Chemical Properties of 1,5-cis-Aromadendr-9-ene

1,5-cis-Aromadendr-9-ene

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InChI
InChI=1S/C15H24/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h6,10-14H,5,7-8H2,1-4H3/t10-,11+,12-,13+,14-/m1/s1
InChI Key
DJAYTQZJAJXFDU-XHJNMGKDSA-N
Formula
C15H24
SMILES
CC1=CCC2C(C3C(C)CCC13)C2(C)C
Molecular Weight1
204.35
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Physical Properties

Property Value Unit Source
Δf 225.18 kJ/mol Joback Calculated Property
Δfgas -146.32 kJ/mol Joback Calculated Property
Δfus 22.56 kJ/mol Joback Calculated Property
Δvap 47.94 kJ/mol Joback Calculated Property
log10WS -4.19 Crippen Calculated Property
logPoct/wat 4.271 Crippen Calculated Property
McVol 185.330 ml/mol McGowan Calculated Property
Pc 1973.55 kPa Joback Calculated Property
Inp [1484.00; 1486.00]   Show Hide
Inp 1484.00 NIST
Inp 1486.00 NIST
I 1716.00 NIST
Tboil 561.73 K Joback Calculated Property
Tc 778.35 K Joback Calculated Property
Tfus 330.05 K Joback Calculated Property
Vc 0.712 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [505.21; 627.64] J/mol×K [561.73; 778.35] Show Hide
Cp,gas 505.21 J/mol×K 561.73 Joback Calculated Property
Cp,gas 528.79 J/mol×K 597.83 Joback Calculated Property
Cp,gas 550.88 J/mol×K 633.94 Joback Calculated Property
Cp,gas 571.64 J/mol×K 670.04 Joback Calculated Property
Cp,gas 591.24 J/mol×K 706.14 Joback Calculated Property
Cp,gas 609.85 J/mol×K 742.24 Joback Calculated Property
Cp,gas 627.64 J/mol×K 778.35 Joback Calculated Property

Similar Compounds

Alloaromadendr-9-ene. Dehydroaromadendrene. «alpha»-Maaliene. Tricyclo[6.3.0.0(2,4)]undec-8-ene, 3,3,7,11-tetramethyl-. 1,1,4,7-Tetramethyl-1a,2,3,4,6,7,7a,7b-octahydro-1H-cyclopropa[e]azulene. cyclocopacamphene. (-)-Aristolene. cis-4-methylcarene. 4-methyl-2-caren. 4-[2,2-Dimethyl-3-(5-methylcyclopenta-1,4-dien-1-yl)-cyclopropyl]-butan- 2-one. epi-Bicyclophellandrene. 6-epi-«alpha»-Cubebene. Cubebene. «alpha»-Cubebene. 1a«alpha»,7«alpha»,7a«alpha»,7b«alpha»-1H-Cyclopropa[a]naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl.

Find more compounds similar to 1,5-cis-Aromadendr-9-ene.

Sources

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