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Trans-2-Hydroperoxy-2-methylpent-3-en is an organic compound with the molecular formula C6H12O2. It is a peroxide derivative of 2-methylpent-3-en, which is an unsaturated hydrocarbon. trans-2-Hydroperoxy-2-methylpent-3-en is characterized by the presence of a hydroperoxy group (-OOH) attached to the trans-2 position of the 2-methylpent-3-en backbone. The trans configuration indicates that the hydroperoxy group and the methyl group are on opposite sides of the double bond. Trans-2-Hydroperoxy-2-methylpent-3-en is a reactive intermediate that can be involved in various chemical reactions, such as oxidation processes, and is typically found in trace amounts in complex mixtures. Due to its instability, it is not commonly used in commercial applications but may be of interest in the study of chemical kinetics and the formation of secondary pollutants in atmospheric chemistry.

3492-80-6

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3492-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3492-80-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3492-80:
(6*3)+(5*4)+(4*9)+(3*2)+(2*8)+(1*0)=96
96 % 10 = 6
So 3492-80-6 is a valid CAS Registry Number.

3492-80-6Upstream product

3492-80-6Downstream Products

3492-80-6Relevant academic research and scientific papers

Studies on the Autoxidation of Branched-chain Olefins. I. Autoxidation of 2-Methylalk-1-enes and 2-Methylalk-2-enes

Bilas, W.,Hoebold, W.,Pritzkow, W.

, p. 125 - 141 (2007/10/02)

The products of the autoxidation of 2-methylpent-1-ene, 2-methylpent-2-ene, 2-methylhex-1-ene, 2-methylhex-2-ene, 2,4,4-trimethylpent-1-ene, and 2,4,4-trimethylpent-2-ene were analyzed by gas chromatography.The identification of the products corresponding to the individual peaks was possible by comparison with authentic substances or by preparative gaschromatographic separation and n.m.r.-spectroscopy of the isolated samples.In this way not only the epoxides and the products of the oxidative cleavage of the C=C double bond but also the allylic alcohols formed by LiAlH4-reduction of the oxidation mixtures could be identified and analyzed.From the results the compositions of the original oxidation mixtures were calculated.

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