Chemical Properties of 3-Ethyl-5b,8,8,11a-tetramethyl-2,3, 5b,6,7,7a,8,9,10,11,11a,11b,12,13-tetradecahydro-1H-cyclopenta[a]chrysene

3-Ethyl-5b,8,8,11a-tetramethyl-2,3, 5b,6,7,7a,8,9,10,11,11a,11b,12,13-tetradecahydro-1H-cyclopenta[a]chrysene

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InChI
InChI=1S/C27H40/c1-6-18-8-9-20-19(18)10-12-22-21(20)11-13-24-26(22,4)17-14-23-25(2,3)15-7-16-27(23,24)5/h10,12,18,23-24H,6-9,11,13-17H2,1-5H3
InChI Key
TYBHAMOKSYDYCY-UHFFFAOYSA-N
Formula
C27H40
SMILES
CCC1CCc2c1ccc1c2CCC2C1(C)CCC1C(C)(C)CCCC12C
Molecular Weight1
364.61
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Physical Properties

Property Value Unit Source
ΔfG° 434.79 kJ/mol Joback Calculated Property
ΔfH°gas -120.73 kJ/mol Joback Calculated Property
ΔfusH° 28.05 kJ/mol Joback Calculated Property
ΔvapH° 76.05 kJ/mol Joback Calculated Property
log10WS -8.37 Crippen Calculated Property
logPoct/wat 7.573 Crippen Calculated Property
McVol 324.090 ml/mol McGowan Calculated Property
Pc 1222.55 kPa Joback Calculated Property
Inp 2951.62 NIST
Tboil 889.93 K Joback Calculated Property
Tc 1134.68 K Joback Calculated Property
Tfus 582.45 K Joback Calculated Property
Vc 1.236 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1149.79; 1384.48] J/mol×K [889.93; 1134.68] Show Hide
Cp,gas 1149.79 J/mol×K 889.93 Joback Calculated Property
Cp,gas 1183.48 J/mol×K 930.72 Joback Calculated Property
Cp,gas 1218.58 J/mol×K 971.51 Joback Calculated Property
Cp,gas 1255.66 J/mol×K 1012.31 Joback Calculated Property
Cp,gas 1295.29 J/mol×K 1053.10 Joback Calculated Property
Cp,gas 1338.04 J/mol×K 1093.89 Joback Calculated Property
Cp,gas 1384.48 J/mol×K 1134.68 Joback Calculated Property

Similar Compounds

3-Ethyl-8,8,11a-trimethyl-2,3,6,7,7 a,8,9,10,11,11a-decahydro-1H-cyclopenta[a]chrysene. Phenanthrene, 1,2,3,4,4a,9,10,10a-octahydro-1,1,4a-trimethyl-7-(1-methylethyl)-, (4aS-trans)-. 7-Isopropyl-1,1,4a-trimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene. 4b,8-Dimethyl-2-isopropylphenanthrene, 4b,5,6,7,8,8a,9,10-octahydro-. 18-norabieta-8,11,13-triene. Chrysene, 1,2,3,4,4a,7,8,9,10,11,12,12a-dodecahydro-. Dehydro abietyl nitrile. 1-Phenanthrenecarboxaldehyde, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1«alpha»,4a«beta»,10a«alpha»)]-. 1-Phenanthrenecarboxaldehyde, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1S-(1«alpha»,4a«alpha»,10a«beta»)]-. 1-Phenanthrenemethanol, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1«alpha»,4a«beta»,10a«alpha»)]-. Epidehydroabietol. Methyl dehydroabietate. Methyl 8,11,13-Abietadien-18-oate. Dehydroabietic acid. 2-Phenanthrenol, 4b,5,6,7,8,8a,9,10-octahydro-4b,8,8-trimethyl-1-(1-methylethyl)-, (4bS-trans)-.

Find more compounds similar to 3-Ethyl-5b,8,8,11a-tetramethyl-2,3, 5b,6,7,7a,8,9,10,11,11a,11b,12,13-tetradecahydro-1H-cyclopenta[a]chrysene.

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