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Cis-jasmone

CAS No.:
488-10-8
Catalog Number:
AG0034MB
Molecular Formula:
C11H16O
Molecular Weight:
164.2441
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$13
- +
5g
95%
In Stock USA
United States
$29
- +
25g
95%
In Stock USA
United States
$74
- +
100g
95%
In Stock USA
United States
$125
- +
500g
95%
In Stock USA
United States
$500
- +
Product Description
Catalog Number:
AG0034MB
Chemical Name:
Cis-jasmone
CAS Number:
488-10-8
Molecular Formula:
C11H16O
Molecular Weight:
164.2441
MDL Number:
MFCD00001402
IUPAC Name:
3-methyl-2-[(Z)-pent-2-enyl]cyclopent-2-en-1-one
InChI:
InChI=1S/C11H16O/c1-3-4-5-6-10-9(2)7-8-11(10)12/h4-5H,3,6-8H2,1-2H3/b5-4-
InChI Key:
XMLSXPIVAXONDL-PLNGDYQASA-N
SMILES:
CCC=CCC1=C(C)CCC1=O
EC Number:
207-668-4
UNII:
RC4W0G9YUK
Properties
Complexity:
233  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1  
Exact Mass:
164.12g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
164.248g/mol
Monoisotopic Mass:
164.12g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.2  
Literature
Title Journal
Fragrance material review on cis-jasmone. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20121001
Activation of defence in sweet pepper, Capsicum annum, by cis-jasmone, and its impact on aphid and aphid parasitoid behaviour. Pest management science 20121001
Aphid antixenosis in cotton is activated by the natural plant defence elicitor cis-jasmone. Phytochemistry 20120601
Emerging roles in plant defense for cis-jasmone-induced cytochrome P450 CYP81D11. Plant signaling & behavior 20110401
Chemical composition of the essential oil of Feronia elephantum Correa. Natural product research 20101101
The transcriptome of cis-jasmone-induced resistance in Arabidopsis thaliana and its role in indirect defence. Planta 20101001
Microwave assisted synthesis of unsaturated jasmone heterocyclic analogues as new fragrant substances. European journal of medicinal chemistry 20090701
Attraction of New Zealand flower thrips, Thrips obscuratus, to cis-jasmone, a volatile identified from Japanese honeysuckle flowers. Journal of chemical ecology 20090601
(+)-7-iso-Jasmonoyl-L-isoleucine is the endogenous bioactive jasmonate. Nature chemical biology 20090501
Delayed cytotoxic effects of methyl jasmonate and cis-jasmone induced apoptosis in prostate cancer cells. Cancer investigation 20081101
The role of JAR1 in Jasmonoyl-L: -isoleucine production during Arabidopsis wound response. Planta 20080501
cis-Jasmone induces Arabidopsis genes that affect the chemical ecology of multitrophic interactions with aphids and their parasitoids. Proceedings of the National Academy of Sciences of the United States of America 20080325
cis-Jasmone induces accumulation of defence compounds in wheat, Triticum aestivum. Phytochemistry 20080101
Iso-OPDA: an early precursor of cis-jasmone in plants? Chembiochem : a European journal of chemical biology 20071217
4-pyridyl carbonyl and related compounds as thrips lures: effectiveness for onion thrips and new zealand flower thrips in field experiments. Journal of agricultural and food chemistry 20070725
[Effects of different elicitors on olfactory response and oviposition selection of Dendrolimus superans (Butler)]. Ying yong sheng tai xue bao = The journal of applied ecology 20070701
Treating hop plants with (Z)-jasmone increases colonization by Phorodon humuli (Hemiptera: Aphididae) spring migrants. Bulletin of entomological research 20070601
Developments in aspects of ecological phytochemistry: the role of cis-jasmone in inducible defence systems in plants. Phytochemistry 20070101
Microwave assisted synthesis of fragrant jasmone heterocyclic analogues. European journal of medicinal chemistry 20060501
Jasmonates induce apoptosis and cell cycle arrest in non-small cell lung cancer lines. Experimental lung research 20060101
Jasmonates--a new family of anti-cancer agents. Anti-cancer drugs 20051001
Ti-crossed-Claisen condensation between carboxylic esters and acid chlorides or acids: a highly selective and general method for the preparation of various beta-keto esters. Journal of the American Chemical Society 20050309
Fragrances in oolong tea that enhance the response of GABAA receptors. Bioscience, biotechnology, and biochemistry 20040901
Dihydrocoronatine, promising candidate for a chemical probe to study coronatine-, jasmonoid- and octadecanoid-binding protein. Bioscience, biotechnology, and biochemistry 20040701
Coronalon: a powerful tool in plant stress physiology. FEBS letters 20040409
cis-Jasmone treatment induces resistance in wheat plants against the grain aphid, Sitobion avenae (Fabricius) (Homoptera: Aphididae). Pest management science 20030901
A new synthesis route to enantiomerically pure jasmonoids. Angewandte Chemie (International ed. in English) 20021104
Properties