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3-methyl-3-p-tolyloxymethyl-oxetane is a complex organic compound with the molecular formula C12H16O2. It features a four-membered oxetane ring, which is a cyclic ether, and is substituted with a methyl group and a p-tolyloxymethyl group. The p-tolyloxymethyl group consists of a tolyl group (a benzene ring with a methyl substituent at the para position) attached to a methylene group. 3-methyl-3-p-tolyloxymethyl-oxetane is characterized by its unique structure, which may contribute to specific chemical properties and potential applications in fields such as pharmaceuticals or materials science. The synthesis and reactivity of such compounds are of interest to chemists due to their potential to form new bonds and participate in various chemical reactions.

3753-52-4

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3753-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3753-52-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3753-52:
(6*3)+(5*7)+(4*5)+(3*3)+(2*5)+(1*2)=94
94 % 10 = 4
So 3753-52-4 is a valid CAS Registry Number.

3753-52-4Relevant academic research and scientific papers

Electro-Oxidative Selective Esterification of Methylarenes and Benzaldehydes

Yu, Congjun,?zkaya, Bünyamin,Patureau, Frederic W.

supporting information, p. 3682 - 3687 (2021/02/01)

A mild and green electro-oxidative protocol to construct aromatic esters from methylarenes and alcohols is herein reported. Importantly, the reaction is free of metals, chemical oxidants, bases, acids, and operates at room temperature. Moreover, the design of the electrolyte was found critical for the oxidation state and structure of the coupling products, a rarely documented effect. This electro-oxidative coupling process also displays exceptional tolerance of many fragile easily oxidized functional groups such as hydroxy, aldehyde, olefin, alkyne, as well as neighboring benzylic positions. The enantiomeric enrichment of some chiral alcohols is moreover preserved during this electro-oxidative coupling reaction, making it overall a promising synthetic tool.

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