Chemical Properties of N-(4-CHLOROPHENYL)-1,2-PHENYLENEDIAMINE

N-(4-CHLOROPHENYL)-1,2-PHENYLENEDIAMINE

InChI
InChI=1S/C12H11ClN2/c13-9-5-7-10(8-6-9)15-12-4-2-1-3-11(12)14/h1-8,15H,14H2
InChI Key
WEUBIWJPIRTWDF-UHFFFAOYSA-N
Formula
C12H11ClN2
SMILES
Nc1ccccc1Nc1ccc(Cl)cc1
Molecular Weight1
218.69
Other Names
  • 1,2-Benzenediamine, N-(4-chlorophenyl)-
  • N-(4-chlorophenyl)benzene-1,2-diamine
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° 28.63 kJ/mol Joback Calculated Property
logPoct/wat 3.666 Crippen Calculated Property
McVol 164.620 ml/mol McGowan Calculated Property
Tboil 628.59 K Relay (1.0) Calculated Property
Tfus 386.74 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.

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [406.30; 468.91] J/mol×K [697.41; 955.95] Show Hide
Cp,gas 406.30 J/mol×K 697.41 Joback Calculated Property
Cp,gas 419.32 J/mol×K 740.50 Joback Calculated Property
Cp,gas 431.21 J/mol×K 783.59 Joback Calculated Property
Cp,gas 442.03 J/mol×K 826.68 Joback Calculated Property
Cp,gas 451.87 J/mol×K 869.77 Joback Calculated Property
Cp,gas 460.80 J/mol×K 912.86 Joback Calculated Property
Cp,gas 468.91 J/mol×K 955.95 Joback Calculated Property

Similar Compounds

1,2-Benzenediamine, N-phenyl-. 4,4'-Dianilino-3,3'-diaminodiphenyl oxide. N-(4-CHLORO-2-NITROPHENYL)ANILINE. Clobazam, hydrolysis. Benzenamine, 2-nitro-N-phenyl-. 3-Chlorodiphenylamine. Benzenamine, 2-nitro-N-(4-nitrophenyl)-. 1,2-Benzenediamine, 4-chloro-. Benzenamine, 2,4-dinitro-N-phenyl-. 2,4-dinitrodiphenylamine. N-Benzoyl-o-aminodiphenylamine. 1,4-Benzenediamine, N-phenyl-. Phenol, 4-[(2,4-dinitrophenyl)amino]-. Clobazam M (norhydroxy-), hydrolysis, acetlyated. 10H-Phenothiazine, 2-chloro-.

Find more compounds similar to N-(4-CHLOROPHENYL)-1,2-PHENYLENEDIAMINE.

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.