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1H-Indole, 1-(4-methylbenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69888-36-4

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69888-36-4 Usage

Usage

Pharmaceutical and chemical research

Derivative of

Indole (heterocyclic compound)

Synthesis applications

Pharmaceutical drugs

Biological activities

Anti-inflammatory, antitumor properties

Organic synthesis

Synthesis of various organic compounds

Value in research

Valuable tool for medicinal chemistry research

Check Digit Verification of cas no

The CAS Registry Mumber 69888-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,8 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69888-36:
(7*6)+(6*9)+(5*8)+(4*8)+(3*8)+(2*3)+(1*6)=204
204 % 10 = 4
So 69888-36-4 is a valid CAS Registry Number.

69888-36-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name indol-1-yl-(4-methylphenyl)methanone

1.2 Other means of identification

Product number -
Other names 1-(4-Methylbenzoyl)indol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69888-36-4 SDS

69888-36-4Relevant academic research and scientific papers

Facile approaches toward the synthesis of 6H-isoindolo[2,1-α]indol-6-ones via palladium-catalyzed carbonylation with carbon monoxide

Han, Qingshuai,Fu, Shurong,Zhang, Xiaofeng,Lin, Shen,Huang, Qiufeng

supporting information, p. 4165 - 4169 (2016/08/24)

Two facile methods for the preparation of 6H-isoindolo[2,1-α]indol-6-ones were developed. In the first protocol, 6H-isoindolo[2,1-α]indol-6-ones were prepared from 2-(2-iodophenyl)-1H-indoles via palladium-catalyzed intramolecular aminocarbonylation. The

Palladium-Catalyzed Carbonylative Synthesis of N -Benzoylindoles with Mo(CO)6 as the Carbon Monoxide Source

Wu, Xiao-Feng,Oschatz, Stefan,Sharif, Muhammad,Langer, Peter

, p. 2641 - 2646 (2015/09/01)

A mild and carbon monoxide gas-free palladium-catalyzed aminocarbonylation of indole has been developed for the synthesis of N-benzoylindoles. This method uses Mo(CO)6 as a convenient CO-precursor and BuPAd2 as the ligand. A number o

A palladium-catalyzed carbonylation approach to acid chloride synthesis

Quesnel, Jeffrey S.,Arndtsen, Bruce A.

supporting information, p. 16841 - 16844 (2013/12/04)

We describe a new approach to acid chloride synthesis via the palladium-catalyzed carbonylation of aryl iodides. The combination of sterically encumbered phosphines (PtBu3) and CO coordination has been found to facilitate the rapid carbonylation of aryl iodides into acid chlorides via reductive elimination from (tBu3P)(CO) Pd(COAr)Cl. The formation of acid chlorides can also be exploited to perform traditional aminocarbonylation reactions under exceptionally mild conditions (ambient temperature and pressure), and with a range of weakly nucleophilic substrates.

Atmospheric pressure aminocarbonylation of aryl iodides using palladium nanoparticles supported on MOF-5

Dang, Tuan T.,Zhu, Yinghuai,Ghosh, Subhash C.,Chen, Anqi,Chai, Christina L. L.,Seayad, Abdul M.

supporting information; experimental part, p. 1805 - 1807 (2012/03/08)

An efficient amide synthesis by atmospheric pressure aminocarbonylation using palladium nanoparticles supported on MOF-5 is reported. Interestingly, only 0.5 wt% palladium loading was required to achieve high yields. The catalyst is recyclable and offers negligible palladium leaching.

A novel one-pot synthesis of N-acylindoles from primary aromatic amides

Abid, Mohammed,De Paolis, Omar,T?r?k, Béla

, p. 410 - 412 (2008/09/17)

A novel one-pot synthesis of N-acylindoles via tandem cycloalkylation- annelation is described. This approach is based on the use of a strong solid-acid catalyst, montmorillonite K-10, and microwave irradiation under solvent-free conditions. The tandem cy

A catalytic antibody programmed for torsional activation of amide bond hydrolysis

Aggarwal, Ranjana,Benedetti, Fabio,Berti, Federico,Buchini, Sabrina,Colombatti, Alfonso,Dinon, Francesca,Galasso, Vinicio,Norbedo, Stefano

, p. 3132 - 3142 (2007/10/03)

Amidase antibody 312d6, obtained against the sulfonamide hapten 4a that mimics the transition state for hydrolysis of a distorted amide, accelerates the hydrolysis of the corresponding amides 1a-3a by a factor of 103 at pH 8. The mechanisms of

Reactions entre l'indole et les chlorures d'acides, en milieu basique: Synthese d'amides de l'ortho -2 ethyl, aniline

Bourgeois, Paul,Mesdouze, Jean,Philogene, Emile

, p. 1043 - 1046 (2007/10/02)

Acid chlorides react with indole in alkaline aqueous medium and yield amides of o-aniline which is in fact a trimer of indole.Their formation can be understood as follows: autocondensation of indole to give 2,3-diindole; acylatio

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