Chemical Properties of Rhodanine, 5-cinnamylidene-

Rhodanine, 5-cinnamylidene-

InChI
InChI=1S/C12H9NOS2/c14-11-10(16-12(15)13-11)8-4-7-9-5-2-1-3-6-9/h1-8H,(H,13,14,15)/b7-4+,10-8+
InChI Key
FPSVMWLWFSURME-WIXOJMCHSA-N
Formula
C12H9NOS2
SMILES
O=C1NC(=S)S/C1=C/C=C\c1ccccc1
Molecular Weight1
247.34
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Physical Properties

Property Value Unit Source
Δfus 33.06 kJ/mol Joback Calculated Property
logPoct/wat 2.732 Crippen Calculated Property
McVol 176.670 ml/mol McGowan Calculated Property

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Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [428.76; 491.29] J/mol×K [768.23; 1061.14] Show Hide
Cp,gas 428.76 J/mol×K 768.23 Joback Calculated Property
Cp,gas 441.44 J/mol×K 817.05 Joback Calculated Property
Cp,gas 453.03 J/mol×K 865.87 Joback Calculated Property
Cp,gas 463.68 J/mol×K 914.69 Joback Calculated Property
Cp,gas 473.52 J/mol×K 963.51 Joback Calculated Property
Cp,gas 482.68 J/mol×K 1012.32 Joback Calculated Property
Cp,gas 491.29 J/mol×K 1061.14 Joback Calculated Property

Similar Compounds

propyl-cannabinolic acid, TMS. Mephenesin, ferroceneboronate derivative. Chlorphenesin, ferroceneboronate derivative. Nadolol tri-TMS derivative. cannabinolic acid, TMS. N-Acetylnornarcotine. Adenosine, 2'-deoxy-N-(trimethylsilyl)-3'-O-(trimethylsilyl)-, 5'-[bis(trimethylsilyl) phosphate]. Cytidine, methyl-TMS derivative. Levophenacylmorphan. 2-(2-furyl)-3-hydroxypiperidine. 5-Methylcytosine riboside, TMS. 2-(5-methyl-2-furyl)-3-hydroxy-piperidine. Nadolol. Atropine, picolinyloxydimethylsilyl ether. 4-[2-(4-Allyl-2,6-dimethoxy-phenoxy)-1-hydroxy-propyl]-2-methoxy-phenol, TPS.

Find more compounds similar to Rhodanine, 5-cinnamylidene-.

Sources

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