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4H-Indol-4-one, 1,5,6,7-tetrahydro-2,3-diphenyl- is a complex organic compound belonging to the indole family. It is characterized by a unique molecular structure, featuring a diphenyl-substituted indolone core with a tetrahydro ring system. 4H-Indol-4-one, 1,5,6,7-tetrahydro-2,3-diphenyl- is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties. The presence of phenyl groups and the indolone core provides a foundation for further functionalization and modification, making it a valuable intermediate in the development of new drugs and chemical compounds.

6206-30-0

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6206-30-0 Usage

Classification

Indole derivative

Main properties

complex molecular structure, potential biological activities, potential therapeutic effects, important target for drug development

Specific content

4H-Indol-4-one, 1,5,6,7-tetrahydro-2,3-diphenylis used in medicinal chemistry and pharmaceutical research, studied for its potential therapeutic effects in treating diseases and disorders, has applications in material science and organic synthesis, versatile and valuable chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 6206-30-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,0 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6206-30:
(6*6)+(5*2)+(4*0)+(3*6)+(2*3)+(1*0)=70
70 % 10 = 0
So 6206-30-0 is a valid CAS Registry Number.

6206-30-0Downstream Products

6206-30-0Relevant academic research and scientific papers

Coumarin-pyrrolizinone synthetic method of compound

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Paragraph 0027; 0064; 0065-0068, (2016/11/21)

The invention discloses a synthetic method of a coumarin-pyrrole compound. The synthetic method comprises the following step of: in a reactive solvent, with 4-amino coumarin compounds and disubstituted acetylene compounds as raw materials, under the catal

Palladium-catalyzed oxidative annulation via C-H/N-H functionalization: Access to substituted pyrroles

Peng, Shiyong,Wang, Lei,Huang, Jiayao,Sun, Shaofa,Guo, Haibing,Wang, Jian

supporting information, p. 2550 - 2557 (2013/10/21)

Pyrroles, ubiquitous bioactive heterocycles in nature, are readily prepared via a palladium-catalyzed oxidative annulation of cyclic trans-enamines to various internal alkynes in the absence of a directing group. Copyright

A catalyst- and solvent-free three-component reaction for the regioselective one-pot access to polyfunctionalized pyrroles

Bhat, Subrahmanya Ishwar,Trivedi, Darshak R.

supporting information, p. 5577 - 5582 (2013/09/23)

A facile method for the regioselective synthesis of tetrasubstituted pyrroles, from readily accessible 1,3-dicarbonyls, benzoin derivatives and ammonium acetate, has been developed. The one-pot three-component reactions were performed to afford tetrasubst

Catalyzed Reaction of Diazodiphenylethanone and Related Diazo Ketones with Enaminones as a Source of Pyrroles

Eberlin, Marcos N.,Kascheres, Concetta

, p. 2084 - 2086 (2007/10/02)

The reaction of copper(II)-stabilized keto carbenes (1, 7, 8), derived from diazo ketones, with enaminones leads to the formation of pyrroles.The cyclic enaminones 3 react with the keto carbenes on nitrogen to form products 5, 9, 11, and/or pyrroles 6, 10

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