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

130406-95-0

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130406-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130406-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,0 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130406-95:
(8*1)+(7*3)+(6*0)+(5*4)+(4*0)+(3*6)+(2*9)+(1*5)=90
90 % 10 = 0
So 130406-95-0 is a valid CAS Registry Number.

130406-95-0Relevant academic research and scientific papers

Synthesis of 4-benzylpyridines via Pd-catalyzed CH3-arylation of 4-picoline

Wu, Jing,Wang, Dadian,Chen, Xiang,Gui, Qingwen,Li, Hua,Tan, Ze,Huang, Genping,Wang, Guangwei

supporting information, p. 7509 - 7512 (2017/09/27)

A highly efficient synthesis of 4-benzylpyridines was developed via Pd-catalyzed C(sp3)-H arylation between 4-picoline and aryl halides. It was found that the best yields were achieved with a simple Pd(PPh3)4 catalyst and Cs2CO3 as the base. Compared with the known methods, our reaction does not require the use of a strong organometallic reagent as the base.

Lewis acid promoted benzylic cross-couplings of pyridines with aryl bromides

Duez, Stephanie,Steib, Andreas K.,Manolikakes, Sophia M.,Knochel, Paul

supporting information; experimental part, p. 7686 - 7690 (2011/10/17)

Either ZnCl2, Sc(OTf)3, or BF3OEt 2 can promote the palladium-catalyzed arylation of methylpyridines and related heterocycles (see example). The complexation of the Lewis acid to the nitrogen atom in the heteroc

Flexible N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine analogues: Synthesis and monoamine oxidase catalyzed bioactivation

Efange,Michelson,Remmel,Boudreau,Dutta,Freshler

, p. 3133 - 3138 (2007/10/02)

Eighteen analogues of N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) were synthesized and evaluated as substrates of monoamine oxidase. In general, the flexible analogues, characterized by the presence of a methylene (or ethylene) bridge between the aryl/heteroaryl and tetrahydropyridyl moieties, were better substrates of the enzyme than the conformationally restricted MPTP. It is suggested that the increased oxidative activity of these flexible analogues reflects enhanced binding due to the ability of the C-4-aryl/heteroaryl substituent to gain access to a hydrophobic pocket within the substrate binding site.

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