ETHYL-3-HYDROXY-3-METHYL-2-METHYLENE-4-OXO-HEXANOATE
Compound with spectra: 2 NMR
| SpectraBase Compound ID | CHWm0j5Ylrg |
|---|---|
| InChI | InChI=1S/C10H16O4/c1-5-8(11)10(4,13)7(3)9(12)14-6-2/h13H,3,5-6H2,1-2,4H3 |
| InChIKey | TZTSWEDZDQANLO-UHFFFAOYSA-N |
| Mol Weight | 200.23 g/mol |
| Molecular Formula | C10H16O4 |
| Exact Mass | 200.104859 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1-Ethoxycarbonyl-5-hydroxy-5-methylcyclopent-1-ene
Methyl (Z)-3-iodo-2-(1-hydroxy-cyclohexyl)prop-2-enoate
4-Methylene-1,2-dioxaspiro[4.4]nonan-3-one
6-HYDROXY-5,6-DIMETHYL-CYCLOHEX-4-ENE-1,3-DIONE
Triethyl citrate
6-Butyl-1-cyclohexenecarboxylic acid ethyl ester
ETHYL-(E)-2-CYClOHEXYL-3-(TRIMETHYLSILYL)-PROP-2-ENOATE
Dimethylethyl citrate
HELZLVLCDGFBJB-UHFFFAOYSA-N
2-(2-cyano-2-oxanyl)acetic acid ethyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Vinylalumination for the Synthesis of Functionalized Allyl Alcohols, Vinylepoxides, and α-Alkylidene-β-hydroxy-γ-lactones | The Journal of Organic Chemistry | 2003 |
| Direct Radical Polymerization of 4-Styryldiphenylphosphine: Preparation of Cross-Linked and Non-Cross-Linked Triphenylphosphine-Containing Polystyrene Polymers | The Journal of Organic Chemistry | 2003 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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