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1,2-Ethanediamine, N-(2-(4-methoxyphenyl)-4-quinolinyl)-N,N-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133671-49-5

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133671-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133671-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,7 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133671-49:
(8*1)+(7*3)+(6*3)+(5*6)+(4*7)+(3*1)+(2*4)+(1*9)=125
125 % 10 = 5
So 133671-49-5 is a valid CAS Registry Number.

133671-49-5SDS

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 N-[2-(4-methoxyphenyl)quinolin-4-yl]-N',N'-dimethylethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names N-(2-(Dimethylamino)ethyl)-2-(4-methoxyphenyl)quinolin-4-amine

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:133671-49-5 SDS

133671-49-5Downstream Products

133671-49-5Relevant academic research and scientific papers

New triple-helix DNA stabilizing agents

Strekowski, Lucjan,Hojjat, Maryam,Wolinska, Ewa,Parker, Alesia N.,Paliakov, Ekaterina,Gorecki, Tadeusz,Tanious, Farial A.,Wilson, W.David

, p. 1097 - 1100 (2007/10/03)

Several substituted quinolin-4-amines and heteroaromatic analogs were synthesized and evaluated for interaction with triplex polydA·2polydT and duplex polydA·polydT by using UV-thermal melting experiments. Excellent triple-helix DNA ligands with high affinity toward T·A·T triplets and triple/duplex selectivity were designed through a rational approach.

Synthesis and quantitative structure-activity relationship analysis of 2-(aryl or heteroaryl)quinolin-4-amines, a new class of anti-HIV-1 agents

Strekowski,Mokrosz,Honkan,Czarny,Cegla,Wydra,Patterson,Schinazi

, p. 1739 - 1746 (2007/10/02)

Thirty-eight 2-(aryl or heteroaryl)quinolin-4-amines, N,N-disubstituted, N-monosubstituted, and without a substituent at the amino group have been synthesized with use of novel chemistries developed by us recently. Some of these derivatives show anti-HIV-

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