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About This Item
Empirical Formula (Hill Notation):
C11H16O
CAS Number:
Molecular Weight:
164.24
EC Number:
207-668-4
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
1907713
MDL number:
InChI key
XMLSXPIVAXONDL-PLNGDYQASA-N
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-
SMILES string
[H]\C(CC)=C(/[H])CC1=C(C)CCC1=O
assay
90%
refractive index
n20/D 1.498 (lit.)
bp
134-135 °C/12 mmHg (lit.)
density
0.94 g/mL at 25 °C (lit.)
application(s)
agriculture
Other Notes
Remainder trans isomer
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
224.6 °F - closed cup
flash_point_c
107 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Eliezer Flescher
Anti-cancer drugs, 16(9), 911-916 (2005-09-16)
Since salicylate, a plant stress hormone, suppresses the growth of various types of cancer cells, it was deemed of interest to investigate whether the jasmonate family of plant stress hormones is endowed with anti-cancer activities. Cell lines representing a wide
John A Pickett et al.
Phytochemistry, 68(22-24), 2937-2945 (2007-11-21)
The challenges and opportunities for protecting agricultural production of food and other materials will be met through exploiting the induction of defence pathways in plants to control pests, diseases and weeds. These approaches will involve processes that can be activated
Toby J A Bruce et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(12), 4553-4558 (2008-03-22)
It is of adaptive value for a plant to prepare its defenses when a threat is detected, and certain plant volatiles associated with insect damage, such as cis-jasmone (CJ), are known to switch-on defense metabolism. We used aphid and aphid
Walter P Suza et al.
Planta, 227(6), 1221-1232 (2008-02-06)
The Arabidopsis thaliana (L.) Heynh. JASMONATE RESISTANT 1( JAR1) locus is essential for pathogen defense, but its role in wound response has not been investigated. JAR1 encodes an enzyme that conjugates jasmonic acid (JA) to isoleucine, which was recently shown
Tomonori Misaki et al.
Journal of the American Chemical Society, 127(9), 2854-2855 (2005-03-03)
Ti-crossed-Claisen condensation between a 1:1 mixture of carboxylic esters and acid chlorides promoted by TiCl4-Bu3N-N-methylimidazole proceeded successfully to give various beta-keto esters in good yields with excellent selectivities (19 examples, approximately 48-95% yield; cross/self-selectivity = approximately 96/4-99/1). The present method
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