Chemical Properties of (-)-15-Acetoxygymnomitr-3-ene

(-)-15-Acetoxygymnomitr-3-ene

Download as PDF file Download as Excel file Download as 2D mole file Predict properties

InChI
InChI=1S/C17H26O2/c1-12(18)19-11-13-6-9-15(2)10-14(13)16(3)7-5-8-17(15,16)4/h6,14H,5,7-11H2,1-4H3/t14?,15-,16+,17-/m0/s1
InChI Key
RNPCIAPLYQGCAJ-HMQMGEFJSA-N
Formula
C17H26O2
SMILES
CC(=O)OCC1=CCC2(C)CC1C1(C)CCCC21C
Molecular Weight1
262.39
Sources

Physical Properties

Property Value Unit Source
Δf 12.54 kJ/mol Joback Calculated Property
Δfgas -361.24 kJ/mol Joback Calculated Property
Δfus 15.79 kJ/mol Joback Calculated Property
Δvap 59.87 kJ/mol Joback Calculated Property
logPoct/wat 4.10 Crippen Calculated Property
Pc 1991.21 kPa Joback Calculated Property
Tboil 693.60 K Joback Calculated Property
Tc 922.67 K Joback Calculated Property
Tfus 481.03 K Joback Calculated Property
Vc 0.85 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 662.58 J/mol×K 693.6 Joback Calculated Property

Molecular Descriptors

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

Similar Compounds

Myrtenyl acetate. 2-pinen-10-yl isobutyrate. myrtenyl 3-methylbutanoate. Myrtenyl caprate. Myrtenyl laureate. Myrtenyl hexanoate. Myrtenyl 3-methylvalerate. Myrtenyl 2-methyl butyrate. Glutaric acid, di(myrtenyl) ester. Myrtenyl angelate. Glutaric acid, myrtenyl 3-methylbut-2-en-1-yl ester. .beta.-Isocyclolavandulyl acetate. Glutaric acid, myrtenyl 8-chlorooctyl ester. Myrtenyl formate. Glutaric acid, myrtenyl 2-ethylhexyl ester.

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

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.