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Trimethylethylene ozonide, also known as 2,2,3-trimethyl-3-oxetanone ozonide, is a highly reactive organic compound with the chemical formula C5H10O3. It is formed by the reaction of ozone with 2,2,3-trimethyl-3-oxetanone, a cyclic ether. Trimethylethylene ozonide is characterized by its strained four-membered ring structure and the presence of an ozonide group, which makes it a potent electrophile and a valuable intermediate in organic synthesis. Trimethylethylene ozonide is used in various chemical reactions, such as the oxidation of alkenes to epoxides, and the cleavage of alkenes to form carbonyl compounds. Due to its high reactivity, it is typically generated in situ and used immediately to avoid hazardous decomposition.

2425-42-5

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2425-42-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2425-42-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2425-42:
(6*2)+(5*4)+(4*2)+(3*5)+(2*4)+(1*2)=65
65 % 10 = 5
So 2425-42-5 is a valid CAS Registry Number.

2425-42-5Downstream Products

2425-42-5Relevant academic research and scientific papers

The Ozonolysis of Tetramethylethylene. Concentration and Temperature Effects

Murray, Robert W.,Kong, Wei,Rajadhyaksha, Shirish N.

, p. 315 - 321 (1993)

The products of the ozonolysis of tetramethylethylene in hexane or methylene chloride are remarkably dependent on the concentration of tetramethylethylene.Ozonolysis in neat tetramethylethylene gives mostly tetramethylene epoxide as product.As the concentration of tetramethylethylene is reduced, more acetone diperoxide is formed until it becomes the major product.The reaction also produces 3-hydroperoxy-2,3-dimethyl-1-butene.The product distribution is also quite dependent on reaction temperature.At a given concentration of the alkene the epoxide yield decreases as the temperature is lowered.Simultaneously the acetone diperoxide yield increases with lower temperature.The results are explained by postulating that energy-rich acetone oxide can be partially converted to dimethyldioxirane which is primarily responsible for the epoxidation.The proposed reaction scheme also has acetone oxide dimerize in a stepwise manner to give an intermediate which can either close to give diperoxide or lose singlet oxygen.The singlet oxygen would then react with tetramethylethylene to give the hydroperoxide.

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