Chemical Properties of L-Valine, N-(3-phenylpropionyl)-, heptyl ester

L-Valine, N-(3-phenylpropionyl)-, heptyl ester

InChI
InChI=1S/C21H33NO3/c1-4-5-6-7-11-16-25-21(24)20(17(2)3)22-19(23)15-14-18-12-9-8-10-13-18/h8-10,12-13,17,20H,4-7,11,14-16H2,1-3H3,(H,22,23)
InChI Key
RXPPSSNUBHLGIK-UHFFFAOYSA-N
Formula
C21H33NO3
SMILES
CCCCCCCOC(=O)C(N=C(O)CCc1ccccc1)C(C)C
Molecular Weight1
347.49
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Physical Properties

Property Value Unit Source
ω 1.0186 Relay (1.0) Calculated Property
Δf -94.18 kJ/mol Relay (1.0-beta) Calculated Property
Δfgas -656.91 kJ/mol Relay (1.0) Calculated Property
Δvap 124.16 kJ/mol Relay (1.0) Calculated Property
IE 8.46 eV Relay (1.0) Calculated Property
log10WS -4.61 Relay (1.0) Calculated Property
logPoct/wat 5.114 Crippen Calculated Property
McVol 301.980 ml/mol McGowan Calculated Property
Pc 1232.01 kPa Joback Calculated Property
Inp [2567.00; 2567.00]   Show Hide
Inp 2567.00 NIST
Inp 2567.00 NIST
Tboil 646.52 K Relay (1.0) Calculated Property
Tc 863.47 K Relay (1.0) Calculated Property
Tfus 371.49 K Relay (1.0) Calculated Property
Vc 1.080 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

L-Valine, N-(3-phenylpropionyl)-, octyl ester. L-Valine, N-(3-phenylpropionyl)-, hexyl ester. L-Valine, N-(3-phenylpropionyl)-, pentyl ester. Thymidine, 5'-O-cyclotetramethylene-tertbutylsilyl. 1-Methyl-6«alpha»,7«alpha»-dihydroxyestrone, TMS. Thymidine, 3'-O-TMS, 5'-O-cyclotetramethylene-isopropylsilyl. Hypoxanthine-7-ethanol, 2,3-dihydro-3-(diphenylmethyl)-, acetate. Thymidine, 3'-O-cyclotetramethylene-tertbutylsilyl, 5'-O-TBDMS. Thymidine, 3'-O-TBDMS, 5'-O-cyclotetramethylene-isopropylsilyl. Thymidine, 3'-O-TFA, 5'-O-cyclotetramethylene-tertbutylsilyl. Thymidine, 3'-O-cyclotetramethylene-tertbutylsilyl, 5'-O-TMS. Thymidine, 5'-O-cyclotetramethylene-isopropylsilyl. Benazepril Me. Thymidine, 3'-O-cyclotetramethylene-tertbutylsilyl, 5'-O-cyclotetramethylene-isopropylsilyl. Thymidine, 3'-O-cyclotetramethylene-isopropylsilyl, 5'-O-TMS.

Find more compounds similar to L-Valine, N-(3-phenylpropionyl)-, heptyl ester.

Sources

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