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N-(2-morpholinophenyl)pyrazine-2-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

793680-20-3

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793680-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 793680-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,3,6,8 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 793680-20:
(8*7)+(7*9)+(6*3)+(5*6)+(4*8)+(3*0)+(2*2)+(1*0)=203
203 % 10 = 3
So 793680-20-3 is a valid CAS Registry Number.

793680-20-3Downstream Products

793680-20-3Relevant academic research and scientific papers

Containing-containing layer C(sp2 Process)-N for the preparation of a bond-containing compound

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Paragraph 0098-0101; 0105-0107, (2020/01/12)

The invention discloses a preparation method of a compound containing C (sp2)-N bonds as shown in a formula I. The preparation method includes the step: performing constant-current electrolysis reaction on a compound as shown in a formula II and a compoun

Copper-Catalyzed Electrochemical C-H Amination of Arenes with Secondary Amines

Yang, Qi-Liang,Wang, Xiang-Yang,Lu, Jia-Yan,Zhang, Li-Pu,Fang, Ping,Mei, Tian-Sheng

supporting information, p. 11487 - 11494 (2018/09/13)

Electrochemical oxidation represents an environmentally friendly solution to conventional methods that require caustic stoichiometric chemical oxidants. However, C-H functionalizations merging transition-metal catalysis and electrochemical techniques are, to date, largely confined to the use of precious metals and divided cells. Herein, we report the first examples of copper-catalyzed electrochemical C-H aminations of arenes at room temperature using undivided electrochemical cells, thereby providing a practical solution for the construction of arylamines. The use of n-Bu4NI as a redox mediator is crucial for this transformation. On the basis of mechanistic studies including kinetic profiles, isotope effects, cyclic voltammetric analyses, and radical inhibition experiments, the reaction appears to proceed via a single-electron-transfer (SET) process, and a high valent Cu(III) species is likely involved. These findings provide a new avenue for transition-metal-catalyzed electrochemical C-H functionalization reactions using redox mediators.

Copper-catalyzed carboxamide-directed ortho amination of anilines with alkylamines at room temperature

Li, Qiong,Zhang, Shu-Yu,He, Gang,Ai, Zhaoyan,Nack, William A.,Chen, Gong

supporting information, p. 1764 - 1767 (2014/04/17)

In this report, a highly efficient method for the room temperature installation of alkyl amino motifs onto the ortho position of anilines via Cu-catalyzed carboxamide-directed amination with alkylamines is described. This method offers a practical solution for the rapid synthesis of complex arylamines from simple starting materials and enables new planning strategies for the construction of arylamine-containing pharmacophores. A single electron transfer (SET)-mediated mechanism is proposed.

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