It seems appealing because there is no concentrated H2SO4/HNO3 nitrations, and all the reagents are fairly cheap and readily available. The most
annoying part might be producing the diaminofurazan.. But hydroxylamine and glyoxal can be bought at a decent price...
I wonder if you could do a one pot reaction from diaminofurazan all the way to dinitroazoxyfurazan.. That would be handy. Hmm, nevermind, references
say the yields are very low..
Also I wonder if it would be possible to make a nitramine deriviative of diaminoazoxyfurazan, and what its properties would be? Nitration would
probably break the N=N or N-O-N linkages no?
By the way, Axt already published a beautiful PDF detailing his experiments with these compounds.
[Edited on 26-7-2009 by 497]basstabone - 26-7-2009 at 12:22
Could you upload it to another site? It says it can only be downloaded ten times and my bet is that more than 10 people wanna view it here CL-20 - 26-7-2009 at 12:32
