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

27904-56-9

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27904-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27904-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,0 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27904-56:
(7*2)+(6*7)+(5*9)+(4*0)+(3*4)+(2*5)+(1*6)=129
129 % 10 = 9
So 27904-56-9 is a valid CAS Registry Number.

27904-56-9Relevant academic research and scientific papers

Molecular modeling and anticholinesterasic activity of novel 2-arylaminocyclohexyl N,N-dimethylcarbamates

Bagatin, Mariane C.,Ca?ndido, Augusto A.,Pinheiro, Glaucia M.S.,Ho?ehr, Nelci F.,Machinski Jr., Miguel,Mossini, Simone A.G.,Basso, Ernani A.,Gauze, Gisele F.

, p. 1798 - 1807 (2014/01/06)

This work reports a detailed theoretical and experimental study of the novel isomer series cis- and trans-2-arylaminocyclohexyl N,N-dimethylcarbamates as potential inhibitors of cholinesterases. In vitro inhibition assay by Ellman's method with human bloo

Catalytic enantioselective Amadori-Heyns rearrangement of racemic α-hydroxy ketones with arylamines: Synthesis of optically active α-arylamino ketones

Frongia, Angelo,Secci, Francesco,Capitta, Francesca,Piras, Pier Paolo,Sanna, Maria Luisa

supporting information, p. 8812 - 8814 (2013/09/24)

A novel synthesis of optically active α-arylamino ketones through an organocatalytic enantioselective Amadori-Heyns rearrangement is described. The Royal Society of Chemistry 2013.

Synthesis of β-amino cyclone catalyzed by alkaline Al 2O3

Xu,Chen,Liu,Ren,Zhou,Lu

experimental part, p. 4165 - 4168 (2012/01/05)

A new method for the synthesis of b-amino cyclone with amines and cyclonene, which was efficiently carried out under solvent free conditions in a short time at room temperature using the catalyst of alkaline Al 2O3 with high yield. T

Highly enantioselective synthesis of chiral cyclic amino alcohols and conhydrine by ruthenium-catalyzed asymmetric hydrogenation

Liu, Sheng,Xie, Jian-Hua,Li, Wei,Kong, Wei-Ling,Wang, Li-Xin,Zhou, Qi-Lin

supporting information; experimental part, p. 4994 - 4997 (2009/12/28)

A highly efficient enantio- and diastereoselective synthesis of chiral cis-β-N-alkyl/arylamino cyclic alcohols has been realized by asymmetric hydrogenation of racemic α-amino cyclic ketones via DKR catalyzed by [RuCl2((S)-Xyl-SDP)((R,R)-DPEN)]. The enantioselectivities of the reaction were up to 99.9% ee with 99:1 cis-selectivities. A practical catalytic asymmetric synthesis of all four isomers of conhydrine was also developed.

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