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(4-methylphenyl)(3-phenyl-1H-2-indolyl)methanone is a complex organic compound with the molecular formula C25H19NO. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a methyl group attached to a phenyl ring, which is further connected to a 2-indolyl group. (4-methylphenyl)(3-phenyl-1H-2-indolyl)methanone is characterized by its unique structure, which includes a carbonyl group (C=O) that bridges the two aromatic rings. It is a white crystalline solid and is often used in the synthesis of various pharmaceuticals and chemical compounds due to its versatile chemical properties. The compound's structure and reactivity make it a valuable intermediate in organic synthesis, particularly in the preparation of indole-based compounds with potential applications in medicine and other industries.

36004-84-9

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36004-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36004-84-9 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 36004-84:
(7*3)+(6*6)+(5*0)+(4*0)+(3*4)+(2*8)+(1*4)=89
89 % 10 = 9
So 36004-84-9 is a valid CAS Registry Number.

36004-84-9Downstream Products

36004-84-9Relevant academic research and scientific papers

Copper-Catalyzed Hydroxyl-Directed Aminoarylation of Alkynes

Sun, Jiaqiong,Zheng, Guangfan,Xiong, Tao,Zhang, Qiao,Zhao, Jinbo,Li, Yan,Zhang, Qian

, p. 3674 - 3678 (2016)

A facile, copper-catalyzed aminoarylation reaction of various aryl/alkyl alkynes was realized by utilizing N-fluoroarylsulfonimides (NFSI) as aminoarylation or amination reagent with hydroxyl as directing group. With this methodology, various α,β-unsatura

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

Microwave Energized Synthesis of 2-Aroylindole Derivatives: Piperidine/DMF as an Effective Medium

Soora Haranath, Jayaprakash,Balam, Satheesh Krishna,Chereddy, Syama Sundar,Sthanikam, Siva Prasad,Sarva, Santhisudha,Gundluru, Mohan,Cirandur, Suresh Reddy

, p. 620 - 625 (2016/04/19)

A convenient and efficient protocol has been developed for the synthesis of 2-aroylindoles (3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j) in good yields by the reaction of 2-aminoketones (1a, 1b, 1c) with phenacyl bromides (2a, 2b, 2c, 2d). The reaction success varied with different bases and solvents in both conventional and microwave methods. But finally, it was established that piperidine in DMF was an effective medium to carry out the reaction under microwave irradiation conditions.

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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