Chemical Properties of 1,2-Benzenediamine, N-phenyl- (CAS 534-85-0)

1,2-Benzenediamine, N-phenyl-

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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
CAS
534-85-0
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
Δf 421.19 kJ/mol Joback Calculated Property
Δfgas 257.84 kJ/mol Joback Calculated Property
Δfus 24.82 kJ/mol Joback Calculated Property
Δvap 64.60 kJ/mol Joback Calculated Property
log10WS -2.91 Crippen 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 655.00 K Joback Calculated Property
Tc 910.40 K Joback Calculated Property
Tfus 426.28 K Joback Calculated Property
Vc 0.555 m3/kmol Joback Calculated Property

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)-. 2,4-dinitrodiphenylamine. Benzenamine, 2,4-dinitro-N-phenyl-. Diphenylamine. Diphenylamine, 5-chloro-2-methylamino. 1,4-Benzenediamine, N,N'-diphenyl-. Benzenamine, 4-chloro-2-nitro-N-phenyl-. N,n'-di-beta-naphthyl-p-phenylene diamine. Benzenamine, 4-nitroso-N-phenyl-. 2-Naphthalenamine, N-phenyl-. Disperse Yellow 1.

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

Sources

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