224033-01-6

Basic information

• Product Name: 1H-1,2,4-Triazol-3-amine,5-azido-(9CI)
• Synonyms: 1H-1,2,4-Triazol-3-amine,5-azido-(9CI);3-azido-1H-1,2,4-triazol-5-amine(SALTDATA: FREE);3-azido-1H-1,2,4-triazol-5-amine
• CAS NO: 224033-01-6
• Molecular Formula: C2H3N7
• Molecular Weight: 125.09212
• Product Categories: AMINEPRIMARY
• Mol File: 224033-01-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-1,2,4-Triazol-3-amine,5-azido-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,4-Triazol-3-amine,5-azido-(9CI)(224033-01-6)
• EPA Substance Registry System: 1H-1,2,4-Triazol-3-amine,5-azido-(9CI)(224033-01-6)

Safety Data

• Hazardous Substances Data: 224033-01-6(Hazardous Substances Data)

Usage

Chemical Family

1H-1,2,4-Triazol-3-amine,5-azido-(9CI) belongs to the triazole family.

Derivative

It is a derivative of 1,2,4-triazole with modifications.

Substituents

The compound has an amine group at position 3 and an azide group at position 5.

Building block

It is used as a building block for the synthesis of various bioactive molecules.

Applications

The compound is used in the synthesis of pharmaceuticals and agrochemicals.

Scientific studies

It has been studied for potential application in organic synthesis and materials science.

Click chemistry

The azido group in the compound makes it useful for click chemistry.

Versatile reactivity

The compound is known for its versatile reactivity.

Potential applications

It has potential applications in various fields of chemistry.

Upstream product

• 1455-77-2 guanazole 
• 21578-85-8 5-amino-3-nitrosamino-1,2,4-triazole 
• 1026782-95-5 N₃-[(1E)-3-(4,5-diamino-4H-1,2,4-triazol-3-yl)-1,2-dioxidotriaz-1-enyl]-4H-1,2,4-triazole-3,4,5-triamine 
• 473-96-1 3,4,5-Triamino-4H-1,2,4-triazole 

Downstream Products

• 22244-55-9 1-methyl-3-nitro-1,2,4-triazol-5-one 
• 224033-10-7 3-azido-2'-methyl-5'-nitro-2'H-[1,3']bi[[1,2,4]triazolyl]-5-ylamine 

Relevant articles and documents

Synthesis of 3-Azido-5-amino-1,2,4-triazole

3-Azido-5-amino-1,2,4-triazole was obtained from 3,5-diamino-1,2, 4-triazole in two ways: by partial diazotization-substitution directly in the substrate or at its primarily nitrosation, and also with the use of direct or indirect protection of an amino g

Selective nitrosation of guanazine: preparation of azidoaminotriazole and nitrosoguanazine anion-Cu(II) complexes

Guanazine (3,4,5-triamino-1,2,4-triazole) is selectively nitrosated on C-NH2 to produce nitrosoguanazine (3-nitrosamino-4,5-diamino-1,2,4-triazole). The nitrosoguanazine is used to prepare 5-azido-3-amino-1,2,4-triazole and nitrosoguanazine anion-Cu(II) complexes.

Synthesis of nitrogen-rich imidazole, 1,2,4-triazole and tetrazole-based compounds

Imidazole, 1,2,4-triazole and tetrazole based molecules were prepared for their possible applications in nitrogen-rich gas generators. The energetic salts of 1-(1H-1,2,4-triazol-3-yl)-1H-tetrazole (9), 5-(1H-tetrazol-1-yl)-1H-1,2,4- triazol-3-amine (10), 1-(3-azido-1H-1,2,4-triazol-5-yl)-1H-tetrazole (11) and 3-azido-1H-1,2,4-triazol-5-amine (12) were prepared with various cationic moieties. Their densities, heats of formation, chemical energy of detonation, detonation velocities and pressures were calculated. All of the compounds possessed high positive heats of formation due to high energy contribution from the molecular backbone of the corresponding compounds. The effect of the azole rings and nitro, amino, and azido groups on their physicochemical properties was examined and discussed. The Royal Society of Chemistry 2014.

Method for azidoaminotriazole, nitrosoguanazine, and related compounds

The present invention includes a method of making of azidoaminotriazole (5-azido-2H-[1,2,4]triazol-3-ylamine), nitrosoguanazine dimer (N3-[(1E)-3-(4,5-diamino-4H-1,2,4-triazol-3-yl)-1,2-dioxidotriaz-1-enyl]-4H-1,2,4-triazole-3,4,5-triamine), novel nitrosoguanazine salts, azidonitraminotriazole/salts and the making of azidonitraminotriazole and salts, and novel metal complexes of an azidonitramine (4,6-diazido-N-nitro-1,3,5-triazin-2-amine) and the making of these metal complexes of this azidonitramine. Azidoaminotriazole, nitrosoguanazine, and azidonitramine compounds, their intermediates, and their salts may generally relate to energetic compounds, while nitrosoguanazine compounds and their metal salts may also have commercial potential in biomedical and pharmaceutical applications.