Chemical Properties of Benzenemethanamine, 4-chloro-«alpha»-phenyl- (CAS 28022-43-7)

Benzenemethanamine, 4-chloro-«alpha»-phenyl-

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InChI
InChI=1S/C13H12ClN/c14-12-8-6-11(7-9-12)13(15)10-4-2-1-3-5-10/h1-9,13H,15H2
InChI Key
XAFODXGEQUOEKN-UHFFFAOYSA-N
Formula
C13H12ClN
SMILES
NC(c1ccccc1)c1ccc(Cl)cc1
Molecular Weight1
217.69
CAS
28022-43-7
Other Names
  • (4-Chlorophenyl)(phenyl)methanamine
  • p-Chlorobenzhydrylamine
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Physical Properties

Property Value Unit Source
Δf 325.85 kJ/mol Joback Calculated Property
Δfgas 162.71 kJ/mol Joback Calculated Property
Δfus 22.99 kJ/mol Joback Calculated Property
Δvap 64.38 kJ/mol Joback Calculated Property
log10WS -4.15 Crippen Calculated Property
logPoct/wat 3.388 Crippen Calculated Property
McVol 168.730 ml/mol McGowan Calculated Property
Pc 3117.52 kPa Joback Calculated Property
Tboil 664.70 K Joback Calculated Property
Tc 925.98 K Joback Calculated Property
Tfus 399.81 K Joback Calculated Property
Vc 0.620 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [409.88; 480.92] J/mol×K [664.70; 925.98] Show Hide
Cp,gas 409.88 J/mol×K 664.70 Joback Calculated Property
Cp,gas 424.67 J/mol×K 708.25 Joback Calculated Property
Cp,gas 438.15 J/mol×K 751.79 Joback Calculated Property
Cp,gas 450.43 J/mol×K 795.34 Joback Calculated Property
Cp,gas 461.58 J/mol×K 838.89 Joback Calculated Property
Cp,gas 471.72 J/mol×K 882.43 Joback Calculated Property
Cp,gas 480.92 J/mol×K 925.98 Joback Calculated Property

Similar Compounds

Benzhydrylamine. Benzhydryl isothiocyanate. 9-Aminofluorene. (p-Chlorophenyl)phenylmethane. Benzene, 1-chloro-4-(chlorophenylmethyl)-. Chlorcyclizine. Triphenylmethane, 4-chloro. Triphenylmethane, 4,4'-dichloro. Benzophenone, 2-methylamino-5-chloro-. Norchlorcyclizine. Methane, bis(p-chlorophenyl)-. 4-(para-Chlorobenzyl)-pyridine. Buclizine M (N-desalkyl), acetylated. Hydroxizine M (N-desalkyl), acetylated. Triphenylmethane, 3,4,4'-trichloro.

Find more compounds similar to Benzenemethanamine, 4-chloro-«alpha»-phenyl-.

Sources

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