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ethyl 2-(p-tolyl)oxazole-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1037597-71-9

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1037597-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1037597-71-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,5,9 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1037597-71:
(9*1)+(8*0)+(7*3)+(6*7)+(5*5)+(4*9)+(3*7)+(2*7)+(1*1)=169
169 % 10 = 9
So 1037597-71-9 is a valid CAS Registry Number.

1037597-71-9Downstream Products

1037597-71-9Relevant academic research and scientific papers

Direct Arylation of Azoles Enabled by Pd/Cu Dual Catalysis

Piou, Tiffany,Slutskyy, Yuriy,Kevin, Nancy J.,Sun, Zhongxiang,Xiao, Dong,Kong, Jongrock

, p. 1996 - 2001 (2021)

A practical approach toward the synthesis of 2-arylazoles via direct arylation is described. The transformation relies on a Pd/Cu cocatalyst system that operates with low catalyst loadings. The reaction conditions were found to be tolerant of a wide range of functional groups and nitrogen-containing heterocycles commonly employed in a drug discovery setting.

Palladium-catalyzed direct C2-arylation of azoles with aromatic triazenes

Liu, Can,Wang, Zhiming,Wang, Lei,Li, Pinhua,Zhang, Yicheng

, p. 9209 - 9216 (2019/11/05)

A highly efficient palladium-catalyzed arylation of azoles at the C2-position using 1-aryltriazenes as aryl reagents was developed. Azoles including oxazoles, thiazoles, imidazoles, 1,3,4-oxadiazoles, and oxazolines could react with 1-aryltriazenes smoothly to generate the corresponding products in good to excellent yields, and various substitution patterns were tolerated toward the reaction.

Palladium-catalyzed deamidative arylation of azoles with arylamides through a tandem decarbonylation-C-H functionalization

Li, Chengliang,Li, Pinhua,Yang, Jin,Wang, Lei

supporting information; experimental part, p. 4214 - 4216 (2012/05/04)

A highly chemo-, regio-selective, and efficient palladium-catalyzed deamidative arylation of azoles with arylamides, as an aryl metal equivalent, has been developed. The reaction proceeds smoothly to generate the corresponding products in good yields via a tandem decarbonylation-C-H activation.

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