Chemical Properties of Oxanilic acid, 2-tert-butyl-, ethyl ester

Oxanilic acid, 2-tert-butyl-, ethyl ester

InChI
InChI=1S/C14H19NO3/c1-5-18-13(17)12(16)15-11-9-7-6-8-10(11)14(2,3)4/h6-9H,5H2,1-4H3,(H,15,16)
InChI Key
DPFZZLSEANVIOP-UHFFFAOYSA-N
Formula
C14H19NO3
SMILES
CCOC(=O)C(=O)Nc1ccccc1C(C)(C)C
Molecular Weight1
249.31
Cheméo is a service of Céondo GmbH, since 2007, we provide simulation, modelling and software development services for the industry. Do not hesitate to contact us for your projects.

Physical Properties

Property Value Unit Source
ΔfusH° 29.32 kJ/mol Joback Calculated Property
logPoct/wat 2.486 Crippen Calculated Property
McVol 203.350 ml/mol McGowan Calculated Property
Tfus 348.14 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, 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.

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [565.13; 638.23] J/mol×K [710.61; 926.66] Show Hide
Cp,gas 565.13 J/mol×K 710.61 Joback Calculated Property
Cp,gas 579.90 J/mol×K 746.62 Joback Calculated Property
Cp,gas 593.57 J/mol×K 782.63 Joback Calculated Property
Cp,gas 606.19 J/mol×K 818.63 Joback Calculated Property
Cp,gas 617.81 J/mol×K 854.64 Joback Calculated Property
Cp,gas 628.47 J/mol×K 890.65 Joback Calculated Property
Cp,gas 638.23 J/mol×K 926.66 Joback Calculated Property

Similar Compounds

Glycinic acid, n-2-tert-butyl-phenyl-, ethyl ester. Acetanilide, 2-tert-butyl-. Carbanilic acid, 2-tert-butyl-, ethyl ester. Acetanilide, 2-tert-butyl-5-methyl. Aniline, 2-tert-butyl-n-beta-cyanoethyl-. Urea, 1-(2'-tert-butylphenyl)-3,3-dimethyl-. Acetanilide, 2-cyclohexyl-. Acetamide, n-[2-[1,1-dimethylethyl)-4-methylphenyl]. Carbanilide, 2,2'-ditertiary butyl-. Aniline, 2-tert-butyl-n-ethyl-. Aniline, n-allyl-o-tert-butyl-. Acetamide, N-[2,4-bis(1,1-dimethylethyl)phenyl]-. Aniline, n-isobutyl-2-tert-butyl-. Carbanilic acid, 2,4-di-tert-butyl-, 2-chloroethyl ester. Aniline, 2-tert-butyl-n-cyclohexyl-.

Find more compounds similar to Oxanilic acid, 2-tert-butyl-, ethyl ester.

Sources

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.
These property values are available through the Cheméo API. A free account gives you an access key.