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2-Amino-3-methylquinoxaline, an organic heterocyclic compound with the molecular formula C9H8N2, features a quinoxaline ring and an amino group. It serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals, and has potential applications in organic electronic materials and dye-sensitized solar cells. While it has been studied for its biological activities, including antitumor properties and as a therapeutic target for neurological disorders, it is also recognized as a carcinogenic compound, necessitating careful handling.

34972-22-0

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34972-22-0 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Amino-3-methylquinoxaline is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs due to its unique chemical structure and reactivity.
Used in Agrochemical Production:
In the agrochemical industry, 2-Amino-3-methylquinoxaline is utilized as a key component in the creation of pesticides and other crop protection agents, enhancing agricultural productivity and crop protection.
Used in Specialty Chemicals:
2-Amino-3-methylquinoxaline is employed as a building block in the synthesis of specialty chemicals, which are used in a wide range of applications, including coatings, adhesives, and other industrial products.
Used in Organic Electronic Materials:
2-AMINO-3-METHYLQUINOXALINE is used in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs), due to its electronic properties and potential for device fabrication.
Used in Dye-Sensitized Solar Cells:
2-Amino-3-methylquinoxaline is utilized in the research and development of dye-sensitized solar cells, where it may contribute to improving the efficiency and performance of these renewable energy technologies.
Used in Biological Research:
2-Amino-3-methylquinoxaline is used as a subject of biological research for its potential as an antitumor agent and a therapeutic target for neurological disorders, despite its carcinogenic properties, which require careful study and handling.
Note: The uses listed are based on the potential applications derived from the compound's properties and should be considered in the context of ongoing research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 34972-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34972-22:
(7*3)+(6*4)+(5*9)+(4*7)+(3*2)+(2*2)+(1*2)=130
130 % 10 = 0
So 34972-22-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3/c1-6-9(10)12-8-5-3-2-4-7(8)11-6/h2-5H,1H3,(H2,10,12)

34972-22-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylquinoxalin-2-amine

1.2 Other means of identification

Product number -
Other names 3-Methyl-2-quinoxalinamine

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:34972-22-0 SDS

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