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N-(4-methoxyphenyl)-2-nitro-4-(trifluoromethyl)aniline is a complex organic compound with the molecular formula C14H11F3N2O3. It is characterized by the presence of a nitro group (-NO2), a trifluoromethyl group (-CF3), and a methoxy group (-OCH3) attached to an aniline moiety. N-(4-methoxyphenyl)-2-nitro-4-(trifluoromethyl)aniline is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and reactivity. The combination of electron-donating and electron-withdrawing groups in its structure can influence its chemical properties, making it a subject of interest in organic chemistry research.

849-58-1

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849-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849-58-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 849-58:
(5*8)+(4*4)+(3*9)+(2*5)+(1*8)=101
101 % 10 = 1
So 849-58-1 is a valid CAS Registry Number.

849-58-1Relevant academic research and scientific papers

Decarboxylative ipso Amination of Activated Benzoic Acids

Pichette Drapeau, Martin,Bahri, Janet,Lichte, Dominik,Goo?en, Lukas J.

supporting information, p. 892 - 896 (2019/01/04)

In the presence of a bimetallic Pd/Cu system with 1,10-phenanthroline as the ligand and either air or N-methylmorpholine N-oxide as the oxidant, electron-deficient benzoic acids undergo oxidative decarboxylative coupling with unprotected amines. This operationally simple aniline synthesis is widely applicable with respect to the amine and gives good yields, even on multigram scale. The orthogonality of this reaction to other Pd-catalyzed cross-couplings allows the concise synthesis of multisubstituted arenes by sequential C?C, C?Cl, and C?N functionalizations. Mechanistic investigations suggest the intermediacy of a hypervalent Pd species.

Polymer-assisted parallel solution phase synthesis of substituted benzimidazoles

Yun, Young K.,Porco Jr., John A.,Labadie, Jeff

, p. 739 - 742 (2007/10/03)

A small library of benzimidazoles was prepared using polymer-bound reagents and scavengers. Polymer-assisted reaction of diphenyl diamines with carboxylic acids yielded o-amido-diphenylamines in the presence of Polystyrene-Carbodiimide (PS-Carbodiimide) u

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