Chemical Properties of Cyclohexanecarboxylic acid, 1-cyclohexyl-

Cyclohexanecarboxylic acid, 1-cyclohexyl-

InChI
InChI=1S/C13H22O2/c14-12(15)13(9-5-2-6-10-13)11-7-3-1-4-8-11/h11H,1-10H2,(H,14,15)
InChI Key
SJSRFXJWBKOROD-UHFFFAOYSA-N
Formula
C13H22O2
SMILES
O=C(O)C1(C2CCCCC2)CCCCC1
Molecular Weight1
210.32
Other Names
  • [1,1'-bicyclohexyl]-1-carboxylic acid
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Physical Properties

Property Value Unit Source
ΔfusH° 16.94 kJ/mol Joback Calculated Property
logPoct/wat 3.602 Crippen Calculated Property
McVol 179.750 ml/mol McGowan Calculated Property
Tboil 581.55 K Relay (1.0) Calculated Property
Tfus 385.90 K Relay (1.0) Calculated Property

Cheméo can also estimate 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, Log10 of Water solubility in mol/l 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.

Correlations

Property Value Unit Temperature (K) Source
Cp,gas [214.72; 678.27] J/mol×K [273.00; 1000.00] Joback Predicted correlation Show Hide
EquationY = A + B·T + C·T² + D·T³ + E·T⁴
Y is Cp,gas in J/mol×K, T in K
Coefficient A-1.85530e+02
Coefficient B1.82570e+00
Coefficient C-1.45060e-03
Coefficient D4.88700e-07
Coefficient E0.00000e+00
Temperature range, min.273.00
Temperature range, max.1000.00
Cp,gas 214.72 J/mol×K 273.00 Calculated Property
Cp,gas 300.45 J/mol×K 353.78 Calculated Property
Cp,gas 374.01 J/mol×K 434.56 Calculated Property
Cp,gas 436.96 J/mol×K 515.33 Calculated Property
Cp,gas 490.84 J/mol×K 596.11 Calculated Property
Cp,gas 537.20 J/mol×K 676.89 Calculated Property
Cp,gas 577.57 J/mol×K 757.67 Calculated Property
Cp,gas 613.51 J/mol×K 838.44 Calculated Property
Cp,gas 646.56 J/mol×K 919.22 Calculated Property
Cp,gas 678.27 J/mol×K 1000.00 Calculated Property

Similar Compounds

4a(2H)-Naphthalenecarboxylic acid, octahydro-, cis-. 4a(2H)-naphthalenecarboxylic acid, octahydro-, trans-. Bicyclo[2.2.2]octane-1-carboxylic acid. D-Campholic acid. Adamantane-1-carboxylic acid. Cyclopentanecarboxylic acid, 1-methyl-3-(1-methylethyl)-, cis-. 1-Methyl-1-cyclohexanecarboxylic acid. Bicyclo[3.3.0]octane-1-carboxylic acid, methyl ester. trans-carbomethoxy-1,2-dimethylcyclohexane. cis-1-carbomethoxy-1,2-dimethylcyclohexane. Cyclohexanecarboxylic acid, 4-(1,1-dimethylethyl)-, trans-. Cyclohexanecarboxylic acid, 4-(1,1-dimethylethyl)-, cis-. Bicyclo[2.2.2]octane-1-carboxylic acid, 4-methyl-. 1-Phenanthrenecarboxylic acid, tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-, methyl ester, [1R-(1«alpha»,4a«beta»,4b«alpha»,7«beta»,8a«beta»,10a«alpha»)]-. Methyl 7-isopropyl-1,4a-dimethyltetradecahydrophenanthrene-1-carboxylate.

Find more compounds similar to Cyclohexanecarboxylic acid, 1-cyclohexyl-.

Sources

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