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

25205-88-3

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25205-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25205-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,0 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25205-88:
(7*2)+(6*5)+(5*2)+(4*0)+(3*5)+(2*8)+(1*8)=93
93 % 10 = 3
So 25205-88-3 is a valid CAS Registry Number.

25205-88-3Downstream Products

25205-88-3Relevant academic research and scientific papers

A novel synthetic method of 2,4-disubstituted oxazoles using carboxylic acid-derived Bu2Sn[OC(O)R]2

Yoneyama, Hiroki,Oka, Naoki,Usami, Yoshihide,Harusawa, Shinya

supporting information, (2020/05/21)

A novel synthetic method for the preparation of 2,4-disubstituted oxazoles was developed, entailing the reaction of dibutyltin diacylates Bu2Sn[OC(O)R]2 with 1-substituted acetylenes and TMSN3 to afford a range of 2,4-disu

Synthesis of 2,4- and 2,4,5-substituted oxazoles via a silver triflate mediated cyclization

Bailey, Jessica L.,Sudini, Ravinder R.

, p. 3674 - 3677 (2014/06/23)

2,4- and 2,4,5-substituted oxazoles were prepared from a broad range of bromo-ketones and amides in high yield and purity.

A versatile synthesis of 2,4-substituted oxazoles

Chudasama, Vijay,Wilden, Jonathan D.

supporting information; experimental part, p. 3768 - 3770 (2009/02/07)

A variety of five-membered ring oxazoles have been synthesised with complete regiocontrol and without the requirement for ring oxidation via a reaction sequence based on a vinyl sulfonamide template. The Royal Society of Chemistry.

Convenient syntheses of 2-alkyl(Aryl)-4,5-diphenyloxazoles and 2-alkyl(Aryl)-4-phepyloxazoles

Pei, Weiwei,Li, Shaohui,Nie, Xiaoping,Li, Yiwei,Pei, Jian,Chen, Bingzi,Wu, Jie,Ye, Xiulin

, p. 1298 - 1304 (2007/10/03)

The synthetic methods to prepare 2-alkyl(aryl)-4,5-diphenyloxazoles and 2-alkyl(aryl)-4-phenyloxazoles were improved on the basis of a mechanistic study of oxazole formation from α-hydroxy ketones (carboxylic esters of benzoin and phenacyl alcohols). By these methods, seven trisubstituted oxazoles and twelve disubstituted oxazoles of the title compounds were prepared.

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