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5-NITROQUINOXALINE, with the molecular formula C8H5N3O2, is a nitro-substituted quinoxaline derivative. It is a significant chemical compound in the pharmaceutical industry, serving as a building block for synthesizing various bioactive compounds and drugs. Recognized for its antitumor, antifungal, and antibacterial properties, 5-NITROQUINOXALINE is a valuable intermediate for the development of new therapeutic agents. Moreover, its intriguing electronic and photophysical properties have led to studies for potential applications in organic electronics and materials science, making it a versatile and important chemical for both pharmaceutical and materials industries.

18514-76-6

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18514-76-6 Usage

Uses

Used in Pharmaceutical Industry:
5-NITROQUINOXALINE is used as a building block for the synthesis of bioactive compounds and drugs due to its antitumor, antifungal, and antibacterial properties. It plays a crucial role in the development of new therapeutic agents.
Used in Organic Electronics:
5-NITROQUINOXALINE is used in the field of organic electronics for its interesting electronic and photophysical properties, which make it a potential candidate for applications in this industry.
Used in Materials Science:
In materials science, 5-NITROQUINOXALINE is utilized for its unique properties, contributing to the advancement of new materials with specific characteristics and functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 18514-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,1 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18514-76:
(7*1)+(6*8)+(5*5)+(4*1)+(3*4)+(2*7)+(1*6)=116
116 % 10 = 6
So 18514-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5N3O2/c12-11(13)7-3-1-2-6-8(7)10-5-4-9-6/h1-5H

18514-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-NITROQUINOXALINE

1.2 Other means of identification

Product number -
Other names 5-Nitro-quinoxaline

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:18514-76-6 SDS

18514-76-6Upstream product

18514-76-6Relevant academic research and scientific papers

Investigation on the photoreactions of nitrate and nitrite ions with selected azaarenes in water

Beitz, Toralf,Bechmann, Wolfgang,Mitzner, Rolf

, p. 351 - 361 (2007/10/03)

The photoreactions of selected azaarenes with nitrate and nitrite ions were investigated under irradiation at λ = 313 nm. The excitation of both anions leads to several photochemical reactions forming mainly hydroxyl radicals and nitrogen oxides. The purification capability of natural waters i.e. the oxidation of inorganic and organic substances results from the formation of hydroxyl radicals. Nitrated isomers of azaarenes were found among the main products of the investigated photoreactions. The nitrogen oxides were responsible for the production of nitrated derivatives which possess a high toxic potential. Their formation was explained by the parallel occurance of two mechanism, a molecular and a radical one. The molecular mechanism became more important with increasing ionisation potentials of the azaarenes. The spectrum of oxidized products corresponded to the one got in the photoreactions of azaarenes with hydrogen peroxide. The formation of several oxidation and nitration products of the pyridine ring with its low electron density was explained by the reaction of excited states of azaarenes. The photoreactions with nitrite ions only led to the formation of oxidized and nitrated products. Nitroso products were not formed. The reactivity of nitrogen monoxide is too low for its reaction with the azaarenes.

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