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1H-Isoindole-1,3(2H)-dione, 2-[2-[2-(4-chlorophenyl)-1H-indol-3-yl]ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192182-28-8

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192182-28-8 Usage

Molecular structure

1H-Isoindole-1,3(2H)-dione, 2-[2-[2-(4-chlorophenyl)-1H-indol-3-yl]ethyl]is a complex organic compound that consists of a 1H-indol-3-yl group attached to a 2-[2-(4-chlorophenyl)ethyl] group, which is connected to the isoindole-1,3(2H)-dione framework.

Isoindole and indole moieties

The compound contains both isoindole and indole parts, which are common structural motifs found in various biologically active compounds and natural products.

Chlorine substitution

The presence of a 4-chlorophenyl group in the molecule indicates a halogen substitution, which can influence the compound's chemical reactivity, stability, and potential pharmaceutical applications.

Biological activity

The indole moiety is often found in biologically active compounds, suggesting that this chemical may have potential pharmaceutical applications.

Isoindole-1,3(2H)-dione scaffold

This specific structural framework is present in certain drugs and natural products, which may contribute to the compound's potential pharmaceutical properties.

Further research needed

The specific properties and potential uses of 1H-Isoindole-1,3(2H)-dione, 2-[2-[2-(4-chlorophenyl)-1H-indol-3-yl]ethyl]are not yet fully understood, and further research is necessary to determine its potential applications and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 192182-28-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,1,8 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 192182-28:
(8*1)+(7*9)+(6*2)+(5*1)+(4*8)+(3*2)+(2*2)+(1*8)=138
138 % 10 = 8
So 192182-28-8 is a valid CAS Registry Number.

192182-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-{2-[2-(4-Chloro-phenyl)-1H-indol-3-yl]-ethyl}-isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names -

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:192182-28-8 SDS

192182-28-8Downstream Products

192182-28-8Relevant academic research and scientific papers

Tryptamine and homotryptamine-based sulfonamides as potent and selective inhibitors of 15-lipoxygenase

Weinstein, David S.,Liu, Wen,Gu, Zhengxiang,Langevine, Charles,Ngu, Khehyong,Fadnis, Leena,Combs, Donald W.,Sitkoff, Doree,Ahmad, Saleem,Zhuang, Shaobin,Chen, Xing,Wang, Feng-Lai,Loughney, Deborah A.,Atwal, Karnail S.,Zahler, Robert,Macor, John E.,Madsen, Cort S.,Murugesan, Natesan

, p. 1435 - 1440 (2007/10/03)

A series of inhibitors of mammalian 15-lipoxygenase based on tryptamine and homotryptamine scaffolds is described. Compounds with aryl substituents at C-2 of the indole core of tryptamine and homotryptamine sulfonamides (e.g., 37a-p) proved to be potent i

Synthesis of 2-aryltryptamines with palladium catalyzed cross-coupling of 2-bromotryptamines and arylboronic acids

Chu, Lin,Fisher, Michael H.,Goulet, Mark T.,Wyvratt, Matthew J.

, p. 3871 - 3874 (2007/10/03)

A versatile and high-yielding synthesis of 2-aryltryptamines employing palladium(0) catalyzed cross-coupling of 2-bromotryptamines and arylboronic acids was developed. The preparation of the intermediate 2-bromotryptamines with pyridine hydrobromide perbromide as the brominating agent, is also reported.

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