3736-26-3 Usage
General Description
1-Hydroperoxyl-1-vinylcyclohexene-3 is a chemical compound that belongs to the class of cyclic organic peroxides. It is a highly reactive and unstable compound, with a molecular formula of C8H12O2. The presence of a vinyl group and a cyclohexene ring in its structure makes it prone to various types of chemical reactions, including polymerization and oxidation. It is primarily used as an intermediate in chemical synthesis, especially in the production of various organic compounds and polymers. However, it should be handled with extreme caution due to its high reactivity and potential for explosive decomposition.
Check Digit Verification of cas no
The CAS Registry Mumber 3736-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3736-26:
(6*3)+(5*7)+(4*3)+(3*6)+(2*2)+(1*6)=93
93 % 10 = 3
So 3736-26-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O2/c1-2-8(10-9)6-4-3-5-7-8/h2-4,9H,1,5-7H2
3736-26-3Relevant articles and documents
Autoxidation of Vinylcyclopentane, Vinylcyclohexane, and 4-Vinylcyclohex-1-ene
Biela, R.,Bilas, W.,Ihsan, U.,Pritzkow, W.,Schmidt-Renner, W.
, p. 893 - 900 (2007/10/02)
The title olefins were oxidized with molecular oxygen at 75-80 deg C.About 40percent of the oxygen absorbed were found by iodometric titration as peroxidic oxygen.The reaction products were analyzed by a combination of chemical methods, gas chromatography, and 13C-n.m.r.-spectroscopy.Vinylcyclopentane and vinylcyclohexane are attacked preferably at the tertiary allylic C-H-bonds giving almost equimolar mixtures of the corresponding allylisomeric hydroperoxides.In the case of 4-vinylcyclohex-1-ene the C-H-bonds in position 6 are preferably attacked, but products of attack on the other allylic C-H-bonds also could be identified.In all cases the amount of products which could not be detected gaschromatographically was determined by balance experiments in the presence of an internal standard.
