Chemical Properties of 1,2-Benzenediamine, N-phenyl-

1,2-Benzenediamine, N-phenyl-

InChI
InChI=1S/C12H12N2/c13-11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9,14H,13H2
InChI Key
NFCPRRWCTNLGSN-UHFFFAOYSA-N
Formula
C12H12N2
SMILES
Nc1ccccc1Nc1ccccc1
Molecular Weight1
184.24
Other Names
  • o-Phenylenediamine, N-phenyl-
  • o-Aminodiphenylamine
  • o-Semidine
  • C.I. 50005
  • N-Phenyl-o-Phenylenediamine
  • 2-Aminodiphenylamine
  • N-Phenyl-1,2-phenylenediamine
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Physical Properties

Property Value Unit Source
ΔfH°gas 207.34 kJ/mol Relay (1.0) Calculated Property
ΔfusH° 24.82 kJ/mol Joback Calculated Property
ΔvapH° 87.02 kJ/mol Relay (1.0) Calculated Property
IE 7.01 eV Relay (1.0) Calculated Property
log10WS -2.83 Relay (1.0) Calculated Property
logPoct/wat 3.012 Crippen Calculated Property
McVol 152.380 ml/mol McGowan Calculated Property
Pc 3659.77 kPa Joback Calculated Property
Tboil 604.47 K Relay (1.0) Calculated Property
Tc 930.51 K Relay (1.0) Calculated Property
Tfus 351.60 K Relay (1.0) Calculated Property

Cheméo can also estimate Critical Volume, Standard Gibbs free energy of formation, Acentric Factor 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 [384.08; 454.44] J/mol×K [655.00; 910.40] Show Hide
Cp,gas 384.08 J/mol×K 655.00 Joback Calculated Property
Cp,gas 398.63 J/mol×K 697.57 Joback Calculated Property
Cp,gas 411.93 J/mol×K 740.13 Joback Calculated Property
Cp,gas 424.08 J/mol×K 782.70 Joback Calculated Property
Cp,gas 435.16 J/mol×K 825.27 Joback Calculated Property
Cp,gas 445.25 J/mol×K 867.84 Joback Calculated Property
Cp,gas 454.44 J/mol×K 910.40 Joback Calculated Property

Similar Compounds

N-(4-CHLOROPHENYL)-1,2-PHENYLENEDIAMINE. 4,4'-Dianilino-3,3'-diaminodiphenyl oxide. Benzenamine, 2-nitro-N-phenyl-. 1,4-Benzenediamine, N-phenyl-. Benzenamine, 2-nitro-N-(4-nitrophenyl)-. Benzenamine, 2,4-dinitro-N-phenyl-. 2,4-dinitrodiphenylamine. Diphenylamine. Clobazam, hydrolysis. 1,4-Benzenediamine, N,N'-diphenyl-. N-(4-CHLORO-2-NITROPHENYL)ANILINE. N,n'-di-beta-naphthyl-p-phenylene diamine. Benzenamine, 4-nitroso-N-phenyl-. 2-Naphthalenamine, N-phenyl-. Phenol, 4-[(2,4-dinitrophenyl)amino]-.

Find more compounds similar to 1,2-Benzenediamine, N-phenyl-.

Sources

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