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1-(4-methylbenzenesulfonyl)-5-(4-methoxyphenyl)-1,2,3-triazole is a complex organic chemical compound with the molecular formula C15H14N2O3S. It is a derivative of the 1,2,3-triazole ring system, which is a five-membered heterocyclic ring containing three nitrogen atoms. The compound features a 4-methylbenzenesulfonyl group attached to the 1-position of the triazole ring and a 4-methoxyphenyl group at the 5-position. The presence of the sulfonyl and methoxy groups imparts unique chemical properties to the molecule, making it potentially useful in various applications, such as pharmaceuticals or agrochemicals, where it may serve as a building block or intermediate in the synthesis of more complex molecules.

5604-42-2

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5604-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5604-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,0 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5604-42:
(6*5)+(5*6)+(4*0)+(3*4)+(2*4)+(1*2)=82
82 % 10 = 2
So 5604-42-2 is a valid CAS Registry Number.

5604-42-2Relevant academic research and scientific papers

Exploring the reactivity of 1,5-disubstituted sulfonyl-triazoles: Thermolysis and Rh(II)-catalyzed synthesis of α-sulfonyl nitriles This article is dedicated to Professor Paul Wender for both his creative contributions to synthetic organic chemistry and u

Meza-Avi?a, Maria Elena,Patel, Mudita Kishor,Croatt, Mitchell P.

, p. 7840 - 7846 (2013/08/23)

The reactivity of a series of 1,5-disubstituted sulfonyl-triazoles was explored using either thermolytic or metal-catalyzed conditions. Both the thermolysis and the Rh(II)-catalyzed reactions led to the synthesis of α-sulfonyl-nitriles, which presumably o

Selective formation of 1,5-substituted sulfonyl triazoles using acetylides and sulfonyl azides

Meza-Avina, Maria Elena,Patel, Mudita Kishor,Lee, Cylivia B.,Dietz, Thomas J.,Croatt, Mitchell P.

supporting information; experimental part, p. 2984 - 2987 (2011/08/06)

The reaction of acetylides with sulfonyl azides was found to selectively form 1,5-substituted sulfonyl triazoles. This reaction thus provides access to the regioisomeric product as compared to the popular copper-catalyzed azide-alkyne cycloaddition. The reaction is efficient and selective with a variety of alkyne sources and sulfonyl azides and can incorporate an additional electrophile to yield 1,4,5-trisubstituted sulfonyl triazoles.

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