1489-04-9

Basic information

• Product Name: 7-Amino-s-triazolo[1,5-a]-s-triazine
• Synonyms: [1,2,4]Triazolo[1,5-a][1,3,5]triazin-7-amine;5-Azaadenine;7-Amino-s-triazolo[1,5-a]-s-triazine;[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-ylamine;[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-amine(SALTDATA: FREE);[1,2,4]triazolo[5,1-f][1,3,5]triazin-7-amine;[1,2,4]triazolo[5,1-f][1,3,5]triazin-7-ylamine
• CAS NO: 1489-04-9
• Molecular Formula: C4H4N6
• Molecular Weight: 136.12
• Mol File: 1489-04-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 320 °C
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 2.05g/cm³
• Refractive Index: 2.04
• PKA: 0.98±0.30(Predicted)
• CAS DataBase Reference: 7-Amino-s-triazolo[1,5-a]-s-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Amino-s-triazolo[1,5-a]-s-triazine(1489-04-9)
• EPA Substance Registry System: 7-Amino-s-triazolo[1,5-a]-s-triazine(1489-04-9)

Safety Data

• Hazard Codes: T
• Statements: 25
• Safety Statements: 45
• RIDADR: UN 2811 6.1 / PGIII
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 1489-04-9(Hazardous Substances Data)

Usage

General Description

7-Amino-s-triazolo[1,5-a]-s-triazine is a chemical compound with a unique structure that includes three triazine rings fused together. It is also known as AAT or AATZ and is used in various research applications as a building block for the synthesis of other compounds. 7-Amino-s-triazolo[1,5-a]-s-triazine has potential uses in pharmaceuticals, agrochemicals, and materials science due to its interesting chemical properties and structural features. It is a white solid at room temperature and is relatively stable under normal conditions, making it suitable for use in laboratory settings. Additionally, it has been studied for its potential as an energetic component in explosives due to its high nitrogen content.

InChI:InChI=1/C4H4N6/c5-3-6-1-7-4-8-2-9-10(3)4/h1-2H,(H2,5,6,7,8,9)

Upstream product

• 420-04-2 CYANAMID 
• 122-51-0 orthoformic acid triethyl ester 
• 61-82-5 3-amino-1,2,4-triazole 
• 78158-91-5 N¹,N¹-dimethyl-N²-(1,2,4-triazolyl-5-yl)formamidine 
• 61-82-5 3⁽⁵⁾-amino-1,2,4-triazole 
• 4428-98-2 N-cyanomethanimidic acid ethyl ester 

Relevant articles and documents

A novel multicomponent microwave-assisted synthesis of 5-aza-adenines

A novel multicomponent strategy for the efficient synthesis of 5-aza-adenines was developed. 5-Aza-adenines were prepared in a one-pot fashion from 5-amino-1,2,4-triazoles, cyanamide and triethyl orthoformate under microwave irradiation. The operational simplicity, efficiency and accessibility of this method make it highly attractive for the generation of bioactive compound libraries.

Reaction of N-Cyanoformimidates with some Heterocyclic Compounds. A New Synthesis of 5-Azaadenine and Related Compounds

3-Amino-1,2,4-triazoles and 2-aminobenzimidazole were reacted with N-cyanoimidates to give 5-amino-1,2,4-triazolo-1,3,5-triazines (5-azaadenines) and 4-aminobenzimidazo-1,3,5-triazines, respectively.The structures of the compounds obtained were confirmed through the comparison with some of the possible isomers prepared by independent methods.