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(S)-1-(4-bromophenyl)-2,2-difluoroethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

887781-85-3

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887781-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 887781-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,7,8 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 887781-85:
(8*8)+(7*8)+(6*7)+(5*7)+(4*8)+(3*1)+(2*8)+(1*5)=253
253 % 10 = 3
So 887781-85-3 is a valid CAS Registry Number.

887781-85-3Relevant academic research and scientific papers

Tuning the reactivity of difluoromethyl sulfoximines from electrophilic to nucleophilic: Stereoselective nucleophilic difluoromethylation of aryl ketones

Shen, Xiao,Zhang, Wei,Ni, Chuanfa,Hu, Jinbo,Gu, Yucheng

, p. 16999 - 17002,4 (2020/09/02)

A stereoselective synthesis of enantiomerically enriched difluoromethyl tertiary alcohols by tuning the reactivity of difluoromethyl sulfoximines from electrophilic to nucleophilic difluoromethylating agents is reported. The key feature of this chemistry is the diastereoselective addition of the difluoromethyl sulfoximine to the prochiral carbon of the ketone. The present method was used to prepare enantiomerically enriched difluoromethyl secondary alcohols and difluorinated analogues of the natural products gossonorol and boivinian B, demonstrating the potency of the method.

The discovery of MK-0674, an orally bioavailable cathepsin K inhibitor

Isabel, Elise,Bateman, Kevin P.,Chauret, Nathalie,Cromlish, Wanda,Desmarais, Sylvie,Duong, Le T.,Falgueyret, Jean-Pierre,Gauthier, Jacques Yves,Lamontagne, Sonia,Lau, Cheuk K.,Leger, Serge,LeRiche, Tammy,Levesque, Jean-Francois,Li, Chun Sing,Masse, Frederic,McKay, Daniel J.,Mellon, Christophe,Nicoll-Griffith, Deborah A.,Oballa, Renata M.,Percival, M. David,Riendeau, Denis,Robichaud, Joel,Rodan, Gideon A.,Rodan, Sevgi B.,Seto, Carmai,Therien, Michel,Truong, Vouy Linh,Wesolowski, Gregg,Young, Robert N.,Zamboni, Robert,Black, W. Cameron

scheme or table, p. 887 - 892 (2010/08/22)

MK-0674 is a potent and selective cathepsin K inhibitor from the same structural class as odanacatib with a comparable inhibitory potency profile against Cat K. It is orally bioavailable and exhibits long half-life in pre-clinical species. In vivo studies

Cathepsin cysteine protease inhibitors

-

Page/Page column 16, (2010/11/08)

This invention relates to a novel class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is i

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