Chemical Properties of 2-Aminopent-4-enoic acid, N-vinyloxycarbonyl-, heptyl ester

2-Aminopent-4-enoic acid, N-vinyloxycarbonyl-, heptyl ester

InChI
InChI=1S/C15H25NO4/c1-4-7-8-9-10-12-20-14(17)13(11-5-2)16-15(18)19-6-3/h5-6,13H,2-4,7-12H2,1H3,(H,16,18)
InChI Key
UBDUKVGLDHQTAQ-UHFFFAOYSA-N
Formula
C15H25NO4
SMILES
C=CCC(NC(=O)OC=C)C(=O)OCCCCCCC
Molecular Weight1
283.37
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° 39.20 kJ/mol Joback Calculated Property
ΔvapH° 87.78 kJ/mol Relay (1.0) Calculated Property
log10WS -3.89 Relay (1.0) Calculated Property
logPoct/wat 3.314 Crippen Calculated Property
McVol 238.470 ml/mol McGowan Calculated Property
Inp [1883.00; 1883.00]   Show Hide
Inp 1883.00 NIST
Inp 1883.00 NIST
Tboil 584.44 K Relay (1.0) Calculated Property
Tfus 264.49 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 [687.75; 764.94] J/mol×K [738.27; 923.61] Show Hide
Cp,gas 687.75 J/mol×K 738.27 Joback Calculated Property
Cp,gas 702.64 J/mol×K 769.16 Joback Calculated Property
Cp,gas 716.70 J/mol×K 800.05 Joback Calculated Property
Cp,gas 729.95 J/mol×K 830.94 Joback Calculated Property
Cp,gas 742.39 J/mol×K 861.83 Joback Calculated Property
Cp,gas 754.05 J/mol×K 892.72 Joback Calculated Property
Cp,gas 764.94 J/mol×K 923.61 Joback Calculated Property

Similar Compounds

2-Aminopent-4-enoic acid, N-vinyloxycarbonyl-, hexyl ester. 2-Aminopent-4-enoic acid, N-vinyloxycarbonyl-, nonyl ester. 2-Aminopent-4-enoic acid, N-vinyloxycarbonyl-, octyl ester. 2-Aminopent-4-enoic acid, N-vinyloxycarbonyl-, pentyl ester. 2-Aminopent-4-enoic acid, N-hexyloxycarbonyl-, nonyl ester. 2-Aminopent-4-enoic acid, N-hexyloxycarbonyl-, pentadecyl ester. 2-Aminopent-4-enoic acid, N-hexyloxycarbonyl-, hexadecyl ester. 2-Aminopent-4-enoic acid, N-decyloxycarbonyl-, octyl ester. 2-Aminopent-4-enoic acid, N-decyloxycarbonyl-, decyl ester. 2-Aminopent-4-enoic acid, N-hexyloxycarbonyl-, butyl ester. 2-Aminopent-4-enoic acid, N-decyloxycarbonyl-, undecyl ester. 2-Aminopent-4-enoic acid, N-decyloxycarbonyl-, tridecyl ester. 2-Aminopent-4-enoic acid, N-hexyloxycarbonyl-, tetradecyl ester. 2-Aminopent-4-enoic acid, N-(but-2-yn-1-yloxycarbonyl)-, heptyl ester. 2-Aminopent-4-enoic acid, N-(but-2-yn-1-yloxycarbonyl)-, hexyl ester.

Find more compounds similar to 2-Aminopent-4-enoic acid, N-vinyloxycarbonyl-, heptyl 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.