592-56-3

Usage

Safety Profile

Low toxicity by inhalation. Whenheated to decomposition it emits toxic vapors of NOx.

InChI:InChI=1/C4H8N2/c1-3-5-6-4-2/h3-4H,1-2H3/b5-3+,6-4+

Upstream product

• 2963-84-0 (Z)-2-hydrazono-propionic acid 
• 131543-46-9 Glyoxal 
• 31909-46-3 Glyoxal semicarbazone 
• 75-07-0 acetaldehyde 
• 22596-53-8 aziridin-1-yl-ethylidene-amine 
• 142267-07-0 3-Methyl-[1,2,4]triazinane 
• 142267-08-1 3,4-Dimethyl-[1,2,4]triazinane 
• 821-14-7 azoethane 

Downstream Products

• 56930-54-2 2-benzhydrylidene-3-ethylideneamino-4-methyl-5,5-diphenyl-[1,3]oxazinan-6-one 
• 56930-56-4 2-benzhydryl-4-methyl-5,5-diphenyl-4,5-dihydro-[1,3]oxazin-6-one 
• 624-80-6 ethylhydrazine 
• 20487-02-9 acetaldehyde ethylhydrazone 
• 85046-73-7 N-Eth-(Z)-ylidene-N'-[1-phenyl-prop-(E)-ylidene]-hydrazine 
• 14531-55-6 3,5-dimethyl-4-nitro-1H-pyrazole 
• 113854-48-1 1-phenyl-3-(4-fluorophenyl)-5-methyl-1,2,4-triazole 
• 113854-52-7 5-Methyl-1-(3-nitro-phenyl)-1H-[1,2,4]triazole-3-carboxylic acid ethyl ester 
• 113854-51-6 1-(3-nitrophenyl)-3-ethoxycarbonyl-4-ethylideneamino-5-methyl-1,2,4-Δ²-triazoline 
• 113854-50-5 1-(4-nitrophenyl)-3-ethoxycarbonyl-4-ethylideneamino-5-methyl-1,2,4-Δ²-triazoline 
• 75-04-7 ethylamine 
• 109-89-7 diethylamine 
• 121-44-8 triethylamine 

Relevant academic research and scientific papers

RING-CHAIN TAUTOMERISM OF SUBSTITUTED HYDRAZONES. 22. SYNTHESIS, STRUCTURE, AND OXIDATION OF ALKYLIDENE DERIVATIVES OF 2-AMINOETHYLHYDRAZINES

Alkylidene derivatives of 2-aminoethylhydrazines exist in solutions either as 2-aminoethylhydrazones or as the ring-chain tautomeric mixtures of the hydrazone-perhydro-1,2,4-triazine depending on the structure.The oxidation of perhydro-1,2,4-triazines leads to the formation of 2,3,4,5-tetrahydro-1,2,4-triazines.

Radical-initiated tautomerization of azoethane to acetaldehyde-ethylhydrazone; Reactivity of the CH3CH=NNC2H5 radical

The N radical centre of the stabilized CH3CH=NNC2H5 radical is capable of H-abstraction from azoethane and radicals at 397-445 K. The tautomerization of azoethane to its hydrazone isomers was observed in both homogeneous and heterogeneous processes.

Decane-1,10-diisocyanates and methods of making the same

Decane-1,10-diisocyanates corresponding to the formula STR1 wherein R1 is an alkyl or cycloalkyl radical, and R2 is a hydrogen atom or an alkyl or cycloalkyl radical and the method of making these diisocyanates by the phosgenation of 1,10-diaminodecanes of the formula STR2

CO-OLIGOMERISATION DE BUTADIENE ET D'HETERODIENES AZOTES CATALYSEE PAR LE NICKEL CONTROLE DE LA SELECTIVITE

Nickel (0) catalysed co-oligomerization of butadiene with heterodienes and hetero-olefins is described.It is shown how the selectivity of these reactions can be controlled by the position of the heteroatom in the heteropartner and also by the nature of th