Chemical Properties of 1,3,6-Dioxathiocane (CAS 2094-92-0)

1,3,6-Dioxathiocane

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InChI
InChI=1S/C5H10O2S/c1-3-8-4-2-7-5-6-1/h1-5H2
InChI Key
QLOPHJMYWXXKTM-UHFFFAOYSA-N
Formula
C5H10O2S
SMILES
C1CSCCOCO1
Molecular Weight1
134.20
CAS
2094-92-0
Other Names
  • Formaldehyde, cyclic thiodiethylene acetal
  • 1,3-Dioxa-6-thiacyclooctane
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Physical Properties

Property Value Unit Source
Δf -133.20 kJ/mol Joback Calculated Property
Δfgas -302.93 kJ/mol Joback Calculated Property
Δfus 14.88 kJ/mol Joback Calculated Property
Δvap 42.64 kJ/mol Joback Calculated Property
IE 8.67 ± 0.05 eV NIST
log10WS -0.36 Crippen Calculated Property
logPoct/wat 0.724 Crippen Calculated Property
McVol 98.540 ml/mol McGowan Calculated Property
Pc 4862.97 kPa Joback Calculated Property
Tboil 448.29 K Joback Calculated Property
Tc 691.93 K Joback Calculated Property
Tfus 287.28 K Joback Calculated Property
Vc 0.322 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [194.22; 270.19] J/mol×K [448.29; 691.93] Show Hide
Cp,gas 194.22 J/mol×K 448.29 Joback Calculated Property
Cp,gas 208.98 J/mol×K 488.90 Joback Calculated Property
Cp,gas 222.88 J/mol×K 529.50 Joback Calculated Property
Cp,gas 235.95 J/mol×K 570.11 Joback Calculated Property
Cp,gas 248.19 J/mol×K 610.72 Joback Calculated Property
Cp,gas 259.60 J/mol×K 651.32 Joback Calculated Property
Cp,gas 270.19 J/mol×K 691.93 Joback Calculated Property

Similar Compounds

1,7-Dioxa-4,10-dithiacyclododecane. bis-(2-Ethoxyethyl) sulfide. 1,4-Oxathiane. 4,7,10-Trioxa-1-thiacyclododecane. 4,7,10,16,19,22-Hexaoxa-1,13-dithiacyclotetracosane. 4,7,13,16-Tetraoxa-1,10-dithiacyclooctadecane. 1,7-Dioxa-4,10-13-trithiacyclopentadecane. O-Mustard. Ethane, 1-chloro-2-[(2-ethoxyethyl)thio]-. 1,4,7-Oxadithionane. 1,10-Dioxa-4,7,13,16-tetrathiacyclooctadecane. 1-Oxa-4,7,10-trithiacyclododecane. 1,14-Dichloro-3,9-dithia-6,12-dioxatetradecane. 2-Chloroethyl (2-chloroethoxy)ethyl sulfide. Ethanol, 2,2'-thiobis-, diacetate.

Find more compounds similar to 1,3,6-Dioxathiocane.

Sources

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