In 2012,Srinivas, Dharavath; Ghule, Vikas D.; Tewari, Surya P.; Muralidharan, Krishnamurthi published 《Synthesis of Amino, Azido, Nitro, and Nitrogen-Rich Azole Substituted Derivatives of 1H-Benzotriazole for High-Energy Materials Applications》.Chemistry – A European Journal published the findings.Recommanded Product: 20154-03-4 The information in the text is summarized as follows:
The amino, azido, nitro, and nitrogen-rich azole substituted derivatives of 1H-benzotriazole were synthesized for energetic material applications. The synthesized compounds were fully characterized by 1H and 13C NMR spectroscopy, IR, MS, and elemental anal. 5-Chloro-4-nitro-1H-benzo[1,2,3]triazole and 5-azido-4,6-dinitro-1H-benzo[1,2,3]triazole crystallize in the Pca21 (orthorhombic) and P21/c (monoclinic) space group, resp., as determined by single-crystal X-ray diffraction. Their densities are 1.71 and 1.77 g cm-3, resp. The calculated densities of the other compounds range between 1.61-1.98 g cm-3. The detonation velocity values calculated for these synthesized compounds range from 5.45-8.06 km s-1, and the detonation pressure ranges from 12.35-28 GPa.3-(Trifluoromethyl)-1H-pyrazole(cas: 20154-03-4Recommanded Product: 20154-03-4) was used in this study.
3-(Trifluoromethyl)-1H-pyrazole(cas: 20154-03-4) belongs to pyrazoles. The application of pyrazole derivatives in the development of anticancer agents has been thoroughly investigated and verified. Moreover, the medicinal features of a number of natural products incorporating pyrazole moiety such as pyrazofurin, pyrazofurin B, pyrazole-3(5)-carboxylic acid and 4-methylpyrazole-3(5)-carboxylic acid have been reported.Recommanded Product: 20154-03-4
Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics