Chemical Properties of 13-ethoxy-8 «alpha»,13-epoxy-14,15,16-trinorlabdane

13-ethoxy-8 «alpha»,13-epoxy-14,15,16-trinorlabdane

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InChI
InChI=1S/C18H32O2/c1-5-19-16-10-7-13-14(20-16)8-9-15-17(2,3)11-6-12-18(13,15)4/h13-16H,5-12H2,1-4H3/t13?,14-,15?,16?,18-/m0/s1
InChI Key
PHUXMFIYWAEFPU-KVODCKKVSA-N
Formula
C18H32O2
SMILES
CCOC1CCC2C(CCC3C(C)(C)CCCC23C)O1
Molecular Weight1
280.45
Sources

Physical Properties

Property Value Unit Source
Δf -2.80 kJ/mol Joback Calculated Property
Δfgas -522.01 kJ/mol Joback Calculated Property
Δfus 26.07 kJ/mol Joback Calculated Property
Δvap 59.95 kJ/mol Joback Calculated Property
logPoct/wat 4.77 Crippen Calculated Property
Pc 1644.42 kPa Joback Calculated Property
Tboil 688.65 K Joback Calculated Property
Tc 915.03 K Joback Calculated Property
Tfus 412.72 K Joback Calculated Property
Vc 0.91 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 769.09 J/mol×K 688.65 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
-O- (ring) 1
-CH2- 1
>C< (ring) 2
-CH3 4
>CH- (ring) 4
-CH2- (ring) 7

Similar Compounds

12-ethoxy-8 «alpha»,12-epoxy-13,14,15,16-tertanorlabdane. Sarsasapogenin. Tigogenin. Smilagenin. Neotigogenin. Gitogenin. Cryptofauronol. 4,7-Methanobenzofuran, 2,2'-oxybis[octahydro-7,8,8-trimethyl-, [2«alpha»(2'R*,3'aS*,4'R*,7'R*,7'aS*),3a«alpha»,4«alpha»,7«alpha»,7a«alpha»]-. 10-Hydroxy-6,10-epoxy-7(14)-isodaucane. 7,10-Epoxy-10-methoxysalvialane. (+)-(4S,5R,6S,7R,10S)-6,11-Epoxyeudesmane. Ambrox. 7,10-Epoxy-10-hydroxysalvianane. 10-Hydroxy-7,10-epoxysalvialane. Ethyl (1R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl carbonate.

Find more compounds similar to 13-ethoxy-8 «alpha»,13-epoxy-14,15,16-trinorlabdane.

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