Chemical Properties of Phthalic acid, 2-(2-nitrophenyl)ethyl propyl ester

Phthalic acid, 2-(2-nitrophenyl)ethyl propyl ester

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InChI
InChI=1S/C19H19NO6/c1-2-12-25-18(21)15-8-4-5-9-16(15)19(22)26-13-11-14-7-3-6-10-17(14)20(23)24/h3-10H,2,11-13H2,1H3
InChI Key
WANANQVIRAUUTN-UHFFFAOYSA-N
Formula
C19H19NO6
SMILES
CCCOC(=O)c1ccccc1C(=O)OCCc1ccccc1[N+](=O)[O-]
Molecular Weight1
357.36
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Physical Properties

Property Value Unit Source
Δf -117.63 kJ/mol Joback Calculated Property
Δfgas -485.73 kJ/mol Joback Calculated Property
Δfus 49.20 kJ/mol Joback Calculated Property
Δvap 98.67 kJ/mol Joback Calculated Property
log10WS -5.48 Crippen Calculated Property
logPoct/wat 3.561 Crippen Calculated Property
McVol 263.350 ml/mol McGowan Calculated Property
Pc 1880.53 kPa Joback Calculated Property
Inp 2756.00 NIST
Tboil 1001.86 K Joback Calculated Property
Tc 1247.36 K Joback Calculated Property
Tfus 669.70 K Joback Calculated Property
Vc 1.014 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [818.17; 857.04] J/mol×K [1001.86; 1247.36] Show Hide
Cp,gas 818.17 J/mol×K 1001.86 Joback Calculated Property
Cp,gas 828.01 J/mol×K 1042.78 Joback Calculated Property
Cp,gas 836.44 J/mol×K 1083.69 Joback Calculated Property
Cp,gas 843.51 J/mol×K 1124.61 Joback Calculated Property
Cp,gas 849.27 J/mol×K 1165.52 Joback Calculated Property
Cp,gas 853.77 J/mol×K 1206.44 Joback Calculated Property
Cp,gas 857.04 J/mol×K 1247.36 Joback Calculated Property

Similar Compounds

Phthalic acid, isobutyl 2-(2-nitrophenyl)ethyl ester. Phthalic acid, butyl 2-(2-nitrophenyl)ethyl ester. Phthalic acid, ethyl 2-(2-nitrophenyl)ethyl ester. Phthalic acid, 2-(2-nitrophenyl)ethyl pentyl ester. Phthalic acid, hexyl 2-(2-nitrophenyl)ethyl ester. Phthalic acid, 2-(2-nitrophenyl)ethyl octyl ester. Phthalic acid, heptyl 2-(2-nitrophenyl)ethyl ester. Phthalic acid, 2-(2-nitrophenyl)ethyl nonyl ester. Phthalic acid, decyl 2-(2-nitrophenyl)ethyl ester. Benzoic acid, 2-(2-nitrophenyl)ethyl ester. Kebuzone, methylated. (-)-2-Aminobutan-1-ol, ferroceneboronate derivative. 12-O-Methylcarnosol. Lycoramine. Thymidine, 3'-O-TMS, 5'-O-cyclotetramethylene-isopropylsilyl.

Find more compounds similar to Phthalic acid, 2-(2-nitrophenyl)ethyl propyl ester.

Sources

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