(3A-ALPHA,8A-ALPHA)-3-ALPHA-BROMO-3-BETA,6-ALPHA-DIMETHYLOCTAHYDRO-2H-CYCLOHEPTA-[B]-FURAN-2-ONE
Compound with spectra: 1 NMR
![(3A-ALPHA,8A-ALPHA)-3-ALPHA-BROMO-3-BETA,6-ALPHA-DIMETHYLOCTAHYDRO-2H-CYCLOHEPTA-[B]-FURAN-2-ONE](/api/compound/LGB2gINoHjj.png?ph=true&h=300&w=458 "(3A-ALPHA,8A-ALPHA)-3-ALPHA-BROMO-3-BETA,6-ALPHA-DIMETHYLOCTAHYDRO-2H-CYCLOHEPTA-[B]-FURAN-2-ONE")
| SpectraBase Compound ID | LGB2gINoHjj |
|---|---|
| InChI | InChI=1S/C11H17BrO2/c1-7-3-5-8-9(6-4-7)14-10(13)11(8,2)12/h7-9H,3-6H2,1-2H3/t7-,8-,9+,11+/m1/s1 |
| InChIKey | TVEQJFFNMRDGJO-REIXXSIJSA-N |
| Mol Weight | 261.16 g/mol |
| Molecular Formula | C11H17BrO2 |
| Exact Mass | 260.041193 g/mol |
| Enantiomer InChIKey | TVEQJFFNMRDGJO-WYOJIJJFSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3-Carbomethoxy-6-isopropyl-1-oxa-3,3a,4,5,6,7,8,8a-octahydroazulen-2(1h)-one
(4-S*,7-R*,8-R*,11-R*)-3-OXOGERMACR-1-(10)-E-EN-8,12-OLIDE
3,8-Dioxo-2,7,11-trimethyl-4-oxabicyclo[8.3.0]tridec-10-ene
(E)-3,6,10-Trimethyl-3a,5,8,10,11,11a-hexahydro-3H,4H-cyclodeca[b]furan-2,9-dione
3-OXO-7-ALPHA,11-ALPHA-H-GERMACRA-1E-EN-12,6-BETA-OLIDE
KETOPELENOLIDE-B;(4R*,6R*,7S*,11R*)-3-OXOGERMACR-1(10)-(E)-EN-12,6-ALPHA-OLIDE
Ethyl (3a.beta.,8a.beta.)-Octahydro-3-methylene-2-oxo-2H-cyclohepta[b]furan-6-carboxylate
(+-)-2,5-Dioxoperhydrocycloocta[b]furan-3-carboxylic acid
4.Xi.-Germacr-9-en-12-oic acid, 6.alpha.-hydroxy-1-oxo-, .gamma.-lactone, (11S)-
| Title | Journal or Book | Year |
|---|---|---|
| Synthetic Method and Biological Activities of cis-Fused α-Methylene γ-Lactones | Journal of Natural Products | 2003 |