Chemical Properties of 4-Chlorobutyric acid, 2,3-dichlorophenyl ester

4-Chlorobutyric acid, 2,3-dichlorophenyl ester

InChI
InChI=1S/C10H9Cl3O2/c11-6-2-5-9(14)15-8-4-1-3-7(12)10(8)13/h1,3-4H,2,5-6H2
InChI Key
GKKJTDZZCWNXHN-UHFFFAOYSA-N
Formula
C10H9Cl3O2
SMILES
O=C(CCCCl)Oc1cccc(Cl)c1Cl
Molecular Weight1
267.54
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Physical Properties

Property Value Unit Source
Δfus 31.88 kJ/mol Joback Calculated Property
log10WS -4.30 Relay (1.0) Calculated Property
logPoct/wat 3.918 Crippen Calculated Property
McVol 172.160 ml/mol McGowan Calculated Property
Inp [1896.00; 1896.00]   Show Hide
Inp 1896.00 NIST
Inp 1896.00 NIST
Tfus 290.21 K Relay (1.0) Calculated Property

Cheméo can also estimate Normal Boiling Point Temperature, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, 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 [369.76; 423.06] J/mol×K [635.55; 859.86] Show Hide
Cp,gas 369.76 J/mol×K 635.55 Joback Calculated Property
Cp,gas 380.51 J/mol×K 672.93 Joback Calculated Property
Cp,gas 390.50 J/mol×K 710.32 Joback Calculated Property
Cp,gas 399.73 J/mol×K 747.70 Joback Calculated Property
Cp,gas 408.22 J/mol×K 785.09 Joback Calculated Property
Cp,gas 415.99 J/mol×K 822.47 Joback Calculated Property
Cp,gas 423.06 J/mol×K 859.86 Joback Calculated Property
η [0.0001658; 0.0013849] Pa×s [386.01; 635.55] Show Hide
η 0.0013849 Pa×s 386.01 Joback Calculated Property
η 0.0008186 Pa×s 427.60 Joback Calculated Property
η 0.0005312 Pa×s 469.19 Joback Calculated Property
η 0.0003698 Pa×s 510.78 Joback Calculated Property
η 0.0002719 Pa×s 552.37 Joback Calculated Property
η 0.0002087 Pa×s 593.96 Joback Calculated Property
η 0.0001658 Pa×s 635.55 Joback Calculated Property

Similar Compounds

4-Chlorobutyric acid, 2,4,5-trichlorophenyl ester. 4-Chlorobutyric acid, 3,4-dichlorophenyl ester. Glutaric acid, di(2,3-dichlorophenyl) ester. Glutaric acid, 2,3-dichlorophenyl 2,6-dichlorophenyl ester. Glutaric acid, 2,3-dichlorophenyl 2,3,5-trichlorophenyl ester. 4-Chlorobutyric acid, 2,3,4,6-tetrachlorophenyl ester. Glutaric acid, 3-chlorophenyl 2,3,5-trichlorophenyl ester. Glutaric acid, 2,3-dichlorophenyl 2,4,5-trichlorophenyl ester. Glutaric acid, 3-chlorophenyl 2,6-dichlorophenyl ester. Glutaric acid, 2,3-dichlorophenyl 1-naphthyl ester. Succinic acid, 2-chlorophenyl 2,3-dichlorophenyl ester. Succinic acid, phenyl 2,3-dichlorophenyl ester. Succinic acid, 2,3-dichlorophenyl 2,6-dichlorophenyl ester. 4-Chlorobutyric acid, 4-chlorophenyl ester. Glutaric acid, 3-chlorophenyl 2,4-dichlorophenyl ester.

Find more compounds similar to 4-Chlorobutyric acid, 2,3-dichlorophenyl ester.

Sources

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