISOPROPYLIDENE-6-C-[METHYL-2,3,4-TRI-O-BENZYL-7-DEOXY-D-GLYCERO-ALPHA-D-GLUCO-HEPTOPYRANOSID-7-(E)-YLIDENE]-ALPHA-D-
3'-SINAPOYL-6-FERULOYLSUCROSE
2-Anthraceneacetic acid, 4,10-dihydroxy-5-methoxy-3-(methoxycarbonyl)-, methyl ester
5,3',4'-TRIHYDROXY-6'',6''-DIMETHYL-PYRANO-[2'',3'':7,6]-ISOFLAVONE
1,4-Epoxyanthracene, 1,2,3,4,4a,10-hexahydro-5-methoxy-2,3-bis(methylene)-, (1.alpha.,4.alpha.,4a.alpha.)-(.+-.)-
6-[8-Methyl-8-(4-methyl-3-pentenyl)-3,4-dihydro-2H,8H-pyrano[2,3-f]chromen-3-yl]-1,3-benzodioxol-5-ol
5,7,2',6'-TETRAHYDROXYFLAVONE-2'-O-BETA-D-GLUCOPYRANOSIDE
TRICIN-5-O-BETA-D-GLUCOPYRANOSIDE
2-Butenedioic acid, 2-[1,2,3,4-tetrahydro-1,3-dimethyl-2,4-dioxo-6-[(triphenylphosphoranylidene)amino]-5-pyrimidinyl]-, diethyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Total Synthesis of Blennolide Mycotoxins: Design, Synthetic Routes and Completion | European Journal of Organic Chemistry | 2014 |