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4-Oxabicyclo[3.2.1]oct-6-en-3-one is a complex organic compound with the molecular formula C8H10O2. It is a cyclic ketone, characterized by the presence of a carbonyl group (C=O) and a six-membered ring with an oxygen atom. 4-oxabicyclo[3.2.1]oct-6-en-3-one is a derivative of bicyclo[3.2.1]octane, where one of the carbon atoms in the ring is replaced by an oxygen atom, forming a six-membered ring with a double bond. The compound has a unique structure that contributes to its chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. Due to its specific structure, 4-oxabicyclo[3.2.1]oct-6-en-3-one may exhibit unique reactivity and can be used as a building block for the synthesis of more complex molecules.

5650-65-7

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5650-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5650-65-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5650-65:
(6*5)+(5*6)+(4*5)+(3*0)+(2*6)+(1*5)=97
97 % 10 = 7
So 5650-65-7 is a valid CAS Registry Number.

5650-65-7Upstream product

5650-65-7Downstream Products

5650-65-7Relevant academic research and scientific papers

Oxygen transfer reactions from an oxaziridinium tetrafluoroborate salt to olefins

Lusinchi, Xavier,Hanquet, Gilles

, p. 13727 - 13738 (2007/10/03)

Oxaziridinium 5 efficiently epoxidises olefins. It reacts as an electrophilic reagent and does not transfer its oxygen to deactivated double-bonds or carbonyl functions. Epoxidation of cyclic allylic acetates shows a remarkable diastereoselectivity leading to the syn isomer. We propose that the epoxidation reaction proceeds through a one-step process.

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