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2-iodo-4-methyl-1-(p-tolyloxy)benzene is an organic compound characterized by its molecular formula C15H15IO2. This aromatic compound features a benzene ring with a methyl group at the 4-position, an iodine atom at the 2-position, and a para-tolyloxy (4-methylphenoxy) group at the 1-position. The presence of the iodine atom and the para-tolyloxy group imparts unique chemical properties to the molecule, making it a potential candidate for various applications in organic synthesis, pharmaceuticals, and materials science. The compound's structure and functional groups contribute to its reactivity and stability, which can be further explored in chemical reactions and transformations.

2236-41-1

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2236-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2236-41-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,3 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2236-41:
(6*2)+(5*2)+(4*3)+(3*6)+(2*4)+(1*1)=61
61 % 10 = 1
So 2236-41-1 is a valid CAS Registry Number.

2236-41-1Downstream Products

2236-41-1Relevant academic research and scientific papers

Four- and Sixfold Tandem-Domino Reactions Leading to Dimeric Tetrasubstituted Alkenes Suitable as Molecular Switches

Tietze, Lutz F.,Waldecker, Bernd,Ganapathy, Dhandapani,Eichhorst, Christoph,Lenzer, Thomas,Oum, Kawon,Reichmann, Sven O.,Stalke, Dietmar

, p. 10317 - 10323 (2015/09/01)

A highly efficient palladium-catalyzed fourfold tandem-domino reaction consisting of two carbopalladation and two C-H-activation steps was developed for the synthesis of two types of tetrasubstituted alkenes 3 and 6 with intrinsic helical chirality starting from substrates 1 and 4, respectively. A sixfold tandem-domino reaction was also developed by including a Sonogashira reaction. 20 compounds with different substitution patterns were prepared with yields of up to 97%. Structure elucidation by X-ray crystallography confirmed helical chirality of the two alkene moieties. Photophysical investigations of some of the compounds showed pronounced switching properties through light-controlled changes of their stereochemical configuration.

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