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167172-14-7

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167172-14-7 Usage

General Description

1H-Indole, 1-(phenylsulfonyl)-3-(2-propenyl)- is a chemical compound with the molecular formula C19H17NO2S. It is a derivative of indole and contains a phenylsulfonyl group and a propenyl group. 1H-Indole, 1-(phenylsulfonyl)-3-(2-propenyl)- is a potential inhibitor of the aryl hydrocarbon receptor and has been studied for its potential use in cancer therapy. It exhibits anti-proliferative and anti-inflammatory properties and has been investigated for its role in the regulation of various cellular processes. Additionally, it has been studied for its potential use in the treatment of neurodegenerative diseases and as a tool for chemical biology research.

Check Digit Verification of cas no

The CAS Registry Mumber 167172-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,1,7 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 167172-14:
(8*1)+(7*6)+(6*7)+(5*1)+(4*7)+(3*2)+(2*1)+(1*4)=137
137 % 10 = 7
So 167172-14-7 is a valid CAS Registry Number.

167172-14-7SDS

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-(benzenesulfonyl)-3-prop-2-enylindole

1.2 Other means of identification

Product number -
Other names 3-allyl-1-(phenylsulfonyl)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:167172-14-7 SDS

167172-14-7Relevant articles and documents

Preparation of highly functionalized heterocyclic zinc organometallics via a Li(acac)-catalysis of the I/Zn-exchange reaction

Gong, Liu-Zhu,Knochel, Paul

, p. 267 - 270 (2005)

The reaction of i-Pr2Zn in the presence of catalytic amount of Li(acac) in NMP with various functionalized heterocyclic iodides provides new polyfunctional diheteroarylzincs, which undergo smooth Negishi cross-coupling reactions and CuCN-2LiCl-

Preparation and reactions of lithium indolyl(dimethyl)zincates

Kondo, Yoshinori,Takazawa, Nobuo,Yoshida, Akihiro,Sakamoto, Takao

, p. 1207 - 1208 (2007/10/02)

Lithium indol-3-yl(dimethyl)zincates, prepared by halogen-zinc exchange of 3-iodo-1-phenylsulfonylindoles with lithium trimethylzincate, reacted with benzaldehyde to give the corresponding alcohols.

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