96907-33-4

Upstream product

• 86663-28-7 4-Amino-1-methyl-bis-1,2,4-triazolium iodide 

Downstream Products

• 116088-23-4 4-(N,N'-bis(4-methoxyphenyl))guanidino-2-methyl-5-methylthio-2H-1,2,4-triazol-3(4H)-one 
• 116088-22-3 4-(N,N'-bis(4-bromophenyl))guanidino-2-methyl-5-methylthio-2H-1,2,4-triazol-3(4H)-one 
• 116088-20-1 4-(N,N'-diphenyl)guanidino-2-methyl-5-methylthio-2H-1,2,4-triazol-3(4H)-one 
• 116088-21-2 4-(N,N'-bis(4-chlorophenyl))guanidino-2-methyl-5-methylthio-2H-1,2,4-triazol-3(4H)-one 

Relevant academic research and scientific papers

Aromatic Systems with 10? Electrons Derived from 3a-Azapentalene. Part 40. Studies on the 1,2,4-Triazolotriazole Series

The synthesis, structure, and reactivity of several 1,2,4-triazolotriazole derivatives have been studied.Structures have been established throughout a careful carbon-13 NMR study, and for the most unusual one (inner salt of 2-methyl-3-methylthio-6-phenyl-7H-1,2,4-triazolotriazolium hydroxide) by X-ray crystallography: the space group is P21/c, the cell constants are a=12.6939(5), b=16.0936(6), c=12.0239(5) and β=107.247(3) deg and Z=8.The S-methyl group is directed towards the fusion of the five-membered rings at +/-syn conformations.Theazapentalene moieties have the first atoms of the substituents on its plane and the 6-phenyl rings make an angle of -26.7 and -4.3 deg with it, in the two independent molecules respectively.