Chemical Properties of Diazene, dicyclohexyl-, 1,2-dioxide

Diazene, dicyclohexyl-, 1,2-dioxide

InChI
InChI=1S/C12H22N2O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h11-12H,1-10H2
InChI Key
IQCWPIHWVLBCTQ-UHFFFAOYSA-N
Formula
C12H22N2O2
SMILES
[O-][N+](C1CCCCC1)=[N+]([O-])C1CCCCC1
Molecular Weight1
226.32
Other Names
  • Azocyclohexane N,N'-dioxide
  • Azocyclohexane, dioxide
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Physical Properties

Property Value Unit Source
ΔvapH° 73.72 kJ/mol Relay (1.0) Calculated Property
logPoct/wat 3.125 Crippen Calculated Property
McVol 185.620 ml/mol McGowan Calculated Property
Tboil 567.33 K Relay (1.0) Calculated Property

Cheméo can also estimate Normal melting (fusion) point, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy, Log10 of Water solubility in mol/l for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Similar Compounds

6,7-Diazatricyclo[3.2.2.0(2,4)]non-6-ene, oxide. 2,3-Diazabicyclo[2.2.2]octa-2,5-diene N-oxide. 2,3-DIAZABICYCLO[2.2.2]OCT-2-ENE. 1-(1-Methoxycarbonylcyclohexyl)-2-methoxydiazen-1-oxide. 1-(1-Methoxycarbonylcyclopentyl)-2-methoxydiazen-1-oxide. 1-(1-Methoxycarbonylcyclohexyl)-2-ethoxydiazen-1-oxide. 1-(1-Methoxycarbonylcyclohexyl)-2-butoxydiazen-1-oxide. Isonipecotinoylisonipecotic acid, N'-pentafluorobenzoyl-, butyl ester. Isonipecotic acid, N-(2-fluoro-6-trifluoromethylbenzoyl)-, ethyl ester. Isonipecotinoylisonipecotic acid, N'-pentafluorobenzoyl-, propyl ester. Isonipecotic acid, N-(2-fluoro-6-trifluoromethylbenzoyl)-, propyl ester. Isonipecotic acid, N-(2-fluoro-6-trifluoromethylbenzoyl)-, butyl ester. Isonipecotic acid, N-(2-fluoro-6-trifluoromethylbenzoyl)-, isobutyl ester. Isonipecotinoylisonipecotic acid, N'-pentafluorobenzoyl-, isobutyl ester. Isonipecotic acid, N-(2-fluoro-6-trifluoromethylbenzoyl)-, undecyl ester.

Find more compounds similar to Diazene, dicyclohexyl-, 1,2-dioxide.

Sources

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