296791-84-9

Basic information

• Product Name: 1-(4-AMINO-1,2,5-OXADIAZOL-3-YL)-5-PHENYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID
• Synonyms: 1-(4-AMINO-1,2,5-OXADIAZOL-3-YL)-5-PHENYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID
• CAS NO: 296791-84-9
• Molecular Formula: C₁₁H₈N₆O₃
• Molecular Weight: 272.22
• Mol File: 296791-84-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(4-AMINO-1,2,5-OXADIAZOL-3-YL)-5-PHENYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-AMINO-1,2,5-OXADIAZOL-3-YL)-5-PHENYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID(296791-84-9)
• EPA Substance Registry System: 1-(4-AMINO-1,2,5-OXADIAZOL-3-YL)-5-PHENYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID(296791-84-9)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 296791-84-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-(4-AMINO-1,2,5-OXADIAZOL-3-YL)-5-PHENYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID is used as a compound with potential medicinal applications due to its unique structural features. Its presence of a 1,2,5-oxadiazole ring, a phenyl group, and a 1,2,3-triazole ring may contribute to its biological activity, making it a candidate for further research and development in the pharmaceutical field.
Used in Chemical Research:
In the field of chemical research, 1-(4-AMINO-1,2,5-OXADIAZOL-3-YL)-5-PHENYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID serves as a subject for investigation into its properties, reactivity, and potential hazards. Understanding these aspects is essential for determining its suitability and safety for various applications, including medicinal chemistry and material science.
Used in Material Science:
1-(4-AMINO-1,2,5-OXADIAZOL-3-YL)-5-PHENYL-1H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID may also find applications in material science, where its unique structural features could be exploited to develop new materials with specific properties. Further research is required to explore its potential in this field.

Downstream Products

• 1382672-07-2 3-nitroamino-4-[5-(3-nitrophenyl)-1H-1,2,3-triazol-1-yl]-1,2,5-oxadiazole 

Relevant articles and documents

Synthesis of 3-nitramino-4-(1 H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles and their salts

Nitration of 3-amino-4-(1 H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles (3-amino-4-triazolyl-furazans) with a mixture of NaNO3 and conc. H2SO4 gave for the first time triazolylfurazans with a primary nitramino group attached to the furazan ring. If the starting amino(triazolyl)-furazan contains an aromatic substituent, the latter also undergoes nitration under the conditions studied. Some of these nitramines were converted into salts (K, Na, and NH4).