ETHYL-2-(1-HYDROXY-2-METHYLPROPYL)-ACRYLATE
Compound with spectra: 2 NMR
| SpectraBase Compound ID | F60j39skb1k |
|---|---|
| InChI | InChI=1S/C9H16O3/c1-5-12-9(11)7(4)8(10)6(2)3/h6,8,10H,4-5H2,1-3H3 |
| InChIKey | KPMZLFYCDSSNIF-UHFFFAOYSA-N |
| Mol Weight | 172.22 g/mol |
| Molecular Formula | C9H16O3 |
| Exact Mass | 172.109944 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 |
ETHYL-2-(2-BROMO-1-HYDROXYETHYL)-ACRYLATE
Butanoic acid, 3-hydroxy-2-methylene-, butyl ester
Isobutyl 2-(1-hydroxyethyl)acrylate
Isopentyl 2-(1-hydroxyethyl)acrylate
ETHYL-2-OXIRAN-2-YLACRYLATE
(-)-3-Methroxy-4-methyl-2-methylenepentanoic acid
Butanoic acid, 3-hydroxy-2-methylene-, 1,1-dimethylethyl ester
3-Hydroxy-4-methyl-2-methylene-4-pentenoic acid methyl ester
2-(1-hydroxy-3-methoxy-propyl)acrylic acid methyl ester
2-(4-Chloro-1-hydroxy-butyl)acrylic acid methyl 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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