Chemical Properties of (+)-5.beta.-Acetoxygymnomitr-3(15)-ene

(+)-5.beta.-Acetoxygymnomitr-3(15)-ene

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InChI
InChI=1S/C17H26O2/c1-11-9-14(19-12(2)18)16(4)10-13(11)15(3)7-6-8-17(15,16)5/h13-14H,1,6-10H2,2-5H3/t13?,14-,15-,16-,17-/m1/s1
InChI Key
JOGWSWZSQXEHIQ-XRZUFTMXSA-N
Formula
C17H26O2
SMILES
C=C1CC(OC(C)=O)C2(C)CC1C1(C)CCCC12C
Molecular Weight1
262.39
Sources

Physical Properties

Property Value Unit Source
Δf 37.58 kJ/mol Joback Calculated Property
Δfgas -343.65 kJ/mol Joback Calculated Property
Δfus 14.87 kJ/mol Joback Calculated Property
Δvap 58.76 kJ/mol Joback Calculated Property
logPoct/wat 4.10 Crippen Calculated Property
Pc 1930.44 kPa Joback Calculated Property
Tboil 683.95 K Joback Calculated Property
Tc 912.08 K Joback Calculated Property
Tfus 477.19 K Joback Calculated Property
Vc 0.84 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 663.97 J/mol×K 683.95 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
>C=O (nonring) 1
=CH2 1
=C< (ring) 1
>C< (ring) 3
-CH3 4
>CH- (ring) 2
-CH2- (ring) 5

Similar Compounds

Epilupeol (20[29]-lupen-3A-ol) acetate. Moretenol (21-epi-22[29]hopenol) acetate. Lup-20(29)-en-3-ol, acetate, (3«beta»)-. larixyl acetate. 6-Camphenol acetate. Bicyclo[2.2.1]heptane-3-methylene-2,2-dimethyl-5-ol acetate. Isoarborinol (9[11]-arborinenol) acetate. 24-Methyl-7-lanosterol acetate. 24-Methyl-24-dihydroparkeol acetate. 31-Nor-9(11)-lanostenol acetate. Lanosta-9(11),24-dien-3-ol, acetate, (3.beta.)-. Butyrospermol acetate. 24-Methyl-31-nor-7-lanostenol acetate. Lanost-7-en-3-ol, acetate, (3«beta»)-. 24,25-Dimethyl-9(11)-lanostenol acetate.

Find more compounds similar to (+)-5.beta.-Acetoxygymnomitr-3(15)-ene.

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