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4-imidazo[1,2-a]pyridin-3-ylbenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1373494-41-7

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1373494-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373494-41-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,4,9 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1373494-41:
(9*1)+(8*3)+(7*7)+(6*3)+(5*4)+(4*9)+(3*4)+(2*4)+(1*1)=177
177 % 10 = 7
So 1373494-41-7 is a valid CAS Registry Number.

1373494-41-7Downstream Products

1373494-41-7Relevant academic research and scientific papers

Direct catalytic C-H arylation of imidazo[1,2-a]pyridine with aryl bromides using magnetically recyclable Pd-Fe3O4 nanoparticles

Lee, Jaewoo,Chung, Jooyoung,Byun, Sang Moon,Kim, B. Moon,Lee, Chulbom

, p. 5660 - 5664 (2013)

The direct C-H arylation of a heteroarene with aryl bromides has been achieved under the catalysis of magnetic nanoparticles. In the presence of bimetallic Pd-Fe3O4 heterodimer nanocrystals (1 mol % in palladium), the reaction of imi

Pd-Catalyzed Tandem Cyclization via C-H Arylation and Acylation for the Construction of Polycyclic Scaffolds

Mu, Bing,Li, Jingya,Zou, Dapeng,Wu, Yusheng,Chang, Junbiao,Wu, Yangjie

supporting information, p. 5260 - 5263 (2016/11/02)

The first Pd-catalyzed tandem cyclization of imidazo[1,2-a]pyridines with 2-chlorobenzaldehydes through C-H arylation and acylation is presented for the efficient synthesis of novel 6H-benzo[b]imidazo[5,1,2-de]quinolizin-6-ones. The direct acylation react

Phosphine-free palladium-catalyzed direct arylation of imidazo[1,2-a] pyridines with aryl bromides at low catalyst loading

Fu, Hai Yan,Chen, Lu,Doucet, Henri

experimental part, p. 4473 - 4478 (2012/06/30)

Ligand-free Pd(OAc)2 was found to catalyze very efficiently the direct arylation of imidazo[1,2-a]pyridines at C3 under very low catalyst concentration. The reaction can be performed employing as little as 0.1-0.01 mol % catalyst with electron-

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