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(4-Methoxyphenyl)(3-phenyl-1H-indol-2-yl)methanone is a complex organic compound with the molecular formula C23H18NO3. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a methanone (ketone) functional group. The molecule consists of a 4-methoxyphenyl group attached to a 3-phenyl-1H-indol-2-yl group through a methylene bridge. (4-methoxyphenyl)(3-phenyl-1H-indol-2-yl)methanone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in the preparation of other organic compounds. Due to its unique structure and properties, it has been the subject of research in the fields of organic chemistry and medicinal chemistry.

36004-82-7

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36004-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36004-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,0 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36004-82:
(7*3)+(6*6)+(5*0)+(4*0)+(3*4)+(2*8)+(1*2)=87
87 % 10 = 7
So 36004-82-7 is a valid CAS Registry Number.

36004-82-7Downstream Products

36004-82-7Relevant academic research and scientific papers

Tandem addition/cyclization for synthesis of 2-aroyl benzofurans and 2-aroyl indoles by carbopalladation of nitriles

Gong, Julin,Hu, Kun,Shao, Yinlin,Li, Renhao,Zhang, Yetong,Hu, Maolin,Chen, Jiuxi

, p. 488 - 494 (2020/02/03)

The first example of the palladium-catalyzed tandem addition/cyclization of 2-(2-acylphenoxy)acetonitriles with arylboronic acids has been developed, providing a new strategy for the synthesis of 2-aroyl benzofurans with excellent chemoselectivity and wid

Reaction of diphenacylanilines with 2-aminobenzophenone: An abnormal friedlander reaction yielding indoles

Paul, Nidhin,Muthusubramanian, Shanmugam

supporting information, p. 1200 - 1209 (2013/04/10)

This article describes an abnormal Friedlander reaction between diphenacylaniline and 2-aminobenzophenone in the presence of a catalytic amount of (±)-camphorsulfonic acid yielding 2-aroyl-3-arylindoles in quantitative yield. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.

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