Chemical Properties of p-Chlorophenylhydroxylamine (CAS 823-86-9)

p-Chlorophenylhydroxylamine

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InChI
InChI=1S/C6H6ClNO/c7-5-1-3-6(8-9)4-2-5/h1-4,8-9H
InChI Key
VVQDMDRAUXFEND-UHFFFAOYSA-N
Formula
C6H6ClNO
SMILES
ONc1ccc(Cl)cc1
Molecular Weight1
143.57
CAS
823-86-9
Other Names
  • Benzenamine, 4-chloro-N-hydroxy-
  • Hydroxylamine, N-(p-chlorophenyl)-
  • N-(p-Chlorophenyl)hydroxylamine
  • N-(4-Chlorophenyl)hydroxylamine
  • 4-Chlorophenylhydroxylamine
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Physical Properties

Property Value Unit Source
Δf 43.06 kJ/mol Joback Calculated Property
Δfgas -56.61 kJ/mol Joback Calculated Property
Δfus 18.33 kJ/mol Joback Calculated Property
Δvap 59.39 kJ/mol Joback Calculated Property
log10WS -1.40 Crippen Calculated Property
logPoct/wat 2.141 Crippen Calculated Property
McVol 99.730 ml/mol McGowan Calculated Property
Pc 5029.93 kPa Joback Calculated Property
Tboil 548.12 K Joback Calculated Property
Tc 758.58 K Joback Calculated Property
Tfus 339.72 K Joback Calculated Property
Vc 0.366 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [202.41; 242.47] J/mol×K [548.12; 758.58] Show Hide
Cp,gas 202.41 J/mol×K 548.12 Joback Calculated Property
Cp,gas 210.29 J/mol×K 583.20 Joback Calculated Property
Cp,gas 217.66 J/mol×K 618.27 Joback Calculated Property
Cp,gas 224.54 J/mol×K 653.35 Joback Calculated Property
Cp,gas 230.95 J/mol×K 688.43 Joback Calculated Property
Cp,gas 236.92 J/mol×K 723.51 Joback Calculated Property
Cp,gas 242.47 J/mol×K 758.58 Joback Calculated Property

Similar Compounds

Benzenamine, N-hydroxy-. p-Chloroaniline. Benzene, 1-chloro-4-nitro-. Benzenamine, 3,4-dichloro-. Benzenamine, 4-chloro-N-methyl-. Benzenamine, 2,4-dichloro-. m-Chloroaniline. Diazene, bis(4-chlorophenyl)-, 1-oxide. Benzene, 1,2-dichloro-4-nitro-. Benzenamine, 2-chloro-5-nitro-. Benzene, 2,4-dichloro-1-nitro-. 5-Chloro-2-nitroaniline. 1,3-Benzenediamine, 4-chloro-. Urea, (4-chlorophenyl)-. 1,2-Benzenediamine, 4-chloro-.

Find more compounds similar to p-Chlorophenylhydroxylamine.

Sources

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