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Acetamide, 2,2,2-trifluoro-N-[2-[3-(trifluoromethyl)phenyl]ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

181514-28-3

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181514-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 181514-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,5,1 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 181514-28:
(8*1)+(7*8)+(6*1)+(5*5)+(4*1)+(3*4)+(2*2)+(1*8)=123
123 % 10 = 3
So 181514-28-3 is a valid CAS Registry Number.

181514-28-3Relevant academic research and scientific papers

SMALL MOLECULE ACTIVATORS OF NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) AND USES THEREOF

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Paragraph 00542, (2018/08/03)

Provided herein are small molecule activators of Nicotinamide Phosphoribosyltransferase (NAMPT), compositions comprising the compounds, and methods of using the compounds and compositions.

Indole, indazole and indoline derivatives as CETP inhibitors

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Page/Page column 23, (2010/02/15)

The present invention relates to compounds of formula (I): wherein —X—Y—, R1 to R11 and n are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prevention of diseases which are mediated by CETP inhibitors.

Substituted phenyl methanones

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Page/Page column 14, (2008/06/13)

The present invention relates to compounds of general formula IA or IB wherein X1 and X2 are each independently N or C—R″ and R1, R2,R3, R4, R5, and R6 are as defined

Preparation of 1,2,3,4-tetrahydroisoquinolines lacking electron donating groups - An intramolecular cyclization complementary to the Pictet-Spengler reaction

Stokker

, p. 5453 - 5456 (2007/10/03)

The synthesis of 1,2,3,4-tetrahydroisoquinolines via an intramolecular cyclization of N-trifluoroacylated phenethylamines devoid of electron donating groups, with paraformaldehyde mediated by acetic/sulfuric acid milieu is described.

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