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N-[5-formyl-2-(pyridin-2-yl)phenyl]benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1581756-80-0

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1581756-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1581756-80-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,1,7,5 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1581756-80:
(9*1)+(8*5)+(7*8)+(6*1)+(5*7)+(4*5)+(3*6)+(2*8)+(1*0)=200
200 % 10 = 0
So 1581756-80-0 is a valid CAS Registry Number.

1581756-80-0Downstream Products

1581756-80-0Relevant academic research and scientific papers

Ortho–C–H amidations enabled by a recyclable manganese-ionic liquid catalytic system

Kong, Xianqiang,Xu, Bo

, (2020)

We described an environmentally benign, recyclable base metal catalyst system (MnBr(CO)5/[Hmim]OAc) for ortho–C–H amidation. The readily available dioxazolones was used as the amidation agents. A broad substrate scope and high functional group

Comparative Catalytic Activity of Group 9 [CpMIII] Complexes: Cobalt-Catalyzed C-H Amidation of Arenes with Dioxazolones as Amidating Reagents

Park, Juhyeon,Chang, Sukbok

, p. 14103 - 14107 (2016/01/25)

A procedure for the [CpCoIII]-catalyzed direct C-H amidation of arenes with dioxazolone has been developed. This reaction proceeds under straightforward and mild conditions with a broad range of substrates, including anilides. A comparative study on the catalytic activity of Group 9 [{CpMCl2}2] complexes revealed the unique efficiency of the cobalt catalyst. Pick of the bunch: A variety of arenes, including anilides, underwent direct C-H amidation with dioxazolones in the presence of a cobalt catalyst with a Cp? ligand under mild and straightforward reaction conditions (see scheme; Piv=pivaloyl). A comparative study of Group 9 [CpMIII] complexes revealed the unique ability of the cobalt catalyst to promote this transformation efficiently.

Mechanistic Studies on the Rh(III)-Mediated Amido Transfer Process Leading to Robust C-H Amination with a New Type of Amidating Reagent

Park, Yoonsu,Park, Kyung Tae,Kim, Jeung Gon,Chang, Sukbok

supporting information, p. 4534 - 4542 (2015/04/22)

Mechanistic investigations on the CpRh(III)-catalyzed direct C-H amination reaction led us to reveal the new utility of 1,4,2-dioxazol-5-one and its derivatives as highly efficient amino sources. Stepwise analysis on the C-N bond-forming process showed th

Cationic Cobalt(III)-Catalyzed Aryl and Alkenyl C-H Amidation: A Mild Protocol for the Modification of Purine Derivatives

Liang, Yujie,Liang, Yu-Feng,Tang, Conghui,Yuan, Yizhi,Jiao, Ning

supporting information, p. 16395 - 16399 (2015/11/09)

A cationic cobalt(III)-catalyzed direct C-H amidation of unactivated (hetero)arenes and alkenes by using 1,4,2-dioxazol-5-ones as the amidating reagent has been developed. This transformation proceeds efficiently under external oxidant-free conditions wit

Orthogonal reactivity of acyl azides in C-H activation: Dichotomy between C-C and C-N amidations based on catalyst systems

Shin, Kwangmin,Ryu, Jaeyune,Chang, Sukbok

, p. 2022 - 2025 (2014/05/06)

The dual reactivity of acyl azides was utilized successfully in C-H activation by the choice of catalyst systems: while selective C-C amidation was achieved under thermal Rh catalysis, a Ru catalyst was found to mediate direct C-N amidation also highly se

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