Chemical Properties of (E)-3,7-Dimethylocta-2,6-dien-1-yl 3-methylbutanoate

(E)-3,7-Dimethylocta-2,6-dien-1-yl 3-methylbutanoate

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InChI
InChI=1S/C15H26O2/c1-12(2)7-6-8-14(5)9-10-17-15(16)11-13(3)4/h7,9,13H,6,8,10-11H2,1-5H3/b14-9+
InChI Key
SOUKTGNMIRUIQN-NTEUORMPSA-N
Formula
C15H26O2
SMILES
CC(C)=CCCC(C)=CCOC(=O)CC(C)C
Molecular Weight1
238.37
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Physical Properties

Property Value Unit Source
Δf -17.60 kJ/mol Joback Calculated Property
Δfgas -388.15 kJ/mol Joback Calculated Property
Δfus 31.65 kJ/mol Joback Calculated Property
Δvap 57.83 kJ/mol Joback Calculated Property
log10WS -4.43 Crippen Calculated Property
logPoct/wat 4.268 Crippen Calculated Property
McVol 221.050 ml/mol McGowan Calculated Property
Pc 1612.88 kPa Joback Calculated Property
Inp [1604.20; 1604.20]   Show Hide
Inp 1604.20 NIST
Inp 1604.20 NIST
Tboil 626.53 K Joback Calculated Property
Tc 813.52 K Joback Calculated Property
Tfus 277.89 K Joback Calculated Property
Vc 0.856 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [580.04; 671.98] J/mol×K [626.53; 813.52] Show Hide
Cp,gas 580.04 J/mol×K 626.53 Joback Calculated Property
Cp,gas 597.38 J/mol×K 657.69 Joback Calculated Property
Cp,gas 613.87 J/mol×K 688.86 Joback Calculated Property
Cp,gas 629.53 J/mol×K 720.02 Joback Calculated Property
Cp,gas 644.42 J/mol×K 751.19 Joback Calculated Property
Cp,gas 658.56 J/mol×K 782.35 Joback Calculated Property
Cp,gas 671.98 J/mol×K 813.52 Joback Calculated Property

Similar Compounds

Neryl isovalerate. Geranyl isovalerate. ( E, E)-farnesyl 3-methylbutanoate. Neryl butyrate. Farnesyl butanoate. Butanoic acid, 3,7-dimethyl-2,6-octadienyl ester, (E)-. Farnesyl butyrate. Geranyl isohexanoate. (2E,6E)-Farnesyl pentanoate. Pentanoic acid, 3,7-dimethyl-2,6-octadienyl ester, (E)-. Neryl valerate. Geranyl isoheptanoate. Hexanoic acid, 3,7-dimethyl-2,6-octadienyl ester, (E)-. Farnesyl hexanoate, (E,E)-. (Z,Z)-Farnesyl caproate.

Find more compounds similar to (E)-3,7-Dimethylocta-2,6-dien-1-yl 3-methylbutanoate.

Sources

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