Chemical Properties of 4-Chloro-N-(2-methyl-4-nitrophenyl)-benzenesulfonamide, N-methyl-

4-Chloro-N-(2-methyl-4-nitrophenyl)-benzenesulfonamide, N-methyl-

InChI
InChI=1S/C14H13ClN2O4S/c1-10-9-12(17(18)19)5-8-14(10)16(2)22(20,21)13-6-3-11(15)4-7-13/h3-9H,1-2H3
InChI Key
MXBOECKBBXIUOS-UHFFFAOYSA-N
Formula
C14H13ClN2O4S
SMILES
Cc1cc([N+](=O)[O-])ccc1N(C)S(=O)(=O)c1ccc(Cl)cc1
Molecular Weight1
340.78
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Physical Properties

Property Value Unit Source
ω 0.7597 Relay (1.0) Calculated Property
Δf -71.21 kJ/mol Joback Calculated Property
Δfgas -192.95 kJ/mol Relay (1.0) Calculated Property
Δfus 48.89 kJ/mol Joback Calculated Property
Δvap 109.95 kJ/mol Relay (1.0) Calculated Property
IE 8.65 eV Relay (1.0) Calculated Property
log10WS -5.31 Relay (1.0) Calculated Property
logPoct/wat 3.382 Crippen Calculated Property
McVol 228.330 ml/mol McGowan Calculated Property
Pc 3028.94 kPa Joback Calculated Property
Inp 2683.00 NIST
Tboil 670.44 K Relay (1.0) Calculated Property
Tc 990.03 K Relay (1.0) Calculated Property
Tfus 407.45 K Relay (1.0) Calculated Property
Vc 0.784 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [619.09; 669.87] J/mol×K [837.51; 1086.13] Show Hide
Cp,gas 619.09 J/mol×K 837.51 Joback Calculated Property
Cp,gas 630.71 J/mol×K 878.95 Joback Calculated Property
Cp,gas 640.99 J/mol×K 920.38 Joback Calculated Property
Cp,gas 649.98 J/mol×K 961.82 Joback Calculated Property
Cp,gas 657.76 J/mol×K 1003.26 Joback Calculated Property
Cp,gas 664.37 J/mol×K 1044.69 Joback Calculated Property
Cp,gas 669.87 J/mol×K 1086.13 Joback Calculated Property

Similar Compounds

4-Chloro-N-(2-methyl-4-nitrophenyl)-benzenesulfonamide, N-trifluoroacetyl-. 4-Chloro-N-(2-methyl-4-nitrophenyl)-benzenesulfonamide, N-pentafluoropropionyl-. 4-Chloro-N-(2-methyl-4-nitrophenyl)-benzenesulfonamide, N-heptafluorobutyryl-. 4-Chloro-N-(2-methyl-4-nitrophenyl)-benzenesulfonamide. Axillarine. Hydroxy-N-methylcytisine. Pumiline A. azadirachtin. Gelsemine. cyclomegistine. Mucronatinine. 1H-Indole-3-ethanol, 2-(5-ethenyl-1-azabicyclo[2.2.2]oct-2-yl)-, [1S-(1«alpha»,2«alpha»,4«alpha»,5«beta»)]-. Nicodicodine. Eburnamenine-14-carboxylic acid, 14,15-dihydro-14-hydroxy-, methyl ester, (3«alpha»,14«alpha»,16«alpha»)-. TCN.

Find more compounds similar to 4-Chloro-N-(2-methyl-4-nitrophenyl)-benzenesulfonamide, N-methyl-.

Sources

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