trans,trans-2,4-Undecadienal
- CasNo:30361-29-6
Product Description
Factory Sells Best Quality trans,trans-2,4-Undecadienal 30361-29-6 with steady supply
- Molecular Formula: C11H18O
- Molecular Weight: 166.263
- Vapor Pressure: 0.0154mmHg at 25°C
- Refractive Index: n20/D 1.514(lit.)
- Boiling Point: 256.4 °C at 760 mmHg
- Flash Point: 111.1 °C
- PSA： 17.07000
- Density: 0.854 g/cm3
- LogP: 3.26810
trans,trans-2,4-Undecadienal(Cas 30361-29-6) Usage
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Synthesis Reference(s) |
The Journal of Organic Chemistry, 55, p. 3679, 1990 DOI: 10.1021/jo00298a061 |
InChI:InChI=1/C11H18O/c1-2-3-4-5-6-7-8-9-10-11-12/h7-11H,2-6H2,1H3/b8-7+,10-9+
30361-29-6 Relevant articles
Method for preparing olefine aldehyde by catalyzing terminal alkyne or terminal conjugated eneyne and diphosphine ligand used in method
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Paragraph 0183-0187, (2021/05/29)
The invention discloses a method for pre...
Selective Rhodium-Catalyzed Hydroformylation of Terminal Arylalkynes and Conjugated Enynes to (Poly)enals Enabled by a π-Acceptor Biphosphoramidite Ligand
Zhao, Jiangui,Zheng, Xueli,Tao, Shaokun,Zhu, Yuxin,Yi, Jiwei,Tang, Songbai,Li, Ruixiang,Chen, Hua,Fu, Haiyan,Yuan, Maolin
, p. 6067 - 6072 (2021/08/16)
The hydroformylation of terminal arylalk...
Two-carbon homologation of aldehydes and ketones to α,β- unsaturated aldehydes
Petroski, Richard J.,Vermillion, Karl,Cosse, Allard A.
experimental part, p. 5062 - 5078 (2011/08/21)
Phosphonate reagents were developed for ...
Highly selective synthesis of conjugated dienoic and trienoic esters via alkyne elementometalation - Pd-catalyzed cross-coupling
Wang, Guangwei,Mohan, Swathi,Negishi, Ei-Ichi
, p. 11344 - 11349 (2011/10/30)
All four stereoisomers (7-10) of ethyl u...
30361-29-6 Process route
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42599-17-7
(E)-1-iodo-1-octene
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-
107-18-6
allyl alcohol
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-
94087-86-2
(2E, 4E)-undeca-2,4-dien-1-ol
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-
30361-29-6
trans,trans-2,4-undecadien-1-al
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-
68820-35-9,160321-33-5
(E)-undec-4-enal
| Conditions | Yield |
|---|---|
|
With
tetra(n-butyl)ammonium hydrogensulfate; silver carbonate;
palladium diacetate;
In
acetonitrile;
Product distribution;
1) rt, overnight, 2) 50 deg C, 5-8 h, various concentrations of nBu4NHSO4; other vinylic halides, other allylic alcohol, high regio- and stereoselectivity;
|
71 % Chromat.
5 % Chromat. 20 % Chromat. |
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-
(4E)-N'-(undeca-2,4-dienylidene)-N,N-dimethyl-hydrazine
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-
30361-29-6,53434-76-7,93614-62-1,93614-63-2,13162-46-4
2,4-undecadien-1-al
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
In
Petroleum ether;
at 25 ℃;
for 24h;
|
30361-29-6 Upstream products
-
111-71-7
heptanal
-
18829-56-6
(E)-2-Nonenal
-
141-82-2
malonic acid
-
93039-04-4
(2E,4E)-N,N-dimethyl-2,4-undecadien-1-amine
30361-29-6 Downstream products
-
94087-86-2
(2E, 4E)-undeca-2,4-dien-1-ol
-
102953-16-2
2-deca-1,3t -dien-t -yl-1,3-diphenyl-imidazolidine
-
21662-16-8
trans,trans-2,4-dodecadienal