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Cyclohexenylperoxycyclohexanhydroperoxid is a complex organic compound with the chemical formula C12H22O2. It is a peroxide derivative, characterized by the presence of an oxygen-oxygen single bond (-O-O-) in its structure. Cyclohexenylperoxycyclohexanhydroperoxid is formed by the reaction of cyclohexanone with hydrogen peroxide in the presence of a catalyst, such as a peroxidase enzyme or a suitable metal catalyst. Cyclohexenylperoxycyclohexanhydroperoxid is an important intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Due to its peroxide nature, it is highly reactive and can be hazardous if not handled properly, as it can decompose and release oxygen gas, potentially leading to explosions. It is crucial to store and handle Cyclohexenylperoxycyclohexanhydroperoxid under controlled conditions to ensure safety.

4096-41-7

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4096-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4096-41-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4096-41:
(6*4)+(5*0)+(4*9)+(3*6)+(2*4)+(1*1)=87
87 % 10 = 7
So 4096-41-7 is a valid CAS Registry Number.

4096-41-7Upstream product

4096-41-7Downstream Products

4096-41-7Relevant academic research and scientific papers

Studies on the Autoxidation of Some Monocyclic Olefins

Blau, K.,Mueller, U.,Pritzkow, W.,Schmidt-Renner, W.,Sedshaw, Z.

, p. 915 - 932 (2007/10/02)

The autoxidations of cyclopentene, cyclohexene, cycloheptene, cyclooctene, cycloocta-1,5-diene, 1-methylcyclopentene, 1-methylcyclohexene, 1-methylcycloheptene, 1-methylcyclooctene, methylene cyclopentene, and methylene cyclohexene with pure oxygen under normal pressure were studied.The epoxides formed were determined gaschromatographically.In most cases also the products of allylic oxidation were analyzed and their structures elucidated after reduction to the corresponding allyl alcohols.The portions of high boiling or polymeric products which could not be detected gaschromatographically and also the real yields of epoxides were determined by balance experiments in the presence of inert internal standards.

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