Chemical Properties of 2-Butenedioic acid (Z)-, dinonyl ester (CAS 2787-64-6)

2-Butenedioic acid (Z)-, dinonyl ester

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InChI
InChI=1S/C22H40O4/c1-3-5-7-9-11-13-15-19-25-21(23)17-18-22(24)26-20-16-14-12-10-8-6-4-2/h17-18H,3-16,19-20H2,1-2H3/b18-17-
InChI Key
PQJYOOFQDXGDDS-ZCXUNETKSA-N
Formula
C22H40O4
SMILES
CCCCCCCCCOC(=O)C=CC(=O)OCCCCCCCCC
Molecular Weight1
368.55
CAS
2787-64-6
Other Names
  • dinonyl maleate
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Physical Properties

Property Value Unit Source
Δf -253.26 kJ/mol Joback Calculated Property
Δfgas -869.79 kJ/mol Joback Calculated Property
Δfus 58.51 kJ/mol Joback Calculated Property
Δvap 82.84 kJ/mol Joback Calculated Property
log10WS -6.61 Crippen Calculated Property
logPoct/wat 6.130 Crippen Calculated Property
McVol 331.420 ml/mol McGowan Calculated Property
Pc 985.16 kPa Joback Calculated Property
Tboil 859.50 K Joback Calculated Property
Tc 1052.62 K Joback Calculated Property
Tfus 476.94 K Joback Calculated Property
Vc 1.296 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1065.82; 1161.02] J/mol×K [859.50; 1052.62] Show Hide
Cp,gas 1065.82 J/mol×K 859.50 Joback Calculated Property
Cp,gas 1084.38 J/mol×K 891.69 Joback Calculated Property
Cp,gas 1101.82 J/mol×K 923.87 Joback Calculated Property
Cp,gas 1118.16 J/mol×K 956.06 Joback Calculated Property
Cp,gas 1133.46 J/mol×K 988.25 Joback Calculated Property
Cp,gas 1147.73 J/mol×K 1020.43 Joback Calculated Property
Cp,gas 1161.02 J/mol×K 1052.62 Joback Calculated Property
η [0.0000347; 0.0006226] Pa×s [476.94; 859.50] Show Hide
η 0.0006226 Pa×s 476.94 Joback Calculated Property
η 0.0002897 Pa×s 540.70 Joback Calculated Property
η 0.0001584 Pa×s 604.46 Joback Calculated Property
η 0.0000972 Pa×s 668.22 Joback Calculated Property
η 0.0000649 Pa×s 731.98 Joback Calculated Property
η 0.0000463 Pa×s 795.74 Joback Calculated Property
η 0.0000347 Pa×s 859.50 Joback Calculated Property

Similar Compounds

Fumaric acid, ditridecyl ester. Fumaric acid, hexyl tridecyl ester. Dioctyl maleate. Maleic acid, dilauryl ester. Maleic acid, dioctadecyl ester. Fumaric acid, pentyl tridecyl ester. Fumaric acid, dioctyl ester. 2-Butenedioic acid (e), dioctyl ester. Dioctyl (2e)-2-butenedioate. Fumaric acid, heptyl tridecyl ester. Fumaric acid, butyl tridecyl ester. Fumaric acid, propyl tridecyl ester. Dihexyl fumarate. Diamyl maleate. di-n-Amylfumarate.

Find more compounds similar to 2-Butenedioic acid (Z)-, dinonyl ester.

Sources

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