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2,3-Quinoxalinediamine, N,N'-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25980-24-9

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25980-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25980-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,8 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25980-24:
(7*2)+(6*5)+(5*9)+(4*8)+(3*0)+(2*2)+(1*4)=129
129 % 10 = 9
So 25980-24-9 is a valid CAS Registry Number.

25980-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N,3-N-diphenylquinoxaline-2,3-diamine

1.2 Other means of identification

Product number -
Other names N2,N3-Diphenyl-chinoxalin-2,3-diyldiamin

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:25980-24-9 SDS

25980-24-9Downstream Products

25980-24-9Relevant academic research and scientific papers

Synthesis and antimicrobial activity of some new substituted quinoxalines

El-Atawy, Mohamed A.,Hamed, Ezzat A.,Alhadi, Mahjoba,Omar, Alaa Z.

, (2019/11/28)

A number of new symmetrically and asymmetrically 2,3-disubstituted quinoxalines were synthesized through functionalization of 2,3-dichloroquinoxaline (2,3-DCQ) with a variety of sulfur and/or nitrogen nucleophiles. The structures of the obtained compounds were established based on their spectral data and elemental analysis. The antimicrobial activity for the prepared compounds was investigated against four bacterial species and two fungal strains. The symmetrically disubstituted quinoxalines 2, 3, 4, and 5 displayed the most significant antibacterial activity, while compounds 6a, 6b, and the pentacyclic compound 10 showed considerable antifungal activity. Furthermore, compounds 3f, 6b showed broad antimicrobial spectrum against most of the tested strains.

ARYLAMINE SUBSTUTUTED QUINOXALINE AND THEIR USE AS ANTICANCER DRUGS

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Paragraph 0053-0055; 0058, (2016/10/09)

The present invention provides new compounds of formula I and II, which have potential of protein phosphatase 2A (PP2A) agonistt, CIP2A inhibitor and SET antagonist. Also provided are treatment methods using the compounds of formula I and II.

ELECTROLUMINESCENT IMIDAZO-QUINOXALINE CARBENE METAL COMPLEXES

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Page/Page column 166; 167, (2016/04/04)

Metal carbene complexes comprising at least one imidazo-quinoxaline ligand, organic electronic devices, especially OLEDs (Organic Light- Emitting Diodes) which comprise such complexes, a light-emitting layer comprising at least one inventive metal carbene complex, an apparatus selected from the group consisting of illuminating elements, stationary visual display units and mobile visual display units comprising such an OLED, the use of such a metal carbene complex for electrophotographic photoreceptors, photoelectric converters, organic solar cells (organic photovoltaics), switching elements, organic light emitting field effect transistors (OLEFETs), image sensors, dye lasers and electroluminescent devices and a process for preparing such metal carbene complexes.

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