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2,3-Diaminoanthracene is an organic compound with the chemical formula C14H12N2. It is a derivative of anthracene, a tricyclic aromatic hydrocarbon, and features two amino groups (-NH2) attached at the 2 and 3 positions of the anthracene core. 2,3-Diaminoanthracene is known for its potential applications in the synthesis of various dyes, pigments, and other organic compounds due to its unique chemical structure. It is also used as an intermediate in the production of certain pharmaceuticals and has been studied for its potential biological activities. The compound is typically synthesized through chemical reactions involving anthracene and ammonia, and it is important to handle it with care due to its potential toxicity and mutagenicity.

5227-67-8

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5227-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5227-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5227-67:
(6*5)+(5*2)+(4*2)+(3*7)+(2*6)+(1*7)=88
88 % 10 = 8
So 5227-67-8 is a valid CAS Registry Number.

5227-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diaminoanthracene

1.2 Other means of identification

Product number -
Other names Anthracene-2,3-diamine

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:5227-67-8 SDS

5227-67-8Downstream Products

5227-67-8Relevant academic research and scientific papers

ORGANIC COMPOUND, ORGANIC LIGHT EMITTING DIODE HAVING THE SAME, AND ORGANIC LIGHT EMITTING DEVICE

-

Paragraph 0229; 0250-0253, (2021/02/05)

The present disclosure relates to an organic compound having the following structure, and an organic light emitting diode (OLED) and an organic light emitting device comprising the same. The organic compound is applied to a light-emitting layer, so that the driving voltage of the OLED and the organic light-emitting device is reduced, and the light-emitting efficiency and the color purity of the OLED and the organic light-emitting device are improved.

Exploration of the Photodegradation of Naphtho[2,3-g] quinoxalines and Pyrazino[2,3-b]phenazines

Kolmer-Anderl, Nicole,Kolmer, Andreas,Thiele, Christina M.,Rehahn, Matthias

supporting information, p. 5277 - 5287 (2016/04/09)

Nitrogen-containing polycyclic aromatic hydrocarbons are very attractive compounds for organic electronics applications. Their low-lying LUMO energies points towards a potential use as n-type semiconductors. Furthermore, they are expected to be more stable under ambient conditions, which is very important for the formation of semiconducting films, where materials with high purity are needed. In this study, the syntheses of naphtho[2,3-g]quinoxalines and pyrazino[2,3-b]phenazines is presented by using reaction conditions, that provide the desired products in high yields, high purity and without time-consuming purification steps. The HOMO and LUMO energies of the compounds are investigated by cyclic voltammetry and UV/Vis spectroscopy and their dependency on the nitrogen content and the terminal substituents are examined. The photostability and the degradation pathways of the naphtho[2,3-g]quinoxalines and pyrazino[2,3-b]phenazines are explored by NMR spectroscopy of irradiated samples affirming the large influence of the nitrogen atoms in the acene core on the degradation process during the irradiation. Finally, by identifying the degradations products of 2,3-dimethylnaphtho[2,3-g]quinoxaline it is possible to track down the most reactive position in the compound and, by blocking this position with nitrogen, to strongly increase the photostability.

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