Chemical Properties of 2,6(E),14(E),18-Icosatriene, 2,6,11,15,19-pentamethyl

2,6(E),14(E),18-Icosatriene, 2,6,11,15,19-pentamethyl

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InChI
InChI=1S/C26H46/c1-8-23(4)17-12-19-26(7)21-13-20-25(6)16-10-9-15-24(5)18-11-14-22(2)3/h14-15,17,21,25H,8-13,16,18-20H2,1-7H3/b23-17+,24-15+,26-21+
InChI Key
HLMYWYJTUIDMOF-YIORQQJGSA-N
Formula
C26H46
SMILES
CCC(C)=CCCC(C)=CCCC(C)CCCC=C(C)CCC=C(C)C
Molecular Weight1
358.64
Sources

Physical Properties

Property Value Unit Source
Δf 452.28 kJ/mol Joback Calculated Property
Δfgas -155.53 kJ/mol Joback Calculated Property
Δfus 55.14 kJ/mol Joback Calculated Property
Δvap 73.23 kJ/mol Joback Calculated Property
logPoct/wat 9.35 Crippen Calculated Property
Pc 826.69 kPa Joback Calculated Property
Tboil 810.00 K Joback Calculated Property
Tc 999.50 K Joback Calculated Property
Tfus 291.62 K Joback Calculated Property
Vc 1.41 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 1117.59 J/mol×K 810.0 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
>CH- 1
-CH2- 10
-CH3 7
=C< 4
=CH- 4

Similar Compounds

2,10-Pristadiene. 2,6,10-Pristatriene. 9,13-Pentadecadien-2-one, 6,10,14-trimethyl-, (E)-. 6«alpha»-Hydroxygermacra-1(10),4-diene. (E)-2,3-Dihydrofarnesal. Z-Dihydro-farnesal. 2,6-Dodecadiene, 2,6-dimethyl-. Dihydrofarnesol. Apofarnesol<(z)-Dihydro->. 6,10-Dodecadien-1-ol, 3,7,11-trimethyl-. 2-Hexadecene, 2,6,10,14-tetramethyl-. 2,6(E),15-Heptadecatriene, 2,6,16-trimethyl-12-methylene-11-(3-methyl-4-pentenyl). phyt-2-ene. 2-Dodecene, 2,6-dimethyl. phytadiene 3.

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