(2E,4Z)-1-(1-Oxo-2,4-decadienyl)-piperidin
Compound with spectra: 4 NMR, and 3 MS (GC)
| SpectraBase Compound ID | HMjlRLgeprA |
|---|---|
| InChI | InChI=1S/C15H25NO/c1-2-3-4-5-6-7-9-12-15(17)16-13-10-8-11-14-16/h6-7,9,12H,2-5,8,10-11,13-14H2,1H3/b7-6+,12-9+ |
| InChIKey | ZPSGREUUQGTKDE-ZICOIJLXSA-N |
| Mol Weight | 235.37 g/mol |
| Molecular Formula | C15H25NO |
| Exact Mass | 235.193614 g/mol |
| Copyright | Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| 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 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | SK-28-247-3 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | SK-28-244-3 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | F-42-4980-7 |
- PIPERIDIDE-2E,4E-DECADIENAMIDE
- (2E,4E)-N-DEC-2,4-DIENOYL-PIPERIDINE
- Achillea Amide
(2E,4Z)-1-(1-Oxo-2,4-octadienyl)-piperidin
SARMENTINE;(2E,4E)-N-DEC-2,4-DIENOYL-PYRROLIDINE
1-(1-Oxo-2,4-decadienyl)pyrolidine
1-[(2-E,4-E)-2,4-DODECADIENOYL]-PYRROLIDINE
(2E,4Z)-1-(1-Oxo-2,4-tetradecadienyl)-pyrrolidin
Trichonine
1-Oxo-1-pyrroridino-icosa-2,4-diene
(2E,4E,6E)-N-DODEC-2,4,6-TRIENOYL-PYRROLIDINE
(E)-1-(1-piperidinyl)-2-octadecen-1-one
| Title | Journal or Book | Year |
|---|---|---|
| Occurrence, biological activities and 13C NMR data of amides from Piper (Piperaceae) | Química Nova | 2012 |
| Two amides from Piper tuberculatum fruits | Fitoterapia | 2001 |
| A facile synthesis of 3,4-dienamides by the reaction of propargyl alcohols with cyclic amide acetals, and their stereoselective rearrangement to 2(E),4(Z)-dienamides promoted with alumina. Total synthesis of isochavicine | The Journal of Organic Chemistry | 1984 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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KnowItAll Mass Spectral Library
Author: Wiley
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