Chemical Properties of 24-Methyl-24-dihydrolanosterol acetate

24-Methyl-24-dihydrolanosterol acetate

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InChI
InChI=1S/C33H56O2/c1-21(2)22(3)11-12-23(4)25-15-19-33(10)27-13-14-28-30(6,7)29(35-24(5)34)17-18-31(28,8)26(27)16-20-32(25,33)9/h21-23,25,28-29H,11-20H2,1-10H3/t22?,23-,25?,28?,29-,31+,32+,33-/m1/s1
InChI Key
SWYDFFCKOFIWAM-LXOXAYJKSA-N
Formula
C33H56O2
SMILES
CC(=O)OC1CCC2(C)C3=C(CCC2C1(C)C)C1(C)CCC(C(C)CCC(C)C(C)C)C1(C)CC3
Molecular Weight1
484.80
Sources

Physical Properties

Property Value Unit Source
Δf 133.85 kJ/mol Joback Calculated Property
Δfgas -689.91 kJ/mol Joback Calculated Property
Δfus 33.95 kJ/mol Joback Calculated Property
Δvap 93.64 kJ/mol Joback Calculated Property
logPoct/wat 9.38 Crippen Calculated Property
Pc 778.51 kPa Joback Calculated Property
Tboil 1073.79 K Joback Calculated Property
Tc 1316.91 K Joback Calculated Property
Tfus 651.67 K Joback Calculated Property
Vc 1.65 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 1762.30 J/mol×K 1073.79 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
>CH- 3
-O- (nonring) 1
-CH3 10
=C< (ring) 2
-CH2- 2
>C< (ring) 4
>C=O (nonring) 1
>CH- (ring) 3
-CH2- (ring) 8

Similar Compounds

5.alpha.-tirucalla-8,23-dien-3.beta.-ol, acetylated. 24-Dihydrotirucallol acetate. butyrospermol acetylated. 24-Methyl-31-norlanosterol acetate. Isoeuphenol acetate. Lanost-8-en-3-ol, acetate, (3«beta»,13«alpha»,14«beta»,17«alpha»)-. 24-Ethyl-31-nor-8,25-lanostadienol acetate. Tirucallol acetate. 24-Methylene-24-dihydrolanosterol acetate. 24-Ethyl-31-nor-8-lanostenol acetate. Isotirucallenol acetate. Euphol acetate. 31-Norlanosterol acetate. Lanost-8-en-3-ol, acetate, (3«beta»)-. 31-Nor-8-lanostenol acetate.

Find more compounds similar to 24-Methyl-24-dihydrolanosterol acetate.

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