Chemical Properties of Rhodanine, 5-p-hydroxybenzylidene- (CAS 6339-79-3)

Rhodanine, 5-p-hydroxybenzylidene-

InChI
InChI=1S/C10H7NO2S2/c12-7-3-1-6(2-4-7)5-8-9(13)11-10(14)15-8/h1-5,12H,(H,11,13,14)/b8-5-
InChI Key
RAYIDZVPIAJJPF-YVMONPNESA-N
Formula
C10H7NO2S2
SMILES
O=C1NC(=S)SC1=Cc1ccc(O)cc1
Molecular Weight1
237.30
CAS
6339-79-3
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Physical Properties

Property Value Unit Source
ω 0.6005 Relay (1.0) Calculated Property
Δf 176.66 kJ/mol Joback Calculated Property
Δfgas -100.21 kJ/mol Relay (1.0) Calculated Property
Δfus 33.46 kJ/mol Joback Calculated Property
Δvap 123.92 kJ/mol Relay (1.0) Calculated Property
IE 7.72 eV Relay (1.0) Calculated Property
log10WS -3.55 Relay (1.0) Calculated Property
logPoct/wat 1.881 Crippen Calculated Property
McVol 158.660 ml/mol McGowan Calculated Property
Pc 5585.83 kPa Joback Calculated Property
Tboil 634.72 K Relay (1.0) Calculated Property
Tc 967.67 K Relay (1.0) Calculated Property
Tfus 514.15 K Relay (1.0) Calculated Property
Vc 0.506 m3/kmol Relay (1.0) Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [390.56; 449.16] J/mol×K [798.93; 1099.60] Show Hide
Cp,gas 390.56 J/mol×K 798.93 Joback Calculated Property
Cp,gas 401.12 J/mol×K 849.04 Joback Calculated Property
Cp,gas 411.10 J/mol×K 899.15 Joback Calculated Property
Cp,gas 420.71 J/mol×K 949.26 Joback Calculated Property
Cp,gas 430.12 J/mol×K 999.37 Joback Calculated Property
Cp,gas 439.54 J/mol×K 1049.49 Joback Calculated Property
Cp,gas 449.16 J/mol×K 1099.60 Joback Calculated Property

Similar Compounds

Rhodanine, 5-p-methoxybenzylidene-. Rhodanine, 5-salicylidene-. 5-Vanillylidene rhodanine. 4-Thiazolidinone, 5-(p-hydroxybenzylidene)-2-imino-. Rhodanine, 5-(p-nitrobenzylidene)-. 5-(4-Diethylaminobenzylidene)rhodanine. 2,4-Thiazolidinedione, 5-[(4-methoxyphenyl)methylene]-. Rhodanine, 5-(m-nitrobenzylidene)-. 2,4-Thiazolidinedione, 5-p-chlorobenzylidene-. 2,4-Thiazolidinedione, 5-benzylidene-. Rhodanine, 5-(p-methoxybenzylidene)-3-(p-methoxybenzylideneamino)-. 2,4-Thiazolidinedione, 5-(p-dimethylaminobenzylidene)-. 4-Thiazolidinone, 5-benzylidene-2-imino-. Rhodanine, 5-benzylidene-3-salicylideneamino-. Rhodanine, 3-amino-5-benzylidene-.

Find more compounds similar to Rhodanine, 5-p-hydroxybenzylidene-.

Sources

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