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Z-Cyclonon-5-enone is a chemical compound with the molecular formula C9H14O and a molecular weight of 138.21 g/mol. It is a cyclic ketone, specifically a cycloalkanone, and features a double bond between the second and third carbon atoms in a nine-membered ring. Z-cyclonon-5-enone is known for its unique structure and properties, which can be relevant in various chemical and industrial applications. It is an important intermediate in the synthesis of certain fragrances and pharmaceuticals due to its ability to form complex molecular structures. Z-Cyclonon-5-enone is also characterized by its distinct chemical reactivity, which can be exploited in organic synthesis to produce a variety of derivatives.

52920-63-5

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52920-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52920-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,9,2 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52920-63:
(7*5)+(6*2)+(5*9)+(4*2)+(3*0)+(2*6)+(1*3)=115
115 % 10 = 5
So 52920-63-5 is a valid CAS Registry Number.

52920-63-5Downstream Products

52920-63-5Relevant academic research and scientific papers

CARBOCYCLIC RING EXPANSION REACTIONS VIA RADICAL CHAIN PROCESSES

Baldwin, Jack E.,Adlington, Robert M.,Robertson, Jeremy

, p. 909 - 922 (2007/10/02)

A free radical mediated ring expansion of cis- and trans-α-alkylated-β-stannylcyclohexanones to provide efficient routes to cis- and trans-cyclononenones and cyclodecenones is described.The cis-/trans- relationship in the precursor was found to have signi

Carbocyclic Ring Expansion Reactions via Radical Chain Processes

Baldwin, Jack E.,Adlington, Robert M.,Robertson, Jeremy

, p. 1404 - 1406 (2007/10/02)

Free radical mediated ring expansion of cis- and trans-α-substituted-β-stannylcyclohexanones provides efficient routes to cis- and trans-cyclononenones and cyclodecenones; the cis-/trans-geometry of the precursor controls the alkene geometry of the ring-e

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