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2-Chloro-N-(4-fluorophenyl)nicotinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57841-99-3

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57841-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57841-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,4 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57841-99:
(7*5)+(6*7)+(5*8)+(4*4)+(3*1)+(2*9)+(1*9)=163
163 % 10 = 3
So 57841-99-3 is a valid CAS Registry Number.

57841-99-3Relevant academic research and scientific papers

Method for preparing amide through electrochemical dechlorination of trichloromethyl pyridine derivative

-

Paragraph 0033-0060, (2020/08/27)

The invention discloses a method for preparing amide by electrochemical dechlorination of a trichloromethylpyridine derivative, the method is characterized by comprising the following steps of: (1) dissolving a polychloropyridine derivative in an amine so

Expedited access to thieno[3,2-c]quinolin-4(5H)-ones and benzo[h]-1,6-naphthyridin-5(6H)-ones via a continuous flow photocyclization method

Fang,Tranmer

supporting information, p. 10799 - 10803 (2016/12/06)

A single-step continuous flow method has been developed that gives expedited access to complex heterocycles via an intramolecular photochemical cyclization. Herein we report the first examples of the photochemically-induced generation of thieno[3,2-c]quin

ALPHA 7 NICOTINIC ACETYLCHOLINE RECEPTOR ALLOSTERIC MODULATORS, THEIR DERIVATIVES AND USES THEREOF

-

Paragraph 00108, (2013/12/03)

The present application is related to compounds represented by Formula I, which are novel positive allosteric modulators of al nAChRs. The application also discloses the treatment of disorders that are responsive to enhancement of acetylcholine action on al nAChRs in a mammal by administering an effective amount of a compound of Formula I.

Nine N-aryl-2-chloronicotinamides: Supramolecular structures in one, two and three dimensions

Cuffini, Silvia,Christopher, Glidewell,Low, John N.,De Oliveira, Aline G.,De Souza, Marcus V. N.,Vasconcelos, Thatyana R. A.,Wardell, Solange M. S. V.,Wardell, James L.

, p. 651 - 665 (2008/02/08)

Structures are reported here for eight further substituted N-aryl-2-chloronicotinamides, 2-ClC5H3NCONHC 6H4X-4′. When X = H, compound (I) (C 12H9ClN2O), the molecules are linked

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