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Pyridine, 2-(4-methyl-2-nitrophenyl)-, also known as 2-(4-methyl-2-nitrophenyl)pyridine, is an organic compound with the chemical formula C12H10N2O2. It is a derivative of pyridine, a heterocyclic aromatic compound containing a nitrogen atom in the ring structure. The molecule features a 4-methyl-2-nitrophenyl group attached to the pyridine ring at the 2-position. Pyridine, 2-(4-methyl-2-nitrophenyl)- is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Due to its potential reactivity and the presence of a nitro group, it should be handled with care, following proper safety protocols.

4422-33-7

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4422-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4422-33-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4422-33:
(6*4)+(5*4)+(4*2)+(3*2)+(2*3)+(1*3)=67
67 % 10 = 7
So 4422-33-7 is a valid CAS Registry Number.

4422-33-7Relevant 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.

Rhodium(III)-catalyzed azidation and nitration of arenes by C-H activation

Xie, Fang,Qi, Zisong,Li, Xingwei

supporting information, p. 11862 - 11866 (2013/11/19)

Getting a handle on it: In the chelation-assisted title reactions in the presence of a hypervalent iodine oxidant, sodium azide and sodium nitrite served as readily available nitrogen sources, and pyridine, pyrimidine, and pyrazole substituents were effic

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.

Synthesis of the New Pyridobenzo-v-triazinium System via Valence Bond Isomerization

Messmer, A.,Hajos, Gy.,Giber, J.,Holly, S.

, p. 1133 - 1135 (2007/10/02)

α-Pyridylphenyl diazonium salts 2 were found to undergo valence bond isomerization and gave the new pyridobenzo-v-triazinium salts 3.The ir and nmr studies on the products showed that isomers 2 and 3 form an equilibrium, and the ring closure is favoured by electron withdrawing substituents.

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