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1,8-bis[(2-hydroxyethyl)amino]anthracene-9,10-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75312-66-2

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75312-66-2 Usage

Chemical structure

1,8-bis[(2-hydroxyethyl)amino]anthracene-9,10-dione

Type of compound

Synthetic chemical compound

Usage

Production of dyes and pigments

Derivative of

Anthraquinone

Color

Deep red

Substituents

Two hydroxyethylamine groups attached to the anthraquinone core

Properties

Hydrophilic and reactive

Industries

Textile and printing

Potential applications

Medicine and materials science

Unique features

Unique chemical structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 75312-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,1 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75312-66:
(7*7)+(6*5)+(5*3)+(4*1)+(3*2)+(2*6)+(1*6)=122
122 % 10 = 2
So 75312-66-2 is a valid CAS Registry Number.

75312-66-2SDS

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 1,8-bis(2-hydroxyethylamino)anthracene-9,10-dione

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:75312-66-2 SDS

75312-66-2Downstream Products

75312-66-2Relevant academic research and scientific papers

Synthesis and antitumor activity of 1,8-diaminoanthraquinone derivatives

Huang, Hsu-Shan,Chiu, Hui-Fen,Lu, Wei-Chih,Yuan, Chun-Lung

, p. 1136 - 1139 (2005)

Continuing our ongoing studies on cytotoxic substances, a series of regioisomeric disubstituted aminoanthraquinone (DAAQ) derivatives have been synthesized as cytotoxic activity based on a proposed bioactive amino conformation. To assess the biological activity of amino-substitution in the side-chains of anthraquinone located at positions 1 and 8 of the anthraquinone ring system. The aim of the study was to determine if members of the anthraquinone family could be used as adjuncts to increase the growth inhibiting effect of anticancer agents in rat glioma C6 cells, human hepatoma G2 cells and 2.2.15 cells. In vitro cytotoxicity data is reported for the compounds and some indications of structure-activity relationships have been discerned. A number of compounds were found to have good cytotoxicity against proliferation in these three cell lines. This has led to the discovery some of the DAAQ as a conformationally constrained structure possessing anticancer properties that displays cytotoxicity for these above cell lines and is being investigated further.

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