In 2020 ORG LETT published article about ENERGETIC MATERIALS; DERIVATIVES; PYRAZOLE; DESIGN; DETONATIONS; PERFORMANCE; INHIBITORS; CHEMISTRY; FRAMEWORK; FAMILY in [Pang, Aimin] Hubei Inst Aerosp Chemotechnol, Sci & Technol Aerosp Chem Power Lab, Xiangyang 441003, Hubei, Peoples R China; [Huang, Haifeng; Shi, Yameng; Li, Hui; Yang, Jun] Chinese Acad Sci, Shanghai Inst Organ Chem, CAS Key Lab Energy Regulat Mat, Shanghai 200032, Peoples R China; [Li, Hongli] Chongqing Med & Pharmaceut Coll, Coll Med Technol, Biochem, Chongqing 401331, Peoples R China in 2020, Cited 36. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Product Details of 61-82-5
Potassium 1,1,3,3-tetranitropropane-1,3-diide (K2TNP) was found to react readily with various (hetero)aryl amines (12 examples) to give corresponding N-(hetero)aryl-3,5-dinitropyrazoles in moderate to excellent yields. The reactions were performed at mild temperature, and most of the reactions completed in less than 4 h. Four potential energetic compounds show high enthalpy of formation, excellent thermal stability, and good sensitivity, with 3-(3,5-dinitropyrazol-1-yl)-1H-1,2,4-triazole (3j) being a potential 2,2′,4,4′,6,6′-hexanitrostibene (HNS) replacement.
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Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics