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2-(Cyclopent-2-enylperoxy)-cyclopentyl-hydroperoxide is a complex organic compound with the molecular formula C10H16O3. It is characterized by a cyclopentyl group (a five-membered ring with five carbon atoms) that has a hydroperoxide group (-OOH) attached to it. Additionally, the molecule features a cyclopent-2-enylperoxy group, which is a cyclopentane ring with a double bond and a peroxy linkage (-O-O-). 2-(Cyclopent-2-enylperoxy)-cyclopentyl-hydroperoxide is of interest in the field of organic chemistry, particularly in the study of peroxides and their reactions. It is known for its potential applications in the synthesis of various organic compounds and may also be relevant in the context of chemical reactions involving peroxides. The specific properties and reactivity of 2-(Cyclopent-2-enylperoxy)-cyclopentyl-hydroperoxide can vary depending on the conditions under which it is studied, making it a subject of ongoing research in chemical science.

4065-77-4

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4065-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4065-77-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4065-77:
(6*4)+(5*0)+(4*6)+(3*5)+(2*7)+(1*7)=84
84 % 10 = 4
So 4065-77-4 is a valid CAS Registry Number.

4065-77-4Upstream product

4065-77-4Downstream Products

4065-77-4Relevant 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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