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4-(2,6-dimethylpyridin-3-yloxy)-3-chlorophenylamine is a complex organic chemical compound with the molecular formula C13H12ClN2O. It features a 3-chlorophenylamine core, which is a derivative of aniline with a chlorine atom attached to the third carbon. The molecule also contains a 2,6-dimethylpyridin-3-yloxy group, which is a pyridine ring with two methyl groups at the second and sixth positions and a hydroxyl group attached to the third position. 4-(2,6-dimethylpyridin-3-yloxy)-3-chlorophenylamine is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as a building block for the development of new compounds with biological activity. Its structure and properties make it a versatile intermediate in organic synthesis, allowing for further functionalization and the creation of a variety of derivatives.

1362703-52-3

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1362703-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1362703-52-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,2,7,0 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1362703-52:
(9*1)+(8*3)+(7*6)+(6*2)+(5*7)+(4*0)+(3*3)+(2*5)+(1*2)=143
143 % 10 = 3
So 1362703-52-3 is a valid CAS Registry Number.

1362703-52-3Relevant academic research and scientific papers

Discovery of 1,4-disubstituted 3-cyano-2-pyridones: A new class of positive allosteric modulators of the metabotropic glutamate 2 receptor

Cid, Jose María,Duvey, Guillaume,Tresadern, Gary,Nhem, Vanthea,Furnari, Rocco,Cluzeau, Philippe,Vega, Juan Antonio,De Lucas, Ana Isabel,Matesanz, Encarnación,Alonso, José Manuel,Linares, María Lourdes,Andrés, José Ignacio,Poli, Sonia M.,Lutjens, Robert,Himogai, Hassan,Rocher, Jean-Philippe,MacDonald, Gregor J.,Oehlrich, Daniel,Lavreysen, Hilde,Ahnaou, Abdelah,Drinkenburg, Wilhelmus,MacKie, Claire,Trabanco, Andrés A.

experimental part, p. 2388 - 2405 (2012/05/05)

The discovery and characterization of compound 48, a selective and in vivo active mGlu2 receptor positive allosteric modulator (PAM), are described. A key to the discovery was the rational exploration of the initial HTS hit 13 guided by an overlay model built with reported mGlu2 receptor PAM chemotypes. The initial weak in vitro activity of the hit 13 was quickly improved, although compounds still had suboptimal druglike properties. Subsequent modulation of the physicochemical properties resulted in compounds having a more balanced profile, combining good potency and in vivo pharmacokinetic properties. Final refinement by addressing cardiovascular safety liabilities led to the discovery of compound 48. Besides good potency, selectivity, and ADME properties, compound 48 displayed robust in vivo activity in a sleep-wake electroencephalogram (sw-EEG) assay consistent with mGlu2 receptor activation, in accordance with previous work from our laboratories.

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