Chemical Properties of Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, decyl ester

Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, decyl ester

InChI
InChI=1S/C22H34ClNO4/c1-3-4-5-6-7-8-9-10-16-28-22(26)13-11-12-21(25)24-19-17-18(23)14-15-20(19)27-2/h14-15,17H,3-13,16H2,1-2H3,(H,24,25)
InChI Key
SSSUPUUNJWNTKP-UHFFFAOYSA-N
Formula
C22H34ClNO4
SMILES
CCCCCCCCCCOC(=O)CCCC(=O)Nc1cc(Cl)ccc1OC
Molecular Weight1
411.96
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Physical Properties

Property Value Unit Source
Δfus 62.45 kJ/mol Joback Calculated Property
Δvap 122.66 kJ/mol Relay (1.0) Calculated Property
log10WS -5.98 Relay (1.0) Calculated Property
logPoct/wat 6.141 Crippen Calculated Property
McVol 334.180 ml/mol McGowan Calculated Property
Inp [3400.00; 3400.00]   Show Hide
Inp 3400.00 NIST
Inp 3400.00 NIST
Tboil 683.38 K Relay (1.0) Calculated Property
Tfus 349.90 K Relay (1.0) Calculated Property

Cheméo can also estimate Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy 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.

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1075.24; 1141.33] J/mol×K [961.71; 1177.82] Show Hide
Cp,gas 1075.24 J/mol×K 961.71 Joback Calculated Property
Cp,gas 1089.65 J/mol×K 997.73 Joback Calculated Property
Cp,gas 1102.65 J/mol×K 1033.75 Joback Calculated Property
Cp,gas 1114.29 J/mol×K 1069.77 Joback Calculated Property
Cp,gas 1124.59 J/mol×K 1105.79 Joback Calculated Property
Cp,gas 1133.59 J/mol×K 1141.81 Joback Calculated Property
Cp,gas 1141.33 J/mol×K 1177.82 Joback Calculated Property

Similar Compounds

Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, hexyl ester. Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, heptyl ester. Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, nonyl ester. Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, pentyl ester. Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, butyl ester. Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, isohexyl ester. Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, propyl ester. Glutaric acid, monoamide, N-(2-methoxyphenyl)-, nonyl ester. Glutaric acid, monoamide, N-(2-methoxyphenyl)-, octyl ester. Glutaric acid, monoamide, N-(2-methoxyphenyl)-, dodecyl ester. Glutaric acid, monoamide, N-(2-methoxyphenyl)-, undecyl ester. Glutaric acid, monoamide, N-(2-methoxyphenyl)-, decyl ester. Glutaric acid, monoamide, N-(2-methoxyphenyl)-, heptyl ester. Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, ethyl ester. Glutaric acid, monoamide, N-(2-methoxyphenyl)-, hexyl ester.

Find more compounds similar to Glutaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, decyl ester.

Sources

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