Chemical Properties of L-Leu, N-ethoxycarbonyl, (S)-1-phenylethylamide

L-Leu, N-ethoxycarbonyl, (S)-1-phenylethylamide

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InChI
InChI=1S/C17H26N2O3/c1-5-22-17(21)19-15(11-12(2)3)16(20)18-13(4)14-9-7-6-8-10-14/h6-10,12-13,15H,5,11H2,1-4H3,(H,18,20)(H,19,21)/t13-,15-/m0/s1
InChI Key
OBRXZDQJVNEAQV-ZFWWWQNUSA-N
Formula
C17H26N2O3
SMILES
CCOC(=O)NC(CC(C)C)C(=O)NC(C)c1ccccc1
Molecular Weight1
306.40
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Physical Properties

Property Value Unit Source
Δf 13.29 kJ/mol Joback Calculated Property
Δfgas -423.96 kJ/mol Joback Calculated Property
Δfus 37.84 kJ/mol Joback Calculated Property
Δvap 83.32 kJ/mol Joback Calculated Property
log10WS -4.36 Crippen Calculated Property
logPoct/wat 3.025 Crippen Calculated Property
McVol 255.600 ml/mol McGowan Calculated Property
Pc 1795.46 kPa Joback Calculated Property
Inp 2176.00 NIST
Tboil 844.22 K Joback Calculated Property
Tc 1056.09 K Joback Calculated Property
Tfus 490.18 K Joback Calculated Property
Vc 0.962 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [792.80; 865.34] J/mol×K [844.22; 1056.09] Show Hide
Cp,gas 792.80 J/mol×K 844.22 Joback Calculated Property
Cp,gas 807.62 J/mol×K 879.53 Joback Calculated Property
Cp,gas 821.28 J/mol×K 914.84 Joback Calculated Property
Cp,gas 833.85 J/mol×K 950.16 Joback Calculated Property
Cp,gas 845.35 J/mol×K 985.47 Joback Calculated Property
Cp,gas 855.83 J/mol×K 1020.78 Joback Calculated Property
Cp,gas 865.34 J/mol×K 1056.09 Joback Calculated Property

Similar Compounds

D-Leu, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Norval, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Norval, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Norleu, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Norleu, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Ile, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Ile, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-«alpha»-Aminobutyric acid, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-«alpha»-Aminobutyric acid, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Pro, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Pro, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Pipecolic acid, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Pipecolic acid, N-ethoxycarbonyl, (S)-1-phenylethylamide. L-Val, N-ethoxycarbonyl, (S)-1-phenylethylamide. D-Val, N-ethoxycarbonyl, (S)-1-phenylethylamide.

Find more compounds similar to L-Leu, N-ethoxycarbonyl, (S)-1-phenylethylamide.

Sources

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