Chemical Properties of e-(Phenylazo)propane (CAS 28053-14-7)

e-(Phenylazo)propane

InChI
InChI=1S/C9H12N2/c1-2-8-10-11-9-6-4-3-5-7-9/h3-7H,2,8H2,1H3/b11-10-
InChI Key
JGHVTEUPGALIRE-KHPPLWFESA-N
Formula
C9H12N2
SMILES
CCCN=Nc1ccccc1
Molecular Weight1
148.21
CAS
28053-14-7
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Physical Properties

Property Value Unit Source
ω 0.5537 Relay (1.0) Calculated Property
Δf 282.79 kJ/mol Relay (1.0-beta) Calculated Property
Δfgas 240.70 kJ/mol Relay (1.0) Calculated Property
Δvap 53.75 kJ/mol Relay (1.0) Calculated Property
IE 8.65 eV Relay (1.0) Calculated Property
log10WS -2.17 Relay (1.0) Calculated Property
logPoct/wat 3.180 Crippen Calculated Property
McVol 129.570 ml/mol McGowan Calculated Property
Pc 2467.81 kPa Joback Calculated Property
Tboil 497.94 K Relay (1.0) Calculated Property
Tc 698.55 K Relay (1.0) Calculated Property
Tfus 248.17 K Relay (1.0) Calculated Property
Vc 0.485 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

3-(Phenylazo)-2,4-pentanedione. Diazene, methylphenyl-. 2,3-Dimethyl-2,3-bis[(E)phenylazo]butane. Diphenyl formazan. Butyronitrile, 2,3,3-trimethyl-2-(4-bromophenyldiazenyl)-. Butyronitrile, 2,3,3-trimethyl-2-(4-nitrophenyldiazenyl)-. N,N-Di-(n-propyl)benzenamine. Trifluoroacetamide, N-phenyl-n-propyl-. Benzonitrile, p-(3-butyl-3-methyl-1-triazeno)-. P-phenylazo carbanilic acid, n-propyl ester. 1-Triazene, 1,3-diphenyl-. Propyl red. (Phenylazo)triphenylmethane. Formic acid, (phenylazo)thio-, 2-phenylhydrazide, manganese derivative-. Trifluoroacetamide, n-butyl-N-phenyl-.

Find more compounds similar to e-(Phenylazo)propane.

Sources

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