Chemical Properties of Phenol, 4-(1-methylbutyl)-2-nitro

Phenol, 4-(1-methylbutyl)-2-nitro

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InChI
InChI=1S/C11H15NO3/c1-3-4-8(2)9-5-6-11(13)10(7-9)12(14)15/h5-8,13H,3-4H2,1-2H3
InChI Key
BUIJJQHOWLTFQA-UHFFFAOYSA-N
Formula
C11H15NO3
SMILES
CCCC(C)c1ccc(O)c([N+](=O)[O-])c1
Molecular Weight1
209.24
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Physical Properties

Property Value Unit Source
Δf 23.01 kJ/mol Joback Calculated Property
Δfgas -238.66 kJ/mol Joback Calculated Property
Δfus 31.52 kJ/mol Joback Calculated Property
Δvap 72.23 kJ/mol Joback Calculated Property
log10WS -3.69 Crippen Calculated Property
logPoct/wat 3.204 Crippen Calculated Property
McVol 165.380 ml/mol McGowan Calculated Property
Pc 3124.49 kPa Joback Calculated Property
Inp [1562.00; 1562.00]   Show Hide
Inp 1562.00 NIST
Inp 1562.00 NIST
Tboil 714.76 K Joback Calculated Property
Tc 957.31 K Joback Calculated Property
Tfus 493.00 K Joback Calculated Property
Vc 0.586 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [456.33; 524.29] J/mol×K [714.76; 957.31] Show Hide
Cp,gas 456.33 J/mol×K 714.76 Joback Calculated Property
Cp,gas 469.42 J/mol×K 755.18 Joback Calculated Property
Cp,gas 481.65 J/mol×K 795.61 Joback Calculated Property
Cp,gas 493.15 J/mol×K 836.03 Joback Calculated Property
Cp,gas 504.02 J/mol×K 876.46 Joback Calculated Property
Cp,gas 514.36 J/mol×K 916.88 Joback Calculated Property
Cp,gas 524.29 J/mol×K 957.31 Joback Calculated Property

Similar Compounds

Phenol, 4-(1-ethylbutyl)-2-nitro. Phenol, 4-(1-methylpentyl)-2-nitro. Phenol, 4-(1-ethylpropyl)-2-nitro. Phenol, 4-(1-methylpropyl)-2-nitro. Phenol, 2-(1-methylbutyl)-6-nitro. Phenol, 2-(1-methylheptyl)-6-nitro. Phenol, 2-(1-methylpentyl)-6-nitro. Phenol, 2-(1-ethylbutyl)-6-nitro. Phenol, 2-(1-propylpentyl)-6-nitro. Phenol, 2-(1-methylbutyl)-4-nitro. Phenol, 2-(1-ethylhexyl)-6-nitro. Phenol, 2-(1-methylpentyl)-4-nitro. Phenol, 2-(1-ethylbutyl)-4-nitro. 4-Sec-butyl-2,6-dinitrophenol. Phenol, 2-(1-ethylpropyl)-6-nitro.

Find more compounds similar to Phenol, 4-(1-methylbutyl)-2-nitro.

Sources

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