39198-34-0 Usage
Uses
Used in Polymer Production Industry:
AZO-TERT-OCTANE is used as a radical initiator for [application reason] the production of various polymers, including acrylics, vinyls, and styrenics. It facilitates the polymerization process by acting as a source of free radicals, which break the double bond and generate highly reactive species, promoting the formation of polymer chains.
Used in Organic Synthesis:
AZO-TERT-OCTANE is used as a reagent in the synthesis of organic compounds for [application reason] its ability to efficiently initiate reactions at relatively low temperatures, making it a valuable tool in the synthesis of various organic compounds.
Used in Industrial Processes:
AZO-TERT-OCTANE is used as a component in industrial processes for [application reason] its high reactivity and efficiency in initiating polymerization at low temperatures, which contributes to the production of polymers with specific properties and characteristics required in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 39198-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,9 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39198-34:
(7*3)+(6*9)+(5*1)+(4*9)+(3*8)+(2*3)+(1*4)=150
150 % 10 = 0
So 39198-34-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H34N2/c1-13(2,3)11-15(7,8)17-18-16(9,10)12-14(4,5)6/h11-12H2,1-10H3/b18-17+
39198-34-0Relevant academic research and scientific papers
Thiadiaziridine 1,1-Dioxides: Synthesis and Chemistry
Timberlake, Jack W.,Alender, Jeff,Garner, Archie W.,Hodges, Melvin L.,Oezmeral, Cenan,et al.
, p. 2082 - 2089 (2007/10/02)
The synthesis and chemical reactions of a series of thiadiaziridine 1,1-dioxides (2) are described.The thermal stability is highly dependent on the R group and in one case (R = tert-octyl) is postulated that the thermolysis initially produces a diradical intermediate which can be trapped or further fragments to give a nitrene.A temperature-dependent NMR study on the coalescence of the diastereotopic α-methyl protons of 2b gives a ΔG = 20 kcal*mol-1.
