Chemical Properties of 2-Ethylbutyric acid, 2-chloro-5-methylphenyl ester

2-Ethylbutyric acid, 2-chloro-5-methylphenyl ester

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InChI
InChI=1S/C13H17ClO2/c1-4-10(5-2)13(15)16-12-8-9(3)6-7-11(12)14/h6-8,10H,4-5H2,1-3H3
InChI Key
AXHQLGNAROZOLY-UHFFFAOYSA-N
Formula
C13H17ClO2
SMILES
CCC(CC)C(=O)Oc1cc(C)ccc1Cl
Molecular Weight1
240.73

Physical Properties

Property Value Unit Source
Δf -96.56 kJ/mol Joback Calculated Property
Δfgas -363.88 kJ/mol Joback Calculated Property
Δfus 26.15 kJ/mol Joback Calculated Property
Δvap 61.28 kJ/mol Joback Calculated Property
log10WS -4.38 Crippen Calculated Property
logPoct/wat 3.990 Crippen Calculated Property
McVol 189.950 ml/mol McGowan Calculated Property
Pc 2167.36 kPa Joback Calculated Property
Inp [1658.00; 1658.00]   Show Hide
Inp 1658.00 NIST
Inp 1658.00 NIST
Tboil 646.76 K Joback Calculated Property
Tc 859.26 K Joback Calculated Property
Tfus 374.81 K Joback Calculated Property
Vc 0.723 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [471.14; 547.07] J/mol×K [646.76; 859.26] Show Hide
Cp,gas 471.14 J/mol×K 646.76 Joback Calculated Property
Cp,gas 485.89 J/mol×K 682.18 Joback Calculated Property
Cp,gas 499.79 J/mol×K 717.59 Joback Calculated Property
Cp,gas 512.83 J/mol×K 753.01 Joback Calculated Property
Cp,gas 525.05 J/mol×K 788.43 Joback Calculated Property
Cp,gas 536.46 J/mol×K 823.84 Joback Calculated Property
Cp,gas 547.07 J/mol×K 859.26 Joback Calculated Property
η [0.0001437; 0.0014216] Pa×s [374.81; 646.76] Show Hide
η 0.0014216 Pa×s 374.81 Joback Calculated Property
η 0.0007896 Pa×s 420.13 Joback Calculated Property
η 0.0004918 Pa×s 465.46 Joback Calculated Property
η 0.0003332 Pa×s 510.78 Joback Calculated Property
η 0.0002405 Pa×s 556.11 Joback Calculated Property
η 0.0001823 Pa×s 601.43 Joback Calculated Property
η 0.0001437 Pa×s 646.76 Joback Calculated Property

Similar Compounds

Adipic acid, di(2-chloro-5-methylphenyl) ester. Sebacic acid, di(2-chloro-5-methylphenyl) ester. 2-Ethylbutyric acid, 3-methylphenyl ester. 2-Ethylbutyric acid, 4-chloro-3-methylphenyl ester. Glutaric acid, di(2-chloro-5-methylphenyl) ester. Diethylmalonic acid, di(2-chloro-5-methylphenyl) ester. 2-Methylvaleric acid, 3-methylphenyl ester. Cyclopentanecarboxylic acid, 3-methylphenyl ester. Glutaric acid, 3-chlorophenyl 2-chloro-5-methylphenyl ester. Diethylmalonic acid, monochloride, 2-chloro-5-methylphenyl ester. Glutaric acid, 2,4,6-trichlorophenyl 2-chloro-5-methylphenyl ester. Glutaric acid, 2,3-dichlorophenyl 2-chloro-5-methylphenyl ester. Cyclohexanecarboxylic acid, 3-methylphenyl ester. 2-Ethylbutyric acid, 2-chlorophenyl ester. Cyclobutanecarboxylic acid, 3-methylphenyl ester.

Find more compounds similar to 2-Ethylbutyric acid, 2-chloro-5-methylphenyl ester.

Sources

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