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2987-66-8

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2987-66-8 Usage

Type of compound

Derivative of anthraquinone

Usage

Dye in textile industry

Affinity

Strong for cellulose fibers

Popularity

Used for dyeing cotton and other cellulose-based materials

Additional uses

Production of colored paper, plastics, and other synthetic materials

Pharmaceutical applications

Fluorescent marker and in the development of certain drugs

Safety concerns

Hazardous effects on human health and the environment if not used and disposed of properly

Check Digit Verification of cas no

The CAS Registry Mumber 2987-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2987-66:
(6*2)+(5*9)+(4*8)+(3*7)+(2*6)+(1*6)=128
128 % 10 = 8
So 2987-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O2/c1-17-11-7-3-5-9-13(11)15(19)10-6-4-8-12(18-2)14(10)16(9)20/h3-8,17-18H,1-2H3

2987-66-8SDS

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 1,5-bis(methylamino)anthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,5-Dimethylaminoanthraquinone

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:2987-66-8 SDS

2987-66-8Relevant articles and documents

STRUCTURE OF THE BORATE COMPLEXES OF α-AMINO AND α-HYDROXY-9,10-ANTHRAQUINONES AND THEIR REACTION WITH AMINES

Gorelik, M. V.,Shapet'ko, N. N.,Arinich, L. V.,Tsurkan, A. I.,Kukushkina, M. L.

, p. 547 - 556 (2007/10/02)

It was shown by 13C NMR that a redistribution of the bonds with partial localization of the 1,5- and 1,10-anthraquinonoid structures occurs during the transition from 1,5-diamino(dihydroxy)- and 1-amino(hydroxy)-9,10-anthraquinones respectively to their borate complexes.For this reason the boroacetates and fluoroborates of 1,5-dihydroxyanthraquinonones, 1-aminoanthraquinones, their N-alkyl and N-aryl derivatives, and 1,5-dihydroxyanthraquinone are capable of entering into amination under the influence of aromatic amines with substitution of the hydrogen atom at position 4 under mild conditions with the participation of atmospheric oxygen as oxidizing agent

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