14779-22-7

Upstream product

• 14792-85-9 μ-disulfido-1,2-diimido-dicarbonic acid bis-(N-methyl-anilide); dihydrobromide 
• 4104-75-0 1-methyl-1-phenylthiourea 
• 22713-97-9 N³,N⁵-diphenyl-1,2,4-thiadiazole-3,5-diamine 
• 74-88-4 methyl iodide 

Downstream Products

• 100-61-8 N-methylaniline 

Relevant academic research and scientific papers

Decomposition Reaction of 3-Aryl-6-disubstituted Amino-1,4,2,5-dithiadiazines in the Solid State

3-Diethylamino-6-phenyl-1,4,2,5-dithiadiazine, on standing in air at room temperature, decomposed to afford 5-diethylamino-3-phenyl- and 3,5-bis(diethylamino)-1,2,4-thiadiazoles, whereas in the melt and in solution it was remarkably stable.With increasing bulkiness of substituents (Ar and /or NR2) in 1,4,2,5-dithiadiazines, their stability in the solid state clearly enhanced.Some interstack interactions in the crystal seem to favor the decomposition.

STRUCTURE ELUCIDATION OF HECTOR'S BASE, DOST'S BASE, AND RELATED COMPOUNDS BY NITROGEN-15 and CARBON-13 N.m.r. SPECTROSCOPY

The structures, in solution, of Hector's Base, Dost's Base, and some related compounds have been deduced by considerations of their 15N and 13C n.m.r. spectra.