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Manufacturer Sells Best Quality 1,9-Decadiene 1647-16-1 with stock
- Molecular Formula: C10H18
- Molecular Weight: 138.253
- Appearance/Colour: clear colorless to slightly yellow liquid
- Vapor Pressure: 2.09mmHg at 25°C
- Melting Point: -69.6°C (estimate)
- Refractive Index: n20/D 1.432(lit.)
- Boiling Point: 169 °C at 760 mmHg
- Flash Point: 41.7 °C
- PSA： 0.00000
- Density: 0.752 g/cm3
- LogP: 3.69900
1,9-Decadiene(Cas 1647-16-1) Usage
|
General Description |
1,9-Decadiene acts as comonomer and undergoes acyclic diene metathesis (ADMET) copolymerization with 1, 5-hexadiene to form random linear polybutadiene –polyoctenamer copolymers. It undergoes ADMET copolymerization with divinyltetraethoxydisiloxane to yield siloxylene–vinylene–alkenylene copolymer. |
InChI:InChI=1/C10H18/c1-3-5-7-9-10-8-6-4-2/h3-4H,1-2,5-10H2
1647-16-1 Relevant articles
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Blomquist,Taussig
, p. 3505,3507 (1957)
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Ethenolysis reactions catalyzed by imido alkylidene monoaryloxide monopyrrolide (MAP) complexes of molybdenum
Marinescu, Smaranda C.,Schrock, Richard R.,Mueller, Peter,Hoveyda, Amir H.
, p. 10840 - 10841 (2009)
(Chemical Equation Presented) Monoarylox...
SYNTHESIS OF METHYL KETONES BY RHODIUM AND RUTHENIUM CATALYZED OXIDATION REACTIONS UNDER PHASE TRANSFER CONDITIONS
Januszkiewicz, Krzysztof,Alper, Howard
, p. 5163 - 5164 (1983)
The use of rhodium and ruthenium complex...
-
Blomquist,Goldstein
, p. 1001 (1955)
-
-
Trent,Zuckrow
, p. 2668,2670 (1952)
-
Luminescent tungsten(vi) complexes as photocatalysts for light-driven C-C and C-B bond formation reactions
Chan, Kaai-Tung,Che, Chi-Ming,Du, Lili,Liu, Yungen,Phillips, David Lee,To, Wai-Pong,Tong, Glenna So Ming,Wu, Liang-Liang,Yu, Daohong
, p. 6370 - 6382 (2020/07/15)
The realization of photocatalysis for pr...
Unprecedented Selectivity of Ruthenium Iodide Benzylidenes in Olefin Metathesis Reactions
Ivry, Elisa,Lemcoff, N. Gabriel,Nechmad, Noy B.,Phatake, Ravindra,Poater, Albert
, p. 3539 - 3543 (2020/02/04)
The development of selective olefin meta...
Nickel-catalyzed deoxygenation of oxiranes: Conversion of epoxides to alkenes
Mori, Takamichi,Takeuchi, Yoshihito,Hojo, Makoto
supporting information, (2020/01/24)
Deoxygenation of epoxides takes place un...
Oxidative Dehydroxymethylation of Alcohols to Produce Olefins
-
Paragraph 0057; 0058, (2019/09/06)
Catalyst compositions for the conversion...
1647-16-1 Process route
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110-52-1
1,4-dibromo-butane
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1730-25-2
allylmagnesium bromide
-
-
1647-16-1
1,10-decadiene
-
-
4117-09-3
7-bromo-hept-1-ene
| Conditions | Yield |
|---|---|
|
With
lithium chloride; copper dichloride;
In
tetrahydrofuran;
at 0 ℃;
for 2.5h;
|
40%
|
-
-
110-52-1
1,4-dibromo-butane
-
-
106-95-6
allyl bromide
-
-
1647-16-1
1,10-decadiene
-
-
592-42-7
1,5-Hexadien
-
-
4117-09-3
7-bromo-hept-1-ene
-
-
21964-49-8
tetradeca-1,13-diene
| Conditions | Yield |
|---|---|
|
Multistep reaction. Further byproducts given;
(i) Mg, THF, (ii) /BRN= 605308/;
|
1647-16-1 Upstream products
-
628-21-7
1,4-Diiodobutane
-
1720-38-3
1,9-decadiyne
-
26118-61-6
1,10-decanediol diacetate
-
96536-94-6
2,13-dioxa-tetradecanedioic acid diethyl ester
1647-16-1 Downstream products
-
24854-67-9
rac/meso-1,2,9,10-diepoxydecane
-
22702-48-3
1.10-Bis-
-decan -
32362-97-3
2-pentylcyclohexanone
-
112-47-0
1,10-Decanediol
