Safety of 3,5-Di(pyridin-2-yl)-4H-1,2,4-triazol-4-amine. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 3,5-Di(pyridin-2-yl)-4H-1,2,4-triazol-4-amine, is researched, Molecular C12H10N6, CAS is 1671-88-1, about Copper-induced N-N bond cleavage results in an octanuclear expanded-core grid-like complex. Author is White, Nicholas G.; Kitchen, Jonathan A.; Joule, John A.; Brooker, Sally.
Reaction of copper(I) acetate and 4-amino-3,5-bis(2-pyridyl)-1,2,4-triazole (adpt) in methanol under ambient conditions yields octanuclear [CuII8(dpt)4(OH)4(OAc)8] (OAc = acetate anion; Hdpt = 3,5-bis(2-pyridyl)-1,2,4-triazole). However, reaction of copper(II) acetate with dptH gives tetranuclear [CuII4(dpt)2(OH)(OMe)(OAc)4].
This compound(3,5-Di(pyridin-2-yl)-4H-1,2,4-triazol-4-amine)Safety of 3,5-Di(pyridin-2-yl)-4H-1,2,4-triazol-4-amine was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.
Reference:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem