Chemical Properties of L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, decyl ester

L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, decyl ester

InChI
InChI=1S/C28H53NO4/c1-8-9-10-11-12-13-14-15-18-32-27(30)25(19-21(2)3)29(7)28(31)33-26-20-23(6)16-17-24(26)22(4)5/h21-26H,8-20H2,1-7H3
InChI Key
CDMBEENWNOORBL-UHFFFAOYSA-N
Formula
C28H53NO4
SMILES
CCCCCCCCCCOC(=O)C(CC(C)C)N(C)C(=O)OC1CC(C)CCC1C(C)C
Molecular Weight1
467.72
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° 63.44 kJ/mol Joback Calculated Property
logPoct/wat 7.614 Crippen Calculated Property
McVol 419.380 ml/mol McGowan Calculated Property
Inp [2862.00; 2862.00]   Show Hide
Inp 2862.00 NIST
Inp 2862.00 NIST

Cheméo can also estimate Normal Boiling Point Temperature, Normal melting (fusion) point, 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, 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 [1505.63; 1597.10] J/mol×K [978.01; 1199.07] Show Hide
Cp,gas 1505.63 J/mol×K 978.01 Joback Calculated Property
Cp,gas 1526.13 J/mol×K 1014.85 Joback Calculated Property
Cp,gas 1544.45 J/mol×K 1051.70 Joback Calculated Property
Cp,gas 1560.65 J/mol×K 1088.54 Joback Calculated Property
Cp,gas 1574.78 J/mol×K 1125.38 Joback Calculated Property
Cp,gas 1586.91 J/mol×K 1162.22 Joback Calculated Property
Cp,gas 1597.10 J/mol×K 1199.07 Joback Calculated Property

Similar Compounds

L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, undecyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, pentadecyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, isohexyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, tridecyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, heptyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, nonyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, dodecyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, butyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, pentyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, hexadecyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, hexyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, octyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, tetradecyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, propyl ester. L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, isobutyl ester.

Find more compounds similar to L-Leucine, N-methyl-N-((1R)-(-)-menthyloxycarbonyl)-, decyl 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.