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ethyl 2-(4-methoxyphenyl)-5-phenyloxazole-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1362690-80-9

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1362690-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1362690-80-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,2,6,9 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1362690-80:
(9*1)+(8*3)+(7*6)+(6*2)+(5*6)+(4*9)+(3*0)+(2*8)+(1*0)=169
169 % 10 = 9
So 1362690-80-9 is a valid CAS Registry Number.

1362690-80-9Downstream Products

1362690-80-9Relevant academic research and scientific papers

miRNA biosynthesis inhibitor

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Paragraph 0158; 0159; 0234-0236, (2019/06/12)

The invention provides a compound shown as a formula I, or a conformational isomer thereof, or an optical isomer thereof, or a pharmaceutically acceptable salt thereof. The compound can be tightly combined with related binding proteins in an miRNA biosynthesis process and can effectively inhibit the synthesis of miRNA-21. The prepared active compound provided by the invention can be used as an miRNA-21 inhibitor, and further as a potential drug for treating malignant tumors. The formula I is shown in the description.

Pd-catalyzed desulfitative arylation for the synthesis of 2,5-diarylated oxazole-4-carboxylates using dioxygen as the terminal oxidant

Tang, Xiaodong,Yang, Kai,Zeng, Liying,Liu, Qiang,Chen, Huoji

supporting information, p. 8504 - 8507 (2017/10/27)

A desulfitative arylation of 2-aryloxazole-4-carboxylate with sodium arylsulfinates under an oxygen (O2) atmosphere to afford 2,5-diarylated oxazole-4-carboxylates is described. This transformation provides a novel approach for the utilization of sodium arylsulfinates as the aryl source and O2 as the sole oxidant.

Regioselective synthesis of oxazole derivatives via palladium-catalyzed and copper-mediated cascade oxidative cyclization

Zheng, Jia,Zhang, Min,Huang, Liangbin,Hu, Xiaohan,Wu, Wanqing,Huang, Huawen,Jiang, Huangfeng

supporting information, p. 3609 - 3611 (2014/04/03)

A novel Pd-catalyzed/Cu-mediated oxidative cyclization has been developed for the synthesis of trisubstituted oxazoles, which is thought to proceed through cascade formation of C-N and C-O bonds. In this protocol, four hydrogen atoms were removed and water was used as the oxygen atom source. This journal is the Partner Organisations 2014.

Mechanism selection for regiocontrol in base-assisted, palladium-catalysed direct C-H coupling with halides: First approach for oxazole- and thiazole-4-carboxylates

Théveau, Laure,Verrier, Cécile,Lassalas, Pierrik,Martin, Thibaut,Dupas, Georges,Querolle, Olivier,Van Hijfte, Luc,Marsais, Francis,Hoarau, Christophe

supporting information; experimental part, p. 14450 - 14463 (2012/01/15)

Both base-assisted non-concerted metallation-deprotonation (nCMD) and concerted metallation-deprotonation (CMD) have been identified as two potent operating mechanisms in palladium-catalysed direct C-H coupling of oxazole and thiazole-4-carboxylate esters

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