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2-(2-Nitro-4-trifluoromethyl-phenyl)-pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

158461-30-4

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158461-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158461-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,4,6 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 158461-30:
(8*1)+(7*5)+(6*8)+(5*4)+(4*6)+(3*1)+(2*3)+(1*0)=144
144 % 10 = 4
So 158461-30-4 is a valid CAS Registry Number.

158461-30-4Relevant academic research and scientific papers

Aerobic oxidation of PdII to PdIV by active radical reactants: Direct C-H nitration and acylation of arenes via oxygenation process with molecular oxygen

Liang, Yu-Feng,Li, Xinyao,Wang, Xiaoyang,Yan, Yuepeng,Feng, Peng,Jiao, Ning

, p. 1956 - 1963 (2015/03/14)

A Pd-catalyzed aerobic oxidative C-H nitration and acylation of arenes with simple and readily available tert-butyl nitrite (TBN) and toluene as the radical precursors has been developed. Molecular oxygen is employed as the terminal oxidant and oxygen source to initiate the active radical reactants. Many different directing groups such as pyridine, pyrimidine, pyrazole, pyridol, pyridylketone, oxime, and azo groups can be employed in these novel transformations. The PdII/PdIV catalytic cycle through a radical process is the most likely pathway for these oxidative C-H nitration and acylation reactions.

Copper-mediated chelation-assisted ortho nitration of (hetero)arenes

Zhang, Lin,Liu, Zhenhua,Li, Huiqin,Fang, Guichun,Barry, Badru-Deen,Belay, Tuemay Abadi,Bi, Xihe,Liu, Qun

supporting information; experimental part, p. 6536 - 6539 (2012/02/04)

A novel copper-mediated chelation-assisted ortho C-H nitration of (hetero)arenes has been developed for the first time, which used dioxygen as terminal oxidant and 1, 2, 3-TCP as solvent, leading to the synthesis of nitroaromatics with excellent regiosele

Synthesis and antiarrhythmic activity of disubstituted phenylpyridine derivative

Shigyo,Sato,Shibuya,Takahashi,Yamaguchi,Sonoki,Ohta

, p. 1573 - 1582 (2007/10/02)

A series of disubstituted phenylpyridine derivatives was synthesized and their antiarrhythmic effects against chloroform-induced ventricular arrhythmias in mice were examined. Among them, 2- and 3-[2-(3- aminobutyramido)-4-(2,2,2-trifluoroethoxy)phenyl]pyridines (23h, 24h) and 3- [2-(3-aminobutyramido)-4-ethoxyphenyl]pyridine (24i) showed potent antiarrhythmic activity. They had approximately twice the potency of mexiletine (III). Compound 24i was selected from this series as a candidate for further development; it was found to have a class I B electrophysiological character and to show a slow kinetic rate-dependent block (RDB) of the sodium channel in cardiac muscle.

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