Chemical Properties of Epilupeol (20[29]-lupen-3A-ol) acetate

Epilupeol (20[29]-lupen-3A-ol) acetate

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InChI
InChI=1S/C32H52O2/c1-20(2)22-12-15-29(6)18-19-31(8)23(27(22)29)10-11-25-30(7)16-14-26(34-21(3)33)28(4,5)24(30)13-17-32(25,31)9/h22-27H,1,10-19H2,2-9H3/t22-,23?,24-,25?,26+,27?,29?,30?,31+,32?/m1/s1
InChI Key
ODSSDTBFHAYYMD-CDDJISFVSA-N
Formula
C32H52O2
SMILES
C=C(C)C1CCC2(C)CCC3(C)C(CCC4C5(C)CCC(OC(C)=O)C(C)(C)C5CCC43C)C12
Molecular Weight1
468.75
Sources

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
logPoct/wat 8.60 Crippen Calculated Property
Pc 880.52 kPa Joback Calculated Property
Tboil 1036.91 K Joback Calculated Property
Tc 1284.48 K Joback Calculated Property
Tfus 669.48 K Joback Calculated Property
Vc 1.55 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 1684.08 J/mol×K 1036.91 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
-CH3 8
=CH2 1
=C< 1
>C< (ring) 5
>C=O (nonring) 1
>CH- (ring) 6
-CH2- (ring) 10

Similar Compounds

Moretenol (21-epi-22[29]hopenol) acetate. Lup-20(29)-en-3-ol, acetate, (3«beta»)-. 24-Methylenedammarenol acetate. 3.beta.-Acetoxylup-20(29)-en-30-al. Acetyl betulinaldehyde. Cyclolaudenol acetate. 31-Norcyclolaudenol acetate. 9,19-Cyclolanostan-3-ol, 24-methylene-, acetate, (3«beta»)-. (+)-5.beta.-Acetoxygymnomitr-3(15)-ene. Lanostan-3-yl acetate. 24-Methyllanostanol acetate. 3«beta»-Acetoxy-30-(trimethylsilyloxy)lup-20(29)-ene. 4,4-Dimethylcholestanol acetate. psi-Taraxasterol (20-taraxastenol) acetate. 24-Methyl-31-nor-7-lanostenol acetate.

Find more compounds similar to Epilupeol (20[29]-lupen-3A-ol) acetate.

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