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1-(3-chlorophenylethynyl)-3-methylbenzene is an organic compound with the molecular formula C15H11Cl. It is a derivative of benzene, featuring a 3-methyl group attached to the benzene ring and a 3-chlorophenylethynyl group connected through an ethynyl (acetylene) bridge. 1-(3-chlorophenylethynyl)-3-methylbenzene is characterized by its unique structure, which combines the properties of both aromatic and acetylenic compounds. It is often used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its versatile chemical reactivity and potential for further functionalization. The presence of the chlorine atom in the 3-chlorophenyl group also allows for further substitution reactions, making it a valuable building block in organic synthesis.

57542-74-2

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57542-74-2 Usage

Structure

Linear with a phenyl group, a methyl group, and an ethynyl group attached to the benzene ring

Derivative

Benzene

Usage

Manufacturing of pharmaceuticals, agrochemicals, and other organic compounds

Chemical properties

Unique chemical properties due to the presence of chlorophenyl and ethynyl groups

Potential use

Reactive intermediate in organic synthesis

Applications

Various fields of chemistry and industry

Building block

Valuable building block for organic synthesis due to the presence of chlorophenyl and ethynyl groups

Check Digit Verification of cas no

The CAS Registry Mumber 57542-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,4 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57542-74:
(7*5)+(6*7)+(5*5)+(4*4)+(3*2)+(2*7)+(1*4)=142
142 % 10 = 2
So 57542-74-2 is a valid CAS Registry Number.

57542-74-2Relevant academic research and scientific papers

Iron-catalyzed sonogashira reactions

Carril, Monica,Correa, Arkaitz,Bolm, Carsten

supporting information; experimental part, p. 4862 - 4865 (2009/02/08)

(Chemical Equation Presented) With an iron will: Terminal alkynes undergo reaction with aryl and heteroaryl iodides in the presence of an iron catalyst formed from FeCl3 and N,N′-dimethylethylenediamine (dmeda, see scheme). The method displays

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