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19721-54-1

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19721-54-1 Usage

Type

Chemical compound

Derivative

4-methoxyphenethylamine

Usage

Production of pharmaceuticals and organic synthesis

Contains

Hydroxyethylamine group

Properties

Unique due to the presence of functional groups

Application

Pharmaceutical research and development, synthesis of potential drug candidates and bioactive molecules

Safety

Handle with caution and according to proper protocols to avoid risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 19721-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,2 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19721-54:
(7*1)+(6*9)+(5*7)+(4*2)+(3*1)+(2*5)+(1*4)=121
121 % 10 = 1
So 19721-54-1 is a valid CAS Registry Number.

19721-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[N-(2-hydroxyethyl)-4-methoxyanilino]ethanol

1.2 Other means of identification

Product number -
Other names 2-[(2-hydroxyethyl)-(4-methoxyphenyl)amino]ethanol

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:19721-54-1 SDS

19721-54-1Relevant articles and documents

-

Ross

, p. 2824,2828, 2830 (1949)

-

Quinolone-based compounds, formulations, and uses thereof

-

Page/Page column 90, (2018/07/02)

Provided herein are quinolone-based compounds that can be used for treatment and/or prevention of malaria and formulations thereof. Also provided herein are methods of treating and/or preventing malaria in a subject by administering a quinolone-based compound or formulation thereof provided herein.

Synthesis, crystal structure and biological activity of novel diester cyclophanes

Zhang, Pengfei,Yang, Bingqin,Fang, Xianwen,Cheng, Zhao,Yang, Meipan

, p. 1771 - 1775 (2013/03/13)

A series of novel diester cyclophanes was synthesized by esterification of 1,2-benzenedicarbonyl chloride with eight different diols under high dilution conditions. The structures of the compounds were verified by elemental analysis, 1H nuclear magnetic resonance (NMR), IR spectroscopy and high resolution mass spectrometry (HRMS). The crystal structures of two compounds were characterized by single crystal X-ray diffractometry (XRD). All the new cyclophanes were evaluated for biological activities and the results showed that some of these compounds have low antibacterial or antifungal activities.

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