Buy Quality (Z,E)-undeca-1,3,5-triene 19883-27-3 In Stock with Immediately Delivery
- Molecular Formula: C11H18
- Molecular Weight: 150.264
- Vapor Pressure: 0.336mmHg at 25°C
- Boiling Point: 206.7°Cat760mmHg
- Flash Point: 65.8°C
- PSA： 0.00000
- Density: 0.78g/cm3
- LogP: 3.86510
(Z,E)-undeca-1,3,5-triene(Cas 19883-27-3) Usage
|
General Description |
(Z,E)-undeca-1,3,5-triene is a chemical compound with the molecular formula C11H16. It is a hydrocarbon consisting of an 11-carbon chain with three double bonds in a specific configuration, giving it both cis (Z) and trans (E) isomers. (Z,E)-undeca-1,3,5-triene is commonly found in essential oils, particularly in plants such as lavender, orange, and tea tree. It is also used in the fragrance industry to add floral and fruity notes to perfumes and other scented products. Additionally, (Z,E)-undeca-1,3,5-triene has potential applications in organic synthesis and pharmaceutical research due to its unique structural properties and reactivity. |
InChI:InChI=1/C11H18/c1-3-5-7-9-11-10-8-6-4-2/h3,5,7,9,11H,1,4,6,8,10H2,2H3/b7-5+,11-9-
19883-27-3 Relevant articles
A simple stereoselective synthesis of "Galbanolene", (3E, 5Z)-1,3,5-undecatriene
Chapuis, Christian
, p. 2461 - 2464 (1992)
A new synthesis of (3E, 5Z)-l,3,5-undeca...
A new efficient and stereoselective synthesis of 1,3E,5Z-undecatriene
Alexakis,Barthel,Normant,Fugier,Leroux
, p. 1839 - 1844 (1992)
1,3E5,Z-Undecatriene is synthesized by c...
METHOD FOR PRODUCING COMPOUND HAVING CONJUGATED DIENE STRUCTURE
-
Paragraph 0045, (2019/08/12)
PROBLEM TO BE SOLVED: To provide a metho...
An approach to the regioselective diamination of conjugated di- and trienes
Lishchynskyi, Anton,Muniz, Kilian
supporting information; experimental part, p. 2212 - 2216 (2012/03/27)
It's do or diaminate: The selective diam...
Synthesis of naturally occurring diene and trienes by Te/Li exchange on (1Z,3Z)-butyltelluro-4-methoxy-1,3-butadiene
Dabdoub, Miguel J.,Dabdoub, Vania B.,Baroni, Adriano C.M.,Hurtado, Gabriela R.,Barbosa, Sandro L.
experimental part, p. 1666 - 1670 (2010/05/19)
(1Z,3Z)-Butyltelluro-4-methoxy-1,3-butad...
A new synthetic route to 1,3,5-undecatrienes and fucoserratene
Garibyan,Ovanesyan,Makaryan,Chobanyan
, p. 455 - 458 (2008/09/20)
A new procedure for preparing natural al...
19883-27-3 Process route
-
-
undeca-1,5-dien-3-yl methanesulfonate
-
-
19883-27-3
(3E,5Z)-1,3,5-undecatriene
-
-
51447-08-6
(1,3Z,5E)-undeca-1,3,5-triene
-
-
16356-11-9,19883-26-2,19883-27-3,51447-08-6,151123-08-9,19883-29-5
(3E,5E)-1,3,5-undecatriene
| Conditions | Yield |
|---|---|
|
With
potassium hydroxide;
In
tert-butyl methyl ether; tert-butyl alcohol;
at 5 - 20 ℃;
for 23h;
Inert atmosphere;
|
43.6%
34.1% 4.7% |
-
-
undeca-1,5-dien-3-yl methanesulfonate
-
-
19883-27-3
(3E,5Z)-1,3,5-undecatriene
-
-
51447-08-6
(1,3Z,5E)-undeca-1,3,5-triene
-
-
16356-11-9,19883-26-2,19883-27-3,51447-08-6,151123-08-9,19883-29-5
(3E,5E)-1,3,5-undecatriene
| Conditions | Yield |
|---|---|
|
With
potassium hydroxide;
In
tert-butyl methyl ether; tert-butyl alcohol;
at 5 - 20 ℃;
for 23h;
Inert atmosphere;
|
43.6%
34.1% 4.7% |
19883-27-3 Upstream products
-
25152-83-4
(2E,4Z)-2,4-decadienal
-
1779-49-3
Methyltriphenylphosphonium bromide
-
1457-42-7
pyridazinyl-N-oxide
-
61307-38-8
1-heptynylmagnesium bromide
19883-27-3 Downstream products
-
56318-85-5
3-((E)-Hept-1-enyl)-4-((1E,3E)-nona-1,3-dienyl)-cyclohexene
-
1379606-27-5
N,N'-((2E,4E)-undeca-2,4-diene-1,6-diyl)bis(4-methyl-N-tosylbenzenesulfonamide)
