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2-isopropyl-4-phenyl-1H-imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31787-73-2

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31787-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31787-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,8 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31787-73:
(7*3)+(6*1)+(5*7)+(4*8)+(3*7)+(2*7)+(1*3)=132
132 % 10 = 2
So 31787-73-2 is a valid CAS Registry Number.

31787-73-2Downstream Products

31787-73-2Relevant academic research and scientific papers

One-pot synthesis of 2-alkyl-4(5)-aryl-1H-imidazoles from 1-aryl-2-bromoethanones, ammonium carbonate and aliphatic carboxylic acids

Liu, Cong,Nie, Yijiao,Yao, Guowei,Dai, Rongji,Deng, Yulin

, p. 208 - 210 (2014)

A simple and efficient protocol for the preparation of 2-alkyl-4(5)-aryl- 1H-imidazoles starting from α-bromo aryl methyl ketones and aliphatic carboxylic acids in the presence of ammonium carbonate has been developed.

Nickel-Catalyzed Construction of 2,4-Disubstituted Imidazoles via C–C Coupling and C?N Condensation Cascade Reactions

Fang, Shengyang,Yu, Haihua,Yang, Xicheng,Li, Jianqi,Shao, Liming

supporting information, p. 3312 - 3317 (2019/06/13)

A convenient Ni(II)-catalyzed C?C and C?N cascade coupling reaction was developed to directly access various 2,4-disubstituted imidazoles. The reaction scope covers a variety of aryl and aliphatic substitutions, which demonstrate moderate-to-excellent yie

Synthesis of Imidazoles and Pyrimidines Using Palladium-Catalyzed Decarboxylative Intramolecular Condensation of 1,2,4-Oxadiazol-5(4 H)-ones

Shimbayashi, Takuya,Okamoto, Kazuhiro,Ohe, Kouichi

supporting information, p. 1916 - 1920 (2014/08/18)

We found that 1,2,4-oxadiazol-5(4H)-ones acted as iminonitrene equivalents in the presence of a palladium catalyst and a stoichiometric amount of phosphine and that aza-Wittig-type condensation with the internal carbonyl moiety occurred to afford the corresponding imidazoles and pyrimidines. Georg Thieme Verlag Stuttgart. New York.

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