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

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

InChI
InChI=1S/C16H23NO4/c1-3-21-16(19)6-4-5-15(18)17-12-11-13-7-9-14(20-2)10-8-13/h7-10H,3-6,11-12H2,1-2H3,(H,17,18)
InChI Key
AHUYPYXQEISPGE-UHFFFAOYSA-N
Formula
C16H23NO4
SMILES
CCOC(=O)CCCC(=O)NCCc1ccc(OC)cc1
Molecular Weight1
293.36
Cheméo is a service of Céondo GmbH, since 2007, we provide simulation, modelling and software development services for the industry. Do not hesitate to contact us for your projects.

Physical Properties

Property Value Unit Source
ΔfusH° 43.10 kJ/mol Joback Calculated Property
IE 8.20 eV Relay (1.0) Calculated Property
log10WS -2.53 Relay (1.0) Calculated Property
logPoct/wat 2.087 Crippen Calculated Property
McVol 237.400 ml/mol McGowan Calculated Property
Inp [2485.00; 2485.00]   Show Hide
Inp 2485.00 NIST
Inp 2485.00 NIST
Tboil 645.54 K Relay (1.0) Calculated Property
Tc 852.74 K Relay (1.0) Calculated Property
Tfus 328.87 K Relay (1.0) Calculated Property

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

Correlations

Property Value Unit Temperature (K) Source
Cp,gas [339.05; 775.74] J/mol×K [273.00; 1000.00] Joback Predicted correlation Show Hide
EquationY = A + B·T + C·T² + D·T³ + E·T⁴
Y is Cp,gas in J/mol×K, T in K
Coefficient A2.57960e+01
Coefficient B1.31564e+00
Coefficient C-6.35060e-04
Coefficient D6.93600e-08
Coefficient E0.00000e+00
Temperature range, min.273.00
Temperature range, max.1000.00
Cp,gas 339.05 J/mol×K 273.00 Calculated Property
Cp,gas 414.83 J/mol×K 353.78 Calculated Property
Cp,gas 483.28 J/mol×K 434.56 Calculated Property
Cp,gas 544.63 J/mol×K 515.33 Calculated Property
Cp,gas 599.09 J/mol×K 596.11 Calculated Property
Cp,gas 646.88 J/mol×K 676.89 Calculated Property
Cp,gas 688.22 J/mol×K 757.67 Calculated Property
Cp,gas 723.33 J/mol×K 838.44 Calculated Property
Cp,gas 752.43 J/mol×K 919.22 Calculated Property
Cp,gas 775.74 J/mol×K 1000.00 Calculated Property

Similar Compounds

Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, propyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, butyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, pentyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, isobutyl 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)-, dodecyl ester. Glutaric acid, monoamide, N-(2-(4-methoxyphenyl)ethyl)-, nonyl 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)-, isohexyl ester. L-Tyrosine, N,O-bis(capryloyl)-, methyl ester. l-Tyrosine, N,O-bis(caproyl)-, methyl ester. Glutaric acid, monoamide, N-(2-phenylpropyl)-, ethyl ester. l-Tyrosine, N,O-bis(butyryl)-, methyl ester.

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

Sources

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.
These property values are available through the Cheméo API. A free account gives you an access key.