Chemical Properties of 2,4-Dinitrobenzaldehyde (CAS 528-75-6)

2,4-Dinitrobenzaldehyde

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InChI
InChI=1S/C7H4N2O5/c10-4-5-1-2-6(8(11)12)3-7(5)9(13)14/h1-4H
InChI Key
ZILXIZUBLXVYPI-UHFFFAOYSA-N
Formula
C7H4N2O5
SMILES
O=Cc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Molecular Weight1
196.12
CAS
528-75-6
Other Names
  • Benzaldehyde, 2,4-dinitro-
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Physical Properties

Property Value Unit Source
Δf 72.79 kJ/mol Joback Calculated Property
Δfgas -81.32 kJ/mol Joback Calculated Property
Δfus 21.18 kJ/mol Calorim...
Δvap 74.68 kJ/mol Joback Calculated Property
log10WS -3.01 Crippen Calculated Property
logPoct/wat 1.315 Crippen Calculated Property
McVol 122.140 ml/mol McGowan Calculated Property
Pc 4498.26 kPa Joback Calculated Property
Tboil 748.54 K Joback Calculated Property
Tc 1021.37 K Joback Calculated Property
Tfus 549.33 K Joback Calculated Property
Vc 0.500 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [305.20; 341.00] J/mol×K [748.54; 1021.37] Show Hide
Cp,gas 305.20 J/mol×K 748.54 Joback Calculated Property
Cp,gas 313.09 J/mol×K 794.01 Joback Calculated Property
Cp,gas 320.14 J/mol×K 839.48 Joback Calculated Property
Cp,gas 326.41 J/mol×K 884.95 Joback Calculated Property
Cp,gas 331.94 J/mol×K 930.43 Joback Calculated Property
Cp,gas 336.79 J/mol×K 975.90 Joback Calculated Property
Cp,gas 341.00 J/mol×K 1021.37 Joback Calculated Property
ΔfusH 21.18 kJ/mol 223.00 NIST

Pressure Dependent Properties

Property Value Unit Pressure (kPa) Source
Tboilr 463.20 K 1.30 NIST

Similar Compounds

Benzaldehyde, 2-nitro-. Benzene, 1-methyl-2,4-dinitro-. 4-Fluoro-2-nitrobenzaldehyde. 2,4-Dinitrobenzoic acid. 2,2',4,4',6-Pentanitrobenzophenone. Benzene, 2,4-dinitro-1-(2-phenylethenyl)-. Benzenamine, 4-methyl-3-nitro-. 3-Nitro-4-methylbenzaldehyde. 5-Hydroxy-2-nitrobenzaldehyde. 2,4-Dinitro-1,3-dimethyl-benzene. Trinitrotoluene. 4,6-Dinitro-1,3-dimethyl-benzene. Benzene, 1-methyl-2-nitro-. Benzenamine, 2-methyl-5-nitro-. 2-Nitrobenzyl bromide.

Find more compounds similar to 2,4-Dinitrobenzaldehyde.

Sources

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