Chemical Properties of Phthalic acid, di(2-methylbenzyl) ester

Phthalic acid, di(2-methylbenzyl) ester

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InChI
InChI=1S/C24H22O4/c1-17-9-3-5-11-19(17)15-27-23(25)21-13-7-8-14-22(21)24(26)28-16-20-12-6-4-10-18(20)2/h3-14H,15-16H2,1-2H3
InChI Key
UJXAWKBKTUXCAE-UHFFFAOYSA-N
Formula
C24H22O4
SMILES
Cc1ccccc1COC(=O)c1ccccc1C(=O)OCc1ccccc1C
Molecular Weight1
374.43
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Physical Properties

Property Value Unit Source
Δf -8.30 kJ/mol Joback Calculated Property
Δfgas -353.11 kJ/mol Joback Calculated Property
Δfus 44.45 kJ/mol Joback Calculated Property
Δvap 96.14 kJ/mol Joback Calculated Property
log10WS -7.13 Crippen Calculated Property
logPoct/wat 5.017 Crippen Calculated Property
McVol 292.620 ml/mol McGowan Calculated Property
Pc 1623.29 kPa Joback Calculated Property
Inp 2880.00 NIST
Tboil 996.08 K Joback Calculated Property
Tc 1242.38 K Joback Calculated Property
Tfus 621.38 K Joback Calculated Property
Vc 1.103 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [906.66; 955.60] J/mol×K [996.08; 1242.38] Show Hide
Cp,gas 906.66 J/mol×K 996.08 Joback Calculated Property
Cp,gas 918.43 J/mol×K 1037.13 Joback Calculated Property
Cp,gas 928.67 J/mol×K 1078.18 Joback Calculated Property
Cp,gas 937.44 J/mol×K 1119.23 Joback Calculated Property
Cp,gas 944.82 J/mol×K 1160.28 Joback Calculated Property
Cp,gas 950.85 J/mol×K 1201.33 Joback Calculated Property
Cp,gas 955.60 J/mol×K 1242.38 Joback Calculated Property
η [0.0000346; 0.0002483] Pa×s [621.38; 996.08] Show Hide
η 0.0002483 Pa×s 621.38 Joback Calculated Property
η 0.0001539 Pa×s 683.83 Joback Calculated Property
η 0.0001034 Pa×s 746.28 Joback Calculated Property
η 0.0000738 Pa×s 808.73 Joback Calculated Property
η 0.0000553 Pa×s 871.18 Joback Calculated Property
η 0.0000431 Pa×s 933.63 Joback Calculated Property
η 0.0000346 Pa×s 996.08 Joback Calculated Property

Similar Compounds

Benzyl o-toluate. 2-Methylbenzyl benzoate. Dibenzyl phthalate. 1(3H)-Isobenzofuranone. 1,2-Benzenedicarboxylic acid, mono(phenylmethyl) ester. Phthalic acid, di(2-trifluorobenzyl) ester. Phthalic acid, di(4-fluorobenzyl) ester. Phthalic acid, 2-methylbenzyl propyl ester. Phthalic acid, isobutyl 2-methylbenzyl ester. Benzoic acid, 2-methyl-, anhydride. Benzoic acid, (2-(trifluoromethyl)phenyl)methyl ester. Benzoic acid, 2-methyl-, methyl ester. Benzyl trimethylsilyl phthalate. Phthalic acid, ethyl 2-trifluoromethylbenzyl ester. Phthalic acid, ethyl 4-fluorobenzyl ester.

Find more compounds similar to Phthalic acid, di(2-methylbenzyl) ester.

Sources

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