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2,3-bis-(4-methoxy-phenyl)-5-methyl-indole is a complex organic compound with the molecular formula C21H19NO2. It is characterized by an indole core, which is a bicyclic structure consisting of a benzene ring fused to a pyrrole ring. The compound features two 4-methoxy-phenyl groups attached to the 2nd and 3rd positions of the indole, which contribute to its lipophilic nature and potential for interaction with biological targets. Additionally, a methyl group is attached to the 5th position of the indole, further modifying its chemical properties. 2,3-bis-(4-methoxy-phenyl)-5-methyl-indole is of interest in the field of organic chemistry and may have applications in the development of pharmaceuticals or other chemical products due to its unique structure and potential biological activity.

5782-05-8

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5782-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5782-05-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,8 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5782-05:
(6*5)+(5*7)+(4*8)+(3*2)+(2*0)+(1*5)=108
108 % 10 = 8
So 5782-05-8 is a valid CAS Registry Number.

5782-05-8Downstream Products

5782-05-8Relevant academic research and scientific papers

Selective Synthesis of Indoles by Cobalt(III)-Catalyzed C-H/N-O Functionalization with Nitrones

Wang, Hui,Moselage, Marc,González, María J.,Ackermann, Lutz

, p. 2705 - 2709 (2016)

The redox-neutral annulation of alkynes by differently decorated nitrones set the stage for a step-economical access to indoles with ample substrate scope. The redox-neutral C-H/N-O functionalization process proceeded through kinetically relevant C-H activation by carboxylate assistance, and displayed an excellent site- and regio-selectivity with unsymmetrical nitrones and alkynes.

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