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2-[amino-(4-propoxyphenyl)methylidene]azaniumylethyl-diethyl-azanium dichloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62979-91-3

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62979-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62979-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,7 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62979-91:
(7*6)+(6*2)+(5*9)+(4*7)+(3*9)+(2*9)+(1*1)=173
173 % 10 = 3
So 62979-91-3 is a valid CAS Registry Number.

62979-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[amino-(4-propoxyphenyl)methylidene]azaniumylethyl-diethylazanium,dichloride

1.2 Other means of identification

Product number -
Other names 2-[amino-(4-propoxyphenyl)methylidene]azaniumylethyl-diethylazanium dichloride

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:62979-91-3 SDS

62979-91-3Downstream Products

62979-91-3Relevant academic research and scientific papers

Synthesis of N1-substituted benzamidines. Effects on blood coagulation, platelet aggregation and antiarrhythmic activity.

Ferroni,Simoni,Manfredini,Guarneri,Orlandini,Barbieri,Franze,Mugelli

, p. 665 - 669 (2007/10/02)

A series of N1-substituted-4-alkoxybenzamidines was synthesized and tested in vitro for their inhibitory effects on blood coagulation and agonist induced platelet aggregation. The antiarrhythmic activity against chloroform-induced arrhythmias in mice was also evaluated. The biological activity of the title compounds is reported in comparison with that of procainamide; among the new products described, IVi and IVe were found to have the most potent anti-platelet and antiarrhythmic activity, respectively. The structure-activity relationships are discussed.

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