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3-(2,6-diphenylpyridin-4-yl)-1-methyl-1H-indole is a complex organic compound characterized by a unique molecular structure. It features a 1H-indole core, which is a bicyclic aromatic system consisting of a benzene ring fused to a pyrrole. The indole is substituted at the 3-position with a 2,6-diphenylpyridin-4-yl group, which adds to its complexity. The pyridine ring in this group is adorned with two phenyl rings at the 2 and 6 positions, enhancing the compound's aromatic character. Additionally, a methyl group is attached to the nitrogen atom of the indole, further modifying its chemical properties. 3-(2,6-diphenylpyridin-4-yl)-1-methyl-1H-indole is of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in the development of new drugs and advanced materials. Its specific properties and reactivity are influenced by the intricate interplay of its constituent functional groups and aromatic systems.

5562-56-1

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5562-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5562-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5562-56:
(6*5)+(5*5)+(4*6)+(3*2)+(2*5)+(1*6)=101
101 % 10 = 1
So 5562-56-1 is a valid CAS Registry Number.

5562-56-1Downstream Products

5562-56-1Relevant academic research and scientific papers

I2-Triggered N-O cleavage of ketoxime acetates for the synthesis of 3-(4-pyridyl)indoles

Gao, Qinghe,Wang, Yakun,Wang, Qianqian,Zhu, Yanping,Liu, Zhaomin,Zhang, Jixia

, p. 9030 - 9037 (2018)

A facile and complementary [3 + 2 + 1] annulation of aryl ketoxime acetates and 3-formylindoles to give pyridine derivatives is reported. The condensation reaction demonstrated that I2 was capable of triggering N-O bond cleavage of ketoxime ace

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