62234-75-7 Usage
Uses
Used in Chemical Production:
5,6,7,8-tetraMethylenebicyclo[2.2.2]oct-2-ene is used as a key component in the production of various organic chemicals, polymers, and adhesives. Its unique structure and properties make it a versatile building block for the synthesis of a wide range of chemical products.
Used in Polymerization:
As a monomer, 5,6,7,8-tetraMethylenebicyclo[2.2.2]oct-2-ene is used in the polymerization of thermoplastic elastomers. These elastomers are valued for their unique combination of properties, such as elasticity, durability, and resistance to heat and chemicals, making them suitable for various applications in the plastics and rubber industries.
Used in Pharmaceutical and Agrochemical Synthesis:
5,6,7,8-tetraMethylenebicyclo[2.2.2]oct-2-ene is also utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its presence in these industries highlights its importance in the development of new drugs and agricultural products.
Used in Adhesive Production:
In the adhesive industry, 5,6,7,8-tetraMethylenebicyclo[2.2.2]oct-2-ene is used as a component in the formulation of various types of adhesives. Its ability to form strong bonds and its compatibility with other materials make it a valuable ingredient in the production of high-performance adhesives.
Overall, 5,6,7,8-tetraMethylenebicyclo[2.2.2]oct-2-ene is a versatile chemical compound with a wide range of applications across different industries, including chemical production, polymerization, pharmaceutical and agrochemical synthesis, and adhesive production. Its low toxicity and proper handling make it a relatively safe compound to work with in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62234-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,3 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62234-75:
(7*6)+(6*2)+(5*2)+(4*3)+(3*4)+(2*7)+(1*5)=107
107 % 10 = 7
So 62234-75-7 is a valid CAS Registry Number.
62234-75-7Relevant academic research and scientific papers
Thermal generation of pentacenes from soluble 6,13-dihydro-6,13- ethenopentacene precursors by a Diels-Alder-retro-Diels-Alder sequence with 3,6-disubstituted tetrazines
Bula, Rafael P.,Oppel, Iris M.,Bettinger, Holger F.
, p. 3538 - 3542 (2012/06/15)
3,6-Substituted tetrazines 2 (a: R2 = 2-pyridyl or b: CO 2Me) react with 2,3,9,10-(R1)4-dihydro-6,13- ethenopentacene 3 in solution at elevated temperature to the corresponding pentacene 1 (a: R1 = H, b: OBn, c: F).
METHOD OF PREPARATION OF A PRECURSOR OLIGOCENE
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Page 9, (2010/02/08)
The synthesis of a precursor oligocene, particularly pentacene, is a two-step process. In the fist step the Diels-Alder adduct of the a,b-dihydro-a,b-etheno-oligocene with a 1,1-dialkoxy-cyclopentadiene is formed. In the second step this Diels-Alder adduct is converted into the precursor oligocene, in that first the corresponding keto-compound is formed, which may be eliminated thereafter. The resulting precursor oligocene can be converted to the oligocene with a heat treatment, particularly after providing a solution hereof on a substrate. It is suitable for use as semiconductor material in a thin-film transistor. Formula (I).
Bicyclically Bridged Cyclopentadienyl Anions: 4,8-Etheno-/Ethano-2,4,6,8-tetrahydro-s-indacene Dianion
Atzkern, Hermann,Koehler, Frank H.,Mueller, Reinhard
, p. 329 - 343 (2007/10/02)
Two cyclopentadienes have been linked in a stereochemically rigid arrangement such that the cyclopentadienes are not coplanar.The key intermediate in the synthesis were tetrakis(methylene)bicyclooct-2-ene (12) or -octane (14).The access to 12 and 1
