cis-Jasmone
cis-Jasmone structure
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Common Name | cis-Jasmone | ||
|---|---|---|---|---|
| CAS Number | 488-10-8 | Molecular Weight | 164.244 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 264.2±0.0 °C at 760 mmHg | |
| Molecular Formula | C11H16O | Melting Point | 203 - 205ºC | |
| MSDS | Chinese USA | Flash Point | 107.2±0.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Comparison of Aroma-Active Volatiles in Oolong Tea Infusions Using GC-Olfactometry, GC-FPD, and GC-MS.
J. Agric. Food Chem. 63 , 7499-510, (2015) The aroma profile of oolong tea infusions (Dongdingwulong, DDWL; Tieguanyin, TGY; Dahongpao, DHP) were investigated in this study. Gas chromatography-olfactometry (GC-O) with the method of aroma intensity (AI) was employed to investigate the aroma-active comp... |
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Chemical composition of the essential oil of Feronia elephantum Correa.
Nat. Prod. Res. 24(19) , 1807-10, (2010) The essential oil composition of Feronia elephantum Correa (family: Rutaceae) was examined by capillary gas chromatography (GC) and gas chromatography-mass spectroscopy (GC-MS). The analysis revealed the presence of 24 constituents, of which 18 constituents w... |
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cis-Jasmone induces accumulation of defence compounds in wheat, Triticum aestivum.
Phytochemistry 69(1) , 9-17, (2008) Liquid phase extraction (LPE) and vapor phase extraction (VPE) methodologies were used to evaluate the impact of the plant activator, cis-jasmone, on the secondary metabolism of wheat, Triticum aestivum, var. Solstice. LPE allowed the measurement of benzoxazi... |
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Aphid antixenosis in cotton is activated by the natural plant defence elicitor cis-jasmone.
Phytochemistry 78 , 81-8, (2012) Upon insect herbivory, plants can release blends of volatile organic compounds (VOCs) that modify herbivore and natural enemy behaviour. We have shown recently that cotton, Gossypium hirsutum, emits a blend of defence VOCs that repels the cotton aphid, Aphis ... |
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Microwave assisted synthesis of fragrant jasmone heterocyclic analogues.
Eur. J. Med. Chem. 41(5) , 586-91, (2006) cis-Jasmone, from jasmonoid group, is an important jasmine odor fragrance compound. The syntheses of new heterocyclic analogues of jasmone were described. Five analogues of this compound were prepared under microwave irradiation and the results of the microwa... |
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Treating hop plants with (Z)-jasmone increases colonization by Phorodon humuli (Hemiptera: Aphididae) spring migrants.
Bull. Entomol. Res. 97(3) , 317-9, (2007) Hop plants were sprayed with (Z)-jasmone, at a rate of 50 g ha(-1), during the spring migration of the damson-hop aphid Phorodon humuli (Schrank) in 2002 and 2003. Numbers of P. humuli spring migrants colonizing hop plants, Humulus lupulus L., 2-6 and 7-11 da... |
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Iso-OPDA: an early precursor of cis-jasmone in plants?
ChemBioChem. 8(18) , 2281-5, (2007) Cis-jasmone is a highly appreciated fragrance and plant-derived signal molecule that controls pollination, attracts parasitoids of attacking herbivores, and serves as an intra- and interspecific signal that controls gene expression. cis-Jasmone is produced fr... |
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Microwave assisted synthesis of unsaturated jasmone heterocyclic analogues as new fragrant substances.
Eur. J. Med. Chem. 44(7) , 3032-9, (2009) Taking the rising interest in jasmone structure based fragrant compounds into account it has been decided to take up an attempt to synthesize the new heterocyclic derivatives of this 2,3-disubstituted cyclopentenone, which could be characterized by the abilit... |
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Fragrance material review on cis-jasmone.
Food Chem. Toxicol. 50 Suppl 3 , S613-8, (2012) A toxicologic and dermatologic review of cis-jasmone when used as a fragrance ingredient is presented. cis-Jasmone is a member of the fragrance structural group ketones cyclopentanones and cyclopentenones. The common characteristic structural element of the g... |
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Attraction of New Zealand flower thrips, Thrips obscuratus, to cis-jasmone, a volatile identified from Japanese honeysuckle flowers.
J. Chem. Ecol. 35(6) , 656-63, (2009) This work was undertaken to identify floral compound(s) produced by honeysuckle flowers, Lonicera japonica (Thunberg), that mediate the attraction of New Zealand flower thrips Thrips obscuratus (Crawford). Volatiles were collected during the day and night and... |