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Benzenesulfonamide,N,N'-[1,3-phenylenebis(methylene)]bis[4-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87338-18-9

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87338-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87338-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,3 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87338-18:
(7*8)+(6*7)+(5*3)+(4*3)+(3*8)+(2*1)+(1*8)=159
159 % 10 = 9
So 87338-18-9 is a valid CAS Registry Number.

87338-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-N-[[3-[[(4-methylphenyl)sulfonylamino]methyl]phenyl]methyl]benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N,N'-m-xylylene-bis-toluene-4-sulfonamide

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:87338-18-9 SDS

87338-18-9Relevant academic research and scientific papers

Chloride-Mediated Apoptosis-Inducing Activity of Bis(sulfonamide) Anionophores

Saha, Tanmoy,Hossain, Munshi Sahid,Saha, Debasis,Lahiri, Mayurika,Talukdar, Pinaki

, p. 7558 - 7567 (2016)

Transmembrane anion transport modality is enjoying a renewed interest because of recent advances toward anticancer therapy. Here we show bis(sulfonamides) as efficient receptors for selective Cl- ion binding and transport across lipid bilayer m

Isolation of Key Organometallic Aryl-Co(III) Intermediates in Cobalt-Catalyzed C(sp2)-H Functionalizations and New Insights into Alkyne Annulation Reaction Mechanisms

Planas, Oriol,Whiteoak, Christopher J.,Martin-Diaconescu, Vlad,Gamba, Ilaria,Luis, Josep M.,Parella, Teodor,Company, Anna,Ribas, Xavi

, p. 14388 - 14397 (2016)

The selective annulation reaction of alkynes with substrates containing inert C-H bonds using cobalt as catalyst is currently a topic attracting significant interest. Unfortunately, the mechanism of this transformation is still relatively poorly understoo

Synthesis, molecular docking, and QSAR study of bis-sulfonamide derivatives as potential aromatase inhibitors

Leechaisit, Ronnakorn,Pingaew, Ratchanok,Prachayasittikul, Veda,Worachartcheewan, Apilak,Prachayasittikul, Supaluk,Ruchirawat, Somsak,Prachayasittikul, Virapong

, (2019/08/14)

A library of bis-sulfonamides (9–26) were synthesized and tested for their aromatase inhibitory activities. Interestingly, all bis-sulfonamide derivatives inhibited the aromatase with IC50 range of 0.05–11.6 μM except for compound 23. The analo

Synthesis of Aza Macrocycles by Nucleophilic Ring Closure with Cesium Tosylamides

Vriesema, Bindert K.,Buter, Jan,Kellogg, Richard M.

, p. 110 - 113 (2007/10/02)

Long-chain diamines as their bis tosylamide derivatives are deprotonated by Cs2CO3 in dimethylformamide solution to give the dicesium salts.These react smoothly with various dibromides or dimesylates to afford the cyclic diamines as their tosyl derivatives.The yields, depending on the size of the ring, range between 25percent and 95percent of isolated product.The largest ring made, 1,12-diazaoctacosane (as the tosylamide derivative) was isolated in 60percent yield.The tosyl groups are readily removed with sodium amalgam in Na2HPO4-buffered methanolic solution.Chiral macrocyclic amines have also been prepared by using this cesium salt method.

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