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115256-12-7

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115256-12-7 Usage

Description

1-(4-methanesulphonamidophenoxy)-2-[N-methyl-N-(4-aminophenethyl)amino]ethane is a complex organic chemical compound characterized by its unique molecular structure. It is composed of various functional groups, including a methanesulphonamidophenoxy group, an N-methyl-N-(4-aminophenethyl)amino group, and an ethane backbone. 1-(4-methanesulphonamidophenoxy)-2-[N-methyl-N-(4-aminophenethyl)amino]ethane's intricate structure suggests that it may possess a range of properties and potential applications, which would require further research and analysis to fully comprehend.

Uses

Used in Pharmaceutical Industry:
1-(4-methanesulphonamidophenoxy)-2-[N-methyl-N-(4-aminophenethyl)amino]ethane is used as a potential pharmaceutical compound for its possible therapeutic effects. 1-(4-methanesulphonamidophenoxy)-2-[N-methyl-N-(4-aminophenethyl)amino]ethane's complex structure, which includes various functional groups, may contribute to its interaction with biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, 1-(4-methanesulphonamidophenoxy)-2-[N-methyl-N-(4-aminophenethyl)amino]ethane serves as a subject of study for understanding its chemical properties, reactivity, and potential applications in various chemical processes. Its unique structure may provide insights into the development of new synthetic methods or the creation of novel materials.
Used in Material Science:
1-(4-methanesulphonamidophenoxy)-2-[N-methyl-N-(4-aminophenethyl)amino]ethane may also find applications in material science, where its specific properties could be harnessed to develop new materials with tailored characteristics. 1-(4-methanesulphonamidophenoxy)-2-[N-methyl-N-(4-aminophenethyl)amino]ethane's functional groups could potentially be utilized in the design of advanced materials for various industries, such as electronics, aerospace, or automotive.

Check Digit Verification of cas no

The CAS Registry Mumber 115256-12-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,5 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115256-12:
(8*1)+(7*1)+(6*5)+(5*2)+(4*5)+(3*6)+(2*1)+(1*2)=97
97 % 10 = 7
So 115256-12-7 is a valid CAS Registry Number.

115256-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methanesulphonamidophenoxy)-2-[N-methyl-N-(4-aminophenethyl)amino]ethane

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

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More Details:115256-12-7 SDS

115256-12-7Downstream Products

115256-12-7Relevant articles and documents

Computer-aided design, synthesis and biological assay of p-methylsulfonamido phenylethylamine analogues

Liu, Hong,Ji, Min,Jiang, Hualiang,Liu, Ligang,Hua, Weiyi,Chen, Kaixian,Ji, Ruyun

, p. 2153 - 2157 (2007/10/03)

Class III antiarrhythmic agents selectively delay the effective refractory period (ERP) and increase the transmembrance action potential duration (APD). Based on our previous studies, a set of 17 methylsulfonamido phenylethylamine analogues were investigated by 3D-QSAR techniques of CoMFA and CoMSIA. The 3D-QSAR models proved a good predictive ability, and could describe the steric, electrostatic and hydrophobic requirements for recognition forces of the receptor site. According to the clues provided by this 3D-QSAR analysis, we designed and synthesized a series of new analogues of methanesulfonamido phenylethylamine (VI(a-i)). Pharmacological assay indicated that the effective concentrations of delaying the functional refractory period (FRP) 10ms of these new compounds have a good correlation with the 3D-QSAR predicted values. It is remarkable that the maximal percent change of delaying FRP in μM of compound VI(c) is much higher than that of dofetilide. The results showed that the 3D-QSAR models are reliable. (C) 2000 Elsevier Science Ltd.

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