Chemical Properties of Thiirane, 2,3-bis(1,1-tert-butyl)-, trans- (CAS 52908-35-7)

Thiirane, 2,3-bis(1,1-tert-butyl)-, trans-

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InChI
InChI=1S/C10H20S/c1-9(2,3)7-8(11-7)10(4,5)6/h7-8H,1-6H3
InChI Key
SUKBJBHRMICECN-UHFFFAOYSA-N
Formula
C10H20S
SMILES
CC(C)(C)C1SC1C(C)(C)C
Molecular Weight1
172.33
CAS
52908-35-7
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Physical Properties

Property Value Unit Source
Δf 131.90 kJ/mol Joback Calculated Property
Δfgas -169.51 kJ/mol Joback Calculated Property
Δfus 9.69 kJ/mol Joback Calculated Property
Δvap 40.68 kJ/mol Joback Calculated Property
IE 8.39 ± 0.05 eV NIST
log10WS -3.53 Crippen Calculated Property
logPoct/wat 3.563 Crippen Calculated Property
McVol 157.250 ml/mol McGowan Calculated Property
Pc 2381.86 kPa Joback Calculated Property
Tboil 471.64 K Joback Calculated Property
Tc 685.03 K Joback Calculated Property
Tfus 304.45 K Joback Calculated Property
Vc 0.576 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [358.22; 458.38] J/mol×K [471.64; 685.03] Show Hide
Cp,gas 358.22 J/mol×K 471.64 Joback Calculated Property
Cp,gas 378.05 J/mol×K 507.20 Joback Calculated Property
Cp,gas 396.50 J/mol×K 542.77 Joback Calculated Property
Cp,gas 413.67 J/mol×K 578.33 Joback Calculated Property
Cp,gas 429.65 J/mol×K 613.90 Joback Calculated Property
Cp,gas 444.52 J/mol×K 649.46 Joback Calculated Property
Cp,gas 458.38 J/mol×K 685.03 Joback Calculated Property

Similar Compounds

1-Thiacycloheptane,3,3,6,6-tetramethyl-. 2-isopropyl-thiacyclopentane. 2,3,4-Trimethylthiolane. trans,trans-2,3,5-trimethyl-thiacyclopentane. trans,cis-2,3,5-trimethyl-thiacyclopentane. cis,cis-2,3,5-trimethyl-thiacyclopentane. cis,trans-2,3,5-trimethyl-thiacyclopentane. trans-2-ethyl-4-methyl-thiacyclopentane. cis-2-ethyl-4-methyl-thiacyclopentane. 3,3-dimethyl-thiacyclohexane. 4,8-dimethyl-2-thiaadamantane. 4-methyl-2-thiaadamantane. 3,3-dimethyl-thiacyclopentane. cis-2-Ethyl-3-methylthiophane. trans-2-Ethyl-3-methylthiophane.

Find more compounds similar to Thiirane, 2,3-bis(1,1-tert-butyl)-, trans-.

Sources

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