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1,5-Bis(phenylamino)-9,10-anthracenedione is an organic compound with the chemical formula C26H18N2O2. It is a derivative of anthraquinone, featuring two phenylamino groups attached to the 1 and 5 positions of the anthraquinone core. This yellow crystalline solid is known for its potential applications in the synthesis of dyes and pigments, as well as in the development of materials for optical and electronic devices. The compound's structure endows it with unique photophysical properties, making it a subject of interest in the field of materials science.

2944-27-6

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2944-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2944-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2944-27:
(6*2)+(5*9)+(4*4)+(3*4)+(2*2)+(1*7)=96
96 % 10 = 6
So 2944-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C26H18N2O2/c29-25-20-14-8-16-22(28-18-11-5-2-6-12-18)24(20)26(30)19-13-7-15-21(23(19)25)27-17-9-3-1-4-10-17/h1-16,27-28H

2944-27-6SDS

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 1,5-Di(phenylamino)-9,10-anthraquinone

1.2 Other means of identification

Product number -
Other names 1,5-dianilino-anthraquinone

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:2944-27-6 SDS

2944-27-6Relevant academic research and scientific papers

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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