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3-(3,4-Dimethoxyphenyl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79445-45-7

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79445-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79445-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79445-45:
(7*7)+(6*9)+(5*4)+(4*4)+(3*5)+(2*4)+(1*5)=167
167 % 10 = 7
So 79445-45-7 is a valid CAS Registry Number.

79445-45-7Relevant academic research and scientific papers

Synthesis of 3-Arylpyridines via Palladium/Copper-Catalyzed Annulation of Allylamine/1,3-Propanediamine and Aldehydes

Yang, Xiaodong,Yang, Shenghua,Xiang, Likui,Pang, Xiaobo,Chen, Baohua,Huang, Guosheng,Yan, Rulong

, p. 3732 - 3736 (2016/01/25)

A novel and efficient method for the synthesis of 3-arylpyridines from allylamine/propanediamine and aldehydes by palladium/copper-catalyzed oxidative tandem cyclization has been developed. With this reaction, a series of desired 3-arylpyridines was synthesized in moderate yields via C-C/C-N bond formation and 6-endo/exo-trig cyclization.

Cross-coupling study of iodo/chloropyridines and 2-chloroquinoline with atom-economic triarylbismuth reagents under Pd-catalysis

Rao, Maddali L.N.,Dhanorkar, Ritesh J.

, p. 338 - 349 (2015/03/04)

This study describes the palladium-catalyzed couplings of iodopyridines, chloropyridines, and chloroquinoline with atom-economic BiAr3 reagents in sub-stoichiometric loadings. Mono-arylations of iodo and chloropyridines produced arylpyridines i

Triarylbismuthanes as threefold aryl-transfer reagents in regioselective cross-coupling reactions with bromopyridines and quinolines

Rao, Maddali L.N.,Dhanorkar, Ritesh J.

supporting information, p. 5214 - 5228 (2014/10/15)

Cross-coupling studies using bromopyridines and bromoquinolines with triarylbismuths as threefold coupling reagents in substoichiometric amounts under Pd-catalysed conditions are disclosed. The reactivity was high with both mono- and dibromopyridyl substrates, and mono- and bis-couplings were carried out regioselectively. A library of monoaryl and diaryl pyridines was formed in high yields. A one-pot strategy provided a simple and straightforward synthesis of both symmetrical and unsymmetrical diarylpyridines. Arylations of 2-bromo- and 3-bromoquinolines were achieved with triarylbismuth reagents. This study demonstrates that triarylbismuths may be used as threefold arylating reagents for the synthesis of aryl pyridines and quinolines through couplings with bromopyridines and bromoquinolines under Pd-catalysed conditions. Copyright

Ti(IV)-centered dynamic interconversion between Pd(II), Ti(IV)-containing ring and cage molecules

Hiraoka, Shuichi,Sakata, Yoko,Shionoya, Mitsuhiko

supporting information; experimental part, p. 10058 - 10059 (2009/02/03)

Heteronuclear, supramolecular ring and cage complexes have been constructed from a pyridyl catechol ligand, TiO(acac)2, and PdCl2(CH3CN)2. These two complexes are quantitatively interconvertible, in which Ti4+-centered coordination changes take place between a well-known Ti(catecholato)3 and a newly established TiH(catecholato)2(acetylacetonato) structures. The Ti4+-centered structural changes arise from the changes in the component fraction and basicity condition. Copyright

3-Phenylpiperidines. Central Dopamine-Autoreceptor Stimulating Activity

Hacksell, Uli,Arvidsson, Lars-Erik,Svensson, Uno,Nilsson, J. Lars G.

, p. 1475 - 1482 (2007/10/02)

Thirty compounds related to the selective dopamine-autoreceptor agonist 3-(3-hydroxyphenyl)-N-n-propylpiperidine have been synthesized and tested for central dopamine-autoreceptor stimulating activity.The 3-(3-hydroxyphenyl)piperidine moiety seems indispensable for high potency and selectivity.Introduction of an additional hydroxyl group into the 4-position of the aromatic ring gives a compound with dopaminergic activity but lacking selectivity for autoreceptors. 3-(3-Hydroxyphenyl)-N-n-propylpyrrolidine, 3-(3-hydroxy)-N-n-propylperhydroazepine, and 3-(3-hydroxyphenyl)quinuclidine were all inactive.The most potent compounds were the N-isopropyl-, N-n-butyl-, N-n-pentyl-, and N-phenethyl-substituted 3-(3-hydroxyphenyl)piperidine derivatives.None of the compounds investigated seemed to have central noradrenaline- or serotonin-receptor stimulating activity.

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