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Benzenesulfonyl chloride, 4-methoxy-3-[(methylsulfonyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

185244-31-9

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185244-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185244-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,2,4 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 185244-31:
(8*1)+(7*8)+(6*5)+(5*2)+(4*4)+(3*4)+(2*3)+(1*1)=139
139 % 10 = 9
So 185244-31-9 is a valid CAS Registry Number.

185244-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-chlorosulfonyl-2-methoxyphenyl) methanesulfonate

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:185244-31-9 SDS

185244-31-9Downstream Products

185244-31-9Relevant academic research and scientific papers

CHEMICAL COMPOUNDS

-

Page/Page column 39, (2008/06/13)

The present invention relates generally to novel therapeutic compounds and AXOR 109 agonists, and processes for the manufacture and use of the same.

Aryl sulfonamides as selective PDE4 inhibitors

Montana, John G.,Buckley, George M.,Cooper, Nicola,Dyke, Hazel J.,Gowers, Lewis,Gregory, Joanna P.,Hellewell, Paul G.,Kendall, Hannah J.,Lowe, Christopher,Maxey, Robert,Miotla, Jadwiga,Naylor, Robert J.,Runcie, Karen A.,Tuladhar, Bishwa,Warneck, Julie B. H.

, p. 2635 - 2640 (2007/10/03)

A series of novel selective phosphodiesterase 4 (PDE4) inhibitors has been developed which displays activity both in vitro and in vivo. These compounds possess good selectivity for the catalytic site of PDE4 over the high affinity Rolipram binding site. In vivo studies demonstrate a reduced propensity to display the emetic side effects which are commonly observed with PDE4 inhibitors.

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