Chemical Properties of 2-Methyl-3,4-dihydro-2H-thiopyran

2-Methyl-3,4-dihydro-2H-thiopyran

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InChI
InChI=1S/C6H8OS/c1-5-4-6(7)2-3-8-5/h2-3,5H,4H2,1H3
InChI Key
KGDMIAZBLYJSSW-UHFFFAOYSA-N
Formula
C6H8OS
SMILES
CC1CC(=O)C=CS1
Molecular Weight1
128.19
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Physical Properties

Property Value Unit Source
Δf -28.68 kJ/mol Joback Calculated Property
Δfgas -147.51 kJ/mol Joback Calculated Property
Δfus 7.52 kJ/mol Joback Calculated Property
Δvap 39.73 kJ/mol Joback Calculated Property
log10WS -1.85 Crippen Calculated Property
logPoct/wat 1.595 Crippen Calculated Property
McVol 98.160 ml/mol McGowan Calculated Property
Pc 4305.56 kPa Joback Calculated Property
Inp [892.00; 892.00]   Show Hide
Inp 892.00 NIST
Inp 892.00 NIST
Tboil 471.04 K Joback Calculated Property
Tc 716.73 K Joback Calculated Property
Tfus 317.19 K Joback Calculated Property
Vc 0.344 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [191.34; 260.31] J/mol×K [471.04; 716.73] Show Hide
Cp,gas 191.34 J/mol×K 471.04 Joback Calculated Property
Cp,gas 204.49 J/mol×K 511.99 Joback Calculated Property
Cp,gas 216.99 J/mol×K 552.94 Joback Calculated Property
Cp,gas 228.83 J/mol×K 593.89 Joback Calculated Property
Cp,gas 240.01 J/mol×K 634.83 Joback Calculated Property
Cp,gas 250.51 J/mol×K 675.78 Joback Calculated Property
Cp,gas 260.31 J/mol×K 716.73 Joback Calculated Property

Similar Compounds

2,4-Dimethyl-3,4-dihydro-2H-thiopyran-3-carbaldehyde. 2-Butyl-2H-thiapyrane. Antheridic acid, MeTMS. 7-(1H-Pyrrol-2-yloxymethyl)-2,3,5,8-tetrahydro-1H-pyrrolizin-1-ol. Cobalt, [(1,2,3,4-«eta»)-2,4-bis(1,1-dimethylethyl)-1,3-diphosphete](«eta»5-2,4-cyclopentadien-1-yl)-. 2-Pentyl-2H-thiapyrane. 2-Hexyl-2H-thiapyrane. Isoflupredone, tetra-TMS. Lysergol. pimaricin. 3'-Hydroxystanozolol, per-TMS. Ethyl 2-(methylamino)-1-phenyl-3-cyclohexene-1-carboxylate. Betamethasone tetra-TMS. 2-(2-furyl)-3-hydroxypiperidine. 2-(5-methyl-2-furyl)-3-hydroxy-piperidine.

Find more compounds similar to 2-Methyl-3,4-dihydro-2H-thiopyran.

Sources

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