Chemical Properties of Moretenol (21-epi-22[29]hopenol) acetate

Moretenol (21-epi-22[29]hopenol) acetate

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InChI Key
Molecular Weight1
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Physical Properties

Property Value Unit Source
Δf 221.37 kJ/mol Joback Calculated Property
Δfgas -551.77 kJ/mol Joback Calculated Property
Δfus 31.84 kJ/mol Joback Calculated Property
Δvap 88.38 kJ/mol Joback Calculated Property
log10WS -9.10 Crippen Calculated Property
logPoct/wat 8.596 Crippen Calculated Property
McVol 410.580 ml/mol McGowan Calculated Property
Pc 880.52 kPa Joback Calculated Property
Inp 3432.00 NIST
Tboil 1036.91 K Joback Calculated Property
Tc 1284.48 K Joback Calculated Property
Tfus 669.48 K Joback Calculated Property
Vc 1.554 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1684.08; 2137.20] J/mol×K [1036.91; 1284.48] Show Hide
Cp,gas 1684.08 J/mol×K 1036.91 Joback Calculated Property
Cp,gas 1743.36 J/mol×K 1078.17 Joback Calculated Property
Cp,gas 1808.04 J/mol×K 1119.43 Joback Calculated Property
Cp,gas 1878.93 J/mol×K 1160.69 Joback Calculated Property
Cp,gas 1956.87 J/mol×K 1201.96 Joback Calculated Property
Cp,gas 2042.68 J/mol×K 1243.22 Joback Calculated Property
Cp,gas 2137.20 J/mol×K 1284.48 Joback Calculated Property

Similar Compounds

Epilupeol (20[29]-lupen-3A-ol) acetate. Lup-20(29)-en-3-ol, acetate, (3«beta»)-. Acetyl betulinaldehyde. 3«beta»-Acetoxylup-20(29)-en-30-al. 24-Methylenedammarenol acetate. Cyclolaudenol acetate. 31-Norcyclolaudenol acetate. 24-Methylene-24-dihydrolanosterol acetate. 9,19-Cyclolanostan-3-ol, 24-methylene-, acetate, (3«beta»)-. Isoarborinol (9[11]-arborinenol) acetate. 24-Methyl-31-norlanosterol acetate. 24-Ethyl-31-nor-8-lanostenol acetate. 31-Nor-8-lanostenol acetate. 24-Ethyl-31-nor-8,25-lanostadienol acetate. Lanost-8-en-3-ol, acetate, (3«beta»)-.

Find more compounds similar to Moretenol (21-epi-22[29]hopenol) acetate.


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