Chemical Properties of L-Methionine, N-pentafluoropropionyl-, propyl ester

L-Methionine, N-pentafluoropropionyl-, propyl ester

InChI
InChI=1S/C11H16F5NO3S/c1-3-5-20-8(18)7(4-6-21-2)17-9(19)10(12,13)11(14,15)16/h7H,3-6H2,1-2H3,(H,17,19)
InChI Key
IZMMKWNAFXBTHN-UHFFFAOYSA-N
Formula
C11H16F5NO3S
SMILES
CCCOC(=O)C(CCSC)NC(=O)C(F)(F)C(F)(F)F
Molecular Weight1
337.31
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Physical Properties

Property Value Unit Source
Δfus 34.91 kJ/mol Joback Calculated Property
logPoct/wat 2.375 Crippen Calculated Property
McVol 210.040 ml/mol McGowan Calculated Property
Inp [1536.00; 1536.00]   Show Hide
Inp 1536.00 NIST
Inp 1536.00 NIST

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Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [594.69; 656.11] J/mol×K [689.64; 871.35] Show Hide
Cp,gas 594.69 J/mol×K 689.64 Joback Calculated Property
Cp,gas 606.78 J/mol×K 719.92 Joback Calculated Property
Cp,gas 618.09 J/mol×K 750.21 Joback Calculated Property
Cp,gas 628.64 J/mol×K 780.49 Joback Calculated Property
Cp,gas 638.47 J/mol×K 810.78 Joback Calculated Property
Cp,gas 647.62 J/mol×K 841.06 Joback Calculated Property
Cp,gas 656.11 J/mol×K 871.35 Joback Calculated Property

Similar Compounds

l-Methionine, n-pentafluoropropionyl-, butyl ester. l-Methionine, n-pentafluoropropionyl-, isobutyl ester. l-Methionine, n-pentafluoropropionyl-, ethyl ester. l-Methionine, n-pentafluoropropionyl-, undecyl ester. L-Methionine, N-pentafluoropropionyl-, pentadecyl ester. L-Methionine, N-pentafluoropropionyl-, nonyl ester. l-Methionine, n-pentafluoropropionyl-, tetradecyl ester. L-Methionine, N-pentafluoropropionyl-, dodecyl ester. l-Methionine, n-pentafluoropropionyl-, heptyl ester. l-Methionine, n-pentafluoropropionyl-, hexyl ester. l-Methionine, n-pentafluoropropionyl-, decyl ester. l-Methionine, n-pentafluoropropionyl-, hexadecyl ester. l-Methionine, n-pentafluoropropionyl-, octyl ester. N-(Heptafluorobutyryl)methionine propyl ester. L-Methionine, N-pentafluoropropionyl-, isohexyl ester.

Find more compounds similar to L-Methionine, N-pentafluoropropionyl-, propyl ester.

Sources

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