Chemical Properties of L-Glutamic acid, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester

L-Glutamic acid, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester

InChI
InChI=1S/C18H33NO6/c1-8-23-18(22)19-15(17(21)25-14(7)12(4)5)9-10-16(20)24-13(6)11(2)3/h11-15H,8-10H2,1-7H3,(H,19,22)/t13-,14-,15?/m1/s1
InChI Key
QOBXCSPBRMIZOJ-GRKKQISMSA-N
Formula
C18H33NO6
SMILES
CCOC(=O)NC(CCC(=O)OC(C)C(C)C)C(=O)OC(C)C(C)C
Molecular Weight1
359.46
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° 38.22 kJ/mol Joback Calculated Property
logPoct/wat 3.057 Crippen Calculated Property
McVol 296.780 ml/mol McGowan Calculated Property
Inp 2148.70 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 [964.55; 1036.50] J/mol×K [888.08; 1090.76] Show Hide
Cp,gas 964.55 J/mol×K 888.08 Joback Calculated Property
Cp,gas 979.82 J/mol×K 921.86 Joback Calculated Property
Cp,gas 993.77 J/mol×K 955.64 Joback Calculated Property
Cp,gas 1006.41 J/mol×K 989.42 Joback Calculated Property
Cp,gas 1017.75 J/mol×K 1023.20 Joback Calculated Property
Cp,gas 1027.77 J/mol×K 1056.98 Joback Calculated Property
Cp,gas 1036.50 J/mol×K 1090.76 Joback Calculated Property

Similar Compounds

D-Glutamic acid, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. D-Norvaline, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. L-«alpha»-Aminoadipic acid, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. D-«alpha»-Aminoadipic acid, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. «alpha»-Aminopimelic acid, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. L-Norleucine, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. D-Norleucine, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. L-Leucine, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. D-Leucine, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. D-Ornithine, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. L-Ornithine, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. D-Lysine, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. L-Lysine, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. L-«alpha»-Aminobutyric acid, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester. D-«alpha»-Aminobutyric acid, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl ester.

Find more compounds similar to L-Glutamic acid, N(O,S)-ethoxycarbonyl, (S)-(+)-3-methyl-2-butyl 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.