Chemical Properties of Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, isohexyl ester

Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, isohexyl ester

InChI
InChI=1S/C20H31NO4/c1-16(2)6-5-15-25-20(23)8-4-7-19(22)21-14-13-17-9-11-18(24-3)12-10-17/h9-12,16H,4-8,13-15H2,1-3H3,(H,21,22)
InChI Key
PJOSTKOKYWKNJZ-UHFFFAOYSA-N
Formula
C20H31NO4
SMILES
COc1ccc(CCNC(=O)CCCC(=O)OCCCC(C)C)cc1
Molecular Weight1
349.46
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Physical Properties

Property Value Unit Source
Δfus 48.36 kJ/mol Joback Calculated Property
IE 8.29 eV Relay (1.0) Calculated Property
logPoct/wat 3.504 Crippen Calculated Property
McVol 293.760 ml/mol McGowan Calculated Property
Inp [2832.00; 2832.00]   Show Hide
Inp 2832.00 NIST
Inp 2832.00 NIST
Tfus 339.01 K Relay (1.0) Calculated Property

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

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [937.60; 1011.95] J/mol×K [890.97; 1097.78] Show Hide
Cp,gas 937.60 J/mol×K 890.97 Joback Calculated Property
Cp,gas 952.96 J/mol×K 925.44 Joback Calculated Property
Cp,gas 967.11 J/mol×K 959.91 Joback Calculated Property
Cp,gas 980.05 J/mol×K 994.38 Joback Calculated Property
Cp,gas 991.82 J/mol×K 1028.85 Joback Calculated Property
Cp,gas 1002.44 J/mol×K 1063.31 Joback Calculated Property
Cp,gas 1011.95 J/mol×K 1097.78 Joback Calculated Property

Similar Compounds

Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, pentyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, heptyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, hexyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, decyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, octyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, dodecyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, nonyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, butyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, propyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, isobutyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, ethyl ester. Glutaric acid, monoamide, N-(2-phenylpropyl)-, isohexyl ester. l-Tyrosine, N,O-bis(3-cyclopentylpropionyl)-, methyl ester. Glutaric acid monoamide, N-(1,2,3,4-tetrahydronaphth-1-yl)-, isohexyl ester. Glutaric acid monoamide, N-(1,2,3,4-tetrahydronaphth-1-yl)-, pentyl ester.

Find more compounds similar to Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, isohexyl ester.

Sources

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