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N-methyl-N-{2-[methyl(1-methyl-1H-benzimidazol-2-yl)amino]ethyl}-4-[(methylsulfonyl)amino]benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138490-53-6

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138490-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138490-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,9 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138490-53:
(8*1)+(7*3)+(6*8)+(5*4)+(4*9)+(3*0)+(2*5)+(1*3)=146
146 % 10 = 6
So 138490-53-6 is a valid CAS Registry Number.

138490-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(methanesulfonamido)-N-methyl-N-[2-[methyl-(1-methylbenzimidazol-2-yl)amino]ethyl]benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-methyl-N-<2-<methyl(1-methyl-1H-benzimidazol-2-yl)amino>ethyl>-4-<(methylsulfonyl)amino>benzenesulfonamide

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:138490-53-6 SDS

138490-53-6Downstream Products

138490-53-6Relevant academic research and scientific papers

Class III Antiarrhythmic Activity of Novel Substituted 4-benzamides and Sulfonamides

Ellingboe, John W.,Spinelli, Walter,Winkley, Michael W.,Nguyen, Thomas T.,Parsons, Roderick W.,et al.

, p. 705 - 716 (2007/10/02)

The synthesis and Class III antiarrhythmic activity of a series of 4-benzamides and sulfonamides are described.Selected compounds shown a potent Class III activity and are devoid of effects on conduction both in vitro (dog Purkinje fibers) and in vivo (anesthetized dogs).Compounds having a 2-aminobenzimidazole group were found to be the most potent, and one compound having the heterocycle (5, WAY-123,398) was selected for further characterization.Compound 5 was shown to have good oral bioavailability and a favorable hemodynamic profile to produce a 3-fold increase of the ventricular fibrillation threshold and to terminate ventricular fibrillation, restoring sinus rhythm in anesthetized dogs.Voltage-clamp studies in isolated myocytes show that 5 is a potent and specific blocker of the delayed rectifier potassium current (IK) at concentrations that cause significant prolongation of action potential duration.

Substituted arylsulfonamides and benzamides

-

, (2008/06/13)

This invention relates to substituted arylsulfonamides and benzamides possessing aniarrhythmic activity, to pharmaceutical compositions and to methods for production thereof.

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