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2,5-dimethyl-2,5-diphenyltetrahydrofuran is a complex organic compound with the molecular formula C18H20O. It is a cyclic ether with a tetrahydrofuran ring structure, which is a type of heterocyclic compound containing an oxygen atom in the ring. The compound is characterized by two methyl groups (-CH3) and two phenyl groups (C6H5) attached to the 2,5-positions of the tetrahydrofuran ring. This specific arrangement of substituents contributes to its unique chemical properties and potential applications in various fields, such as pharmaceuticals, materials science, and organic synthesis. Due to its structural complexity, 2,5-dimethyl-2,5-diphenyltetrahydrofuran may exhibit interesting reactivity patterns and can be a subject of study for chemists interested in exploring the properties of complex cyclic ethers.

2963-52-2

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2963-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2963-52-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2963-52:
(6*2)+(5*9)+(4*6)+(3*3)+(2*5)+(1*2)=102
102 % 10 = 2
So 2963-52-2 is a valid CAS Registry Number.

2963-52-2Upstream product

2963-52-2Downstream Products

2963-52-2Relevant academic research and scientific papers

Selective Functionalization of Styrenes with Oxygen Using Different Electrode Materials: Olefin Cleavage and Synthesis of Tetrahydrofuran Derivatives

Imada, Yasushi,Okada, Yohei,Noguchi, Keiichi,Chiba, Kazuhiro

, p. 125 - 129 (2019)

Electrode materials can have a significant impact on the course of an electrolysis reaction. Of particular interest is that different electrodes can generate different products from the same substrate. The electrode-material-selective transformations of styrene derivatives with molecular oxygen are reported. Platinum electrodes afford carbonyl products via cleavage of olefins, whereas tetrahydrofuran formation is achieved with carbon electrodes. A variety of different styrenes are available for both reactions. Electrolysis allows straightforward and mild chemical conversions that are metal- and oxidant-free. Electrochemical measurements illuminate the different effects of platinum and carbon electrodes on styrenes. The key to the differing reactions is probably that the oxidation potentials of the substrates are lower (higher HOMO energy) on carbon electrodes than on platinum electrodes. The adsorption of the substrates on carbon electrodes can also promote tetrahydrofuran formation.

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