Chemical Properties of p-Dimethylaminobenzylidene-p-chlorophenylacetonitrile

p-Dimethylaminobenzylidene-p-chlorophenylacetonitrile

InChI
InChI=1S/C17H15ClN2/c1-20(2)17-9-3-13(4-10-17)11-15(12-19)14-5-7-16(18)8-6-14/h3-11H,1-2H3/b15-11+
InChI Key
JYSGNKFGNNTQNO-RVDMUPIBSA-N
Formula
C17H15ClN2
SMILES
CN(C)c1ccc(/C=C(\C#N)c2ccc(Cl)cc2)cc1
Molecular Weight1
282.77
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Physical Properties

Property Value Unit Source
Δfus 34.71 kJ/mol Joback Calculated Property
IE 7.30 eV Relay (1.0) Calculated Property
logPoct/wat 4.470 Crippen Calculated Property
McVol 222.170 ml/mol McGowan Calculated Property
Tboil 676.49 K Relay (1.0) Calculated Property

Cheméo can also estimate Normal melting (fusion) point, 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, 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 [591.12; 658.24] J/mol×K [807.67; 1057.23] Show Hide
Cp,gas 591.12 J/mol×K 807.67 Joback Calculated Property
Cp,gas 604.50 J/mol×K 849.26 Joback Calculated Property
Cp,gas 616.84 J/mol×K 890.86 Joback Calculated Property
Cp,gas 628.26 J/mol×K 932.45 Joback Calculated Property
Cp,gas 638.89 J/mol×K 974.04 Joback Calculated Property
Cp,gas 648.84 J/mol×K 1015.63 Joback Calculated Property
Cp,gas 658.24 J/mol×K 1057.23 Joback Calculated Property

Similar Compounds

BENZENE, 1-DIMETHYLAMINO-4(2-CYANO-2-PHENYLETHENYL). p-Dimethylaminobenzylidene-p-isopropylphenylacetonitrile. p-Nitrobenzylidene-p-chlorophenylacetonitrile. «alpha»-(p-Chlorophenyl)cinnamonitrile. m-Chlorobenzylidene-p-chlorophenylacetonitrile. p-Methoxybenzylidene-p-chlorophenylacetonitrile. BENZENE, 1-CHLORO-4-(2-CYANO-2-PHENYLETHENYL). m-Nitrobenzylidene-p-chlorophenylacetonitrile. Alpha-(p-chlorophenyl)-o-chlorocinnamonitrile. o-Nitrobenzylidene-p-chlorophenylacetonitrile. NITROBENZENE, 4-(2-CYANO-2-PHENYLETHENYL). p-Nitrobenzylidene-p-isopropylphenylacetonitrile. 3,4-Dioxymethylenebenzylidene-p-chlorophenylacetonitrile. m-Chlorobenzylidene-2-methylphenylacetonitrile. p-Chlorobenzyliden-5,6,7,8-tetrahydronaphthyl-2-acetonitrile.

Find more compounds similar to p-Dimethylaminobenzylidene-p-chlorophenylacetonitrile.

Sources

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