Chemical Properties of (o-Nitrobenzylidene)phenylacetonitrile (CAS 19016-67-2)

(o-Nitrobenzylidene)phenylacetonitrile

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InChI
InChI=1S/C15H10N2O2/c16-11-14(12-6-2-1-3-7-12)10-13-8-4-5-9-15(13)17(18)19/h1-10H/b14-10+
InChI Key
QKDHOOPDLFPJKV-GXDHUFHOSA-N
Formula
C15H10N2O2
SMILES
N#CC(=Cc1ccccc1[N+](=O)[O-])c1ccccc1
Molecular Weight1
250.25
CAS
19016-67-2
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Physical Properties

Property Value Unit Source
Δcsolid [-7519.00; -7515.64] kJ/mol Show Hide
Δcsolid -7519.00 kJ/mol NIST
Δcsolid -7515.64 kJ/mol NIST
Δf 531.01 kJ/mol Joback Calculated Property
Δfgas 370.21 kJ/mol Joback Calculated Property
Δfsolid [183.80; 187.00] kJ/mol Show Hide
Δfsolid 187.00 kJ/mol NIST
Δfsolid 183.80 kJ/mol NIST
Δfus 34.06 kJ/mol Joback Calculated Property
Δvap 81.30 kJ/mol Joback Calculated Property
log10WS -5.01 Crippen Calculated Property
logPoct/wat 3.659 Crippen Calculated Property
McVol 189.190 ml/mol McGowan Calculated Property
Pc 2584.59 kPa Joback Calculated Property
Tboil 858.90 K Joback Calculated Property
Tc 1137.09 K Joback Calculated Property
Tfus 513.73 K Joback Calculated Property
Vc 0.749 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [514.14; 569.03] J/mol×K [858.90; 1137.09] Show Hide
Cp,gas 514.14 J/mol×K 858.90 Joback Calculated Property
Cp,gas 525.21 J/mol×K 905.26 Joback Calculated Property
Cp,gas 535.30 J/mol×K 951.63 Joback Calculated Property
Cp,gas 544.57 J/mol×K 997.99 Joback Calculated Property
Cp,gas 553.19 J/mol×K 1044.36 Joback Calculated Property
Cp,gas 561.29 J/mol×K 1090.72 Joback Calculated Property
Cp,gas 569.03 J/mol×K 1137.09 Joback Calculated Property

Similar Compounds

o-Nitrobenzilidene-2-naphthylacetontrile. o-Nitrobenzylidene-p-chlorophenylacetonitrile. o-Nitrobenzylidene-2-methylphenylacetonitrile. o-Nitrobenzylidene-2,5-dimethylphenylacetonitrile. Nitrobenzene, 3-(2-cyano-2-phenylethenyl). m-Nitrobenzilidene-2-naphthylacetonitrile. m-Nitrobenzylidene-p-chlorophenylacetonitrile. Nitrobenzene, 4-(2-cyano-2-phenylethenyl). o-Nitrobenzylidene-5,6,7,8-tetrahydronaphthyl-2-acetonitrile. m-Nitrobenzylidene-2-methylphenylacetonitrile. m-Nitrobenzylidene-p-isopropylphenylacetonitrile. m-Nitrobenzylidene-2,5-dimethylphenylacetonitrile. p-Nitrobenzylidene-2-methylphenylacetonitrile. p-Nitrobenzylidene-p-chlorophenylacetonitrile. p-Nitrobenzylidene-2,5-dimethylphenylacetonitrile.

Find more compounds similar to (o-Nitrobenzylidene)phenylacetonitrile.

Sources

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