Chemical Properties of Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 4-isopropoxyphenyl ester

Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 4-isopropoxyphenyl ester

InChI
InChI=1S/C20H20ClNO5/c1-13(2)26-15-5-7-16(8-6-15)27-20(24)11-10-19(23)22-17-12-14(21)4-9-18(17)25-3/h4-13H,1-3H3,(H,22,23)/b11-10+
InChI Key
MDDFRWTXOCFFMH-ZHACJKMWSA-N
Formula
C20H20ClNO5
SMILES
COc1ccc(Cl)cc1NC(=O)C=CC(=O)Oc1ccc(OC(C)C)cc1
Molecular Weight1
389.83
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Physical Properties

Property Value Unit Source
Δfus 48.79 kJ/mol Joback Calculated Property
log10WS -5.04 Relay (1.0) Calculated Property
logPoct/wat 4.236 Crippen Calculated Property
McVol 283.810 ml/mol McGowan Calculated Property
Inp 3299.00 NIST
Tfus 410.91 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, 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 [847.17; 888.37] J/mol×K [973.75; 1209.87] Show Hide
Cp,gas 847.17 J/mol×K 973.75 Joback Calculated Property
Cp,gas 857.50 J/mol×K 1013.10 Joback Calculated Property
Cp,gas 866.39 J/mol×K 1052.46 Joback Calculated Property
Cp,gas 873.89 J/mol×K 1091.81 Joback Calculated Property
Cp,gas 880.04 J/mol×K 1131.16 Joback Calculated Property
Cp,gas 884.85 J/mol×K 1170.52 Joback Calculated Property
Cp,gas 888.37 J/mol×K 1209.87 Joback Calculated Property

Similar Compounds

Fumaric acid, monoamide, N-(2-methoxy-5-chlorophenyl)-, 4-bromophenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 2-chlorophenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 3-fluorophenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 3,5-difluorophenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 2,4,6-trichlorophenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 2-fluorophenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, isopropyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 2-bromo-4-fluorophenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 4-chloro-2-methylphenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, neopentyl ester. Fumaric acid, monoamide, N-(2,4-dimethoxyphenyl)-, 2-chlorophenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 2-pentyl ester. Fumaric acid, monoamide, N-(2,4-dimethoxyphenyl)-, 3-fluorophenyl ester. Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, pentafluorobenzyl ester. naringin.

Find more compounds similar to Fumaric acid, monoamide, N-(5-chloro-2-methoxyphenyl)-, 4-isopropoxyphenyl ester.

Sources

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