4974-27-0 Usage
Uses
Used in Chemical Synthesis:
2,6-Octadiene is used as a building block in the chemical synthesis of various compounds due to its reactive double bonds. The presence of these double bonds allows for a range of chemical reactions, such as addition, polymerization, and cyclization, which can lead to the formation of a wide array of products.
Used in Polymer Industry:
In the polymer industry, 2,6-Octadiene is used as a monomer for the production of specialty polymers. Its unique structure allows for the creation of polymers with specific properties, such as improved flexibility, strength, or chemical resistance, which can be tailored for various applications.
Used in Pharmaceutical Industry:
2,6-Octadiene can be used as a starting material in the synthesis of pharmaceutical compounds. Its reactive double bonds can be exploited to create complex molecular structures with potential therapeutic properties.
Used in Flavor and Fragrance Industry:
Due to its unique chemical structure, 2,6-Octadiene can be used as a precursor in the synthesis of various flavor and fragrance compounds. These compounds can be used in the production of perfumes, cosmetics, and other consumer products to provide specific scents or tastes.
Used in Fuel Industry:
2,6-Octadiene, being a hydrocarbon, can be used as a component in the fuel industry. Its high energy content and reactivity make it a valuable addition to the development of advanced fuel formulations for various applications, such as automotive, aviation, or industrial use.
Synthesis Reference(s)
Journal of the American Chemical Society, 73, p. 2654, 1951 DOI: 10.1021/ja01150a068
Check Digit Verification of cas no
The CAS Registry Mumber 4974-27-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,7 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4974-27:
(6*4)+(5*9)+(4*7)+(3*4)+(2*2)+(1*7)=120
120 % 10 = 0
So 4974-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-3-5-7-8-6-4-2/h3-6H,7-8H2,1-2H3/b5-3+,6-4+
4974-27-0Relevant academic research and scientific papers
REACTIONS INVOLVING TRANSITION METALS. XVII. REACTION OF ORGANIC HALOGEN COMPOUNDS WITH 2 AND 2 (S = CH2Cl2, THF)
Booth, Brian L.,Casey, Geoffrey C.,Haszeldine, Robert N.
, p. 197 - 205 (2007/10/02)
The complexes 2 and 2 (S=CH2Cl2, THF) have been shown to react with CXCl3 (X=Cl, H) to form with generation of both dichlorocarbene and trichloromethyl radical.Reaction of 2 with CF3I, allyl- and benzyl-halides takes a different course giving organic coupling products and .The THF solvate complex also causes coupling of gem-dihalides, and dehalogenation of vic-dihalides to produce alkenes.Possible mechanisms for these reactions are discussed.
THERMISCHE STABILITAET VON BIS(ALK-2-ENYL)ZINK-VERBINDUNGEN
Lehmkuhl, Herbert,Doering, Ingo,Nehl, Hans
, p. 7 - 12 (2007/10/02)
The dialk-2-enylzinc compounds I-III react slowly at 20 to 50 deg C by addition of the Zn-C bond to the C=C bond of an alk-2-enyl group to give oligomers from which the alkenes XIII-XV are released on hydrolysis.For I-III homolytic cleavage of the Zn-Callyl bond, followed by coupling of the allyl radicals to give the alkadienes V-VII, IX and XI predominates above 50 deg C.IV decomposes mainly homolytically even at 20 deg C.
