Chemical Properties of Isophthalic acid, hexadecyl 2,2,3,3,4,4,5,5-octafluoropentyl ester

Isophthalic acid, hexadecyl 2,2,3,3,4,4,5,5-octafluoropentyl ester

InChI
InChI=1S/C29H40F8O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-40-24(38)22-17-16-18-23(20-22)25(39)41-21-27(32,33)29(36,37)28(34,35)26(30)31/h16-18,20,26H,2-15,19,21H2,1H3
InChI Key
SPCKDHHGZIWXHA-UHFFFAOYSA-N
Formula
C29H40F8O4
SMILES
CCCCCCCCCCCCCCCCOC(=O)c1cccc(C(=O)OCC(F)(F)C(F)(F)C(F)(F)C(F)F)c1
Molecular Weight1
604.61
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Physical Properties

Property Value Unit Source
ω 1.3423 Relay (1.0) Calculated Property
Δfus 72.13 kJ/mol Joback Calculated Property
log10WS -9.84 Relay (1.0) Calculated Property
logPoct/wat 9.652 Crippen Calculated Property
McVol 424.750 ml/mol McGowan Calculated Property
Pc 634.16 kPa Joback Calculated Property
Inp 3062.00 NIST
Tboil 706.59 K Relay (1.0) Calculated Property
Tc 869.13 K Relay (1.0) Calculated Property
Tfus 322.56 K Relay (1.0) Calculated Property
Vc 1.599 m3/kmol Relay (1.0) Calculated Property

Cheméo can also estimate Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Ionization energy 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 [1469.37; 1560.41] J/mol×K [995.25; 1239.20] Show Hide
Cp,gas 1469.37 J/mol×K 995.25 Joback Calculated Property
Cp,gas 1487.91 J/mol×K 1035.91 Joback Calculated Property
Cp,gas 1504.85 J/mol×K 1076.57 Joback Calculated Property
Cp,gas 1520.38 J/mol×K 1117.22 Joback Calculated Property
Cp,gas 1534.68 J/mol×K 1157.88 Joback Calculated Property
Cp,gas 1547.96 J/mol×K 1198.54 Joback Calculated Property
Cp,gas 1560.41 J/mol×K 1239.20 Joback Calculated Property

Similar Compounds

Isophthalic acid, 2,2,3,3,4,4,5,5-octafluoropentyl tridecyl ester. Isophthalic acid, octadecyl 2,2,3,3,4,4,5,5-octafluoropentyl ester. Isophthalic acid, heptyl 2,2,3,3,4,4,5,5-octafluoropentyl ester. Isophthalic acid, heptadecyl 2,2,3,3,4,4,5,5-octafluoropentyl ester. Isophthalic acid, 2,2,3,3,4,4,5,5-octafluoropentyl octyl ester. Isophthalic acid, 2,2,3,3,4,4,5,5-octafluoropentyl pentadecyl ester. Isophthalic acid, 2,2,3,3,4,4,5,5-octafluoropentyl undecyl ester. Isophthalic acid, nonyl 2,2,3,3,4,4,5,5-octafluoropentyl ester. Isophthalic acid, 2,2,3,3,4,4,5,5-octafluoropentyl tetradecyl ester. Isophthalic acid, dodecyl 2,2,3,3,4,4,5,5-octafluoropentyl ester. Isophthalic acid, decyl 2,2,3,3,4,4,5,5-octafluoropentyl ester. Terephthalic acid, 2,2,3,3,4,4,4-heptafluorobutyl octyl ester. Terephthalic acid, decyl 2,2,3,3,4,4,4-heptafluorobutyl ester. Terephthalic acid, dodecyl 2,2,3,3,4,4,4-heptafluorobutyl ester. Terephthalic acid, heptadecyl 2,2,3,3,4,4,4-heptafluorobutyl ester.

Find more compounds similar to Isophthalic acid, hexadecyl 2,2,3,3,4,4,5,5-octafluoropentyl ester.

Sources

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