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1373889-89-4

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1373889-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373889-89-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,8,8 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1373889-89:
(9*1)+(8*3)+(7*7)+(6*3)+(5*8)+(4*8)+(3*9)+(2*8)+(1*9)=224
224 % 10 = 4
So 1373889-89-4 is a valid CAS Registry Number.

1373889-89-4Upstream product

1373889-89-4Downstream Products

1373889-89-4Relevant academic research and scientific papers

SULFONE DERIVATIVES AND THEIR USE AS PKM2 MODULATORS FOR THE TREATMENT OF CANCER

-

, (2013/03/26)

Provided herein is novel compound of the general formula (I), its tautomeric forms, its stereoisomers, its analogs, its prodrugs, its isotopes, its N- oxides, its metabolites, its pharmaceutically acceptable salts, its polymorphs, its solvates, its optical isomers, its clathrates, its co-crystals, its combinations with suitable medicament and pharmaceutical compositions comprising the same. Also provided is method of treating a disease responsive to activation of human PKM2 by administration of said compound and its use as PKM2 modulator in various pathological conditions.

Cyanoacetamides (IV): Versatile one-pot route to 2-quinoline-3-carboxamides

Wang, Kan,Herdtweck, Eberhardt,Doemling, Alexander

scheme or table, p. 316 - 322 (2012/06/18)

Cyanoacetic acid derivatives are the starting materials for a plethora of multicomponent reaction (MCR) scaffolds. Herein, we describe scope of a valuable general protocol for the synthesis of arrays of 2-aminoquinoline-3-carboxamides from cyanoacetamides and 2-aminobenzaldehydes or heterocyclic derivatives via a Friedlaender reaction variation. In many cases, the reactions involve a very convenient work up by simple precipitation and filtration. More than 40 new products are described. We foresee our protocol and the resulting derivatives becoming very valuable to greatly expanding the scaffold space of cyanoacetamide derivatives.

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