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2-Benzoyl-1-methyl-1H-indole is an organic compound with the molecular formula C16H13NO. It is a derivative of indole, a heterocyclic aromatic organic compound that contains a benzene ring fused to a pyrrole. The molecule features a methyl group attached to the nitrogen atom and a benzoyl group (a benzene ring with a carbonyl group) attached to the second carbon of the indole ring. 2-Benzoyl-1-methyl-1H-indole is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and reactivity. It is typically synthesized through various chemical reactions, such as Friedel-Crafts acylation, and can be further functionalized to create a wide range of compounds with different properties and applications.

1025-99-6

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1025-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1025-99-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1025-99:
(6*1)+(5*0)+(4*2)+(3*5)+(2*9)+(1*9)=56
56 % 10 = 6
So 1025-99-6 is a valid CAS Registry Number.

1025-99-6Relevant academic research and scientific papers

One-Pot Assembly of 3-Hydroxycarbazoles via Uninterrupted Propargylation/Hydroxylative Benzannulation Reactions

Reddy, Chada Raji,Subbarao, Muppidi,Sathish, Puppala,Kolgave, Dattahari H.,Donthiri, Ramachandra Reddy

, p. 689 - 693 (2020/01/31)

A novel strategy for the synthesis of 3-hydroxycarbazoles involving the consecutive propargylation/palladium-catalyzed hydroxylative benzannulation of indole-2-carbonyls with propargylic alcohols has been exploited. This one-pot procedure leads to a wide range of substituted 3-hydroxycarbazoles in high yield with a broad substrate scope. The method was further extended to access furano-carbazole derivatives from dialkynols via tandem annulations.

Beta-carboline derivatives, gamma-carboline derivatives as well as preparation methods and use thereof

-

Paragraph 0098; 0100, (2017/08/29)

The invention relates to beta-carboline derivatives, gamma-carboline derivatives as well as preparation methods and use thereof. The general structural formulas of the beta-carboline derivatives and the gamma-carboline derivatives are respectively describ

Syntheses of 1-alkyl-2-acylindoles, 1-alkyl-2-acylindole-3-carboxylic acids, and their esters, in superbasic media

Rekhter

, p. 408 - 417 (2007/10/03)

2-Acylindoles and 2-acylindole-3-carboxylic acids are readily alkylated at the nitrogen atom by haloalkanes in a superbasic medium (DMSO + NaOH). For the carboxylic acids, this reaction may proceed either entirely at the nitrogen atom, or at both the the

Oxidation of Indoles with Lead Tetra-acetate and Hydrolysis of 1,2-Disubstituted Indol-3-yl Acetates

Sukari, Mohamed A.,Vernon, John M.

, p. 2219 - 2224 (2007/10/02)

Oxidation of some 1,2-disubstituted indoles with lead tetra-acetate gives the corresponding 3-acetoxy derivatives.Similar oxidation of ethyl indole-2-carboxylate affords an acetoxylated 3,3'-bi-indolyl product; methyl 1-methylindol-3-yl acetate is acetoxylated at the benzylic position of the side-chain.Alkaline hydrolysis of 1,2-disubstituted indol-3-yl acetates is accompanied by autoxidation and rearrangement to give dioxindoles, but hydrolysis of 2-ethoxycarbonyl-1-methylindol-3-yl acetate gives N,N'-dimethyl derivatives of indigo and indirubin.

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