Chemical Properties of 24-Methyl-31-norlanosterol acetate

24-Methyl-31-norlanosterol acetate

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InChI
InChI=1S/C32H54O2/c1-10-21(2)11-12-22(3)24-15-19-32(9)26-13-14-27-29(5,6)28(34-23(4)33)17-18-30(27,7)25(26)16-20-31(24,32)8/h21-22,24,27-28H,10-20H2,1-9H3/t21?,22-,24?,27?,28-,30+,31+,32-/m1/s1
InChI Key
GZIUSEKAVIUXEE-OQTLQYEJSA-N
Formula
C32H54O2
SMILES
CCC(C)CCC(C)C1CCC2(C)C3=C(CCC12C)C1(C)CCC(OC(C)=O)C(C)(C)C1CC3
Molecular Weight1
470.77
Sources

Physical Properties

Property Value Unit Source
Δf 127.87 kJ/mol Joback Calculated Property
Δfgas -663.99 kJ/mol Joback Calculated Property
Δfus 34.88 kJ/mol Joback Calculated Property
Δvap 91.80 kJ/mol Joback Calculated Property
logPoct/wat 9.13 Crippen Calculated Property
Pc 818.20 kPa Joback Calculated Property
Tboil 1051.35 K Joback Calculated Property
Tc 1290.99 K Joback Calculated Property
Tfus 655.40 K Joback Calculated Property
Vc 1.60 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 1680.25 J/mol×K 1051.35 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
>CH- 2
-CH3 9
=C< (ring) 2
-CH2- 3
>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. 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»)-. 24-Methyl-24-dihydrolanosterol acetate. 31-Nor-8-lanostenol acetate.

Find more compounds similar to 24-Methyl-31-norlanosterol acetate.

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