20966-34-1 Usage
Uses
Used in Polymer and Plastics Industry:
BUTADIENE-2,2,5,5-D4 SULFONE is utilized as a key component in the production of polymers and plastics due to its high reactivity and stability. Its incorporation enhances the performance characteristics of the final products, such as durability, heat resistance, and chemical resistance.
Used in High-Temperature Processes:
BUTADIENE-2,2,5,5-D4 SULFONE is employed as a stable and reliable material in high-temperature processes, where its thermal stability ensures consistent performance and prevents degradation under extreme conditions.
Used in Harsh Chemical Environments:
BUTADIENE-2,2,5,5-D4 SULFONE is used as a chemically stable compound in environments with aggressive chemicals, where its resistance to chemical reactions protects it from degradation and maintains its structural integrity.
Used as a Precursor in Organic Chemistry:
In the field of organic chemistry research and development, BUTADIENE-2,2,5,5-D4 SULFONE serves as a crucial precursor for the synthesis of a variety of organic compounds. Its unique structure and properties make it an ideal starting material for creating new molecules with specific functionalities and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 20966-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,6 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20966-34:
(7*2)+(6*0)+(5*9)+(4*6)+(3*6)+(2*3)+(1*4)=111
111 % 10 = 1
So 20966-34-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O2S/c5-7(6)3-1-2-4-7/h1-2H,3-4H2/i3D2,4D2
20966-34-1Relevant academic research and scientific papers
Hydrogen Transfer Reactions, 9. Synthesis and Analytics of Selectively Deuterated 1,4-Cyclohexadienes and 1,4-Dihydronaphthalenes
Brock, Martin,Hintze, Horst,Heesing, Albert
, p. 3718 - 3726 (2007/10/02)
Five isotopomers of 1,4-cyclohexadiene (1a - e) and four of 1,4-dihydronaphthalene (2a - d) have been synthesized in an isotopomeric purity sufficient for mechanistic experiments.
Study of the Alkylation Reactions of Sulphol-3-enes
Chou, Ta-shue,Tso, Hsi-Hua,Chang, Lee-Jean
, p. 515 - 520 (2007/10/02)
Sulphol-3-ene can be deprotonated with sodium hydride in DMF to form the α-anion which reacts with various alkyl halides to give the 2-alkylsulpholenes.This approach provides a regiospecific preparation of disubstituted sulphol-3-enes and sulphol-2-enes.
