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1-iodo-4,5-dimethoxy-2-[2-(4-methylbenzenesulfonylamino)ethyl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

950676-25-2

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950676-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 950676-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,6,7 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 950676-25:
(8*9)+(7*5)+(6*0)+(5*6)+(4*7)+(3*6)+(2*2)+(1*5)=192
192 % 10 = 2
So 950676-25-2 is a valid CAS Registry Number.

950676-25-2Relevant academic research and scientific papers

Asymmetric synthesis of 1-vinyltetrahydroisoquinoline through Pd-catalyzed intramolecular allylic amination

Shi, Ce,Ojima, Iwao

, p. 8563 - 8570 (2007)

Asymmetric synthesis of 6,7-dimethoxy-1-vinyltetrahydroisoquinolines through Pd-catalyzed intramolecular allylic amination of 3-(amidoethylphenyl)prop-2-enyl carbonates was studied, using a library of fine-tunable monodentate phosphoramidite ligands. Unde

Synthesis of Functionalized Indolines and Dihydrobenzofurans by Iron and Copper Catalyzed Aryl C-N and C-O Bond Formation

Henry, Martyn C.,Senn, Hans Martin,Sutherland, Andrew

, p. 346 - 364 (2019/01/08)

A simple and effective one-pot, two-step intramolecular aryl C-N and C-O bond forming process for the preparation of a wide range of benzo-fused heterocyclic scaffolds using iron and copper catalysis is described. Activated aryl rings were subjected to a highly regioselective, iron(III) triflimide-catalyzed iodination, followed by a copper(I)-catalyzed intramolecular N-or O-arylation step leading to indolines, dihydrobenzofurans, and six-membered analogues. The general applicability and functional group tolerance of this method were exemplified by the total synthesis of the neolignan natural product, (+)-obtusafuran. DFT calculations using Fukui functions were also performed, providing a molecular orbital rationale for the highly regioselective arene iodination process.

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