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60316-43-0

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60316-43-0 Usage

Appearance

Dark green solid

Textile industry

Dye for fabric printing and dyeing

Photography and motion pictures

Production of color films

Organic electronics

Potential applications in organic photovoltaic devices and organic light-emitting diodes

Type

Anthraquinone dye

Characteristics

a. Vibrant and long-lasting color
b. High stability
c. Good solubility in organic solvents

Industrial and technological applications

Versatile and useful due to its stability and solubility properties

Check Digit Verification of cas no

The CAS Registry Mumber 60316-43-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,1 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60316-43:
(7*6)+(6*0)+(5*3)+(4*1)+(3*6)+(2*4)+(1*3)=90
90 % 10 = 0
So 60316-43-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O2/c1-17-11-7-3-5-9-13(11)16(20)14-10(15(9)19)6-4-8-12(14)18-2/h3-8,17-18H,1-2H3

60316-43-0SDS

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 1,8-bis(methylamino)anthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 9,10-Anthracenedione,1,8-bis(methylamino)

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:60316-43-0 SDS

60316-43-0Relevant 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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