DICYCLOETHER,EN-YNE
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 103031
Name
DICYCLOETHER,EN-YNE
Also reported as
DICYCLOETHER,EN-YNE: CIS; DICYCLOETHER,EN-YNE: TRANS; DIOXASPIRO-(4-4)-NON-3-ENE,1-6: 2-(HEXA-2-4-DIYNYLIDENE)
IUPAC name
2-(hexa-2,4-diyn-1-ylidene)-1,6-dioxaspiro[4.4]non-3-ene
SMILES
CC#CC#CC=C1C=CC2(O1)CCCO2
Molecular formula
C13H12O2
Molecular weight
200.24 g/mol
Monoisotopic mass
200.0837 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Matricaria chamomilla L. | aerial parts | - |
Mericli, A.H. (1990). The lipophilic compounds of a turkish Matricaria chamomilla variety with no chamazulene in the volatile oil. Int J Crude Drug Res, 28(2), 145-147 doi:10.3109/13880209009082799
|
| Matricaria chamomilla L. | essential oil | - |
Hethelyi, E., Palfineledniczky, M., Wilde, P.F., Zambo, I., Palinkas, J. (1999). Gas chromatography analysis of the essential oil and extract of the chamomile. Olaj Szappan Kozmet, 48(1), 26-32
|
| Matricaria chamomilla L. | essential oil | - |
Repcak, M., Imrich, J., Garcar, J. (1999). Quantitative evaluation of the main sesquiterpenes and polyacetylenes of Chamomilla recutita essential oil by high-performance liquid chromatography. Phytochem Anal, 10(6), 335-338 doi:10.1002/(sici)1099-1565(199911/12)10:6
|
| Matricaria chamomilla L. | flower | - |
Debska, W., Wasiewiczowa, E., Bartkowiakowa, T. (1977). Method for detection and determination of chamazulene,bisabolol, and spiroether(2-(2,4-hexadiynylidene)-1,6-dioxaspiro(4,4-)non-3-ene) in chamomile (Matricaria chamomila) flower heads. Acta Pol Pharm, 34, 681
|
| Matricaria chamomilla L. | flower | - |
Scalia, S., Giuffreda, L., Pallado, P. (1999). Analytical and preparative supercritical fluid extraction of chamomile flowers and its comparison with conventional methods. J Pharm Biomed Anal, 21(3), 549-558 doi:10.1016/s0731-7085(99)00152-1
|