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5-methyl-2-(4-trifluoromethoxyphenyl)-2H-pyrazol-3-ylamine is a complex organic compound with the molecular formula C11H9F3N3O. It features a pyrazol-3-ylamine core, which is a heterocyclic ring system containing nitrogen. The molecule is characterized by a methyl group at the 5-position, a trifluoromethoxyphenyl group at the 2-position, and an amino group attached to the pyrazole ring. 5-methyl-2-(4-trifluoromethoxyphenyl)-2H-pyrazol-3-ylamine is of interest in medicinal chemistry due to its potential as a building block for the development of new pharmaceuticals, particularly in the area of kinase inhibitors. Its specific structure allows for interactions with biological targets, making it a candidate for further research and development in drug discovery.

497141-59-0

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497141-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497141-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,1,4 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 497141-59:
(8*4)+(7*9)+(6*7)+(5*1)+(4*4)+(3*1)+(2*5)+(1*9)=180
180 % 10 = 0
So 497141-59-0 is a valid CAS Registry Number.

497141-59-0Downstream Products

497141-59-0Relevant academic research and scientific papers

Oxidative Ring-Opening of 1H-Pyrazol-5-amines and Its Application in Constructing Pyrazolo–Pyrrolo–Pyrazine Scaffolds by Domino Cyclization

Bao, Xiaoguang,Fu, Rui,Gao, Ke,Jin, Feng,Pan, Lei,Zhou, Shaofang

, p. 2956 - 2961 (2020)

Herein, an oxidative ring-opening of 1H-pyrazol-5-amines to form 3-diazenylacrylonitrile derivatives under mild and transition-metal-free conditions is described. In addition, the nucleophilic addition of deprotonated 1H-pyrrole-2-carbaldehydes to the vinyl moiety of the yielded 3-diazenylacrylonitriles could trigger domino cyclization to afford the 3H-pyrazolo[3,4-e]pyrrolo[1,2-a]pyrazine derivatives. Computational studies suggest that the oxidation of 1H-pyrazol-5-amines in the presence of PhIO is through the formation of a hydroxylamine intermediate followed by elimination of H2O to result in the ring-opening product. The detailed domino cyclization pathway leading to the pyrazolo–pyrrolo–pyrazine scaffolds is revealed.

NEW POSITIVE ALLOSTERIC MODULATORS OF NICOTINIC ACETYLCHOLINE RECEPTOR

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Page/Page column 14, (2013/02/28)

The present invention relates to compounds useful in therapy, to compositions comprising said compounds, and to methods of treating diseases comprising administration of said compounds. The compounds referred to are positive allosteric modulators (PAMs) of the nicotinic acetylcholine alpha7 receptor.

PYRAZOLOPYRIDINES USEFUL IN THE TREATMENT OF DISORDERS OF THE CENTRAL NERVOUS SYSTEM

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Page/Page column 31; 33, (2013/03/26)

The present invention relates to compounds useful in therapy, to compositions comprising said compounds, and to methods of treating diseases comprising administration of said com- pounds. The compounds referred to are positive allosteric modulators (PAMs) of the nicotinic acetylcholine α7 receptor.

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