(5'R)-5'-hydroxy-1'-[[(5'R)-5'-hydroxy-4'-keto-2',5',7'-trimethyl-spiro[cyclopropane-1,6'-indene]-1'-yl]methoxymethyl]-2',5',7'-trimethyl-spiro[cyclopropane-1,6'-indene]-4'-one
Compound with spectra: 1 NMR
![(5'R)-5'-hydroxy-1'-[[(5'R)-5'-hydroxy-4'-keto-2',5',7'-trimethyl-spiro[cyclopropane-1,6'-indene]-1'-yl]methoxymethyl]-2',5',7'-trimethyl-spiro[cyclopropane-1,6'-indene]-4'-one](/api/compound/JQ5xiIIZCvy.png?ph=true&h=300&w=458 "(5'R)-5'-hydroxy-1'-[[(5'R)-5'-hydroxy-4'-keto-2',5',7'-trimethyl-spiro[cyclopropane-1,6'-indene]-1'-yl]methoxymethyl]-2',5',7'-trimethyl-spiro[cyclopropane-1,6'-indene]-4'-one")
| SpectraBase Compound ID | JQ5xiIIZCvy |
|---|---|
| InChI | InChI=1S/C30H34O5/c1-15-11-19-23(17(3)29(7-8-29)27(5,33)25(19)31)21(15)13-35-14-22-16(2)12-20-24(22)18(4)30(9-10-30)28(6,34)26(20)32/h11-12,33-34H,7-10,13-14H2,1-6H3/t27-,28-/m0/s1 |
| InChIKey | LALKVQWTTJQTQA-NSOVKSMOSA-N |
| Mol Weight | 474.6 g/mol |
| Molecular Formula | C30H34O5 |
| Exact Mass | 474.240624 g/mol |
| Enantiomer InChIKey | LALKVQWTTJQTQA-VSGBNLITSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(5'R)-1'-(2-bromoethoxymethyl)-5'-hydroxy-2',5',7'-trimethylspiro[cyclopropane-1,6'-indene]-4'-one
(5'R)-1'-(ethoxymethyl)-5'-hydroxy-2',5',7'-trimethylspiro[cyclopropane-1,6'-indene]-4'-one
(5'R)-5'-hydroxy-1'-(2-hydroxyethoxymethyl)-2',5',7'-trimethylspiro[cyclopropane-1,6'-indene]-4'-one
(5'R)-1'-(glyceryloxymethyl)-5'-hydroxy-2',5',7'-trimethyl-spiro[cyclopropane-1,6'-indene]-4'-one
(5'R)-5'-hydroxy-1'-(methoxymethyl)-2',5',7'-trimethylspiro[cyclopropane-1,6'-indene]-4'-one
acetic acid [(5'R)-5'-hydroxy-4'-keto-2',5',7'-trimethyl-spiro[cyclopropane-1,6'-indene]-1'-yl]methyl ester
(5'R)-5'-hydroxy-1'-(3-hydroxypropyl)-2',5',7'-trimethylspiro[cyclopropane-1,6'-indene]-4'-one
3-[(5'R)-5'-hydroxy-4'-keto-2',5',7'-trimethyl-spiro[cyclopropane-1,6'-indene]-1'-yl]propionaldehyde
RUTAECARPINE-ALKALOID
ACHIFOLIDIEN,ISO
| Title | Journal or Book | Year |
|---|---|---|
| Structure−Activity Studies of Antitumor Agent Irofulven (Hydroxymethylacylfulvene) and Analogues | The Journal of Organic Chemistry | 2001 |