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

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

PDF Excel Molecule Calculator
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
ΔfG° -523.89 kJ/mol Joback Calculated Property
ΔfH°gas -1122.18 kJ/mol Joback Calculated Property
ΔfusH° 38.22 kJ/mol Joback Calculated Property
ΔvapH° 87.63 kJ/mol Joback Calculated Property
log10WS -3.96 Crippen Calculated Property
logPoct/wat 3.057 Crippen Calculated Property
McVol 296.780 ml/mol McGowan Calculated Property
Pc 1317.52 kPa Joback Calculated Property
Inp [2138.50; 2138.50]   Show Hide
Inp 2138.50 NIST
Inp 2138.50 NIST
Tboil 888.08 K Joback Calculated Property
Tc 1090.76 K Joback Calculated Property
Tfus 486.76 K Joback Calculated Property
Vc 1.121 m3/kmol Joback Calculated Property

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

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

Find more compounds similar to D-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.