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

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

InChI
InChI=1S/C13H21NO4/c1-4-7-8-10-18-12(15)11(9-5-2)14-13(16)17-6-3/h5-6,11H,2-4,7-10H2,1H3,(H,14,16)
InChI Key
CZPUGDABXVNVPJ-UHFFFAOYSA-N
Formula
C13H21NO4
SMILES
C=CCC(NC(=O)OC=C)C(=O)OCCCCC
Molecular Weight1
255.31
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° 34.02 kJ/mol Joback Calculated Property
log10WS -3.16 Relay (1.0) Calculated Property
logPoct/wat 2.534 Crippen Calculated Property
McVol 210.290 ml/mol McGowan Calculated Property
Inp [1675.00; 1675.00]   Show Hide
Inp 1675.00 NIST
Inp 1675.00 NIST
Tboil 561.52 K Relay (1.0) Calculated Property
Tfus 258.72 K Relay (1.0) Calculated Property

Cheméo can also estimate 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 [578.64; 651.65] J/mol×K [692.51; 878.92] Show Hide
Cp,gas 578.64 J/mol×K 692.51 Joback Calculated Property
Cp,gas 592.65 J/mol×K 723.58 Joback Calculated Property
Cp,gas 605.92 J/mol×K 754.65 Joback Calculated Property
Cp,gas 618.44 J/mol×K 785.72 Joback Calculated Property
Cp,gas 630.22 J/mol×K 816.79 Joback Calculated Property
Cp,gas 641.29 J/mol×K 847.86 Joback Calculated Property
Cp,gas 651.65 J/mol×K 878.92 Joback Calculated Property

Similar Compounds

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

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