Methyl 4-methyl-5-oxo-5-phenylpentanoate
Compound with spectra: 2 NMR, and 1 MS (GC)
| SpectraBase Compound ID | LnyEqVOVyl4 |
|---|---|
| InChI | InChI=1S/C13H16O3/c1-10(8-9-12(14)16-2)13(15)11-6-4-3-5-7-11/h3-7,10H,8-9H2,1-2H3 |
| InChIKey | HBNYOKFRSJKPRE-UHFFFAOYSA-N |
| Mol Weight | 220.27 g/mol |
| Molecular Formula | C13H16O3 |
| Exact Mass | 220.109944 g/mol |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | C-125-7298-3da |
| 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-Hexanone, 2-methyl-1,6-diphenyl-
1,5-Pentanedione, 2,4-dimethyl-1,5-diphenyl-
(2R)-2-methyl-1-phenyl-hexane-1,4-dione
Benzenepentanoic acid, .gamma.-bromo-.delta.-oxo-
(2S)-2-METHYL-1,3-DIPHENYL-PROPAN-1-ONE
2-Methyl-1,3-diphenyl-1-propanone
2-Methyl-3-oxidanyl-1-phenyl-pentan-1-one
2-METHYL-1-PHENYL-PENTAN-1,3-DIONE
(2-Methyl-3-diethylamino)propiophenone
Methyl 3-methyl-5-oxo-5-phenylpentanoate
| Title | Journal or Book | Year |
|---|---|---|
| Michael Addition of Stannyl Ketone Enolate to α,β-Unsaturated Esters Catalyzed by Tetrabutylammonium Bromide and an ab Initio Theoretical Study of the Reaction Course | Journal of the American Chemical Society | 2003 |
| The First Michael Addition of Metal Ketone Enolates to α,β-Unsaturated Esters under Catalytic Conditions: Tin Enolate with a Catalytic Amount of Tetrabutylammonium Bromide | The Journal of Organic Chemistry | 1999 |
Wiley Registry of Mass Spectral Data 12th Edition
Author: Wiley
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