(3,5-dimethylisoxazol-4-yl)-(2-methylolpyrrolidin-1-yl)methanone
Compound with spectra: 2 NMR
| SpectraBase Compound ID | 2rSUnnfo7o0 |
|---|---|
| InChI | InChI=1S/C11H16N2O3/c1-7-10(8(2)16-12-7)11(15)13-5-3-4-9(13)6-14/h9,14H,3-6H2,1-2H3 |
| InChIKey | XWKYMBLGGCOTCQ-UHFFFAOYSA-N |
| Mol Weight | 224.26 g/mol |
| Molecular Formula | C11H16N2O3 |
| Exact Mass | 224.116092 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. |
|---|
N,N,3-trimethyl-5-phenyl-1,2-oxazole-4-carboxamide
(R)-(+)-1-(2-Methoxybenzoyl)-2-pyrrolidinemethanol
(S)-(-)-1-(2-Methoxybenzoyl)-2-pyrrolidinemethanol
(2-methoxyphenyl)-(2-methylolpyrrolidin-1-yl)methanone
5-Methyl-3,4-isoxazoledicarboxylic acid, 4-T-buty L amide 3-methyl ester
3-ethyl-5-methyl-N-(5-methyl-3-isoxazolyl)-4-isoxazolecarboxamide
N,5-dimethyl-3-(4-fluorophenyl)-4-isoxazolecarboxamide
1-(2,6-Dichlorobenzoyl)proline
1,2,4-oxadiazole-5-carboxamide, N-[(3,5-dimethyl-4-isoxazolyl)methyl]-3-(4-pyridinyl)-
| Title | Journal or Book | Year |
|---|---|---|
| Selective lateral metalation and electrophilic quenching of c-4 functionalized isoxazoles.IX. Direct formation of the C-N bond utilizing an electrophilic nitrogen source | Journal of Heterocyclic Chemistry | 1990 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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