3711-34-0

Usage

Physical state

Colorless, flammable liquid

Primary use

Rocket propellant for spacecraft and satellite engines

Secondary use

Fuel additive in automotive and aviation industries

Reactivity

Highly reactive

Hazard

Can react violently with oxidizing agents, posing a potential fire and explosion hazard

Safety precautions

Must be handled and stored with caution, following proper safety procedures

Classification

Hazardous material

Transportation and disposal

Must be done according to regulations to minimize environmental impact and ensure safety

InChI:InChI=1/C6H16N2/c1-5(2)7-8-6(3)4/h5-8H,1-4H3

Upstream product

• 7423-01-0 acetone isopropylhydrazone 
• 693-13-0 diisopropyl-carbodiimide 
• 2684-60-8 2-diazopropane 
• 627-70-3 propan-2-one azine 
• 67-64-1 acetone 
• 67-63-0 isopropyl alcohol 
• 75-26-3 isopropyl bromide 

Downstream Products

• 693-13-0 diisopropyl-carbodiimide 
• 60678-71-9 N,N'-diisopropyl-N,N'-dimethyl-hydrazine 
• 36286-44-9 6β-(2-phenyl-acetylamino)-penicillanic acid N,N'-diisopropyl-hydrazide 
• 40028-67-9 C₂₀H₂₆N₄O₂ 
• 78211-42-4 1,2-Diisopropyl-4-phenyl-[1,2,4]diazaphospholidine 
• 6400-42-6 3,4-diisopropyl-[1,3,4]oxadiazolidine 
• 934750-67-1 1,2-diisopropyl-1,2-diaza-3,5-diphenyldiborolidine 
• 142842-10-2 4-benzyl-3,5-di-tert-butyl-1,2-diisopropyl-1,2,4,3,5-triazadiborolidine 
• 1356370-29-0 1,2-diisopropyl-1,2-diaza-3,5-diphenyl-3,5-diborolyltrimethylsilane 
• 1356370-27-8 Bis(1,2-diisopropyl-1,2-diaza-3,5-diphenyl-3,5-diborolyl)(C-C) (Germ_.) 
• 1356370-26-7 (1,2-Diisopropyl-1,2-diaza-3,5-diphenyl-3,5-diborolyl)kalium (Germ_.) 
• 1356370-21-2 1,2-diisopropyl-1,2-diaza-3,5-diphenyl-3,5-diborolidine 
• 934750-69-3 (1,2-diisopropyl-1,2-diaza-3,5-diphenyldiborolyl)sodium 
• 934750-70-6 (4-methyl-1,2-diisopropyl-3,5-diphenyl-1,2-diaza-3,5-diborolyl)potassium 

Relevant academic research and scientific papers

Asymmetric nitrogen 78. Sterically hindered inversion of nitrogen atoms in cyclic hydrazines: N,N'-dialkyl-1,3,4-oxadiazolidines; 1,3,4-thiadiazolidine; and 4,5-benzo-1,2,3,6-tetrahydropyridazine

N,N'-Diisopropyl-substituted 1,3,4-oxadiazolidine 3c, 1,3,4-thiadiazolidine 6, 4,5-benzo-1,2,3,6-tetrahydropyridazine 8, and new 3,4-dialkyl-1,3,4-oxadiazolines 9-14 were synthesized and studied.The configurational stability of the N atoms does not change on going from compounds 3c to its S-analog 6 and decreases in the case of pyridazine 8. 3,4-Di-tert-alkyl-1,3,4-oxadiazolidines 3d and 11-14 were found to be promising objects for optical resolution. - Keywords: N,N'-dialkyl-substituted 1,3,4-oxadiazolidines; 1,3,4-thiadiazolidine; 4,5-benzo-1,2,3,6-tetrahydropyridazine; nitrogen inversion; 1H, 13C NMR.