7206-16-8 Usage
Description
(E)-5-Dodecene, also known as 5-dodecene, is a long-chain, unsaturated hydrocarbon with the chemical formula C12H24. It is categorized as an alpha-olefin, which is a type of organic compound commonly used in the production of plastics, synthetic lubricants, and surfactants. (E)-5-Dodecene is a colorless, flammable liquid with a mild, sweet odor and is often used as an intermediate in the production of various chemical products. It is primarily obtained by the oligomerization of ethylene, a process that involves combining multiple ethylene molecules to form longer-chain hydrocarbons. Due to its multiple industrial applications, (E)-5-Dodecene is considered an important chemical in the manufacturing and production of a wide range of materials and products.
Uses
Used in Plastics Industry:
(E)-5-Dodecene is used as a monomer for the production of various types of plastics. Its long-chain structure and unsaturated nature make it suitable for polymerization, resulting in the formation of durable and versatile plastic materials.
Used in Synthetic Lubricants Industry:
(E)-5-Dodecene is used as a base oil for the synthesis of high-quality lubricants. Its ability to form long-chain hydrocarbons contributes to the development of lubricants with excellent viscosity and thermal stability, which are essential for various mechanical applications.
Used in Surfactants Industry:
(E)-5-Dodecene is used as a raw material for the production of surfactants, which are compounds that lower the surface tension of a liquid. These surfactants are widely used in the manufacturing of detergents, cleaners, and other products that require emulsification or foaming properties.
Used in Chemical Intermediates:
(E)-5-Dodecene is used as an intermediate in the synthesis of various chemical products, such as additives, coatings, and adhesives. Its versatile chemical structure allows for further reactions and modifications, leading to the creation of a diverse range of specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 7206-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7206-16:
(6*7)+(5*2)+(4*0)+(3*6)+(2*1)+(1*6)=78
78 % 10 = 8
So 7206-16-8 is a valid CAS Registry Number.
7206-16-8Relevant articles and documents
A General and Stereospecific Synthesis of Trans Alkenes and Regiospecific Synthesis of Ketones via Stepwise Hydroboration
Brown, Herbert C.,Basavaiah, D.,Kulkarni, Surendra U.
, p. 3808 - 3810 (1982)
The hydroboration of 1-bromo-1-alkynes with alkylbromoboranes (RBHBr*SMe2), conveniently obtained via the controlled hydridation of alkyldibromoboranes (RBBr2*SMe2), followed by treatment with sodium methoxide produces B-(trans-1-alkyl-1-alkenyl)boronate esters that provide the corresponding trans alkenes on protonolysis and ketones on oxidation
Stereoretentive Pd-catalyzed kumada-corriu couplings of alkenyl halides at room temperature
Krasovskiy, Arkady L.,Haley, Stephen,Voigtritter, Karl,Lipshutz, Bruce H.
, p. 4066 - 4069 (2014/10/15)
Stereoselective palladium-catalyzed Kumada-Corriu reactions of functionalized alkenyl halides and a variety of Grignard reagents, including those bearing β-hydrogen atoms and sensitive functional groups, can be carried out at room temperature using a new combination of reagents.
Nickel-catalyzed cross-coupling reactions of alkyl aryl sulfides and alkenyl alkyl sulfides with alkyl grignard reagents using (Z)-3,3-dimethyl-1,2- bis(diphenylphosphino)but-1-ene as ligand
Kanemura, Shigenari,Kondoh, Azusa,Yorimitsu, Hideki,Oshima, Koichiro
scheme or table, p. 2659 - 2664 (2009/04/05)
A combination of nickel(II) acetylacetonate and (Z)-3,3-dimethyl-1,2- bis(diphenylphosphino)but-1-ene catalyzes cross-coupling reactions of alkyl aryl sulfides and alkenyl alkyl sulfides with alkyl Grignard reagents. Not only primary but also secondary alkyl Grignard reagents can be employed. Georg Thieme Verlag Stuttgart.
