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1H-Indole, 1-[(4-methoxyphenyl)sulfonyl]-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88939-68-8

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88939-68-8 Usage

Chemical class

Indole derivatives

Type of compound

Sulfonyl compound

Substituent at 1-position

4-Methoxyphenyl group

Substituent at 3-position

Methyl group

Potential applications

Organic synthesis, medicinal chemistry

Unique structure

Attractive for pharmaceutical development

Functional groups

Influential in the synthesis of other organic compounds

Properties and reactivity

Valuable for research in chemical and pharmaceutical sciences

Check Digit Verification of cas no

The CAS Registry Mumber 88939-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,3 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88939-68:
(7*8)+(6*8)+(5*9)+(4*3)+(3*9)+(2*6)+(1*8)=208
208 % 10 = 8
So 88939-68-8 is a valid CAS Registry Number.

88939-68-8SDS

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 1-(4-methoxyphenyl)sulfonyl-3-methylindole

1.2 Other means of identification

Product number -
Other names 1-(4-methoxyphenylsulfonyl)-3-methyl-1H-indole

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:88939-68-8 SDS

88939-68-8Relevant academic research and scientific papers

ZnO-mediated regioselective C-arylsulfonylation of indoles: A facile solvent-free synthesis of 2- and 3-sulfonylindoles and preliminary evaluation of their activity against drug-resistant mutant HIV-1 reverse transcriptases (RTs)

Tocco, Graziella,Begala, Michela,Esposito, Francesca,Caboni, Pierluigi,Cannas, Valeria,Tramontano, Enzo

, p. 6237 - 6241 (2013/10/22)

A ZnO-mediated one-pot solvent-free protocol for the regioselective C-arylsulfonylation of indoles is described and some novel derivatives were tested on wild type and non-nucleoside inhibitor resistant K103N and Y181C HIV-1 reverse transcriptases (RTs).

INDOLE-2,3-QUINODIMETHANES. SYNTHESIS OF INDOLOCARBAZOLES FOR THE SYNTHESIS OF THE FUSED DIMERIC INDOLE ALKALOID STAUROSPORINONE

Magnus, Philip D.,Exon, Christopher,Sear, Nancy L.

, p. 3725 - 3730 (2007/10/02)

N--3-ethyl-2-formylindole, made by direct electrophilic formylation of N--3-ethylindole using α,α-dichloromethylmethylether/TiCl4, was converted into the imine 23 by treatment with 2-aminostyrene.The i

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