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2,2,6,6-Tetramethyl-piperidinium cation, also known as TMPD, is a chemical compound with the formula [C9H18N]+. It is a cationic derivative of the piperidine molecule, featuring four methyl groups attached to the 2, 2, 6, and 6 positions of the piperidine ring. TMPD is a stable, colorless, and odorless substance that is soluble in organic solvents. It is commonly used as a redox mediator in various chemical reactions, particularly in the field of electrochemistry, where it facilitates electron transfer between the electrode and the reactants. Additionally, TMPD has applications in the synthesis of other organic compounds and as a stabilizer in the production of certain polymers. Its stability and reactivity make it a valuable component in a range of industrial and research settings.

79855-30-4

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79855-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79855-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,5 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79855-30:
(7*7)+(6*9)+(5*8)+(4*5)+(3*5)+(2*3)+(1*0)=184
184 % 10 = 4
So 79855-30-4 is a valid CAS Registry Number.

79855-30-4Downstream Products

79855-30-4Relevant academic research and scientific papers

Copper-Catalyzed Radical N-Demethylation of Amides Using N-Fluorobenzenesulfonimide as an Oxidant

Yi, Xuewen,Yi, Xuewen,Lei, Siyu,Liu, Wangsheng,Che, Fengrui,Yu, Chunzheng,Liu, Xuesong,Wang, Zonghua,Zhou, Xin,Zhang, Yuexia

supporting information, p. 4583 - 4587 (2020/05/05)

An unprecedented N-demethylation of N-methyl amides has been developed by use of N-fluorobenzenesulfonimide as an oxidant with the aid of a copper catalyst. The conversion of amides to carbinolamines involves successive single-electron transfer, hydrogen-atom transfer, and hydrolysis, and is accompanied by formation of N-(phenylsulfonyl)benzenesulfonamide. Carbinolamines spontaneously decompose to N-demethylated amides and formaldehyde, because of their inherent instability.

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