Chemical Properties of THIAZOLIDINE-2,4-DIONE

THIAZOLIDINE-2,4-DIONE

InChI
InChI=1S/C3H3NO2S/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)
InChI Key
ZOBPZXTWZATXDG-UHFFFAOYSA-N
Formula
C3H3NO2S
SMILES
O=C1CSC(=O)N1
Molecular Weight1
117.13
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Physical Properties

Property Value Unit Source
ΔfusH° 8.66 kJ/mol Joback Calculated Property
logPoct/wat -0.031 Crippen Calculated Property
McVol 71.740 ml/mol McGowan Calculated Property

Cheméo can also estimate Normal Boiling Point Temperature, Normal melting (fusion) point, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy, Log10 of Water solubility in mol/l for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Correlations

Property Value Unit Temperature (K) Source
Cp,gas [88.02; 206.55] J/mol×K [273.00; 1000.00] Joback Predicted correlation Show Hide
EquationY = A + B·T + C·T² + D·T³ + E·T⁴
Y is Cp,gas in J/mol×K, T in K
Coefficient A4.53400e+01
Coefficient B1.11410e-01
Coefficient C2.07700e-04
Coefficient D-1.57900e-07
Coefficient E0.00000e+00
Temperature range, min.273.00
Temperature range, max.1000.00
Cp,gas 88.02 J/mol×K 273.00 Calculated Property
Cp,gas 103.76 J/mol×K 353.78 Calculated Property
Cp,gas 120.02 J/mol×K 434.56 Calculated Property
Cp,gas 136.30 J/mol×K 515.33 Calculated Property
Cp,gas 152.11 J/mol×K 596.11 Calculated Property
Cp,gas 166.95 J/mol×K 676.89 Calculated Property
Cp,gas 180.31 J/mol×K 757.67 Calculated Property
Cp,gas 191.69 J/mol×K 838.44 Calculated Property
Cp,gas 200.61 J/mol×K 919.22 Calculated Property
Cp,gas 206.55 J/mol×K 1000.00 Calculated Property

Similar Compounds

4(5H)-Thiazolone, 2-imino-. 2,4-Thiazolidinedione, 5-isopropylidene. 4-Thiazolidinone, 3-ethyl-2-thioxo-. Carbamothioic acid, S-[2-oxo-2-(phenylamino)ethyl] ester. 4-Thiazolidinone, 3-amino-2-thioxo-. N-Methylrhodanine. Thiazolidin-4-one, 3-phenylamino-2-thioxo-. Rhodanine, n-diacetylamino-. 2,4-Thiazolidinedione, 5-benzylidene-. 2,4-Thiazolidinedione, 5-p-hydroxybenzylidene-. N-Carboxyethylrhodanine. 2,4-Thiazolidinedione, 5-p-chlorobenzylidene-. Thiazolidine-2,4-dione, 5-(4-methoxyphenyl)methylene-. Ethanethioic acid, S-[2-(acetylamino)ethyl] ester. 2,4-Thiazolidinedione, 5-(p-dimethylaminobenzylidene)-.

Find more compounds similar to THIAZOLIDINE-2,4-DIONE.

Sources

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