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4-(1H-imidazol-1-yl)-3-(trifluoromethyl)benzamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

351324-53-3

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351324-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 351324-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,3,2 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 351324-53:
(8*3)+(7*5)+(6*1)+(5*3)+(4*2)+(3*4)+(2*5)+(1*3)=113
113 % 10 = 3
So 351324-53-3 is a valid CAS Registry Number.

351324-53-3Relevant academic research and scientific papers

IMIDAZOQUINOLINES AS LIPID KINASE INHIBITORS

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Page/Page column 91, (2008/06/13)

The invention relates to novel organic compounds of formula (I) processes for the preparation thereof, the application thereof in a process for the treatment of the human or animal body, the use thereof - alone or in combination with one or more other pharmaceutically active compounds - for the treatment of an inflammatory or obstructive airway disease, such as asthma, disorders commonly occurring in connection with transplantation, or a proliferative disease, such as a tumor disease.

Preparation of Substituted N-Phenyl-4-aryl-2-pyrimidinamines as Mediator Release Inhibitors

Paul, Rolf,Hallett, William A.,Hanifin, John W.,Reich, Marvin F.,Johnson, Bernard D.,et al.

, p. 2716 - 2725 (2007/10/02)

The role of immunologically released mediators, such as histamine, leukotrienes, and platelet-activating factor, is well-established for asthma and other allergic disorders.Developing therapeutic agents which would block mediator release from mast cells and other relevant cell types would provide a rational approach to asthma therapy.Using human basophil as a screen, a series of 4-aryl-2-(phenylamino)pyrimidines was found which inhibited mediator release.These compounds were prepared by condensing acetyl heterocycles with dimethylformamide dimethyl acetal to form enaminones which are cyclized with aryl guanidines to give pyrimidines.After examining a large number of analogs, N--4-(2-pyridinyl)-2-pyrimidinamine (1-27) was chosen for toxicological evaluation.

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