QVKJQJVJMKVRGS-MQIPJXDCSA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 3tWpWFMLuLw |
|---|---|
| InChI | InChI=1S/C16H24O3/c1-14(2)9-18-15(19-10-14)7-12-4-3-11-5-6-13(17)16(11,12)8-15/h11-12H,3-10H2,1-2H3/t11-,12-,16+/m0/s1 |
| InChIKey | QVKJQJVJMKVRGS-MQIPJXDCSA-N |
| Mol Weight | 264.36 g/mol |
| Molecular Formula | C16H24O3 |
| Exact Mass | 264.172545 g/mol |
| Enantiomer InChIKey | QVKJQJVJMKVRGS-HSMVNMDESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
GSPDFRQMJHXKCZ-JKIFEVAISA-N
Tricyclo[6.3.0.0(2,6)]undecan-10-one, 3-[(2-methoxyethoxy)methoxy]-2-methyl-
[[(3AS',4'R,5'R,6A'R)-4'-ALLYL-5,5-TRIMETHYLHEXAHYDRO-1'H-SPIRO-(1,3-DIOXANE-2,2'-PENTALEN)-5'-YL]-OXY]-(TERT.-BUTYL)-DIMETHYLSILANE
(Tetrahydro-5,5-dimethylspiro[1,3-dioxane-2,2'-(1'H)-pentalen]-5'(3'H)-ylidene)-5-methyl-2-(1'-methyl-1'-phenylethyl)cyclohexyl acetate
5-(t-Butyldimethylsilyloxy)-{4'-ethynyl-octahydro-5,5-dimethyl)-spiro[1,3-dioxan-2,2(1'H)-pentalene]}
(+-)-trans-(4a.alpha.,8a.beta.-4,4-(2,2-Dimethylpropylenedioxy)-6.alpha./.beta.,8.alpha./.beta.-dihydroxy-2,3,4,4a,5,6,7,8,8a-octahydro-1-naphthylenone
(+-)cis-(4a.alpha.,8a.alpha.-4,4-(2,2-Dimethylpropylenedioxy)-6.alpha.,7.alpha.-dihydroxy-2,3,4,4a,5,6,7,8,8a-octahydro-1-naphthylenone
4-Oxa-hexacyclo(5.4.1.0/2,6/.0/3,10/.0/5,9/.0/8,11/)dodecan-12-one
(3aS,6R,6aR)-6a-[(1,3-Dioxolan-2-yl)methyl]-3,3,6-trimethylhexahydro-1H-cyclopenta[c]furan-1-one
Spiro(bicycl[3.3.0]octan-8-one)-2,2'-(1',3'-dioxolane), 1,4',5'-trimethyl-
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of a Highly Functionalized Triquinane: Studies Towards a Total Synthesis of Subergorgic Acid and Its Analogues | Molecules | 2000 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.