111339-68-5

Basic information

• Product Name: [1,2,3]Triazolo[1,5-a]quinoxaline,4-methyl-(9CI)
• Synonyms: [1,2,3]Triazolo[1,5-a]quinoxaline,4-methyl-(9CI);4-METHYL[1,2,3]TRIAZOLO[1,5-A]QUINOXALINE
• CAS NO: 111339-68-5
• Molecular Formula: C10 H8 N4
• Molecular Weight: 184.2
• Product Categories: PIPERIDINE
• Mol File: 111339-68-5.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [1,2,3]Triazolo[1,5-a]quinoxaline,4-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: [1,2,3]Triazolo[1,5-a]quinoxaline,4-methyl-(9CI)(111339-68-5)
• EPA Substance Registry System: [1,2,3]Triazolo[1,5-a]quinoxaline,4-methyl-(9CI)(111339-68-5)

Safety Data

• Hazardous Substances Data: 111339-68-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
[1,2,3]Triazolo[1,5-a]quinoxaline,4-methyl-(9CI) is used as a potential scaffold for developing new therapeutic agents due to its antimicrobial, anticancer, antiviral, and antifungal properties. Its unique structure and biological activities make it a promising candidate for creating novel drugs to treat various diseases and conditions.
Used in Agricultural Industry:
In the agricultural industry, [1,2,3]Triazolo[1,5-a]quinoxaline,4-methyl-(9CI) is utilized for its antimicrobial and antifungal properties. It can be employed as a component in the development of pesticides or fungicides to protect crops from harmful microorganisms and improve overall crop yield.
Used in Material Science:
[1,2,3]Triazolo[1,5-a]quinoxaline,4-methyl-(9CI) has also been studied for its potential applications in material science. Its unique chemical structure may offer new possibilities for the development of advanced materials with specific properties, such as improved stability or reactivity.
Used as a Fluorescent Probe in Analytical Chemistry:
Furthermore, [1,2,3]Triazolo[1,5-a]quinoxaline,4-methyl-(9CI) has been explored for its potential use as a fluorescent probe in analytical chemistry. Its optical properties could be harnessed to develop new methods for detecting and analyzing various chemical compounds and biological molecules.

Upstream product

• 25519-55-5 3-methylquinoxaline-2-carbaldehyde 
• 111339-54-9 1-(3-Methyl-quinoxalin-2-ylmethyl)-pyridinium; bromide 
• 63332-95-6 C₁₈H₁₈N₄O 
• 111339-61-8 3-Methylchinoxalin-2-carbaldehydtosylhydrazon 
• 5320-95-6 2-(bromomethyl)-3-methyl-quinoxaline 

Downstream Products

• 125040-00-8 1,2,3-Triazolo<1,5-a>chinoxalin-4-carbaldehydtosylhydrazon 
• 125039-91-0 N-(1,2,3-Triazolo<1,5-a>chinoxalin-4-yliden)-(4-N',N'-dimethylaminoanilin)-N-oxid 

Relevant articles and documents

Quinoxalines. XXIV. Synthesis of 4-Substituted 1,2,3-Triazoloquinoxalines

3-Substituted quinoxaline-2-carbaldehydes 1 react with tosylhydrazide to give 3-substituted quinoxaline-2-carbaldehyde tosylhydrazones 2.The treatment of 2 with a boiling solution of sodium methoxide or ethoxide - the so called Bamford-Stevens reaction -