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5-Bromoquinoxaline is a heterocyclic aromatic organic compound with the molecular formula C8H5BrN2. It features a quinoxaline core with a bromine atom attached at the 5-position, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. This versatile chemical has demonstrated potential as an antibacterial and antifungal agent, as well as a reagent in organic synthesis for introducing the quinoxaline core into various compounds. Its diverse potential applications make it of significant interest in the pharmaceutical and chemical industries.

76982-23-5

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76982-23-5 Usage

Uses

Used in Pharmaceutical Industry:
5-Bromoquinoxaline is used as a building block for the synthesis of various pharmaceutical compounds due to its unique chemical structure and properties. Its ability to be incorporated into a wide range of molecules makes it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Bromoquinoxaline is utilized as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its potential as an antibacterial and antifungal agent makes it a promising candidate for the development of new products to protect crops and enhance agricultural productivity.
Used in Medicinal Chemistry:
5-Bromoquinoxaline is used as a research compound in medicinal chemistry to explore its potential as an antibacterial and antifungal agent. Scientific studies have shown its effectiveness in inhibiting the growth of various microorganisms, making it a valuable tool in the search for new treatments for infectious diseases.
Used in Organic Synthesis:
As a reagent in organic synthesis, 5-Bromoquinoxaline is used to introduce the quinoxaline core into a variety of compounds. This allows chemists to create new molecules with unique properties and potential applications in various industries, including pharmaceuticals, materials science, and more.
Overall, 5-Bromoquinoxaline's diverse applications across different industries highlight its importance as a versatile chemical compound with significant potential for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 76982-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,8 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76982-23:
(7*7)+(6*6)+(5*9)+(4*8)+(3*2)+(2*2)+(1*3)=175
175 % 10 = 5
So 76982-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrN2/c9-6-2-1-3-7-8(6)11-5-4-10-7/h1-5H

76982-23-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromoquinoxaline

1.2 Other means of identification

Product number -
Other names 5-bromoquinoxaline

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:76982-23-5 SDS

76982-23-5Downstream Products

76982-23-5Relevant academic research and scientific papers

Bromination of quinoxaline and derivatives: Effective synthesis of some new brominated quinoxalines

U?ar, Sefa,E?siz, Sel?uk,Da?tan, Arif

, p. 1618 - 1632 (2017/03/08)

The synthesis of brominated quinoxaline derivatives starting from several kinds of quinoxaline by different bromination strategies was studied. First the synthesis of some brominated quinoxalines was accomplished along with the development of an alternative and effective synthesis of some known compounds. A new, clean, and effective synthetic method for selective reduction of quinoxaline to 1,2,3,4-tetrahydroquinoxaline was also developed. The products obtained were characterized by means of NMR spectroscopy, elemental analyses, and mass spectrometry.

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